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Reduction in dietary crude protein and addition of fiber could mitigate the incidence and severity of post-weaning diarrhea, a common gastrointestinal condition in newly weaned pigs. Therefore, 360 weanling pigs, initially 5.0 ± 0.10 kg, were used to evaluate the effects of crude protein (CP) level and fiber source on growth performance and fecal microbial communities. At weaning, pigs were randomly assigned to pens and allotted to 1 of 8 dietary treatments in a 2 × 4 factorial with main effects of CP (21 or 18%) and fiber source (none, coarse wheat bran, oat hulls, or cellulose). There were 5 pigs per pen and 9 pens per treatment. Experimental diets were formulated in two dietary phases from d 0 to 10 and 10 to 24, with a common post-treatment diet fed from 24 to 45. The 21% CP diets contained 1.40% standardized ileal digestible (SID) Lys in phase 1 and 1.35% SID Lys in phase 2. By using a maximum SID Lys:digestible CP ratio of 6.35%, the 18% CP diets contained 1.25% SID Lys in both phases. Diets containing a fiber source were formulated to the level of insoluble fiber provided by 4% coarse wheat bran, resulting in the addition of 1.85% oat hulls and 1.55% cellulose. No fiber source × CP level interactions (P > 0.05) were observed. Decreasing CP (and subsequently SID lysine) decreased (P = 0.05) ADG and G:F during the experimental period. From d 0 to 45, ADG decreased (P = 0.05) for pigs fed 18% CP diets compared to pigs fed 21% CP. No effect of fiber source was observed for growth performance. Fecal DM on d 17 increased (P < 0.001) for pigs fed 18% CP diets compared to pigs fed 21% CP diets. Pigs fed diets with added cellulose had increased (P < 0.05) fecal dry matter during the experimental period compared to pigs fed no fiber source or wheat bran. Bacterial community structure was investigated by sequencing the V4 region of the 16S rRNA gene. Analysis indicated a significant difference between CP content at d 24 (P = 0.023) using a Weighted UniFrac distance matrix. Further investigation identified five differential Amplicon Sequence Variants associated with CP content at d 24. In conclusion, reducing crude protein (and subsequently SID Lys) decreased growth performance but increased fecal dry matter content. The source of dietary fiber in nursery diets had no impact on growth performance; but pigs fed added cellulose had increased fecal DM compared with other treatments. Microbial analysis identified differential taxa associated with CP content.

Dietary fibers can influence a dog’s overall health, but high concentrations of soluble dietary fibers can cause soft stools. An in vitro model could be useful to predict the rate fibers are fermented once they reach the colon. Pet food companies are constantly searching for new ingredients to differentiate their products from competitors. Miscanthus grass (MG), pea fiber (PF), and sorghum bran (SB) are novel fiber sources that could be alternatives to standards like cellulose (CE) and beet pulp (BP). The objectives of the study were to determine the effects of fiber source on organic matter disappearance (OMD), estimated organic matter disappearance (EOMD), and fermentation end-product concentrations using an in vitro fermentation procedure and dog fecal inoculum. Total dietary fiber (TDF) residues from MG, CE, BP, PF, and SB were fermented in vitro with buffered dog feces. Fecal samples were collected and maintained in anaerobic conditions until the dilution and inoculation. Test tubes containing the fibrous substrates were incubated for 4, 8, and 12 h at 39 °C. Short-chain fatty acids (SCFA), branched-chain fatty acids (BCFA), OMD, and EOMD were determined for each fiber source and time point. Beet pulp had the highest OMD, EOMD, and SCFA production of all tested fiber sources (38.6% OMD, 26.2% EOMD, 2.72 mmol SCFA/g of substrate). Sorghum bran led to greater concentrations of BCFA (59.86 µmol/g of substrate) and intermediate OMD and EOMD compared to the other tested fibers. Cellulose and MG were poorly fermented with the lowest OMD, EOMD, SCFA, and BCFA compared to other fibers. In conclusion, MG could be used as an insoluble minimally fermentable replacement fiber for CE in dog foods.

Phytase is added to swine diets to improve the utilization of phytate-bound P in swine diets. This provides financial and environmental benefits to the pig industry. However, it is unclear if phytase works equally well in all dietary circumstances. The objective of this experiment was to determine if insoluble fiber affects the efficacy of the phytase enzyme in nursery pigs when fed diets limiting in P content. A total of 480 pigs (initial BW 5.48 ± 0.14 kg) were blocked by BW and randomly assigned (10 pigs per pen) to treatment within the block. A common nutrient-adequate diet was fed from days −14 to −5, and two basal P deficient diets (either a corn-soy diet containing 0.16% standardized total tract digestible [STTD] P [low insoluble fiber [LF]], or a corn-soybean meal plus 20% corn bran containing 0.14% STTD P [high insoluble fiber [HF]]) were fed from days −5 to 0 to acclimate pigs to a P deficient diet. From days 0 to 21, pigs received eight dietary treatments (six pens per treatment: n = 6). Experimental diets consisted of LF supplemented with one of four levels of added phytase (0, 109, 218, and 327 phytase units [FTU]/kg; Quantum Blue 5 G, AB Vista, Wiltshire, United Kingdom) expected to provide 0.16, 0.21, 0.26, and 0.31% STTD P, respectively, or HF supplemented with one of the same four levels of added phytase expected to provide 0.14, 0.19, 0.24, and 0.29% STTD P. Titanium dioxide was added to the diet at 0.4% as an indigestible marker. On day 21, one pig representing the average BW for each pen was euthanized, and fibulae were collected and analyzed for bone ash. Fecal samples were collected from each pen on days 19–20. Data were analyzed using PROC MIXED of SAS. There were no interactions between insoluble fiber and phytase for any of the variables evaluated. For days 0–21, adding phytase increased ADG (P < 0.001) with the response being linear (P < 0.001), whereas insoluble fiber decreased ADG (P = 0.033). There were no effects of phytase or insoluble fiber on ADFI (P = 0.381 and P = 0.632, respectively). Phytase improved G:F ratio (P < 0.001) with the response being linear (P < 0.001). Insoluble fiber tended to decrease G:F ratio (P = 0.097). Phytase increased bone ash (P = 0.005) with the response being linear (P = 0.001), but there was no effect of insoluble fiber (P = 0.949). Phytase did not affect the apparent total tract digestibility of DM, NDF, or ADF (P > 0.050), whereas insoluble fiber decreased the ATTD of DM (P < 0.001), NDF (P < 0.001), and ADF (P < 0.001). In conclusion, the addition of insoluble fiber did not affect the ability of phytase to improve growth performance and bone mineralization in nursery pigs fed a P deficient diet.

In theory, supplementing xylanase in corn-based swine diets should improve nutrient and energy digestibility and fiber fermentability, but its efficacy is inconsistent. The experimental objective was to investigate the impact of xylanase on energy and nutrient digestibility, digesta viscosity, and fermentation when pigs are fed a diet high in insoluble fiber (>20% neutral detergent fiber; NDF) and given a 46-d dietary adaptation period. A total of 3 replicates of 20 growing gilts were blocked by initial body weight, individually housed, and assigned to 1 of 4 dietary treatments: a low-fiber control (LF) with 7.5% NDF, a 30% corn bran high-fiber control (HF; 21.9% NDF), HF + 100 mg xylanase/kg (HF + XY [Econase XT 25P; AB Vista, Marlborough, UK]) providing 16,000 birch xylan units/kg; and HF + 50 mg arabinoxylan-oligosaccharide (AXOS) product/kg (HF + AX [XOS 35A; Shandong Longlive Biotechnology, Shandong, China]) providing AXOS with 3–7 degrees of polymerization. Gilts were allowed ad libitum access to fed for 36-d. On d 36, pigs were housed in metabolism crates for a 10-d period, limit fed, and feces were collected. On d 46, pigs were euthanized and ileal, cecal, and colonic digesta were collected. Data were analyzed as a linear mixed model with block and replication as random effects, and treatment as a fixed effect. Compared with LF, HF reduced the apparent ileal digestibility (AID), apparent cecal digestibility (ACED), apparent colonic digestibility (ACOD), and apparent total tract digestibility (ATTD) of dry matter (DM), gross energy (GE), crude protein (CP), acid detergent fiber (ADF), NDF, and hemicellulose (P < 0.01). Relative to HF, HF + XY improved the AID of GE, CP, and NDF (P < 0.05), and improved the ACED, ACOD, and ATTD of DM, GE, CP, NDF, ADF, and hemicellulose (P < 0.05). Among treatments, pigs fed HF had increased hindgut DM disappearance (P = 0.031). Relative to HF, HF + XY improved cecal disappearance of DM (162 vs. 98 g; P = 0.008) and NDF (44 vs. 13 g; P < 0.01). Pigs fed xylanase had a greater proportion of acetate in cecal digesta and butyrate in colonic digesta among treatments (P < 0.05). Compared with LF, HF increased ileal, cecal, and colonic viscosity, but HF + XY decreased ileal viscosity compared with HF (P < 0.001). In conclusion, increased insoluble corn-based fiber decreases digestibility, reduces cecal fermentation, and increases digesta viscosity, but supplementing xylanase partially mitigated that effect.

Two experiments were conducted to determine the effects of crude protein (CP) level in diets containing coarse wheat bran (CWB) with or without pharmacological levels of Zn (provided by zinc oxide: ZnO) on growth performance and fecal DM of nursery pigs. In experiment 1, 360 barrows (Line 200 × 400, DNA, Columbus, NE, initially 5.6 kg) were allotted to 1 of 6 dietary treatments from d 0 to 21 after weaning with 5 pigs per pen and 12 pens per treatment. Treatments included a positive control diet (21% CP) with 3,000 mg/kg Zn in phase 1 and 2,000 mg/kg in phase 2; negative control (21% CP) with 110 mg/kg added Zn, and 4 diets containing 4% CWB and 110 mg/kg added Zn formulated to contain 21%, 19.5%, 18%, or 16.5% CP. The 2 control diets and 21% CP CWB diet contained 1.40% standardized ileal digestible (SID) Lys in phase 1 and 1.35% SID Lys in phase 2, while the 19.5%, 18%, and 16.5% CP diets contained 1.33, 1.25 and 1.20% Lys, respectively, in both phases. Pigs fed the positive control diet containing pharmacological ZnO had increased (P < 0.05) ADG and G:F compared with the negative control and the 21% CP CWB diet. Reducing CP (concurrently with SID Lys) in diets containing CWB decreased ADG and G:F (linear, P = 0.002); however, fecal DM increased (linear, P = 0.005). In experiment 2, two groups of 300 and 350 pigs, initially 7.0 and 6.2 kg, respectively, were used with 5 pigs per pen and 26 pens per treatment. The objective was to determine if adding back essential AA would improve growth performance of pigs fed the low CP diets. All dietary treatments were fed for 13 days, contained 4% CWB, and consisted of: (1) positive control with 2,000 mg/kg of Zn and 21% CP (1.35% SID Lys); (2) no ZnO and 21% CP; and 3 diets with no ZnO formulated to 18% CP and (3) 1.2% SID Lys; (4) 1.35% SID Lys by the addition of feed grade amino acids (AA), and (5) diet 4 with non-essential amino acids (NEAA; Gly and Glu). Pigs fed 21% CP with ZnO had increased (P = 0.001) ADG compared to those fed 18% CP (1.35% SID Lys) with high levels of feed grade amino acids or those fed the reduced SID Lys (1.2%) diet. Overall, G:F was improved (P < 0.001) for pigs fed 21% CP diets and those fed the 18% CP diet with NEAA compared to pigs fed 1.2% SID Lys and pigs fed high levels of feed grade amino acids. Fecal DM was increased for pigs fed the reduced SID Lys diet. In summary, pharmacological levels of Zn improve pig growth performance, but reducing CP (and subsequently SID Lys) decreased nursery pig growth performance.

Three experiments (exp.) were conducted to determine and compare the digestibility of nutrients and energy of corn distillers dried grains with solubles (DDGS) from the United States (USDDGS), a dried mixture of corn bran with solubles (CBS) from Brazil (BRCBS), and high protein corn distillers dried grains (HP-DDG) from the United States (USHPDG) and Brazil (BRHPDG) in growing pigs. The feed ingredients were evaluated for apparent total tract digestibility (ATTD) of gross energy (GE), dry matter (DM), crude protein (CP), ether extract, neutral and acid detergent fiber (NDF and ADF, respectively), and digestible and metabolizable energy (DE and ME, respectively) using the total collection and index methods in exp. 1; ATTD and standardized total tract digestibility (STTD) of phosphorus (P) in exp. 2; and apparent (AID) and standardized (SID) ileal digestibilities of CP and amino acids (AA) in exp. 3. Fifty crossbred barrows (32.4 ± 6.9, 38.3 ± 5.2, and 46.2 ± 5.3 kg body weight [BW], in exp. 1, 2, and 3, respectively) were fed a corn basal diet in exp. 1, a P-free diet in exp. 2, and an N-free diet in exp. 3 or diets with 40% inclusion of test ingredients to provide 10 replications per treatment. Pigs were housed individually in metabolism cages (exp. 1) or in pens (exp. 2 and 3) and fed at 2.8 times the maintenance DE requirement (110 kcal/kg BW0.75) based on their BW at the beginning of each experiment. Except for ATTD of NDF, which tended (P = 0.058) to be greater by the index method compared with the total collection method, no difference between the total collection and index methods was observed for ATTD of remaining nutrients and DE. The ATTD of DM, GE, NDF, and DE content of BRHPDG were greater (P < 0.001) than USHPDG, BRCBS, and USDDGS. The AID of CP, Arg, His, Ile, Leu, Lys, Thr, and Val and the SID of His, Leu, Lys, and Val of BRHPDG were 8% to 36% greater (P < 0.05) than those from USHPDG. Except for Trp, all AID and SID AA values were greater (P < 0.05) in BRHPDG than in USHPDG. The ATTD of DM, GE, NDF, and ADF; DE and ME content; AID of CP, Arg, Ile, Leu, Phe, Thr, and Trp; and SID of CP, Arg, Phe, and Thr of USDDGS were 9% to 45% greater (P < 0.05) than those in BRCBS. The ATTD and the STTD of P in USHPDG and USDDGS were 26% to 42% greater (P < 0.05) compared with BRHPDG and BRCBS. In conclusion, BRHPDG had a greater digestibility of energy and most of the AA than USHPDG, while the BRCBS evaluated had lower nutritional value than the USDDGS source.

The objective of this study was to evaluate the effects of different defatted rice bran (DFRB) sources and processing technologies on nutrient digestibility in different intestinal segments of pigs. Nine barrows with T-cannula in the distal ileum were randomly allotted to nine different sources in which oil was pressed extracted for seven sources and was solvent extracted for two sources. The experiment contained 6 periods of 12 d, including 8 d for diet adaptation, 2 d for fecal collection, and 2 d for digesta collection. The apparent ileal digestibility (AID) of dry matter (DM), ash, total dietary fiber (TDF), insoluble dietary fiber (IDF), neutral detergent fiber (NDF), acid detergent fiber (ADF), and hemicellulose in different sources of DFRB was quite variable. There were no differences in the AID of dietary gross energy (GE), organic matter (OM), ether extract (EE), crude protein (CP), and soluble dietary fiber (SDF) between different sources of DFRB. There were no differences in the AID of dietary EE, TDF, IDF, and hemicellulose between different processing technologies. Pressed DFRBs have greater (P < 0.05) average AID of dietary GE, DM, ash, OM, CP, SDF, and NDF and lower (P < 0.01) ADF compared with solvent-extracted DFRBs. The apparent total tract digestibility (ATTD) of most of the dietary nutrients, except for the ATTD of dietary EE, SDF, and hemicellulose, significantly varied in different sources of DFRB (P < 0.05). In addition, pressed DFRB had greater (P < 0.05) ATTD of dietary SDF, NDF, ADF, and hemicellulose compared with solvent-extracted DFRB. The apparent hindgut digestibility (AHD) of dietary DM, SDF, NDF, and ADF significantly varied (P

Cotton byproducts can be an economical source of protein, fat, and fiber in cattle finishing diets. The objectives of this study were 1) to assess the effects of including whole cottonseed (WCS) and cotton gin trash (CGT) in finishing diets on in situ ruminal degradability and 2) to determine the effects of including cotton byproducts in a finishing diet on rumen fluid pH, lactate, and volatile fatty acid concentrations. Six ruminally cannulated steers were used in a crossover design. Treatments included a control diet (CON; 7% prairie hay [PH], 15% Sweet Bran, 67.25% rolled corn, and 5% liquid supplement) and a cotton byproduct diet (CTN; 7% CGT, 15% WCS, 72.25% rolled corn, and 5% water). Both diets included 0.75% urea and 5% dry supplement. In situ bags containing individual diet ingredients and whole diet samples were incubated in the rumen for up to 96 h. Rumen fluid samples were collected over a 24-h period. No treatment × substrate interactions were detected for any fraction of dry matter (DM) or organic matter (OM) degradability for individual ingredients or whole diets (P ≥ 0.14). The A, B, and C fractions, disappearance rate (Kd), and effective degradability of DM and OM differed between diet ingredients (P ≤ 0.04) but were not different between CON and CTN substrates (P ≥ 0.25). A treatment × substrate interaction (P = 0.04) was detected for the effective degradability of neutral detergent fiber (NDF) of CGT and PH but there was no interaction for other fractions (P ≥ 0.27). The A fraction of NDF was greater (P < 0.001) for CGT than PH; however, the B fraction of NDF tended to be greater (P = 0.08) for PH than CGT. No differences (P ≥ 0.37) were detected for the % NDF disappearance at 48 h between CON and CTN substrates. A tendency for a treatment × substrate interaction (P = 0.10) was observed for the effective degradability of starch among diets; however, when the CON substrate was incubated in steers consuming the CON diet, effective degradability of starch was not different (P = 0.84) from when the CTN diet was incubated in steers consuming the CTN diet. There was no treatment × time interaction or treatment effect for rumen pH; however, there was a time effect (P = 0.03). Steers consuming the CTN diet had greater molar proportions of acetate and decreased molar proportions of propionate compared with CON steers (P < 0.01). This experiment suggests that there are minimal differences between the digestibility of finishing diets containing cotton byproducts and those comprised of traditional finishing diet ingredients.

The experimental objective was to investigate the impact of xylanase on the bioavailability of energy, oxidative status, and gut function of growing pigs fed a diet high in insoluble fiber and given a longer adaptation time than typically reported. Three replicates of 20 gilts with an initial body weight (BW) of 25.43 ± 0.88 kg were blocked by BW, individually housed, and randomly assigned to one of four dietary treatments: a low-fiber control (LF) with 7.5% neutral detergent fiber (NDF), a 30% corn bran without solubles high-fiber control (HF; 21.9% NDF), HF + 100 mg/kg xylanase (HF + XY; Econase XT 25P), and HF + 50 mg/kg arabinoxylan-oligosaccharide (HF + AX). Gilts were fed ad libitum for 36 d across two dietary phases. Pigs and feeders were weighed on days 0, 14, 27, and 36. On day 36, pigs were housed in metabolism crates for a 10-d period, limit fed (80% of average ad libitum intake), and feces and urine were collected the last 72 h to determine the digestible energy (DE) and metabolizable energy (ME). On day 46, serum and ileal and colonic tissue were collected. Data were analyzed as a linear mixed model with block and replication as random effects, and treatment, time, and treatment × time as fixed effects. There was a significant treatment × time interaction for BW, average daily gain (ADG), and gain to feed (G:F; P < 0.001). By design, BW at day 0 did not differ; at day 14, pigs fed LF were 3.5% heavier, and pigs fed HF + XY, when compared with HF, were 4% and 4.2% heavier at days 27 and 36, respectively (P < 0.001). From day 14 to 27 and day 27 to 36, when compared with HF, HF + XY improved ADG by 12.4% and 10.7% and G:F by 13.8% and 8.8%, respectively (P < 0.05). Compared with LF, HF decreased DE and ME by 0.51 and 0.42 Mcal/kg, respectively, but xylanase partially mitigated that effect by increasing DE and ME by 0.15 and 0.12 Mcal/kg, over HF, respectively (P < 0.05). Pigs fed HF + XY had increased total antioxidant capacity in the serum and ileum (P < 0.05) and tended to have less circulating malondialdehyde (P = 0.098). Pigs fed LF had increased ileal villus height, and HF + XY and HF + AX had shallower intestinal crypts (P < 0.001). Pigs fed HF + XY had increased ileal messenger ribonucleic acid abundance of claudin 4 and occludin (P < 0.05). Xylanase, but not AX, improved the growth performance of pigs fed insoluble corn-based fiber. This was likely a result of the observed increase in ME, improved antioxidant capacity, and enhanced gut barrier integrity, but it may require increased adaptation time to elicit this response.

Two experiments were conducted to estimate standardized mineral (Ca, P, Cu, Fe, Mn, and Zn) availabilities (SMA) in commonly used feedstuffs and verify the additivity of SMA for diet formulation of broilers. In Exp. 1, after 3 d of acclimation, a total of 96 22-d-old Arbor Acres male broilers were fasted for 24 h. Then the broilers were fed a mineral-free, corn, soybean meal (SBM), or corn-soybean meal (C-SBM) diet for 4 h and the excreta samples were collected for 48 h after feed withdrawal (totally 52 h). The results showed that the endogenous losses of Ca, P, Cu, Fe, Mn, and Zn for chickens fed the mineral-free diet were 13.7, 113, 0.064, 0.593, 0.094, and 0.132 mg/52 h per bird, respectively. The standardized availability values of Ca, P, Cu, Fe, Mn, and Zn were 20.8%, 39.6%, 37.8%, 47.4%, 10.7%, and 45.2% in corn as well as 54.3%, 51.1%, 39.7%, 27.6%, 26.1%, and 51.0% in SBM, respectively. The determined values of SMA in C-SBM diet were close (P > 0.09) to the predicted summations of SMA from corn and SBM (Ca, 48.6% vs. 48.1%; P, 44.9% vs. 46.0%; Cu, 41.7% vs. 39.1%; Fe, 35.3% vs. 33.2%; Mn, 22.7% vs. 22.2%; Zn, 46.2% vs. 48.4%). In Exp. 2, a total of 144 22-d-old Arbor Acres male broilers were used to estimate the SMA values in 6 feedstuffs by using the above procedure. The results showed that the standardized availability values in wheat, wheat bran, corn distillers dried grains with solubles, cottonseed meal, rapeseed meal, and corn gluten meal diets were 24.7% to 55.8% for Ca, 35.6% to 46.6% for P, 24.5% to 45.7% for Cu, 21.6% to 43.5% for Fe, 9.3% to 34.5% for Mn, and 22.9% to 52.9% for Zn, respectively. The results from the present study indicated that the mineral-free diet could be used for estimating the endogenous losses of the above minerals and SMA values of feedstuffs for broilers, and the estimates of SMA in feedstuffs for the C-SBM diet formulation were additive.

The aim of this study was to investigate the growth performance and nutrient utilization responses of broiler chickens and the nutrient utilization of pigs to xylanase, experimental diet formulation method for energy (FME), and digestibility index marker (DIM). In Exp. 1, a total of 448 male broiler chickens were used in a randomized complete block design with body weight (BW) as a blocking factor. Seven dietary treatments were prepared in a 3 × 2 + 1 factorial arrangement with inclusion of sand, diatomaceous earth (DAE), or wheat bran (WB) as FME and without or with xylanase (26,400 units/kg of diet) plus positive control. Each of chromic oxide and titanium dioxide was incorporated at 5 g/kg in diets. There were eight replicate cages of eight birds per cage. Birds were weighed on d 7, 14, and 21, and feed intake was recorded. Excreta samples were collected from d 19 to 21. On d 21, birds were euthanized, and ileal digesta samples were collected. In Exp. 2, twenty-one barrows (initial BW = 33.0 ± 0.3 kg), fitted with simple T-cannulas at the distal ileum, were used in a triplicate 7 × 2 incomplete Latin Square design with seven dietary treatments, which were prepared by the same arrangement as in broiler chickens, and two periods giving six replicates per diet. Fecal samples were collected on d 4 and 5, and ileal digesta samples were collected on d 6 and 7 of each period. In Exp. 1, the growth performance of birds was not affected by xylanase. There were interactions (P < 0.05) between xylanase and FME for apparent ileal digestibility (AID) of crude protein, His, Met, Thr, and Trp. Inclusion of xylanase decreased (P < 0.05) the AID of crude protein and Trp in sand diet and AID of His and Thr in DAE diet, but increased (P < 0.05) AID of Met in WB diet. The AID of energy and nutrients except Arg and Met were greater (P < 0.05) observed with Cr than Ti as DIM. In Exp. 2, there were interactions (P < 0.05) between xylanase and FME for AID of dry matter, energy, Arg, and Lys. Inclusion of xylanase decreased (P < 0.05) the AID of Lys in DAE or WB diet, but increased (P < 0.05) AID of Arg in sand diet and AID of energy in WB diet. The DIM type had no effect on responses in pigs. In conclusion, the efficacy of xylanase on ileal energy and amino acids digestibility depends on the choice of FME in broiler chickens and pigs, and DIM affects the determination of ileal digestibility in broiler chickens.

The study was conducted to determine the effects of multicarbohydrase (MC) preparation (700 U α-galactosidase, 2,200 U galactomannanase, 3,000 U xylanase, and 22,000 U β-glucanase per kg of diet) and phytase (Phy, 500 FTU per kg of diet) supplementation on the nutritive value of wheat bran (WB) in broiler chicks. Trial 1 determined retention of nutrients and apparent metabolizable energy corrected by nitrogen (AMEn). One reference diet (RD) protein-free (85% corn based) was fortified to determine the WB nutrient retention coefficient. Trial 2 determined standardized ileal digestibility (SID) of AA, when pancreas and liver were weighed. An additional group of bird was fed with an RD with 5% casein-corn starch diet, fortified with vitamins and minerals to quantify the endogenous fraction and determine SID of AA. For each trial, the test diets were made by mixing RD and WB 7:3 (wt/wt) and fed without or with MC or Phy or combination. Male broilers (Cobb 500), 245 d old, were allocated to five treatments to give seven replicates (seven birds/cage). The birds were fed a commercial diet from day 0 to10 followed by Trial 1 diets from day 11 to 18 and finally Trial 2 diets from day 19 to 21. Excreta samples were collected on days 15-18 and all birds were slaughtered on day 21 for ileal digesta. There was an interaction (P < 0.05) between MC and Phy on retention of DM, N, P, and AMEn. An interaction (P < 0.05) was also observed on SID of Arg, His, Leu, Lys, Phe, Thr, Val, Asp, Cys, Glu, and Ser. Responses of MC plus Phy supplementation were higher (P < 0.05) on overall SID of AA by 6.05% (75.18 to 94.26%), compared with responses for MC (2.35%; 72.04 to 88.97) or Phy (3.46%; 73.27 to 92.13). Liver and pancreas weights were affected (P < 0.05) by the single MC supplementation. The MC and Phy combination may be an effective strategy to improve AA utilization of WB in broiler chickens.

The objective of this experiment was to determine the effects of increased fiber content in diets on heat production (HP) and NE:ME ratio and to determine the NE content and NE:ME ratio of full-fat rice bran (FFRB), defatted rice bran (DFRB), corn gluten feed (CGF), and corn germ meal (CGM) fed to growing barrows using indirect calorimetry (IC). Thirty growing barrows (28.5 ± 2.4 kg BW) were allotted in a completely randomized design to 5 dietary treatments that included a corn–soybean meal basal diet and 4 experimental diets with a constant ratio of corn and soybean meal (difference method) containing 30% FFRB, DFRB, CGF, and CGF. Pigs were housed in individual metabolism crates for 20 d including 14-d adaptation to the diet and 6 d to determine the HP and total collection of feces and urine in respiration chambers. Pigs were fed their respective diets at 550 kcal ME·kg BW(0.60−1)·d(−1) on the basis of BW measured on days 0, 7, and 14. The apparent total tract digestibility (ATTD) of DM, GE, and OM were greater (P < 0.01) in pigs fed the basal diet. The ATTD of DM, GE, and OM in pigs fed the DFRB diet were lesser (P < 0.01) when compared with those fed the basal and FFRB diets. The ATTD of ether extract (EE) in pigs fed the FFRB diet was greater (P < 0.01) compared with those fed basal, DFRB, CGF, and CGM diets. The HP adjusted for the same ME intake was greater (P < 0.01) in pigs fed the DFRB, CGF, and CGM diets compared with those fed basal and FFRB diets. The NE:ME ratio in pigs fed the FFRB diet was greater (P < 0.01) when compared with those fed the DFRB, CGF, and CGM diets. The NE content of FFRB, DFRB, CGF, and CGM determined using the IC method were 2,952, 1,100, 1,747, and 2,079 kcal/kg DM, respectively. The NE content of FFRB, CGF, and CGM determined using the IC method were 3.5%, 3.8%, and 1.8% greater, respectively, than the predicted values, whereas NE content of DFRB determined using the IC method was 2.1% lower than the predicted values. In conclusion, pigs fed the fiber-rich ingredients had greater HP and lower nutrient digestibility. However, pigs fed FFRB diets containing greater fat content had a lower heat increment and, therefore, higher utilization efficiency. The NE:ME ratio ranged from 71.6% to 82.4%. The NE of FFRB, DFRB, CGF, and CGM determined using the IC method were 2,952, 1,100, 1,747, and 2,079 kcal/kg DM, respectively.

The objective was to test the hypothesis that increasing inclusion levels of full fat rice bran (FFRB) or defatted rice bran (DFRB) are not detrimental to growth or carcass characteristics, longissimus muscle (LM) quality, or fat quality when fed to growing-finishing pigs. A total of 224 barrows and gilts were randomly allotted to 7 treatments, with 4 pigs per pen and 8 pen replicates per treatment. Pigs had an average initial BW of 28.2 ± 4.1 kg and a 3-phase feeding program was used. A basal diet containing corn and soybean meal, 3 diets containing corn, soybean meal, and 10, 20, or 30% FFRB, and 3 diets containing corn, soybean meal, and 10, 20, or 30% DFRB were formulated within each phase. Daily feed allotments and pig BW at the start of the experiment and at the conclusion of each phase were recorded. On the last day of the experiment, 1 pig per pen was harvested and carcass characteristics, LM quality, and fat quality were determined. For the overall experimental period, no effects of dietary treatments were observed for average daily gain. However, average daily feed intake (ADFI) decreased (linear, P < 0.05) and gain to feed ratio (G:F) increased (linear, P < 0.05) for pigs fed diets with increasing concentrations of FFRB. In contrast, ADFI increased linearly (P < 0.05) and G:F decreased (linear, P < 0.05) as DFRB was included in the diets. There were no effects of dietary treatments on LM quality. The length of the bellies decreased (linear and quadratic, P < 0.05) as the inclusion of FFRB or DFRB increased in the diets. The concentration of crude fat in the adipose tissue of pigs increased linearly (P < 0.05) as the concentration of FFRB or DFRB increased in the diets. The concentration of saturated fatty acids in the adipose tissue of pigs fed diets containing FFRB decreased (linear, P < 0.05), whereas the concentration of polyunsaturated fatty acids (PUFA) increased (linear, P < 0.05). In contrast, addition of DFRB did not affect the concentration of fatty acids in adipose tissues. In conclusion, 30% FFRB included in diets for growing-finishing pigs may improve G:F without affecting carcass characteristics or LM quality with the exception that PUFA in adipose tissues will increase. However, inclusion of DFRB in diets for growing-finishing pigs will reduce G:F without affecting the LM quality or composition of adipose tissues.

An experiment was conducted to determine the standardized ileal digestibility (SID) of CP and AA in brewers rice, full-fat rice bran (FFRB), defatted rice bran (DFRB), peanut meal, sesame meal, rapeseed meal, rapeseed expellers, soybean expellers, cassava meal, and bakery meal fed to young growing pigs. Twenty-two barrows (initial BW: 14.09 ± 1.48 kg) were surgically fitted with a T-cannula in the distal ileum and randomly allotted to a replicated 11 × 4 incomplete Latin square design with 11 diets and four 7-d periods in each square. Eleven experimental diets were prepared and test ingredients were the sole source of CP and AA in 10 diets and the eleventh diet was a N-free diet used to measure basal ileal endogenous losses of CP and AA. Chromic oxide (0.4%) was included in all diets as an indigestible marker and ileal digesta were collected on day 6 and 7 of each period. Results indicated that the SID of CP and AA was greatest (P < 0.05) in brewers rice and sesame meal and least (P < 0.05) in cassava meal. The SID of indispensable AA was greater (P < 0.05) in sesame meal compared with all other ingredients except brewers rice. Full-fat rice bran had greater (P < 0.05) SID of Arg, Ile, Leu, Lys, and Met compared with DFRB. The SID of CP and most AA was not different among rapeseed meal, rapeseed expellers, and soybean expellers. Bakery meal had the least (P < 0.05) SID of most AA compared with all other ingredients, with the exception of cassava meal. The concentration of standardized ileal digestible CP was greater (P < 0.05) in sesame meal and peanut meal (482.32 and 452.44 g/kg DM, respectively) than in all other ingredients. Soybean expellers had the greatest (P < 0.05) concentration of standardized ileal digestible Lys (22.98 g/kg DM) followed by rapeseed meal (16.11 g/kg DM) and rapeseed expellers (16.17 g/kg DM). Cassava meal and bakery meal had the least (P < 0.05) concentration of standardized ileal digestible CP and most AA compared with the other ingredients. Concentrations of standardized ileal digestible CP and AA in brewers rice, FFRB, and DFRB were less (P < 0.05) than in rapeseed meal, rapeseed expellers, and soybean expellers. In conclusion, peanut meal and sesame meal have greater concentrations of standardized ileal digestible CP and most AA, with the exception of Lys, than other ingredients. Rapeseed meal, rapeseed expellers, and soybean expellers have the greatest concentrations of standardized ileal digestible Lys.

Rice bran is a common feed/food stuff for animals and humans; however, it usually contains a substantial amount of arsenic that is a class-I, non-threshold carcinogen to humans. This study was to investigate the fecal arsenic excretion pattern from the pigs fed an arsenic-containing rice bran. Twenty growing gilts (26.3 kg) were randomly assigned to 3 dietary treatments (n = 6 or 7) with Diets I, II, and III containing 0, 36.7, and 73.5% rice bran, and 0, 306, and 612 ppb arsenic, respectively. The feeding trial lasted 6 weeks, and fresh fecal samples were collected on Days 0, 14, 28, and 42 post-treatments. Fecal arsenic concentrations were analyzed using an ICP-MS protocol standardized by the U.S. Environmental Protection Agency. Tobit statistical model was employed for data analysis because some censored values were obtained from the laboratory sample analysis. Results (Table 1) showed that there were no differences in fecal arsenic concentrations from Day 0 through 42 post-treatment in pigs fed Diet I (a control diet). Nevertheless, the fecal arsenic concentration was increased significantly (P < 0.05) on Days 14 and 28 when compared to Day 0 post-treatment with Diet II (a moderate level of rice bran inclusion), and it was further increased (P < 0.05) on Day 42 post-treatment. The fecal arsenic excretion pattern in pigs fed Diet III (a high level of rice bran inclusion) was the same as that in pigs fed Diet II. The dietary treatment effects on fecal arsenic excretion were already reported previously. In short, the results of this study suggest that the fecal arsenic excretion is increased in the first 4 weeks and then further increased around the 6th week since the start of feeding arsenic-containing rice bran. This further increase may be due to the saturation of arsenic retention in pig body.

This study investigated substituting groundnut cake with wheat bran mixed with cattle blood at ratio1:1 in broilers and it lasted for eight weeks. Seventy-five broiler chicks were allotted randomly to five treatment replicated thrice. Control had 15% GNC, 0% blood meal wheat bran (BMWB) in diets II -V GNC was replaced with BMWB at graded levels of 25,50,75 and 100%. Results revealed that body weight gain and feed intake of diets II and III were similar and (P = 0.05) higher than other diets at both phases. Feed efficiency of diet II was better than others at the starter phase while diet III was better at finisher phase. Haematology and serum chemistry at the finisher phase showed that heamoglobin, white blood cell lymphocyte heterophil and plasma of the birds fed diets II, III, IV and V were (P < 0.05) higher than those on control. The kidney liver and spleen histopathology revealed hepatic and renal degeneration, necrosis and inflammatory responses in diets IV and V. Carcass characteristics showed the wings shanks drumstick leg heart and spleen of birds on BMWB were higher than control. Conclusively it seems BMWB could replace GNC without adverse effect on the broilers at 25% inclusion level

Four experiments evaluated the use of a complete starter feed (RAMP; Cargill Corn Milling, Blair, NE) for grain adaptation. In Exp. 1, 229 yearling steers (397 ± 28.4 kg BW) were used to compare a traditional adaptation program (CON) with adapting cattle with RAMP in either a 1- (RAMP-1RS) or 2- (RAMP-2RS) ration system. From d 23 to slaughter, cattle were fed a common finishing diet. In Exp. 2, 390 yearling steers (341 ± 14 kg BW) were used to compare accelerated grain adaptation programs with RAMP with 2 control treatments where RAMP was blended with a finishing diet containing either 25 (CON25) or 47.5% (CON47) Sweet Bran (Cargill Corn Milling) in 4 steps fed over 24 d to adapt cattle. Rapid adaptation treatments involved feeding RAMP for 10 d followed by a blend of RAMP and a 47% Sweet Bran finishing diet to transition cattle with 3 blends fed for 1 d each (3-1d), 2 blends fed for 2 d each (2-2d), or 1 blend fed for 4 d (1-4d). From d 29 to slaughter, all cattle were fed a common finishing diet. In Exp. 3, 300 steer calves (292 ± 21 kg BW) were used to compare the CON47 and 1-4d adaptation programs with directly transitioning cattle from RAMP, which involved feeding RAMP for 10 d and then switching directly to F1 on d 11 (1-STEP). From d 29 until slaughter, F2 was fed to all cattle. In Exp. 4, 7 ruminally fistulated steers (482 ± 49 kg BW) were used in a 35-d trial to compare the CON47 and 1-STEP adaptation programs. Ruminal pH and intake data from the first 6 d of F1and first 6 d of F2 were used to compare adaptation systems. Adaptation with RAMP-1RS and RAMP-2RS increased ( 0.11) among treatments in Exp. 2. Daily gain, DMI, and G:F were not different ( > 0.20) among treatments on d 39 or over the entire feeding period in Exp. 3. When F1 or F2 was being fed, DMI was similar ( ≥ 0.40) for CON47 and 1-STEP in Exp. 4. When F1 or F2 was being fed, 1-STEP cattle had lower average ruminal pH ( ≤ 0.03) and greater time below a pH of 5.3 ( ≤ 0.03). Using RAMP for grain adaptation improved performance compared with traditional adaptation. Rapid adaptation with RAMP decreased pH, but no performance differences were observed between long and rapid RAMP adaptation programs. Therefore, cattle started on RAMP do not require extensive adaptation before feeding a finishing diet with Sweet Bran.

The objective of this study was to compare the effect of source (corn DDGS, rice bran, or soybean) or form of oil (extracted or intact) on apparent total tract digestibility (ATTD) and true total tract digestibility (TTTD) of acid-hydrolyzed ether extract (AEE) and fatty acids. The study determined and compared the ATTD or TTTD of AEE and fatty acids in extracted corn oil, rice oil, and soybean oil with intact oil in corn DDGS, full-fat rice bran, and full-fat soybean. Seventy-eight barrows (initial BW = 47.2 ± 3.9 kg; Duroc × Landrace × Yorkshire) were allotted to 1 of 13 dietary treatments in a randomized complete block design with 6 barrows in each dietary treatment. The 13 experimental diets included 1 cornstarch-soybean meal basal diet (AEE, 0.56%) and 3 diets containing 6% extracted oils (corn oil, rice oil, and soybean oil) and 9 diets supplemented with 3 levels of corn DDGS (17%, 34%, and 51%), full-fat rice bran (14%, 28%, and 42%), and full-fat soybean (12%, 24%, and 36%). These diets provided about 2%, 4%, and 6% intact oil, respectively. The barrows were housed in individual metabolism crates and were fed the assigned test diets at 4% of initial BW per day. A 5-d total collection of feces followed a 7-d diet adaptation period. The ATTD of AEE were calculated for each diet. The endogenous flow of AEE associated with each ingredient and values for TTTD were calculated using regression methods. The ATTD of AEE were greater ( < 0.05) for extracted oil than for intact oil. Compared to extracted oil, intact oil had lower ( < 0.01) ATTD of palmitic acid (C16:0), stearic acid (C18:0), oleic acid (C18:1), linoleic acid (C18:2), and linolenic acid (C18:3). However, a source by form interaction ( < 0.01) was observed for ATTD of C18:0, C18:2, and C18:3. The ATTD of C18:0, C18:2, and C18:3 in extracted corn and rice oil were greater compared with intact corn DDGS and rice oil ( < 0.05), while there was no significant difference for the ATTD of C18:0, C18:2, and C18:3 between extracted soybean oil and intact oil in full-fat soybean. In conclusion, lipids that are extracted have a greater digestibility compared with intact lipids, and this is especially true regarding saturated fatty acids. The ATTD of AEE in 2 forms of rice oil (intact oil and extracted oil) was less than the values in corn oil and soybean oil. The TTTD of AEE in corn DDGS and full-fat soybeans were greater than in full-fat rice bran.

The effects of dietary feeding different levels of recycled poultry bedding (RPB) and dried orange pulp (DOP) on the performance of fattening Shal lambs (initial BW of 28 ± 2.2 kg) were assessed using a factorial experiment (2 × 3) with a completely randomized design. Six diets, containing different levels of RPB (0 or 160 g/kg of DM) and DOP (0, 110, or 220 g/kg of DM), were randomly assigned to 6 groups of 6 lambs each for a 74-d period (14 d for adaptation and 60 d for data collection). Diets were offered as total mixed ration to ensure 10% of orts. Feed intake, growth, diet digestibility, microbial nitrogen (N) synthesis (MNS), N retention, rumen fermentation parameters, and blood metabolites were determined. Data were analyzed using the PROC MIXED of SAS. Increasing RPB and DOP levels in the diet of the lambs improved ( 0.05), but increased as DOP level increased in the diet ( 0.05) on the ruminal pH. The ruminal total VFA concentration, molar proportion of acetic acid, and acetate-to-propionate ratio increased ( 0.05) by feeding RPB, but increased ( < 0.05) with increasing DOP level in diet. The animal performance reached its greatest value with simultaneous feeding of 160 g of RPB and 220 g of DOP per kg of diet DM. It has been concluded that the partial dietary substitution of RPB (instead of soybean meal, wheat bran, and sugar beet pulp) or/and DOP (instead of barley grain and corn grain) in fattening Shal lambs had positive effects on feed intake, diet digestibility, ruminal microbial N, growth, and N retention. Synchronized feeding of the great levels of RPB (as an N source) and DOP (as an energy source) increased utilization efficiency of these byproducts in the fattening lambs.

A total of 355 pigs (DNA 200x400; initially 5.6 kg) were used to evaluate the effects of coarse wheat bran and crude protein (CP) level in diets without pharmacological levels of zinc oxide on nursery pig performance and fecal dry matter (DM%). Pigs were allotted to 1 of 6 treatments in a completely randomized design with 5 pigs per pen and 12 pens per treatment. Treatment diets were fed in two phases (d 0 to 7 and 7 to 21) followed by a common diet fed d 21 to 45. Treatments included a positive control diet with ZnO, negative control without ZnO, and negative control with 4% wheat bran and formulated to contain 21, 19.5, 18, or 16.5% CP. All diets contained 1.35% SID lysine except the 18 and 16.5% (1.25 and 1.20% lysine) CP diets. Data were analyzed using the lmer function from the lme4 package in R. During the experimental period, decreasing CP decreased (linear, P< 0.05) ADG, G:F, and d 21 BW, but increased (linear, P=0.005) fecal DM%. Pigs fed the diet containing ZnO had increased (P< 0.050) ADG, ADFI, and G:F compared to the negative control and diet with 21% CP and wheat bran. From d 21 to 45, pigs previously fed the 21% CP diet with wheat bran had increased (P< 0.05) ADG compared to the positive control. Fecal DM on d 45 and G:F increased (P< 0.05) for pigs fed the 21% CP, wheat bran diet and negative control compared to those fed the positive control. Overall, pigs fed low CP diets had decreased (P< 0.05) ADG while pigs fed the positive control had greater (P< 0.05) ADG compared to the negative control. Additional research is needed to determine if modifying low CP, wheat bran diets will elicit benefits of increased fecal DM% while maintaining growth performance.

Increased cotton production in the Southwestern United States has increased the availability of cotton byproducts for use in cattle diets. The objective of this experiment was to evaluate the inclusion of cotton byproducts in feedlot finishing diets on the performance, carcass traits, fecal characteristics, and plasma metabolites of steers. Crossbred beef steers (n = 64; BW = 318 ± 12.3 kg) were assigned to 1 of 2 experimental treatments in a randomized complete block design (8 pens per treatment; 4 steers per pen). Treatments included a control (CON) diet, which included prairie hay, Sweet Bran, rolled corn, and a corn steep and molasses-based liquid fat supplement, and a cotton byproduct (CTN) diet, which included cotton gin trash, whole cottonseed, rolled corn, and water. Both diets contained urea and dry supplement. Over the entire feeding period, DMI (P = 0.04) was greater for CTN steers than CON steers with no difference in the gain to feed ratio (P = 0.86) between treatments. The CTN steers tended to have heavier final BW (P = 0.09) and greater overall average daily gain (P = 0.08). The CTN steers had heavier hot carcass weight (P = 0.02) and greater fat thickness (P = 0.03) than CON steers, but marbling score and rib eye area were not different between treatments (P ≥ 0.64). Steers fed the CON diet tended to have a lower yield grade (P = 0.07), less kidney, pelvic and heart fat (P = 0.09), and decreased dressing percentage (P = 0.10) than CTN steers. Liver scores did not differ (P ≥ 0.17) between treatments. Fecal consistency scores were decreased for CTN steers on day 56 (P = 0.03) and fecal pH tended to be greater for the CTN steers on day 28 (P = 0.09) compared with CON steers, but neither differed during other periods (P ≥ 0.18). A treatment × day interaction (P = 0.04) was detected for plasma urea nitrogen (PUN) concentrations, where PUN concentrations differed between treatments only on days 28 and 56. On both days 28 and 56, CTN steers had lower PUN concentrations (P = 0.03, P = 0.002, respectively). No treatment × day interaction was detected for plasma glucose or lactate concentrations. A day effect was observed for both metabolites (P < 0.01). Results from this experiment suggest that cotton byproducts can be effectively used as a source of fiber, fat, and protein in feedlot rations without adverse effects on performance or carcass characteristics.

The objective of this study was to evaluate the effects of feeding high-protein corn distillers grains on fresh beef quality. Steers (n = 60) were fed one of five diets for 190 d (six pens with 10 cattle/pen/diet): a corn control (Control), 40% high-protein dry distillers grains plus solubles (HP-DDGS), 40% dry distillers grains plus solubles (DDGS), 40% wet distillers grains plus solubles (WDGS), or 40% bran plus solubles (Bran). Eighteen Choice carcasses (three cattle per pen) were randomly selected within each treatment; however, two carcasses were lost during carcass selection. Strip loins (Longissimus lumborum, IMPS # 180) were collected, divided into three equal portions, and aged for 2, 9, or 23 d. Steaks were fabricated following each aging period and placed under retail display (RD) conditions for 0, 4, or 7 d. Pen was the experimental unit. Hot carcass weight at harvest was 391 kg (SD 31.6 kg). Dietary treatment had no effect on tenderness (Warner-Bratzler shear force) within each aging period (P > 0.05). After 7 d of RD, following all aging periods, steaks from cattle fed HP-DDGS had the greatest visual discoloration except for DDGS and Bran after 23 d (P < 0.05). The steaks from cattle fed HP-DDGS had lower (P < 0.05) redness (a*) values than all other treatments following 7 d of RD. Lipid oxidation increased (P < 0.001) during RD at all aging periods, as measured via thiobarbituric acid reactive substance (TBARS). A day of RD-by-dietary treatment effect (P < 0.001) was observed for lipid oxidation. After 7 d of RD, steaks from cattle fed HP-DDGS had higher TBARS than all other treatments except WDGS (P < 0.01). A trend was found for sarcomere length (P = 0.07), with steaks from cattle fed Bran having the longest sarcomere length compared with all other treatments. An aging effect was found for free calcium content (P < 0.001) where steaks aged 9 and 23 d had significantly higher levels of free calcium than those aged 2 d. There was a tendency (P = 0.07) that steaks from cattle fed WDGS contained more free calcium than steaks from cattle fed DDGS or Bran. Although there were no statistical differences, there was a trend (P = 0.07) that steaks from cattle fed HP-DDGS had higher levels of PUFAs and C18:2. These results suggest that feeding high protein distillers grains has no detriment on tenderness, but may alter the lipid profile of the muscle, resulting in decreased color stability, increased lipid oxidation, and decreased shelf life.

This experiment evaluated replacing dietary corn (50:50 blend of dry-rolled and high-moisture) with corn bran plus condensed distillers solubles (CBCDS) on finishing phase growth performance, efficiency of dietary net energy (NE) utilization, comparative NE value, and carcass trait responses in finishing beef steers. This study used 30 pens of 8 steers/pen assigned to one of three treatments in a randomized complete block design (initial BW=401±43.2 kg); pen served as the experimental unit. Treatments included: 1) finishing diet that contained no corn co-product (Control); 2) finishing diet that contained a dry-corn milling bio-refinery product (20% DM basis inclusion) that replaced corn in the diet: CBCDS; 3) finishing diet that contained a wet-corn milling co-product (20% DM basis inclusion) that replaced corn in the diet: wet corn gluten feed (WCGF). For all analyses, an α of 0.05 determined significance and an α of 0.06 to 0.10 was a tendency. No differences were detected (P ≥ 0.58) among treatments for carcass-adjusted final BW (HCW/0.6433), ADG, or G:F. Observed NE for maintenance and gain was not impacted (P ≥ 0.28) by treatment. No appreciable influence for treatment was detected for the ratio of observed to expected dietary NE for maintenance or gain (P ≥ 0.40). Replacement NEm and NEg values (Mcal/45.4 kg) were determined to be 93.5 and 62.3 for CBCDS and 91.5 and 60.5 for WCGF. There was no influence (P ≥ 0.16) of treatment on DP, HCW, REA, RF, USDA Marbling, KPH, EBF, or final BW at 28% EBF. Treatment tended to influence (P = 0.10) YG, where steers fed WCGF had lesser YG than Control; however, CBCDS diet was intermediate, not differing from WCGF or Control. Distribution of USDA Quality and Yield Grade did not differ (P ≥ 0.29) among treatments. Substitution of corn for CBCDS at 20% of dietary DM can occur without detriment to growth performance or carcass traits.

This study assessed the effect of Sweet BranTM (SWBR; 40% DM inclusion; Cargill Corn Milling, Blair, NE) or modified distiller’s grains (MDGS; 25% DM inclusion) in the diet of newly received feedlot steers on feeding behavior and growing period performance. Diets were formulated for similar metabolizable protein and DM. Two hundred sixteen freshly weaned Angus-cross steers (253 kg ± 18.1) were stratified by BW to 36 pens (n = 18 per treatment; 6 steers/pen). Individual BW were recorded on d 0, 28, and 60. Eight pens per treatment were utilized to assess rate of feed disappearance early (day 5 and 6) and late (53 and 54) during growing by weighing feed in bunks every 2 hours post-delivery for 12 consecutive hours. Feed weights were averaged across consecutive days within pen and timepoint. Slopes were calculated between each timepoint to determine rate of feed disappearance. Data were analyzed with Proc Mixed of SAS 9.4; diet was fixed effect and pen was experimental unit. Feed disappearance slopes were analyzed as repeated measures with the repeated effect of time. Body weights did not differ on d 28 (P ≥ 0.29), but d 60 BW and d 0 to 60 ADG were greater for SWBR than MDGS (P < 0.05). Steers fed SWBR had greater DMI throughout the trial (P < 0.05). Feed efficiency (G:F) did not differ throughout the trial (P ≥ 0.31). Rate of feed disappearance on d 5/6 was greater for SWBR between hours 6–8, and greater for MDGS from hours 10–12. On d 53/54, SWBR had increased feeding rate during hours 0–2, while MDGS was increased from hours 8–10. Steers fed SWBR had a greater rate of feed disappearance earlier in the day and had improved DMI and growth than steers fed MDGS.

A study was conducted to evaluate the effects of replacing corn by full-fat rice bran (FFRB) on performance and meat quality characteristics of growing-finishing pigs. A total of 728 pigs [Duroc x (Yorkshire x Landrace); initial body weight (BW) = 24.1 ± 0.11 kg] were randomly distributed to 4 dietary treatments with 7 replicate pens (26 pigs/pen) per treatment. Diets 1, 2, 3 and 4 were formulated replacing corn by 5%, 15%, 30%, and 45% of FFRB, respectively. Growth phases include, phase 1 (24 - 60 kg BW), and phase 2 (61 - 105 kg BW). Data were analyzed as a completely randomized design, and each pen was considered as an experimental unit. During phase 1 and 2, average daily gain (ADG) did not differ (P >0.05) when FFRB was increased from 5 to 30% in the diets. Pigs fed 45% FFRB had lower (P< 0.05) ADG in phase 1 and higher in phase 2 than other dietary treatments. Throughout the study, feed intake was not affected (P > 0.05) by dietary treatments. During phase 1, feed conversion ratio (FCR) was similar (P >0.05) among the treatments, however, during phase 2, pigs fed increasing levels of FFRB linearly improved (P< 0.05) FCR. The overall growth performance was similar (P >0.05) among the dietary treatments. Back-fat thickness and meat color were not affected (P >0.05) by treatments. Saturated fatty acids (palmitic acid, stearic acid) in pig muscle (Longissimus) significantly decreased (linear; P< 0.05) with increasing levels of FFRB in pig diets. Pigs fed increasing levels of FFRB had increased linoleic acid (linear; P< 0.05) and linolenic acid (quadratic; P< 0.05) in meat. In conclusion, FFRB could be used as an alternative feed ingredient for corn up to 45% in swine diets without compromising overall growth performance, back-fat thickness and favoring improved unsaturated to saturated fatty acid profile.

The objective of this experiment was to determine the effect of increased concentrations of full fat rice bran (FFRB) or defatted rice bran (DFRB) in diets without or with supplementation of an exogenous xylanase on growth performance and blood characteristics in weanling pigs. A total of 532 pigs (9.3 ± 0.5 kg initial BW) were allotted to 14 diets in 4 blocks and 8 replicate pens per diet in a randomized complete block design. There were 4 or 5 pigs per pen. A basal diet containing corn, soybean meal, and whey powder and 6 diets containing corn, soybean meal, whey powder, and 10, 20, or 30% FFRB or 10, 20, or 30% DFRB were used. Seven additional diets that were similar to the initial 7 diets with the exception that they also contained 16,000 units/kg of microbial xylanase were also formulated. On the last day of the 23-d experiment, 2 blood samples were collected from 1 pig in each pen. Tumor necrosis factor-α (TNF-α), IgA, and peptide YY (PYY) were measured in plasma samples and blood urea nitrogen (BUN), total protein, and albumin were measured in serum samples. Initial and final BW were not affected by the inclusion level of FFRB or DFRB or by the addition of xylanase. The ADFI linearly decreased ( < 0.05) as inclusion of FFRB increased in diets and there was a tendency ( = 0.08) for reduced ADFI as DFRB was increased in the diets. Pigs fed diets containing DFRB had greater ADFI ( < 0.05) than pigs fed diets containing FFRB. The ADG increased and then decreased (quadratic, < 0.05) with increasing level of FFRB or DFRB in the diets. The G:F linearly and quadratically increased ( < 0.05) as the inclusion of FFRB increased, and the G:F was greater ( < 0.05) in pigs fed diets containing FFRB than in pigs fed diets containing DFRB. The concentration of BUN linearly decreased ( < 0.05) when pigs were fed diets containing increasing levels of FFRB or DFRB. There was a tendency for the concentrations of TNF-α and PYY to linearly decrease ( = 0.09 and = 0.075, respectively) as the inclusion of FFRB increased in the diet. In conclusion, ADG of weanling pigs was not affected by at least 20% FFRB or DFRB and inclusion of 30% DFRB had no effect on the G:F whereas 30% FFRB increased the G:F. However, microbial xylanase did not influence growth performance under the conditions of this experiment and there was minimal influence of rice coproducts or xylanase on blood characteristics.

This study aimed to determine the impact of replacing soybean meal with peanut cake in the diets of crossbred Boer goats as determined by carcass characteristics and quality and by the fatty acid profile of meat. Forty vaccinated and dewormed crossbred Boer goats were used. Goats had an average age of 5 mo and an average BW of 15.6 ± 2.7 kg. Goats were fed Tifton-85 hay and a concentrate consisting of corn bran, soybean meal, and mineral premix. Peanut cake was substituted for soybean meal at levels of 0.0, 33.33, 66.67, and 100%. Biometric and carcass morphometric measurements of crossbred Boer goats were not affected by replacing soybean meal with peanut cake in the diet. There was no influence of the replacement of soybean meal with peanut cake on weight at slaughter ( = 0.28), HCW ( = 0.26), cold carcass weight ( = 0.23), noncarcass components of weight ( = 0.71), or muscularity index values ( = 0.11). However, regression equations indicated that there would be a reduction of 18 and 11% for loin eye area and muscle:bone ratio, respectively, between the treatment without peanut cake and the treatment with total soybean meal replacement. The weights and yields of the commercial cuts were not affected ( > 0.05) by replacing soybean meal with peanut cake in the diet. Replacing soybean meal with peanut cake did not affect the pH ( = 0.79), color index ( > 0.05), and chemical composition ( > 0.05) of the meat (). However, a quadratic trend for the ash content was observed with peanut cake inclusion in the diet ( = 0.09). Peanut cake inclusion in the diet did not affect the concentrations of the sum of SFA ( = 0.29), the sum of unsaturated fatty acids (UFA; = 0.29), or the sum of PUFA ( = 0.97) or the SFA:UFA ratio ( = 0.23) in goat meat. However, there was a linear decrease ( = 0.01) in the sum of odd-chain fatty acids in the meat with increasing peanut cake in the diet. Soybean meal replacement with peanut cake did not affect the n-6:n-3 ratio ( = 0.13) or the medium-chain fatty acid ( = 0.76), long-chain fatty acid ( = 0.74), or atherogenicity index values ( = 0.60) in the meat. The sensory attributes of the longissimus lumborum did not differ with the inclusion of peanut cake in the diet as a replacement for soybean meal. These results suggest that based on carcass and meat characteristics, peanut cake can completely substitute soybean meal in the diet of crossbred Boer goats.

The objective of this experiment was to test the hypothesis that the apparent total tract digestibility (ATTD) of DM, OM, fiber, and GE by weanling pigs and the concentration of DE and ME in full-fat rice bran (FFRB), defatted rice bran (DFRB), brown rice, and broken rice is improved if microbial xylanase is added to the diet. Eighty pigs (13.6 ± 0.8 kg initial BW) were allotted to 10 diets with 8 replicate pigs per diet in a randomized complete block design with 2 blocks of 40 pigs. A basal diet based on corn and soybean meal and 4 diets containing corn, soybean meal, and each of the 4 rice coproducts were formulated. The rice coproducts and corn and soybean meal were the only sources of energy in the diets. Five additional diets that were similar to the initial 5 diets with the exception that they also contained 16,000 units of xylanase (Econase XT-25; AB Vista, Marlborough, UK) were also formulated. All diets also contained 1,500 units of microbial phytase (Quantum Blue 5G; AB Vista). The DE and ME and the ATTD of DM, OM, fiber, and GE in diets and ingredients were calculated using the direct method and the difference method, respectively. Results indicated that the concentrations of DE and ME (DM basis) in FFRB and DFRB increased ( < 0.05) if xylanase was used. Broken rice had a greater ( < 0.05) concentration of DE and ME than FFRB and DFRB if no xylanase was added to the diets, but if xylanase was used, no differences in ME among FFRB, brown rice, and broken rice were observed. The ATTD of DM was greater ( < 0.05) in ingredients with xylanase than in ingredients without xylanase and there was a tendency ( = 0.067) for the ATTD of OM to be greater if xylanase was used. The ATTD of NDF in FFRB was greater ( < 0.05) when xylanase was added than if no xylanase was used, whereas the ATTD of NDF in DFRB was not affected by the addition of xylanase. In conclusion, if no xylanase was used, broken rice and brown rice have greater concentrations of DE and ME than FFRB and DFRB, and these values were not increased by microbial xylanase. However, xylanase increased the concentration of DE and ME (DM basis) in FFRB and DFRB.

Two trials evaluated adapting cattle to a finishing diet using wet corn gluten feed compared with traditional methods using forage. A 33-d grain adaptation metabolism trial (Exp. 1) compared decreasing wet corn gluten feed (Sweet Bran; Corn Milling unit, Cargill Corn Milling, Blair, NE) while increasing corn inclusion (SB) and a traditional grain adaptation system decreasing alfalfa hay while increasing corn with no Sweet Bran inclusion (CON). Ruminal pH, intake characteristics, and 24-h in situ digestibility were evaluated using 8 ruminally fistulated steers (291 kg BW [SD 19]). Steers (4/treatment) were adapted to finishing diets across 4 periods consisting of 5, 7, 7, and 7 d and then fed a finishing diet for 7 d. No period × adaptation diet interactions were observed ( ≥ 0.12). Average ruminal pH decreased ( < 0.01) whereas time and area below a pH of 5.6 increased ( ≤ 0.02) for the SB adaptation system compared with the CON adaptation system. Cattle adapted using SB had greater DMI than cattle adapted using CON ( < 0.01). As steers were adapted to finishing diets, DMI increased ( = 0.01), average ruminal pH decreased ( = 0.05), and time and area below a pH of 5.6 increased ( ≤ 0.04) for both treatments. Ruminal pH for CON steers decreased from 6.59 to 6.12 across periods as corn replaced alfalfa hay whereas ruminal pH decreased from 6.00 to 5.79 for SB steers. Steers adapted using SB had greater ( ≤ 0.05) in situ digestion of adaptation diets than steers adapted using CON for adaptation periods 3, 4, and 5. The SB diets were more digestible than the CON diets when incubated in either CON- or SB-fed steers for adaptation periods 1 and 2 ( < 0.01). Experiment 2 used 240 finishing steers (273 kg BW [SD 14]) to determine performance impacts of using Sweet Bran instead of forage to adapt cattle to finishing diets. Steers were fed either decreasing Sweet Bran inclusion while increasing corn (SB) or decreasing alfalfa hay inclusion while increasing corn (CON). Treatments were applied only during grain adaptation (26 d) and all steers were finished on a common diet containing 35% Sweet Bran for an additional 147 d. Steers adapted using SB had greater ( ≤ 0.01) final BW, ADG, G:F, and HCW compared with steers adapted using CON, even though treatments differed only the first 26 d. Grain adaptation treatment had no effect ( ≥ 0.13) on carcass quality. These results indicate that Sweet Bran can be used to adapt cattle to finishing diets instead of forage and improves ADG and G:F while decreasing the forage needs of feedlots.

High dietary fiber (DF) and immune system stimulation (ISS) are thought to limit amino acid availability for protein deposition (PD) in growing pigs. A nitrogen-balance study was conducted to determine Thr requirement for optimal PD when DF and ISS were present alone and in combination. A total of 90 barrows (20.5 kg initial BW; SD = 0.75 kg) were randomly assigned to one of 10 dietary treatments (n = 9) in nine blocks. Diets consisted of a low fiber (LF; 12.5% total DF) or high fiber (HF; 18.5% total DF by adding 10% sugar beet pulp and 5% wheat bran to the LF diet) with graded levels of Thr (0.49%, 0.57%, 0.65%, 0.73%, and 0.81% standardized ileal digestible [SID]) fed at 2.2 × maintenance ME requirements. After an 8-d adaptation, two 4-d nitrogen balance collection periods (pre-ISS and ISS) were conducted. ISS was induced by repeated injections (i.m.) of increasing doses of Escherichia coli lipopolysaccharide. Blood samples were taken during both periods to assess acute phase proteins and complete blood cell count. Data were analyzed by PROC MIXED with fixed effects of period, Thr, fiber, and their interactions, with block as a random effect. Nitrogen balance was analyzed separately for each period. Threonine requirement was estimated using PROC NLIN quadratic break-point model. Serum concentration of albumin, haptoglobin, fibrinogen, whole blood white blood cell, and platelet count were affected by ISS (P < 0.001) confirming successful ISS. During pre-ISS, PD increased linearly (P < 0.01) as Thr concentration in the diet increased, with a significant interaction (P < 0.05) between fiber and Thr. During ISS, PD increased linearly (P < 0.05) as Thr concentration in the diet increased. Quadratic break-point model estimated SID Thr required to maximize PD of pigs fed LF and HF diets during pre-ISS period was 0.68% (R2 = 0.88) and 0.78% (R2 = 0.99), respectively. During ISS, the SID Thr requirement was estimated at 0.76% (R2 = 0.76) for LF diet and 0.72% (R2 = 0.95) for HF fed pigs. HF and ISS independently increased Thr requirement for maximum PD, but these effects were not additive. HF may therefore mask the effects of ISS on Thr requirement for immune response and PD.

This study was conducted to determine and compare available energy and apparent ileal digestibility (AID) and standardized ileal digestibility (SID) of CP and AA in 9 samples of defatted rice bran (DFRB) fed to growing pigs and to generate prediction equations for DE and ME based on chemical analysis. In Exp. 1, 60 crossbred growing pigs (Duroc × Landrace × Yorkshire; 40.7 ± 3.5 kg BW) were fed 1 of 10 diets in a completely randomized design to determine the available energy of DFRB. The diets included a corn-soybean meal-basal diet and 9 experimental diets formulated by replacing the corn and soybean meal with 29.16% DFRB. In Exp. 2, 6 growing pigs (initial BW = 28.5 ± 2.8 kg) were surgically equipped with a T-cannula in the distal ileum and arranged in a 6 × 6 Latin square design with 6 diets and 6 periods. The diets included an N-free diet based on cornstarch and sucrose and 5 experimental diets containing 60% DFRB as the sole source of AA. Chromic oxide (0.3%) was used as an indigestible marker. Among the 9 samples, the concentrations of ether extract (EE), crude fiber (CF), NDF, ADF, starch, Ca, and P averaged 1.33 (0.50% to 4.14%), 14.54 (9.78% to 23.85%), 28.62 (20.19% to 38.85%), 14.22 (9.32% to 23.99%), 38.80% (30.62% to 47.55%), 0.16% (0.09% to 0.24%), and 1.96% (1.11% to 2.28%), respectively. The average DE and ME were 2,643 and 2,476 kcal/kg DM, respectively, and ranged from 2,039 to 3,157 kcal/kg DM and 1,931 to 2,978 kcal/kg DM, respectively. In Exp. 2, there were significant differences in the AID and SID of CP and most AA except for His, Tyr, and Met (P < 0.05). The AID and SID of CP averaged 67.75% and 76.37%, respectively. The digestibility of Met was the greatest, averaging 86.15% and 90.08% for AID and SID, respectively. The AID and SID of Lys ranged from 51.88% to 71.43% (mean = 63.27%) and from 61.93% to 79.98% (mean = 72.97%), respectively. These results indicated that there is significant variability in chemical composition, energy content, and the SID and AID of CP and most AA among the selected DFRB. The DE and ME of DFRB are primarily related to their NDF and starch concentrations.

This study investigated the amount of energy available to growing pigs from fermentation of dietary fiber in the hindgut. Eighteen growing barrows, fitted with a simple T-shaped cannula at the terminal ileum, were allocated to 3 experimental diets in a completely randomized design. The 3 diets were a standard-fiber diet (SFD), which contained 75.1 g NDF/kg diet; a medium-fiber diet (MFD) of 105.7 g NDF/kg diet; and a high-fiber diet (HFD), which contained 146.9 g NDF/kg diet. Each diet had 6 replicate pigs. After a 5-d period of adjustment of the pigs to the cage environment, feces were collected on d 6 and 7 and ileal digesta on d 8 and 9 and subsequently freeze-dried. Fecal slurry from a pig was used to inoculate the ileal digesta from the same pig. The amount of energy available was calculated from the amount of short-chain fatty acids (SCFA) produced from a 48-h in vitro fermentation of the ileal digesta. Increasing NDF enhanced ( < 0.01) the ileal DM flow and DM in feces. The energy available in the foregut was reduced ( < 0.05) from 3,360 to 2,974 kcal/kg feed DM and increased ( < 0.01) from 619 to 1,009 kcal/kg feed DM produced in the hindgut with increasing dietary NDF. The amount of SCFA increased ( < 0.01) with higher dietary NDF. Acetic acid was highest ( < 0.01) in the HFD whereas propionic and valeric acids were highest ( < 0.05) in the SFD. The amount of butyric acid was not affected by diet. The amount of energy contributed from SCFA fermentation to total tract digestible energy increased ( < 0.01) from 10.7 to 24.2% as dietary NDF level increased from 75 to 147 g/kg feed. The results of the study showed that increasing level of dietary NDF resulted in reduced energy digestibility in the foregut of growing pigs with a corresponding increase in the amount of energy from microbial fermentation in the hindgut.

The aim of this work was to evaluate the effects of the inclusion of whole-ear corn silage (WECS) in diets for advanced fattening heavy pigs (substitution for part of the dry corn and wheat bran) allocated or not in metabolic cages on the main blood parameters. The high-moisture shelled corn is largely used in pig feeding while WECS is less often used despite the fact that it increases the DM crop yield. Three experimental diets were fed to 27 barrows (Italian Large White × Italian Duroc), with an average BW of 98.2 (±5.6) kg at the start of the trial, and randomly allotted to 3 experimental groups including a control diet (CON) containing cereal meals (corn, barley, and wheat, 80.2% DM in total), soybean meal (9% DM), wheat bran (8% DM), minerals and supplements (2.8% DM), and 2 diets containing WECS (15 or 30% DM referred to as 15WECS and 30WECS, respectively) in partial or complete substitution for wheat bran and corn meal. The pigs were randomly housed in 9 pens with 3 animals per pen and 3 pens per dietary treatment. Six pigs per each of the 3 treatments were moved from the pens to individual metabolic cages for 3 consecutive periods (2 pigs per treatment per period). Each period lasted 14 d, and blood was collected at the start and at the end of the periods. Blood was drawn from the jugular vein before feed distribution in the morning, at 14 d intervals, and analyzed for hematological, metabolic, and serum protein profiles. The effect of the metabolic cage housing was included in the statistical model to compare the results obtained in the 2 different environments of restrained and group-housed barrows. The WECS affected the neutrophil to lymphocyte ratio and mean corpuscular hemoglobin concentration. The main diet effect on plasma metabolites was recorded for plasma NEFA, with higher values in WECS diets compared with the CON. The metabolic cage housing affected both hematological (red blood cell count, hemoglobin, hematocrit) and metabolic (protein and its fractions) items, which can be markers of hemodilution. These results indicate the possibility to use this feed in the diet of heavy pigs without negative effects on physiology. The absolute values from metabolic profile of pigs in metabolic cages must be considered with caution for possible comparisons with values obtained on-field in group pens, particularly because a different hemodilution may affect the results.

The objectives of this experiment were to determine the apparent total tract digestibility (ATTD) and the standardized total tract digestibility (STTD) of P and the effect of microbial phytase on ATTD and STTD of P in full-fat rice bran (FFRB), defatted rice bran (DFRB), brown rice, broken rice, and rice mill feed when fed to pigs. Ninety-six barrows (initial BW of 19.4 ± 1.4 kg) were allotted to 12 diets with 8 replicate pigs per diet in a randomized complete block design. A basal diet based on corn and soybean meal was formulated. Five additional diets containing corn, soybean meal, and each rice coproduct were also formulated, and the ratio between corn and soybean meal in these diets was similar to that in the basal diet. Six additional diets that were similar to the initial 6 diets with the exception that 1,000 units of microbial phytase were added to the diets were also formulated. The ATTD and STTD of P were calculated for each diet using the direct procedure, and the ATTD and STTD of P in each rice coproduct were calculated using the difference procedure. Results of the experiment indicated that the concentration of P in feces was reduced (P < 0.05) from pigs fed diets with microbial phytase compared with pigs fed diets without phytase. No differences were observed between the basal diet and the broken rice diet, but the ATTD and the STTD of P in those diets was greater (P < 0.05) than in all other diets both without and with phytase. Among the rice coproducts, the greatest (P < 0.05) ATTD and STTD of P were observed for broken rice regardless of inclusion of phytase. If no microbial phytase was used, the values for STTD of P in brown rice, FFRB, DFRB, and rice mill feed were not different, but if microbial phytase was included in the diet, ATTD and STTD of P in brown rice was greater (P < 0.05) than in FFRB, DFRB, and rice mill feed. The STTD of P in brown rice, FFRB, and rice mill feed was greater (P < 0.05) if microbial phytase was used than if no microbial phytase was used. Addition of microbial phytase to the diets also increased (P < 0.05) the ATTD of Ca regardless of the rice coproducts used. In conclusion, the STTD of P is greater in broken rice than in all other rice coproducts. The STTD of P in brown rice, FFRB, DFRB, and rice mill feed is relatively low due to the high concentration of phytate in these ingredients, but addition of microbial phytase will increase the STTD of P in most rice coproducts.

This study aimed to test the hypothesis that peanut cake can substitute for soybean meal in the feed of ruminants on the basis of the intake, performance, digestion, and serum urea and glucose concentration in crossbred Boer × indigenous goat kids. Forty intact vaccinated and dewormed crossbred Boer × indigenous goat kids (average age = 5 mo, average BW = 15.6 ± 2.7 kg) were used. The goats were fed Tifton-85 (Cynodon dactylon) hay and concentrate mixes of corn bran, soybean meal, premix mineral, and peanut cake substituted for soybean meal at rates of 0.0%, 33.33%, 66.67%, and 100%. The animals were confined for 62 d, and the digestibility trial was performed from d 27 to 31 of confinement. Samples of orts and feces were quantified and collected from each animal during this period. On the d 32 of confinement, a blood sample was taken from animals to measure urea N and glucose. Data were analyzed with a regression model. Substitution of soybean meal with peanut cake in the diet of the animals resulted in a reduction in intake of DM (P = 0.02), CP (P = 0.03), NDF (P = 0.03), nonfiber carbohydrate (NFC; P = 0.01), and TDN (P = 0.02) and an increase in intake of ether extract (P < 0.001). The total and daily average weight gains decreased (P = 0.02) with substitution, whereas G:F was not influenced (P = 0.11). With the exception of ether extract digestibility, which increased (P < 0.001) with substitution, digestibility of DM (P = 0.13), OM (P = 0.18), CP (P = 0.54), NDF (P = 0.20), and NFC (P = 0.73) was not influenced by diets. The concentration of serum urea N was influenced quadratically by the postprandial time for treatments with 33.33%, 66.67%, and 100.00% substitution. Peanut cake is not a complete, equal substitute for soybean meal in goat feed. However, peanut cake may represent an eventual replacer able to reduce goat producers’ dependence on traditional ingredients in the feed of growing goat kids.

The first objective of this experiment was to test the hypothesis that apparent total tract digestibility (ATTD) of GE and nutrients in full fat rice bran (FFRB) and defatted rice bran (DFRB) determined in gestating sows is greater if feed is provided at 1.5 × the ME required for maintenance than at 3.5 × the ME requirement. The second objective was to test the hypothesis that the ATTD of GE and nutrients and the concentrations of DE and ME in FFRB and DFRB is not different between growing gilts and gestating sows if both groups of animals are fed 3.5 × the maintenance requirement for ME. Forty eight gestating sows (parity 2 to 6) were allotted to 3 diets and 2 levels of feed intake (i.e., 1.5 or 3.5 × the maintenance requirement for ME) in a randomized complete block design, with 4 blocks of 12 sows and 2 replicate sows per block for a total of 8 replicate sows per diet. Twenty four growing gilts (51.53 ± 3.1 kg BW) were randomly allotted to the same 3 diets, but all gilts were fed at 3.5 × the maintenance requirement for ME. A basal diet containing corn and soybean meal and 2 diets that consisted of 60% basal diet and 40% FFRB or DFRB were used. Results of the experiment indicated that there were no effects of level of feed intake of sows on ATTD of GE, DM, OM, or NDF, or on concentrations of DE and ME. However, concentrations of DE and ME were greater ( < 0.05) in FFRB than in DFRB regardless of feed intake level. The ATTD of GE, OM, DM, and NDF of diets containing FFRB or DFRB was less ( < 0.05) than in the basal diet, regardless of the physiological stage of the animals. However, the ATTD of GE, OM, and NDF of the basal diet and diets containing FFRB or DRFB was greater ( < 0.05) in gestating sows than in growing gilts. Concentrations of DE and ME in the diets were also greater ( < 0.05) if determined in gestating sows than in growing gilts. The ATTD of GE and the concentrations of DE and ME of FFRB were greater ( < 0.05) than in DFRB and these values were also greater ( < 0.05) in gestating sows than in growing gilts. In conclusion, the level of feed intake by gestating sows did not affect the digestibility of GE and nutrients or the concentrations of DE and ME in diets or in FFRB or DFRB, but the ATTD of GE and the concentration of DE and ME in diets and in FFRB and DFRB were greater in gestating sows than in growing gilts.

Two experiments were conducted to evaluate the effect of full-fat rice bran (FFRB) inclusion in dry diets with and without enzyme blend (EB) supplementation for adult dogs. The diets contained 0, 20, or 40% of FFRB, replacing the equivalent amount of wheat flour (WF). Experiment 1 evaluated the consumption and preference of diets using a simple choice method with 3 comparisons (0 vs. 20, 0 vs. 40, and 20 vs. 40% FFRB). Experiment 2 investigated the effect of EB supplementation on the apparent digestibility coefficients (ADC) of nutrients and GE, fecal characteristics, urinary pH, Ca and P balance, and ME of the diets. In Exp. 1, the results indicated that FFRB included in diets up to 40% did not affect the preference or consumption of food by dogs (P < 0.05). In Exp. 2, increasing levels of FFRB in the diet linearly reduced the ADC of nutrients, GE, and ME (P < 0.05). The addition of EB had no effect on any of the variables examined. Regression analysis enabled estimation of the ADC in FFRB; and ADC of DM, CP, ether extract, GE; and the apparent coefficient of ME were 60.5, 74.8, 88.4, 70.8, and 66.4%, respectively. The inclusion of 20 or 40% FFRB in the diets did not affect urinary pH but caused an imbalance in the Ca and P metabolism when included at 40% (P < 0.05), which could be one of the limitations for greater inclusion of FFRB. The ME of FFRB was estimated to be 3,443 kcal/kg DM. The FFRB appears to be palatable for adult dogs, and although ADC was reduced by 40% FFRB in the diet, this ingredient has the potential for inclusion at 20% of diets for dogs, depending on the other ingredients used to achieve adequate Ca and P balance. The inclusion greater than 20% tends to increase P in the diet and reverse the relationship between Ca and P.

Two experiments were conducted to determine DE and ME and the apparent ileal digestibility (AID) and the standardized ileal digestibility (SID) of CP and AA in corn and corn coproducts (high-fat corn germ [HFCG], corn bran, liquid corn extractives [LCE], and a mixture of corn germ meal and LCE [CGM-LCE]) fed to growing pigs. In Exp. 1, 40 growing barrows (initial BW: 33.4 ± 5.77 kg) were housed individually in metabolism cages and randomly allotted to 1 of 5 diets. A corn-based diet (97.4% corn) and 4 diets that contained both corn and each of the corn coproducts were formulated. Each diet was fed to 8 pigs. Feces and urine samples were collected using the marker to marker method with 5-d adaptation and 5-d collection periods. The DE and ME were calculated using the difference procedure. The concentrations of DE and ME in HFCG, corn bran, LCE, and CGM-LCE were less (P < 0.05) than in corn. Among corn coproducts, the concentration of DE in HFCG was greater (P < 0.05) than in corn bran, but the DE in corn bran was not different from DE values in LCE and CGM-LCE. No differences were observed in the ME concentrations among corn coproducts. In Exp. 2, 6 growing barrows (initial BW: 96.6 ± 1.16 kg) with a T-cannula in the distal ileum were randomly allotted to a 6 × 6 Latin square design with 6 diets and 6 periods. A N-free diet and 5 diets that contained corn, HFCG, corn bran, LCE, or CGM-LCE as the sole source of CP and AA were formulated. Each period lasted 7 d and ileal digesta were collected on d 6 and 7 of each period. The SID of CP and all indispensable AA was greater (P < 0.05) in corn than in all corn coproducts with the exception that the SID of Lys in corn was not different from the SID of Lys in HFCG, and the SID of Trp in corn was also not different from the SID of Trp in CGM-LCE. Among corn coproducts, the SID of CP, Arg, and Lys were greater (P < 0.05) in HFCG and CGM-LCE than in corn bran, the SID of Lys and Val was greater (P < 0.05) in LCE than in corn bran, and the SID of Arg was greater (P < 0.05) in HFCG and CGM-LCE than in LCE, but for the remaining indispensable AA, no differences among corn coproducts were observed. In conclusion, the corn coproducts used in these experiments contain less ME and have reduced SID of most AA compared with corn, but there are no differences in ME among corn coproducts and only few differences in the SID of indispensable AA among HFCG, corn bran, LCE, and CGM-LCE.

The objectives of this experiment were to evaluate in vitro DE (IVDE) of selected feed ingredients using a computer-controlled simulated digestion system (CCSDS) and predict DE of ingredients for growing pigs. Samples of 6 ingredients with a wide range in energy and nutrient profile were collected. The CP and GE contents ranged from 9.9 to 50.9% and 4,493 to 4,841 kcal/kg (DM basis), respectively. Two control diets were formulated to achieve different CP contents (12.5 and 20.0%). Three experimental diets were formulated by replacing 20% of the high-CP control diet with corn, wheat, or wheat bran, whereas 3 additional diets were formulated by replacing 20% of the low-CP control diet with soybean meal, rapeseed meal, or cottonseed meal. The DE was determined using barrows (n = 24; initial BW = 35.9 ± 1.9 kg) in 2 periods with 6 observations per diet treatment and ranged from 2,769 to 4,368 kcal/kg. The equation for the DE content (kcal/kg of DM) using chemical components as independent variables was DE = 4,186 + 0.06 × CP + 79.33 × ether extract - 14.57 × NDF - 47.99 × ADF, with R(2) = 0.995, residual SD (RSD) = 89.5 kcal/kg, CV = 2.4%, and P = 0.10 (chemical component values; %). The IVDE ranged from 2,289 to 3,724 kcal/kg and was highly related to the determined DE content of the ingredients (R(2) = 0.91, RSD = 193 kcal/kg, and CV = 5.2%). The relationship between IVDE:GE and DE:GE was very high (R(2) = 0.93, RSD = 3.8%, and CV = 4.7%). The average values of CV for IVDE (0.75%) and IVDE:GE (0.73%) were less than that for determined DE (2.58%) and DE:GE (2.54%), respectively. In conclusion, the IVDE content determined, using a CCSDS with relatively high accuracy and acceptable repeatability, might be used to predict DE of feed ingredients for growing pigs.

A study was conducted to evaluate the effect of 2 hulless barley varieties, with or without the addition of a nonstarch polysaccharide (NSP) enzyme complex (β-glucanase and xylanase), on growth performance of weaned piglets in a 42-d feeding study. The study was conducted with 140 piglets (PIC × Duroc). Pigs were allocated to pens (4 castrated males or 4 females per pen) based on BW and sex, and pens were assigned to 5 experimental diets with 4 pens of castrated males and 3 pens of females per treatment. Five isonitrogenous and isoenergetic diets were compared: 1) control corn-based diet (CTR), 2) diet with corn and wheat bran replaced by the Astartis hulless barley variety (AS), 3) diet with corn and wheat bran replaced by the AS supplemented with the NSP enzyme complex (ASE), 4) diet with corn and wheat bran replaced by the Alamo hulless barley variety (AL), and 5) diet with corn and wheat bran replaced by the AL supplemented with the NSP enzyme complex (ALE). The diets were formulated to meet or exceed nutrient requirements and offered in 2 phases: d 0 to 14 and d 14 to 42. At the end of the study, pigs fed AS and AL had equal weights as pigs fed CTR. Pigs fed the hulless barley diets had greater (P < 0.05) ADG during the second phase (P2) and overall phase, BW at d 42, and G:F during the P2 than those fed the CTR. Pigs fed the ASE and ALE had greater (P < 0.05) ADFI during the P2 and overall ADG than those fed the AS and AL. The increases in ADG during the P2 and final BW obtained with NSP enzyme supplementation were greater in pigs fed the AS than those fed the AL (barley × enzyme, P < 0.05). On the other hand, the NSP enzyme complex increased G:F in pigs fed the AS during the P2 and overall phase, but it had no effect on those fed the AL (barley × enzyme, P < 0.05). In conclusion, hulless barley with or without the NSP enzyme complex can be a replacement ingredient for corn and wheat bran in weaned pig diets. Addition of the NSP enzyme complex to AS variety, but not AL variety, improved growth performance of weanling pigs.