OBJECTIVE: To evaluate effects of vaccination with a killed whole-cell vaccine against Mycobacterium avium subsp paratuberculosis (MAP) on fecal shedding of the organism, development of clinical paratuberculosis (Johne's disease [JD]), milk production, measures of reproduction, and within-herd longevity of dairy cattle naturally exposed to MAP. DESIGN: Controlled clinical trial. ANIMALS: 200 vaccinated and 195 unvaccinated (control) dairy cows from 3 herds in Wisconsin. PROCEDURES: Every other heifer calf born in each herd received the MAP vaccine; 162 vaccinates and 145 controls that had ≥ 1 lactation were included in analyses. Bacteriologic culture of fecal samples for MAP was performed annually for 7 years; results were confirmed via histologic methods and PCR assay. Production records and culture results were evaluated to determine effects of vaccination on variables of interest in study cows. Annual whole-herd prevalence of MAP shedding in feces was also determined. RESULTS: Vaccinates had a significantly lower hazard of testing positive for MAP via culture of fecal samples than did controls over time (hazard ratio, 0.57; 95% confidence interval, 0.34 to 0.97). Fewer vaccinates developed clinical JD than did controls (n = 6 and 12, respectively), but these differences were nonsignificant. Overall within-herd longevity, total milk production, and calving-to-conception intervals were similar between vaccinates and controls. In all herds, prevalence of MAP shedding in feces decreased over time. CONCLUSIONS AND CLINICAL RELEVANCE: Vaccination with a killed whole-cell MAP vaccine appeared to be an effective tool as part of a program to control the spread of JD in dairy cattle.
OBJECTIVE: To evaluate effects of vaccination with a killed whole-cell vaccine against Mycobacterium avium subsp paratuberculosis (MAP) on fecal shedding of the organism, development of clinical paratuberculosis (Johne's disease [JD]), milk production, measures of reproduction, and within-herd longevity of dairy cattle naturally exposed to MAP. DESIGN: Controlled clinical trial. ANIMALS: 200 vaccinated and 195 unvaccinated (control) dairy cows from 3 herds in Wisconsin. PROCEDURES: Every other heifer calf born in each herd received the MAP vaccine; 162 vaccinates and 145 controls that had ≥ 1 lactation were included in analyses. Bacteriologic culture of fecal samples for MAP was performed annually for 7 years; results were confirmed via histologic methods and PCR assay. Production records and culture results were evaluated to determine effects of vaccination on variables of interest in study cows. Annual whole-herd prevalence of MAP shedding in feces was also determined. RESULTS: Vaccinates had a significantly lower hazard of testing positive for MAP via culture of fecal samples than did controls over time (hazard ratio, 0.57; 95% confidence interval, 0.34 to 0.97). Fewer vaccinates developed clinical JD than did controls (n = 6 and 12, respectively), but these differences were nonsignificant. Overall within-herd longevity, total milk production, and calving-to-conception intervals were similar between vaccinates and controls. In all herds, prevalence of MAP shedding in feces decreased over time. CONCLUSIONS AND CLINICAL RELEVANCE: Vaccination with a killed whole-cell MAP vaccine appeared to be an effective tool as part of a program to control the spread of JD in dairy cattle.
Authors: Deepanker Tewari; Ernest Hovingh; Rick Linscott; Edmond Martel; John Lawrence; David Wolfgang; David Griswold Journal: Clin Vaccine Immunol Date: 2014-03-12
Authors: John P Bannantine; Murray E Hines; Luiz E Bermudez; Adel M Talaat; Srinand Sreevatsan; Judith R Stabel; Yung-Fu Chang; Paul M Coussens; Raúl G Barletta; William C Davis; Desmond M Collins; Yrjö T Gröhn; Vivek Kapur Journal: Front Cell Infect Microbiol Date: 2014-09-09 Impact factor: 5.293
Authors: Marie-Eve Fecteau; Dipti W Pitta; Bonnie Vecchiarelli; Nagaraju Indugu; Sanjay Kumar; Susan C Gallagher; Terry L Fyock; Raymond W Sweeney Journal: PLoS One Date: 2016-08-05 Impact factor: 3.240
Authors: John P Bannantine; Jamie L Everman; Sasha J Rose; Lmar Babrak; Robab Katani; Raúl G Barletta; Adel M Talaat; Yrjö T Gröhn; Yung-Fu Chang; Vivek Kapur; Luiz E Bermudez Journal: Front Cell Infect Microbiol Date: 2014-07-01 Impact factor: 5.293