Comparison of D-alanine and diaminopimelic acid as bacterial markers in young calves

D-alanine (DAL) and diaminopimelic acid (DAP) were compared as markers to estimate proportion of bacterial N in total N reaching the abomasum of young calves. Sixteen Holstein bull calves fed complete pelleted starter or unpelleted starter plus hay and weaned at 4 or 8 wk of age were fitted with ruminal and abomasal cannulas and sampled twice weekly from 2 to 11 wk of age. Isolated ruminal bacterial cells contained more DAL than DAP at all weeks and averaged 7.0 and 5.4 mg N/g N, respectively. Weekly mean marker concentrations were highly correlated (.89) in ruminal bacteria, except at 3 wk of age. Concentration of DAL in abomasal digesta was greater than that of DAP at all weeks and averaged 5.2 and 2.4 mg N/g N, respectively. Weekly mean DAL correlated with DAP .61 in abomasal digesta and correlated .57 and .89 with starter intake, respectively. The proportion of bacterial N in total abomasal N was greater at all weeks when estimated by DAL than by DAP and averaged 77% and 46%, respectively. Estimates by DAL exceeded 100% in several cases and reflected large variation in analytical estimates. Estimates by DAL and DAP correlated .33 and .92 with starter intake. D-alanine was not an acceptable bacterial marker in this study.     

Occurrence of 2-aminoethylphosphonic acid in feeds, ruminal bacteria and duodenal digesta from defaunated sheep

A quantitative method of analysis for 2-aminoethylphosphonic acid (AEP) was developed using reverse-phase HPLC. The detection limit for AEP was 15 nM, and the detector response (peak area) was linear from AEP levels up to 100 microM (R = .99). Mean recovery of AEP added to strained ruminal fluid from faunated sheep was 98.2%. When AEP was added to a fermentation mixture at a concentration of 22.6 micrograms/ml, 78% disappeared during a 24-h incubation. 2-Aminoethylphosphonic acid was readily detected in preparations of mixed ruminal ciliate protozoa as well as in mixed and pure strains of ruminal bacteria, feedstuffs, and ruminal fluid and duodenal digesta from defaunated sheep. The occurrence of AEP in feed and bacterial hydrolysates was confirmed by organic phosphorus analyses. The concentration of AEP in mixed ruminal protozoa was three times greater than its concentration in mixed ruminal bacteria (4,304 vs 1,383 micrograms/g DM, respectively). The AEP values for pure ruminal bacterial cultures ranged from 733 micrograms/g DM in Bacteroides succinogenes B21a to 1,166 micrograms/g DM in Butyrivibrio fibrisolvens H17c. Ruminal fluid and duodenal digesta from defaunated sheep contained AEP concentrations of 30 micrograms/ml and 90 micrograms/g DM, respectively. The concentration of AEP in feedstuffs ranged from 25 micrograms/g DM in wheat straw to 263 micrograms/g DM in oats. Because AEP occurrence is not limited to ruminal ciliate protozoa, it is of little value as a marker for protozoal presence in or passage out of the rumen.     

The effects of frequency of feeding on some quantitative aspects of digestion in the rumens of growing steers

Three steers with simple rumen and abomasal cannulas were given ground and pelleted diets containing predominantly dried grass meal (DG) or rolled barley (RB). Diets were given at frequencies of two or eight feeds/d in a simple changeover design. Chromic oxide and polyethylene glycol were given as flow markers and flows (g/24 h) of organic matter (OM), nitrogenous and carbohydrate compounds were calculated. Ribonucleic acid and 35S were used as microbial markers and diaminopimelic acid (DAP) as a bacterial marker. Frequency of feeding had no significant effect on mean rumen pH, ammonia levels or liquid outflow rates with either diet. Rumen volume was decreased and abomasal digesta flow increased on Diet DG with more feeds but these parameters were unaffected with Diet RB. Increased feeding frequency with both feeds resulted in increased numbers of protozoa. There were no significant effects of feeding frequency of Diet DG on the abomasal flows of any of the nitrogenous constituents measured. However, there was a significant increase in microbial-N flow from 33 to 43 g/d with more frequent feeding of diet RB which was not reflected in bacterial-N flow as measured by DAP. The apparent digestion of OM in the rumen, expressed as g/g intake with diet DG was 0.41 and 0.31 for two feeds and eight feeds/d respectively. Corresponding values for diet RB were 0.56 and 0.63 respectively. The reduction in OM digestion with frequent feeding of diet DG was reflected in similarly reduced rumen digestibilities of all dietary carbohydrate components whereas the increase in OM digestion with diet RB was reflected only by the component sugars of the dietary fibre. The efficiencies of microbial protein synthesis (expressed as gMN/kg ADOM) increased from 36 to 46 when the feeding frequency of diet DG was increased from two to eight times/d. No significant effect of frequency of feeding was found for diet RB. Mouth to abomasum degradation of feed-N (expressed as g/g intake) of 0.64 was unaffected by the number of feeds of diet DG but was significantly increased from 0.55 to 0.82 when eight rather than two feeds/d of diet RB were given.     

Determination of bacterial N portions in feces and differently collected ileum chymus from swine]

In faeces and ileal digesta samples of 31 intact (INT) as well as 73 surgically differently prepared pigs bacterial fractionations and 2.6-diaminopimelic acid (DAP) estimations were carried out in order to calculate the bacterial N proportion in faeces N and digesta N after feeding various diets. Because of a high individual variability and the analytical variation width of the DAP/N-ratios no distinct influences of the fed diets could be found. The average DAP/N-values in the faeces (0.224) of INT pigs ranged in the same magnitude as in the digesta (0.0272) of ileorectostomized (IRA) pigs with open colon descendens (IRAo), where a digesta backflow is possible. Distinct lower DAP/N-ratios (0.0125 resp. 0.0043), however, were found in the digesta of pigs with ileo-caecal cannulae (IZB) or IRA pigs with closed colon (IRAg). On the base of various premises (N of the "bacterial fraction" C is only bacterial N; the DAP found in fraction A originates from intestinal bacteria adhering to feed particles) conducted calculations of the bacterial N proportions (in per cent of total N) led to the following data: Faeces of INT pigs: 43.0 ... 68.2 vs. 69.6 ... 89.0; digesta of operated pigs (except protein free diet) IRAo: 22.3 ... 57.0 vs. 46.2 ... 73.8; IZB: 17.0 ... 35.7 vs. 25.2 ... 53.6; IRAg (only 3 pigs): 23.6 vs. 24.2. The proportion of bacterial N in the digesta N of protein free fed IRAo pigs was 22.0 vs. 22.6%.     

Determination of 2,6-diaminopimelic acid in swine feces and chymus

A method is described for estimation of 2.6-diaminopimelic acid (DAP) using an automated amino acid analyzer and MOORE and STEIN ninhydrin reagent. Investigations were made concerning the influence of sample treatment on DAP content of faeces and ileal digesta of pigs and isolated bacteria. Oxidation before hydrolysis did not change DAP content of faeces and bacterial samples, but increased DAP of digesta. Since analytical reasons were excluded, different accessibility of DAP in faeces and digesta for hydrolysis is suggested. Lyophilization or preservation of fresh samples with formaldehyde and phenolic solution, resp., resulted in no significant influence on DAP content.     

Use of quantitative real‐time PCR to assess the in vitro survival of specific DNA gene sequences of rumen microbes under simulated abomasal conditions

The use of specific DNA sequences (DS) as a microbial marker in post‐rumen digesta requires their persistence and integrity throughout gastric digestion. The aim of this study was to evaluate in vitro the survival of microbial DS during gastric digestion and the factors involved. Gastric pH had a highly significant effect on the integrity of DS. pH 4.2 allows for a significant growth of microbes in the medium, but at pH 1.2, almost all of the DS were hydrolysed. In the presence of carboxymethylcellulose, the effect of pH was reduced, pepsin activity was inhibited and gene survival increased considerably. In the simulated abomasal conditions (pH = 2.3, 2 g/l of carboxymethylcellulose, and 40‐min retention time), almost all of the bacterial genes and around 78% of the protozoa gene sequences retained their molecular integrity throughout gastric digestion, although factors such as acidity and viscera retention time might compromise the utilisation of DS as a microbial marker.     

The effects of different sources of nitrogen supplementation on the post ruminal flows of organic matter and different nitrogenous constituents in steers

Friesian steers, virtually protozoa free, were equipped with simple rumen and abomasal cannulas. They were given diets consisting of approximately equal proportions of ground, pelleted alkali treated straw and a rolled barley, tapioca mixture supplemented with urea + casein (UC), soybean meal (SBM), 'normal' white fishmeal (NDF) or white fishmeal designated as being of 'low' rumen degradability (LDF). The diets were isoenergetic (the protein sources replacing part of the tapioca) and they were given in amounts to supply sufficient metabolizable energy (ME) to support an average growth rate of 0.5 kg/d. Rumen degradable nitrogen (RDN): ME values were estimated to be 2.08, 1.40, 1.90 and 1.66 for diets UC, SBM, NDF and LDF respectively. RNA, alpha-epsilon-diaminopimelic acid and 35S (added as sulphate) were used as bacterial markers. Chromic oxide and polyethylene glycol (PEG) were given as flow markers and flows (g/24 h) at the abomasum of organic matter (OM) and nitrogenous constituents were calculated. Rumen volumes and ruminal liquid fractional outflow rates were measured using PEG. Samples of mixed rumen bacteria separated from strained rumen digesta from animals receiving diet UC contained significantly less DAP-N (0.322 g/kg DM) than those from animals receiving diets SBM, NDF or LDF (0.530 g/kg DM). Mean rumen volume (approximately 15 l) and liquid fractional outflow rates (approximately 0.105/h) were similar on all diets but there was appreciable variation between animals. The proportion of OM intake digested in the rumen was similar on all diets. The proportional contribution of bacterial-N to the total non-ammonia-N passing the abomasum based on mean values derived from DAP and 35S as markers was 0.57, 0.47, 0.39 and 0.31 for diets UC, SBM, NDF and LDF respectively. Corresponding values based on RNA were 0.71, 0.50, 0.48 and 0.35 respectively. Bacterial-N (RNA) flows at the abomasum were 31, 25, 26 and 20 g/d for diets UC, SBM, NDF and LDF respectively. Corresponding values for 35S and DAP were 26, 24, 21 and 18 g/d respectively. Values derived from RNA flows were consistently and significantly higher (P less than 0.01) than those based on DAP or 35S. Mean estimated efficiencies of bacterial protein synthesis (g bacterial-N/kg OM truly digested) were 15, 15, 14 and 12 for diets UC, SBM, NDF and LDF respectively.(ABSTRACT TRUNCATED AT 400 WORDS)     

Supplementing barley or rapeseed meal to dairy cows fed grass-red clover silage: II. Amino acid profile of microbial fractions

Four ruminally cannulated dairy cows were used to examine the effect of diet on the AA composition of rumen bacteria and protozoa, and the flow of microbial and nonmicrobial AA entering the omasal canal. Cows were offered grass-red clover silage alone, or that supplemented with 5.1 kg DM of barley, 1.9 kg DM of rapeseed meal, or 5.1 kg DM of barley and 1.9 kg DM of rapeseed meal according to a 4 x 4 Latin square design with a 2 x 2 factorial arrangement of treatments. During the first 10 d of each period, cows had free access to silage and, thereafter intake was restricted to 95% of ad libitum intake. Postruminal digesta flow was assessed using the omasal canal sampling technique in combination with a triple marker method. Liquid- (LAB) and particle- (PAB) associated bacteria were isolated from digesta in the reticulorumen and protozoa from digesta entering the omasal canal. Microbial protein flow was determined using 15N as a microbial marker. Flows of AA entering the omasal canal were similar in cows fed silage diets supplemented with barley or rapeseed meal. However, rapeseed meal increased nonmicrobial AA flow while barley increased the flow of AA associated with LAB and protozoa. Diet had negligible effects on the AA profile of microbial fractions. Comparison of AA profiles across diets indicated differences between LAB and PAB for 10 out of 17 AA measured. Rumen bacteria and protozoa were found to be different for 14 out of 15 AA measured. For grass silage-based diets, energy and protein supplementations appear to alter postruminal AA supply through modifications in the proportionate contribution of microbial and nonmicrobial pools to total protein flow rather than as a direct result of changes in the AA profile of microbial protein.     

Effects of bentonite on wool growth and nitrogen metabolism in fauna-free and faunated sheep.

Two experiments were carried out with sheep that originated from a fauna-free flock and were fed a soybean meal-corn silage diet with or without a bentonite supplement. One-half of the sheep fed each diet in each experiment were faunated with a mixed population of ruminal protozoa, whereas the other half of the sheep remained fauna-free until the end of both experiments. Wool growth and daily gain were measured in Exp. 1. (eight rams per treatment), which lasted 110 d, and the metabolic effects in the rumen and intestinal tract of protozoa and dietary bentonite supplement were tested with cannulated wethers (four wethers per treatment) in Exp. 2. The results of Exp. 1 showed decreased wool growth (P less than .05) due to the presence of protozoa in the rumen. Dietary supplementation with bentonite partly offset the decreased wool growth in sheep with protozoa, but there were no effects of dietary bentonite and no protozoa x bentonite interaction (P greater than .05). Daily gain was decreased by the dietary bentonite (P less than .05) supplement but was not affected (P greater than .05) by the ruminal presence of protozoa. In Exp. 2, protozoa increased (P less than .01) the ruminal concentrations of ammonia and decreased (P less than .05) the acetic:propionic acid molar ratio. Fractionation of N in the duodenal digesta flowing from the stomach to the small intestine showed that protozoa decreased (P less than .05) the flow of nonammonia N and bacterial N, and there was a protozoa x bentonite interaction for these effects (P less than .05).(ABSTRACT TRUNCATED AT 250 WORDS)     

Study of the effect of presence or absence of protozoa on rumen fermentation and microbial protein contribution to the chyme

The aim of this study was to investigate the effect of presence or absence of protozoa on rumen fermentation and efficiency of microbial protein synthesis under different diets. Of 20 twin paired lambs, 1 lamb of each pair was isolated from the ewe within 24 h after birth and reared in a protozoa-free environment (n = 10), whereas their respective twin-siblings remained with the ewe (faunated, n = 10). When lambs reached 6 mo of age, 5 animals of each group were randomly allocated to 1 of 2 experimental diets consisting of either alfalfa hay as the sole diet, or 50:50 mixed with ground barley grain according to a 2 × 2 factorial arrangement of treatments. After 15 d of adaptation to the diet, the animals were euthanized and total rumen and abomasal contents were sampled to estimate rumen microbial synthesis using C(31) alkane as flow marker. Different ((15)N and purine bases) and a novel (recombinant DNA sequences) microbial markers, combined with several microbial reference extracts (rumen protozoa, liquid and solid associated bacteria) were evaluated. Absence of rumen protozoa modified the rumen fermentation pattern and decreased total tract OM and NDF digestibility in 2.0 and 5.1 percentage points, respectively. The effect of defaunation on microbial N flow was weak, however, and was dependent on the microbial marker and microbial reference extract considered. Faunated lambs fed with mixed diet showed the greatest rumen protozoal concentration and the least efficient microbial protein synthesis (29% less than the other treatments), whereas protozoa-free lambs fed with mixed diet presented the smallest ammonia concentration and 34% greater efficiency of N utilization than the other treatments. Although (15)N gave the most precise estimates of microbial synthesis, the use of recombinant DNA sequences represents an alternative that allows separate quantification of the bacteria and protozoa contributions. This marker showed that presence of protozoa decrease the bacterial-N flow through the abomasum by 33%, whereas the protozoa-N contribution to the microbial N flow increased from 1.9 to 14.1% when barley grain was added to the alfalfa hay. Absolute data related to intestinal flow must be treated with caution because the limitations of the sampling and maker system employed.     

Effect of dietary protein content on ileal amino acid digestibility, growth performance, and formation of microbial metabolites in ileal and cecal digesta of early-weaned pigs

Diarrhea incidence in weaned pigs may be associated with the concentration of intestinal microbial metabolites (ammonia, amines, and VFA) that are influenced by dietary CP content. Three experiments were conducted to determine effects of a low-protein, AA-supplemented diet on ileal AA digestibility, growth performance, diarrhea incidence, and concentration of microbial metabolites in ileal and cecal digesta of pigs weaned at 14 d of age. In Exp. 1, 8 pigs fitted with a simple T-cannula at the distal ileum were assigned in a crossover design to 2 diets containing 24 or 20% CP using wheat, corn, full-fat soybeans, whey powder, fish meal, and blood plasma as the main ingredients. Supplemental AA were added to the diets to meet the AA standards according to the 1998 NRC recommendations. Chromic oxide was used as an indigestible marker. Diets were fed at 2.5 times the ME requirement for maintenance. The reduction of dietary CP decreased (P < 0.05) the apparent ileal digestibility of most AA, except Lys, Met, Thr, Val, and Pro. Dietary CP content did not affect the pH of ileal digesta or ileal concentrations of ammonia N, cadaverine, putrescine, or VFA. In Exp. 2, 8 pigs fitted with a simple T-cannula in the cecum were assigned to 2 diets, similar to Exp. 1. Dietary CP content did not affect the pH of cecal digesta. The reduction in CP content decreased (P < 0.05) cecal ammonia N, acetic acid, isobutyric acid, isovaleric acid, total VFA, and putrescine concentrations by 28 to 39%. In Exp. 3, 32 pigs were assigned to 2 diets, similar to Exp. 1, according to a randomized complete block design. Pigs had free access to feed and water. Dietary CP content did not affect growth performance or fecal consistency scores during the 3-wk study, and diarrhea was not observed. The results of these experiments indicate that lowering the dietary CP content combined with supplementation of AA markedly reduced the production of potentially harmful microbial metabolites in cecal digesta of early-weaned pigs without affecting growth performance.     

Effects of zinc sulfate concentration and feeding frequency on ruminal protozoal numbers, fermentation patterns and amino acid passage in steers

Effects of zinc sulfate (0 vs 1,142 ppm supplemental zinc from zinc sulfate) and feeding frequency (1 x vs 12x daily) on ruminal protozoa numbers, fermentation patterns and amino acid passage were investigated using four ruminally and abomasally cannulated mature Jersey steers in a 4 x 4 Latin square experiment. Steers (530 kg) were fed a 50:50 roughage:concentrate diet at 1.5 times their NEm requirement. Experimental periods were 14 d in duration; ruminal, abomasal and fecal samples were collected at 6-h intervals during the last 3 d of each period. Protozoa numbers tended to be lowest (1.82 x 10(6)/ml) in steers fed zinc 1 x and tended to be highest (3.83 x 10(6)/ml) in steers fed zinc 12 x daily (P less than .10). Frequent feeding decreased ruminal pH .24 units and increased total VFA 20.7%, ammonia 22.7% and ruminal digestion of dietary amino acids (AA) 61.6% (P less than .05). Zinc supplementation decreased ruminal digestion of dietary AA 35.8% (P less than .05) and the abomasal passage of bacterial OM and AA 21.2% (P less than .05) and increased ruminal output of amino acids as a percentage of intake 15.1% (P less than .05). Although it increased escape of dietary AA, zinc sulfate decreased postruminal passage of bacterial AA and resulted in a net negative effect on total postruminal AA passage as a percentage of intake. The effects of zinc on ruminal AA digestion may be more closely related to an interaction of zinc with dietary CP rather than to an effect of Zn on ruminal microbial populations.     

Short-term effect of dietary yeast nucleotide supplementation on small intestinal enzyme activities, bacterial populations and metabolites and ileal nutrient digestibilities in newly weaned pigs

In previous studies, dietary nucleotides have been shown to improve performance in single-stomached animals by promoting the renewal of small intestine epithelial cells and by influencing the activity and composition of the microbial community in the digestive tract. The present experiment was carried out with 12 barrows weaned at the age of 18 days and fitted with a simple T-cannula at the distal ileum. To determine short-term effects of dietary yeast nucleotides, the piglets received a grain-soybean meal-based basal diet with or without supplementation of 1 g/kg of a dried yeast product containing free nucleotides. Dietary supplementation with yeast did not affect bacterial numbers in the ileum as well as ileal concentrations of individual short-chain fatty acids (SCFA), total SCFA and total lactic acid (p > 0.05). Moreover, there was no effect of supplemental yeast nucleotides on ileal α-amylase, leucine amino peptidase, maltase and lactase activities (p > 0.05), as well as on ileal dry matter, crude protein and crude fibre digestibilities (p > 0.05). In conclusion, short-term supplementation with dietary yeast nucleotides did not affect microbial metabolite concentrations, bacterial numbers and enzyme activities in the ileal digesta as well as ileal nutrient digestibilities of newly weaned pigs.     

Comparative characterization of reticular and duodenal digesta and possibilities of estimating microbial outflow from the rumen based on reticular sampling in dairy cows

The objective of this experiment was to investigate the possibility of estimating the outflow of nutrients and microbial protein from the rumen based on sampling reticular contents as an alternative to duodenal sampling. Microbial protein flow estimates were also compared with a third method based on sampling of ruminal contents. Reticular and duodenal digesta and ruminal contents were recovered from 4 cows used in a 4 x 4 Latin square design experiment, in which the ruminal effects of 4 exogenous enzyme preparations were studied. Large and small particulate and fluid markers were used to estimate digesta flow in a triple-marker model; 15N was used as a microbial marker. Reticular and duodenal digesta were segregated into small and large particles (SP and LP, respectively) and a fluid phase, and ruminal digesta was segregated into particulate and fluid phases. Compared with digesta recovered at the duodenum, reticular digesta had lower OM and greater NDF contents. The proportion of microbial N was notably greater in the fluid phase of reticular digesta. Ruminal outflow of DM and OM was greater (by 17 and 28%) and that of NDF was lower (by 14%) when estimated from duodenal compared with reticular samples. There was no difference in the estimated flow of starch and nonammonia and microbial N between the reticular and duodenal techniques. Microbial N flow estimated based on ruminal sampling was similar to those based on duodenal and reticular sampling. The ruminal method, however, grossly overestimated flow of DM, OM, and NDF. This study supports the concept that microbial protein outflow from the rumen can be measured based on sampling of ruminal or reticular digesta. The reticular sampling technique can also provide reliable estimates for ruminal digestibility of OM, N, and fiber fractions. These findings need to be confirmed in experiments with basal diets varying in structure and forage-to-concentrate ratios.     

Lysine requirement of growing steers

Eight Limousin-cross steers (355 kg) were used in a replicated 4 x 4 Latin-square designed to estimate lysine requirements. Steers were fed a semipurified diet containing little ruminal escape protein. Treatments were abomasal infusions of 0, 8, 16, or 24 g/day L-lysine. All steers were additionally infused with 400 g/day dextrose and 285.9 g/day of an amino acid mix that contained (g/day) L-methionine (12.0), L-histidine (8.1), L-arginine (10.5), L-threonine (12.0), L-valine (18.0), L-isoleucine (13.8), L-leucine (27.3), L-phenylalanine (28.2), L-glutamic acid (76.5), glycine (76.5) and L-tryptophan (3.0); it had been demonstrated previously that when lysine was included in this infusion mixture, nutritional requirements of steers for maximal N retention were met or exceeded. Nitrogen retention averaged 38 g/day and was not affected by treatment, implying that the lysine requirement of steers was less than the 37.8 g/day lysine estimated to be absorbed from the small intestine when the basal diet was fed.     

柑橘提取物对肥育猪后肠食糜蛋白质代谢产物的影响

【目的】通过研究柑橘提取物对肥育猪后肠食糜蛋白质代谢产物的影响,旨在为柑橘提取物从源头调控臭气的产生提供依据。【方法】选取108头56日龄(19.73±0.39)kg杜×长×大猪,公母各半,随机分为3组,每组分6栏,每栏6头猪。对照组饲喂基础饲粮,抗生素组在基础饲粮中添加75 g/t金霉素,柑橘提取物组在基础饲粮中添加柑橘提取物(56～112日龄添加250 mL/t柑橘提取物,113～194日龄添加200 mL/t柑橘提取物)。194日龄时收集肥育猪盲肠和结肠食糜,测定食糜中游离氨基酸、酚和吲哚类物质、生物胺的含量。【结果】(1)在盲肠食糜中,与对照组相比,柑橘提取物组和抗生素组牛磺酸、天冬氨酸、丙氨酸、缬氨酸、亮氨酸、赖氨酸、组氨酸、精氨酸、吲哚和甲胺含量均显著降低(P<0.05)。与对照组相比,柑橘提取物有降低苏氨酸、丝氨酸、谷氨酸、甘氨酸、瓜氨酸、异亮氨酸、脯氨酸和粪臭素含量的趋势(0.05≤P<0.10),苯酚、腐胺、酪胺和精胺含量均显著降低(P<0.05)。与抗生素组相比,柑橘提取物组腐胺和酪胺含量均显著减少(P<0.05)。(2)在结肠食糜中,与对照...     

不同粗蛋白质水平日粮对育肥羊小肠养分吸收率的影响

本研究旨在比较不同粗蛋白质（CP）水平日粮对育肥羔羊小肠养分吸收率的影响。选用体重30 kg左右,安装有瘤胃、十二指肠近端和回肠末端瘘管的3只哈萨克育肥羊为试验动物,采用3×3拉丁方试验设计,采用醋酸镱（Yb-Ac）、锂铬乙二胺四乙酸（LiCr-EDTA）分别作为消化道固相和液相食糜标记物测定小肠食糜流量。结果显示,增加全混合日粮中CP水平可显著提高育肥羊N的进食量、全消化道表观消化率和N沉积（P<0.05）,显著提高干物质（DM）和有机物（OM）的表观消化率（P<0.05）,但对小肠食糜流量无显著影响（P>0.05）;提高日粮CP水平对十二指肠食糜除EE和嘌呤外的营养成分流量均产生显著的影响（P<0.05）,仅对回肠食糜中CP、粗灰分（Ash）、DM、中性洗涤纤维（NDF）和酸性洗涤纤维（ADF）流量的影响显著（P<0.05）,且对CP、Ash、DM、NDF和ADF的小肠吸收率影响显著（P<0.05）。本试验为进一步深入分析增加日粮CP水平对其在育肥羊体内的消化利用奠定基础。     

Effects of Different Dietary Crude Protein Levels on the Nutrient Absorbability in the Small Intestine of Lambs

This experiment was conducted to study the effects of different dietary crude protein levels on the nutrient absorbability in the small intestine of lambs.Three Kazakh lambs (30 kg body weight) fitted with permanent ruminal,duodenal and ileal fistula were selected.3×3 Latin square design was adopted.A dual-phase marker system with LiCr-EDTA and Yb-Ac as the liquid-phase or particulate-phase digesta flows maker was adopted to measure the true digesta flows at duodenal and ileal fistula,respectively.The results showed that nitrogen intake,total tract apparent digestibility,N deposition,the apparent digestibility of dry matter and organic matter were significantly increased with increasing levels of dietary crude protein (P<0.05),but had no significant effects on intestinal digesta flows (P>0.05).Increasing dietary crude protein levels had significant effects on most part of nutrients of duodenal digesta except fat and purine (P<0.05),while it only significantly effected CP,Ash,dry matter,neutral detergent fibre and acid detergent fiber of ileal digesta flows (P<0.05).In addition,intestinal absorbability of nutrients except for CP,Ash,dry matter,neutral detergent fibre and acid detergent fiber were significantly affected with increasing levels of dietary crude protein(P<0.05).The test provided basis for further study of the effects of dietary CP level on the digestibility and utilization of lamb.     

Evaluation of dairy food processing wash water solids as a protein source: III. Nitrogen utilization by heifers fed medium-concentrate diets

Eight multicannulated heifers (average BW 415 +/- 34 kg) were used in a replicated 4 x 4 Latin square to evaluate fluid milk processing wash water solids (WWS) as a dietary N source. Heifers were fed corn/cottonseed hull-based diets containing soybean meal (control, 0% WWS N) or WWS replacing soybean meal at 33, 67, or 100% of supplemental dietary N. Total tract and ruminal DM and OM digestibilities decreased linearly or cubically (P less than .05) as dietary WWS N increased. Total ruminal VFA concentration (P less than .05) and propionic acid molar proportion (P less than .10) were greater in heifers fed 0 vs 100% WWS N. Heifers fed 0% WWS N had the greatest (P less than .05) ruminal ammonia concentration at all sampling times. Dietary WWS did not affect (P greater than .10) ruminal pH, fluid dilution rate, fluid flow, fluid volume, or turnover time. Total tract N digestibility decreased quadratically (P less than .10) with increasing WWS N in the diet. Supplemental WWS N did not affect (P greater than .10) flow of duodenal ammonia N or bacterial N, or efficiency of microbial N synthesis. Diets containing WWS N resulted in a cubic increase (P less than .10) in duodenal flow of essential amino acids compared with 0% WWS N; however, there were no differences in small intestinal amino acid disappearance. Data indicate that WWS can replace 33% of the soybean meal N in a corn/cottonseed hull-based diet without decreasing ruminal fermentation, fluid digesta kinetics, microbial efficiency, or small intestinal amino acid utilization.     

Comparison of three markers for the determination of bacterial protein in terminal ileal digesta in the growing pig

The aim of the study was to compare three methods commonly used to determine the concentrations of bacterial protein in digesta collected from the terminal ileum of growing pigs that had been fed a casein‐based diet. The amounts of bacterial protein in terminal ileal digesta were determined using three different markers: 2.6‐diaminopimelic acid (DAPA) and the d ‐amino acids, d ‐aspartic acid (d ‐Asp) and d ‐glutamic acid (d ‐Glu). The effectiveness of each marker was compared against a control based on physical fractionation by centrifugation. The total bacterial protein concentrations derived from the markers d ‐Asp and d ‐Glu were significantly different (p = 0.05) to those calculated from DAPA and the control, but there was no difference between DAPA and the control. The percentage of bacterial nitrogen ranged from 40% to 52% dependent on the marker used. Bacterial protein expressed as a percentage of the total protein, ranged from 48% to 62%, a substantial proportion of which (12–28%) was derived from lysed bacterial cells. Statistical correlations between the estimation methods were low. Such poor correlation between the markers may be the result of random errors such as variance in the epimerization of the two d ‐amino acids during protein hydrolysis. DAPA was accepted as a reliable marker for determining microbial protein in ileal digesta.