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Made available in DSpace on 2018-12-11T16:50:56Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-12-01 This experiment compared performance and physiological responses of the offspring from cows supplemented with Ca salts of PUFA or SFA + MUFA during late gestation. Ninety-six multiparous, nonlactating, pregnant Angus × Hereford cows were ranked by BW, BCS, and age and divided into 24 groups of 4 cows/group at the end of their second trimester of gestation (d −7). Cows conceived during the same estrus synchronization + AI protocol, with semen from a single sire; hence, gestation length was 195 d for all cows at the beginning of the experiment (d 0). Groups were randomly assigned to receive (DM basis) 405 g/cow daily of soybean meal in addition to 1) 190 g/cow daily of Ca salts of PUFA based on eicosapentaenoic, docosahexaenoic, and linoleic acids or 2) 190 g/cow daily of Ca salts of SFA + MUFA based on palmitic and oleic acids (CON). Groups were maintained in 2 pastures (6 groups of each treatment/pasture) and received daily 10.1 kg/cow (DM basis) of grass–alfalfa hay. Groups were segregated into 1 of 12 drylot pens (6 by 18 m) and individually offered treatments 3 times/wk from d 0 until calving. Cow BW and BCS were recorded, and blood samples were collected on d −7 of the experiment and also within 12 h after calving. Calf BW was also recorded within 12 h of calving. Calves were weaned on d 280 of the experiment, preconditioned for 45 d (d 280 to 325), transferred to a growing lot on d 325, and moved to a finishing lot on d 445, where they remained until slaughter. At calving, PUFA-supplemented cows had a greater (P < 0.01) proportion (as % of total plasma fatty acids) of PUFA, including linoleic, linolenic, arachidonic, docosapentaenoic, and docosahexaenoic acids. At weaning, calves from CON-supplemented cows were older (P = 0.03), although no treatment differences were detected (P = 0.82) for calf weaning BW. During both growing and finishing phases, ADG was greater (P ≤ 0.06) in calves from PUFA-supplemented cows. Upon slaughter, HCW and marbling were also greater (P ≤ 0.05) in calves from PUFA-supplemented cows. Collectively, these results indicate that supplementing eicosapentaenoic, docosahexaenoic, and linoleic acids to late-gestating beef cows stimulated programming effects on postnatal offspring growth and carcass quality. Therefore, supplementing late-gestating beef cows with Ca salts of PUFA appears to optimize offspring productivity in beef production systems. Oregon State University – Eastern Oregon Agricultural Research Center UNESP – Faculdade de Medicina Veterinária e Zootecnia University of Florida – Range Cattle Research and Education Center South Dakota State University Department of Animal Science Michigan State University Department of Animal Science São Paulo State University(UNESP) School of Veterinary Medicine and Animal Science Texas A&M University Department of Animal Science UNESP – Faculdade de Medicina Veterinária e Zootecnia São Paulo State University(UNESP) School of Veterinary Medicine and Animal Science

Made available in DSpace on 2018-12-11T16:50:31Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-11-01 One hundred eight Angus × Hereford steers, originating from 7 cow–calf were obtained from an auction yard on d −2 and transported by road (800 km; 12 h) to an experimental feedlot facility. Upon arrival on d −1, shrunk BW was recorded and steers were grouped with free-choice access to grass hay, mineral supplement, and water. On d 0, steers were ranked by source and shrunk BW and assigned to 1 of 18 pens (6 steers/pen). Pens were allocated to 1) no immunomodulatory ingredient supplementation during feedlot receiving (CON), 2) supplementation with OmniGen-AF (OMN; 22 g/steer daily, as-fed basis; Phibro Animal Health Corp., Teaneck, NJ) from d 0 to 30, or 3) 2 oral capsules of Stocker Immune Primer on d 0 + 15 g/ steer daily (as-fed basis) of Stocker Preconditioned Premix (Ramaekers Nutrition, Santa Cruz, CA) from d 7 to 30 (IPF). From d 0 to 80, steers had free-choice access to grass hay and water and received a corn-based concentrate. Feed DMI was recorded from each pen, and steers were assessed for bovine respiratory disease (BRD) signs daily. Steers were vaccinated against BRD pathogens on d 0 and 21. Final shrunk BW was recorded on d 81, and blood samples were collected on d 0, 3, 7, 10, 14, 21, 31, 42, 56, and 73. Steer ADG and final BW were greater (P ≤ 0.05) in CON steers than in OMN and IPF steers (1.23, 0.76, and 1.06 kg/d [SEM 0.06], respectively, and 320, 282, and 307 kg [SEM 4], respectively) and (P < 0.01) in IPF steers than in OMN steers. No treatment effects were detected (P ≥ 0.76) for BRD incidence (66 ± 4%) and DMI, whereas G:F was greater (P < 0.01) in OMN steers than in CON steers. Mean plasma cortisol concentration was greater (P = 0.01) in CON steers than in OMN and IPF steers. Plasma haptoglobin concentrations tended (P = 0.10) to be greater in CON steers than in IPF steers on d 3, were greater (P = 0.04) in IPF steers than in CON steers on d 7, and tended (P = 0.10) to be less in OMN steers than in IPF and CON steers on d 21. Blood mRNA expression of interleukin 8 was greater (P ≤ 0.05) in OMN and IPF steers than in CON steers on d 3 and in OMN steers than in CON and IPF steers on d 14. Blood mRNA expression of tumor necrosis-α was greater (P ≤ 0.05) in OMN and IPF steers than in CON steers on d 10. Plasma IGF-I concentrations, serum antibody titers to BRD pathogens, and blood mRNA expression of chemokine ligand 5, cyclooxygenase 2, interleukin 8 receptor, and L-selectin did not differ (P ≥ 0.21) among treatments. Collectively, the immunomodulatory feed ingredients evaluated herein impacted adrenocortical and innate immune responses but failed to mitigate BRD incidence and improve performance of receiving cattle. Oregon State University Eastern Oregon Agricultural Research Center São Paulo State University (UNESP) School of Veterinary Medicine and Animal Science Texas A&M University Department of Animal Science São Paulo State University (UNESP) School of Veterinary Medicine and Animal Science

Made available in DSpace on 2018-12-11T16:48:20Z (GMT). No. of bitstreams: 0 Previous issue date: 2017-01-01 This experiment compared DMI, ruminal forage degradability, and liquid parameters as well as physiological responses in beef cattle receiving a lipopolysaccharide (LPS) challenge or not. Eight ruminally cannulated Angus × Hereford steers (485 ± 16 kg BW) were housed in individual pens on d −7, ranked by BW, and allocated to 1 of 2 treatments administered on d 0: 1) an intravenous (i.v.) bolus dose (0.5 μg/kg of BW, diluted in 5 mL of 0.9% sterile saline) of bacterial LPS (Escherichia coli 0111:B4) or 2) a 5-mL i.v. injection of 0.9% sterile saline (CON). Steers had free-choice access to mixed alfalfa–grass hay, water, and a commercial vitamin + mineral mix during the experiment (d −7 to 6). Hay DMI was evaluated daily from d −5 to 6. Immediately prior to treatment administration (h 0), polyester bags containing 4 g of ground dietary hay (DM basis) were immersed into the rumen of each steer and incubated for 0, 4, 8, 12, 24, 36, and 48 h for DM and NDF degradability evaluation. Steers were also intraruminally pulse-dosed with 5 g of Co-EDTA immediately prior to treatment administration, and rumen fluid samples were collected at 0, 2, 4, 6, 8, 12, 16, and 24 h for ruminal liquid volume and dilution rate calculations. Blood was collected every 2 h from −2 to 8 h, every 4 h from 8 to 16 h, every 12 h from 24 to 72 h, and every 24 h from 96 to 144 h relative to treatment administration. Values obtained before treatment administration were used as a covariate within each respective analysis. Steers receiving LPS had less (P ≤ 0.03) DMI on d 0 and 1 compared with CON steers. Steers receiving LPS had reduced (P ≤ 0.05) rumen liquid volume and dilution rate as well as ruminal disappearance rate and effective degradability of DM and NDF compared with CON steers. Steers receiving LPS had greater (P ≤ 0.05) plasma tumor necrosis factor α at 2 h, greater plasma hapto-globin from 24 to 72 h, greater plasma cortisol from 12 to 16 h, greater serum NEFA from 6 to 48 h, greater plasma insulin and glucose at 2 h, reduced plasma glucose from 4 to 12 h, greater plasma cholecystokinin at 16 h, and greater plasma leptin concentrations at 8, 12, 16, 36, 48, and 60 h after treatment administration compared with CON steers. Hence, LPS administration transiently reduced DMI in steers via physiological reactions that modulate gastrointestinal motility and satiety centers in the central nervous system, in addition to potential host–microbiome endocrine interactions that impaired ruminal hay DM and NDF degradability. Oregon State University – Eastern Oregon Agricultural Research Center Programa de Pós-Graduação em Zootecnia/Faculdade de Medicina Veterinária e Zootecnia UNESP – Univ. Estadual Paulista Programa de Pós-Graduação em Zootecnia/Faculdade de Medicina Veterinária e Zootecnia UNESP – Univ. Estadual Paulista

Made available in DSpace on 2018-11-26T15:37:27Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-09-01 Made available in DSpace on 2018-12-11T16:44:00Z (GMT). No. of bitstreams: 0 Previous issue date: 2016-09-01 Item merged in doublecheck by Luana Priscila Costa (luana@reitoria.unesp.br) on 2019-02-15T18:16:28Z Item was identical to item(s): 171292, 161437 at handle(s): http://hdl.handle.net/11449/169013, http://hdl.handle.net/11449/159219 USDA-NIFA Oregon Ninety Angus × Hereford calves were ranked by sex, BW, and age and assigned to 1 of 3 vaccination schemes against the bovine respiratory disease complex: 1) vaccination at weaning (d 0) and a booster at feedlot entry (d 30; CON; n = 30), 2) vaccination 15 d before weaning (d −15) and a booster 15 d before feedlot entry (d 15; EARLY; n = 30), and 3) vaccination 15 d after weaning (d 15) and a booster 15 d after feedlot entry (d 45; DELAYED; n = 30). From d −15 to 7, calves were maintained as a single group on pasture. On d 8, calves were placed into 1 of 18 drylot pens (6 pens/treatment; 5 calves/pen) and fed alfalfa–triticale hay. On d 29, calves were transported 1,440 km in a livestock trailer and unloaded on d 30 at the same feed yard with the same pen arrangement used prior to transport. From d 30 to 75, calves were fed a receiving diet based on alfalfa–triticale hay + corn-based concentrate. Calf BW was recorded on 2 consecutive days (d −15, −14, 0, 1, 28, 29, 75, and 76). Blood samples were collected on d −15, 0, 15, 30, 45, 60, and 75. The EARLY calves had less (P ≤ 0.09) ADG before weaning (d −15 to −1); however, they had greater (P ≤ 0.01) ADG during feedlot receiving (d 30 to 75) compared with calves with the other treatments. During preconditioning (d 0 to 29), CON calves had greater (P ≤ 0.04) DMI compared with EARLY and DELAYED calves. During feedlot receiving, no treatment differences were detected (P ≥ 0.17) for hay or concentrate DMI, G:F, and morbidity and mortality rates. There were no treatment effects on calf BW at weaning and at the end of the preconditioning or receiving periods (P ≥ 0.65). Plasma concentrations of antibodies against Mannheimia haemolytica were greater (P ≤ 0.05) in EARLY calves than in CON and DELAYED calves on d 0, greater (P ≤ 0.04) for CON calves than for EARLY and DELAYED calves on d 15, greater (P ≤ 0.02) in DELAYED and EARLY calves than in CON calves on d 30, and greater (P = 0.03) in EARLY calves than in CON calves on d 75. Plasma concentrations of antibodies against bovine viral diarrhea viruses were greater (P ≤ 0.04) in EARLY calves than in CON and DELAYED calves on d 15 and greater for EARLY and CON calves than for DELAYED calves on d 30 and 45. Collectively, EARLY calves had greater plasma concentrations of antibodies against the evaluated pathogens at feedlot entry and increased ADG during receiving compared with their CON and DELAYED cohorts. Hence, anticipating initial and booster vaccinations against respiratory pathogens to provide both doses prior to feedlot entry appears to be a valid strategy to enhance cattle health and performance during feedlot receiving. Oregon State University Eastern Oregon Agricultural Research Center UNESP Faculdade de Medicina Veterinária e Zootecnia Faculdade de Medicina Veterinária e Zootecnia UNESP - Univ. Estadual Paulista UNESP Faculdade de Medicina Veterinária e Zootecnia Faculdade de Medicina Veterinária e Zootecnia UNESP - Univ. Estadual Paulista USDA-NIFA Oregon: ORE00142