Attenuation of a Brucella abortus mutant lacking a major 25 kDa outer membrane protein in cattle

Citation
Md. Edmonds et al., Attenuation of a Brucella abortus mutant lacking a major 25 kDa outer membrane protein in cattle, AM J VET RE, 62(9), 2001, pp. 1461-1466
Citations number
27
Categorie Soggetti
Veterinary Medicine/Animal Health
Journal title
AMERICAN JOURNAL OF VETERINARY RESEARCH
ISSN journal
00029645 → ACNP
Volume
62
Issue
9
Year of publication
2001
Pages
1461 - 1466
Database
ISI
SICI code
0002-9645(200109)62:9<1461:AOABAM>2.0.ZU;2-T
Abstract
Objective-To determine the virulence of a Brucella abortus mutant, BA25, la cking a major 25 kd outer membrane protein (Omp25) In cattle. Animals-20 mixed-breed heifers in late gestation. Procedure-10 heifers were inoculated with 1 x 10(7) colony-forming units of the Omp25 mutant via the conjunctival sac, and an equal number were Infect ed with the virulent parental strain B abortus 2308. The delivery status of the dams was recorded, and colonization was assessed following necropsy. T he ability of BA25 to replicate Inside bovine phagocytes and chorionic trop hoblasts was also evaluated in vitro because of the propensity of virulent brucellae to replicate inside these cells in vivo. Results-The parental strain Induced abortions in 5 of 10 Inoculated cattle, whereas only 1 of 10 dams exposed to BA25 aborted. Brucella abortus strain 2308 colonized all of the cow-calf pairs and induced Brucella-specific ant ibodies In 100% of the dams. In contrast, BA25 was isolated by bacteriologi c cultural technique from 30% of the calves and 50% of the inoculated dams (n=10). Of the 10 heifers inoculated with BA25, 4 did not develop Brucella- specific antibodies nor were they colonized by the mutant strain. In bovine macrophages and chorionic trophoblasts, BA25 replicated in significantly l ower numbers than the virulent parental strain (n=3). Conclusions and Clinical Relevance-The 25 kd outer membrane protein may be an important virulence factor for B abortus in cattle. The attenuation of t he Omp25 mutant in cattle may involve the inability of BA25 to replicate ef ficiently in bovine phagocytes and chorionic trophoblasts.