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Nutrients derived from ruminal fermentation supply a substantial amount of metabolizable nutrients for ruminants. These include amino acids, carbohydrates, fatty acids, vitamins, and fermentation end products, such as ammonia and volatile fatty acids. Furthermore, ruminal fermentation modifies dietary nutrients in such a way that nutrients reaching the small intestine for absorption may substantially differ from those being consumed in the diet. Therefore, understanding ruminal fermentation kinetics and quantification of nutrients flowing out of the rumen is an important aspect of ruminant nutrition. Accurate quantification of these nutrients, using in vivo experiments, is laborious, costly, and invasive, requiring surgical procedures such as ruminal, abomasal, and intestinal cannulas. To decrease the time and cost of experiments as well as the use of animals, in vitro methodologies are important tools in ruminant nutrition. Therefore, the objectives of this presentation are i) describe different in vitro methodologies, ii) discuss the advantages of in vitro methodologies, iii) discuss shortcomings of in vitro methodologies, and iv) describe potential developments that may improve in vitro methodologies. Having been used for decades, in vitro methodologies such as pure, batch, and continuous cultures have been well documented to investigate a wide array of aspects of nutrition, including the effects of different dietary compositions, individual fermentation end products, and impacts on the microbiome. However, both batch and pure cultures can result in a build-up of end products that may inhibit fermentation. Continuous culture, however, allows for the removal of end products but, similar to pure and batch cultures, is applicable only to ruminal fermentation and cannot provide information regarding intestinal digestion. The dual-flow continuous culture system (DFCC), developed in the 1970s and used by various laboratories in the USA and Europe consists of fermentation vessels of approximately 1.5 L that are capable of simulating ruminal fermentation for periods longer than 10 d. It has been extensively used and evaluated by meta-analyses. When compared with other in vitro methodologies, the DFCC has longer fermentation time, larger volume, and the possibility of sampling from the liquid and the solid flows. When compared with in vivo experiments the DFCC is faster, less costly, less invasive, allows for greater range of treatments, allows for more controlled condition, and isolates ruminal function. Limitations of the DFCC include it does not predict in vivo response, it assumes equal saliva flow and concentration, no effects of intake, no ruminal absorption, less retention of protozoa, possible differences in microbiome, and limited gas emission data. Therefore, while in vitro methodologies provide useful data into the field of ruminant nutrition, some in vitro methodologies are more robust than others. Furthermore, in vivo experiments are still the ideal approach for assessing nutrient utilization and necessary to evaluate animal responses. [ABSTRACT FROM AUTHOR]

The objective of this study was to determine the fecal characteristics, microbiota, and metabolites of dogs fed a Saccharomyces cerevisiae fermentation product (SCFP) and subjected to exercise challenge in untrained and trained states. Thirty-six adult dogs (18 male, 18 female; mean age: 7.1 yr; mean body weight: 29.0 kg) were randomly assigned to control or SCFP-supplemented (250 mg/dog/d) diets and fed for 10 wk. After 3 wk, dogs were given an exercise challenge (6.5 km run), with fresh fecal samples collected pre- and post-challenge. Dogs were then trained by a series of distance-defined running exercise regimens over 7 wk (two 6.4 km runs/wk for 2 wk; two 9.7 km runs/wk for 2 wk; two 12.9 km runs/wk for 2 wk; two 3.2 km runs/wk). Dogs were then given exercise challenge (16 km run) in the trained state, with fresh fecal samples collected pre- and post-challenge. Fecal microbiota data were evaluated using QIIME2, while all other data were analyzed using the Mixed Models procedure of SAS. Effects of diet, exercise, and diet*exercise were tested with P  < 0.05 considered significant. Exercise challenge reduced fecal pH and ammonia in both treatments, and in untrained and trained dogs. After the exercise challenge in untrained dogs, fecal indole, isobutyrate, and isovalerate were reduced, while acetate and propionate were increased. Following the exercise challenge in trained dogs, fecal scores and butyrate decreased, while isobutyrate and isovalerate increased. SCFP did not affect fecal scores, pH, dry matter, or metabolites, but fecal Clostridium was higher in controls than in SCFP-fed dogs over time. SCFP and exercise challenge had no effect on alpha or beta diversity in untrained dogs. However, the weighted principal coordinate analysis plot revealed clustering of dogs before and after exercise in trained dogs. After exercise challenge, fecal Collinsella , Slackia , Blautia , Ruminococcus , and Catenibacterium were higher and Bacteroides , Parabacteroides , Prevotella , Phascolarctobacterium , Fusobacterium , and Sutterella were lower in both untrained and trained dogs. Using qPCR, SCFP increased fecal Turicibacter , and tended to increase fecal Lactobacillus vs. controls. Exercise challenge increased fecal Turicibacter and Blautia in both untrained and trained dogs. Our findings show that exercise and SCFP may affect the fecal microbiota of dogs. Exercise was the primary cause of the shifts, however, with trained dogs having more profound changes than untrained dogs. [ABSTRACT FROM AUTHOR]

In the current study, we hypothesized that an increase in dietary ileal indigestible protein concentration induces an increase in hindgut nitrogen utilization and nitrogen excretion and a shift in fecal microbiota in growing pigs, when compared to pigs given a high total protein diet. Three diets were prepared: 1) standard protein diet based on corn and soybean meal, 2) high-indigestible protein diet in which autoclaved, low-digestible soybean meal replaced soybean meal in the first diet, and 3) high protein diet where the inclusion rate of soybean meal was greater than that of the other diets. The 3 diets were fed to 18 barrows that were fitted with T-cannula at the ileo-cecal junction (initial body weight = 63.4 ± 8.0 kg) in a randomized complete block design with body weight as a blocking factor. Pigs were individually housed in pens and the experiment lasted for 23 d. On days 7 and 21, fecal samples were collected by rectal massage for microbiota analysis. Grab samples of feces were collected on days 20 and 21, and ileal digesta were collected on days 22 and 23 for the determination of energy and nitrogen utilization. Lower apparent ileal digestibility of nitrogen in the high-indigestible protein diet containing autoclaved soybean meal resulted in greater ileal indigestible nitrogen concentration (P  < 0.05). Apparent total tract digestibility of nitrogen was lower (P  < 0.05), and correspondingly nitrogen concentration and daily fecal nitrogen output were greater (P  < 0.05) in the high-indigestible protein diet compared with the other diets. Apparent post-ileal digestibility and hindgut disappearance of nitrogen and gross energy were the greatest (P  < 0.05) in the high protein diet, whereas a statistical difference was not observed in those variables between the standard protein diet and the high-indigestible protein diet. Beta diversity metrics of feces in the high-indigestible protein diet on day 21 were different (q  < 0.05) from those in the other two diets, which indicates a shift in microbial communities. According to the results of the DESeq2, the direction of microbiota shift induced by the high-indigestible protein diet may have reduced fiber utilization in the hindgut. In conclusion, an increase in dietary ileal indigestible protein concentration increased fecal nitrogen excretion and shifted fecal microbial communities but did not increase nitrogen utilization in the hindgut. [ABSTRACT FROM AUTHOR]

Five ruminally and duodenally cannulated red angus steers (n = 5; initial body weight [ BW ] = 542 kg, SD = 40 kg) were used in a three-period Youden square design consisting of three 21-d periods, three treatments, and five steers (one or two steers per treatment within each period) to evaluate the effect of feeding hempseed cake on ruminal fermentation parameters, organic matter (OM) intake, total tract nutrient digestion, and nitrogen (N) balance in steers fed finishing diets. The control (CON) diet contained 75% dry-rolled corn, 20% corn silage, and 5% supplement (DM basis). The dried corn distillers grains plus solubles (DDGS) and hempseed cake (HEMP) diets contained 55% dry-rolled corn, 20% corn silage, 20% dried corn distillers grains plus solubles or hempseed cake, and 5% supplement (DM basis). Total ruminal volatile fatty acid concentration was greater (P < 0.01) in steers fed the HEMP diet than in steers fed the DDGS or CON diets. Ruminal fluid pH was not influenced (P = 0.93) by treatment. Organic matter intake tended (P = 0.07) to be greater and OM total tract digestibility was less (P = 0.03) in steers fed the HEMP diet compared with steers fed the DDGS or CON diets. Ruminal true and total tract apparent N digestibility was greater (P < 0.01) in steers fed the HEMP diet than steers fed the DDGS or CON diets. Duodenal flow of essential, nonessential, and total amino acids was not influenced (P ≥ 0.37) by dietary treatment, but the lack of response was likely because ruminally degradable protein (RDP) supply exceeded the RDP requirement. Steers fed the HEMP diet had greater (P < 0.01) N retention (g/d) than steers fed the DDGS diet, which was greater (P < 0.01) than steers fed the CON diet, suggesting that feeding hempseed cake improved utilization of N. Although inclusion of hempseed cake decreased total tract OM digestibility compared with dried corn distillers grains or corn, improvements in N utilization suggest that hempseed cake could be a useful alternative feed ingredient for finishing cattle diets. [ABSTRACT FROM AUTHOR]

The objective of this trial was to evaluate the fermentation parameters, gas production and dry matter (DM) disappearance in vitro of two corn hybrids with two particle sizes. A 2 × 2 factorial design study was carried out to evaluate two types of Flint corn with or without high amylase concentration (Enogen flint or Tropical Flint, respectively), and two particle sizes (1.5 or 2.5 mm). Incubations were carried out for a total period of 24 h using the automatic gas pressure system (ANKOM, RF). The ruminal liquid was combined with buffer in a 1:4 ratio respectively and each bottle received 150 mL of this mixture plus 1.5 g of DM corn sample. At the end of the 24-h period, a gas sample was taken for methane analysis, a sample was taken for short chain fatty acid (SCFA) analysis, and DM was performed on the final residue from the bottles to estimate the disappearance of DM. Data were analyzed using SAS Proc Mixed (9.4). There was no interaction effect between corn hybrid and particle size for the variables evaluated. Enogen Flint corn increased the proportion of propionate (30.7 vs. 28.1 mM/100 mM; P = 0.03) and reduced isovalerate (1.23 vs. 1.65 mM/100 mM; P = 0.01), and acetate: propionate ratio (1.85 vs. 2.11; P = 0.04), with no effect on the other fermentation variables evaluated. The particle size affected the pH of the fluid, with lower pH observed when using 1.5 mm particle size (6.64 vs. 6.70; P < 0.01). Regarding the disappearance of DM, Enogen Flint corn increased disappearance compared with Tropical Flint (80.8 vs. 77.5%; P < 0.01), and the 1.5 mm particle size also resulted in an increase in DM disappearance (81.9 vs. 76.4%; P < 0.01), with no interaction between the factors studied. (P = 0.80). Corn hybrids did not affect total gas production and methane production. However, the 1.5 mm particle size increased the total gas production (117.5 vs. 103.2 mL/24 h; P < 0.01), with no effect on methane production. In conclusion, Enogen technology optimizes the rumen fermentation process and increases corn dry matter degradability, and 1.5 mm particle size of the corn grain also increases degradability. [ABSTRACT FROM AUTHOR]

This article examines the effects of Saccharomyces cerevisiae fermentation product (SCFP) on methane production in steers fed a finishing diet. The study found that supplementing SCFP did not lead to greater methane production, but instead showed a trend toward reduced methane emission per kilogram of dry matter intake (DMI). The results suggest that SCFP may have a potential role in mitigating methane emissions in cattle, but further research using larger experimental units is needed to confirm these findings. [Extracted from the article]

Metronidazole is a potent antibiotic often prescribed to treat gastrointestinal enteropathies, but is known to induce loose stools, negatively alter the fecal microbiome, and affect fecal metabolite production. Dietary intervention may aid in post-antibiotic recovery, but little research has been conducted regarding the potential of fiber utilization for microbial recovery in canines. Using an in vitro fermentation assay, the objective was to investigate the fermentation characteristics of dietary fibers using fecal inocula from dogs treated with metronidazole. All procedures were approved by the University of Illinois IACUC prior to experimentation. Healthy male beagles (n = 4) were fed a commercial canned diet for 2 wk, then administered metronidazole [20 mg/kg body weight (BW) twice a day] for 2 wk. Fresh fecal samples were collected at wk 2 [diet only (CTL)] and 4 [antibiotic treatment (ANT)], stabilized in a 20% glycerol solution, and then frozen. On the in vitro fermentation day, feces from each time point were thawed and used to inoculate tubes. At baseline and after 6, 12, and 18 h of fermentation, pH, short-chain fatty acid (SCFA) concentrations, and microbiota populations were measured. SCFA were measured by gas chromatography and fecal microbiota populations were analyzed by 16S rRNA sequencing. All blank tube-corrected changes from baseline data were analyzed using repeated measures and the MIXED procedure of SAS 9.4, with significance set at P < 0.05. QIIME2 analysis was used for bacterial diversity measures. As expected, metronidazole administration heavily influenced microbiota populations and fiber fermentability characteristics. Pectin fermentation reduced (P < 0.001) pH and increased (P < 0.001) SCFA concentrations over time, but responses were less (P < 0.001) in ANT tubes than CTL tubes. Beet pulp fermentation also reduced (P < 0.001) pH and increased (P < 0.001) SCFA concentrations over time. Whereas the magnitude of pH change was small between inoculum sources, SCFA concentrations were different (P < 0.001) between ANT tubes and CTL tubes. Propionate and butyrate concentrations were greater (P < 0.001) in CTL tubes than ANT tubes at all time points, but acetate concentrations varied over time. Chicory pulp fermentation reduced (P < 0.001) pH over time, with greater (P < 0.01) reductions in ANT tubes than CTL tubes. Chicory pulp fermentation increased SCFA concentrations, but had different patterns based on inoculum source. Metronidazole altered microbiota populations by reducing (P < 0.001) bacterial alpha diversity. The analysis of bacterial beta diversity revealed separate clusters for dogs in the absence and presence of metronidazole. Beta diversity analysis also showed that tubes containing chicory pulp clustered separately from those containing the other fibers. Relative abundances of over 50 bacterial genera differed (P < 0.05) among inoculum sources. In summary, interesting fermentation patterns in response to varying fiber sources were observed, allowing for improved insight into their potential abilities when provided to antibiotic-treated dogs. [ABSTRACT FROM AUTHOR]

Insects like the black soldier fly larvae (Hermetia illucens; BSFL) have been proposed as protein-rich feed ingredients to support the growing demand for meat. The BSFL hold also promise for use as a protein source in pet foods and, as such, it has been studied for palatability, nutritional quality and health effects in dogs and cats. This study aimed to evaluate the effects of including BSFL meal in a dry, extruded food on nutritional quality and health in healthy adult cats. Two similar compositions of dry, extruded foods were formulated to meet the FEDIAF nutrition guidelines for adult cats of which one was chicken mealbased (control, with 34.3% chicken meal) and the other BSFL meal-based (inclusion of 37.5% BSFL meal). BSFL meal contained 95.0% dry matter, 53.1% crude protein, 14.3% crude fat, 6.0% ash (Protix, Dongen, The Netherlands). Two groups of four cats were each fed one of the two foods for two 28-d periods in a crossover design, with sample collection during the last 7 d of each period. Cats were housed in groups of the same sex during the first 21 d of each period. Both foods were well-accepted by the cats. No health problems (including coat and skin condition) were noted throughout the study. Food type did not impact body weight (P = 0.850). Food intake was greater when cats were fed the BSFL-based food (P < 0.001). Consistency scores of fresh feces were optimal and did not differ between the foods. Compared with the control food, the food with BSFL meal had decreased apparent fecal digestibility values for dry matter, organic matter, nitrogen, and gross energy (P < 0.05) although all values were high. Digestibility values for acid-hydrolyzed fat were similar for both foods (P = 0.628). Diets resulted in changes in fermentation product concentrations, like fecal ammonia was less when cats fed this food compared with the control food (P < 0.001), but the fecal concentrations of the short-chain fatty acids and biogenic amines were generally increased (P < 0.05). Moreover, reduced fecal bacterial diversity and affected bacterial relative abundance suggested that inclusion of BSFL meal steered the microbial composition in the distal gut of cats. It was observed increased relative abundance of bacteria genus considered beneficial for host health like Bifidobacterium (P < 0.001) and Megasphaera (P < 0.036); and inhibition of genus Negativibacillus and Lachnoclostridium (P < 0.001), previously associated to digestive issues and negative for gut health. Overall, the data gathered in this study suggests that BSFL meal is an adequate alternative ingredient for extruded dry cat foods and may exert a prebiotic effect on intestinal microbiota. [ABSTRACT FROM AUTHOR]

Feeding Saccharomyces cerevisiae fermentation product (SCFP) has previously altered fecal microbiota, fecal metabolites, and immune function of adult dogs. The objective of this study was to investigate measures of skin and coat health, changes in circulating immune cell numbers and activity, antioxidant status, and oxidative stress marker concentrations of healthy adult dogs fed a SCFP-supplemented extruded diet. Sixteen adult English Pointer dogs (8 M, 8 F; mean age = 6.7 ± 2.1 yr; mean BW = 25.9 ± 4.5 kg) were used in a randomized crossover design study. All dogs were fed a control diet for 4 wk, then randomly assigned to either the control or SCFP-supplemented diet (0.13% of active SCFP) and fed to maintain BW for 10 wk. A 6-wk washout preceded the second 10-wk experimental period with dogs receiving opposite treatments. After baseline/washout and treatment phases, skin and coat were scored, and pre and postprandial blood samples were collected. Transepidermal water loss (TEWL), hydration status, and sebum concentrations were measured (back, inguinal, ear) using external probes. Oxidative stress and immune cell function were measured by ELISA, circulating immune cell percentages were analyzed by flow cytometry, and mRNA expression of oxidative stress genes was analyzed by RT-PCR. Change from baseline data was analyzed using the Mixed Models procedure of SAS 9.4. Sebum concentration changes tended to be higher (P < 0.10; inguinal, ear) in SCFP-fed dogs than in controls. TEWL change was lower (P < 0.05) on the back of controls, but lower (P = 0.054) on the ear of SCFP-fed dogs. Delayed-type hypersensitivity response was affected by diet and time post-inoculation. Other skin and coat measures and scores were not affected by diet. Changes in unstimulated lymphocytes and stimulated IFN-γ secreting T cells were lower (P < 0.05) in SCFP-fed dogs, while changes in stimulated T cells were lower (P < 0.05) in control-fed dogs. Upon stimulation, the percentage of cytotoxic T cells delta trended lower (P < 0.10) in SCFP-fed dogs. Change in serum superoxide dismutase concentrations was higher (P < 0.05) and change in catalase mRNA expression was lower (P < 0.05) in SCFP-fed dogs. All other measurements of immune cell populations, oxidative stress markers, and gene expression were unaffected by treatment. In conclusion, our data suggest that SCFP positively impacts indicators of skin and coat health of dogs, modulates immune responses, and enhances some antioxidant defense markers. [ABSTRACT FROM AUTHOR]

As the demand of nutrients by the population will continue to grow over the years, efficient practices are required in the food chain to satisfy the demand. This practice involves the intensification of production systems. Moreover, intensification can potentially harm the animal or environment if the resources are used to the limit. The latter, product of pushing to the limit the ruminal environment. Dietary buffers and tannins offer a key role addressing issues related to intensification. This study aimed to evaluate the effects of two dietary buffers and tannins. Ruminal fermentation parameters, in vitro methane production, ruminal pH, in vitro organic matter digestibility were measured. Eight ruminally cannulated steers were used in a duplicated 4 x 4 Latin square design. Steers were fed with a basal diet comprised of 35.5% corn silage, 18.7% protein supplement, 21.5% corn grain, 22% bermuda hay, 1% mineral supplement (DM basis). Four treatments were used: BICARB (Basal diet + 1.2% DM Sodium Bicarbonate), BRIC-050 (Basal diet + 1.2% DM BRIC), BRIC-150 (Basal diet + 1.2% DM BRIC + 0.15 % DM Tannins), TAN (Basal diet + 0.15% DM Tannins). Steers were housed in individual pens and received every morning a TMR and water ad libitum. The experiment consisted of 4 periods with 16 days total, composed by 3 d of covariates, 7 d of treatment adaptation, 1 d of 50% feed restriction, 1 d SARA challenge, 4 d of recovery, and 20 d of washout between periods. Two in vitro batch culture were performed in every period at the last day of covariates and last day of recovery, collecting ruminal fluid from each animal. Treatments with BICARB promoted a higher pH than TAN during the adaptation at 4 h after feeding (P = 0.01). Moreover, BRIC-150 showed similar results with a tendency to increase (P = 0.07) when compared with TAN. During the feed restriction BRIC-150 showed a greater pH (P = 0.01) when compared with TAN. While, for BICARB and BRIC-050 pH tended to be greater (P = 0.06) than TAN. During the SARA challenge and the recovery, treatments with buffer tended to have greater pH (P < 0.1). A significant reduction ammonia nitrogen was observed for BICARB and TAN compared with BRIC-050 and BRIC-150 (P < 0.01). Overall, the three buffers tested showed similar results in terms of maintaining a greater pH than treatment without buffer. [ABSTRACT FROM AUTHOR]

The objective of the experiment was to evaluate a commercial Saccharomyces cerevisiae fermentation product (SCFP; NaturSafe, Dimond V, Cedar Rapids, IA) on performance, plasma metabolites, rumen parameters, and fecal pathogen shedding in feedlot steers. Crossbred steers (n = 61; 271 ± 48.1 kg) were sourced from 3 different research units at Oklahoma State University and assigned to 1 of 3 experimental treatments in a randomized complete block design. Steers were group housed in pens equipped with an automated individual feed intake system. Treatments consisted of a negative control (CON), CON with tylosin phosphate (TYL; 9.9 mg ⋅ kg-1 of diet DM), or CON with SCFP (1.63 g ⋅ kg-1 of diet DM). Body weight and feed efficiency did not differ among treatments (P ≥ 0.12). However, steers fed SCFP tended to have greater ADG from d 35 to 56 (P = 0.10). In addition, steers fed SCFP exhibited increased DMI from d 56 to 112 (P = 0.03), a tendency for increased DMI from d 112 to final (P = 0.07), and increased DMI overall (P = 0.05). There was no treatment x time interaction for pH, pH change, or lactate concentrations in rumen fluid (P ≥ 0.11), but all were impacted by time (P < 0.01). A treatment x time interaction (P < 0.01) was detected for fecal pH and fecal pH change, with the pH being greater in TYL fed steers on d 56 and in CON fed steers on the final day. Steers that consumed CON had a reduced fecal pH (P < 0.01) and steers consuming SCFP tended to have a reduced fecal pH (P = 0.08) from d 35 to 56 compared with TYL fed steers, while both CON and SCFP fed steers experienced an increase in fecal pH from d 56 to 112 (P < 0.01). A time effect was detected (P ≤ 0.04) for plasma glucose, lactate, urea nitrogen, and non-esterified fatty acid concentrations among treatment groups. A treatment x time interaction was observed (P < 0.02) for stx2 genes of Shiga toxin producing Escherichia coli (STEC) in individual fecal samples where SCFP and TYL fed steers tended to exhibit an increased concentration compared with CON fed steers on d 14, while on d 190 CON and SCFP fed steers exhibited an increased concentration compared with TYL fed steers. Overall, STEC, E. coli O157:H7, and Salmonella concentrations were all impacted by time (P < 0.001). This experiment suggests that SCFP could be utilized as a potential alternative to TYL in feedlot cattle without adversely affecting cattle performance. However, SCFP did not impact pathogen shedding. In addition, CON fed steers performed similarly to both SCFP and TYL fed steers. [ABSTRACT FROM AUTHOR]

Several studies have evaluated the effects of the dietary application of exogenous alpha-amylase preparations (AMA) as a strategy to increase total tract starch digestibility (TTSD) and milk yield (MY) in dairy cows, but the results have been inconsistent. Thus, the objective of this study was to evaluate the effects of the dietary application of AMA on the performance, digestibility, and rumen fermentation of lactating dairy cows using a meta-analytic method. A total of 18 peer-reviewed manuscripts (N = 32 treatment comparisons) from 2003 to 2019 were systematically identified following the PRISMA method. The weighted raw mean differences between dietary AMA and control treatments were compared with a robust variance estimation. Likewise, diet characteristics like crude protein (CP) content, NDF content, starch content, days in milk (DIM), experimental design (Latin square and continuous), and AMA dose (0 to 732 Kilo Novo units [KNU]/kg TMR) were used as covariates in a meta-regression, subgrouping, and dose–response analysis. Compared to the control, dietary AMA increased (P < 0.05) DM digestibility (69.32% vs. 68.30%), TTSD (94.62% vs. 94.10%), milk protein concentration and yield (3.11% vs. 3.08%; 1.14 vs. 1.10 kg/d) and tended to increase (P = 0.09) fat-corrected milk (35.96 vs. 35.10 kg/d), but no effects were observed on DM intake (22.99 vs. 22.90 kg/d) and feed efficiency (1.50 vs. 1.48). Dietary AMA tended (P = 0.10) to reduce rumen pH (6.27 vs. 6.30). Both the enzyme dose and DIM strongly influenced (P < 0.05) the effects of AMA on digestibility and performance. The dose–response analysis revealed that feeding 600 KNU/kg to high-producing early lactation (< 70 DIM) dairy cows increased FCM and milk protein. Accounting for the type of experimental design was associated with a lower between-studies-variance among comparisons. Overall, this meta-analysis supports the hypothesis that dietary AMA supplementation is associated with a better lactational performance in dairy cows. However, these effects are only suitable for high-producing early lactation dairy cows. [ABSTRACT FROM AUTHOR]

The objective of this study was to examine the enzyme activities of an enzymatic complex produced by Pleurotus ostreatus in different pH and the effects of adding increased application rates of this enzymatic complex on the fermentation profile, chemical composition, and in situ ruminal disappearance of whole-plant corn silage (WPCS) at the onset of fermentation and 30 d after ensiling. The lignocellulolytic enzymatic complex was obtained through in vitro cultivation of P. ostreatus. In the first experiment, the activities of laccase, lignin peroxidase (LiP), manganese peroxidase, endo- and exo-glucanase, xylanase, and mannanase were determined at pH 3, 4, 5, and 6. In the second experiment, five application rates of enzymatic complex were tested in a randomized complete block design (0, 9, 18, 27, and 36 mg of lignocellulosic enzymes/kg of fresh whole-plant corn [ WPC ], corresponding to 0, 0.587, 1.156, 1.734, and 2.312 g of enzymatic complex/kg of fresh WPC, respectively). There were four replicates per treatment (vacuum-sealed bags) per opening time. Bags were opened 1, 2, 3, and 7 d after ensiling (onset of fermentation period) and 30 d after ensiling to evaluate the fermentation profile, chemical composition, and in situ dry matter and neutral fiber detergent disappearance of WPCS. Laccase had the greatest activity at pH 5 (P < 0.01), whereas manganese peroxidase and LiP had the greatest activity at pH 4 (P < 0.01; P < 0.01). There was no effect of the rate of application of enzymatic complex, at the onset of fermentation, on the fermentation profile (P > 0.21), and chemical composition (P > 0.36). The concentration of water-soluble carbohydrate quadratically decreased (P < 0.01) over the ensiling time at the onset of fermentation, leading to a quadratic increase of lactic acid (P = 0.02) and a linear increase of acetic acid (P = 0.02) throughout fermentation. Consequently, pH quadratically decreased (P < 0.01). Lignin concentration linearly decreased (P = 0.04) with the enzymatic complex application rates at 30 d of storage; however, other nutrients and fermentation profiles did not change (P > 0.11) with the enzymatic complex application rates. Addition of lignocellulolytic enzymatic complex from P. ostreatus cultivation to WPC at ensiling decreased WPCS lignin concentration 30 d after ensiling; however, it was not sufficient to improve in situ disappearance of fiber and dry matter. [ABSTRACT FROM AUTHOR]

Six ruminally cannulated steers (average BW = 791 ± 71 kg) were used in a replicated 3 × 3 Latin square experiment to determine the effects of roughage type on rumination, fiber mat characteristics, and rumen fermentation variables. Three roughages were included at 7% (DM basis) in a steam flaked corn-based diet: cotton burrs (CB), wheat silage (WS), or corn stalks (CS). Steers were fitted with a sensory collar to record rumination behaviors in 2-h intervals at the beginning of the experiment. Each 30-d period consisted of 7 d of recovery, 14 d of diet adaptation, 7 d of rumination data collection (daily and bi-hourly average rumination), 1 d of rumen fluid collection, and 1 d of rumen evacuations. In situ degradation of individual roughages was determined for 4 d after period 3 evacuations. During rumen evacuations, ruminal contents were removed; the rumen fiber mat (RF) was separated from the liquid portion with a 2-mm sieve, weighed, and a subsample was dried. Data were analyzed using the MIXED procedure of SAS with steer as the experimental unit and roughage (CB, WS, and CS) as the main effect. Dry matter intake (DMI) was not different for CB and WS (P = 0.25) and greatest for steers consuming CS diet (P ≤ 0.01). Roughage type did not influence the weight of the RF dry matter (%; DM; P = 0.92), RF weight (P = 0.69), or RF:DMI ratio (P = 0.29). Daily rumination (min/d) did not differ among roughages (P = 0.40), but min of rumination/kg of DMI was greatest for CS (18.0 min), min/kg of NDF was greatest for WS (89.8 min; P = 0.02), and min/kg of peNDF was greatest for CS (132.4 min; P ≤ 0.01). Wheat silage had the greatest percentage of soluble and degradable DM. Rumen fiber mat did not differ for roughages, although rumination min/kg of DMI and peNDF was greatest for steers consuming CS and WS. In situ degradation determined that CB-R and CS-R had the greatest percentage of ruminal undegraded DM. Based on the objective of the experiment, roughage type did not influence daily rumination or fiber mat characteristics. [ABSTRACT FROM AUTHOR]

We evaluated the effects of different types of additives on the fermentation and aerobic stability of alfalfa (Medicago sativa) ensiled at 2 dry matters (DM). Alfalfa was untreated (CTRL) or treated with sodium benzoate, potassium sorbate, and sodium nitrite (SFE), or microbial inoculants (Lactobacillus plantarum MTD1 [ LP ] or L. buchneri 40788 and Pediococcus pentocaseus 12455 [ LBPP ]) at a moderate (38%) and high (46%) DM using a completely randomized design with a 2 × 4 factorial arrangement of treatments. High DM silage was higher (P < 0.01) in pH, had less lactic and acetic acid (P < 0.01) and had more yeasts (P < 0.05) and molds (P < 0.01) than moderate DM silage. Recovery of DM declined (P  < 0.01) for CTRL and LP treated silages with increasing DM but was not different between LBPP and SFE treatments. Compared to CTRL, LBPP had a lower (P  < 0.01) DM recovery at the moderate DM, but SFE had the greatest (P  < 0.01) recovery of all treatments at the high DM. Treatment with LBPP increased (P  < 0.05) the concentrations of acetic acid and 1,2 propanediol (PD) compared with other treatments (P  < 0.01). Numerically, fewer yeasts were found in additive treated silages compared with CTRL, but they were statistically (P  < 0.01) lower only when treated with SFE. Treatment with LP resulted in a small improvement in aerobic stability at the moderate but not high DM. In contrast, treatment with SFE and LBPP markedly improved (P  < 0.01) the aerobic stability of alfalfa silage at both DM. Whereas SFE and LBPP were similar in their improvements in aerobic stability at the DM, LBPP was better (P  < 0.01) than SFE at the high DM. A higher (P  < 0.01) concentration of acetic acid in LBPP compared with other treatments was most likely responsible for better stability. This study showed that LBPP and SFE resulted in increases in the aerobic stability of alfalfa silage and it is the first study showing SFE, can markedly improve the aerobic stability of alfalfa silage. [ABSTRACT FROM AUTHOR]

Creating ensiled forage on a laboratory-scale is a tedious and cumbersome process. One must ensure an anaerobic environment for the success of the fermentation while also striving to replicate field-scale conditions. The objective of this experiment was to determine the effect of laboratory-scale silo type on nutritive value and fermentation profiles of grass-legume silage. This experiment was conducted as a generalized complete block design. There was one treatment factor (silo type) with 11 levels: field-scale baleage control (CON), miniature wrapped baleage (MINI), large fermentation bucket (6GAL), small fermentation bucket (2GAL), miniature silo (PVC), pint-sized Mason-type jar with "BurpLid" (BURP), pint-sized Mason-type jar with Ball-brand fermentation lid (BALL), pint-sized Mason-type jar with an airlock lid (LOCK), single-layered vacuum-sealed bag using a chamber-style sealer (CHMB), double-layered vacuum-sealed bag using a chamber-style sealer (HCHMB), single-layered vacuum-sealed bag using a suction-style sealer (FOOD), or double-layered vacuum-sealed bag using a suction-style sealer (HFOOD). Harvest served as the random blocking factor. Forage was harvested from a single alfalfa-bermudagrass pastures at the Wiregrass Research and Extension Center in Headland, AL. Forage was cut 24 h before collection and allowed to sun-cure. After allocation to treatment, samples were allowed to ferment for 56 d. Following fermentation, samples were assayed for NDF, ADF, ADL, CP, pH, mold, and yeast. Dunnett's test revealed a difference (P < 0.05) from CON for NDF, ADF, and pH. Samples from PVC had 26% greater NDF and 45% greater ADF than CON (58 and 37%, respectively). Samples from BALL were 3 units greater and samples from LOCK were 2 units greater in pH than CON (4.8). When comparing alternative treatments exclusive of CON, there were differences (P ≤ 0.01) in NDF, ADF, ADL, pH, and mold counts among treatments. Results are interpreted to mean that BALL and LOCK are not effective representatives of field-scale silage production due to lack of pH drop, while PVC alters the fiber profiles. All other methods showed promise as prospects for laboratory silage procedures. [ABSTRACT FROM AUTHOR]

Including Saccharomyces cerevisiae fermentation product (SCFP) into the diets of young, exercising horses may prolong their performance career by optimizing the intra-articular environment. Our objective was to evaluate the effect of dietary SCFP on joint inflammation in yearlings undergoing regular exercise, challenged with intra-articular lipopolysac-charide (LPS). Thirty Quarter Horse yearlings (374 ± 25 kg BW; 562 ± 16 d of age; 15 fillies and 15 geldings) were used in a 60-d study to test the hypothesis that dietary SCFP (TruEquine C, Diamond V Mills, Inc.) ameliorates joint inflammation following an acute inflammatory insult. Horses were stratified by BW, age, sex, and randomly assigned to dietary treatments (n = 10/treatment): Control (0), 46, or 92 mg/kg BW SCFP. Treatments were top-dressed onto a custom-formulated concentrate void of added microbials offered at 1% BW/d (as-fed) every 12 h. Horses were individually stalled (3.6 m x 7.3 m) and offered ad libitum Coastal bermudagrass hay. Using a free-stall exerciser, horses were exercised following a progressive workload regimen for 30 min/d, 5 d/wk. On d 46, all horses underwent an intra-articular LPS challenge where each horse had one radial carpal joint randomly assigned to receive either 0.8 mL of a 0.5 ng LPS solution or sterile lactated Ringer's solution (LRS) as a contralat-eral control. Synovial fluid samples were obtained pre-injection (h 0) and at 6, 12, 24, and 336 h post-injection and analyzed for prostaglandin E2 (PGE2), a proinflammatory prostaglandin via commercial ELISA, and for chemokine-concentration (signaling proteins that direct immune cells; CCL2, and CCL11) and cytokines (inflammatory mediators; TNFα and IL-10) using a multiplex platform via commercial laboratory. Non-normal data (PGE2, IL-10, and CCL2) were log transformed, and all markers were analyzed using MIXED procedure of SAS v9.4. Mean separation was achieved with orthogonal contrasts, and contralateral control carpi were used as a covariate across all hours. There was no effect of SCFP on synovial logPGE2 (P = 0.42), logCCL2 (P = 0.90), CCL11 (P = 0.26), or logIL-10 (P = 0.23). However, there was a treatment x hour interaction for CCL11 (P = 0.04) where the Control had increased concentrations compared with SCFP treatment groups at 6 h post-injection. Furthermore, logIL-10 also had a treatment x hour interaction (P = 0.05) where the 46mg/kg BW group had decreased concentrations at h 12 compared with the Control and 92mg/kg BW group. The main effect of treatment for TNFa (P = 0.04) revealed that the 92mg/kg BW group had less concentrations than the 46mg/kg BW group and tended to have less concentrations than the Control group across all hours. Results indicate that SCFP may help mitigate inflammation markers following an acute intra-articular inflammatory insult. [ABSTRACT FROM AUTHOR]

Ewes transitioning from late gestation to early lactation face a number of challenges including physiological stress, dietary changes, and metabolic adaptations, particularly when bearing and rearing multiple offspring. Furthermore, rumen microbial composition and function has been correlated with milk production and nutrient density in transitioning dairy cows. However, limited research has evaluated the rumen microbial community of ewes during early lactation. The objective of this study was to conduct a functional microbiological survey of the ewe rumen from parturition to weaning. We hypothesized that ewes would experience fermentative disturbances post-parturition and that the rumen microbiota, and consequently, circulating metabolites, would recover over time. Nine multiparous Polypay ewes bearing triplets were fed a lactation diet consisting of alfalfa hay and concentrate mix to meet protein and energy requirements. One lamb of each triplet set was randomly selected and placed on milk replacer 24 h after birth. The two lambs remaining on the ewe were weaned at 56 d of age. Blood and rumen samples from ewes were collected via jugular venipuncture and oral intubation, respectively, at 2, 7, and 15 d of lactation in addition to at the time of weaning. Rumen bacterial functional guilds were enumerated via serial dilution. Ruminal short-chain fatty acids (SCFA) were quantified via HPLC and serum metabolites by LC-MS. All data were analyzed using PROC Mixed with repeated measures in SAS (v. 9.4, SAS Inst. Inc., Cary, NC). Total starch-utilizing bacteria remained steady during early lactation but increased 100-fold by weaning (P = 0.03). In contrast, the starch-utilizing guild sub-population lactobacilli increased 10-fold by d 15 of lactation (P < 0.01) and remained constant through weaning (P > 0.05). No differences were found in the viable number of rumen cellulolytic bacteria (P = 0.37) throughout the study. Ruminal propionate concentrations increased 35% (P = 0.04) from d 2 to weaning and serum propionate (36.8 ± 4.42 µM; P = 0.08) and glucose (59.8 ± 2.97 mg dL-1; P < 0.01) peaked on d 15 of lactation. While ruminal acetate did not fluctuate in early lactation, it increased 58% by weaning (P < 0.01) leading to an 88% increase in serum acetate (P < 0.01). Ruminal butyrate increased 49% by d 15 (P = 0.01) and this was reflected in a 7-fold increase in serum butyrate (P = 0.02). However, serum P-hydroxybutyrate did not differ from parturition through weaning (P = 0.51). Results of this experiment demonstrate that rumen bacterial functional guilds, as well as rumen and serum metabolites, were lowest two days post-parturition and increased over the course of lactation. This may suggest that ruminal fermentation is suppressed post-parturition, which could have implications for early lactation management strategies of triplet-bearing ewes. [ABSTRACT FROM AUTHOR]

The individual and combined effects of 3-nitrooxypropanol (3-NOP) and canola oil (OIL) supplementation on enteric methane (CH4) and hydrogen (H2) emissions, rumen fermentation and biohydrogenation, and total tract nutrient digestibility were investigated in beef cattle. Eight beef heifers (mean body weight ± SD, 732 ± 43 kg) with ruminal fistulas were used in a replicated 4 × 4 Latin square with a 2 (with and without 3-NOP) × 2 (with and without OIL) arrangement of treatments and 28-d periods (13 d adaption and 15 d measurements). The four treatments were: control (no 3-NOP, no OIL), 3-NOP (200 mg/kg dry matter [ DM ]), OIL (50 g/kg DM), and 3-NOP (200 mg/kg DM) plus OIL (50 g/kg DM). Animals were fed restrictively (7.6 kg DM/d) a basal diet of 900 g/kg DM barley silage and 100 g/kg DM supplement. 3-NOP and OIL decreased (P < 0.01) CH4 yield (g/kg DM intake) by 31.6% and 27.4%, respectively, with no 3-NOP × OIL interaction (P = 0.85). Feeding 3-NOP plus OIL decreased CH4 yield by 51% compared with control. There was a 3-NOP × OIL interaction (P = 0.02) for H2 yield (g/kg DM intake); the increase in H2 yield (P < 0.01) due to 3-NOP was less when it was combined with OIL. There were 3-NOP × OIL interactions for molar percentages of acetate and propionate (P < 0.01); individually, 3-NOP and OIL decreased acetate and increased propionate percentages with no further effect when supplemented together. 3-NOP slightly increased crude protein (P = 0.02) and starch (P = 0.01) digestibilities, while OIL decreased the digestibilities of DM (P < 0.01) and neutral detergent fiber (P < 0.01) with no interactions (P = 0.15 and 0.10, respectively). 3-NOP and OIL increased (P = 0.04 and P < 0.01, respectively) saturated fatty acid concentration in rumen fluid, with no interaction effect. Interactions for ruminal trans -monounsaturated fatty acids (t-MUFA) concentration and percentage were observed (P = 0.02 and P < 0.01); 3-NOP had no effect on t-MUFA concentration and percentage, while OIL increased the concentration (P < 0.01) and percentage (P < 0.01) of t-MUFA but to a lesser extent when combined with 3-NOP. In conclusion, the CH4-mitigating effects of 3-NOP and OIL were independent and incremental. Supplementing ruminant diets with a combination of 3-NOP and OIL may help mitigate CH4 emissions, but the decrease in total tract digestibility due to OIL may decrease animal performance and needs further investigation. [ABSTRACT FROM AUTHOR]

The aim of the present study was to evaluate the inclusion of narasin, salinomycin, or flavomycin for 140 d on ruminal fermentation parameters, apparent nutrient digestibility, and performance of Nellore cattle offered a forage-based diet. In experiment 1, 32 rumen-cannulated Bos indicus Nellore steers [initial body weight (BW) = 220 ± 12.6 kg] were assigned to individual pens in a randomized complete block design according to their initial shrunk BW. Within block, animals were randomly assigned to 1 of 4 treatments: (1) forage-based diet without feed additives (CON ; n = 8), (2) CON diet plus 13 ppm of narasin (NAR ; n = 8), (3) CON diet plus 20 ppm of salinomycin (SAL ; n = 8), or (4) CON diet plus 3 ppm of flavomycin (FLA ; n = 8). The experimental period lasted 140 d and was divided into 5 periods of 28 d each. The inclusion of feed additives did not impact (P ≥ 0.17) dry matter intake (DMI), nutrient intake, and apparent total tract digestibility of nutrients. Nonetheless, steers fed NAR had lower (P < 0.01) molar proportion of acetate compared with CON, SAL, and FLA steers, whereas ruminal acetate tended to be greater (P < 0.09) for SAL vs. CON and FLA, but did not differ (P = 0.68) between CON vs. FLA steers. Ruminal propionate was the highest (P < 0.01) for steers fed NAR and did not differ (P > 0.20) between CON, SAL, and FLA. Consequently, NAR steers had the lowest (P < 0.01) Ac:Pr ratio, whereas Ac:Pr did not differ (P > 0.18) among CON, SAL, and FLA. Total volatile fatty acids were greater (P < 0.04) for NAR and CON vs. SAL and FLA, but did not differ (P > 0.67) among NAR vs. CON and SAL vs. FLA. In experiment 2, 164 Nellore bulls (initial shrunk BW = 299 ± 2.5 kg) were assigned to feedlot pens for 140 d in a randomized complete block design. Within block (n = 10), animals were randomly assigned to the same treatments used in experiment 1. Average daily gain was greater (P < 0.01) in NAR vs. CON, SAL, and FLA bulls, and did not differ (P > 0.12) between CON, SAL, and FLA bulls. Bulls fed NAR had greater (P < 0.02) DMI (as kg/d or % BW) and final shrunk BW compared with CON, SAL, and FLA bulls, whereas DMI and final shrunk BW did not differ (P > 0.26) between CON, SAL, and FLA bulls. Feed efficiency, however, was not impacted (P = 0.51) by any feed additives used herein. Collectively, narasin was the only feed additive that benefited performance and ruminal fermentation of Nellore animals fed a forage-based diet. [ABSTRACT FROM AUTHOR]

Sixteen Angus crossbred steers (531 ± 22.7 kg), fitted with rumen canulae, were used to determine the impact of trace mineral (TM) source, diet type, and Rumensin (R) or Rumensin + Tyolsin (RT) supplementation on rumen fermentation characteristics. In experiment 1, steers were individually housed and fed a high concentrate finishing diet for 21 d. Steers were then blocked (n = 4 steers/block) based on mean dry matter intake (DMI) over the acclamation period. Steer blocks were then randomly assigned to 4 dietary treatments for 28 d. A 2 x 2 factorial arrangement of treatments was used. Factors included: 1) TM source (Sulfate or Hydroxy Cu, Mn, and Zn TM supplemented at 18, 40, and 90, mg/kg DM, respectively), and 2) with or without RT (supplemented at 36.3 and 11 g/metric ton DM, respectively). Following the 28-d feeding period, rumen samples were collected at 0, 2, and 4 h post-feeding. On experiment 2, all steers were then transitioned to a lactating dairy diet for 21 d. Steers were then blocked and assigned to treatments for 28 d. Treatments included: 1) TM source (Sulfate or Hydroxy Cu, Mn, and Zn TM supplemented at 10, 50, and 60, mg/kg DM, respectively) and 2) with or without R (0.0 or 24.2 g of R/metric ton DM). Following the 28-d feeding period, rumen samples were collected as described previously. Rumen fluid samples from both experiments were analyzed for short chain fatty acids (SCFA), pH, and ammonia concentrations. Within an experiment, data over the three time periods (0, 2, and 4 h) were averaged for each parameter measured before statistical analysis. In experiment 1, Molar proportions of acetate were lesser (P < 0.04) and propionate greater (P < 0.01) in steers receiving Hydroxy TM compared with steers receiving Sulfate TM. All other rumen fermentation characteristics measured in this experiment were similar across TM source. Rumen molar concentrations of acetic acid were less in steers receiving RT than steers not receiving RT. Steers receiving RT and Hydroxy TM tended (P < 0.10) to have decreased rumen ammonia concentrations compared with steers receiving RT and Sulfate TM. In experiment 2, there were no TM source impacts on the rumen fermentation characteristics measured. Supplementation of R reduced molar concentrations (P < 0.02) and proportions (P < 0.01) of acetate and increased molar concentrations and proportions of propionate (P < 0.01, P < 0.01, respectively) and butyrate (P < 0.02, P < 0.04, respectively). These data indicate that TM source, R, and RT may modulate rumen fermentation characteristics but their impacts on rumen fermentation may be diet dependent. [ABSTRACT FROM AUTHOR]

The objective was to compare the effect of applying silage additives to male sterile sorghum hybrids on temperature production during ensiling time (30 d) and at feed-out period after 30 or 90 d of ensiling period. Two male-sterile sorghum hybrids; F430 and F465, with and without BMR12 trait, respectively (Richardson Seed Ltd.); were randomly allocated in plots blocked by irrigation section in a dairy farm in West Texas. During harvest, duplicate samples from each plot were obtained, placed on plastic trays, and transported to one of three stations to be treated with chemical silage preservative (SG, SiloGuard), heterofermentative bacteria inoculant with mold inhibitor solution (SM, Silage Maker 250) or distilled water (DW, control). Treatments were applied with spray bottles following a protocol that consisted of two sets of 5 sprays (1.1 mL each and 11 mL total) followed by mixing of the forage. Personnel applying the treatment were blind as to which treatment they were applying and all spray bottles, trays and tables from each station were color coded to prevent cross contamination. After treated, 3.63 kg of forage was packed in three consecutive steps using a manual press on 4.7L buckets (Uline) and a temperature data logger was placed in the center of each of the 30 d mini silos. The amount of material packed was estimated to achieve a 230 kg of DM/m³ compaction at 30% DM of the forage. At opening, the material from each silo was moved to a tray and mixed to be homogenized and exposed to oxygen. Then, the material was added back to its correspondent bucket until it filled up to the border without compressing. Heat production during the feed-out period and air-stability were assessed for both ensiling periods, whereas fermentation heat production during ensiling period was only assessed for 30 d silos. Statistical analysis was performed using mixed linear regression models (GLIMMIX procedure of SAS) with ensiling period, hybrid, treatment and the interaction of day and treatment included in the model as independent variables. Fourth root and natural log transformation were performed to obtain a normal distribution of residuals, back transformed LSM and 95% CI are reported in Table 1. Treatment effected the silage temperature during the feed-out period (P < 0.0001) and air-stability test (P = 0.02). Whereas a tendency was observed for daily heat production during the ensiled period (P = 0.07). Male-sterile sorghum silage treated with SG had the least temperature during the ensiling period and longer air-stability than SM. [ABSTRACT FROM AUTHOR]

Nitrogen fertilizing of hemp varietals in high the high desert may assist in ensuring that production levels match the demand for growing hemp varietals. However, altering fertilizer levels may differently affect plant biomass and cannabinoid concentrations of plant tissues which changes the potential by-product utilizable for livestock feed. This study aimed to determine the influence of hemp fractions [flower (FL) vs stem and leaves (SL)] under three nitrogen fertilization regimens (0, 100, and 200 kg· ha-1) on in vitro rumen fermentation. Incubations runs consisted of triplicates of 500-mL bottles containing approximately 0.5 g of either ground SL or FL of hemp at the three nitrogen fertilization regimens. Rumen fluid was collected from two ruminally cannulated Angus steers, filtered through four layers of cheesecloth, and diluted to 4:1 with a standard buffer solution. A total incubation volume of 75 mL of the buffer: rumen fluid mix was added to each flask. Flasks were then placed in a rotating incubator (55 rpm) at 39°C, connected to an Ankom RF gas production system (Ankom Technology, Macedon, NY), and removed after 24, 48, and 96h. Total gas production (TGP), metabolizable energy (ME), ammonia nitrogen concentration (N-NH3), and total volatile fatty acids (VFA) were determined. Data were analyzed as a completely randomized design using lmer function in lme4 package in R with treatment and time as a fixed effect and replicates as a random effect. Statistical significance was established at P < 0.05 (Table 1). No differences were observed for N-NH3 (P > 0.05). Overall, SL samples had greater total VFA than FL, with T0SL having the greatest concentration among all treatments (P < 0.01). In congruence, acetate, isobutyrate, isovalerate, and the ratio between acetate and propionate concentrations were also greater for T0SL (P < 0.01). Concentrations of butyrate were greater for T200SL (P < 0.01), while T100SL had the greatest concentration of butyrate among all the treatments (P < 0.01). Overall, SL fractions of hemp seem to be more suitable as a ruminant feed source. The greater fat content of the FL compared with SL may detrimentally affect microbial populations and should further be explored. From our results, N supplementation significantly alters fermentation patterns during in vitro, which further warrants the evaluation of these feeds on in vivo experiments. [ABSTRACT FROM AUTHOR]

Canola meal (CM) has become an increasingly available high protein feed source for beef cattle in North America, thanks to the expansion of the canola crushing industry in Western Canada and the United States. The inclusion of CM in diets has been reported to improve nutrient utilization and the performance of growing beef cattle. However, the energy value of CM was not as high as barley grain finishing diets, resulting in poorer performance of finishing feedlot steers. Pea starch and pea molasses are available as food industry by-products of industrial pea protein extraction. However, the utilization of these food industry by-products as a component of livestock feed has not been well evaluated. The strategic blending of food industry by-products, such as pea starch and pea molasses, with canola meal (CM) is a novel approach to improving the energy density of CM as animal feed. Nutrient synchrony, where the energy and protein availability in the rumen is synchronized to maximize the ruminal microbial fermentation, has been proposed to improve animal performance. The objectives of our study were to evaluate the in vitro and in situ fermentation and nutrient degradability of novel blended CM. Pea starch and pea molasses were added at 5% (CM5) and 10% (CM10) levels in CM (DM basis), with regular CM serving as control (CON). The in vitro study consisted of two runs of 24 h incubations with three replicates per treatment. The in situ study utilized three cannulated beef heifers and used the same number of replicates of samples and time periods as for the in vitro study. Results indicated a numerical improvement in DM degradation for CM5 and CM10 than CON both in vitro and in situ incubations. Total gas production (mmol) was numerically greater, while the proportion of methane (mmol and g/DM) was less for CM5 than CON. Results indicated that in vitro fermentation of CM5 was enhanced, while greater propionate production from CM5 likely reduced methane production. Further evaluation of these food industry by-products for beef cattle growth performance studies could provide valuable information about rumen fermentation, nutrient digestibility, and energy value of these novel blended CM. [ABSTRACT FROM AUTHOR]

We assessed the effects of a postbiotic program consisting of liquid and solid Saccharomyces cerevisiae fermentation products (SCFP) on the ruminal microbiome and fermentation characteristics of beef steers. Eight Holstein steers (BW 467 ± 13.9 kg) with rumen cannulas were used in a crossover design study with 21-d per period and 7-d washout in between periods. Steers were blocked based on initial BW and assigned to one of two treatments: 1) Control, basal diet, or 2) SCFP, basal diet plus one day feeding of LiquiCare RTU (Diamond V, Cedar Rapids, IA; dosed via rumen cannula at 11 mL/100 kg BW), followed by daily feeding of 12 g/d NaturSafe (Diamond V, topdressed). Rumen fluid samples were collected on d 0, 1, 2, 3, 5 and 21 at 0, 4, 8, or 12 h post morning feeding via rumen cannula for pH, VFA and NH3-N analyses. Samples collected at 4 h post morning feeding on d 0, 2 and 21 were subjected to DNA extraction and shotgun Nanopore sequencing to determine microbiome composition and carbohydrate active enzymes (CAZy) functional potential. Statistical model included the fixed effects of treatment, period, day and their interactions and random effect of animal. Feeding SCFP tended to reduce ruminal lactate (0.09 vs. 0.02 mM, P = 0.10), and reduced ruminal NH3-N (4.86 vs. 6.83 mg/dL, P = 0.04) on d 21. Ruminal total VFA concentration was increased (P = 0.01) by feeding SCFP 4-h post-feeding on d 5 and numerically increased 4-h post-feeding on day 21 (133.3 vs. 151.2 mM, P = 0.12). Treatments did not affect species or CAZy alpha- and beta-diversity. Steers received liquid postbiotic on d 2 exhibited a positive correlation (P < 0.05) between propionate molar proportion and glycosyl transferases (GT), glycoside hydrolases (GH), carbohydrate esterases, and carbohydrate binding modules (CBM); and a negative correlation (P < 0.05) between acetate molar proportion and polysaccharide lyases, GT, GH, and CBM, whichwas not observed in Control. Additionally, SCFP steers had higher (P = 0.05) CBM functional potential on d 21 than on d 0, while CAZy class abundances did not change over time in Control steers. Differential network analysis indicated a greater normalized degree for GT in the SCFP steers compared with Control on d 21. There were 2, 6 and 12 differently abundant species (P < 0.01) between SCFP and Control on d 0, 2 and 21, respectively, suggesting supplementing SCFP altered the abundances of more species over time. Our results showed that the postbiotic program altered the metabolic pathways of ruminal microbes toward greater propionate production, and improved abundance of carbohydrate binding modules. Our results also showed that glycosyl transferases had a greater promotive role in the ruminal enzymatic network of SCFP steers. [ABSTRACT FROM AUTHOR]

The objective of this study was to determine the effects of a postbiotic feeding program consisting of liquid and solid Saccharomyces cerevisiae fermentation products (SCFP) on digestibility, ruminal fermentation, and plasma metabolome of finishing beef steers. Eight Holstein steers (BW 467 ± 13.9 kg) equipped with rumen cannulas were used in a crossover design study, with 21-d per period and 7-d washout period in between periods. Steers were blocked based on initial BW to one of two treatments: 1) Control, basal diet only (CON), or 2) SCFP, one day feeding of LiquiCare RTU (Diamond V, dosed via rumen cannula at 11 mL/100 kg BW) followed by daily feeding of 12 g NaturSafe (Diamond V, top-dressed). Feed and fecal samples were collected during d 17 to 20 for determination of digestibility and fecal excretion of N, P, Cu and Zn using acid-insoluble ash as an internal marker. Blood samples were collected on d 21 before morning feeding. Rumen fluid samples were collected on d 0, 1, 2, 3, 5 and 21 at 0, 4, 8, or 12 h post morning feeding via rumen cannula. Results were analyzed with the GLIMMIX procedure of SAS 9.4 (SAS, 2022). BW, DMI and digestibility were not affected by treatment. There was a tendency of treatment by period interaction (P = 0.09) on feed efficiency, which was improved by feeding SCFP only in period 1. Feeding SCFP did not affect (P > 0.10) ruminal pH. Feeding SCFP tended to reduce ruminal lactate concentration on d 21 (0.09 vs. 0.02 mM, P = 0.10). Supplementing SCFP reduced ruminal NH3-N concentration on d 2 (4.24 vs. 7.31 mg/dL, P = 0.03) and d 21 (4.86 vs. 6.83 mg/dL, P = 0.04). By feeding SCFP, ruminal total VFA concentration was increased 4-h post-feeding on d 5 (139.7 vs. 126.7 mM, P = 0.01) and numerically increased 4-h post-feeding on d 21 (151.2 vs. 133.3 mM, P = 0.12). For VFA composition, no treatment differences were observed on day 21. However, feeding SCFP reduced (P = 0.01) propionate proportion and increased (P = 0.05) butyrate proportion on day 3. The enriched plasma metabolic pathways (P ≤ 0.05) by feeding SCFP are citric acid cycle, pyrimidine metabolism, glycolysis/gluconeogenesis, retinol metabolism, and inositol phosphate metabolism pathways. Overall, our results indicated potential benefits of the SCFP feeding program on improving ruminal fermentation, preventing acidosis and improving N utilization in the rumen. Furthermore, feeding SCFP enriched several important pathways in lipid, protein, and glucose metabolism, which may improve feed efficiency of energy and protein in finishing beef cattle. [ABSTRACT FROM AUTHOR]

The objective was to evaluate a novel brewer's yeast product on ruminal fiber fermentation in vitro. The experiment was a completely randomized design and included 4 treatments. Treatments included a negative control (NCON), a commercial brewer's yeast product (Emprove MX; EMX), and a prototype concentrated brewer's yeast (T1R8) fed at low and high inclusions (T1R8-L and T1R8-H, respectively). Inclusions for low and high treatments were 0.0008 and 0.0015 g, respectively, to correspond with 7 and 14 g inclusion in a lactating cow diet. Treatments were evaluated in duplicate flasks in 2 replicated runs for a total of four observations per treatment. Flasks contained 2.5 grams dry matter (DM) of substrate to represent a lactating cow diet (30% haylage, 25% corn silage, 20% corn, 15% canola meal, and 10% soybean hulls), and 150mL of rumen fluid mixture (2 McDougall's buffer:1 rumen fluid ratio). Four F57 sealed Ankom bags were filled with 0.25 grams DM of substrate each to facilitate measuring in vitro DM and neutral detergent fiber disappearance (IVDMD and IVNDFD, respectively). Flasks were incubated at 39℃ for 30 hours with sample aliquots collected at hour 0, 8, 16, and 30 to determine pH and volatile fatty acids (VFA). Data were analyzed using the MIXED procedure of SAS 9.4 with IVDMD and IVNDFD considered a main effect of treatment while pH and VFA were analyzed with effects of treatment, time, and their interaction. No differences in IVDMD were observed (P = 0.31) among treatments. Treatment affected (P = 0.01) IVNDFD with EMX (50.6%), T1R8-L (48.6%), and T1R8-H (50.3%) being greater than NCON (45.7%). A treatment by hour interaction (P < 0.01) was observed for total VFA concentration; EMX (71.8 mM), T1R8-L (72.6 mM), and T1R8-H (66.0 mM) were greater than NCON (47.8 mM) at h 8, but all treatments were not different at h 16. A treatment by hour interaction (P < 0.01) was also observed for acetate and propionate; EMX, T1R8-H, and T1R8-L were greater than NCON at h 8, but all treatments were not different at h 16. At h 30, greater propionate was observed for T1R8-H compared with all treatments. No effects of treatment or treatment by hour (P = 0.89) were observed for acetate:propionate ratio. Although a treatment by hour interaction was not observed for pH (P = 0.12), a treatment effect (P = 0.03) indicated T1R8-L was the greatest with EMX being intermediate, and NCON and T1R8-H being the least. Novel brewer's yeast product T1R8 increased the rate of substrate fermentation in the initial 8 h and increased the extent of fiber degradation after a 30 h in vitro fermentation. [ABSTRACT FROM AUTHOR]

The objective was to determine the effect of replacing forage with coproducts in transition diets on rumen microbiome composition and ruminal fermentation ex vivo after steers consumed a common finishing diet. A random subset of 30 steers were selected from a larger, separate pen study. Steers were blocked by initial BW and allotted into 9 pens. Pens were then assigned to 1 of 3 dietary treatments for the 35 d adaptation period: a forage-based diet (FO; alfalfa and grass hay), a coproduct-based diet (CO; soybean hulls and modified wet distillers grains with solubles), and a coproduct-based diet pair-fed (CO-P) to isoenergetic levels of FO. Dry-rolled corn inclusion increased with either decreasing forage or coproduct inclusion. Both FO and CO were fed with slick bunk management. At d 35 and 63, rumen fluid was collected by esophageal tubing to determine differences in fermentation of the finishing diet as the substrate in an ex vivo model. Rumen fluid was also utilized for microbiome analysis using 16S rRNA sequencing on the Illumina MiSeq platform with 2 × 300 bp paired-end sequencing. Sequencing reads were analyzed within QIIME2. Statistical analyses were conducted using SAS 9.4. Fermentation data were analyzed using the MIXED procedure, while bacterial relative abundance data were analyzed in the GLIMMIX procedure. Correlations were analyzed using the CORR procedure. A treatment × sampling day interaction (P = 0.02) was observed for in vitro dry matter disappearance; on d 35, it was greater in steers fed CO compared with CO-P (58 vs. 53%, respectively), but no differences were observed on d 63. Within the rumen microbiome, there was a tendency (P = 0.06) for alpha diversity to have a treatment × day interaction. Specifically, CO steers had the greatest decrease in alpha diversity from d 35 to 63, but there was no change in alpha diversity in FO steers and CO-P steers over time. Final pH in from the ex vivo model was positively correlated (r = 0.32) with Bacteroidetes relative abundance but negatively correlated (r = -0.25) with Proteobacteria (P = 0.05). In vitro dry matter disappearance was positively correlated (r = 0.38) with relative abundance of Firmicutes, but negatively correlated (r = -0.43) with Proteobacteria (P < 0.01). Dietary treatment did not affect (P = 0.21) richness within the rumen microbiome. Rumen microbiome composition and ex vivo fermentation results suggest all treatments were adapted for the finishing diet at the conclusion of the 35-d adaptation period. [ABSTRACT FROM AUTHOR]

The effect of hay type on the microbiome of the equine gastrointestinal tract is relatively unexplored. Our objective was to characterize the cecal and fecal microbiome of mature horses consuming alfalfa or Smooth Bromegrass (brome) hay. Six cecally cannulated horses were used in a split-plot design run as a crossover in two periods. The whole plot treatment was ad libitum access to brome or alfalfa hay fed over two 21-d acclimation periods with subplots of sampling location (cecum and rectum) and sampling hour. Each acclimation period was followed by a 24-h collection period where cecal and fecal samples were collected every 3 h for analysis of pH and volatile fatty acids (VFA). Fecal and cecal samples were pooled and sent to a commercial lab (MR DNA, Shallowater, TX) for the amplification of the V4 region of the 16S rRNA gene and sequenced using Illumina HiSeq. The main effects of hay on VFA, pH, and taxonomic abundances were analyzed using the MIXED procedure of SAS 9.4 with fixed effects of hay, hour, location, period, and all possible interactions and random effect of horse. Alpha and beta diversities were analyzed using the R Dame package. Horses fed alfalfa had greater fecal than cecal pH (P ≤ 0.05), whereas horses fed brome had greater cecal than fecal pH (P ≤ 0.05). Regardless of hay type, total VFA concentrations were greater (P ≤ 0.05) in the cecum than in feces, and alfalfa resulted in greater (P ≤ 0.05) VFA concentrations than brome in both sampling locations. Alpha diversity was greater (P ≤ 0.05) in fecal compared with cecal samples. Microbial community structure within each sampling location and hay type differed from one another (P ≤ 0.05). Bacteroidetes were greater (P ≤ 0.05) in the cecum compared with the rectum, regardless of hay type. Firmicutes and Firmicutes: Bacteroidetes were greater (P ≤ 0.05) in the feces compared with cecal samples of alfalfa-fed horses. In all, fermentation parameters and bacterial abundances were impacted by hay type and sampling location in the hindgut. [ABSTRACT FROM AUTHOR]

A 16-wk growth trial was conducted to examine the effects of dietary replacement of fish meal by defatted soybean meal (SBM) and fermented soybean meal (FSBM) with taurine supplementation on growth performance, nutrient apparent digestibility coefficient (ADC) and biological parameters of pompano fish. The FSBM was produced by fermenting SBM with Lactobacillus spp. Seven isonitrogenous and isoenergetic diets were formulated to replace 35% or 50% of fish meal by SBM or FSBM with taurine supplementation. The diets are denoted as follows: FM, SBM35, SBM35T, FSBM35T, SBM50, SBM50T, and FSBM50T. The FM (the basal diet) contained fish meal as a main source of dietary protein. Taurine was supplemented to SBM35T, FSBM35T, SBM50T, and FSBM50T at the level of 15 g/kg diet. Pompano juveniles with an initial body weight (BW) of 80 g reared in floating net cages were fed the experimental diets twice daily for 16 wk. Results showed that the final BW, weight gain, and feed conversion ratio of fish fed SBM35 and SBM50 were significantly lower than those of fish fed FM (P < 0.05), indicating that the replacement of fish meal by SBM at the rate of 35% in the diet is excessive for pompano. Supplementation of taurine to the SBM-included diets significantly increased growth performance and feed utilization (P < 0.05); however, these diets did not restore the performance back to a level equivalent to that of fish offered the basal diet. Meanwhile, fish fed FSBM35T had comparable growth and feed performances to those fed FM. Hematocrit values, total biliary bile acid levels, whole body lipid contents, and tissue taurine concentrations of fish fed SBM35 and SBM50 were the lowest among the treatments, but these parameters were improved by taurine supplementation and FSBM inclusion in the diet. Taurine supplementation increased lipid ADC, and SBM fermentation slightly enhanced both lipid and protein ADCs of the fish. These findings suggest that the combination of FSBM and taurine supplementation is an effective way to improve growth performance, nutrient digestibility, and biological parameters, and that FSBM with taurine supplementation can replace 35% of fish meal in pompano diets without any negative effects on growth and feed performances in a long-term feeding period. [ABSTRACT FROM AUTHOR]

Our objective was to examine the effects of processing, moisture, and anaerobic storage length of reconstituted corn grain (RCG) on the fermentation profile, geometric mean particle size (GMPS), and ruminal dry matter disappearance (DMD). Dry corn kernels were ground (hammer mill, 5-mm screen) or rolled, then rehydrated to 30%, 35%, or 40% moisture, and stored for 0, 14, 30, 60, 90, 120, or 180 d in laboratory silos. Rolled corn had an increased GMPS compared with ground corn (2.24 and 1.13 mm, respectively, at ensiling). However, there was a trend for an interaction between processing and moisture concentration to affect particle size, with GMPS increasing with increased moisture concentration, especially in ground corn. Longer storage periods also slightly increased GMPS. Processing, moisture, and storage length interacted to affect the fermentation pattern (two- or three-way interactions). Overall, pH decreased, whereas lactic acid, acetic acid, ethanol, and NH3-N increased with storage length. RCG with 30% moisture had less lactic acid than corn with 35% and 40% moisture, indicating that fermentation might have been curtailed and also due to the clostridial fermentation that converts lactic acid to butyric acid. Ensiling reconstituted ground corn with 30% of moisture led to greater concentrations of ethanol and butyric acid, resulting in greater DM loss than grain rehydrated to 35% or 40% of moisture. Ammonia-N and in situ ruminal DMD were highest for reconstituted ground corn with 35% or 40% of moisture, mainly after 60 d of storage. Therefore, longer storage periods and greater moisture contents did not offset the negative effect of greater particle size on the in situ ruminal DMD of rolled RCG. Nonetheless, RCG should be ensiled with more than 30% moisture and stored for at least 2 mo to improve the ruminal DMD and reduce the formation of ethanol and butyric acid. [ABSTRACT FROM AUTHOR]

We evaluated the effects of a chemical additive on the microbial communities, fermentation profile, and aerobic stability of whole-plant corn silage with or without air stress during storage. Whole-plant corn was either untreated or treated with a chemical additive containing sodium benzoate, potassium sorbate, and sodium nitrite at 2 or 3 liters/t of fresh forage weight. Ten individually treated and replicated silos (7.5 liters) were made for each treatment. Half of the silos remained sealed throughout a 63-d storage period, and the other half was subjected to air stress for 2 h/wk. The composition of the bacterial and fungal communities of fresh forage and silages untreated or treated with 2 liters/t of fresh forage weight was analyzed by Illumina Miseq sequencing. Treated silage had greater (P < 0.05) aerobic stability than untreated, even when subjected to air stress during storage, but the numbers of yeasts culturable on selective agar were not affected. However, the additive reduced the relative abundance (RA) of the lactating-assimilating yeast Candida tropicalis (P < 0.01). In air-stressed silages, untreated silage had a greater (P < 0.05) RA of Pichia kudriavzevii (also a lactate assimilator) than treated silage, whereas treated silage was dominated by Candida humilis , which is usually unable to assimilate lactate or assimilates it slowly. The additive improved the aerobic stability by specifically preventing the dominance of yeast species that can consume lactate and initiate aerobic spoilage. To the best of our knowledge, this is the first work that identifies the specific action of this additive on shifting the microbial communities in corn silage. [ABSTRACT FROM AUTHOR]

A replicated 5 × 5 Latin square design with a 2 × 2 + 1 factorial arrangement of treatments was used to determine the effects of bismuth subsalicylate (BSS) and encapsulated calcium ammonium nitrate (eCAN) on ruminal fermentation of beef cattle consuming bahiagrass hay (Paspalum notatum) and sugarcane molasses. Ten ruminally cannulated steers (n = 8; 461 ± 148 kg of body weight [ BW ]; average BW ± SD) and heifers (n = 2; 337 ± 74 kg of BW) were randomly assigned to one of five treatments as follows: 1) 2.7 g/kg of BW of molasses (NCTRL), 2) NCTRL + 182 mg/kg of BW of urea (U), 3) U + 58.4 mg/kg of BW of BSS (UB), 4) NCTRL + 538 mg/kg of BW of eCAN (NIT), and 5) NIT + 58.4 mg/kg of BW of BSS (NITB). With the exception of NCTRL, all treatments were isonitrogenous. Beginning on day 14 of each period, ruminal fluid was collected and rectal temperature was recorded 4× per day for 3 d to determine ruminal changes every 2 h from 0 to 22 h post-feeding. Ruminal gas cap samples were collected at 0, 3, 6, 9, and 12 h on day 0 of each period followed by 0 h on days 1, 2, 3, and 14. Microbial N flow was determined using Cr-Ethylenediaminetetraacetic acid, YbCl3, and indigestible neutral detergent fiber for liquid, small particle, and large particle phases, respectively. Data were analyzed using the MIXED procedure of SAS. Orthogonal contrasts were used to evaluate the effects of nonprotein nitrogen (NPN) inclusion, NPN source, BSS, and NPN source × BSS. There was no treatment effect (P > 0.05) on concentrations of H2S on day 0, 1, 2, or 14; however, on day 3, concentrations of H2S were reduced (P = 0.018) when NPN was provided. No effect of treatment (P = 0.864) occurred for ruminal pH. There was an effect of NPN source on total concentrations of VFA (P = 0.011), where a 6% reduction occurred when eCAN was provided. There were effects of NPN (P = 0.001) and NPN source (P = 0.009) on the concentration of NH3-N, where cattle consuming NPN had a greater concentration than those not consuming NPN, and eCAN reduced the concentration compared with urea. Total concentrations of VFA and NH3-N were not affected (P > 0.05) by BSS. There was an effect of BSS (P = 0.009) on rectal temperature, where cattle not consuming BSS had greater temperatures than those receiving BSS. No differences for NPN, NPN source, nor BSS (P > 0.05) were observed for microbial N flow. In conclusion, eCAN does not appear to deliver equivalent ruminal fermentation parameters compared with urea, and BSS has limited effects on fermentation. [ABSTRACT FROM AUTHOR]

An experiment was conducted during the winter of two consecutive years to evaluate the effects of feeding green-chopped cool-season forages on digestibility, ruminal fermentation, and blood parameters in beef steers. Nine ruminally cannulated Angus crossbred steers (year 1: 359 ± 79 kg; year 2: 481 ± 105 kg) received ad libitum green-chopped forages from pastures planted with one of the following mixtures: 1) OAT = Horizon 201 oats (Avena sativa L.)/Prine annual ryegrass (Lolium multiflorum Lam.) at 95 and 17 kg/ha, respectively; 2) RYE = FL401 cereal rye (Secale cereale L.)/Prine annual ryegrass (Lolium multiflorum Lam.) at 78 and 17 kg/ha, respectively; or 3) TRIT = Trical 342 triticale (X Triticosecale spp.)/Prine annual ryegrass (Lolium multiflorum Lam.) at 95 and 17 kg/ha, respectively. Intake was measured using the GrowSafe system and orts were discarded prior to subsequent feeding. After a 14-d adaptation, feed and fecal samples were collected twice daily for 4 d to determine apparent total tract nutrient digestibility using indigestible neutral detergent fiber (NDF) as an internal marker. On day 19, blood and ruminal fluid samples were collected every 3 h during a 24-h period to analyze plasma urea nitrogen (PUN) and glucose, ruminal pH, and concentration of ruminal ammonia nitrogen (NH3 -N) and volatile fatty acids (VFA). Data were analyzed as a generalized randomized block design with repeated measures using the PROC MIX of SAS. No effect of treatment (P > 0.05) was observed for intake of dry matter, organic matter (OM), crude protein, NDF, or acid detergent fiber. Apparent total tract digestibility of nutrients was greater (P < 0.05) for OAT and TRIT when compared with RYE, with OM digestibility being 82.7%, 79.6%, and 69.5%, respectively. An effect of time (P < 0.01) was observed for ruminal pH. Plasma concentration of glucose was greater (P < 0.01) in steers consuming OAT, whereas steers fed RYE had greater (P < 0.05) concentrations of ruminal NH3 -N and PUN, and the least concentration of total ruminal VFA (P < 0.05), despite having the greatest (P > 0.05) molar proportion of acetate, branched-chain VFA, and acetate:propionate. Increased nutrient digestibility and favorable ruminal fermentation and blood metabolites of OAT and TRIT are potentially conducive to enhanced growth performance when compared with RYE. [ABSTRACT FROM AUTHOR]

Enteric methane (CH4) emissions are not only an important source of greenhouse gases but also a loss of dietary energy in livestock. Corn oil (CO) is rich in unsaturated fatty acid with >50% PUFA, which may enhance ruminal biohydrogenation of unsaturated fatty acids, leading to changes in ruminal H2 metabolism and methanogenesis. The objective of this study was to investigate the effect of CO supplementation of a diet on CH4 emissions, nutrient digestibility, ruminal dissolved gases, fermentation, and microbiota in goats. Six female goats were used in a crossover design with two dietary treatments, which included control and CO supplementation (30 g/kg DM basis). CO supplementation did not alter total-tract organic matter digestibility or populations of predominant ruminal fibrolytic microorganisms (protozoa, fungi, Ruminococcus albus , Ruminococcus flavefaciens , and Fibrobacter succinogenes), but reduced enteric CH4 emissions (g/kg DMI, −15.1%, P = 0.003). CO supplementation decreased ruminal dissolved hydrogen (dH2, P < 0.001) and dissolved CH4 (P < 0.001) concentrations, proportions of total unsaturated fatty acids (P < 0.001) and propionate (P = 0.015), and increased proportions of total SFAs (P < 0.001) and acetate (P < 0.001), and acetate to propionate ratio (P = 0.038) in rumen fluid. CO supplementation decreased relative abundance of family Bacteroidales_BS11_gut_group (P = 0.032), increased relative abundance of family Rikenellaceae (P = 0.021) and Lachnospiraceae (P = 0.025), and tended to increase relative abundance of genus Butyrivibrio_2 (P = 0.06). Relative abundance (P = 0.09) and 16S rRNA gene copies (P = 0.043) of order Methanomicrobiales , and relative abundance of genus Methanomicrobium (P = 0.09) also decreased with CO supplementation, but relative abundance (P = 0.012) and 16S rRNA gene copies (P = 0.08) of genus Methanobrevibacter increased. In summary, CO supplementation increased rumen biohydrogenatation by facilitating growth of biohydrogenating bacteria of family Lachnospiraceae and genus Butyrivibrio_2 and may have enhanced reductive acetogenesis by facilitating growth of family Lachnospiraceae. In conclusion, dietary supplementation of CO led to a shift of fermentation pathways that enhanced acetate production and decreased rumen dH2 concentration and CH4 emissions. [ABSTRACT FROM AUTHOR]

This study evaluated the effects of supplementing dry live yeast (LY ; Saccharomyces cerevisiae) on in vitro gas production (IVGP) fermentation dynamics, pH, and CH4 concentration at 48 h, and in situ rumen parameters and digestibility of DM (DMD) and NDF (NDFD) of growing cattle during 3 feeding phases: grower (GRW) for 17 d (38% steamed-flaked corn; SFC), transition (TRANS) for 15 d (55.5% SFC: 1.2 Mcal/kg NEg), and finisher (FIN) for 13 d (73% SFC: 1.23 Mcal/kg NEg). Twenty British-crossbred, ruminally cannulated steers (183 kg ± 44 kg) 6 mo of age were blocked by weight into 5 pens containing Calan gate feeders and received a control (CON) diet (17.2% CP, 35.8% NDF, 86.7% DM) without LY on days −12 to 0. After that, animals were randomly assigned to treatments (TRT), 5 animals per TRT: CON or LY at inclusion rates of 5 g/d (LY1), 10 g/d (LY2), or 15 g/d (LY3) top dressed every morning at 0800 for 45 d. The DMD and NDFD were assessed during 7 separate collection days using in situ nylon bags containing 5 g of GRW, TRANS, or FIN diets, incubated at 1200 for 48 h. Protozoa counts (PC) were determined during 5 collection periods. Data were analyzed as a repeated measure within a randomized complete block design, assuming a random effect of the pen. For GRW, TRT altered the total gas production of the nonfiber carbohydrate (NFC ; P = 0.045) and the fractional rate of degradation (kd) of the fiber carbohydrate (FC) pool (P = 0.001) in a cubic pattern (P ≤ 0.05): LY2 had the most gas production and fastest kd. TRT also influenced DMD (P = 0.035) and NDFD (P = 0.012) with LY2 providing the greatest digestibility. For TRANS, TRT tended to affect the NFC kd (P = 0.078) and influenced pH (P = 0.04) and DMD (P < 0.001) in which LY2 yielded the fastest kd, highest pH, and greatest DMD. For FIN, there was an effect of TRT on total gas production (P < 0.001) and kd (P = 0.004) of the NFC pool, FC kd (P = 0.012), in vitro CH4 concentration (P < 0.001), PC (P < 0.001), DMD (P = 0.039), and NDFD (P = 0.008). LY1 had the highest PC and provided the greatest DMD and NDFD. LY2 had the fastest kd of both the NFC and FC pools and had the least CH4 concentration. LY3 had the greatest NFC gas production. No specific dose–response pattern was observed, but 10 g/d provided the most beneficial result for all diets. We concluded that supplementation with LY affected IVGP as well as ruminal parameters and digestibilities. [ABSTRACT FROM AUTHOR]

Two experiments were conducted to determine: 1) the impact of strained rumen fluid (SRF) alone or SRF with particle-associated microorganisms (PAO) included and dilution on in vitro dry matter digestibility (DMD) and 2) the impact of trace mineral (TM) source on in vitro fermentation characteristics and TM solubility under simulated abomasal and intestinal conditions. In experiment 1, 3 cannulated steers were adapted to a diet formulated to meet the nutrient requirements for lactating dairy cows. Strained RF was obtained by straining rumen content through 2 layers of cheesecloth. Half of the remaining digesta was washed with McDougall's buffer and filtered through 2 layers of cheesecloth to obtain PAO. Both SRF and PAO were filtered again through 8 layers of cheesecloth. Strained RF was mixed with either McDougall's buffer (SRF) or PAO (SRF+ + PAO) at a ratio of 1:2 or 1:4 and incubated at 39 °C for 12 h using the ground basal diet as the substrate. Digestibility of DM was greater in digestion tubes containing SRF and SRF + PAO at a 1:2 ratio. In experiment 2, 8 steers fitted with a ruminal cannula were blocked by body weight and assigned to 1 of the 2 treatment groups. Treatments consisted of 10 mg Cu, 40 mg Mn, and 60 mg Zn/kg DM from either: 1) sulfate (STM) or 2) hydroxychloride (HTM) sources. Steers were housed in individual pens and fed the same diet as described in experiment 1. Dietary TM treatments were mixed with dried distiller grains and mixed in the diet, by hand, immediately after basal diet delivery. Dietary treatments were fed for 14 d. On day 15, SRF + PAO was collected from each steer (STM-RF and HTM-RF) and used in a series of in vitro crossover experiments. In vitro substrates (S) used were the ground diets consumed by the animals on each treatment (STM-S and HTM-S). Incubations containing HTM-S had greater (P < 0.01) total volatile fatty acid (VFA) concentration and propionic acid molar proportions, but lesser (P < 0.01) acetic acid molar proportions than STM-S. Rumen fluid from steers supplemented with HTM had a greater (P < 0.03) total VFA than STM-RF at 24 h post incubation. After 12 h post incubation, the molar proportion of propionic acid in HTM-RF was lesser (P = 0.04) than in STM-RF. After simulated abomasal digestion, soluble Mn concentration in HTM-S was greater (P < 0.01) than in STM-S. These data indicate that the source of TM can influence in vitro rumen fermentation characteristics and Mn solubility under simulated abomasal conditions., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science.)

Previous research has demonstrated that decreasing starch availability of steam-flaked corn by increasing flake density or increasing the degree of starch retrogradation influences in vitro gas production kinetics. However, it is unclear if increasing flake density or the degree of starch retrogradation influences end-products of in vitro ruminal fermentation (methane, volatile fatty acids, ammonia). The objective of this experiment was to evaluate the effects of increasing flake density and the degree of starch retrogradation on in vitro gas production kinetics, digestibility, and ruminal fermentation characteristics of steam-flaked corn. Three ruminally cannulated steers were fed a high-concentrate diet and sampled for ruminal digesta for an in vitro fermentation experiment with a 5 × 2 factorial arrangement of treatments. Steam-flaked corn was produced to flake densities of 257, 296, 335, 373, and 412 g/L by adjusting the rolls of a steam-flaker. Samples were stored for 3 d at either 23 °C to produce fresh steam-flaked corn or at 55 °C in heat-sealed foil bags to produce retrograded steam-flaked corn. In vitro fermentation vessels were incubated for 24 h and then assessed for fermentation parameters including dry matter digestibility, volatile fatty acid concentrations, and total gas and methane production. Increasing the degree of starch retrogradation decreased (P < 0.01) the rate of gas production across all flake densities of steam-flaked corn but did not decrease the extent of gas production. In vitro methane production, dry matter digestibility, and microbial biomass concentration were not influenced by increasing flake density or starch retrogradation. Increasing the degree of starch retrogradation decreased (P = 0.03) the molar propionate proportion and increased (P < 0.06) the molar proportions of butyrate, isobutyrate, and isovalerate and the acetate:propionate ratio. Enzymatic starch availability of steam-flaked corn was positively correlated with mean propionate proportion (r2 = 0.93) and negatively correlated with the mean butyrate proportion (r2 = 0.89). Results from the current study demonstrate that increasing the degree of starch retrogradation of steam-flaked corn decreased the rate of in vitro gas production and altered volatile fatty acid profiles in the ruminal fermentation media., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

The objectives of this study were to evaluate the levels of supplemental salt on low-quality forage intake, water intake, dry matter (DM) digestibility, and rumen fermentation. Six ruminally cannulated, Angus crossbred heifers (14 mo of age; 449 kg ± 24 kg body weight [BW]) were used in a dual 3 × 3 Latin square design. The heifers were housed in individual stalls with 2 animals assigned to each treatment per period. Salt treatments were mixed into a protein supplement of 50% cracked corn and 50% soybean meal and fed at 0.3% of shrunk BW. Salt treatments consisted of 1) control, no salt (CON), 2) 0.05% of BW salt (LOW), and 3) 0.1% of BW salt (HIGH). Chopped, low-quality (CP = 7.4%; NDF = 64.2%), grass hay was used as the base ration and was provided daily at 120% of the average daily intake of the previous 3 d. Each period included a 14-d diet adaptation, 6 d of sample collection, 1 d collection of rumen fluid samples for ruminal and microbial profiles. Individual forage dry matter intake, water intake, and DM digestibility were measured during the 6-d collection period. Rumen pH, ammonia levels, and volatile fatty acid (VFA) concentrations were measured during the 1-d ruminal profile. Rumen DM and liquid fill were determined with a 5-h post-feeding rumen evacuation. Supplemental salt had no influence on forage intake (P = 0.19) expressed on a kg/d basis yet tended to decrease linearly (P = 0.06) with increasing levels of salt when expressed on a grams/kg BW basis. DM digestibility was not influenced by salt levels (P > 0.05), but DM fill tended to increase linearly with increasing salt levels (P = 0.06). Water intake and liquid fill, however, increased linearly with increasing levels of salt (P < 0.01) with an 18.9% increase in water intake and 17.0% increase in liquid fill compared to control animals. Ruminal pH and ammonia levels both decreased linearly with increasing salt (P < 0.01). Acetate concentration and acetate: propionate ratio increased linearly with increasing levels of salt (P < 0.01). In contrast, isobutyrate and butyrate concentrations decreased linearly with increasing levels of salt (P < 0.01). Our research suggests that increasing levels of salt tends to influence dry matter intake, DM fill, liquid kinetics, and rumen fermentation characteristics. Results from this research provide additional information on how salt-limited supplements may impact beef cattle consuming low-quality forage diets., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science.)

This study investigated the effects of a blend of bacillus-fermented soybean meal, functional amino acids, and nucleotides (Functional protein blend-FP Blend) as a replacement for animal protein sources in a weaner pig diet without antibiotic growth promoters on nutrient digestibility, blood profiles, intestinal morphology, diarrhea incidence, and growth performance. A total of 288 crossbred weaned piglets [♂ Duroc x ♀ (Yorkshire × Landrace)] with an average body weight (BW) of 6.89 ± 0.71 kg were randomly allocated to 6 groups based on initial BW and sex (8 replicate pens per treatment; 3 gilts and 3 barrows/pen). The experiment lasted for 5 wk. Dietary treatments included PC [standard diet with 3% fish meal (FM) and 2% plasma protein (PP)], NC (nonanimal protein, AP), T1 (3% FM replaced with 5% FP Blend), T2 (3% FM and 1% PP replaced with 5% FP Blend), T3 (2% PP replaced with 5% FP Blend), and T4 (3% FM and 2% PP replaced with 5% FP Blend). Data were analyzed using Minitab version 17 software. Key results indicated that FP Blend improved the apparent ileal digestibility (AID) coefficient of dry matter, gross energy, lysine, and valine in T4 compared with NC treatment (P < 0.05), whereas AID coefficient of crude protein and other amino acids remained constant (P > 0.05). Compared with NC diet, the weaned pigs fed T4 diet reduced malondialdehyde, serum IL8, TNF-α, and increased IgG (P < 0.05), while showing no effect on serum IL6, IL10, white blood cells, IgA, and endotoxin (P > 0.05). Furthermore, FP blend significantly increased villus height in the duodenum and ileum in T4 compared with NC (P < 0.05). The average daily gain (ADG) was highest in T4 (502.73 g/d), followed by T1 (477.96 g/d) and T2 (475.85 g/d), compared with PC (450.86 g/d) and NC (439.79 g/d). T4's ADG significantly differed from PC and NC (P < 0.001), whereas no significant differences were observed in T1, T2, and T3 (P > 0.05). The feed conversion ratio (FCR) was significantly lower in T4 (1.45) compared with PC (1.57) and NC (1.59) (P < 0.001), with no significant differences among other groups. In conclusion, FP Blend demonstrated efficacy in improving nutrient digestibility, optimizing intestinal morphology, bolstering immune responses, reducing diarrhea incidence, alleviating the adverse effects of weaning stress, and enhancing growth performance of weaned piglets., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

There is an increasing concern about using limited high-quality protein sources in the aquafeed industry. The alternative solution to this problem is cost-effective plant proteins such as soybean meal (SBM). However, it is better to improve plant protein-containing diets through processing and supplemental amino acids. This study aimed to examine the effects of fermented soybean meal (FSBM) and supplemental methionine and lysine (ML) in diets on growth, digestibility, and body and amino acid composition in Beluga (Huso huso). Two basal diets (490 g FM Kg-1) of fish meal (FM) and FM with ML (FM + ML) were replaced by 40%, 60%, and 80% of FSBM and FSBM + ML (FM, FSBM40, FSBM60, FSBM80, FM + ML, FSBM40 + ML, FSBM60 + ML and FSBM80 + ML; 444 g kg-1 crude protein and 19.77 MJ kg-1 gross energy). The diets were fed to triplicate groups of Beluga (394.6 ± 4.3 g) three times daily for 56 d. The results showed that Beluga fed 80% FSBM and FSBM + ML had lower growth and feed utilization. Moreover, Beluga-fed FSBM + ML performed poorer than those fed FSBM (P < 0.05). No interactions between fermented SBM and ML were observed in apparent digestibility coefficients (ADC) and body proximate composition except for ADC of crude lipid. ADC in Beluga fed 80% were less than other diets. Substitution of FSBM and FSBM + ML in diets significantly reduced dry matter, ash and crude lipid; Crude lipid increased in groups fed FSBM + ML (P < 0.05). FSBM and FSBM + ML in 60% had higher and lower total amino acids in muscle and feces (P < 0.05), respectively. Also, excreted total amino acids in feces increased with ML (P < 0.05). Generally, in Beluga, FSBM-containing diets showed better effects on growth, feed utilization, whole-body lipid, and muscle and fecal amino acids than those with FSBM + ML. Fermented SBM could be replaced up to 60%., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

Co-products from the ethanol industry, such as distillers dried grains with solubles (DDGS), can provide alternative protein sources for pet food. Corn fermented protein (CFP) is produced using postfermentation technology to split the protein and yeast from fiber prior to drying. This results in a higher protein ingredient compared to DDGS, increasing its appeal for pet food. In addition, the substantial yeast component, at approximately 20% to 25%, may promote gut health through modulation of the microbiome and the production of short-chain fatty acids. Therefore, the objective of this study was to determine the effect of CFP on the fecal microbiome of cats. The 4 experimental diets included a control with no yeast (T1) and diets containing either 3.5% brewer's dried yeast (T2), 2.5% brewer's dried yeast plus 17.5% DDGS (T3), or 17.5% CFP (T4). All diets except T1 were formulated to contain 3.5% yeast. Diets were fed to adult cats (n = 11) in an incomplete 4 × 4 replicated Latin square design. Cats were adapted to diet for 9 d followed by a 5-d total fecal collection. During each collection period, fresh fecal samples from each cat were collected and stored at -80 °C until analysis. Fresh fecal samples (n = 44) were analyzed by 16S rRNA gene sequencing. Raw sequences were processed through Mothur (v.1.44.1). Community diversity was evaluated in R (v4.0.3). Relative abundance was analyzed within the 50 most abundant operational taxonomic unitsusing a mixed model of SAS (v9.4, SAS Institute, Inc., Cary, NC). Diet was the fixed effect and cat and period were random effects. Results were considered significant at P < 0.05. Alpha-diversity indices (Observed, Chao1, Shannon, Simpson) and beta-diversity metric (principal coordinate analysis) were similar for all treatments. Predominant phyla were Firmicutes (66%), Bacteroidetes (25%), Actinobacteria (8%), Proteobacteria (0.64%), and Desulfobacteria (0.54%). The relative abundance of Firmicutes and Actinobacteria was lower (P < 0.05) for T3 compared to T4 and T2, respectively. On a more specific phylogenic level, 17 genera resulted in differences (P < 0.05) among dietary treatments. Overall, this data indicates that compared to traditional yeast and distillers dried grains, CFP did not alter the overall diversity of the fecal microbiome of healthy adult cats over a 14-d period., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science.)

Observed improvements in animal and sward performance, coupled with a desire for more sustainable pasture-based feeding systems, has triggered a surge in the implementation of more botanically diverse pastures. However, thus far, there has been limited research investigating the effects of botanically diverse sward types on enteric methane (CH4) or nitrogen (N) excretion, alongside the ruminal microbiota and fermentation profile, in sheep. Hence, this study investigates the effect of sward type on CH4 production and N excretion, in addition to assessing the rumen microbiome, volatile fatty acid proportions, and ammonia nitrogen (NH3-N) concentration in sheep. A 5 × 5 Latin square design experiment was implemented to investigate 5 dietary treatments; perennial ryegrass (Lolium perenne L.; PRG) only or PRG plus white clover (Trifolium repens L.; PRG + WC), red clover (Trifolium pratense L.; PRG + RC), chicory (Chicorium intybus L.; PRG + Chic) or plantain (Plantago lanceolata L.; PRG + Plan). Diets were mixed at a ratio of 75% PRG and 25% of the respective companion forage and 100% PRG for the PRG treatment, on a dry matter basis. Twenty castrated male sheep were housed in metabolism crates across 5 feeding periods. Methane measurements were acquired utilizing portable accumulation chambers. Rumen fluid was harvested using a transoesophageal sampling device. Microbial rumen DNA was extracted and subjected to 16S rRNA amplicon sequencing and fermentation analysis. Data were analyzed using PROC MIXED in SAS. Results show that animals consuming PRG + WC ranked lower for CH4 production (g/d) than sheep offered PRG, PRG + Chic or PRG + Plan (P < 0.01) while the addition of any companion forage ranked CH4 yield (g/kg dry matter intake (DMI)) lower (P < 0.001) than PRG. There was a moderate positive correlation between DMI and CH4 (g/d; r = 0.51). Ruminal NH3-N was lowest in animals consuming the PRG diet (P < 0.01). There was a greater abundance of Methanobrevibacter and reduced abundance of Methanosphaera (P < 0.001) in sheep offered PRG, compared with any binary sward. On average, herb diets (PRG + Chic or PRG + Plan) reduced the urinary nitrogen concentration of sheep by 34% in comparison to legume diets (PRG + WC or PRG + RC) and 13% relative to the PRG diet (P < 0.001). Sheep offered PRG + Chic had a greater dietary nitrogen use efficiency than PRG + RC (P < 0.05). This study demonstrates the potential for sward type to influence rumen function and the microbial community, along with CH4 and N output from sheep., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science.)

Fermented liquid feed (FLF) can improve dietary nutrient absorption levels, degrade antinutrient factors in diets, and increase beneficial bacteria abundance in animal guts. However, few systematic studies have been conducted on wheat-based fermented liquid feed (WFLF) in pigs. The present study evaluates the effects of WFLF on the growth performance, nutrient digestibility, gastric volume, intestinal morphology, intestinal health, intestinal barrier function, serum biochemical immunity, gut microbiota, and intestinal microbial diversity of grower-finisher pigs. In total, 80 weaned pigs were randomly allocated to two treatment groups based on their initial body weight: a basal diet with pellet dry feeding (CON) and a basal diet with WFLF, with four replicate pens per group. The experiment lasted 82 d. Compared with CON pigs, those fed WFLF were significantly heavier at 60 to 82 d and had significantly higher average daily feed intake, average daily gain, and gain: feed ratio at 60 to 82 d and 1 to 82 d. WFLF pigs had significantly greater jejunum, total tract, and ileal digestibility for all nutrients and amino acids, excluding arginine, than CON pigs. WFLF intake influenced villus height, villus height:crypt depth ratio of the anterior segment of the jejunum (A-jejunum), crypt depth, and redox potential of the posterior segment of the jejunum (P-jejunum) while significantly affecting body weight. Additionally, FLF improved gastric capacity significantly. Furthermore, mRNA expression of occludin and claudin-1 in the mucosa of the ileum and jejunum was significantly higher in WFLF pigs than in CON pigs. WFLF increased serum concentrations of alanine transaminase and reduced low-density lipoprotein cholesterol, total cholesterol, and total bile acid content. The alpha diversity (Shannon and Simpson indices) in the stomachs of WFLF pigs was significantly higher than in CON pigs. Microbial diversity in the stomach, ileum, and cecum, as well as the abundance of lactic acid bacteria, were increased in WFLF pigs compared to CON pigs. In conclusion, WFLF intake may positively influence intestinal ecology by improving digestive tract structure, upregulating intestinal barrier-related genes, and improving intestinal morphology to enhance intestinal digestive function and health. Collectively, the present study shows that WFLF intake can increase growth performance while maintaining beneficial nutrient digestibility in grower-finisher pigs., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

The study aimed to determine the effects of a postbiotic feeding program consisting of liquid and dry Saccharomyces cerevisiae fermentation product (SCFP) on ruminal fermentation, digestibility, and plasma metabolome of Holstein steers receiving a grain-based diet. Eight Holstein steers (body weight, BW, 467 ± 13.9 kg) equipped with rumen cannulas were used in a crossover design study, with 21 d per period and a 7-d washout period in between periods. Steers were stratified by initial BW and assigned to 1 of 2 treatments. The treatments were 1) Control, basal finishing diet only (CON); 2) SCFP, 1-d feeding of liquid SCFP (infused into the rumen via the cannula at 11 mL/100 kg BW) followed by daily feeding of dry SCFP (12 g/d, top-dressed). Feed and spot fecal samples were collected during days 17 to 20 for determination of digestibility and fecal excretion of N, P, Cu, and Zn. Digestibility was measured using acid-insoluble ash as an internal marker. Blood samples were collected on day 21 before the morning feeding. Rumen fluid samples were collected on days 0, 1, 2, 3, 5, and 21 via rumen cannula. Results were analyzed with the GLIMMIX procedure of SAS 9.4 (SAS, 2023). Treatment did not affect dry matter intake (P = 0.15) and digestibility (P ≥ 0.62). The fecal output and absorption of Zn, Cu, P, and N were not affected (P > 0.22) by treatment. On day 1, the liquid SCFP supplementation tended to reduce (P = 0.07) ruminal VFA concentration and increased (P < 0.01) the molar proportion of valerate. Feeding SCFP tended to increase total ruminal VFA on day 5 (P = 0.08) and significantly increased total VFA on day 21 (P = 0.05). Ruminal NH3-N was reduced (P = 0.02) on day 21 by supplementing SCFP. Treatment did not affect the production of proinflammatory cytokines, interleukin (IL)-1β (P > 0.19), and IL-6 (P > 0.12) in the whole blood in response to various toll-like receptor stimulants in vitro. Feeding SCFP enriched (P ≤ 0.05) plasma metabolic pathways, including citric acid cycle, pyrimidine metabolism, glycolysis/gluconeogenesis, retinol metabolism, and inositol phosphate metabolism pathways. In summary, supplementing liquid SCFP with subsequent dry SCFP enhanced ruminal total VFA production and reduced NH3-N concentration in the rumen. Furthermore, feeding SCFP enriched several important pathways in lipid, protein, and glucose metabolism, which may improve feed efficiency of energy and protein in Holstein steers., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

The study aimed to investigate the effect of supplementing polyclonal antibodies (PAP) of avian origin against the ruminal methanogens Methanobrevibacter gottschalkii Ho (PAP-Ho) and M. ruminantium M1 (PAP-M1) on ruminal fermentation profile and methane production in Angus crossbred cattle (13 steers and 1 heifer). The experiment was conducted using a randomized block design with a 3 × 2 + 1 factorial arrangement, replicated in 3 periods. The factors included proportions of PAP against Ho and M1 in the mixture (100:0, 50:50, and 0:100 Ho:M1) and level of each mixture (3- or 6-mL per d). Cattle in control treatment did not receive PAP supplementation. Ruminal fluid was collected from the animals on days 0, 14, and 21 of treatment to determine of ruminal fermentation profile and ex vivo methane production. There was no effect of level of inclusion on ex vivo methane production. Supplementation with PAP-M1, either alone or in combination with PAP-Ho, decreased ex vivo methane output compared to the control group. Furthermore, in vivo molar proportion of propionate tended to be greater with PAP-M1, alone or combined with PAP-Ho, when compared with the control group. The study concluded that polyclonal antibodies against ruminal methanogens have the potential to decrease enteric methane emissions in cattle. The research provided important insights into the potential use of PAP as a strategy for reducing greenhouse gas emissions from cattle. Further research is needed to confirm these findings and to determine the practicality and feasibility of using PAP., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

Understanding ruminal microbiota and diet-host breed interactions under forage feeding conditions is essential for optimizing rumen fermentation and improving feed efficiency in small ruminants. This study aimed to investigate the effects of different ratios of condensed tannin-rich Sericea lespedeza (SL; Lespedeza cuneata) in the diets on changes and interactions of ruminal microbiota and host species (i.e., sheep and goats). Katahdin sheep (n = 12) and Alpine goats (n = 12) at approximately 10 to 12 mo of age were blocked by body weight (BW = 30.3 and 25.5 kg, respectively) and randomly assigned to one of the 3 treatments. Diets contained 75% coarsely ground forage and 25% concentrate. The forages were 1) 100% alfalfa hay (AL), 2) 100% SL, and 3) 50% AL + 50% SL (ASL). In the present study, the diversity and composition of ruminal microbiota differed between sheep and goats fed similar diets. Based on the taxonomic analysis, there was a distinct clustering pattern (P < 0.05) for sheep by diets, but such a pattern was not observed for goats (P > 0.1). The most predominant phyla were Firmicutes, Bacteroidetes, Ascomycota, and methanogen species of Methanobrevibactor sp. in the rumen of sheep and goats, regardless of diets. The Bacteroidetes and Ascomycota were enriched in sheep fed AL and ASL. In contrast, these microbial phyla were enhanced in goats fed tannin-rich SL diets, with the diet-by-host species interaction (P < 0.02) for the Bacteroidetes phylum. Sheep rumen fluid samples showed a higher degree of variability in microbial community composition compared to goat rumen fluid samples. The relative proportion of the Aspergillus fungi population was reduced to 90.7% in the SL group compared with the AL group, regardless of host species. The antimicrobial activity of tannins and greater sensitivities of selected microbiota species to these tannin compounds during SL feeding in sheep and goats perhaps caused this difference. The results from this study suggest that differences in the microbiota were associated with differences in diets and host species. Therefore, this study provides a better understanding of ruminal microbiota and diet-host species interactions under various tannin-rich diets, which could advance consolidative information on rumen microbiome community diversity changes and may improve sheep and goat production., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

This experiment was conducted to evaluate the effects of including a mixed-dimensional attapulgite clay (MDA) into a naturally moldly diet for Hu lambs. Fifty male Hu lambs with similar initial body weight (28.24 ± 1.80 kg) were randomly allocated into five dietary treatments: a basal diet containing naturally occurring mycotoxins with 0, 0.5, 1.0, and 2.0 kg/t MDA, and basal diet with a commercial mycotoxin adsorbent Solis with montmorillonite as the major component at 1 kg/t. Both MDA and Solis increased average daily gain (ADG) and dry matter intake (DMI; P ≤ 0.004), and there was no difference in growth performance between MDA and Solis (P ≥ 0.26). The final body weight, DMI, and ADG were linearly increased with increasing MDA supplementation (P < 0.01). Lambs treated with both MDA and Solis demonstrated greater apparent digestibility of dry matter (DM), organic matter (OM), and energy compared with the control group (P ≤ 0.03), and there were no differences in nutrient digestibilities between MDA and Solis (P ≥ 0.38). Digestibility of CP was linearly increased with the increasing MDA supplementation (P = 0.01). Neither MDA nor Solis affected rumen total volatile fatty acid (TVFA) concentration (P ≥ 0.39), but decreased the acetate-to-propionate ratio and molar proportion of n-butyrate (P ≤ 0.01), and MDA also increased the concentration of ammonia (P = 0.003). Besides, increasing MDA supplementation linearly reduced the acetate-to-propionate ratio and molar proportion of n-butyrate (P = 0.01), but linearly and quadratically increased the concentration of ammonia (P ≥ 0.003). These results showed that the incorporation of MDA into a naturally moldy diet of Hu lambs yielded comparable results to the Solis product, with higher growth performance and nutrient digestibility but lower acetate-to-propionate ratio observed. In conclusion, including ≥ 1 kg/t of MDA in high mycotoxin risk diets for growing lambs improves feed intake and rumen fermentation., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

Soybeans can provide ruminally degradable protein, lipid, and metabolizable amino acid (AA) to lactating dairy cows; however, soy-based trypsin inhibitors can limit protein digestion in nonruminants. Eight ruminally cannulated lactating Holstein cows were used to evaluate the impacts of soy-based trypsin inhibitors on nutrient disappearance, lactation, and plasma AA bioavailability. Treatments were abomasal infusion of 0 or 400 g/d casein or a crystalline AA analog of casein with unroasted or roasted soybeans fed at 10% dry matter (DM). Data were analyzed using the MIXED procedure of SAS. Measures of digestion were determined from fecal output determined with acid detergent insoluble ash and urine output determined from measures of urine creatinine. Neither soybean processing (P ≥ 0.20) nor the source of abomasal infusion (P ≥ 0.60) impacted nutrient digestibility. Ruminal ammonia, isobutyrate, and isovalerate were increased (P ≤ 0.01) among cattle consuming unroasted soybeans. Source of infusion did not affect (P ≥ 0.38) ruminal volatile fatty acids or nitrogen metabolism. Ruminal N metabolism was largely unaffected by soybean processing although microbial N efficiency was greater (P < 0.01) among cows fed unroasted soybeans. DM intake and energy-corrected milk were greater (P < 0.01) in cows fed roasted compared to unroasted soybeans. The proportion of fat, protein, lactose, and solids not fat (SNF) in milk did not differ between soybean processing or postruminal AA source, but fat, protein, lactose, and SNF yield was greater (P ≤ 0.01) when cows were fed roasted soybeans because milk yields were greater when cows were fed roasted vs. unroasted soybeans. As expected, infusion of casein or its crystalline AA analog increased plasma essential AA and milk urea nitrogen concentration. The rate of increase in essential AA concentration in plasma was 2.9× greater for casein than for crystalline AA. These data seem to indicate that soy-based trypsin inhibitors have no impacts on postruminal AA bioavailability when fed to cows and that metabolizable protein from casein is greater than from crystalline AA., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)

Pelleted total mixed ration (P-TMR) feeding, which has become a common practice in providing nutrition for fattening sheep, requires careful consideration of the balance between forage neutral detergent fiber (FNDF) and rumen degradable starch (RDS) to maintain proper rumen functions. The present study aimed to investigate the effects of the dietary FNDF/RDS ratio (FRR) on chewing activity, ruminal fermentation, ruminal microbes, and nutrient digestibility in Hu sheep fed a P-TMR diet. This study utilized eight ruminally cannulated male Hu sheep, following a 4 × 4 Latin square design with 31 d each period. Diets consisted of four FRR levels: 1.0 (high FNDF/RDS ratio, HFRR), 0.8 (middle high FNDF/RDS ratio, MHFRR), 0.6 (middle low FNDF/RDS ratio, MLFRR), and 0.4 (low FNDF/RDS ratio, LFRR). Reducing the dietary FRR levels resulted in a linear decrease in ruminal minimum pH and mean pH, while linearly increasing the duration and area of pH below 5.8 and 5.6, as well as the acidosis index. Sheep in the HFRR and MHFRR groups did not experience subacute ruminal acidosis (SARA), whereas sheep in another two groups did. The concentration of total volatile fatty acid and the molar ratios of propionate and valerate, as well as the concentrate of lactate in the rumen linearly increased with reducing dietary FRR, while the molar ratio of acetate and acetate to propionate ratio linearly decreased. The degradability of NDF and ADF for alfalfa hay has a quadratic response with reducing the dietary FRR. The apparent digestibility of dry matter, organic matter, neutral detergent fiber, and acid detergent fiber linearly decreased when the dietary FRR was reduced. In addition, reducing the dietary FRR caused a linear decrease in OTUs, Chao1, and Ace index of ruminal microflora. Reducing FRR in the diet increased the percentage of reads assigned as Firmicutes, but it decreased the percentage of reads assigned as Bacteroidetes in the rumen. At genus level, the percentage of reads assigned as Prevotella, Ruminococcus, Succinivibrio, and Butyrivibrio linearly decreased when the dietary FRR was reduced. The results of this study demonstrate that the dietary FRR of 0.8 is crucial in preventing the onset of SARA and promotes an enhanced richness of ruminal microbes and also improves fiber digestibility, which is a recommended dietary FRR reference when formulating P-TMR diets for sheep., (© The Author(s) 2024. Published by Oxford University Press on behalf of the American Society of Animal Science. All rights reserved. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.)