Identification of a mutant bovine herpesvirus-1 (BHV-1) in post-arrival outbreaks of IBR in feedlot calves and protection with conventional vaccination
Svl. Van Den Hurk et al., Identification of a mutant bovine herpesvirus-1 (BHV-1) in post-arrival outbreaks of IBR in feedlot calves and protection with conventional vaccination, CAN J VET R, 65(2), 2001, pp. 81-88
Citations number
15
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
CANADIAN JOURNAL OF VETERINARY RESEARCH-REVUE CANADIENNE DE RECHERCHE VETERINAIRE
Outbreaks of infectious bovine rhinotracheitis (IBR) have recently been obs
erved in vaccinated feedlot calves in Alberta a few months post-arrival. To
investigate the cause of these outbreaks, lung and tracheal tissues were c
ollected from calves that died of IBR during a post-arrival outbreak of dis
ease. Bovine herpesvirus-1 (BHV-1), the causative agent of IBR, was isolate
d from 6 out of 15 tissues. Of these 6 isolates, 5 failed to react with a m
onoclonal antibody specific for one of the epitopes on glycoprotein D, one
of the most important antigens of BHV-1. The ability of one of these mutant
BHV-1 isolates to cause disease in calves vaccinated with a modified-live
IBR vaccine was assessed in an experimental challenge study. After one vacc
ination, the majority of the calves developed humoral and cellular immune r
esponses. Secondary vaccination resulted in a substantially enhanced level
of immunity in all animals. Three months after the second vaccination, calv
es were either challenged with one of the mutant isolates or with a convent
ional challenge strain of BHV-1. Regardless of the type of virus used for c
hallenge, vaccinated calves experienced significantly (P < 0.05) less weigh
t loss and temperature rises, had lower nasal scores, and shed less virus t
han non-vaccinated animals. The only statistically significant (P < 0.05) d
ifference between the 2 challenge viruses was the amount of virus shed, whi
ch was higher in non-vaccinated calves challenged with the mutant virus tha
n in those challenged with the conventional virus. These data show that cal
ves vaccinated with a modified-live IBR vaccine are protected from challeng
e with either the mutant or the conventional virus.