A. Bach

Quantitative review of in situ starch degradation in the rumen

The partition of starch digestion in the digestive tract of ruminants has a great influence on various animal responses. There is a need to more accurately estimate and control the amount of starch degraded in the rumen. A quantitative review on starch degradability in situ was conducted from a database built from 48 references corresponding to 302 observations. Appropriate statistical analyses have been performed, particularly to correct for the variations among laboratories. The estimated values for the in situ starch parameters and for the effective degradability were calculated for 22 ingredients. The effect of some chemical or physical treatments was also investigated and quantified. The data confirmed that large differences occurred due to intrinsic properties of the feed. Furthermore, there was a strong influence of processing, especially on feedstuffs containing slowly degrading starch. This study updated the data on starch degradability in situ. The values presented have an interest for feedstuffs evaluation, for diet formulation and also for modeling ruminal digestion.

Effects of forage provision to young calves on rumen fermentation and development of the gastrointestinal tract.

Fifteen Holstein male calves were randomly assigned to 1 of 3 dietary treatments according to age and body weight (BW) to determine the effects of feeding different forages sources on rumen fermentation and gastrointestinal tract (GIT) development. Treatments consisted of a starter (20% crude protein, 21% neutral detergent fiber) fed alone (CON) or supplemented with alfalfa (AH) or with oat hay (OH). All calves received 2L of milk replacer (MR) at 12.5% dry matter twice daily until 49 d of age. Calves received 2L of the same MR from 50 to 56 d of age and were weaned at 57 d of age. Individual starter, forage, and MR intakes were recorded daily and BW was recorded weekly. A rumen sample was taken weekly to determine rumen pH and volatile fatty acid concentrations. Three weeks after weaning, animals were harvested and each anatomical part of the GIT was separated and weighed with and without contents. Rumen pH was lower in CON than in OH and AH calves. Furthermore, acetate proportion in the rumen liquid tended to be greater in AH than in CON and OH treatments. Total GIT weight, expressed as a percentage of BW, tended to be greater in AH compared with the other 2 treatments. Rumen tissue tended to weigh more in CON than in OH animals. Animals with access to forage tended to have a greater expression of monocarboxylate transporter 1 than CON calves. In conclusion, calves supplemented with oat hay have a better rumen environment than calves offered no forage and do not have an increased gut fill.

Performance and health responses of dairy calves offered different milk replacer allowances.

Eighty female Holstein calves (12±4.1 d of age and 42±4.3 kg of BW) were collected from different herds, brought to the study site, and blocked by age and assigned to either a 6 L/d maximum daily milk replacer (MR) allowance (LMR) or a maximum MR allowance of 8 L/d (HMR). Calves were kept in individual hutches until 52 d of age and then moved into pens, forming groups of 10. All calves had ad libitum access to a mash starter feed. Calves in both treatments received the MR distributed in 3 separate allotments between 1 wk after the beginning of the study and 52 d of age. Then, all calves were moved to group pens and preweaned by offering 2 L/calf of the same MR twice daily in a trough until the age of 59 d, when MR offer was further reduced to a single dose of 2 L until the age of 73 d, when all calves were completely weaned. Individual starter feed and MR consumption was recorded on a daily basis until 52 d of age, and on a group basis until weaning time. Body weight was measured at the beginning of the study and at 52 (preweaning), 73 (weaning), and 110, 160, and 228 d of age. Solid feed consumption (mean ± SE) was greater in LMR (821±42.1 g/d) than in HMR calves (462±42.1 g/d) between 42 d of age and 52 d (preweaning). As expected, as age increased, solid feed consumption increased, and LMR showed a more marked increase than HMR calves. Despite the greater solid feed intake of LMR calves, HMR grew faster than LMR calves until preweaning time, but from preweaning to weaning, LMR calves grew more than HMR calves (977 vs. 857±30.7 g/d, respectively; mean ± SE). No differences in feed efficiency were observed. While calves were individually housed, no differences were observed in the incidence of bovine respiratory disease or diarrhea between treatment groups. We concluded that, under the milk regimen, age range of calves, and weaning method used in the current study, before preweaning, HMR calves grow more than LMR calves, but between preweaning and weaning, LMR grow more than HMR calves, overcoming the difference in BW at preweaning. As a result, with the weaning scheme followed herein, providing more milk does not ensure greater performance; no differences are obtained in BW at weaning and at 228 d of life. Also, based on solid feed consumption patterns seen in this study, we determined that the optimum age to reduce MR allowances and foster solid feed intake is around 45 d of age.

Short communication: lying behavior of lactating dairy cows is influenced by lameness especially around feeding time.

Lameness is considered one of the most common welfare and productive problems in dairy cattle. The objective of this study was to evaluate differences in lying behavior between moderately lame and nonlame lactating cows under commercial conditions. Data were collected from 10 free-stall commercial herds, which were feeding on exactly the same ration once daily. All lactating cows were scored for lameness according to a 1 to 5 locomotion scoring system. Only cows with a lameness score between 1 and 4 were considered in the study. In each herd, between 10 and 15 lame cows (scored as 3 or 4) were chosen, and for each lame cow, a nonlame cow (scored as 1) within the same parity and similar days in milk was also selected. Pendant data loggers were then placed on the right hind leg of each cow for 10 d to record lying behavior at 1-min intervals. In addition, the time of feed delivery was recorded in each herd on a daily basis. Total daily lying time, daily number of lying bouts, lying bout duration, laterality (side of recumbence), and lying behavior around feed delivery time were evaluated using a mixed-effects model that accounted for the fixed effects of lameness, days in milk, parity, and the interaction between parity and lameness, plus the random effects of herd. Total daily lying time (721±24.2 min/d) tended to increase with days in milk, but it was not affected by lameness or parity. Likewise, no differences were found in the number of lying bouts (9.6±0.49/d) or laterality (47±2.6% of time lying on the right side). However, the mean bout duration was longer in lame (89.3±3.89 min) compared with nonlame (80.7±3.90 min) cows. It is interesting that lame cows stood up 13 min later than nonlame cows relative to the time when the ration was delivered. In addition, lame cows lay down 19 min earlier than nonlame ones after the feed was delivered, which implies that nonlame cows spent more time standing, and probably eating, than did lame cows. It was concluded that lame cows have longer lying bouts than nonlame animals, and that lying behavior around feed delivery time may be an effective proxy to identify moderately lame cows.

Evaluation of the fermentation dynamics of soluble crude protein from three protein sources in continuous culture fermenters

Eight dual-flow continuous culture fermenters (1.03 +/- 0.05 L) were used to assess differences in microbial degradation of the soluble CP fraction of canola meal (CMSCP), soybean meal (SBMSCP), and fish meal (FMSCP) using a completely randomized design with two 9-d experimental periods and a solution of tryptone as a control treatment (control). All fermenters received the same basal diet (58% ground corn, 40% canary grass hay, 0.4% vitamin-mineral premix, 1% CaCO(3), 0.6% salt on a DM basis) in 8 equal portions daily. During sampling on the last 3 d of each period, 90-mL doses containing soluble CP were infused into the fermenters 30 min after the beginning of the first and last feedings of the day. The total amount of soluble CP supplied by the infusions of FMSCP, CMSCP, and SBMSCP was 3.2 g/d, representing 24% of the daily dietary CP intake. Infusion of FMSCP resulted in the greatest (P < 0.05) NH(3)-N concentration (4.6 +/- 0.40 mg/dL) compared with the other treatments (0.5 +/- 0.40 mg/dL). Microbial N flow (g/d) from the fermenters was also greatest (P < 0.05) with FMSCP (1.42 +/- 0.062) compared with the other soluble CP fractions (1.08 +/- 0.062). The efficiency of microbial protein synthesis tended to be lowest with the control diet, and the efficiency of N utilization was lowest with FMSCP treatment. These results indicate that N was limiting microbial growth in the control diet, and there was more rumen-available N with the FMSCP diet compared with the other dietary treatments. The extent of degradation of the soluble CP fraction from fish meal, soybean meal, and canola meal was determined to be 99, 30, and 37% of soluble CP, respectively. These results indicate that the soluble CP fraction is not 100% degraded in all feeds and that assuming a high degradation extent of the soluble CP fraction from soybean meal and canola meal may result in an underestimation of the supply of undegradable protein from these protein sources.

Measuring resistance to ruminal degradation and bioavailability of ruminally protected methionine

The objectives of this study were to evaluate ruminal degradation and intestinal digestion of two ruminally protected methionine (RPM) products and to assess the potential use of changes in plasma methionine concentrations as an indication of methionine availability to the animal. Ruminal degradation of the protected methionine was assessed using the in situ technique. The intestinal availability of methionine after ruminal incubation was determined in vitro using an enzymatic procedure. Four Holstein cows receiving a typical mid-lactation ration (16.5% CP, 1.6 Mcal NEL/kg) were supplemented with 0, 30, and 60 g per day of a slowly degraded ruminally protected methionine (SDM), or 60 g per day of a moderately slowly degradable ruminally protected methionine (MSDM) in a 44 Latin square design. Blood samples were collected from the jugular vein at 0, 6, 12, 18, 24, and 36 h after feeding the RPM sources. Ruminal degradation rates of SDM and MSDM were 0.03 h ˇ1 and 0.07 h ˇ1 , respectively. The calculated amount of methionine available for absorption, based on the in situ and in vitro results, was 17.9, 11.9 and 23.8 g per day when dosing 60 g of MSDM, 30 and 60 g of SDM, respectively. The highest (p<0.05) methionine plasma concentration (133.9 mM) was measured with 60 g of SDM, followed by 30 g of SDM, and 60 g of MSDM. Plasma methionine concentrations were affected by an interaction (p<0.05) between time after dosing methionine and rate of ruminal degradation of the methionine dosed. Methionine plasma concentration peaked 12 h after dosing SDM, whereas methionine plasma concentration appeared to peak between 6 and 12 h after feeding MSDM. There was a good relationship (r 2 a0.86) between the grams of methionine escaping from the RPM products and the greatest area under the curve describing plasma methionine concentration. Data from this study show that the lower the ruminal degradation rate, the later the maximum plasma concentration of methionine will occur, and that the plasma methionine concentrations or their area

Short communication: Comparison of pH, volatile fatty acids, and microbiome of rumen samples from preweaned calves obtained via cannula or stomach tube

The objective of this study was to compare rumen samples from young dairy calves obtained via a stomach tube (ST) or a ruminal cannula (RC). Five male Holstein calves (46±4.0 kg of body weight and 11±4.9 d of age) were ruminally cannulated at 15 d of age. Calves received 4 L/d of a commercial milk replacer (25% crude protein and 19.2% fat) at 12.5% dry matter, and were provided concentrate and chopped oats hay ad libitum throughout the study (56 d). In total, 29 paired rumen samples were obtained weekly throughout the study in most of the calves by each extraction method. These samples were used to determine pH and volatile fatty acids (VFA) concentration, and to quantify Prevotella ruminicola and Streptococcus bovis by quantitative PCR. Furthermore, a denaturing gradient gel electrophoresis was performed on rumen samples harvested during wk 8 of the study to determine the degree of similarity between rumen bacteria communities. Rumen pH was 0.30 units greater in ST compared with RC samples. Furthermore, total VFA concentrations were greater in RC than in ST samples. However, when analyzing the proportion of each VFA by ANOVA, no differences were found between the sampling methods. The quantification of S. bovis and P. ruminicola was similar in both extraction methods, and values obtained using different methods were highly correlated (R(2)=0.89 and 0.98 for S. bovis and P. ruminicola, respectively). Fingerprinting analysis showed similar bacteria band profiles between samples obtained from the same calves using different extraction methods. In conclusion, when comparing rumen parameters obtained using different sampling techniques, it is recommended that VFA profiles be used rather than total VFA concentrations, as total VFA concentrations are more affected by the method of collection. Furthermore, although comparisons of pH across studies should be avoided when samples are not obtained using the same sampling method, the comparison of fingerprinting of a bacteria community or a specific rumen bacterium is valid.

Associations between subclinical hypocalcemia and postparturient diseases in dairy cows

Dairy cows suffer blood Ca losses as lactation begins and might be affected by hypocalcemia in its clinical (total serum Ca concentration <1.50 mM) or subclinical form (total serum Ca concentration ≤2.14 mM). Several studies have suggested that hypocalcemia is associated with different health problems of the cow but results from different studies are not consistent. The objective of this study was to assess potential associations between subclinical hypocalcemia (SCHC) and displaced abomasum, intramammary infections, metritis, retained placenta, and ketosis. Also, the associations between SCHC and milk yield and reproductive function were evaluated. After discarding cows (32) with clinical hypocalcemia, a total of 764 cows from 6 different commercial farms were enrolled in this study. Blood samples were collected at 24 to 48 h postcalving and analyzed for total Ca concentration. Odds ratios of the different afflictions potentially associated with SCHC were calculated. Seventy-eight percent of the analyzed cows incurred SCHC. The occurrence of displaced abomasum, ketosis, retained placenta, and metritis was 3.7, 5.5, 3.4, and 4.3 times more likely, respectively, in cows that had SCHC than in cows with normocalcemia. Furthermore, the risk of incurring retained placenta or metritis increased in multiparous cows as serum Ca concentrations decreased compared with that in primiparous cows. Normocalcemic cows, independent of parity, were more likely to show their first estrus sooner after calving than SCHC cows, but no correlation was found between SCHC and other reproductive parameters. Different serum Ca concentration cutoffs were identified for several postpartum afflictions (≤1.93, ≤2.05, ≤2.05, and ≤2.10 mM for ketosis, retained placenta, metritis, and displaced abomasum, respectively). In conclusion, SCHC, defined as serum Ca ≤2.14 mM, is a frequent illness affecting the majority of the dairy cows with important repercussions on health. However, if SCHC were to be used to predict postpartum disease, different serum Ca cutoff points are likely to be needed because best predictive cutoff values varied among postpartum ketosis, displaced abomasum, retained placenta, and metritis.

Trends in recombinant protein use in animal production

Recombinant technologies have made possible the production of a broad catalogue of proteins of interest, including those used for animal production. The most widely studied proteins for the animal sector are those with an important role in reproduction, feed efficiency, and health. Nowadays, mammalian cells and fungi are the preferred choice for recombinant production of hormones for reproductive purposes and fibrolytic enzymes to enhance animal performance, respectively. However, the development of low-cost products is a priority, particularly in livestock. The study of cell factories such as yeast and bacteria has notably increased in the last decades to make the new developed reproductive hormones and fibrolytic enzymes a real alternative to the marketed ones. Important efforts have also been invested to developing new recombinant strategies for prevention and therapy, including passive immunization and modulation of the immune system. This offers the possibility to reduce the use of antibiotics by controlling physiological processes and improve the efficacy of preventing infections. Thus, nowadays different recombinant fibrolytic enzymes, hormones, and therapeutic molecules with optimized properties have been successfully produced through cost-effective processes using microbial cell factories. However, despite the important achievements for reducing protein production expenses, alternative strategies to further reduce these costs are still required. In this context, it is necessary to make a giant leap towards the use of novel strategies, such as nanotechnology, that combined with recombinant technology would make recombinant molecules affordable for animal industry.

Effects of acarbose on ruminal fermentation, blood metabolites and microbial profile involved in ruminal acidosis in lactating cows fed a high-carbohydrate ration.

The objective was to evaluate the effects of an inhibitor of alpha-amylase and glucosidase (acarbose, Pfizer Limited, Corby, UK) on ruminal fermentation, blood metabolism and microbial profile in dairy cows in a 2x2 cross-over experiment. Eight Holstein cows fitted with rumen cannulas (milk yield, 24.3+/-2.35 kg/d, body weight, 622+/-54 kg, days in milk, 183+/-67, 5 multiparous and 3 primiparous) were used. Treatments were: control (no additive, CTR) and alpha-amylase and glucosidase inhibitor (0.75 g acarbose-premix/cow per d, AMI). Animals were given ad-libitum access to a high non-fibre carbohydrate (NFC) partial mixed ration (PMR) containing 17.6% crude protein, 28.3% neutral detergent fibre, and 46.5% NFC in the dry matter and supplementary concentrate during milking. Blood samples were taken to determine blood glucose, insulin and urea within the first hour after the morning feeding on two separate days in each period. Samples of ruminal contents were collected during 3 d in each period at 0, 4 and 8 h after feeding to determine volatile fatty acid and ammonia-N concentrations and to quantify protozoa, Streptococcus bovis and Megasphaera elsdenii. Rumen pH was recorded electronically at 22-min intervals during 6 d in each period. Results were analysed using a mixed-effects model. Cows on AMI treatment spent less time with ruminal pH <5.6 compared with cows in the CTR group (3.74 and 6.52+/-0.704 h/d, respectively). Cows in the AMI group had greater daily average pH compared with those in the CTR group (6.05 and 5.92+/-0.042, respectively). AMI animals tended (P=0.09) to have lower Str. bovis to Meg. elsdenii ratio than CTR (4.09 and 26.8+/-12.0, respectively). These results indicate that dietary supplementation with acarbose in dairy cattle fed high-production rations may be effective in reducing the time for which rumen pH is suboptimal, with no negative effects on ruminal fermentation and blood metabolites.