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Vitamin E is important for animal production because of its effects on health and product quality, but the amount and form required remains controversial. Our objective was to quantify the absolute bioavailability of oral all-rac-α-tocopheryl acetate (α-TAc) in swine (22 ± 1 kg and 8 wk old, fitted with jugular catheters) adapted to a diet supplemented with 75 mg/kg all-rac-α-TAc; 75 mg/kg was chosen because this level represents the nonweighted average inclusion level in piglet diets across Western key swine-producing countries. For this, a 350-g test meal (6% fat) was supplied at time 0 containing 75 mg deuterated (D9) all-rac-α-TAc to 9 animals, and 8 animals received an intravenous (i.v.) dose containing deuterated (D6) RRR-α-tocopherol (α-T) at one-eighth the oral dose and a test meal without supplemental vitamin E. Plasma samples (12 to 13 per animal) were obtained at incremental intervals over 75 h for analysis of deuterated α-T using liquid chromatography–tandem mass spectrometry. Surprisingly, the i.v. dose rapidly disappeared from plasma and then reappeared. The half-life for this first peak was only 1.7 ± 0.3 min. The second peak had an appearance rate (Ka) of 0.10 ± 0.06 d−1and a half-life of 5.9 ± 1.2 h. Oral dosing resulted, after a lag of 56 min, in a Ka of 0.91 ± 0.21 d−1and a half-life of 2.6 ± 0.8 h. The bioavailability for oral α-TAc was 12.5%, whereas the area under the curve was only 5.4%. This low bioavailability, small area under the curve, and short half-life are likely because of various factors, that is, the use of only 6% fat in the diet, the use of the acetate ester and all-rac, and the high dose relative to requirements. In conclusion, i.v. dosed vitamin E shows both a rapid and a very slow pool, whereas orally dosed vitamin E shows a single slow pool. The oral material has a very short half-live (44% of i.v. or 2.6 h), low bioavailability (12.5%), and a very small area under the curve (5.4%), bringing into question the efficacy of typical doses of vitamin E in swine diets for alleviating oxidative stress.

Intestinal barrier function in pigs after weaning is almost exclusively determined in terminal experiments with Ussing chambers. Alternatively, the recovery in urine of orally administered lactulose can be used to assess intestinal permeability in living animals. This experiment was designed to study the barrier function of the small intestine of pigs over time after weaning. The aim was to relate paracellular barrier function (measured by lactulose recovery in the urine) with macromolecular transport [measured by horseradish peroxidase (HRP) using Ussing chambers] and bacterial translocation to assess whether lactulose recovery is related to possible causes of infection and disease. Forty gonadectomized male pigs (6.7 ± 0.6 kg) were weaned (d 0) at a mean age of 19 d, fitted with urine collection bags, and individually housed. Pigs were dosed by oral gavage with a marker solution containing lactulose (disaccharide) and the monosaccharides L-rhamnose, 3-O-methylglucose, and D-xylose at 2 h and at 4, 8, and 12 d after weaning. The recovery of sugars in the urine was determined over 18 h after each oral gavage. The day after each permeability test, the intestines of 10 pigs were dissected to determine bacterial translocation to the mesenteric lymph nodes and jejunal permeability for HRP in Ussing chambers. Recovery of L-rhamnose in urine was affected by feed intake and by the time after weaning (P≤ 0.05). Recovery of lactulose from the urine was greater (P≤ 0.05) at 4, 8, and 12 d after weaning compared with the first day after weaning and was negatively correlated with feed intake (r = −0.63, P≤ 0.001). The mean translocation of aerobic bacteria to the mesenteric lymph nodes was greater at 5 and 13 d after weaning compared with d 1 (P≤ 0.05). Lactulose recovery showed no correlation with permeability for HRP nor with bacterial translocation (P> 0.05). Although both lactulose recovery and bacterial translocation increased over time after weaning, lactulose recovery did not correlate with the permeability for HRP nor bacterial translocation within a pig (P> 0.05). Therefore, we conclude that lactulose recovery in the urine of pigs after weaning is not associated with risk factors for infections. However, it appears to be possible to measure paracellular barrier function with orally administered lactulose in pigs shortly after weaning. Further studies will reveal whether this variable is relevant for the long-term performance or health of pigs after weaning.

The experiment was designed to assess whether corn fractions or extrusion of corn can result in feed ingredients with a greater nutritional value than corn. Corn grain (8.0% CP, 0.21% P, 9.8% NDF) was processed by extrusion (82.8°C, 345 kPa steam pressure for 12 s) or by dry milling to derive fractions rich in germ (13.1% CP, 1.19% P, 17.2% NDF), hulls (8.1% CP, 0.27% P, 32.6% NDF), and endosperm, namely tails (6.6% CP, 0.07% P, 3.6% NDF) and throughs (7.4% CP, 0.15% P, 4.5% NDF). Relative recovery in each fraction was 16, 20, 44, and 20%, respectively. Ileal digestibility of DM, P, and amino acids was determined using diets containing 7.0% CP from soybean meal and 5.3% CP from one of the test products. To allow for determination of standardized ingredient, ileal digestibility, basal endogenous AA losses were determined using a protein-free diet (74.6% cornstarch and 18.7% sucrose). Soybean meal ileal digestibility was determined using a diet (12.3% CP) based on soybean meal (23.3%). Eight barrows (27 ± 2 kg) fitted with T-cannulas were fed 8 experimental diets (5-d adaptation and 2-d collection period) such that each diet was evaluated in at least 5 barrows. Relative to corn (77.9 ± 1.2%), ileal digestibility of DM was greater for extruded corn (82.5%; P= 0.02), tails (85.9%; P< 0.01), and throughs (85.0%; P< 0.01), but it was lower for hulls (62.2%; P< 0.01) and germ (51.1%; P< 0.01). For P, corn (41.6 ± 9.5%), throughs (47.2%), and hulls (57.3%) had similar ileal digestibility, but germ (7.9%) had lower ileal digestibility (P= 0.02) than corn; tails (27.6%) and extruded corn (23.5%) were not different from corn or germ but were lower than throughs and hulls. For total AA, corn (84.7 ± 2.4%), throughs (84.3%), and hulls (85.8%) had similar ileal digestibility, but germ (76.6%) had lower ileal digestibility (P< 0.01) than corn; tails (82.0%) and extruded corn (81.7%) were intermediate. In conclusion, germ and hulls have a low ileal DM digestibility; germ also has low AA and P digestibility. Extrusion improved the ileal DM digestibility of corn. To maximize the ileal digestibility, removal of germ and hull from corn or extrusion of corn may thus be of interest.

As environmental constraints become more important issues for the animal industry, selecting feed ingredients that yield good animal performance but also minimize environmental impact of animal production becomes critical. The objective of this research was to identify which compositional features would be desirable for soybean meal to maximize nutritional value and minimize animal waste. Eight soybean samples were selected from a database of 72, such that maximal variability for CP, NDF, and ADF content was obtained. Samples were subsequently processed into meal using standardized procedures. In Experiment 1, 8 cannulated pigs were used to determine ileal digestibility following a Latin square design. In Experiment 2, 5 of the samples were used in complete feeds and 10 pigs were used in a crossover Latin square design to determine the total tract digestibility, odorants in fresh and 5-d-old manure, and ammonia emission from manure. Differences up to 6% in ileal DM digestibility and 8% in ileal CP digestibility were observed. This difference was reduced to 1.1% for total tract DM digestibility and 4% for total tract CP digestibility. Differences in odorant concentration were 3-fold and for in vitro ammonia emission were 42%. The only compositional variable with a significant effect on digestibility was stachyose, which negatively affected ileal digestibility of DM (r = −0.80, P= 0.02) and energy (r = −0.73, P= 0.04). None of the compositional variables measured affected ileal CP digestibility. Ileal CP digestibility, however, was correlated with estimated CP fermentation in the large intestine (r = −0.86, P= 0.06) and with in vitro ammonia emission after 48h (r = −0.81, P= 0.09). In conclusion, nutritionally relevant variability exists in soy varieties. Low stachyose content is important for maximizing ileal energy digestibility of soybean meal. Although no compositional variable was identified that explained differences in ileal CP digestibility, maximizing ileal CP digestibility is of interest for maximizing the nutritional value of soybean meal and possibly for reducing ammonia and odor emissions.

The objective of this study was to compare three infrared spectroscopy techniques for routine evaluation of AA in animal meals. Animal meals (n = 54) with known AA contents were scanned with a near (NIRS), mid (FTIR), and Raman infrared spectrometer. For NIRS and Raman, samples were scanned “as is”, whereas for FTIR, samples had to be finely ground before scanning to obtain reasonable spectra. Both FTIR and Raman data suffered from noise; for Raman, this prevented the development of calibrations. Using derivatized spectral data and a standardized outlier removal procedure, calibrations for nutritionally relevant AA could be developed that were equivalent for both NIRS and FTIR. The variation across AA tested explained (r2) by these calibrations was 70% for NIRS and 68 ± 3% for FTIR. Removing spectral data between 4,000 and 2,000 cm−1from the FTIR data improved calibrations (P= 0.09) and explained an average of 77% of the variation with prediction errors lower than obtained with NIRS (P< 0.01). However, FTIR calibrations based on the entire or the shortened spectrum contained fewer samples than did NIRS calibrations (41 and 39 vs. 48, respectively; P< 0.01) because more samples were removed as outliers. In conclusion, Raman did not yield acceptable spectra for animal meals. For FTIR, sample preparation was more time-consuming because the samples required grinding before analysis. Using the entire mid-infrared range, FTIR calibrations were comparable to NIRS calibrations. Calibrations for FTIR were improved by eliminating wave numbers that exhibited more noise, resulting in prediction errors better than those for NIRS. Thus, FTIR has the potential to yield better calibrations for AA in animal meals than NIRS, but it requires greater care in sample preparation and scanning.

Typically, in vitro methods used for estimating the amount of ileal digestible AA do not exhaustively digest samples, and arbitrary methods for separating digestible from indigestible protein are used. This may lead to over- or underestimation of digestibility coefficients. A method that exhaustively digests proteins using pepsin and pancreatin was developed, and the first objective of this research was to confirm that exhaustive digestion was indeed appropriate and to determine the fractionation method for separating digestible from indigestible proteins. For this, three homoarginine-labeled animal proteins were prepared. Samples were subsequently digested in vivo and in vitro to determine which fraction should be considered indigestible, and in vitro followed by in vivo to determine whether the extent of digestion in vivo was improved by predigestion. In vivo, soluble but unabsorbed peptides were smaller than 1 kDa, suggesting that the size of soluble peptides is not what prevents their absorption. Thus, all in vitro-soluble proteins should be considered digestible. In vitro, 88 ± 3% of the soluble peptides were smaller than 1 kDa, with the remainder between 1 and 5 kDa, suggesting that in vitro digestion is less complete. Predigested samples were digested in vivo to the same size distribution as the nonpredigested samples. The second objective was to test whether in vitro digestibility assays based on these principles equaled in vivo digestibility. For this, digestibility data for 25 animal proteins were compared. Results showed a lack of correlation between lysine digestibility coefficients; however, across samples, the extent of digestion did not differ for lysine (P= 0.71), threonine (P= 0.26), methionine (P= 0.18), or valine (P= 0.66), whereas in vitro digestibility coefficients were lower for (the less water-soluble) histidine (P= 0.05), isoleucine (P< 0.01), leucine (P< 0.01), and phenylalanine (P= 0.05). In conclusion, in vitro digestibility assays should exhaustively digest proteins to mimic in vivo digestibility. All in vitro-soluble peptides could be considered digestible, because in vivo, no large soluble peptides were observed whose size prevented them from being absorbed. However, an in vitro assay based on these principles lacked precision for highly water-soluble AA, and underestimated digestibility for other AA. Better solubilization of the digesta and more replicates may improve the in vitro assay further.

Quantifying odor is important for objectively assessing the impact of animal production systems on surrounding areas. A possible method that has received little attention is Fourier transform (mid) infrared spectroscopy (FTIR). Gases that contribute to odor have unique infrared spectra, and the advantage of FTIR over electronic nose technology or gas chromatography is that theoretically all these gases can be analyzed instantaneously. To determine the feasibility of FTIR for predicting odor, 71 air samples analyzed by olfactometry were scanned in a spectrometer using an 84-m path-length gas cell. Scans were obtained over a period of about 1 min and from 4,000 to 740 cm(-1) with a resolution of 0.5 cm(-1). Calibrations for predicting odor were developed using partial least squares regression with full cross-validation. Air samples were obtained from experiments with pigs fed diets formulated to alter odor emission or from stored manure. Odor threshold dilution ratios averaged 676+/-491 units, with a range from 120 to 2,161. Using these samples, a prediction error for odor sensation of 344 units (R2 = 0.51) was obtained. Log transformation of the odor data improved the R2 to 0.61. Based on the olfactometry data, it is estimated that the measurement error of olfactometry is 250 units, which limits the R2 of any method to approximately 0.74. Thus, this calibration is very encouraging. In conclusion, FTIR shows promise as a practical means for objectively assessing swine odor.

The amount of nutrients (i.e., N, P, Zn, and Cu) and associated odors emitted from production animals into the environment can be modulated by several different nutritional strategies, but their practical application is dependent on costs and biological limitations. In general, nutrient excretion may be reduced by avoiding the overfeeding of specific nutrients or by using nutritional manipulations to enhance nutrient utilization in the animal. Loss to the environment can be avoided by manufacturing and handling the feed in a pelletized form that will minimize waste and improve feed/gain. Other strategies for minimizing nutrient losses include: 1) the development of feeding programs that are specific for sex and strain of the animal; 2) increasing the number of feed phases to better meet the animal's age-related requirements; 3) formulating diets to include the minimal amounts of nutrients required to satisfy production goals; 4) meeting the animal's amino acid requirements; 5) using synthetic amino acid supplements to feed to reduce N emission; 6) using feed ingredients with high digestibility and nutrient bioavailability; and 7) formulating diets based on nutrient availability instead of total nutrient content. Nutrient digestibility of feedstuffs is dependent on processing conditions, genetic characteristics of the grains and oilseeds, and the presence of nutritional antagonists in specific feedstuffs used in the diet. Feed ingredients that lead to odor production can be avoided (e.g., fishmeal and some easily fermentable feed ingredients). Feed additives, such as antibiotics, nonstarch polysaccharides, direct-fed microbials, organic acids, microbial enzymes (i.e., phytase, carbohydrases, and proteases) can be used to increase the digestibility and absorption of nutrients or to modulate the microflora. Finally, a cost factor for the control or disposal of nutrients or odor should be considered in the feed formulation to optimize the various nutritional strategies discussed above. Regardless of biological and economic limitations, significant reductions in nutrient and odor emission from nonruminants can be achieved by appropriate nutritional strategies, but response may differ for swine and poultry.

This study was designed to determine the effects of hydrolyzed feather meal inclusion on growth performance, carcass characteristics, nutrient digestibility and fecal odorous compounds in modern lean growth genotype pigs. Two hundred forty pigs (BW = 23.2 +/- 1.3 kg) were allotted based on BW and sex to a 2 x 6 factorial arrangement of treatments (four pens per treatment; five pigs per pen) in a randomized complete block design. Factors consisted of 1) sex (barrows or gilts) and 2) dietary treatment (0, 2, 4, 6, 8, or 10% hydrolyzed feather meal). Diets were formulated to contain 1.00, 0.90, 0.75, or 0.60% apparent ileal digestible lysine for phases 1 to 4, respectively, with other amino acids provided at an ideal ratio. Available P and ME were kept constant within each phase. No significant interactions between feather meal inclusion and sex were observed for growth performance (P > 0.15). Body weight gain was reduced (P < 0.05) for pigs fed 10% feather meal compared to pigs fed 0, 4, or 8% feather meal. Feed intake of pigs fed 10% feather meal was reduced (P < 0.05) compared to pigs fed 0 or 4% feather meal. Ultrasound backfat measurements tended (P = 0.12) to increase with increasing levels of feather meal. Daily lean gain was less (P < 0.05) in pigs fed 10% feather meal than in pigs fed either 0, 2, 4, or 8% feather meal. Digestibility of N measured on wk 9 decreased quadratically (P < 0.001) with increasing levels of feather meal. Phosphorus digestibility increased in a linear fashion (P < 0.02), however, the improvement in P digestibility with increasing levels of feather meal was more pronounced in barrows compared to gilts (interaction, P < 0.05). Fecal samples obtained from pigs fed 0, 4, or 8% feather meal were analyzed for odorous compounds. Concentrations of butanoic, pentanoic, and 3-methylbutanoic acid were greater (P < 0.05) and concentrations of 3-methylphenol, 4-methylphenol, indole, and decane were less (P < 0.05) in feces from pigs fed feather meal. These results suggest that feather meal can be included in diets for growing-finishing pigs at a rate of 8%. Excretion of N in feces increased but P excretion decreased with increasing levels of feather meal. Odorous compounds in feces can be affected by the inclusion of hydrolyzed feather meal, but the exact impact of these changes on odor perception remains to be elucidated.

To assess differences in soybean meal quality related to region of production, researchers in Illinois, Kansas, North Carolina, The Netherlands, and Ohio collected four soybean meal samples processed locally at least 15 d apart. These samples were assayed for ileal amino acid digestibility by pigs using a common soybean meal and a soy protein concentrate as references, and a low-protein casein diet for determination of endogenous amino acid losses. Digestibility was determined at each university using seven barrows surgically fitted with ileal cannulas in a 7 x 7 Latin square design. The experimental diets contained 17% CP from the test material except for the low-protein casein diet. Animals were fed twice daily, 12 h apart, at a level of 45 g x kg(-0.75) BW for each meal. Following a 5-d adaptation period, ileal digesta were collected for two 12-h periods for 2 d to be used for determination of ileal digestibility. Variation in amino acid digestibility was very small among and within sites and was much smaller than variation in the concentration of amino acids. Among sites, samples from The Netherlands had less total and thus digestible lysine and methionine than the U.S. samples (P < 0.05). The soybean meals tested in this experiment were approximately 4% higher in amino acids than that reported in the NRC (1998). True (standardized) digestibilities, however, were very similar to NRC values except for cysteine and threonine, which were 5 and 3 percentage points lower in this experiment, respectively. In conclusion, soybeans grown in the United States and locally processed into soybean meal were very similar in nutritional composition. Soybean meals produced in The Netherlands were lower in lysine and methionine (P < 0.05) but had a digestibility similar to that produced in the United States.

Adipic acid is only partially catabolized when it is fed to animals, and a portion of it is excreted in urine. The excreted portion may lower urinary pH and, as a result, ammonia emission. The present study tested this hypothesis. In Exp. 1, nursery pigs (n = 14) were fed (for a period of 7 d) either a standard nursery diet or the same diet supplemented with 1% adipic acid to assess effects on urinary pH (collected on d 5 or 6) and in vitro ammonia emission from the collected urine samples that were mixed with control feces. In Exp. 2, grower pigs housed 10 each in one of two chambers were fed a control diet or the same diet supplemented with 1% adipic acid. Ventilated air was quantified and analyzed for ammonia using Fourier transform infrared spectroscopy to determine the effects of feeding 1% adipic acid on ammonia emission. The results from Exp. 1 showed that adipic acid strongly reduced urinary pH (from 7.7 to 5.5, P< 0.05). In vitro ammonia emission from these urine samples was significantly reduced at all the time points evaluated (1, 3, 18, and 46 h with reductions of 94, 93, 70, and 39%, respectively, P< 0.05). Experiment 2 showed that adipic acid supplementation reduced ammonia emission by 25% (P< 0.05), which corresponded to the predicted reduction in ammonia emission based on the reduction in manure pH observed. In conclusion, feeding adipic acid lowers urinary pH and reduces ammonia emission. The reduction in ammonia emission, though, does not correspond to the reduction in urinary pH but corresponds to the reduction in fecal pH as a result of mixing the urine and feces, in which feces act as a strong buffer.

Adipic acid, upon catabolism, results in intermediates that bear a structural similarity to lysine degradation products. The objectives of this research were to determine whether adipic acid affects lysine concentrations in plasma and to evaluate whether adipic acid improves the efficiency of lysine utilization in pigs. In Exp. 1, nursery pigs (n = 14) were fed (for a period of 7 d) either a standard nursery diet or the same diet supplemented with 1% adipic acid to assess effects on plasma amino acid concentrations (plasma collected on d 7). In Exp. 2, nursery pigs (n = 56) were fed (for a period of 15 d) either a control diet or the same diet but deficient in either lysine, threonine, or tryptophan with or without supplemental adipic acid to assess the effects of adipic acid on the efficiency of amino acid utilization. The results from Exp. 1 showed that adipic acid increased plasma lysine (by 18%) but not alpha-amino adipic acid, an intermediate in lysine degradation. Experiment 2 demonstrated that adipic acid did not increase the efficiency of utilization of lysine, threonine, or tryptophan. The lack of effects on α-amino adipic acid in Exp. 1 and the lack of a positive effect on the efficiency of utilization of lysine, threonine, and tryptophan suggest that adipic acid does not inhibit the mitochondrial uptake of lysine and(or) its degradation in the mitochondrion. It is concluded that feeding adipic acid increases plasma lysine but does not improve the efficiency of lysine utilization.