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Thirty-three colostrum-deprived Holstein bull calves (initial BW of 131 ± 4 kg) were used to determine the effect of timing of anthelmintic administration relative to vaccination on antibody titer response to vaccine component antigens. When calves were at least 3 mo of age, they were sorted randomly into individual pens and assigned to 1 of 3 treatment groups, treatments consisted of 1) dewormed 2 wk before vaccination (DPV), 2) dewormed at the time of vaccination (DV), or 3) control, vaccinated but not dewormed (CONT). All calves were inoculated with infective larvae of brown stomach worms (Ostertagia ostertagi) and intestinal worms (Cooperia spp.) on d 1, 7, 10, 14, and 18 for a total dose of 235,710 infective larvae per calf. Calves (DPV and DV) were dewormed on d 21 or 35 with a 10% fenbendazole suspension at 5 mg/kg of BW. On d 35, all calves were vaccinated with a modified-live virus respiratory vaccine containing IBRV (infectious bovine rhinotracheitis virus), BVDV-1 (bovine viral diarrhea virus genotype 1), BVDV-2 (BVDV genotype 2), PI-3 (parainfluenza-3), and BRSV (bovine respiratory syncytial virus). During the 103-d experiment, weekly fecal egg counts, blood, and rectal temperatures were collected and health status was recorded daily. Blood samples were obtained weekly to determine serum neutralizing (SN) antibody titers to IBRV, BVDV-1, BVDV-2, and PI-3 and cytokine levels for IL-4, IL-6, TNF-α (tumor necrosis factor-α), and IFN-γ (interferon-gamma). There was a tendency (P < 0.09) for CONT calves to have greater IL-4 concentrations. By design, control calves had greater (P < 0.01) fecal egg counts during the experiment. All calves developed antibody titers to IBRV, BVDV-1, BVDV-2, and PI-3 by d 15 postvaccination. On d 88, all calves were challenged with IBRV and blood samples were obtained on d 88, 89, 90, 93, 95, 98, 99, and 103. All calves had increased rectal temperatures during the final 7 d of the IBRV challenge. However, the CONT group had greater (P < 0.01) rectal temperatures on each sampling day except d 90 compared with the DPV and DV treatments. Therefore, deworming before or at vaccination reduced parasite burden and decreased rectal temperature increase after an IBRV challenge. Deworming strategy had no effect on antibody response to vaccination or IBRV challenge.

Performance of Angus cows and calves was compared between two methods of bahiagrass (Paspalum notatum Flügge) grazing management, rotational stocking (ROT) and continuous intensive stocking (CIS), where stocking rate was varied by adjusting available pasture area as forage growth rate changed during the growing season. Effects of sire type (low [LO] vs high [HI] EPD for nematode egg shedding rate [EPG]) also were studied. Data were analyzed for two complete cycles of calf production from breeding through weaning. There was no effect of pasture grazing management method on cow BW, cow body condition score, adjusted 205-d calf weaning weight, and preweaning calf ADG. Five genera of nematodes (Ostertagia, Haemonchus, Trichostrongylus, Cooperia, and Oesophagostomum) were recovered from calves removed and killed at times throughout the grazing season. Mean nematode numbers recovered increased (P < .05) for all species as the grazing season progressed from spring to fall, consistent with results on EPG (P < .001). Effect of sire type on EPG was not significant; however, sire type did affect mean EPG (P < .05) from a subset of calves placed in drylot after weaning and sampled for three consecutive days. Sire type affected IgG1 titer to H. placei (LO = .50 +/- .012, HI = .45 +/- .011) and IgA titer to O. radiatum (LO = .28 +/- .006, HI = .26 +/- .005), and there was a sire type x pasture grazing method interaction on IgG1 titer to H. placei (LO-ROT = .49 +/- .016, HI-ROT = .49 +/- .017, LO-CIS = .50 +/- .017, HI-CIS = .41 +/- .014). Increased anti-parasite antibody titers in progeny of sires with EPD for low nematode egg shedding rates may reflect increased host resistance to these parasites.