Metabolizable Protein Requirements Research Articles

Effects of late gestational nutrient restriction on uterine artery blood flow, placental size, and cotyledonary mRNA expression in primiparous beef females.

Fall-calving primiparous beef females [body weight (BW): 451 ± 28 (SD) kg; body condition score (BCS): 5.4 ± 0.7] were individually-fed either 100% (control; CON; n = 13) or 70% (nutrient restricted; NR; n = 13) of metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to parturition. Doppler ultrasonography of both uterine arteries was conducted pre-treatment and every 21 d from days 181 to 265 of gestation. Expelled placentas were collected, and ipsilateral cotyledonary tissue was sampled to assess relative messenger ribonucleic acid (mRNA) expression. Placentas were separated into ipsilateral and contralateral sides, dissected (cotyledonary vs. intercotyledonary), and dried. Data were analyzed with nutritional plane, treatment initiation date, and calf sex (when P < 0.25) as fixed effects. Uterine blood flow included day and nutritional plane × day as repeated measures. We previously reported that post-calving, NR dams weighed 64kg less and were 2.0 BCS lower than CON, but calf birth weight was not affected. Maternal heart rate was less (P < 0.001) for NR dams than CON after nutritional planes began. Nutritional plane did not affect (P ≥ 0.20) uterine artery hemodynamics, but all variables were affected (P ≤ 0.04) by day. Contralateral cotyledonary and placental weight were less (P ≤ 0.04) and contralateral intercotyledonary weight and number of cotyledons tended to be less (P ≤ 0.10) for NR dams than CON, but ipsilateral and whole placental weights were not affected (P ≥ 0.13). Ipsilateral placental weight as a percentage of total placental weight was greater (P = 0.03) for NR dams than CON. Whole placental cotyledonary:intercotyledonary weight was less (P = 0.01) for NR dams than CON. Placental efficiency was not affected (P = 0.89) by nutritional plane. Cotyledonary relative mRNA expression of GLUT3 and SNAT2 was greater (P ≤ 0.05) and relative expression of GLUT1, GLUT4, and NOS3 tended to be greater (P ≤ 0.07) for NR dams than CON. Nutritional plane did not affect (P ≥ 0.13) relative mRNA expression of GLUT5, 4F2hc, CAT1, LAT1, LAT2, VEGFA, FLT1, KDR, GUCY1B3, and PAG2. Despite less contralateral placental growth, beef heifers experiencing late gestational nutrient restriction maintained uterine artery blood flow and total placental mass and had 4 nutrient transporters and 1 angiogenic factor upregulated in cotyledons, all which likely contributed to conserving fetal growth.

81 Effects of udder quarter location on colostrum yield, nutrients, and immunoglobulin G in beef heifers

Abstract We hypothesized that colostrum total nutrients and immunoglobulin G (IgG) would not be affected by side of the udder, but that they would be greater in the rear versus the front half of the udder due to difference in volume of colostrum produced. Complete colostrum yield was collected individually from each quarter pre-suckling [40.5 ± 21.0 min (SD)] from fall-calving crossbred beef heifers (body weight = 472 ± 34 kg; body condition score (= 5.3 ± 0.4) that were either individually-fed 100% (control; n = 12) or 70% (nutrient restricted; n = 12) of NASEM metabolizable energy and metabolizable protein requirements from d 160 of gestation to calving. Analysis of colostrum lactose, protein, triglycerides, and free glucose was performed using colorimetric assays on a UV-visible light microplate reader. Colostrum IgG was analyzed using a commercially available ELISA kit. Quarter yield, nutrient or IgG concentration, and total nutrients or IgG were analyzed using the mixed procedure of SAS with fixed effects of udder location, nutritional plane, and their interaction in the model. Nutritional plane was not part of the current objective, but was included to account for variation in colostrum yield due to nutrient restriction, as we have previously reported. Separate statistical comparisons were made between the front and rear quarters and between the right and left quarters of the udder, with each quarter considered a sampling unit within each experimental unit (half) for both analyses. The interaction of udder location × nutritional plane did not affect (P ≥ 0.11) any variable. Nutrient restriction decreased (P ≤ 0.03) colostrum yield, total lactose, and total free glucose compared with controls. Front quarters produced less volume (P &amp;lt; 0.001; 36.2% of total); total lactose, protein, and free glucose (P ≤ 0.02; 34.3 to 43.3%); and total IgG (P &amp;lt; 0.001; 33.7%) than rear quarters. Front quarters tended to produce less (P = 0.07; 43.3%) total triglycerides than rear quarters. Lactose concentration was 10.5% greater (P = 0.05) in front compared with rear quarters, but other nutrient or IgG concentrations were not affected (P ≥ 0.18). Udder side did not affect total volume (P = 0.78), total nutrients (P ≥ 0.36), or total IgG (P = 0.79). The left side represented 50.7% of the total volume and 50.1 to 53.4% of total nutrients and IgG produced. Concentration of nutrients and IgG also were not affected (P ≥ 0.31) by udder side. In conclusion, colostrum did not differ between udder sides, but, relative to front quarters, rear quarters produced greater nutrient and IgG yield due to greater colostrum volume with minimal differences in nutrient or IgG concentrations.

PSIV-A-4 Effect of late gestational nutrient restriction on locomotor activity of beef heifers

Abstract The objective of this study was to determine the effects of nutrient restriction on locomotor behavior during late gestation. Fall-calving crossbred beef heifers were moved to 3.7 × 15.8 m partially-covered pens and individually-fed 100% (control; n = 13) or 70% (nutrient restricted; n = 13) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from d 160 of gestation to calving. Diets were based on chopped sorghum sudan hay fed in Calan gates and supplemented to meet targeted nutritional planes. IceQube accelerometers (iceRobotics, Edinburgh, UK) were placed on the left hind fetlock between d 158 and 168 of gestation to determine standing time, lying time, step count, number of lying bouts, and motion index. Daily behavior data were averaged for 5 distinct periods (period 1: IceQube placement to d 180 of gestation; period 2: d 181 to 201 of gestation; period 3: d 202 to 222 of gestation; period 4: d 223 to 243 of gestation; and period 5: 244 to 264 of gestation). Days in which animals were moved from their pens were excluded from the data set, resulting in an average of 17.2 ± 2.35 d per period. Data were analyzed with fixed effects of nutritional plane, period, and their interaction in the model. Maternal sire and day of treatment initiation were included as covariates. The number of lying bouts was affected (P = 0.02) by the nutritional plane × period interaction. Within period, there was no effect (P ≥ 0.20) of nutritional plane on lying bouts. Lying bouts in control heifers decreased (P = 0.008) from period 1 to 2, whereas lying bouts in nutrient restricted heifers decreased (P = 0.002) from period 1 to 2 before increasing (P = 0.02) again from period 2 to 3. Motion index and step count were affected (P ≤ 0.05) by nutritional plane, where both were greater in control heifers. Motion index and step count were affected (P &amp;lt; 0.001) by period, while standing time and lying time tended to be affected (P ≤ 0.09) by period. Motion index and step count decreased (P &amp;lt; 0.001) between periods 1 and 2 and periods 3 and 4 but increased (P ≤ 0.004) between periods 2 and 3 and periods 4 and 5. Standing time decreased (P = 0.02), while lying time increased (P = 0.02), between periods 3 and 4. These data suggest that nutrient restricted heifers may have reduced locomotor behavior in late gestation compared with control heifers. Throughout all periods of gestation, control heifers took more daily steps and had a greater motion index, suggesting that nutrient availability in late gestation may directly impact locomotor behavior of beef heifers.

PSIV-A-7 Effects of late gestational nutrient restriction of beef heifers on small intestinal crypt depth in neonatal calves

Abstract We hypothesized that late gestational nutrient restriction would impair small intestinal development in neonatal calves, including crypt cell depth and proliferation. Fall-calving crossbred beef heifers [body weight (BW) = 466 ± 30 (SD) kg; BCS: 5.4 ± 0.5] bred to a single sire were individually-fed 100% (control; n = 10) or 70% (nutrient restricted; n = 12) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from d 160 of gestation to calving. Calves were removed from their dams immediately post-calving and fed artificial colostrum and milk replacer relative to body weight until euthanasia at 48.7 ± 0.4 h of age. The gastrointestinal tract was removed, and proximal jejunum samples were dissected from each calf and immersion-fixed in 10% neutral buffered formalin. Tissues were embedded in paraffin blocks and cut into 5-µm sections that were mounted on glass slides. Slides were incubated with Ki-67 (marker of nuclear proliferation) and counterstained with Hematoxylin using an autostainer. Images were taken at 5× magnification using an upright microscope. QuPath software was used to measure crypt depth, starting at the base of the crypt region and ending at the furthest cluster of Ki-67 positive cells, perpendicular to the base of the mucosa. For each calf, 10 crypt depth measurements were taken from 4 images, resulting in 40 crypt depth measurements that were averaged. Nutritional plane was a fixed effect in the model, and maternal sire, date of study initiation, and calf sex (when P &amp;lt; 0.25) were considered covariates. We previously reported that calves born to nutrient restricted dams weighed less (P ≤ 0.05) at birth and 48 h than calves born to control dams. Small intestinal mass tended to be less (P = 0.11) in offspring of nutrient restricted dams but was not affected (P = 0.58) when expressed relative to body weight. Calves born to nutrient restricted dams also tended to have less (P = 0.11) small intestinal mass relative to brain weight. Maternal nutrient restriction did not affect (P = 0.95) jejunal crypt depth. Additionally, crypt depth relative to body weight was not affected (P = 0.20) by nutrient restriction. Although crypt depth was not affected, further analysis of proliferation and morphology will help to understand the relationship between maternal nutrient restriction and small intestine development in neonatal calves.

Late gestational nutrient restriction in primiparous beef females: Performance and metabolic status of lactating dams and pre-weaning calves.

Fall-calving primiparous beef females [body weight (BW): 451 ± 28 (SD) kg; body condition score (BCS): 5.4 ± 0.7] were individually-fed 100% (control; CON; n = 13) or 70% (nutrient restricted; NR; n = 13) of estimated metabolizable energy and metabolizable protein requirements from day 160 of gestation to calving. Post-calving, all dams were individually-fed tall fescue hay supplemented to meet estimated nutrient requirements for maintenance, growth, and lactation in Calan gates until day 149 of lactation, which limited calves to milk only. From day 150 of lactation until weaning at day 243, dams and calves were group-fed in drylots. Dam BW and metabolic status were determined every 21 d, and BCS and backfat (BF) were determined every 42 d of lactation until weaning. Pre-weaning calf BW, size, and metabolic status were determined every 21 d. Data were analyzed with nutritional plane, calving date, and calf sex (when P < 0.25) as fixed effects. Circulating metabolites included day and nutritional plane × day as repeated measures. We previously reported that post-calving, NR dams were 64kg and 2.0 BCS less than CON, but calf BW and size at birth were not affected. During the first 147 d of lactation, NR dams gained more (P < 0.01) BW than CON and increased (P < 0.01) BCS, while CON decreased (P ≤ 0.01) BCS and BF. Previously, NR dams had lower (P < 0.01) circulating triglycerides on day 1 of lactation, tended to have lower (P = 0.08) triglycerides on day 21, and had lower (P ≤ 0.04) non-esterified fatty acids (NEFA) on days 21 and 243 than CON. Maternal glucose and urea N were not affected (P ≥ 0.73). At weaning, NR dams weighed 17kg less (P = 0.15), were 0.67 BCS lower (P < 0.01), and tended to have less (P = 0.06) BF. Calves born to NR dams weighed less (P = 0.02) than CON by day 42 of age and were 13% smaller (P < 0.01) at weaning. Calf girth measures diverged (P ≤ 0.05) by day 21 of age, and skeletal size measures were less (P ≤ 0.08) for calves born to NR dams at most timepoints after day 63 of age. Calves born to NR dams tended to have lower (P = 0.09) circulating urea N pre-weaning than CON, but glucose, triglycerides, and NEFA were not affected (P ≥ 0.16). In summary, first-parity beef females that were nutrient restricted during late gestation experienced compensatory growth and gained body condition during lactation but were still thinner at weaning. Nutrient restriction reduced pre-weaning calf growth, likely due to decreased milk production.

Influence of metabolizable protein and methionine supplementation on growth-performance of Holstein steer calves during the initial 112-d feedlot growing phase.

The objective was to examine the effects of metabolizable protein (MP) and ruminal-protected methionine supplementation on growth performance of Holstein steer calves during the initial feedlot growing phase (112 d). One hundred eighty Holstein steer calves (122 ± 7kg) were blocked by weight and assigned to 30 pens (6 steers per pen). Five treatments were applied: 1) control, a diet based on steam-flaked corn containing urea and dry distillers grains plus solubles as supplemental N sources with no amino acid addition; 2) control diet plus blood meal supplementation; 3) diet from treatment 2, with 0.064% Smartamine M (70% methionine; Adisseo, Alpharetta, GA) supplementation; 4) diet from treatment 2 with 0.096% Smartamine M supplementation; 5) diet from treatment 2 with 0.128% Smartamine M supplementation. All diets were formulated to exceed the estimated MP requirements. The estimated metabolizable lysine, as well as methionine, was deficient in the control diet. Blood meal was added to the control diet to meet estimated lysine requirements (diet 2), the other diets had increasing concentrations of supplemental methionine. Supplemental MP enhanced (10%, P < 0.02) interim and overall 112-d average daily gain (ADG). Additional effects of supplemental methionine on ADG were not appreciable (P > 0.10). Supplemental MP did not affect (P > 0.10) dry matter intake (DMI) during the first 56-d period; however, it tended to increase (P = 0.08) DMI during the subsequent 56-d period. Overall, supplemental MP or methionine had no appreciable effect (P > 0.10) on DMI. Supplemental MP improved (P < 0.01) gain efficiency and estimated dietary net energy (NE) values during the initial 56-d period (11 and 7%, respectively) and overall (7 and 4%, respectively). Supplemental MP did not affect (P > 0.10) gain efficiency during the second 56-d period, although it tended to enhance (P = 0.08) estimated dietary NE. Supplemental methionine did not appreciably affect (P > 0.10) gain efficiency or estimated dietary NE. Therefore, adding MP to cover the estimated limiting amino acid supply in diets may enhance the gain efficiency and dietary energetics of growing Holstein calves. However, amino acid addition supplementation beyond the requirements may not produce extra productive performance of steer calves.

Crude protein requirements of light-weight feedlot steersduring a 35-d receiving period

The influence of dietary crude protein (CP) levels on growth performance, morbidity, and estimated dietary net energy (NE) of light-weight crossbreed feedlot calves during a 35-d receiving period was evaluated. For the above, 108 crossbred steers (196±13 kg) were used in 35-d receiving trial. Steers were randomly allocated to 18 pens (6 steers/pen, 6 replicas/treatment). Treatments consisted of a steam flaked corn-based receiving diet (72:28 concentrate to forage ratio) containing 12.5, 13.5 and 14.5% CP. Crude protein level in diet was manipulated by replacing steam flaked corn by canola meal. Steers were allowed ad lib. access to their experimental diets. Morbidity averaged 32%, and was not affected by treatments. Increasing the level of dietary CP improved average daily weight gain, gain efficiency and tended to increase the ratio of observed-to expected dietary NE. Furthermore, in CP range from 12.5 to 13.5%, these effects were evident, but were not apparent at 13.5 to 14.5% CP. It can be concluded that high-energy receiving diet formulations containing 13.5 to 14.5% CP will optimise initial growth performance of light-weight (~200 kg BW) feedlot calves. However, present effect may be more a function of achieving metabolisable amino acid rather than metabolisable protein requirements.

328 Comparison of Predicted Nutritional Requirements of Two Feeding Systems for Dairy Cattle Implemented in a Monte-Carlo Simulation Model of Herd Dynamics

Abstract There is increased interest in precision-feeding systems that account for individual-animal variation and temporal dairy herd dynamics to increase feed-efficiency and reduce environmental footprints. The Ruminant Farm Systems (RuFaS; Hansen et al., 2021) model simulates individual animals on a daily timestep using a stochastic, Monte Carlo framework to represent the phenotypic diversity and population dynamics expected in a dairy herd. Within RuFaS, individual animal nutrient requirements are used to inform pen-level diet formulations and feed delivery. However, nutritional requirements for feeding dairy cattle were recently updated via consideration of both animal and diet-related factors. Our aim was to calculate individual animal predictions for dry matter intake (DMI), as well as energy and metabolizable protein requirements, and compare the methods described in the 7th (NRC, 2001) and 8th (NASEM, 2021) editions of the Nutrient Requirements for Dairy Cattle. For that purpose, we simulated dairy herds (ca. 6,000 individual Holstein animals per simulation, mean adult body weight = 671 kg, standard deviation = 79, mean daily milk production = 39.8 kg·day-1·cow-1 , standard deviation = 7.5) for 10+ year time periods with an updated version of RuFaS. The simulated herds provided a wide range of values with which to test the nutrient requirement models, and their implications. The NASEM DMI estimates were less across the board but began to converge towards NRC calculated values at the larger simulated animal body weights. The principal differences in energy requirements between the two models (NRC vs. NASEM) were: 1) predicted requirements for pregnancy were significantly greater for NASEM than NRC across all life history stages; 2) NASEM displayed slightly greater energy requirements for growth in first and second lactation cows, and; 3) NASEM predicted decreased maintenance requirements for all heifer stages but the opposite was true for mature cows. Metabolizable protein requirements were greater following NASEM calculations in heifers over 300 kg, but strikingly similar to NRC-computed values for lactating cows. Overall, results from this modeling study align with our expectations and demonstrate successful implementation of the two nutrition models within the RuFaS model. These outputs confirm the usefulness of data obtained to explore applications of the two nutrient requirement models under different precision feeding management practices and, to some extent, to quantitatively evaluate their viability of the models in edge cases that can occur within the expected variation of a herd’s population. Future work will explore downstream consequences of the nutrient requirement models within the automated, least-cost ration formulation framework using nonlinear programming and metrics related to manure output and storage. These data will guide further developments of RuFaS as whole farm simulation model and provide insights into expected variation in nutritional requirements within a dynamic set of animals.

329 Evaluation and Prediction of Site and Extent of Protein Digestion of Feedstuffs Commonly Fed in Beef Cattle Finishing Diets

Abstract Meeting metabolizable protein requirements of finishing cattle without overfeeding protein requires reliable estimates of site and extent of digestion. Current estimates of rumen degradable (RDP) and undegradable protein (RUP), as well as intestinal digestibility of RUP (dRUP) may be inadequate. Thus, the objectives of this experiment were to quantify RDP, RUP, and dRUP of common feedstuffs and evaluate nutrient composition as a predictor of RDP, RUP, and dRUP. Ruminally cannulated steers (n = 6) consuming a finishing diet were enrolled in replicated 3 × 3 Latin squares. Within each Latin square period, steers were assigned a feedstuff classification for in situ ruminal incubation. Single-source ingredients were classified as grain (steam-flaked and whole-shelled corn, wheat, and milo), protein (wet and dried corn distillers grains, Sweet Bran, cottonseed meal, canola meal, and soybean meal), and roughage (cotton burrs, alfalfa hay, wheat hay, sorghum × sudangrass hay, wheat silage, and corn stalks). Nutrient composition was determined for all feedstuffs using wet chemistry procedures. Feedstuffs were lyophilized, ground through a 2-mm screen, aliquoted into in situ bags, and ruminally incubated for 0, 4, 8, 12, 24, or 48 h. Samples were composited within incubation time point, analyzed for crude protein (CP), corrected for microbial contamination, and fit to non-linear models to estimate RDP and RUP using calculated passage rate. Subsamples of in situ digested feedstuffs underwent in vitro pepsin-pancreatin digestion and CP analysis to estimate dRUP. Statistical analyses were conducted using JMP Pro 16.0 and R (v4.1.0). On average, RUP estimates were 37.0% decreased (P &amp;lt; 0.05) for protein ingredients, yet grains and roughages were not different (P &amp;gt; 0.73) compared with NASEM (2016) empirical values, respectively. However, average dRUP was 11.9% and 33.1% reduced (P &amp;lt; 0.01) for protein ingredients and roughages, yet grain dRUP was not different (P = 0.16) compared with NASEM (2016) values, respectively. Neutral detergent fiber (NDF) and CP explained a substantial portion of the variation in RDP (P &amp;lt; 0.01, R2 = 0.94, RMSE = 2.26). Acid detergent fiber, NDF, and CP explained considerable variation in dRUP (P &amp;lt; 0.01, R2 = 0.91, RMSE = 5.43). Models were predictive when applied to independent data from the literature for estimates of RDP (R2 = 0.93; RMSE = 3.72) and dRUP (R2 = 0.83; RMSE = 6.06). There was slope (-0.09; P &amp;lt; 0.05) and mean bias (-1.30; P &amp;lt; 0.01) for RDP prediction validation but only mean bias (4.90; P &amp;lt; 0.01) in dRUP prediction validation models. Collectively, these data suggest that dRUP of protein ingredients and roughages are less than values reported by the NASEM (2016). Furthermore, CP and NDF may be useful for predicting RDP, RUP, and dRUP.

PSIV-14 Effects of Maternal Nutrient Restriction During Late Gestation on Expelled Cotyledonary Mrna Expression in Primiparous Beef Females

Abstract To determine the effects of late gestational nutrient restriction on expelled cotyledonary mRNA expression, fall-calving Hereford × Simmental-Angus heifers [single-sired; BW: 451 ± 28 (SD) kg; BCS: 5.4 ± 0.7] bred to a single sire were allocated by fetal sex and expected calving date to receive either 100% (control; CON; n = 12) or 70% (nutrient restricted; NR; n = 11) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth. Beginning on d 160 of gestation, heifers were individually fed chopped sorghum sudan hay (1.74 Mcal ME/kg, 6.69% CP, 72.0% NDF; DM basis) and based on individual intakes, supplemented to meet targeted nutritional planes. Calving was observed for all females and placentas were collected at natural expulsion. Immediately after collection (average: 4.5 h post-calving; range: 2.3 to 12.1 h post-calving), 2 representative cotyledons on the ipsilateral side were cleaned with phosphate buffered saline, and cotyledonary tissue was flash frozen. Total RNA was extracted, and RT-qPCR was performed for mRNA expression of glucose transporters (SLC2A1, SLC2A3, SLC2A4), a fructose transporter (SLC2A5), amino acid transporters (SLC1A1, SLC3A2, SLC7A1, SLC7A5, SLC7A8, SLC38A2), angiogenic factors/receptors (VEGFA, NOS3, FLT1, KDR, GUCY1B3), and pregnancy-associated glycoprotein 2 (PAG2). Relative mRNA expression was analyzed with nutritional plane, treatment initiation date, time to cotyledon sampling, and calf sex (when P &amp;lt; 0.25) as fixed effects. We have previously reported that total uterine blood flow during late gestation was not affected (P ≥ 0.20) by nutritional plane or the nutritional plane × day of gestation interaction. Post-calving, NR dams were 64 kg BW less (P &amp;lt; 0.001) and 2.0 BCS less (P &amp;lt; 0.001), but calf birth weight was not affected (P = 0.72) by nutritional plane. Contralateral placental dry weight tended to be less (P = 0.07) in NR dams, but total placental weight was not affected (P = 0.86) by late gestational nutritional plane. Cotyledonary relative mRNA expression of SLC2A3 and SLC38A2 was greater (P ≤ 0.05) and relative expression of SLC2A1, SLC2A4, and NOS3 tended to be greater (P ≤ 0.07) in NR dams compared with CON. Late gestational nutritional plane did not affect (P ≥ 0.13) cotyledonary relative mRNA expression of FLT1, GUCY1B3, KDR, PAG2, SLC1A1, SLC2A5, SLC3A2, SLC7A1, SLC7A5, SLC7A8, and VEGFA. In summary, first parity beef females who experienced late gestational nutrient restriction maintained uterine blood flow and placental mass and had 4 nutrient transporters and 1 angiogenic factor upregulated in cotyledons, all which likely contributed to their conservation of fetal growth.

71 Effects of Late Gestational Nutrient Restriction on Calf pre-Weaning Growth, Backgrounding and Feedlot Performance, and Carcass Composition

Abstract Fall-calving Hereford-SimAngus heifers [single-sired; BW: 451 ± 28 (SD) kg; BCS: 5.4 ± 0.7] bred to a single sire were individually fed 100% (control; CON; n = 12) or 70% (nutrient restricted; NR; n = 13) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to calving. Post-calving, all females were fed chopped tall-fescue hay supplemented to meet lactational nutrient requirements in Calan gates to constrain diets of calves to milk only until day 147, then pen-fed in drylots until weaning at day 242 ± 3 (SD). Post-weaning, calves were fed a tall fescue hay-based backgrounding diet in the same large drylots for 53 ± 12 d, then moved to partially covered pens with GrowSafe feeding systems in 2 groups and fed a corn-based feedlot diet (formulated to be 18.3% CP, 1.21 Mcal NEg/kg, DM basis; 89% DM) for 255 ± 3 d (similar days on feed rather than carcass endpoint). Cattle were harvested in a commercial plant, and camera carcass grading was performed. Data were analyzed with maternal treatment, calving date, and calf sex (when P &amp;lt; 0.25) as fixed effects; feedlot group was included for feedlot and carcass measures. We previously reported that birth weight was not affected (P = 0.72), but NR decreased (P &amp;lt; 0.04) milk production by 15%. Calves born to NR dams had reduced ADG from birth to day 147 (P = 0.02), day 147 to weaning (P = 0.08), and birth to weaning (P = 0.003), resulting in NR calves having 13% lighter (P = 0.004) weaning weight. Backgrounding ADG was not affected (P = 0.80) by maternal treatment; thus, feedlot entry BW was 11% less (P = 0.009) in NR calves. On day 28, 56, 84, and 112 on feed, NR calves weighed less (P ≤ 0.09) than control. Final BW was not affected (P = 0.91) by maternal treatment. Feedlot ADG was greater for NR calves from day 168 to slaughter (P = 0.02) and the overall feeding period (P = 0.03), but not before day 168 on feed (P ≥ 0.22). Calves born to NR dams had less (P = 0.02) dressing percentage, but improved (P = 0.02) yield grade and backfat thickness. Hot carcass weight, ribeye area, marbling score, and KPH were not affected (P ≥ 0.26) by maternal treatment. Percent prime, yield grade ≤ 2, and yield grade ≥ 4 were not affected (P ≥ 0.29) by maternal treatment. Overall, late gestational nutrient restriction decreased growth pre-weaning but increased late finishing growth, without affecting backgrounding or early feedlot growth. These cattle had leaner carcasses after similar days on feed, suggesting that late gestational nutrient restriction altered growth patterns or body composition.

70 Nutrient Restriction During Late Gestation Alters Maternal Circulating Amino Acid Concentrations in Primiparous Beef Females

Abstract We hypothesized that maternal circulating AA concentrations would be reduced by late gestational nutrient restriction, indicating less available nutrients for transport by the uteroplacenta to the growing fetus. Fall-calving Hereford-SimAngus heifers [single-sired; BW: 451 ± 28 (SD) kg; BCS: 5.4 ± 0.7] bred to a single sire were allocated by fetal sex and expected calving date to receive either 100% (control; CON; n = 12) or 70% (NR; n = 13) of NASEM metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to calving. Heifers were individually fed chopped sorghum sudan hay (1.74 Mcal ME, 6.66% CP, 72.0% NDF; DM basis) and based on individual intakes, supplemented to meet targeted nutritional planes. Jugular blood samples were obtained on days 159 (Pre-treatment), 202, and 244 of gestation, and 1 h post-calving to determine serum concentrations of the 20 common AA (except cysteine), 1-methyl histidine, and 3-methyl histidine. Gestational and post-calving AA were analyzed separately with nutritional plane, treatment initiation date, and calf sex (when P &amp;lt; 0.25) as fixed effects. Gestational AA included day and nutritional plane x day using repeated measures. We have previously reported that dam BCS was less (P ≤ 0.04) by day 202 of gestation and dam BW was less (P ≤ 0.01) by day 223 of gestation for NR dams. Post-calving, NR dams were 64 kg BW and 2.0 BCS lless (P &amp;lt; 0.001), but calf birth weight was not affected (P = 0.72) by nutritional plane. Histidine, lysine, and methionine were greater (P ≤ 0.03) in NR dams on day 202 of gestation. Tryptophan and valine were less (P ≤ 0.05) while methionine and total AA tended to be less (P ≤ 0.08) on day 244 of gestation in NR dams. Aspartic acid, glutamic acid, and tyrosine were less (P ≤ 0.03), but 3-methyl histidine was greater (P ≤ 0.01) on days 202 and 244 of gestation in NR dams. 1-methyl histidine was greater (P ≤ 0.05) at all 3 gestational timepoints but leucine was less (P = 0.03) in NR dams during gestation. Post-calving, glutamic acid, leucine, and valine were less (P ≤ 0.04), and methionine, threonine, tryptophan, tyrosine, and total AA tended to be less (P ≤ 0.10) in NR dams. Histidine, 1-methyl histidine, 3-methyl histidine, and serine were greater (P ≤ 0.03) in NR dams post-calving. In summary, late gestational nutrient restriction reduced total maternal circulating AA and altered the maternal serum AA profile, but calf birth weight was not affected. Individual AA that were greater or unaffected in NR dams were likely indicative of body protein catabolism occurring to meet nutrient requirements.

Energy and protein requirements for maintenance and weight gain of Canindé goats supplemented on pasture in the semi-arid region

The purpose of this study was to estimate the carcass composition, and energy and protein requirements for maintenance and weight gain of Canindé goats supplemented on pasture in a semi-arid region. Forty-six castrated animals, with initial body weight (BW) of 15.7 ± 0.96 kg, grazing in Caatinga were used. Six animals were slaughtered at the beginning of the experiment representing the initial carcass composition (reference animals; 16.1 ± 1.15 kg BW), while the other animals were randomly distributed in four treatments (concentrate supplementation at 0%, 0.5%, 1.0%, and 1.5% BW), with ten animals per treatment. When one of the animals of each group reached 25 kg BW, all animals in that group were slaughtered. The whole empty body was weighed, ground, homogenized, and sampled for further chemical analyses. The level of supplementation influenced dry matter intake, retained energy, and body weight gain of Canindé goats. The energy (kcal/kg) and fat (g/kg EBW) contents in the carcass of goats of 15, 20, and 25 kg were 2.29 and 86.11, 2.39 and 113.48, and 2.47 and 140.53, respectively. The minimum nitrogen losses were 188 mg N/EBW0.75. The net and metabolizable energy for maintenance were 72.11 kcal/EBW0.75/day and 2.19 g/kg EBW0.75/day, respectively. The net and metabolizable protein requirements were 2.19 and 1.88 g/kg EBW0.75, respectively. The net energy and protein requirements for weight gain ranged from 2.61 to 2.81 Mcal/kg EBW gain and 194.37–222.55 g protein/kg EBW, respectively, for animals from 15 to 25 kg BW. It is concluded that the energy and protein nutritional requirements of Canindé goats supplemented on pasture in the semi-arid region vary according to body weight.

Protein requirements for pregnant dairy cows

We aimed to estimate the protein requirements of pregnant Holstein × Gyr cows. Sixty-one Holstein × Gyr (HG) cows were used, with an average initial BW of 480 ± 10.1 kg and 5 ± 0.5 yrs of age. Cows were divided into 3 groups: pregnant (n = 43), non-pregnant (n = 12), and baseline (n = 6). Baseline animals were slaughtered before starting the experiment to estimate the initial body composition of the remaining animals. Pregnant and non-pregnant cows received 2 diets: maintenance and ad libitum. Pregnant cows were slaughtered at 139, 199, 241, and 268 gestation days (GD). First, we used data only from non-pregnant cows to determine the requirements for maintenance and growth in adult cows. The requirements of metabolizable protein for maintenance (MPm; g/EBW0.75/d) were estimated using a linear regression between the metabolizable protein intake (MPI, g/d) and average daily gain (g/d), and the MPm was defined as the intercept divided by the average BW0.75. Net protein requirements for gain (NPg; g/d) were estimated by the first derivative of the allometric equation between final crude protein (CP) in the body (kg) and the final EBW (kg). The efficiency of use of metabolizable protein for gain (k) was calculated from the regression between the retained protein (g/EBW0.75/d) and the MPI (g/EBW0.75/d), and k was the slope of this regression. The MPI was estimated by combining microbial protein synthesis (purine derivatives) with the digestible rumen undegradable protein [(total protein intake minus RDP) × intestinal digestibility]. Second, an exponential model was used to fit the protein accumulation in the gestational components in the function of GD. The first derivative of that model was considered the net requirement for gestation (NPgest). The efficiency of protein utilization for gestation (kgest) was calculated by the iterative method using the equation: Δ = MPI - (MPm + NPg/kg + NPgest/kgest). The iteration was performed aiming at a zero deviation between observed MPI and MP estimated by the requirements determined herein. We obtained a value of 3.88 g/EBW0.75/d for MPm. The estimation of NPg can be calculated according to the following equation: NPg = 0.716 × (EBWopen-0.308) × EBGcorrected, where EBWopen is the empty BW (kg) for non-pregnant animals and EBGcorrected is the empty body gain (kg/d) corrected for the gestational component. The k was determined as 0.347. The net protein requirements for gestation (NPgest) were determined as NPgest (g/d) = 0.0008722 × exp(0.01784 ×GD) × (calfweight/35). The efficiency of using metabolizable protein for gestation (kgest) was 0.625. It is important to highlight that different methods of MP estimates should not be mixed and that the proposed method requires the estimate of microbial protein (estimate it via urinary estimates) and might be a limitation for practical application. In conclusion, new studies should be conducted to validate our results and the methodology adopted to determine protein requirements for pregnancy in dairy cows. Due to the pattern of protein accumulation in the gestational components, we suggest that exponential model to describe protein requirements for pregnancy for dairy cows.

Dose response to postruminal urea in lactating dairy cattle

Inclusion of urea in dairy cattle diets is often limited by negative effects of high levels of feed urea on dry matter intake (DMI) and efficiency of rumen N utilization. We hypothesized that supplying urea postruminally would mitigate these limitations and allow greater inclusion of urea in dairy cattle diets. Four rumen-fistulated Holstein-Friesian dairy cows (7 ± 2.1 lactations, 110 ± 30.8 d in milk; mean ± standard deviation) were randomly assigned to a 4 × 4 Latin square design to examine DMI, milk production and composition, digestibility, rumen fermentation, N balance, and plasma constituents in response to 4 levels of urea continuously infused into the abomasum (0, 163, 325, and 488 g/d). Urea doses were targeted to linearly increase the crude protein (CP) content of total DMI (diet plus infusion) by 0%, 2%, 4%, and 6% and equated to 0%, 0.7%, 1.4%, and 2.1% of expected DMI, respectively. Each 28-d infusion period consisted of a 7-d dose step-up period, 14 d of adaptation, and a 7-d measurement period. The diet was fed ad libitum as a total mixed ration [10.9% CP, 42.5% corn silage, 3.5% grass hay, 3.5% wheat straw, and 50.5% concentrate (dry matter basis)] and was formulated to meet 100%, 82%, and 53% of net energy, metabolizable protein, and rumen-degradable protein requirements, respectively. Linear, quadratic, and cubic effects of urea dose were assessed using polynomial regression assuming the fixed effect of treatment and random effects of period and cow. Dry matter intake and energy-corrected milk yield responded quadratically to urea dose, and milk urea content increased linearly with increasing urea dose. Apparent total-tract digestibility of CP increased linearly with increasing urea dose and ruminal NH3-N concentration responded quadratically to urea dose. Mean total VFA concentration was not affected by urea dose. The proportion of N intake excreted in feces decreased linearly and that excreted in urine increased linearly in response to increasing urea dose. The proportion of N intake excreted in milk increased linearly with increasing urea dose. Urinary urea excretion increased linearly with increasing urea dose. Microbial N flow responded cubically to urea dose, but the efficiency of microbial protein synthesis was not affected. Plasma urea concentration increased linearly with increasing urea dose. Regression analysis estimated that when supplemented on top of a low-CP diet, 179 g/d of postruminal urea would maximize DMI at 23.4 kg/d, corresponding to a dietary urea inclusion level of 0.8% of DMI, which is in line with the current recommendations for urea inclusion in dairy cattle diets. Overall, these results indicate that postruminal delivery of urea does not mitigate DMI depression as urea dose increases.

Bioavailability of a novel rumen protected methionine supplement and its effect on milk production and body composition in dairy cows

Our objective was to evaluate the bioavailability of a rumen-protected Met product (EMT 3.4) using milk selenium (Se) marker method and its impact on milk production and body composition in dairy cows. Twelve multiparous Holstein cows (82 ± 27 days in milk, 38.7 ± 3.4 kg/d of milk; mean ± SD) were used in a replicated 3 × 3 Latin-square design with 21 d periods. Prior to the study, cows were fed Se-yeast for 2 wk to reach stable milk Se concentration. Treatments were 1; a negative control diet (NCT) providing 100% of the metabolizable protein (MP) requirement and 90% of the metabolizable Lys and Met requirements, 2; a positive control diet (PCT) providing 101% of the MP, and 110% of the Met and Lys requirements (Met supplied by Smartamine M, Adisseo), and 3; an experimental Met treatment (EMT; Met supplied by EMT 3.4, Ajinomoto Inc.) that was formulated to provide 101% of the MP, and 110% of the metabolizable Met and Lys requirements (AMTS.Cattle.Professional utilizing CNCPS 6.5.5 models). The NCT cows were not supplemented with additional Met or Lys, whereas supplemental Lys for both the EMT and PCT diets was supplied by Aji-Pro L (Ajinomoto). The PCT and EMT treatments decreased milk Se-to-N ratio (i.e. bioavailability; Se:N), by 11% and 9.5% respectively compared with NCT (P < 0.05). The PCT increased DMI and tended to increase milk yield compared to NCT and EMT. The PCT treatment increased yields of milk protein, solids, lactose, and milk lactose concentration compared to NCT and EMT treatments. The EMT treatment increased milk urea nitrogen (MUN) concentration compared with NCT and PCT. However, the potential for milk Se to be inconsistently diluted due to differences in MUN and DMI poses challenges with interpretation. The lack of measurable production responses when supplementing EMT compared to NCT, may indicate less bioavailable Met than the bioavailability calculation assumes.

Performance and milk fatty acid profile of beef cows with a different energy status with short nutrient restriction and refeeding.

Our study objective was to determine the effect of a short feed restriction (4 d) and subsequent refeeding (4 d) on the performance and metabolism of beef cows with a different nutritional status by particularly focusing on their milk fatty acid (FA) profile, to consider its potential use as biomarker of metabolic status. Thirty-two Parda de Montaña multiparous lactating beef cows were individually fed a diet based on the average cow's net energy (NE) and metabolizable protein requirements. At 58 d in milk (DIM, day 0), cows underwent a 4 d feed restriction (55% requirements, restriction period). Before and after the restriction, diets met 100% of their requirements (basal and refeeding periods). Cow performance, milk yield and composition, and plasma metabolites, were determined on day -2, 1, 3, 5, 6, and 8. Cows were classified into two status clusters according to their pre-challenge performance and energy balance (EB) (Balanced vs. Imbalanced). All traits were statistically analyzed considering the fixed effect of status cluster and feeding period or day, with cow as a random effect. Imbalanced cows were heavier and had a more negative EB (P < 0.001), but similar milk yield, milk composition, and circulating metabolites (except for greater urea) than Balanced cows (P > 0.10). Milk contents of C18:1 cis-9, monounsaturated FA (MUFA), and mobilization FA were greater (P < 0.05), whereas saturated FA (SFA) and de novo FA were lesser in Imbalanced than Balanced cows (P < 0.05). Restriction decreased body weight (BW), milk yield, and milk protein compared to the basal period, but increased milk urea and plasma nonesterified fatty acids (NEFA) (P < 0.001). Milk contents of SFA, de novo, and mixed FA decreased immediately during the restriction, while MUFA, polyunsaturated FA and mobilization FA increased (P < 0.001). Basal milk FA contents were recovered on day 2 of refeeding, and all their changes strongly correlated with differences in EB and NEFA (P < 0.05). The general lack of interactions between status clusters and feeding periods implied that the response mechanisms to diet changes did not differ between cows with a different pre-challenge nutritional status.

Maternal nutrient restriction during late gestation reduces vigor and alters blood chemistry and hematology in neonatal beef calves.

Fall-calving primiparous beef females [body weight: 451 ± 28 (SD) kg; body condition score: 5.4 ± 0.7] were individually-fed either 100% (control; CON; n = 13) or 70% (nutrient restricted; NR; n = 13) of metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to parturition. Calves were reared naturally by their dams and monitored for latency times from birth to first sternal recumbency, attempt to stand, and stand; vigor scores were assigned at 2, 5, 10, and 20min of age. Rectal temperatures and jugular blood were obtained at 0 (pre-suckling), 6, 12, 24, and 48h of age, and blood chemistry, hematology, cortisol, and insulin were determined. Data were analyzed with fixed effects of late gestational nutritional plane (single data point) or nutritional plane, hour, and their interaction (data over time, repeated measures). Calving date was a fixed effect; calf sex was included when P < 0.25. We previously reported that late gestational nutritional plane did not affect gestation length or calf size at birth, but calving assistance and fetal malpresentations occurred more often in NR. Nutritional plane did not affect (P = 0.65) duration of parturition, but calves born to NR dams had slower times to attempt to stand (P = 0.09), slower times to stand (P = 0.02), and had poorer 20min vigor scores (P = 0.05). Serum immunoglobulin G and A concentrations at 48h were greater (P ≤ 0.03) for NR calves. Rectal temperature of NR calves was less (P = 0.02) at 0h, but greater (P = 0.04) at 24h compared with CON. Circulating glucose, non-esterified fatty acids, triglycerides, cortisol, and insulin were not affected by nutritional plane (P ≥ 0.18). Total protein and globulin from 6 to 48h were greater (P ≤ 0.02) in NR calves. Calves from NR dams had greater (P < 0.08) gamma-glutamyl transferase at 6, 12, and 48h. Serum aspartate aminotransferase was greater (P ≤ 0.07) from 0 to 24h and creatine kinase was greater (P ≤ 0.04) from 6 to 24h in NR calves. At 0h, potassium was greater (P = 0.03) in NR calves. Calves born to CON had greater chloride (P = 0.08; main effect), sodium (P ≤ 0.09) from 0 to 48h, and anion gap (P = 0.02) at 6h. Hematocrit from 6 to 24h and red blood cells and hemoglobin at 6 and 12h were greater (P ≤ 0.09) in CON calves. These data indicate that nutrient restriction during late gestation resulted in less vigorous calves with more indicators of trauma in early life.

Late gestational nutrient restriction in primiparous beef females: nutrient partitioning among the dam, fetus, and colostrum during gestation.

Fall-calving primiparous crossbred beef females [body weight (BW): 451 ± 28 (SD) kg; body condition score (BCS): 5.4 ± 0.7] were allocated by fetal sex and expected calving date to receive either 100% (control; CON; n = 13) or 70% (nutrient restricted; NR; n = 13) of metabolizable energy and metabolizable protein requirements for maintenance, pregnancy, and growth from day 160 of gestation to calving. Heifers were individually-fed chopped poor quality hay and supplemented to meet targeted nutritional planes based on estimated hay intakes. Dam BW, BCS, backfat, and metabolic status were determined pre-treatment, every 21 d (BW and metabolic status) or 42 d (BCS and backfat) during gestation, and post-calving. At birth, calf BW and size were measured, and total colostrum from the most full rear quarter was collected pre-suckling. Data were analyzed with nutritional plane, treatment initiation date, and calf sex (when P < 0.25) as fixed effects. Gestational metabolites included day and nutritional plane × day as repeated measures. During late gestation, CON dams gained (P < 0.01) maternal (non-gravid) BW and maintained (P ≥ 0.17) BCS and backfat, while NR dams lost (P < 0.01) maternal BW, BCS, and backfat. Circulating glucose, urea N, and triglycerides were less (P ≤ 0.05) in NR dams than CON at most late gestational timepoints after treatment initiation. Circulating non-esterified fatty acids were greater (P < 0.01) in NR dams than CON. Post-calving, NR dams weighed 63.6 kg less (P < 0.01) and were 2.0 BCS less (P < 0.01) than CON. At 1 h post-calving, NR dams had less (P = 0.01) plasma glucose and tended to have less (P = 0.08) plasma triglycerides than CON. Nutrient restriction did not affect (P ≥ 0.27) gestation length, calf birth weight, or calf size at birth. Colostrum yield was 40% less (P = 0.04) in NR dams than CON. Protein and immunoglobulin concentrations were greater (P ≤ 0.04), but free glucose and urea N concentrations were less (P ≤ 0.03), in colostrum of NR dams than CON. Colostrum total lactose, free glucose, and urea N were less (P ≤ 0.03) in NR dams than CON, but total protein, triglycerides, and immunoglobulins were not affected (P ≥ 0.55). In summary, beef heifers experiencing late gestational nutrient restriction prioritized partitioning nutrients to fetal growth and colostrum production over maternal growth. During undernutrition, fetal and colostral nutrient demands were largely compensated for by catabolism of maternal tissue stores.

A new protein requirement system for dairy cows

Accurate prediction of protein requirements for maintenance and lactation is needed to develop more profitable diets and reduce N loss and its environmental impact. A new factorial approach for accounting for net protein requirement for maintenance (NPM) and metabolizable protein (MP) efficiency for lactation (EMPL) was developed from a meta-analysis of 223 N balance trials. We defined NPM as the sum of the endogenous protein fecal and urinary excretion and estimated it from the intercept of a nonlinear equation between N intake and combined total N fecal and urinary excretion. Our model had a strong goodness-of-fit to estimate NPM (6.32 ± 0.15 g protein/kg metabolic body weight; n = 807 treatment means; r = 0.91). We calculated the EMPL as a proportion of the N intake, minus N excreted in feces and urine, that was secreted in milk. A fixed-EMPL value of 0.705 ± 0.020 was proposed. In a second independent data set, nonammonia-nonmicrobial-N and microbial-N ruminal outflows were measured, and the adequacy of the MP prediction (51 studies; n = 192 means treatments) was assessed. Our system based on the fixed-EMPL model predicted the MP requirement for lactation and maintenance with higher accuracy than several North American and European dairy cattle nutrition models, including the INRA (2018) and NASEM (2021). Only the NRC (2001), CNCPS 6.5, and Feed into Milk (2004) models had similar accuracy to predict MP requirement. Our system may contribute to improve the prediction for MP requirements of maintenance and lactation. However, most refined predictive models of intestinal digestibility for rumen undegradable protein and microbial protein are still needed to reduce the evaluation biases in our model and external models for predicting the MP requirements of dairy cows.