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Simple Summary: Understanding placental vascularity is vital for ensuring the proper nourishment of the fetus and, therefore, a healthy offspring. We aimed to investigate the impact of vitamin and mineral supplementation and/or different rates of body weight gain on placental vascularity in beef heifers. To this end, in the first experiment, heifers were divided into groups that received vitamin and mineral supplementation or did not at least 72 days before breeding. At breeding, they were further divided into low or moderate-weight gain groups, resulting in four different treatments maintained until day 83 of pregnancy when tissue collection was performed. In the second experiment, another group of heifers received a basal diet or a diet with vitamin and mineral supplementation from breeding until parturition. We evaluated placental blood vessel density in both experiments and the placental expression of genes related to blood vessel growth in the first experiment. Results showed that supplementation and the rate of body weight gain during early pregnancy did not significantly affect placental vascularity or the expression of angiogenic factors. On the other hand, placental vascularity measured at parturition was increased in the fetal placenta of the supplemented group. These findings suggest that supplementation with vitamins and minerals throughout all gestation may impact placental function at a later stage of pregnancy. The effect of vitamins and minerals supplementation (VTM) and/or two rates of body weight gain (GAIN) on bovine placental vascular development and angiogenic factors gene expression were evaluated in two experiments: In Exp. 1, crossbred Angus heifers (n = 34) were assigned to VTM/NoVTM treatments at least 71 days before breeding to allow changes in the mineral status. At breeding, through artificial insemination (AI), heifers were assigned to low-gain (LG) 0.28 kg/d or moderate-gain (MG) 0.79 kg/d treatments, resulting in NoVTM-LG (Control; n = 8), NoVTM-MG (n = 8), VTM-LG (n = 9), and VTM-MG (n = 9) until day 83 of gestation; In Exp. 2, crossbred angus heifers (n = 28), were assigned to control (CON; n = 12), receiving a basal total mixed ration (TMR) or TMR + VTM (VTM; n = 16) from breeding until parturition. Placentomes from Exp. 1 and cotyledons (COT) from Exp. 2 were evaluated by immunohistochemistry for COT vascular density area. COTs from Exp. 1 were evaluated for angiogenic factor (ANGPT-1, ANGPT-2, eNOS2, eNOS3, FLT1, KDR, TEK, VEGFA) gene expression. In Exp. 1, COT vascularity was not affected by the interaction of VTM and GAIN (p = 0.67) or the main effects of VTM (p = 0.50) and GAIN (p = 0.55). Likewise, angiogenic factors were not differentially expressed between treatments (p < 0.05). In Exp. 2, COT vascularity was greater in VTM vs. CON (p = 0.07). In conclusion, there is a suggested later-stage influence of vitamin and mineral supplementation on placental vascularity, emphasizing the importance of supplementation beyond early pregnancy. [ABSTRACT FROM AUTHOR]

To evaluate the effects of feeding hempseed cake on digestive enzymes, crossbred heifers (n = 32; 494 ± 10 kg body weight) were fed diets containing 20% (dry matter basis) dried corn distillers grains plus solubles or hempseed cake for 111 days. There was greater (P = 0.05) pancreatic mass relative to body weight in heifers fed hempseed cake. No differences (P ≥ 0.19) in digestive enzyme activity in the pancreas (α-amylase, trypsin, and lipase) and jejunum (maltase, glucoamylase, and isomaltase) were observed between treatments. Our results suggest that feeding hempseed cake did not influence digestive enzyme activity. [ABSTRACT FROM AUTHOR]

Traditional heifer feeding strategies typically involve modest rates of body weight (BW) gain and include a relatively low proportion of concentrate feeds. In situations of limited forage or high feed costs, additional concentrates may be included in the diets and fed at a limited rate. High-concentrate diets can enhance the efficiency of nutrient utilization, alter characteristics of the gastrointestinal tract (GIT), and influence the composition of gain. The objective of this study was to evaluate the strategy of limit-feeding highconcentrate diets on feeding behavior, carcass characteristics, and GIT morphometrics in replacement beef heifers. Crossbred beef heifers (n = 20) began receiving either a high forage (75% forage:25% concentrate; HF, n =10) or high concentrate (25% forage:75% concentrate; HC, n =10) diet 74 ± 4 d before breeding. Heifers were inseminated with sexed male semen from a single bull. Individual intake and feeding behavior data were recorded using the Insentec Roughage Intake Control system, and heifers were weighed, and diet deliveries were adjusted every 2 wk to target a BW gain of 0.45 kg/d for both groups. Heifers were harvested at 180 d of gestation, where the viscera were removed, and weights of the full gastrointestinal tract, including the stomach complex, and small and large intestines were recorded. After removing digesta, weights of the empty gastrointestinal tract, rumen-reticulum, omasum, abomasum, small and large intestine, and mesenteric fat were recorded. Carcass characteristics were assessed 24 h after slaughter. Data were analyzed using the MIXED procedure of SAS, with heifer as the experimental unit. No differences were observed in final BW, average daily gain, or body condition score (P ≥ 0.18) between treatments (Table 1). Reflecting that HC heifers were limit-fed to a greater extent than HF heifers, therefore, dry matter intake, number of meals, visits to the feed bunk, time spent eating, and time per meal were less in HC heifers than in the HF group (P ≤ 0.001). In contrast, HC heifers had greater (P ≤ 0.001) eating rates of DM per minute, per visit and per meal compared with HF heifers. Though no differences were observed in back (P = 0.31) or rib fat (P = 0.37), HC heifers had greater (P = 0.04) marbling score and tended to have greater carcass weight (P = 0.06) and ribeye area (P = 0.07) as compared with HF heifers (Table 2). Greater (P < 0.001) full weights of GIT and stomach complex, empty weight of rumen-reticulum, weight of total digesta, and digesta as a proportion of BW (i.e., fill) were observed in HF heifers. In contrast, HC heifers had greater (P < 0.001) weights of full small intestine and mesenteric fat than HF heifers. These findings demonstrate that, despite similar rates of gain, limit-feeding high-concentrate diets can alter the composition of weight gain, favoring fat, muscle, and GIT development, potentially altering dam efficiency throughout her productive life. [ABSTRACT FROM AUTHOR]

Ruminal methane (CH4) emission from cattle represents about 2 to 12% gross energy loss and is considered as one of the main contributors to the greenhouse gas emissions by the livestock industry. Recent multiple lines of research indicated that maternal gut microbiome may influence offspring ruminal CH4 emission phenotype via potential influence on fetal programming and transmission of methanogens from the dam to calf perinatally. Our objective was to evaluate the effects of altering maternal microbiota via feeding high forage (HF) and high concentrate (HC) diets during the entire gestation on the maternal ruminal CH4 emissions in beef heifers. For this, Crossbred replacement beef heifers (n = 61) bred with male sexed semen were randomly assigned into two groups and were fed either a high forage (75% forage:25% concentrate; HF, n = 29) or high concentrate (25% forage:75% concentrate; HC, n = 32) diet with limited feed intake to gain 0.45 kg/d during the gestation. Individual feed intake was monitored and body weight (BW) were measured bi-weekly and diet deliveries were adjusted to ensure the target BW gain. A subset of pregnant heifers (n = 10 per treatment group) was harvested at 180 d of gestation. Ruminal fluid was collected by stomach tubing on d 180 (20 heifers slaughtered), d 238 of gestation, and at the postpartum (within 3 h of calving). The ruminal fluid was placed in 15 mL falcon tube, kept in a warm thermos and immediate processing for the in vitro CH4 production assay. About 12.5 mL of ruminal fluid was placed into separate 120 mL serum bottles each containing 0.62g of feed (HC or HF diet) and 50 mL of McDougall buffer under CO2 infusion before the bottle sealed with stoppers. The cultures were incubated at 39°C for 24h. Immediately after incubation, total biogas production, headspace CH4 concentration (using Gas chromatography), and pH of the 24 h culture was measured. Overall, the mean total volume of gas produced over 24 h was not statistically different (P > 0.05) between HF and HC heifers at any of the day measured, although it was numerically greater on d 238 (219 vs. 197 mL) and at postpartum (246 vs. 219 mL) in HC than HF heifers. Methane concentration in per milliliter gas was ranged between 13.3 and 16.3% but was not different between HF and HC heifers on any of the day evaluated (P > 0.05). Total volume of CH4 gas produced over 24 h was tended (P = 0.067) to be greater in HC heifers on d 238 (37.5 vs. 25. 7 mL). The culture pH from the ruminal fluid of HC heifers was less on d 238 (6.08 vs. 6.57) and at postpartum (P < 0.05). Overall, in vitro ruminal CH4 was not different in the ruminal fluid of HF and HC pregnant heifers. [ABSTRACT FROM AUTHOR]

Our objectives were to develop a Mobile Cow Command Center (MCCC) capable of precision monitoring of grazing heifers to 1) examine the relationship between supplement intake on concentrations of liver mineral and blood metabolites and 2) examine activity, reproductive, and health behavior. Yearling crossbred Angus heifers (N = 60; initial BW = 400.4 ± 6.2 kg) were fitted with radio frequency identification ear tags that allowed access to electronic feeders (SmartFeed system; C-Lock Inc. Rapid City, SD), and with activity monitoring tags (CowManager B.V. the Netherlands) that monitored reproductive, feeding, and health-associated behaviors. Heifers were assigned randomly to one of three treatments for a 57-day monitoring period: 1) no supplement (CON ; N = 20), 2) free choice mineral (MIN ; Purina Wind and Rain Storm [Land O'Lakes, Inc.], N = 20), or 3) free choice energy and mineral supplement (NRG ; Purina Accuration Range Supplement 33 with added MIN [Land O'Lakes, Inc.], N = 20). Consecutive day body weights, blood, and liver biopsies were collected at pasture turnout and final day of monitoring. By design, mineral intake was greatest in MIN heifers (49 ± 37 g/d) and energy supplement intake was greatest in NRG heifers (1,257 ± 37 g/d). Final BW and ADG were similar among treatments (P > 0.42). Concentrations of glucose on day 57 were greater (P = 0.01) in NRG compared with CON and MIN heifers. Liver concentrations of Se and Fe on day 57 were greater (P < 0.05) in NRG heifers than CON, with MIN being intermediate. Activity tags reported NRG heifers spent less time eating (P < 0.0001) and more time (P < 0.0001) being "highly active" than MIN with CON heifers being intermediate. Data retrieved from activity tags identified 16 of 28 pregnant heifers exhibiting some type of estrus-associated behavior even after confirmation of established pregnancy. The activity monitoring system triggered a total of 146 health alerts from 34 of the 60 heifers monitored, but only 3 heifers of the heifers initiating an electronic health alert needed clinical treatment. However, animal care staff identified nine additional heifers that required treatment for which no electronic health alert was generated. The electronic feeders successfully controlled intake of individual heifers managed in groups pastures; however, the activity monitoring system misrepresented estrus and health events. [ABSTRACT FROM AUTHOR]

The objective of this study was to determine the dose of folate and vitamin B12 in beef heifers fed rumen protected methionine and choline required to maintain increased B12 levels and intermediates of the methionine-folate cycle in circulation. Angus heifers (n = 30; BW = 392.6 ± 12.6 kg) were individually fed and assigned to one of five treatments: 0XNEG : Total mixed ration (TMR) and saline injections at day 0 and 7 of the estrous cycle, 0XPOS : TMR, rumen protected methionine (MET) fed at 0.08% of the diet DM, rumen protected choline (CHOL) fed at 60 g/d, and saline injections at day 0 and 7, 0.5X : TMR, MET, CHOL, 5 mg B12, and 80 mg folate at day 0 and 7, 1X : TMR, MET CHOL, 10 mg vitamin B12, and 160 mg folate at day 0 and 7, and 2X : TMR, MET, CHOL, 20 mg B12, and 320 mg folate at day 0 and 7. All heifers were estrus synchronized but not bred, and blood was collected on day 0, 2, 5, 7, 9, 12, and 14 of a synchronized estrous cycle. Heifers were slaughtered on day 14 of the estrous cycle for liver collection. Serum B12 concentrations were greater in the 0.5X, 1X, and 2X, compared with 0XNEG and 0XPOS on all days after treatment initiation (P  < 0.0001). Serum folate concentrations were greater for the 2X treatment at day 5, 7, and 9 of the cycle compared with all other treatments (P  ≤ 0.05). There were no differences (P  ≥ 0.19) in hepatic methionine-cycle or choline analyte concentrations by treatment. Concentrations of hepatic folate cycle intermediates were always greater (P  ≤ 0.04) in the 2X treatment compared with the 0XNEG and 0XPOS heifers. Serum methionine was greater (P  = 0.04) in the 0.5X and 2X heifers compared with 0XNEG, and S-adenosylhomocysteine (SAH) tended (P  = 0.06) to be greater in the 0.5X heifers and the S-adenosylmethionine (SAM):SAH ratio was decreased (P  = 0.05) in the 0.5X treatment compared with the 0XNEG, 0XPOS, and 2X heifers. The hepatic transcript abundance of MAT2A and MAT2B were decreased (P  ≤ 0.02) in the 0.5X heifers compared with the 0XNEG, 0XPOS, and 2X heifers. These data support that beef heifers fed rumen protected methionine and choline require 20 mg B12 and 320 mg folate once weekly to maintain increased concentrations of B12 and folate in serum. Furthermore, these data demonstrate that not all supplementation levels are equal in providing positive responses, and that some levels, such as the 0.5X, may result in a stoichiometric imbalance in the one-carbon metabolism pathway that results in a decreased SAM:SAH ratio. [ABSTRACT FROM AUTHOR]

Simple Summary: Trace minerals play a critical role in several biological functions, being essential for fetal growth and development. Maternal nutrition influences the supply of trace minerals to the fetus, which can lead to long-term consequences on offspring performance and health. Our study shows that a maternal vitamin and mineral supplementation (VTM) pre-breeding and during the first trimester of gestation resulted in greater concentrations of Se, Cu, and Co in the liver of beef heifers and their fetuses. These minerals are an essential component of the antioxidant system, which may have positive impacts on the immune system of the future offspring. In addition, we reported that low rates of gain (LG, 0.28 kg/d) from breeding to d 83 of gestation resulted in greater concentrations of Mo and Co in fetal liver compared with moderate rates of gain (MG, 0.79 kg/d). Having a greater fetal trace mineral reserve may be beneficial for neonates, as the immune system of newborn calves is underdeveloped and minerals play a role in that development. Therefore, our study shows that liver weight and concentrations of hepatic trace minerals are affected by maternal dietary treatments, which may impact the performance and health of the future offspring. We evaluated the effects of vitamin and mineral supplementation (from pre-breeding to day 83 of gestation) and two rates of gain (from breeding to day 83 of gestation) on trace mineral concentrations in maternal and fetal liver, fetal muscle, and allantoic (ALF) and amniotic (AMF) fluids. Crossbred Angus heifers (n = 35; BW = 359.5 ± 7.1 kg) were randomly assigned to one of two vitamin and mineral supplementation treatments (VMSUP; supplemented (VTM) vs. unsupplemented (NoVTM)). The VMSUP factor was initiated 71 to 148 d before artificial insemination (AI), allowing time for the mineral status of heifers to be altered in advance of breeding. The VTM supplement (113 g·heifer−1·d−1) provided macro and trace minerals and vitamins A, D, and E to meet 110% of the requirements specified by the NASEM, and the NoVTM supplement was a pelleted product fed at a 0.45 kg·heifer−1·day−1 with no added vitamin and mineral supplement. At AI, heifers were assigned to one of two rates of gain treatments (GAIN; low gain (LG) 0.28 kg/d or moderate gain (MG) 0.79 kg/d) within their respective VMSUP groups. On d 83 of gestation fetal liver, fetal muscle, ALF, and AMF were collected. Liver biopsies were performed prior to VMSUP factor initiation, at the time of AI, and at the time of ovariohysterectomy. Samples were analyzed for concentrations of Se, Cu, Zn, Mo, Mn, and Co. A VMSUP × GAIN × day interaction was present for Se and Cu (p < 0.01 and p = 0.02, respectively), with concentrations for heifers receiving VTM being greater at AI and tissue collection compared with heifers not receiving VTM (p < 0.01). A VMSUP × day interaction (p = 0.01) was present for Co, with greater (p < 0.01) concentrations for VTM than NoVTM at the time of breeding. VTM-MG heifers had greater concentrations of Mn than all other treatments (VMSUP × GAIN, p < 0.01). Mo was greater (p = 0.04) for MG than LG, while Zn concentrations decreased throughout the experiment (p < 0.01). Concentrations of Se (p < 0.01), Cu (p = 0.01), Mn (p = 0.04), and Co (p = 0.01) were greater in fetal liver from VTM than NoVTM. Mo (p ≤ 0.04) and Co (p < 0.01) were affected by GAIN, with greater concentrations in fetal liver from LG than MG. In fetal muscle, Se (p = 0.02) and Zn (p < 0.01) were greater for VTM than NoVTM. Additionally, Zn in fetal muscle was affected by GAIN (p < 0.01), with greater concentrations in LG than MG. The ALF in VTM heifers (p < 0.01) had greater Se and Co than NoVTM. In AMF, trace mineral concentrations were not affected (p ≥ 0.13) by VMSUP, GAIN, or their interaction. Collectively, these data suggest that maternal nutrition pre-breeding and in the first trimester of gestation affects fetal reserves of some trace minerals, which may have long-lasting impacts on offspring performance and health. [ABSTRACT FROM AUTHOR]

The objective of this study was to evaluate the effects of feeding heifers a vitamin and mineral supplement and targeting divergent rates of weight gain during early gestation on the fetal liver amino acid, carbohydrate, and energy profile at d 83 of gestation. Seventy-two crossbred Angus heifers were randomly assigned in a 2 × 2 factorial arrangement to one of four treatments comprising the main effects of vitamin and mineral supplementation (VTM or NOVTM) and feeding to achieve different rates of weight gain (low gain [LG] 0.28 kg/day vs. moderate gain [MG] 0.79 kg/day). Thirty-five gestating heifers with female fetuses were ovariohysterectomized on d 83 of gestation and fetal liver was collected and analyzed by reverse phase UPLC-tandem mass spectrometry with positive and negative ion mode electrospray ionization, as well as by hydrophilic interaction liquid chromatography UPLC-MS/MS with negative ion mode ESI for compounds of known identity. The Glycine, Serine, and Threonine metabolism pathway and the Leucine, Isoleucine, and Valine metabolism pathway had a greater total metabolite abundance in the liver of the NOVTM-LG group and least in the VTM-LG group (p < 0.01). Finally, both the TCA Cycle and Oxidative Phosphorylation pathways within the Energy Metabolism superpathway were differentially affected by the main effect of VTM, where the TCA cycle metabolites were greater (p = 0.04) in the NOVTM fetal livers and the Oxidative Phosphorylation biochemicals were greater (p = 0.02) in the fetal livers of the VTM supplemented heifers. These data demonstrate that the majority of metabolites that are affected by rate of weight gain or vitamin/mineral supplementation are decreased in heifers on a greater rate of weight gain or vitamin/mineral supplementation. [ABSTRACT FROM AUTHOR]

Simple Summary: Cow-calf operations rely mostly in forage-based systems. Different supplementation strategies are used by beef producers in order to overcome nutrient deficiencies and achieve targeted growth or reproductive performances. This study provides information on the impacts of feeding pregnant replacement heifers with vitamin/mineral and protein/energy supplements on heifer performance and fetal outcomes. Our study shows that moderate rates of gain (achieved via protein/energy supplementation) resulted in fetuses with heavier femurs and reduced liver mass relative to fetal body weight. Moreover, vitamin and mineral supplementation increased fetal liver mass, and vitamin and mineral supplementation combined with moderate gain treatments resulted in greater fetal intestinal weights. These findings indicate that replacement heifer nutrition during early gestation can alter the development of organs in the fetus that are relevant for future offspring performance. Liver and intestines are key organs related to energy metabolism; therefore, this study shows that compensatory mechanisms are in place in the developing conceptus that can alter the growth rate of key metabolic organs possibly in an attempt to increase or decrease energy utilization. Thirty-five crossbred Angus heifers (initial BW = 359.5 ± 7.1 kg) were randomly assigned to a 2 × 2 factorial design to evaluate effects of vitamin and mineral supplementation [VMSUP; supplemented (VTM) vs. unsupplemented (NoVTM)] and different rates of gain [GAIN; low gain (LG), 0.28 kg/d, vs. moderate gain (MG), 0.79 kg/d] during the first 83 d of gestation on dam hormone and metabolic status, fetal tissue and organ mass, and concentration of glucose and fructose in fetal fluids. The VMSUP was initiated 71 to 148 d before artificial insemination (AI), allowing time for mineral status of heifers to be altered in advance of breeding. At AI heifers were assigned their GAIN treatment. Heifers received treatments until the time of ovariohysterectomy (d 83 ± 0.27 after AI). Throughout the experiment, serum samples were collected and analyzed for non-esterified fatty acids (NEFA), progesterone (P4), insulin, and insulin-like growth factor 1 (IGF-1). At ovariohysterectomy, gravid reproductive tracts were collected, measurements were taken, samples of allantoic (ALF) and amniotic (AMF) fluids were collected, and fetuses were dissected. By design, MG had greater ADG compared to LG (0.85 vs. 0.34 ± 0.04 kg/d, respectively; p < 0.01). Concentrations of NEFA were greater for LG than MG (p = 0.04) and were affected by a VMSUP × day interaction (p < 0.01), with greater concentrations for NoVTM on d 83. Insulin was greater for NoVTM than VTM (p = 0.01). A GAIN × day interaction (p < 0.01) was observed for IGF-1, with greater concentrations for MG on d 83. At d 83, P4 concentrations were greater for MG than LG (GAIN × day, p < 0.01), and MG had greater (p < 0.01) corpus luteum weights versus LG. Even though fetal BW was not affected (p ≥ 0.27), MG fetuses had heavier (p = 0.01) femurs than LG, and VTM fetuses had heavier (p = 0.05) livers than those from NoVTM. Additionally, fetal liver as a percentage of BW was greater in fetuses from VTM (P = 0.05; 3.96 ± 0.06% BW) than NoVTM (3.79 ± 0.06% BW), and from LG (p = 0.04; 3.96 ± 0.06% BW) than MG (3.78 ± 0.06% BW). A VMSUP × GAIN interaction was observed for fetal small intestinal weight (p = 0.03), with VTM-MG being heavier than VTM-LG. Therefore, replacement heifer nutrition during early gestation can alter the development of organs that are relevant for future offspring performance. These data imply that compensatory mechanisms are in place in the developing conceptus that can alter the growth rate of key metabolic organs possibly in an attempt to increase or decrease energy utilization. [ABSTRACT FROM AUTHOR]

As the hemp industry continues to develop in the United States, there is an increasing interest in feeding byproducts of industrial hemp production to livestock. A completely randomized design experiment using crossbred finishing heifers (initial body weight [ BW ] ± SE = 494 ± 10 kg) was conducted to determine the effects of feeding hempseed cake in a corn-based finishing diet (10% forage) formulated to meet or exceed ruminally degradable and metabolizable protein requirements on growth performance, carcass characteristics, feeding behavior, and plasma parameters. Dietary treatments were the inclusion of 20% (dry matter [ DM ] basis) of dried corn distillers grains plus solubles (DDGS , n  = 16) or hempseed cake (HEMP , n  = 15). Cattle were housed in two pens, had ad libitum access to feed and water, and individual intakes and feeding behavior were monitored using the Insentec feeding system. Cattle were fed treatment diets for 111 d, and every 14 d BW were measured and blood samples were collected. Blood plasma was analyzed for glucose, urea nitrogen, and individual amino acids, and results were analyzed using repeated-measures analysis in SAS. Final BW, average daily gain, gain:feed, and hot carcass weight decreased (P  ≤ 0.05) by 2.3%, 7.7%, 7.7%, and 2.6%, respectively, in heifers fed the HEMP diet than in heifers fed the DDGS diet. Net energy for maintenance and gain (Mcal/kg of feed, DM basis), estimated based on heifer intake and performance, were greater (P  = 0.02) for the DDGS diet than for the HEMP diet. All other performance and carcass characteristics were not different (P  ≥ 0.20) between treatments. Heifers fed the HEMP diet had greater (P  < 0.05) plasma urea nitrogen concentration in samples from each collection day compared with heifers fed the DDGS diet, although there was a treatment-by-day interaction (P  < 0.01) because of variability in the magnitude of treatment differences over time. Plasma glucose concentration was not influenced (P  = 0.17) by dietary treatment. Plasma concentrations of total amino acids, nonessential amino acids, and essential amino acids were not different between treatments (P  ≥ 0.09), although there were several interactions between treatment and day (P  ≤ 0.04) for individual amino acids. These data suggest that hempseed cake has a lower net energy for maintenance and gain relative to DDGS when adequate metabolizable protein is supplied, while still providing adequate nutrition to support the acceptable performance of finishing cattle. [ABSTRACT FROM AUTHOR]

Interest is growing in methods to apply precision nutritional supplements strategically during the peri-conceptual period to enhance progeny performance of beef females. Studies where supplemental methionine (MET) was provided to bovine females in the peri-conceptual period demonstrated epigenetic modifications in muscle of the progeny. Guanidinoacetic acid (GAA) has been fed directly to livestock to increase creatine synthesis, but has not been evaluated for use in fetal programming. We fed MET and GAA to crossbred heifers during the peri-conceptual period as a 2 x 2 factorial design to influence carcass characteristics of their steer calves. It was, therefore, important to determine if the interactions of dietary MET and GAA in the peri-conceptual period would alter reproductive efficiency. The null hypothesis was that these supplements would not alter reproductive efficiency of beef heifers when fed in the peri-conceptual period. Heifers were divided into four breeding groups for management purposes. On day -63, heifers (n = 20/diet, age = 384.1 ± 1.1 d) were assigned HeatTime collars and individually fed MET (10 g/d), GAA (40 g/d), the combination (MET + GAA), or ground corn carrier (CON) for 126 days. On day -9, heifers received 100 mg of gonadotropin releasing hormone and a CIDR. On day -2, the CIDR was removed and luteolysis was initiated with 25 mg of prostaglandin F2a. All heifers were inseminated with male sexed semen from a single sire and administered a second 100 mg injection of gonadotropin releasing hormone on day 0. On day 63, a blood sample was collected from all pregnant heifers (CON n = 10; MET n = 8; GAA n = 7; MET + GAA n =10) to evaluate circulating progesterone concentrations. Reproductive tracts were collected to determine CL weight, gravid uterine weight, and placentome number. Data were analyzed using the MIXED procedure of SAS with group, MET, GAA, and the interaction of MET and GAA as fixed effects. Days to first estrus were greater and number of estrus events prior to synchronization were fewer in CON heifers compared with supplemented heifers (P < 0.05). Luteal weight tended to be greater in heifers supplemented with MET compared with CON and GAA heifers (P = 0.09), but peak intensity of estrus, concentration of progesterone at day 63 of pregnancy, gravid uterine weight, and placentome number did not differ due to diet (P > 0.10). Supplementation with MET or GAA may improve onset of puberty but does not negatively alter reproductive performance in crossbred beef heifers. These supplements can be used for fetal programming of muscle development in steer progeny without negatively impacting reproductive performance in the breeding herd. USDA is an equal opportunity provider and employer. Funded in part by USDA-NIFA-AFRI # 2022-67015-36196. [ABSTRACT FROM AUTHOR]

Two experiments were conducted to evaluate the impacts of feeding a vitamin/mineral supplement to beef heifers throughout gestation on concentrations of immunoglobulin (Ig) in colostrum and in calf serum 24 h after consumption of maternal colostrum (Exp. 1) or a colostrum replacement product (Exp. 2). Angusbased beef heifers [n = 72, initial body weight (BW) = 380.4 ± 50.56 kg] were managed in an individual feeding system and randomly assigned to a basal diet targeting gain of 0.45 kg·heifer-1·d-1 (CON; n = 36) or the basal diet plus 113 g·heifer-1·d-1 of a vitamin/mineral supplement (VTM; n = 36). For Exp. 1 treatments began at the time of artificial insemination (AI) to sexed semen, and heifers becoming pregnant after first service AI (CON, n = 14; VTM, n = 17) continued treatments throughout gestation. At calving, heifer calves were allowed to nurse their dams and remained alongside their dams until weaning. For Exp 2. non-pregnant heifers were rebred 60 d after initial dietary treatments began and continued treatments throughout gestation, with resultant heifer calves (CON, n = 7; VTM, n = 7) being removed from their dams at birth and receiving 1.5 L of colostrum replacer containing 150 g globulin protein via an esophageal feeder, followed every 12 h by 1.9 L of milk replacer. In both experiments samples of colostrum were collected after completely milking the rear-right quarter of the udder. Blood samples were collected from calves before (within 2 h of birth) and 24 h after colostrum consumption. Concentrations of IgG, IgM, and IgA were quantified in colostrum and serum via bovine radial immunodiffusion plates. Data for both experiments were analyzed for the effect of treatment using the MIXED procedure in SAS, with additional analysis of data from Exp. 1 using the CORR procedure to determine correlations among dam colostrum and calf serum Ig concentrations at 24 h. In both experiments, maternal treatment did not affect (P = 0.21) concentrations of IgG, IgM, or IgA in colostrum at calving or in calf serum at 24 h. All calves from both experiments had undetectable concentrations of these respective immunoglobulins at birth. Concentrations of IgG at 24 h in calves that received maternal colostrum were 2,595.8 ± 535.38 mg/dL (Exp. 1), whereas those that received colostrum replacer were 1,610.6 ± 335.09 mg/dL (Exp. 2). Concentrations of IgG, IgM, and IgA were positively correlated (r = 0.34; P = 0.05) with concentrations of calf serum IgG, IgM, and IgA at 24 h after suckling. Our results suggest that maternal vitamin/mineral supplementation throughout gestation did not impact Ig concentrations in colostrum or the resultant serum Ig concentrations in calves either 24 h after suckling or after delivery of a commercial colostrum replacer. [ABSTRACT FROM AUTHOR]

Vitamin B12 and folate are involved in the metabolic process known as one-carbon metabolism, which among other things, has a role in DNA, RNA, and protein methylation. This methylation connects one-carbon metabolism to epigenetics, which influences fetal development. Thus, an adequate supply of one-carbon metabolites (OCM) is important during fetal development. We hypothesized that differing planes of nutrition, along with supplementation of OCM, would impact concentrations of B12, folate, and folate intermediates in maternal liver, maternal serum, fetal liver, allantoic fluid (ALF), and amniotic fluid (AMF). Specifically, OCM supplementation would increase circulating and hepatic B12 and folate concentrations compared with non-supplemented heifers. Heifers (n = 72) were individually fed on one of two planes of nutrition: control (CON; 0.45 kg/d gain) or restricted (RES; -0.23 kg/d gain). To complete the 2 × 2 factorial arrangement, heifers were also given either OCM supplementation (10 g/d rumen-protected methionine + 60 g/d rumen-protected choline in the diet plus 20 mg B12 + 320 mg folic acid; weekly intramuscular injections) or no supplementation (grain carrier + saline injection). Thus, the final treatments were CONOCM, CON+OCM, RES-OCM, and RES+OCM. Heifers were bred to a single sire via artificial insemination with sexed semen. Heifers pregnant with female calves (n = 31) were selected for slaughter on d 63. Samples of maternal liver, ALF, AMF, and fetal liver were collected at slaughter. Maternal serum was collected at breeding (d 0) and at slaughter. For B12 and folate concentration analysis, maternal serum was sent to IDEXX BioAnalytics (N. Grafton, MA). For analysis of folate intermediate concentrations in maternal and fetal liver, ALF, and AMF, samples were analyzed using LC-MS/MS. There were treatment × day interactions (P ≤ 0.05) for B12 and folate in maternal serum; on d 63, R+OCM was greater compared with C-OCM and R-OCM and all treatments at d 0 (Table 1). For folate intermediate concentrations, no plane of nutrition × supplement interactions (P = 0.06) were found in fetal liver, ALF, or AMF; however, 5-methyl THF in ALF tended (P = 0.06) to be greater in R+OCM compared with all other treatments (Table 2). No interactions were found for concentrations in maternal liver when corrected for total liver weight; however, there was a supplement effect (P ≤ 0.05) where the concentrations of folic acid, dihydrofolate, tetrahydrofolate, 5-methyltetrahydrofolate, 5,10-methylenetetrahydrofolate and 5,10-methenyltetrahydrofolate were increased in +OCM compared with -OCM, and a plane of nutrition effect (P ≤ 0.05) with increased 5,10-methenyltetrahydrofolate and 5,10-methylenetetrahydrofolate concentrations in RES. We conclude that supplementing OCM increases concentrations of B12, folate and its intermediates in maternal liver and serum. USDA is an equal opportunity provider and employer. [ABSTRACT FROM AUTHOR]

Due to the unique nature of the rumen, unlike monogastric animals, ruminants like cattle largely depend on microbial hydrolysis of feed rather than postruminal enzymatic degradation. However, in ruminants fed high-grain diets, significant amounts of starch can bypass ruminal fermentation, where pancreatic and small intestinal enzymes play a vital role in digestion. Ruminal microbiota, as well as the host animal, require protein as a nitrogen source to optimize digestibility. Hempseed cake (containing >30% of crude protein) is a by-product of hempseed oil production, but currently is not used as a feed source as it is not an FDAapproved feed ingredient. Presently, the availability and costs of protein supplements are volatile, and sourcing alternative protein sources is needed. Therefore, information is necessary on the effect of feeding hempseed cake on ruminant digestive function. This study aimed to evaluate the effects of feeding hempseed cake on pancreatic and intestinal enzymatic activity in finishing heifers. Angus-crossbred finishing heifers (494 ± 10 kg BW) were fed for 111 days with one of two dietary treatments: 20% [dry matter (DM) basis] of dried corn distillers grains plus solubles (n = 16, control) or hempseed cake (n = 16, hemp). All animals were slaughtered at the end of treatment. Intestinal tissues for digestive enzyme assays were isolated and stored at -800C following immediate flash freezing with liquid nitrogen. The MIXED procedure in SAS was used to analyze the data. There was a tendency (P = 0.09) of greater pancreatic tissue mass in the hemp group than in the control group. The activity of pancreatic α-amylase, trypsin, and lipase relative to protein (U/g protein) was less (P < 0.01) in heifers fed hemp than in heifers fed distillers grains primarily because protein concentration (mg/g) and content (g/pancreas) were greater (P < 0.01) in the hemp group than the control group. However, there were no differences (P ≥ 0.2) in digestive enzyme activity (U/g of tissue) in pancreatic and small intestinal tissues. Overall, our results suggest that there was no adverse effect of feeding hemp on the enzymes responsible for nutrient digestion in the small intestine and that hempseed cake may be useful as an alternative source of protein in cattle fed finishing diets. [ABSTRACT FROM AUTHOR]

We hypothesized that maternal nutrition during the first 50 d of gestation would influence the abundance of hexose transporters, SLC2A1, SLC2A3, and SLC2A5, and cationic amino acid transporters, SLC7A1 and SLC7A2, in heifer uteroplacental tissues. Angus-cross heifers (n = 43) were estrus synchronized, bred via artificial insemination, and assigned at breeding to 1 of 2 dietary intake groups (CON = 100% of requirements to achieve 0.45 kg/d of BW gain or RES = 60% of CON intake) and ovariohysterectomized on day 16, 34, or 50 of gestation (n = 6 to 9/d) in a completely randomized design with a 2 × 3 factorial arrangement of treatments. Uterine cross-sections were collected from the horn ipsilateral to the corpus luteum, fixed in 10% neutral buffered formalin, sectioned at 5 µm, and stained via immunofluorescence for transporters. For each image, areas of fetal membrane (FM ; chorioallantois), luminal epithelium (ENDO), superficial glands (SG), deep glands (DG), and myometrium (MYO) were analyzed separately for relative intensity of fluorescence as an indicator of transporter abundance. Analysis of FM was only conducted for days 34 and 50. No transporters in target areas were influenced by a day × treatment interaction (P ≥ 0.06). In ENDO, all transporters were differentially abundant from days 16 to 50 of gestation (P ≤ 0.04), and SLC7A2 was greater (P = 0.05) for RES vs. CON. In SG, SLC7A1 and SLC7A2 were greater (P ≤ 0.04) at day 34 vs. day 16. In DG, SLC2A3 and SLC7A1 were greater (P ≤ 0.05) for CON vs. RES heifers; furthermore, SLC7A1 was greater (P < 0.01) at day 50 vs. days 16 and 34 of gestation. In MYO, SLC7A1 was greater (P < 0.01) for CON vs. RES and was greater (P = 0.02) at days 34 and 50 vs. day 16. There were no differences in FM (P ≥ 0.06). Analysis of all uterine tissues at day 16 determined that SLC2A1, SLC2A3, and SLC7A2 were all differentially abundant across uterine tissue type (P < 0.01), and SLC7A1 was greater (P = 0.02) for CON vs. RES. Analysis of all uteroplacental tissues at days 34 and 50 demonstrated that all transporters differed (P < 0.01) across uteroplacental tissues, and SLC7A1 was greater (P < 0.01) for CON vs. RES. These data are interpreted to imply that transporters are differentially affected by day of gestation, and that hexose and cationic amino acid transporters are differentially abundant across utero-placental tissue types, and that SLC7A1 is responsive to maternal nutritional treatment. [ABSTRACT FROM AUTHOR]

We hypothesized that maternal nutrition and day of gestation would influence the abundance of the neutral amino acid transporters SLC1A1, SLC1A5, SLC7A5, SLC38A2, and SLC38A7 in heifer utero-placental tissues. Angus-cross heifers (n = 43) were estrus synchronized and bred via AI. At breeding, heifers were assigned to one of two dietary intake groups (CON = 100% of requirements to achieve 0.45 kg/d gain or restricted heifers (RES) = 60% of CON intake) and ovariohysterectomized on day 16, 34, or 50 of gestation (n = 6 to 9/d). Thus, the experimental design was a completely randomized design with a 2 × 3 factorial arrangement of treatments. Uterine cross sections were taken from the horn ipsilateral to the CL, fixed in 10% NBF, sectioned at 5 µm, and stained for transporters. For each image, the areas of fetal membrane (FM; chorioallantois), endometrium (ENDO), superficial glands (SG), deep glands (DG), and myometrium (MYO) were analyzed separately for relative intensity of fluorescence as an indicator of transporter abundance. Analysis of FM was only conducted on days 34 and 50. In ENDO, SLC7A5 was greater (P < 0.01) in CON compared with RES heifers. In SG, SLC1A1 was greater (P = 0.02) in day 16 RES compared with day 16 CON and days 34 and 50 RES. In DG, SLC1A1 was greater (P = 0.02) on day 16 compared with 50 of gestation. In MYO, SLC1A1 was greater (P = 0.02) in day 50 CON compared with day 16 CON and day 50 RES. Additionally, in MYO SLC38A2 was greater (P = 0.02) in day 16 RES compared with day 16 CON and day 34 RES. In FM, SLC7A5 tended (P = 0.08) to be greater in CON vs RES. Analysis of all uterine tissues on day 16 determined that expression of SLC1A1, SLC1A5, SL38A2, and SL38A7 differed across uterine tissue type (P < 0.01); however, only SLC7A5 tended (P = 0.10) to differ and be greater in CON compared with RES heifers. Analysis of all utero-placental tissues on days 34 and 50 determined that SLC1A1, SLC7A5, SLC38A2, and SLC38A7 were greater (P ≤ 0.03) in CON compared with RES heifers. Furthermore, abundance of all transporters investigated on days 34 and 50 differed across utero-placental tissue types (P < 0.01). These data support our hypothesis that maternal nutrition and day of gestation influence the abundance of neutral amino acid transporters in utero-placental tissues from days 16 to 50 of gestation. Additionally, these data combined with previously published works help further elucidate nutrient supply and demands of the maternal and fetal system during early gestation in beef heifers. [ABSTRACT FROM AUTHOR]

The article presents a study on one-carbon metabolite supplementation improves growth of bovine embryonic fibroblasts cultured in divergent glucose media. Topics discussed include the one-carbon metabolism (OCM), that is the network of biochemical pathways that regulates amino acid metabolism, nucleotide synthesis, and epigenetic processes; moderate global nutrient restriction of heifers; and OCM supplementation to bovine embryonic cells.

We examined the hypothesis that maternal nutrition and day of gestation would affect the concentrations of AAs and hexoses in bovine utero-placental fluids and maternal serum from days 16 to 50 of gestation. Forty-nine cross-bred Angus heifers were bred via artificial insemination and fed a control diet (CON = 100% of requirements for growth) or a restricted diet (RES = 60% of CON) and ovariohysterectomized on days 16, 34, or 50 of gestation; nonpregnant controls were not bred and ovariohysterectomized on day 16 of the synchronized estrous cycle. The resulting design was a completely randomized design with a 2 × 3 factorial + 1 arrangement of treatments. Maternal serum, histotroph, allantoic fluid, and amniotic fluid were collected at time of ovariohysterectomy. Samples were then analyzed for concentrations of AAs and intermediary metabolites: alanine (Ala), arginine, asparagine (Asn), aspartate (Asp), citrulline, cysteine, glutamine, glutamate (Glu), glycine (Gly), histidine, isoleucine, leucine (Leu), lysine, methionine (Met), ornithine, phenylalanine (Phe), proline (Pro), serine (Ser), threonine (Thr), tryptophan, tyrosine (Tyr), and valine (Val). The concentrations of Gly, Ser, and Thr in maternal serum were greater (P ≤ 0.05) in CON compared with RES. Furthermore, day of gestation affected (P ≤ 0.05) concentrations of Asn, Glu, Phe, Thr, and Tyr in maternal serum. Status of maternal nutrition affected the Asp concentration of histotroph where RES was greater (P = 0.02) than CON. In histotroph, Ala, Leu, Met, and Val concentrations were greater (P ≤ 0.05) on day 50 compared with day 16. Additionally, Glu and Pro concentrations in histotroph were greater (P < 0.01) on days 34 and 50 compared with day 16. A day × treatment interaction was observed for the concentration of Val in allantoic fluid where day 34 CON was greater (P = 0.05) than all other days and nutritional treatments. In addition, the concentration of Gln in amniotic fluid experienced a day × treatment interaction where day 34 RES was greater (P ≤ 0.05) than day 34 CON, which was greater (P ≤ 0.05) than day 50 CON and RES. These data support our hypothesis that day of gestation and maternal nutrition affect the concentrations of various neutral and acidic AA in beef heifer utero-placental fluids and maternal serum from days 16 to 50 of gestation. [ABSTRACT FROM AUTHOR]

Maternal nutrition is critical during pregnancy as the fetus relies on the nutrients from the dam. Fetal organogenesis starts during the first trimester. Thus, an appropriate supply of nutrients, including vitamins and minerals, is indispensable. In the field of fetal developmental programming, there is still a lack of knowledge based on appropriate livestock models to explain the role of regulatory factors in translating the effect of maternal minerals and vitamins on fetal development and metabolic function. Therefore, this study was designed to investigate the effect of maternal vitamin and mineral supplementation (VTM -d 71 periconceptual to d 83 of pregnancy) on fetal liver expression of long non-coding RNAs (lncRNAs) and their potential regulatory metabolic pathways. Angus crossbreed beef heifers (n = 16) were supplemented (VTM, n = 8) or not (NoVTM, n = 8) with 113 g· heifer-1· day-1 of mineral premix (Purina Wind & Rain Storm All-Season 7.5 Complete) and all heifers were bred with female sexed semen from a single sire. Transcriptomic profiles were determined with RNA-Seq in fetal livers collected on d 83 ± 0.27 of gestation. After data quality control and read mapping, lncRNAs were predicted using the FEELnc pipeline. Using the DESeq2 software, we identified 50 differentially expressed novel lncRNAs (expression of 32 lncRNAs was upregulated and 18 were downregulated; FDR < 0.05) located either downstream, upstream, or in exonic, or intronic regions of 51 genes (including PFKP, SLC30A10, KCNH8, ZNF451, MINPP1, BCL9, PAH, ITPR2, AHCY, and ABCG8), potentially regulating their expression. These genes could affect pathways (FDR < 0.1) such as PI3K signaling, mineral storage and transport, and amino acids biosynthetic pathways (i.e., cysteine and methionine biosynthesis). Collectively, these results suggest that periconceptual maternal vitamin and mineral supplementation affects the expression of lncRNAs and potentially regulates the expression of genes involved in fetal liver development and function. [ABSTRACT FROM AUTHOR]

The objective was to determine if changes in DMI, time spent eating (TIME), and number of meals per day (MEALS) within interactions of frame score group (FSG) or primary ancestral breed type (PAB) with day relative to estrus (DRE) exist. We hypothesized that different FSG or PAB responses would vary between d -3 to d +3 surrounding estrus (d 0). Over four years, 295 crossbred heifers (347.03 ± 47.39 kg) were monitored. Using calculated frame score, heifers were classified as FSG small (< 4.00), moderately small (4.00 to 5.50), moderately large (5.50 to 6.50), and large (> 6.50). Admixture analysis classified heifers into five PAB (greatest proportion; Angus and Red Angus, American Aberdeen, Shorthorn, Simmental, and crossbred). Estrus was detected using visual checks [patches or chin ball markers, bull present (BP), year 1, n = 87] or heat detection devices (BP or absent, year 2 to 4, n = 208). The last 45 d of the feeding trial had BP. Conception date was estimated using ultrasound fetal size captured at pregnancy checks. Heifers were fed a forage-based diet using the Insentec feeding system. Software errors were removed; then estrus and feeding data were paired based on calendar date. A 7-d range was kept for each heifer using estrus categories (EC) of: 1) last without a BP (n = 195), 2) first with a BP (n = 285), and 3) at estimated conception date (n = 247). The statistical model included fixed effects of year, PAB, FSG, DRE, interactions of FSG x DRE (n = 28) and PAB x DRE (n = 42), and fixed covariate of calendar date. Repeated measures were modeled with unstructured covariance structure and heifer as experimental unit. Square root transformation for TIME and MEALS was used due to normality concerns. Across EC, no interactions for DMI were found (P = 0.5529). For TIME, differences existed within FSG x DRE (P = 0.0375; EC-3) suggesting large heifers responded differently than others. All EC showed DMI (P = 0.0083) and TIME (P = 0.0373) declined on d 0, with less reduction observed when BP (DMI, TIME: 1) -17.09%, -21.56%; 2) -9.01%, -15.02%; 3) -9.21%, -13.45%). A recovery surge occurred on d +1 (> 15%). For MEALS, PAB x DRE (P = 0.0495; EC-1,2) and FSG x DRE (P = 0.0494; EC-2,3) were different. A similar trend as DMI and TIME in response to estrus was observed in small heifers but no other FSG. Size did influence MEALS (P = 0.0024), where smaller heifers ate more MEALS than larger heifers. Results indicate differences in TIME and MEALS likely exist between small and large heifers in response to estrus, but all respond similarly in DMI. [ABSTRACT FROM AUTHOR]

Emerging evidence suggests that urogenital microbiome-targeted approaches may provide a novel opportunity to reduce the incidence of reproductive failures in cattle. The objectives of this study were to: 1) characterize the vaginal and uterine microbiota between beef cattle that became pregnant via artificial insemination (AI) and those that did not; 2) identify differentially abundant taxa between pregnant and non-pregnant cattle; and 3) characterize the culturable fraction of the vaginal and uterine microbiota using extensive culturing. Vaginal and uterine swab samples were collected from two cohorts of Angus-crossbred cattle: mature cows (n =100) and heifers (n = 72, vaginal swab only) at the time of AI. At 35 days post-AI, pregnancy diagnoses were made via ultrasound. A subset of vaginal and uterine swabs from cows (27 non-pregnant and 31 pregnant) and heifers (26 non-pregnant and 33 pregnant) were selected and processed for microbiota assessment using 16S rRNA gene (V3-V4) sequencing. For culturing, a subset of cryopreserved vaginal and uterine swabs (128) were plated onto three different agar types and cultured, and isolates were identified by nearfull length 16S rRNA gene sequencing. Sequencing results revealed 11 taxa that were more abundant in the vaginas of heifers that failed to become pregnant via AI than heifers that did become pregnant. While there was no significant difference in vaginal microbiota community structure (P = 0.21) between pregnant and non-pregnant cows, non-pregnant cows tended to have greater microbial richness and Shannon diversity (P ≤ 0.08) compared with pregnant cows. No differentially abundant taxa were detected in the vaginas of pregnant versus non-pregnant cows. Pregnant cows had a distinct uterine microbiota community structure (R² = 0.032, P = 0.008) but similar alpha diversity (P > 0.1) compared with non-pregnant cows. Twenty-eight differentially abundant taxa were observed in the uterine microbiota between pregnant and non-pregnant groups, with 11 of them more abundant in pregnant cows. Methanobrevibacter ruminantium (archaea) and Fusobacterium necrophorum were among these 11 positive pregnancy-associated taxa. Although community structure was significantly different between the vagina and uterus, 277 "core taxa" (present in = 80% of all samples) were shared between the two communities. A total of 733 bacterial isolates were recovered from vaginal (512) and uterine (221) swabs under aerobic (n = 363, 83 different species) and anaerobic (n = 370, 69 species) culturing. Potential pathogenic isolates within the Trueperella, Mannheimia and Histophilus genera were most exclusively identified from vaginal swabs. Only two Lactobacillus isolates were recovered. Overall, our results indicate that pregnancy-associated taxonomic signatures are present in the bovine uterine and vaginal microbiota. Among 39 pregnancy statusassociated taxa, 41% were unclassified at the genus level, suggesting that shotgun metagenomics and culturomics are needed to identify and characterize the pregnancy-associated taxa in cattle. [ABSTRACT FROM AUTHOR]

Two experiments were conducted to evaluate the effects of a high concentrate, s.c. PGF2α compared with a conventionally concentrated, i.m. PGF2α in estrus synchronization protocols for heifers. In Exp. 1, 869 Angus-based beef heifers were enrolled at 8 locations. All heifers were exposed to the 7-d CO-Synch + controlled internal drug release (CIDR) estrus synchronization protocol. On day 7 of the protocol heifers received 100 pg of GnRH i.m., and a CIDR insert for 7 d. On day 0, at CIDR removal, estrous detection patches were applied to heifers and, within location, heifers randomly received 1 of 2 PGF2α treatments: 5 mL of Lutalyse i.m. (CONTROL; n = 434) or a 2 mL of Lutalyse HighCon s.c. (HiCON; n = 435). A second GnRH injection was administered at 54 ± 2 h and heifers were fixed-time AI (TAI). Heifers were evaluated for estrous activity at TAI by determining the activation of estrous detection patches. Pregnancy rates to AI (PR/AI) were diagnosed by transrectal ultrasonography between 35 and 55 d after TAI. The percentage of heifers exhibiting estrus between day 0 and TAI did not differ (P = 0.68) between CONTROL and HiCON treatments (47 vs. 46 ± 4%, respectively). Additionally, PR/AI were similar (P = 0.65) between CONTROL and HiCON treatments (46 vs. 45 ± 3%). In Exp. 2, 190 Angus-based beef heifers were enrolled at 2 locations. Heifers were exposed to the melengestrol acetate (MGA)--PGF2α protocol where they were offered 0.5 mg MGA per day from days 1 to 14. On day 33, heifers were randomly assigned to receive CONTROL (n = 95) or HiCON (n = 95) treatment, and estrous detection aids were applied. Heifers were exposed to AI 12 h after detection of estrus. Heifers not detected in estrus at location 1 received a second PGF2α injection 6 d after the initial PGF2α injection and were placed with fertile bulls. Heifers at location 2 that did not express estrus were administered 100 pg of GnRH i.m. and exposed to TAI 96 h after the initial PGF2α injection. Transrectal ultrasonography was used to diagnose PR/AI between 51 and 57 d after the initial PGF2α injection. The percentage of heifers exhibiting estrus during the estrus detection period was similar (P = 0.40) between CONTROL and HiCON treatments (82 vs. 87 ± 4%). Furthermore, PR/AI were similar (P = 0.62) between CONTROL and HiCON treatments (60 vs. 65 ± 5%). In summary, the 2 concentrations and corresponding routes of administration of PGF were similar in 2α efficacy at synchronizing estrus in beef heifers. [ABSTRACT FROM AUTHOR]

To determine the effects of administration of 25 mg of PGF2α7 d prior to the initiation of the 7-d CO-Synch + controlled internal drug release (CIDR) fixed-time AI (TAI) protocol, 985 Bos taurus beef heifers were enrolled in a completely randomized design at 9 locations from April to July of 2016. Within location, all heifers were randomly assigned to 1 of 2 treatments: 1) CONTROL (n = 496); 100 pg injection of GnRH and a CIDR insert for 7 d [day 7], administration of 25 mg of PGF2α at CIDR removal [day 0], followed by a second injection of GnRH and TAI 54 ± 2 h later; or 2) PRESYNCH (n = 489); same as CONTROL but heifers received an additional injection of 25 mg of PGF2α 7 d prior [day 14] to CIDR insertion. Estrous detection patches were applied to all heifers on day 14 and were evaluated for estrual activity on day 7. Similarly, estrus alert patches were placed on all heifers on day 0 and evaluated for estrual activity at the time of TAI. Pregnancy was diagnosed via transrectal ultra-sonography between 35 and 55 d after TAI. The percentage of heifers exhibiting estrus between days 14 and 7 was greater (P < 0.001) for the PRESYNCH (70.1 ± 2.4%) than the CONTROL (41.1 ± 2.3%) treatment, whereas the percentage of heifers exhibiting estrus between day 0 and TAI was greater (P < 0.001) for the CONTROL (55.6 ± 2.4%) than the PRESYNCH (39.7 ± 2.5%) treatment. Estrus response rates differed (P < 0.001) among locations. Pregnancy rates to TAI differed (P = 0.023) among locations; however, they did not differ (P = 0.739) between CONTROL and PRESYNCH treatments (45.4 ± 2.5 vs. 43.2 ± 2.5%, respectively). Final breeding season pregnancy rates did not differ (P = 0.811) between treatments. Therefore, an injection of PGF2α 7 d prior to initiation of the 7-d CO-Synch +" CIDR protocol failed to improve pregnancy rates to TAI in replacement beef heifers. [ABSTRACT FROM AUTHOR]

We hypothesize that syncytin-Rum1, bovine endogenous retrovirus-K1 (BERV-K1), pregnancy-specific protein-B (PSP-B), and interferon-τ (IFN-τ) will be influenced by maternal nutrient restriction and be differentially expressed during key stages (day 16, 34, and 50) of the establishment of gestation when fed to meet industry standards. Commercial crossbred heifers (n = 49) were maintained on a total mixed ration and supplemented with dried distillers grains with solubles. All heifers were subjected to 5-d CO-Synch + CIDR estrus synchronization protocol. Non-pregnant, non-bred control (NP-NB) heifers (n = 6) were ovariohysterectomized on day 16, and the remaining heifers were AI to a single Angus sire (day of breeding = day 0). On the day of breeding, heifers were randomly assigned to dietary treatments. One half were assigned to control treatment (CON) targeted to gain 0.45 kg/d, and the remaining half were assigned to restricted treatment (RES), which received 60% of control diets. Heifers were subjected to ovariohysterectomy on day 16, 34, or 50 of gestation. Utero-placental tissues were obtained from the uterine horn ipsilateral (P) and contralateral (NP) to the corpus luteum and separated into maternal caruncle (CAR), maternal endometrium, inter-caruncle, (ICAR), and fetal membrane (FM). There were no interactions between stage of gestation and nutritional treatment for syncytin-Rum1 or PSP-B (P > 0.22). Expression of BERV-K1 was influenced by a treatment x stage of gestation interaction (P = 0.03) in NP-CAR. On day 50, heifers fed the CON diet had greater BERV-K1 expression compared with CON heifers on day 16 and 34 and RES heifers at all sampling time points. There was a treatment x stage of gestation interaction (P < 0.01) for IFN-τ in FM tissue. On 16 d, mRNA expression of IFN-τ was greater (P < 0.01) compared with day 34 and 50 for both CON and RES heifers, but RES FM had greater (P < 0.01) IFN-τ expression compared with CON FM. In P-CAR, PSP-B expression increased (P < 0.01) by 18 000-fold on day 50 compared with NP-NB heifers. In P-ICAR, expression of syncytin-Rum1 in P-ICAR was greater (P = 0.01) on day 16 with a 14.14-fold increase compared with relative expression on day 34 and 50; whereas, PSP-B was increased (P < 0.01) on day 34 and 50 compared with day 16. In conclusion, 40% nutrient restriction had limited influence on mRNA of ERVs, PSP-B, and IFN-τ but stage of gestation differences reinforced the importance of these genes during the establishment of pregnancy. [ABSTRACT FROM AUTHOR]

The objective of these studies was to evaluate if vascularity of the fetal part of the placenta, termed cotyledon (COT), of crossbreed Angus heifers is affected by vitamin and mineral (VTM) and/or energy (NRG) supplementation during pregnancy. We hypothesized that dietary supplementation with VTM and/or NRG would improve fetoplacental vascular development, which is an important index of placental function. Two experiments were conducted: In Exp. 1, 34 heifers were randomly assigned to VTM/NoVTM supplementation 71 days before artificial insemination (AI). At breeding, the diet was maintained and heifers were randomly assigned to receive NRG, resulting in the following treatments combinations: NoVTM-NoNRG (n=8), NoVTM-NRG (n=8), VTMNoNRG (n=9), and VTM-NRG (n=9). Dietary supplementation was maintained until d 83 when heifers were ovariohysterectomized and COT was collected. On Exp. 2, 72 heifers were randomly assigned to VTM supplementation (n=36) or control (CON) (n=36) treatments at breeding and continuing until parturition when COT from a subset of 28 heifers was collected. The COT from both experiments was evaluated by immunohistochemistry using rabbit anti-CD34 and anti-CD31 antibodies as markers for vascularity along with DAPI for background nuclear staining. In the d 83 group, BS1 lectin was used as a marker of fetal placental tissue. Three images per animal were captured and the percentage/number of blood vessels within the tissue area was analyzed. The data were analyzed using the GLM procedure of SAS. Results indicated that on d 83 COT vascularity was not affected by VTM (P-value = 0.5030), NRG (P-value = 0.5450), or their interaction (P-value = 0.6664), whereas on parturition there was a tendency for COT vascularity to be greater in VTM than CON (P- value=0.0723). These results suggest that dietary VTM supplementation from breeding until parturition potentially has a beneficial effect on placental vascular development in crossbred Angus heifers [ABSTRACT FROM AUTHOR]

Objectives were to evaluate the effects of feeding a vitamin and mineral (VTM) supplement to beef heifers during gestation on calf performance, body measurements, trace mineral status, and organ weights at 30 h after birth. We hypothesized that VTM supplementation during gestation would improve mineral status in the neonatal calf but not impact calf performance parameters and body and organ weights at 30 hours after birth. Fourteen Angus-based heifers [initial body weight (BW)] = 273.7 ± 1.10 kg) were randomly assigned to receive either a basal diet (CON; n = 7) or a basal diet plus a VTM supplement (VTM; n = 7; 113 g•heifer-1•d-1, targeting gain of 0.45 kg/day) from 60 d pre-breeding through gestation. Immediately after parturition, blood samples were collected from dams and calves, then calves were separated from their dams. Calves were fed one feeding of colostrum replacer, followed by milk replacer every 12 h, then euthanized at 30 h. Body weight and measurements were recorded, then organs and viscera were removed, weighed, and sampled. Dam serum and neonatal serum, liver, and blood were analyzed for concentrations of minerals. Data were analyzed using the GLM Procedure of SAS with individual animal as the experimental unit. Dietary treatments did not impact calf weight (0 h or 30 h), calf body measurements, or body weight of the dam at calving (P ≥ 0.32). Further, neonatal organ weights were not influenced (P ≥ 0.21) by maternal VTM treatment. Concentrations of Se and Co in calf serum and Se in calf liver were increased (P ≤ 0.02) by VTM treatment; however, concentrations of Cu, Mn, Mo, and Zn in calf muscle, liver, and serum were not impacted (P ≥ 0.07) by VTM treatment. Concentrations of Co in serum of the dam was the only mineral affected by dietary treatments, being greater (P = 0.001) in VTM than CON dams. In the current experiment providing trace mineral supplementation throughout gestation did not impact calf weight or body measurements at birth. However, the implications of altered mineral status of the neonatal calves at birth, and presumably throughout gestation, may have additional postnatal effects that warrant further investigation. [ABSTRACT FROM AUTHOR]

Vitamins and minerals are essential for proper fetal and placental development and function. However, the impact of micronutrient supplementation on placental function and gene expression remains unclear. Herein, we performed a transcriptomic analysis to determine the impact of pre-breeding maternal micronutrient supplementation on the gene expression of placental caruncles (CAR; maternal placenta). Crossbred Angus beef heifers were supplemented (VTM, n = 7) or not (CON, n = 7) with 113 g•heifer-1•d-1 of mineral premix (Purina® Wind & Rain® Storm® All-Season 7.5 Complete) from d 71 to 148 before breeding and until d 83 of gestation. After breeding, heifers were fed a diet to gain 0.79 kg/d. Uteroplacental tissues were collected at d 83. The largest placentome closest to the fetus was collected, and CAR was manually dissected from the cotyledon. Total RNA was isolated from CAR, and gene expression was measured with RNA-Seq. After data quality control and read mapping, differential expression was performed using DESeq2. We identified 46 upregulated and 19 downregulated genes in the VTM group (adj.Pval < 0.1). ShinyGO pathway analysis software was used to identify genes in the Ca and CGMP-PKG signaling pathways, including CALM2 and CAMK2G, which were down and upregulated, respectively. Calcium-mediated systems may activate steroidogenic activity in bovine placentomes, while the cGMP-PKG pathway plays a key role in vascular homeostasis mediated by nitric oxide and decreased Ca concentrations. Furthermore, biological processes underlying blood circulation were among those over-represented. Previous studies report that maternal nutrition may impact placental vascularity and uterine blood flow. ATP2B, that is upregulated in the VTM group, is a calcium/calmodulin-regulated, magnesiumdependent protein involved in intracellular Ca homeostasis. In summary, pre-breeding and early gestation maternal micronutrient supplementation leads to differential expression of genes involved in Ca homeostasis and has a putative effect on placenta vascular function. [ABSTRACT FROM AUTHOR]

As cannabinoid production continues to increase, there is increasing interest in feeding byproducts of industrial hemp production to livestock. An experiment using crossbred heifers (n = 31; initial BW= 494 kg, SE = 10) was conducted to determine the effects of feeding hempseed cake in a corn-based finishing diet (10% forage) formulated to meet or exceed ruminally degradable and metabolizable protein requirements on growth, performance, carcass characteristics, and feeding behavior. Heifers were assigned randomly to one of two treatments: 1.) diet containing 20% dried distillers grains plus solubles (CON, n = 16), or 2.) diet containing 20% hempseed cake (HEMP, n = 15) on a dry-matter basis. Cattle were housed in two pens, had ad-libitum access to feed and water, and individual intakes and feeding behavior were captured using the Insentec BV feeding system across the feeding period (111 d). Final BW was not different (P = 0.28) between CON (696 kg, SE = 12) and HEMP (683 kg, SE = 12) heifers. Dry matter intake was not different between treatments (P = 0.99), while CON cattle had improved ADG and feed efficiency (G:F; P ≤ 0.04) compared to HEMP cattle. Carcass characteristics were not different (P ≥ 0.20) between treatments for all parameters measured. Control and HEMP cattle were not different (P ≥ 0.34) for number of meals, time spent eating, number of visits to the bunk per day, meal size, or eating rate. Feeding hempseed cake reduced ADG and G:F while having no effect on other performance measures, carcass characteristics, or feeding behavior. Overall, these data suggest hempseed cake could be a viable alternative feed source for ruminants depending on availability and cost. Further understanding of hempseed cakes' nutrient utilization is critical to determining this products viability as a feedstuff for cattle. [ABSTRACT FROM AUTHOR]

Thirty-five crossbred Angus heifers (body weight = 359.5 >± 7.1 kg) were randomly assigned to a 2 × 2 factorial design to evaluate the effects of vitamin and mineral supplementation [VMSUP; supplemented (VTM) vs. unsupplemented (NoVTM)] and rate of gain [GAIN; low gain (LG), 0.28 kg/d vs. moderate gain (MG), 0.79 kg/d] during the first 83 d of gestation on trace mineral concentrations in fetal liver, muscle, and allantoic (ALF) and amniotic (AMF) fluids. The VTM treatment (113 g supplement•heifer-1•d-1) was initiated a minimum 71 d before breeding. At breeding, heifers were either maintained on the basal diet (LG) or received the MG diet by adding a protein/energy supplement to the basal diet. On d 83 of gestation, samples of fetal liver, muscle, ALF, and AMF were collected and analyzed for trace mineral concentrations. In fetal liver, Se, Cu, Mn, and Co concentrations were greater (P ≤ 0.04) for VTM than NoVTM, while Mo and Co greater (P ≤ 0.04) for LG than MG. In fetal muscle, VTM increased (P ≤ 0.02) concentrations of Se and Zn, whereas LG increased (P < 0.01) Zn. In ALF, Mo concentrations were affected (P = 0.03) by a VMSUP × GAIN interaction, with VTM-MG greater than NoVTM-MG; while VTM increased (P < 0.01) concentrations of Se and Co. Trace mineral concentrations were not affected (P ≥ 0.13) in AMF. In conclusion, VTM increased fetal liver Se, Cu, Mn, and Co concentrations; fetal muscle Se and Zn; and ALF Se and Co; while LG increased fetal liver Mo and Co concentrations and fetal muscle Zn. Our results confirm that managerial decisions associated with vitamin and mineral supplementation and rate of gain can alter fetal reserves of trace elements during early pregnancy. [ABSTRACT FROM AUTHOR]

In the present study, we evaluated whether the nasopharyngeal, ruminal, and vaginal microbiota would diverge (1) in virgin yearling beef heifers (9 months old) due to the maternal restricted gain during the first trimester of gestation; and (2) in pregnant beef heifers in response to the vitamin and mineral (VTM) supplementation during the first 6 months of pregnancy. As a secondary objective, using the microbiota data obtained from these two cohorts of beef heifers managed at the same location and sampled at the same time, we performed a holistic assessment of the microbial ecology residing within the respiratory, gastrointestinal, and reproductive tract of cattle. Our 16S rRNA gene sequencing results revealed that both α and β-diversity of the nasopharyngeal, ruminal and vaginal microbiota did not differ between virgin heifers raised from dams exposed to either a low gain (targeted average daily gain of 0.28 kg/d, n = 22) or a moderate gain treatment (0.79 kg/d, n = 23) during the first 84 days of gestation. Only in the vaginal microbiota were there relatively abundant genera that were affected by maternal rate of gain during early gestation. Whilst there was no significant difference in community structure and diversity in any of the three microbiota between pregnant heifers received no VTM (n = 15) and VTM supplemented (n = 17) diets, the VTM supplementation resulted in subtle compositional alterations in the nasopharyngeal and ruminal microbiota. Although the nasopharyngeal, ruminal, and vaginal microbiota were clearly distinct, a total of 41 OTUs, including methanogenic archaea, were identified as core taxa shared across the respiratory, gastrointestinal, and reproductive tracts of both virgin and pregnant heifers. [ABSTRACT FROM AUTHOR]

We evaluated effects of rate of gain during the first 84 d of gestation on composition of colostrum and milk. At breeding, forty-five Angus-based heifers received either a basal total mixed ration allowing 0.28 kg/d gain [low gain (LG), n = 23] or basal diet plus starchbased supplement allowing 0.79 kg/d gain [moderate gain (MG), n = 22] for 84 days. Heifers were then managed on a common diet until parturition. Colostrum samples (50 mL) were collected before first suckling. Milk samples (50 mL) were collected 6 hours after calf removal on d 62 ± 10 and 103 ± 10 postpartum. Samples were collected by stripping each teat 15 to 20 times after discarding the first 5 strips. At d 103 sampling techniques were compared by collecting a second sample after 1 mL oxytocin administration and 90 sec lag. Data were analyzed using the GLM procedure of SAS. Fat, protein, somatic cell count (SCC), milk urea nitrogen, and other solids were analyzed in colostrum for effect of treatment, whereas milk was evaluated for effects of treatment, day and their interaction. Heifer was experimental unit and significance was set at P ≤ 0.05. Colostrum SCC was greater (P = 0.05) in LG (6,949 ± 739 cells/mL) than MG (4,776 ± 796 cells/mL). In milk, protein and other solids were greater (P ≤ 0.03) in MG (3.02 ± 0.03 and 6.20 ± 0.02 %, respectively) than LG (2.87 ± 0.03 and 6.14 ± 0.02 %, respectively). On d 103, oxytocin administration and extended lag time after teat stimulation (0.96 ± 0.05 %) increased fat content in milk (P < 0.01) compared with immediate milk sample collection (0.34 ± 0.05 %). Nutrition during early gestation had a sustained impact on milk composition and techniques of oxytocin administration results in greater milk fat content. [ABSTRACT FROM AUTHOR]

The objective was to determine if genetic markers related to mitochondrial function are associated with growth and feed intake of Bos taurus heifers fed foragebased diets. Weight data collected at birth, weaning, and as yearlings were available on 373 heifers. As yearlings, feed intake was measured using an Insentec system. Primary ancestral breeds of heifers included 204 British, 66 Continental European, 68 American Aberdeen, 29 British mix, and 6 American Aberdeen mix. Traits included DMI, ADG, G:F, adjusted birth weight (BWT), adjusted 205 weaning weight (WW), and average of start and end feed trial weight (FWT) and body volume (VOL). Heifers were genotyped using Neogen GGP150HD for beef cattle. Markers (n=56) were extracted if located within or flanking AMPK, PPARGC1A, FGF2, and SIRT1 or on mitochondrial DNA using ARS-UCD1.2 coordinates. After quality checks (minor allele frequency and call rate), 44 markers remained. No mitochondrial markers passed quality checks. For each trait, each marker was fit independently as a fixed effect in a model including year and group based on frame score (n=4), ancestry (n=5), and dam age (n=4; non-adjusted traits only). Pairwise comparisons were done using Tukey-Kramer method. No markers within FGF2 or SIRT1 had significant associations. Two markers were found significant for PPARGC1A, where Hapmap24121-BTC-039009 (P=0.0344) showed the C allele increased DMI. For weight traits, significant markers surrounding AMPK and within PPARGC1A (n=5; 0.0009=P= 0.0468) identified dominance gene actions that indicate certain variants of the AMPK and PPARGC1A increased weight across time-points. For VOL, 16 of 22 markers within PPARGC1A were significant (0.0068=P=0.0467). Of the 16 markers, 14 identified a recessive variant that increased volume, but did not translate to increased weight. Further research is needed to better understand the roles that genetic markers for AMPK and PPARGC1A have on tissue level mitochondrial function and energy metabolism. [ABSTRACT FROM AUTHOR]

Objectives were to determine the influence of a vitamin and mineral supplement (VTM), an energy supplement (NRG), and day post-artificial insemination (DPAI) on concentrations of glucose and non-esterified fatty acids (NEFA) in beef heifers. Cross-bred heifers (n = 72; initial weight = 351.2 kg) were assigned to 4 treatments arranged as a 2 × 2 factorial with main factors of VTM and NRG supplement. Treatments were: 1) control (no VTM or NRG), 2) VTM (initiated 71 to 106 before breeding) only, 3) NRG (initiated at breeding) only, and 4) VTM and NRG. Heifers were synchronized then bred via artificial insemination on d 0. Blood was drawn on d -9, 14, 28, and 42 from all heifers and on d 56, 70, and 84 from pregnant heifers (n = 31). Plasma samples were analyzed for concentrations of glucose and NEFA. Data were analyzed using the MIXED procedure in SAS. There were no interactions between VTM, NRG, or DPAI (P > 0.05). In addition, pregnancy status did not influence concentrations of glucose or NEFA (P > 0.05). There were no effects (P > 0.35) of VTM on glucose or NEFA concentrations. Energy supplementation increased (P = 0.012) glucose and decreased (P = 0.013) NEFA concentrations. Glucose concentrations were greatest at d -9, decreased through d 42, and then, on d 70 and 84 increased to levels similar to d -9 (81.9, 76.1, 73.6, 73.7, 74.3, 76.2, and 78.4 ± 2.97 for d -9, 14, 28, 42, 56, 70, and 84, respectively). Concentrations of NEFA were greater (P < 0.01) at d -9 compared with 14, 28, 42, 56, and 70, and concentrations on d 84 were greater (P < 0.01) than all other days. In conclusion, glucose and NEFA were affected by NRG and DPAI, but not VTM. [ABSTRACT FROM AUTHOR]

Leptin is a 16-kDa-peptide hormone product of the leptin gene (LEP) that is predominantly synthesized by adipose tissues and has known involvement in regulation of feed intake, energy expenditure, reproduction, and immune functions. The objective was to determine the association of leptin genotype (LEP c.73C >T), leptin diplotype (LEPD) and plasma leptin hormone (LEPH) concentration with growth, feed intake, feed efficiency, and behavior characteristics in developing beef heifers. A total of 336 commercial beef heifers were genotyped for the LEP c.73C >T marker. Four single nucleotide polymorphism markers including LEP c.73C >T, ARSBFGL-NGS-59298 (intron 1), BovineHD0400026029 (upstream) and BovineHD0400026063 (downstream) of LEP were considered for haplotype analysis. Eleven LEPD were identified for this study using parsimonybased analyses. Circulating levels of LEPH were measured on 333 heifers prior to their first breeding season and used to assign low or high concentration group based on population median. Data were analyzed using the mixed procedure of SAS for repeated measures, fixed effects of ancestral breed group (n = 4), dam age category (n = 4), frame size group (n = 4), project cycle nested within birth year (n = 6), week of feed trial × year, LEP (n = 3) or LEPD (n = 11) or LEPH (n = 2), as well as week × LEPH (only for LEPH). There were no significant differences between LEP genotypes (P = 0.11) or LEPD (P = 0.33) for any of the studied traits. Heifers with low LEPH ate fewer meals per day (P = 0.02) and had more DMI per meal (P = 0.04) compared to those with high plasma leptin. Further research is needed to better understand plasma LEPH concentration and its role in feeding behavior attributes. However, circulatory LEPH before the breeding season may serve as a predictor for feeding behavior. [ABSTRACT FROM AUTHOR]

The cotyledon and caruncle tissues provide a functional bridge between the fetus and the dam. However, the relationship between these tissues and the transcriptomic profile that underlies the tissue functions remains elusive. Herein we investigate the expression profile of cotyledon and caruncle from nulliparous beef heifers carrying female fetuses at day 83 of pregnancy to identify changes occurring across tissues that contribute to placental function and their tissue-specific roles. We identified 2654 differentially expressed genes [ padj ≤ 0.05, abs(log2FC) ≥ 1], including nutrient transporters and paternally imprinted genes. We found key regulators of tissue function and differentiation, including FOXO4 , GATA2 , GATA3 , and HAND1, rewired between the tissues. Finally, we shed light on the over-represented pathways related to immune tolerance, tissue differentiation and remodeling. Our findings highlighted the intricate and coordinated cross-talk between fetal-maternal tissues. They provided evidence of a fine-tuned gene regulatory network underlying pregnancy and tissue-specific function in the bovine placenta. • Genes involved with nutrient transport and tissue differentiation and remodeling were differentially expressed between the fetal and maternal tissues. • The Wnt pathway is likely repressed in cotyledon at day 83 of pregnancy. • Downregulated differentially expressed genes are involved with immune tolerance in the fetal placental tissue. • Key transcription factors play a key role in modulating gene expression between cotyledon and caruncle. • Paternally imprinted genes were upregulated in the cotyledon tissue. [ABSTRACT FROM AUTHOR]

Abstract: We determined whether source of trace mineral supplementation prior to embryo collection affected embryo production and quality. Angus half-sibling heifers (n =20) originating from a common herd were assigned to three treatment groups using a 3×3 latin square design replicated in time (3×) and space (6× complete and 1× incomplete): (1) heifers received no added mineral to their diet (control; n =53); (2) heifers received a commercially available organic mineral supplement (organic; n =52); or (3) heifers received an all inorganic mineral supplement (inorganic; n =55). All heifers had ad libitum access to hay and were fed a supplement containing corn and soybean meal. Treatments were initiated 23 days prior to embryo recovery. Heifers were given a 45-day adaptation period of no mineral supplementation before initiating a new treatment. Ovarian structures were evaluated using transrectal ultrasonography to determine the presence and number of follicles and CL on each ovary. The mean number of recovered ova/embryos was similar among treatments (4.1±0.7, 3.8±0.7, and 3.3±0.7 for control, inorganic, and organic treatments, respectively), the number of unfertilized oocytes was greater (P <0.05) for inorganic (2.3±0.5) and control (1.6±0.5) treated heifers than organic (0.4±0.4) treated heifers. No differences among treatments existed for the number of degenerate or transferable embryos, but individual heifer influenced the total number of embryos/ova, unfertilized ova, and transferable embryos recovered. We conclude that heifer accounted for the greatest differences in embryo production and quality. Source of trace mineral supplementation did not significantly alter embryo number or quality in superovulated purebred Angus heifers fed a well-balanced diet, meeting all trace mineral requirements. [Copyright &y& Elsevier]