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Biomedical subjects

G C Fahey

Publications and source records attributed to G C Fahey.

At least 73 records · Page 4Linked to original sources

Alteration of the fiber and lipid components of a defined-formula diet: effects on stool characteristics, nutrient digestibility, mineral balance, and energy metabolism in humans.

Eighteen healthy males with a body weight of 70.0 +/- 3.1 kg consumed three defined-formula diets that varied only in their fiber and/or lipid components: 1) 6.4% fiber (100% soy polysaccharides) and 13.1% lipid [50% medium-chain triacylglycerols (MCTs), 40% corn oil, and 10% soy oil]; 2) 3.4% fiber (75% oat fiber, 17.5% gum arabic, and 7.5% carboxymethylcellulose) and 15.6% lipid (20% MCTs, 50% canola oil, and 30% high oleic acid safflower oil); and 3) 4.4% fiber (same as diet 2) and 14.5% lipid (same as diet 1). Consumption of diet 2 resulted in slightly firmer stools and provided the greatest amount of fecal output per unit fiber intake. Total dietary fiber (TDF) digestibility was lowest for men fed diets 2 and 3, but nitrogen and lipid digestibilities and energy metabolism criteria were not different among diets. Although mineral excretion patterns differed among treatments, fiber and lipid components of the diets appeared not to be responsible for these differences. Results indicate that fecal output can be maintained with a lower intake of a blend of oat fiber, gum arabic, and carboxymethylcellulose compared with soy polysaccharides. Except for TDF digestibility, alteration of amounts and/or sources of fiber and lipid components of defined-formula diets used in this experiment did not alter nutrient digestibility, energy metabolism, or mineral retention.

Adult↗

Effects of glycine and bovine serum albumin on inhibition of propionate metabolism in ovine hepatocytes caused by reduced phenolic monomers.

Hepatocytes isolated from sheep were incubated in the presence of reduced phenolics and glycine to determine the effects of these compounds on hepatic propionate metabolism in vitro. 3-Phenyl-propionic (PPA) or t-cinnamic (CA) acids, but not benzoic (BA) or 3-(4-hydroxyphenyl)propionic (4OHPPA) acids, decreased conversion of propionate to glucose at .05 mM in the absence of supplemental glycine. At 1.2 mM, all reduced phenolics decreased conversion of propionate to glucose in the absence of supplemental glycine. Addition of glycine to the incubation medium linearly alleviated the inhibition by BA, PPA, or CA, suggesting that physiological glycine concentrations limited alleviation of inhibition of propionate metabolism. Hippuric acid production increased as glycine concentration increased in the presence of PPA, CA, or 4OHPPA. Bovine serum albumin did not alleviate inhibition of conversion of propionate to glucose caused by BA, PPA, or CA and slightly alleviated inhibition caused by 4OHPPA (.4 mM). Of the reduced phenolics tested, PPA is the most likely to inhibit gluconeogenesis from propionate in ovine liver in vivo.

Animals↗

In vitro fermentation of cellulose, beet pulp, citrus pulp, and citrus pectin using fecal inoculum from cats, dogs, horses, humans, and pigs and ruminal fluid from cattle.

We evaluated the influence of gastrointestinal tract microflora from several species on fiber fermentation characteristics in vitro. Selected fibrous substrates (cellulose, beet pulp, citrus pulp, and citrus pectin) were incubated for 6, 12, 24, and 48 h with ruminal fluid from cattle or feces from dogs, cats, pigs, horses, or humans. When data were pooled across all substrates and fermentation times, OM disappearance (29.4%) and acetate, propionate, butyrate, and total short-chain fatty acid (SCFA) production (1.09, .41, .12, and 1.61 mmol/g of OM, respectively) were lowest (P < .05), and lactate production (.23 mmol/g of OM) was greatest (P < .05) for horse fecal microflora compared with samples from the other species. The greatest (P < .05) acetate production resulted when substrates were fermented by cat fecal microflora (2.38 mmol/g of OM). The greatest (P < .05) propionate productions resulted from pig fecal and cattle ruminal microflora (.88 and .83 mmol/g of OM, respectively), and the greatest (P < .05) butyrate productions resulted from human and pig fecal microflora (.39 and .40 mmol/g of OM, respectively). Total SCFA production was greatest (P < .05) for cat fecal microflora (3.38 mmol/g of OM). When data were pooled across the species, substrate OM disappearance and SCFA production ranked from least to greatest in the following order: cellulose < beet pulp < citrus pulp < citrus pectin. The fermentability of different fibrous substrates by fecal or ruminal microflora from various species seems to be dependent not only on the fermentative activity of the microbial population but on other factors as well, perhaps lag time and rate of digesta passage.

Adult↗

Dietary fiber for dogs: IV. In vitro fermentation of selected fiber sources by dog fecal inoculum and in vivo digestion and metabolism of fiber-supplemented diets.

Two experiments were conducted to evaluate single sources and blends of dietary fiber in dog food. In Exp. 1, 14 fibrous substrates were fermented in vitro using dog feces as the source of inoculum. Organic matter disappearance was lowest (P < .05; < 10%) for Solka Floc and oat fiber and greatest (P < .05; > 80%) for fructooligosaccharides (FOS) and lactulose. Solka Floc, oat fiber, gum karaya, and xanthan gum produced the least (P < .05; < 1 mmol/g of substrate OM) total short-chain fatty acids (SCFA). Lactulose, citrus pectin, and guar gum produced the greatest (P < .05; > 6.8 mmol/g of substrate OM) total SCFA. In Exp. 2, six diets were formulated based on results obtained in Exp. 1. Treatments included 1) beet pulp (BP), 2) Solka Floc (SF), 3) citrus pulp (CP), 4) stool blend (SB), 5) SCFA blend (SC), and 6) combination blend (CB). Digestibility of DM and total dietary fiber (TDF) was greatest (P < .05; 87.3 and 60.8%, respectively) for dogs consuming the SC diet. Feces from dogs fed SC were scored as more unformed and liquid in consistency than feces from dogs fed the other diets. Dogs consuming the SF and SB diets had the lowest (P < .05; 11.0 and 4.1%, respectively) TDF digestibilities. Organic matter disappearance values derived from substrates fermented in vitro reasonably predicted the fiber digestibility of diets fed to dogs. Moderately fermentable dietary fiber sources, such as BP, promote excellent stool characteristics without compromising nutrient digestibility, and may promote gastrointestinal tract health by optimizing SCFA production.

Animals↗

In vitro fermentation of selected fibrous substrates by dog and cat fecal inoculum: influence of diet composition on substrate organic matter disappearance and short-chain fatty acid production.

Two in vitro fermentation experiments were conducted to evaluate the influence of source of dietary fiber fed to dogs and cats on fermentative activity of their fecal microflora. In Exp. 1, six English Pointer dogs were fed a diet containing either a non-fermentable fiber (Solka Floc) or a fermentable fiber (citrus pulp). A fecal sample from each dog was used as the inoculum source to determine in vitro OM disappearance (OMD) and short-chain fatty acid (SCFA) production from selected fibrous substrates. When data were pooled across substrates and fermentation times, a lower (P = .02) OMD (24.8 vs 29.4%) and a higher (P = .01; 3.8 vs 2.2) acetate to propionate ratio (A:P) occurred for the Solka Floc than for the citrus pulp diet. In Exp. 2, six short-hair cats were fed a diet containing no supplemental fiber (NF) or a diet containing beet pulp (BP). When data were pooled across substrates and fermentation times, NF resulted in a greater (P < .01) A:P than the BP diet (3.4 vs 1.5). The BP treatment resulted in a slightly higher (P = .07) OMD (42.0 vs 39.3%) and a higher (P = .07) propionate production (.74 vs .47 mmol/g of OM) than the NF diet. In summary, in vitro substrate OMD increased and A:P decreased when fecal inoculum from dogs and cats fed diets containing a supplemental source of fermentable fiber was used. In vitro fermentation of fibrous substrates by fecal microflora from dogs and cats increased with inclusion of fermentable fiber in the diet.

Animal Feed↗

Portal and hepatic fluxes in sheep and concentrations in cattle ruminal fluid of 3-(4-hydroxyphenyl)propionic, benzoic, 3-phenylpropionic, and trans-cinnamic acids.

Extraction methods and HPLC procedures were developed for analysis of potential ruminal metabolites of dietary phenolics (reduced phenolics). Hepatic portal venous blood from wethers fed bromegrass, bermudagrass, ryegrass-wheat, and alfalfa hays also was analyzed for hippuric (HA), 3-(4-hydroxyphenyl)propionic (4OHPPA), benzoic (BA), 3-phenylpropionic (PPA), and t-cinnamic (CA) acids. Additionally, mesenteric arterial and hepatic venous blood was analyzed and, in conjunction with blood flow measurements, fluxes for portal-drained viscera (PDV) and liver were calculated. Ruminal fluid from four steers fed two levels of forage and two forage particle sizes in a Latin square design was analyzed for PPA and CA. 3-Phenylpropionic and benzoic acids were the most concentrated reduced phenolics identified in hepatic portal venous blood. Concentrations of PPA in ruminal fluid varied with ruminal disappearance of p-coumaric and ferulic acids. Additionally, hepatic portal venous concentrations of PPA were correlated (P < .05) with p-coumaric acid (r = .57) and ferulic acid (r = .67) intakes. Net release of PPA from PDV was observed, suggesting absorption of PPA from the gut. The liver removed PPA and BA with less efficiency. Given the relatively high concentrations of PPA in blood of ruminants, specific effects of this reduced phenolic on liver metabolism of ruminants should be assessed.

Animals↗

Dietary fiber for cats: in vitro fermentation of selected fiber sources by cat fecal inoculum and in vivo utilization of diets containing selected fiber sources and their blends.

Two experiments were conducted to evaluate the addition of single sources and blends of dietary fibers to cat diets. In Exp. 1, fermentability of selected fibrous substrates by cat fecal microflora was evaluated. After 24 h of fermentation, OM disappearance (OMD) and total short-chain fatty acid (SCFA) production were greatest (P < .05) for citrus pectin, guar gum, and locust bean gum, whereas Solka Floc resulted in the least (P < .05) OMD and total SCFA production. In Exp. 2, six diets were formulated based on results of Exp. 1. The highest (P < .05) digestibilities of DM and OM occurred when cats consumed the diet with no supplemental fiber, and the lowest (P < .05) digestibilities occurred when cats consumed the SCFA blend (SC) diet. Nitrogen and lipid digestibilities also were lowest (P < .05) for cats consuming the SC diet, whereas total dietary fiber (TDF) digestibility (P < .05) was greatest for cats consuming the beet pulp, SC, and combination blend diets. Fecal consistency scores were highest (P < .05) for cats consuming the SC diet, indicating liquid, unformed stools. In conclusion, the in vitro fermentation technique was reasonably accurate in predicting in vivo digestion of fiber. The SC diet, which contained the most fermentable fibers, severely decreased nutrient digestibility and resulted in poor stool characteristics. Diets that contain moderately fermentable fiber provide fermentation end products that may be important in maintaining the health of the gastrointestinal tract of the cat.

Animal Feed↗

Influence of altering ruminal degradation of soybean meal protein on in situ ruminal fiber disappearance of forages and fibrous byproducts.

The objective was to determine the effects of altering ruminal CP degradation of soybean meal (SBM) by roasting (Exp. 1) on ruminal characteristics and extents of in situ disappearance of DM, OM, and fiber components (Exp. 2). A control diet (8.2% CP) containing oat hulls, corn silage, starch grits, ammoniated corn cobs, and molasses was supplemented to 17.1% CP with unroasted SBM (SBM-0) or SBM roasted at 165 degrees C for 75, 150, or 210 min (SBM-75, SBM-150, and SBM-210, respectively). In Exp. 1, SBM was incubated for 0, 2, 4, 8, 12, 16, and 24 h in the rumen of two steers that were fed the SBM-0 diet. Extents of ruminal CP degradation and rates of N disappearance decreased (P < .05) linearly with increasing roasting time of SBM. In Exp. 2, five ruminally cannulated steers were used in a 5 x 5 Latin square design and were fed the five diets listed above during five 11-d periods. On d 11, five substrates (alfalfa hay, orchardgrass hay, corn silage, soy hulls, and wheat straw) were incubated in the rumen for 24 h. Extents of in situ disappearance of DM, OM, and fiber (NDF, ADF, cellulose, hemicellulose, and total dietary fiber) were analyzed as a split-plot design. No substrate x diet interaction (P > .05) was observed for any of the measurements evaluated. Extents of in situ disappearance (24 h) of DM, OM, and fiber were highest (P < .05) when the control diet was fed and were lowest (P < .05) when the SBM-0 diet was fed. Decreasing the availability of SBM protein in the diet by roasting increased (P < or = .10) extents of in situ disappearance of DM, OM, and fiber linearly. These extents were similar for steers fed the control diet or the diet containing SBM-210. Ruminal concentrations of NH3 N, branched-chain VFA, and valerate were highest (P < .05) and ruminal pH lowest (P < .05) when the SBM-0 diet was fed. Results indicated a rapid ruminal fermentation of both protein and readily available carbohydrates of SBM (resulting in pH below 6.0) during the first 4.5 h after feeding the SBM-0 diet. Making both protein and readily available carbohydrates of SBM more slowly fermentable by roasting slowed early fermentation processes, maintained higher ruminal pH, and encouraged earlier and faster ruminal fiber digestion.

Animal Feed↗

Effects of forage level and canola seed supplementation on site and extent of digestion of organic matter, carbohydrates, and energy by steers.

The objective of this study was to determine the effects of fat supplementation from canola seed (CS) on ruminal fermentation and postruminal digestion of OM, carbohydrates, and energy of diets containing different levels of forage. Six ruminally and duodenally cannulated beef steers (354 kg +/- 18) were given ad libitum access to six isonitrogenous diets that were offered twice daily in a 6 x 6 Latin square design. Treatments were arranged as a 2 x 3 factorial with two forage levels (70 vs 30% of dietary DM as corn silage) and three forms of CS supplementation including no CS or CS added at 10% of dietary DM as whole CS treated with alkaline hydrogen peroxide or untreated crushed CS. Fat from CS provided 5% of dietary DM. The remaining dietary ingredients were corn, canola meal, molasses, and urea. No interactions (P > .05) between dietary forage level and CS supplementation were observed for ruminal characteristics or digestion of OM, carbohydrates, and energy in the rumen, postruminally, or in the total tract. Fat supplementation from CS did not affect (P > .05) DMI. With few exceptions, fat supplementation did not affect (P > .05) ruminal, postruminal, or total tract digestibilities of OM, structural and nonstructural carbohydrates, and GE. Ruminal disappearance of GE was decreased (P < .05) when diets were supplemented with fat from whole treated CS, and total tract digestibilities of OM and GE were decreased (P < .05) when diets were supplemented with fat from CS in either form. Ruminal pH, concentrations of NH3 N and total VFA, and molar proportions of acetate, propionate, and butyrate were not affected (P > .05) by fat supplementation. Results suggest that fat supplementation from CS (at 5% of dietary DM) as whole treated or untreated crushed had no negative effects on ruminal fermentation of OM, carbohydrates, or energy when steers were given ad libitum access to diets containing high or low forage.

Animal Feed↗

Composition of ruminal bacteria harvested from steers as influenced by dietary forage level and fat supplementation.

The objective of this study was to examine the effects of dietary forage level and fat supplementation on the chemical composition of mixed ruminal bacteria (MRB). Six ruminally cannulated beef steers (354 kg +/- 18) were given ad libitum access to six diets (13.2% CP; DM basis) that were offered twice daily in a 6 x 6 Latin square design. Treatments were arranged as a 2 x 3 factorial with two forage levels (70 vs 30% of dietary DM as corn silage) and three forms of fat supplementation including no canola seed or canola seed added at 10% of dietary DM as whole treated with alkaline hydrogen peroxide or untreated crushed. Canola seed contributed 5% added fat to the total diet. The remaining dietary ingredients were corn, canola meal, molasses, and urea. No interactions (P > .05) between dietary forage level and canola seed supplementation were observed. Concentrations of OM, N, and all amino acids were higher (P < .05) in MRB from steers fed low forage than in MRB from steers fed high forage. Concentrations of purines and GE and the N:purines ratio in MRB were not affected (P > .05) by dietary forage level or canola seed supplementation. Canola seed supplementation did not affect (P > .05) concentrations of OM, N, or most of the amino acids in MRB. Concentrations of four essential amino acids (i.e., isoleucine, leucine, lysine, and phenylalanine) in MRB were decreased (P < .05) due to canola seed supplementation. Dietary forage level did not affect (P > .05) concentrations of long-chain fatty acids in MRB.(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

Utilization of supplemental fat by dairy cows fed diets varying in content of nonstructural carbohydrates.

Sixteen Jersey cows were used in a Latin square design to determine milk production and composition when the cows were fed supplemental fat in diets varying in nonstructural carbohydrate content. Eight cows were used in a second experiment to assess ruminal fermentation and nutrient digestibilities. Diets were 1) high nonstructural carbohydrates, no added fat; 2) high nonstructural carbohydrates, 2.5% added fat; 3) low nonstructural carbohydrates, no added fat; and 4) low nonstructural carbohydrates, 2.5% added fat. Diets consisted of alfalfa haylage, corn silage, and concentrate (22:22:56, DM basis). Soyhulls replaced corn grain in diets 3 and 4; high and low diets contained 37.3 and 27.2% nonstructural carbohydrate. The DMI, milk production, and milk fat content were not affected by fat or nonstructural carbohydrates, although milk production tended to be higher when cows were fed fat. Fatty acid composition and N distribution of milk were unchanged by nonstructural carbohydrates. Supplemental fat decreased contents of CP, casein N, and true protein N in milk. Low nonstructural carbohydrates increased total VFA concentration and percentage of acetate and decreased percentages of propionate and butyrate in ruminal fluid. Total fatty acid digestibility decreased when cows were fed fat. Digestibilities of fiber components and total fatty acids were higher for diets low in nonstructural carbohydrates. Dietary content of nonstructural carbohydrates did not affect production of milk or milk components by Jersey cows fed supplemental fat.

Animal Nutritional Physiological Phenomena↗

Forage level and particle size effects on orchardgrass digestion by steers: I. Site and extent of organic matter, nitrogen, and cell wall digestion.

Four steers (502 +/- 49 kg) with ruminal, duodenal, and ileal cannulas were used in a 4 x 4 Latin square experimental design with a 2 x 2 factorial arrangement of treatments to determine the effects of dietary forage:concentrate ratio (96:4 [96F] and 60:40 [60F]) and forage particle size (long hay [L] and coarsely ground hay [G]) on site and extent of digestion of OM, N, and plant cell wall monomeric components. Orchardgrass hay was the forage source used and was the sole source of cell wall material fed to steers (DMI = 88.6 g/kg BW.75). Diurnal variation in ruminal pH was greater when steers consumed 60F vs 96F (P < .01) and greater for G vs L (P < .10). Ruminal fluid volumes (liters) and daily outflows (liters/day) were greater (P < .05) when steers consumed 96F or L. True ruminal OM digestion (percentage of intake) was greater (P < .05) when steers consumed 60F (69.0) vs 96F (59.5) or L (65.8) vs G (62.7). Efficiency of net bacterial CP synthesis (grams of N/kilogram of true ruminal OM disappearance) was greater (P < .05) when steers consumed 60F (33.8) vs 96F (30.8). Total tract digestibilities of NDF and ADF were 63.3 and 53.0% when steers consumed 96F and were decreased (P < .05) to 52.3 and 43.8% when steers consumed 60F. Total tract digestibilities of plant cell wall arabinose, galactose, glucose, xylose, and uronic acids were 78.7, 69.7, 70.8, 67.6, and 79.7% when steers consumed 96F and were decreased (P < .05) when steers consumed 60F. Ruminal digestion accounted for greater than 90% of total tract digestion of all cell wall monosaccharide components when steers consumed 96F but accounted for 6 to 20 percentage units less of total digestion when steers consumed 60F. Total tract disappearances of cell wall acetyl groups, ferulic acid, and p-coumaric acid were 62.4, 79.4, and 50.6% when steers consumed 96F and were decreased (P < .05) to 49.7, 73.2, and 42.2% when steers consumed 60F. Addition of concentrate to diets, but not forage processing, decreased total tract digestibilities of cell wall components and shifted site of digestion to the lower gastrointestinal tract.

Animal Feed↗

Forage level and particle size effects on orchardgrass digestion by steers: II. Ruminal digestion kinetics of cell wall components.

Four steers (502 +/- 49 kg) with ruminal cannulas were used in a 4 x 4 Latin square experimental design with a 2 x 2 factorial arrangement of treatments to determine the effects of the dietary forage:concentrate ratio (96:4 and 60:40) and forage particle size (long hay and coarsely ground hay) on in situ ruminal digestion kinetics of orchardgrass hay DM and cell wall neutral monosaccharides, uronic acids, acetyl groups, and hydroxycinnamic acids. Dacron in situ bags containing orchardgrass hay were fermented for 0, 4, 8, 12, 18, 24, 48, and 96 h. Digestion profiles of DM and cell wall monomers in undigested residues recovered from the rumen were analyzed using a first-order, exponential equation to estimate the indigestible fraction (fi), the insoluble, potentially digestible fraction (fd), and the fractional rate constant (kd) of digestion of fd. Initial results indicated that fi was not consistently influenced by diet fed to the steers; thus, in situ digestion profiles were analyzed to estimate single fi and fd values common to all steers and diets and different estimates of kd for each steer x diet combination (16 total). Estimates of fi (percentage of original) for cell wall components were ranked in the following order: galactose (12.6), ferulic acid (13.9), arabinose (14.5), total uronic acids (15.4), glucose (19.8), xylose (28.4), p-coumaric acid (34.6), and acetyl groups (35.8).(ABSTRACT TRUNCATED AT 250 WORDS)

Animal Feed↗

Ruminal digestion and glycosyl linkage patterns of cell wall components from leaf and stem fractions of alfalfa, orchardgrass, and wheat straw.

Samples of alfalfa, orchardgrass, and wheat straw were hand-separated into leaf and stem fractions that were subjected to in situ ruminal fermentation for various lengths of time to assess the rate and extent of degradation of cell wall neutral monosaccharides, uronic acids, acetyl groups, and hydroxycinnamic acids. A second objective was to measure the glycosyl linkage patterns of leaf and stem fractions of substrates before and after ruminal fermentation. Samples were fermented for 0, 6, 12, 24, 48, 96, and 192 h in each of two ruminally cannulated steers. In situ disappearance data were fitted to a first-order exponential equation to estimate the following substrate parameters: insoluble, potentially digestible fraction (fd), indigestible fraction (fi), and fractional rate constant of degradation of the potentially digestible fraction (k). Leaves contained larger concentrations of crude protein and smaller concentrations of cell wall components than did stem fractions. Estimates of fi were 7.3, 39.2, 22.1, 49.3, 27.7, and 36.3 for dry matter disappearances for alfalfa leaf, alfalfa stem, orchardgrass leaf, orchardgrass stem, wheat straw leaf, and wheat straw stem, respectively. Averaged across substrates, estimates of fi for arabinose, galactose, glucose, xylose, uronic acids, acetyl groups, and p-coumaric acid were 16.5, 11.4, 14.8, 31.2, 12.8, 25.3, and 22.6% in leaf fractions and 29.5, 19.9, 37.5, 56.2, 35.0, 52.4, and 44.6% in stem fractions. Rates of digestion of all monomeric components except galactose and xylose were greater (P < .05) for alfalfa than for orchardgrass or wheat straw. Differences in digestibility of cell wall components from leaf and stem fractions were greater in alfalfa and orchardgrass than in wheat straw. Glycosyl linkage analysis indicated that xylans in leaf and stem fractions of alfalfa, orchardgrass leaf, and wheat straw stem that resisted degradation had a lower degree of substitution with acid-labile constituents (i.e., other monosaccharides) than was found in original substrates. Different rates and extents of digestion of leaf and stem fractions of forages explain part, but not all, of the observed differences in digestibilities of cell wall monomers by ruminants.

Animals↗

Effects of chemically treated, recycled newsprint on feed intake and nutrient digestibility by growing lambs.

In situ experiments and two lamb digestion trials were conducted to evaluate the effects of chemically treating recycled newsprint (NP). Treatment of NP with 2% HCl (percentage of NP DM) followed by autoclaving for 4 h was most efficacious and was used in an in vivo digestion trial with 25 ram and wether lambs in a randomized complete block design (RCB). On a DM basis treatment diets were: 1) control, 95% alfalfa hay (AH); 2) 75% AH, 20% HCl-treated NP (HCl-NP); 3) 55% AH, 40% HCl-NP; 4) 75% AH, 20% untreated NP; and 5) 55% AH, 40% untreated NP on a DM basis. Lambs fed Treatments 2 and 3 had ad libitum DMI (1,043 and 1,036 g/d, respectively) similar to the DMI of those fed the control treatment (1,024 g/d); however, lambs fed Treatments 4 and 5 had lower (P < .05) ad libitum DMI (578 and 426 g/d, respectively) than lambs fed Treatments 1, 2, and 3. Apparent DM digestibilities were lower (P < .05) by lambs consuming Treatments 2, 3, 4, and 5 (52.6, 44.5, 52.0, and 48.2%, respectively) than by those consuming Treatment 1 (60.7%). Apparent OM, CP, NDF, and ADF digestibilities followed trends similar to DM. In the second digestion trial, 15 ram and wether lambs were used in a RCB to compare Treatments 1, 2, and 3. For this second digestion study, NP was treated with 4% HCl (percentage of NP DM), autoclaved for 4 h, and diets were fed at 2% of BW. As in Trial 1, apparent nutrient digestibilities decreased (P < .05) with increasing amounts of HCl-NP. Our results suggest that HCl-NP can be fed to sheep at 40% of the diet without a decrease in DMI; however, apparent nutrient digestibility decreases with increasing levels of HCl-NP.

Animal Feed↗

Effect of fiber source on short-chain fatty acid production and on the growth and toxin production by Clostridium difficile.

BACKGROUND: Fermentable fiber promotes the growth of resident gut microbes, which modify the environment of the gastrointestinal tract and thus prevent colonization by Clostridium difficile. METHODS: An in vitro system with pigs as fecal inoculum donors was used to estimate fiber fermentability and changes in intestinal microbiota. RESULTS: Acetate and propionate production (mumol/mg substrate fermented/day) was greatest for gum arabic (1013.4 and 704.1, respectively); butyrate production was greatest for xylo-oligosaccharide (345.6). Growth of total anaerobes and clostridia was greatest for gum arabic (21.2 and 16.2 x 10(8) counts/ml, respectively) and xylo-oligosaccharides (21.0 and 19.6 x 10(8) respectively); growth of acidogenic bacteria was greatest with fructo-oligosaccharide (6.7 x 10(8) counts/ml). No culturable counts of C. difficile were obtained, nor was toxin A detected. CONCLUSIONS: Fermentable fibers support the growth of indigenous intestinal bacteria, particularly acidogenic bacteria, and yield large amounts of short-chain fatty acids with decreased gut pH. These factors contribute to the prevention of growth and toxin elaboration by C. difficile.

Animals↗