Published research suggests that it might be beneficial to increase the amount of rumen undegradable protein (RUP) that passes out of the rumen, through manipulation of rumen fermentation to establish a lower rumen pH. To test this hypothesis, a study was conducted in which three ruminally cannulated Holstein cows, 722 kg ±25.6 kg fed three different diets (treatments) were used in a Latin square design experiment to determine effects of increasing levels of dietary concentrate on some rumen parameters and ruminal crude protein (CP) degradability. The in situ method was used to determine the ruminal protein degradability of sunflower oilcake, cottonseed oilcake and roasted soya. The three treatments differed in roughage:concentrate ratio, being 60:40 (Treatment UP 60), 45:55 (Treatment UP 45) and 30:70 (Treatment UP 30). Intake of dry matter (DM) (kg/day) did not differ between treatments. The mean rumen pH in cows receiving the three experimental diets differed and was 6.00, 6.27 and 6.44 for treatments UP 30, UP 45 and UP 60 respectively. The time (hours) below pH 5.8, which is considered to be the pH where fibre degradation is substantially negatively affected, was approximately 2.5 hours, but only on treatment UP 30. Mean rumen ammonia nitrogen (N) and total volatile fatty acid (VFA) concentrations did not differ among cows receiving different treatments but, cows fed treatment UP 30 had a lower ruminal acetic acid:propionic acid (A:P) ratio compared to the other treatments. There were no differences in ruminal CP degradation within the three feedstuffs when incubated in cows fed diets with different roughage:concentrate ratios. Results suggest that roughage:concentrate ratios ranging from 60:40 to 30:70, which resulted in mean pH values ranging from 6.4 to 6.0, did not affect ruminal CP degradation of sunflower oilcake, cottonseed oilcake and roasted soya. / Dissertation (MSc(Agric))--University of Pretoria, 2009. / Animal and Wildlife Sciences / unrestricted

Within the South African feedlot industry, there are currently several different roughage sources available for use in feedlot finishing diets. To evaluate the influence of dietary energy and fibre source on rumen function in feedlot animals, four roughage sources (wheat straw, Eragrostis curvula hay, cottonseed hulls and maize silage) were used in combination with hominy chop or dry rolled maize in two experiments. Four Beefmaster steers (270kg ±15kg) fitted with ruminal cannulae were used in two separate experiments in a 4 x 4 Latin square design. Experiment 1 was conducted to evaluate each roughage source in combination with hominy chop namely: wheat straw, hominy chop (WSHC); Eragrostis hay, hominy chop (EHHC); cottonseed hulls, hominy chop (CHHC); and maize silage, hominy chop (MSHC). Experiment 2 was conducted to evaluate each roughage source in combination with dry rolled maize (DRM) namely: wheat straw, dry rolled maize (WSDRM); Eragrostis curvula hay, dry rolled maize (EHDRM); cottonseed hulls, dry rolled maize (CHDRM); and maize silage, dry rolled maize (MSDRM). Diets were designed to contain equal amounts of energy, starch, crude protein, neutral detergent fibre (NDF) and 7.5% roughage source in both experiments. All diets were evaluated for particle size distribution through the Penn State Forage Particle Separator (PSPS) and ruminal fermentation parameters (volatile fatty acid composition, VFA; rumen ammonia nitrogen, NH3-N; lactate and ruminal pH) were compared for each experiment. Results from experiment 1 showed that animals fed the MSHC had the lowest (P<0.05) concentration of VFA while animals fed the CHHC diet produced the highest (P<0.05) ruminal propionate concentration, lowest (P<0.05) acetate: propionate ratio and had the lowest (P<0.05) ruminal pH during the 24h observation period. Time intervals below pH 5.6 and pH5.2 for CHHC was 940 minutes (P<0.05) and 388.75 minutes respectively. Measurements for rumen NH3-N concentrations and lactate did not differ between treatments. Results from experiment 2 revealed that animals fed WSDRM had numerically the lowest concentration of VFA and differed (P<0.05) from CHDRM and MSDRM diets. Propionate and acetate as well as A:P ratios for CHDRM were numerically higher than other treatments but differed (P<0.05) from the WSDRM diet. Rumen NH3-N concentrations did not differ but lactate concentrations were higher for EHDRM when compared to the MSDRM and WSDRM diets (P>0.05). Ruminal pH observations showed steers consuming the MSDRM diet to have the lowest mean ruminal pH of 5.53 which differed (P<0.05) from the WSDRM diet with a mean ruminal pH of 6.1. Time periods spent below pH 5.6 and 5.2 for steers consuming the MSDRM diet was highest at 703.75 and 306 minutes respectively and differed from steers consuming the WSDRM diet. Results from these experiments indicated that different roughage sources in combination with specific energy sources resulted in different rumen fermentation characteristics. Evaluation of particle size distribution from the roughage source, particularly the large pool (upper and middle sieve sizes on PSPS) further revealed that particle size alone does not explain all variation in fermentation patterns alone but the digestible NDF as percentage of total NDF for these fractions could be a valuable predictor for chewing and rumination activity to ultimately establish a more optimal ruminal pH. / Dissertation (MSc(Agric))--University of Pretoria, 2011. / Animal and Wildlife Sciences / unrestricted

Thirty high-producing multiparous Holstein cows were used in a completely randomized block design to compare a lysine deficient total mixed ration, which was sufficient in methionine, to the same diet supplemented with a rumen protected lysine product. The CPM-Dairy prediction model was used to estimate the nutrient requirements and adequacy or deficiency of amino acids. During the 21-day prepartum transition period, cows were fed 4 kg (dry basis) of the lysine deficient diet plus Eragrostis curvula hay ad lib. After calving, cows were fed the lysine deficient diet for the first three weeks and were then blocked according to the average production from day 19-21. Fifteen cows were allocated to each treatment and blocked into 15 groups of two each. Data on production parameters were analyzed for all cows and also separately for cows in the 10 highest production blocks. The experimental period was from day 22 to 120 postpartum. Lysine supplementation resulted in an optimal dietary lysine : methionine ratio in metabolisable protein of 7.2 : 2.4. Lysine supplementation did not affect dry matter intake, milk production, milk fat percentage, milk protein percentage, milk urea nitrogen, body weight or body condition score; but decreased the non-casein nitrogen and whey content of milk. Furthermore, milk casein, which is the milk nitrogen fraction most sensitive towards increased duodenal supply of lysine and methionine, was not affected. The rumen protected lysine product evaluated did not improve cow productivity, probably because the product was either unprotected from rumen degradation, or overprotected to the extent that the lysine was not available for absorption in the small intestine; or absorbed but could not be metabolised. Copyright / Dissertation (MSc(Agric))--University of Pretoria, 2009. / Animal and Wildlife Sciences / unrestricted

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The objectives of this research were to: 1) evaluate the accuracy of the Molly cow model predictions of ruminal metabolism and nutrient digestion when simulating dairy and beef cattle diets, 2) advance representations of N recycling between blood and the gut and urinary N excretion in the model, 3) improve the representation of pH and to refit parameters related to ruminal metabolism and nutrient digestion in the model, 4) investigate how ruminal pH affects the microbial community, expression of carbohydrate-active enzyme transcripts (CAZymes), fiber degradation, and short chain fatty acid (SCFA) concentrations. To achieve the first objective, a total of 229 studies (n = 938 treatments) including dairy and beef cattle data, published from 1972 through 2016, were collected from the literature and used to assess the model accuracy and precision based on root mean squared errors (RMSE) and concordance correlation coefficients (CCC). Only slight mean and slope bias were exhibited for ruminal outflow of NDF, starch, lipid, total N, and non-ammonia N, and for fecal output of protein, NDF, lipid, and starch. However, ruminal pH was poorly simulated and contributed to problems in ruminal nutrient degradation and VFA production predictions. To achieve the second objective, representations including ruminal ammonia outflow, intestinal urea entry, microbial protein synthesis in the hindgut, and fecal urea N excretion, were added in the model. Total urea entry, gut urea entry, and urinary urea elimination rates collected from 15 published urea kinetics studies were used to derive related parameters. Significant improvements in predictions of variables describing ruminal N metabolism, blood urea metabolism and urinary N secretion were exhibited after the modifications. To achieve the third objective, a dataset assembled from the literature containing 284 peer reviewed studies with 1223 treatment means was used to derive parameter estimates for ruminal metabolism and nutrient digestions. After refitting the parameters, the model is even more robust in representing ruminal nutrient degradation compared to the initial model. Adding ammonia concentration as a driver to the pH equation increased the precision of predicted ruminal pH, and thereby, the precision of predicted VFA concentrations due to an improved representation of pH regulation of VFA production rates. To achieve the fourth objective, six cannulated Holstein heifers with an initial BW of 362 ± 22 kg (mean ± SD) were subjected to 2 treatments in a cross-over design. The treatments were 10 days of intraruminal infusions of both 1) distilled water (Control), and 2) a dilute blend of hydrochloric and phosphoric acids to achieve a pH reduction of 0.5 units (LpH). Statistical analyses indicated 19 bacterial genera and 4 protozoal genera were affected by low ruminal pH. We observed significant correlations between 54 microbes (43 bacterial and 11 protozoal genera) and 25 enzymes, of which 8 key enzymes participated in reactions leading to SCFA production, suggesting that the ruminal microbial community alters fiber catalysis and fermentation in response to altered pH through a shift in carbohydrate-active enzyme transcripts (CAZymes) expression. Overall, after the modifications and reparameterizations, 19.7 to 37.5% of RMSE with essentially no slope bias and minor mean bias were exhibited for of ruminal and fecal outflow of ADF, NDF, fat, and protein, suggesting the model is properly to represent nutrient degradation and digestion in the bovine. Considering ruminal microbes and CAZymes in predicting ruminal volatile fatty acid concentrations could explain more variance of observations. / Ph. D. / The purpose of this research was to improve ruminal nutrient metabolism and nutrient digestion representations in the Molly cow model. First, the model accuracy and precision were assessed using a dataset including 229 studies (n = 938 treatments) conducted with dairy and beef cattle. The model evaluation results indicated the mechanisms encoded in the model relative to ruminal and total tract nutrient digestion are properly represented. However, ruminal pH was very poorly represented in the model with a RMSE of 4.6% and a concordance correlation coefficient (CCC) of 0.0. Although VFA concentrations had negligible mean (2.5% of MSE) and slope (6.8% of MSE) bias, the CCC was 0.28 implying that further modifications with respect to VFA production and absorption are required to improve model precision. As identified by the residual analyses, the representations of N recycling between blood and the gut were improved by considering ruminal ammonia outflow, intestinal urea entry, microbial protein synthesis in the hindgut, and fecal urea N excretion in the model. Observations of total urea entry, gut urea entry, and urinary urea elimination rates were collected from 15 published urea kinetics studies were used to derive related parameters. After the modifications, prediction errors for ruminal outflows of total N, microbial N, and non-ammonia non-microbial N were 39.5, 27.8 and 35.9% of the respective observed mean values. Prediction errors of each were approximately 10% units less than the corresponding values before model modifications and fitting due primarily to decreased slope bias. The revised model predicted ruminal ammonia and blood urea concentrations with substantially decreased overall error and reductions in slope and mean bias. After that, ammonia concentration as a driver was added to the pH equation, and a dataset assembled from the literature containing 284 peer reviewed studies with 1223 treatment means was used to derive parameter estimates for ruminal metabolism and nutrient digestions. Refitting the parameters significantly improved the accuracy and precision of the model predictions for ruminal nutrient outflow (ADF, NDF, total N, microbial N, non-ammonia N, and non-ammonia, non-microbial N), ammonia concentrations, and fecal nutrient outflow (protein, ADF, and NDF). Therefore, the improved model can be used to simulate nutrient degradation and digestion in the bovine. Although minor mean and slope bias were observed for ruminal pH and VFA concentrations, the small values for concordance correlations indicated much of the observed variation in these variables remains unexplained. To further explain variance in ruminal metabolism and understand how ruminal pH affects the microbial community, expression of carbohydrate-active enzyme transcripts (CAZymes), fiber degradation, and short chain fatty acid (SCFA) concentrations, six cannulated Holstein heifers with an initial BW of 362 ± 22 kg (mean ± SD) were subjected to 2 treatments in a cross-over design. We observed 19 bacterial genera and 4 protozoal genera were affected by low ruminal pH, and significant correlations between 54 microbes (43 bacterial and 11 protozoal genera) and 25 enzymes, of which 8 key enzymes participated in reactions leading to SCFA production. In summary, after the modifications and reparameterizations, the model is even more robust to represent nutrient degradation and digestion in bovine compared to the initial model. More variance of observations of ruminal volatile fatty acid concentrations could be explained by considering ruminal microbes and CAZymes expressions in further study.

The quality of early milk produced by dams is affected by various factors (i.e. breed, age, parity, environment, nutrition, management). The impact of these factors on the quality of milk then have subsequent effects on calf health and development. Producers are responsible for following guidelines in order to ensure that they feed calves optimal quality milk in order to produce a healthy animal. They can also regulate factors such as environment and nutrition of the dam in order to produce better quality early milk. However, even after maximizing these factors there is still high mortality rate among pre-weaned calves, therefore, other factors such as mode of birth and genetics need to be studied to determine impacts on early milk quality and make further improvements to calf health and decrease mortality. Two experiments were conducted in order to study the effects of maternal and genetic factors on early milk production and to determine relationships that exist with calf health. The objective of the first study was to determine the effects that the mode of delivery had on early milk composition, and on the rumen microbiome of calves. We hypothesized that mode of birth would impact early milk composition, and, in turn, influence the microbial phyla in the calf gut. The second study had three objectives: 1) establish phenotypic relationships between colostrum composition traits, milk production traits, and calf health, 2) determine impact of breed and season on colostrum production and 3) ) elucidate the genetic parameters (i.e. heritability, genotypic, and phenotypic correlations) among colostrum production and milk production We hypothesized that colostrum composition and production differ among breeds and by season and that individual components influence calf health. Additionally, we hypothesized that colostrum quality traits (i.e. Brix score and volume) are heritable. For the first study Charolaise (CHAR; n = 23) and Angus (ANG; n = 15) dams were divided into two experimental groups; dams underwent vaginal (VD; n= 25) or cesarean (CD; n= 13) deliveries. Early milk samples were collected and quantified for protein, lactose, somatic cell count, and fatty acid concentrations. After parturition calves were separated based on dams experimental group. Rumen fluid was collected from calves on d 1, 3, and 28 post-partum. Extracted DNA from fluid were used for metagenomic sequencing (ANG calves, n=11; CHAR calves, n=13). Samples were run on the HiSeq 2500 platform as paired end reads according to Ilumina's standard sequencing protocol. A regression analysis was done in SAS using PROC GLM and regressing mode of birth on milk components for d 1,3, and 28. After, milk components found to be significantly impacted by mode of birth were regressed against microbial counts. Results showed that VD dams were more likely to have increased (P  0.05) protein, solids non-fat, and lactose on d 1 and 3, but decreased (P < 0.05) urea concentrations. Similarly, short, medium, and long-chain fatty acids were increased (P  0.05) in VD d 3 milk. Changes in true protein elicited a decrease (P  0.05) in rumen fluid Actinobacteria and Proteobacteria; whereas, both solids non-fat and lactose were associated with an increased (P  0.05) response in d 1 transition milk. No significant results for d 28 of sampling were observed. Based on our results we suggest that mode of birth influences protein concentrations in early milk. However, only a slight impact on the overall dynamics of the calf rumen was observed with the microbiome remaining relatively stable on the phyla level in response to changes in protein concentration. The second study looked into relationships between colostrum composition traits, management practices, and calf health, as well as determined heritability and genetic correlations for colostrum quality traits. Values for test-day milk, protein, fat, and somatic cell count (SCS) for Holstein (HO, n= 250) and Jersey (JE, n=289) cows were obtained from the Animal Genomic and Improvement laboratory server at the USDA. Brix score, colostrum weight, dam age, parity, and 3-month season of calving were also recorded. After, colostrum samples from JE cows were sent to DHIA where compositional measurements were obtained (i.e. true protein, fat, lactose, SCS, solid non-fats). Lactoferrin concentration for JE colostrum samples was also determined via ELISA. Calf blood samples were collected within 72 h post-partum and total serum protein (TSP) quantified to determine success of passive immunity transfer. Additionally, farm staff were instructed to record colostrum source for 1st feeding (i.e. dam, mix, other), freshness for 1st feeding (frozen vs fresh), Brix score of colostrum fed, volume of colostrum fed, and birth weight. A PROC Mixed with LSMEANS was performed in SAS to determine relationships between colostrum components, test day components, and quality traits for season, breed, and the interaction between season and breed. Also, PROC Mixed with LSMEANS was used to determine relationships of calf health with environment, management, and colostrum components. Additionally, a Pearson correlation was used to determine relationships between colostrum components and quality traits. Results for Holstein and Jersey showed that both colostrum Brix and volume (P < 0.001) differed by breed. Colostrum volume (P < 0.001), lactose (P < 0.001), and lactoferrin (P = 0.002) varied significantly by season. Additionally, test day milk (P = 0.046), fat (P = 0.012), and protein (P = 0.003) varied significantly by season. Moreover, a significant season and breed interaction (P = 0.028) was observed solely for colostrum volume. Calf health models indicated that TSP, colostrum total protein and solid non-fats impacted incidence of respiratory illness, but no factor significantly impacted incidence of scours. Results for Pearson correlation indicated strong correlations between true protein and solid non-fats and Brix (r = 0.99; 0.86). Lactoferrin also had moderate negative correlations with volume and lactose (r = -0.35; -0.33). Heritability and repeatability's were calculated using BLUPF90 family of programs. A single-trait repeatability animal model was used and included a 1-vector phenotype (Brix or Colostrum weight), fixed effects (i.e. calving year, parity, 3-month season of calving, and age at calving), additive genetic variance, random permanent environment effects, and random residual effects. A series of bivariate models were used to calculate genetic correlations of Brix score and colostrum weight with test-day compositional traits. Heritability estimates results for Holstein cow Brix and colostrum weight, were 0.25 and 0.15. Jersey cow heritability estimates were 0.36 and 0.47 respectively. We also observed some significant genetic correlations with Holstein Brix score and test-day milk (-0.23), fat (0.54), and SCS (0.29) having moderate correlations. Holstein colostrum weight had a strong correlation with test-day milk (0.96). Jerseys had strong genetic correlation of Brix score with colostrum weight (-0.98). Low to moderately heritability was observed for Brix score and colostrum weight in both breeds making them receptive to genetic selection in order to improve breeding programs. In conclusion, mode of birth significantly impacted colostrum composition which had subsequent effects on abundance of rumen microbiota. Colostrum Brix and volume were impacted by breed, season, and interaction, and calf incidence of disease was impacted by colostrum composition and environment. Additionally, two factors influencing colostrum quality (Brix score and colostrum weight) were found to be low to moderately heritable and have moderate to strong genetic correlations to compositional traits. Strong significant relationships were also found between colostrum compositional traits and colostrum quality traits. Therefore, incorporating quality traits into breeding programs has the potential to influence compositional traits which, in turn, can impact calf health and development by the interactions that exist between composition and microbial abundance in the rumen. / Master of Science in Life Sciences / Factors like breed, age, parity, nutrition, environment, and management can affect the quality of early milk produced. Many of these factors have been studied and guidelines developed in order to ensure producers feed the best quality milk to their calves which will allow for calves to develop properly. However, there is still a high mortality rate in pre-weaned calves and factors like mode of birth and genetics have not been readily studied. The purpose of our studies were to determine mode of birth impacts on composition of early milk and establish relationships between composition and rumen microbial phyla abundance. Additionally, establish relationships between colostrum composition traits, management practices, and calf health, and determine heritability and genetic correlations of colostrum quality traits to test-day composition traits. Our hypothesis was that colostrum quality traits such as Brix score and colostrum weight are heritable. We also hypothesized that mode of birth influences early milk composition and changes to composition has secondary effects to calf rumen microbial abundance. Charolaise (CHAR; n = 23) and Angus (ANG; n = 15) dams were divided into two experimental groups; dams underwent vaginal (VD; n= 25) or cesarean (CD; n= 13) delivery. Early milk samples were collected and sent to DHIA to quantify components. After parturition calves were separated based on dam's experimental group. Rumen fluid was collected from calves on d 1, 3, 28 post-partum and DNA extracted from fluid (ANG calves, n=11; CHAR calves, n=13). Results showed that VD significant differences in composition of VD and CD cows. Dams in VD group were more likely to have increased (P  0.05) protein, solids non-fat, and lactose but decreased (P < 0.05) urea concentrations. Similarly, short, medium, and long-chain fatty acids were increased (P  0.05) in VD. Changes in true protein elicited a decrease (P  0.05) in rumen fluid Actinobacteria and Proteobacteria. Results suggest that mode of birth influences protein concentrations in early milk and induces a slight impact on the overall dynamics of the calf rumen microbiome. A second study was conducted to establish relationships between colostrum components, management and calf health as well as determine genetic parameters of colostrum quality traits. Holstein (HO, n= 250) and Jersey (JE, n=289) cow test-day data was obtained from the Animal Genomic and Improvement laboratory server at the USDA. Brix score, colostrum weight, dam age, parity, and 3-month season of calving were also recorded. Colostrum samples from JE cows were sent to DHIA where compositional measurements were obtained (i.e. true protein, fat, lactose, SCS, solid non-fats). Lactoferrin concentration for JE cow colostrum samples was also determined via ELISA. Calf blood samples were collected within 72 h post-partum and TSP quantified. Farm staff recorded colostrum source for 1st feeding and colostrum freshness for 1st and feeding. A PROC Mixed was performed to determine impact of test-day milk composition traits on colostrum quality traits by breed, PROC Mixed with LSMEANS was used to determine relationships of environment, colostrum management, and colostrum components with incidence of scours and respiratory disease in calves. A Pearson correlation was used to determine relationships between colostrum components and quality traits Heritability and repeatability's were calculated using BLUPF90 family of programs. A series of bivariate models were used to calculate genetic correlations of Brix score and colostrum weight with test-day compositional traits. Results indicated that colostrum Brix and volume were impacted by season, breed, and the interaction of breed and season. Calf incidence of disease was impacted by colostrum components and total serum protein levels. Results for Pearson correlation indicated strong correlations between true protein and solid non-fats and Brix (r = 0.99; 0.86). Lactoferrin also had moderate negative correlations with volume and lactose (r = -0.35; -0.33). Heritability estimates results for Holstein Brix and colostrum weight were 0.25 and 0.15. Jersey cow heritability estimates were 0.36 and 0.47, respectively. We also observed some significant genetic correlations with Holstein Brix score and test-day milk (-0.23), fat (0.54), and SCS (0.29) having moderate correlations. Holstein colostrum weight had a strong correlation with test-day milk (0.96). Jerseys had strong genetic correlation of Brix score with colostrum weight (-0.98). Results indicated a low to moderately heritability for Brix score and colostrum weight in both breeds making them receptive to genetic selection in order to improve breeding programs. Strong significant relationships were also found between colostrum compositional traits and colostrum quality traits.