A M O'Connor1, S Brace, S Gould, R Dewell, T Engelken. 1. Department of Veterinary Diagnostics and Production Animal Medicine, Iowa State University College of Veterinary Medicine, Ames, IA 50011, USA. oconnor@iastate.edu
Abstract
BACKGROUND: A randomized, masked, 2-arm parallel trial was conducted to assess the efficacy of a Moraxella bovis (M. bovis) autogenous vaccine to prevent naturally occurring infectious bovine keratoconjunctivis (IBK) in beef calves. HYPOTHESIS: The null hypothesis was that treatment group was not associated with either risk of IBK or last observed weight. ANIMALS: The trial was conducted between May and November 2009 and 2010 on a university-owned farm in Iowa. The vaccine contained 2 randomly selected M. bovis from IBK cases that occurred at the farm in 2008. Calves born between January and May 2009 and 2010 without visible corneal lesions were randomly allocated to receive vaccine (n = 191) or placebo (n = 178). METHODS: Two s.c. doses were administered 21-28 days apart. Allocation to treatment was concealed using bottles marked A or B. Staff observing the animals for IBK could not determine the treatment grouping. The herd met the "at-risk" criteria (ie, >15% IBK in unvaccinated calves and M. bovis detection in IBK cases). Analysis was "per-protocol". RESULTS: The risk of IBK was 58/185 (31%) in vaccinated calves and 66/173 (38%) in unvaccinated calves (adjusted risk ratio = 0.78; 95% CI, 0.49-1.24). Average weight before sale did not differ between the vaccinated calves (196.6 kg, SD ± 39.9) and unvaccinated calves (198.1 kg, SD ± 42.7) (P value = .19). No adverse effects were noted. CONCLUSION AND CLINICAL IMPORTANCE: Combination of the study results with previous studies suggests that autogenous M. bovis vaccines often are ineffective in controlling naturally occurring IBK.
BACKGROUND: A randomized, masked, 2-arm parallel trial was conducted to assess the efficacy of a Moraxella bovis (M. bovis) autogenous vaccine to prevent naturally occurring infectious bovine keratoconjunctivis (IBK) in beef calves. HYPOTHESIS: The null hypothesis was that treatment group was not associated with either risk of IBK or last observed weight. ANIMALS: The trial was conducted between May and November 2009 and 2010 on a university-owned farm in Iowa. The vaccine contained 2 randomly selected M. bovis from IBK cases that occurred at the farm in 2008. Calves born between January and May 2009 and 2010 without visible corneal lesions were randomly allocated to receive vaccine (n = 191) or placebo (n = 178). METHODS: Two s.c. doses were administered 21-28 days apart. Allocation to treatment was concealed using bottles marked A or B. Staff observing the animals for IBK could not determine the treatment grouping. The herd met the "at-risk" criteria (ie, >15% IBK in unvaccinated calves and M. bovis detection in IBK cases). Analysis was "per-protocol". RESULTS: The risk of IBK was 58/185 (31%) in vaccinated calves and 66/173 (38%) in unvaccinated calves (adjusted risk ratio = 0.78; 95% CI, 0.49-1.24). Average weight before sale did not differ between the vaccinated calves (196.6 kg, SD ± 39.9) and unvaccinated calves (198.1 kg, SD ± 42.7) (P value = .19). No adverse effects were noted. CONCLUSION AND CLINICAL IMPORTANCE: Combination of the study results with previous studies suggests that autogenous M. bovis vaccines often are ineffective in controlling naturally occurring IBK.
Authors: Annette O'Connor; Vickie Cooper; Laura Censi; Ella Meyer; Mac Kneipp; Grant Dewell Journal: J Vet Intern Med Date: 2019-10-12 Impact factor: 3.333
Authors: Matthew M Hille; Matthew L Spangler; Michael L Clawson; Kelly D Heath; Hiep L X Vu; Rachel E S Rogers; John Dustin Loy Journal: Vaccines (Basel) Date: 2022-06-09