Affiliation:
1. Schering Plough Animal Health Corporation, Elkhorn, Nebraska 68022
2. Gundersen Lutheran Medical Center, La Crosse, Wisconsin 54601
3. University of Wisconsin, Madison, Wisconsin 53706
Abstract
ABSTRACT
Groups of 15 laboratory-bred beagles were vaccinated and boosted with either a placebo or adjuvanted bivalent bacterin comprised of a traditional
Borrelia burgdorferi
strain and a unique
ospA
- and
ospB
-negative
B. burgdorferi
strain that expressed high levels of OspC and then challenged with
B. burgdorferi
-infected
Ixodes scapularis
ticks. The vaccinated dogs produced high titers of anti-OspA and anti-OspC borreliacidal antibodies, including borreliacidal antibodies specific for an epitope within the last seven amino acids at the OspC carboxy terminus (termed OspC7) that was conserved among pathogenic
Borrelia
genospecies. In addition, spirochetes were eliminated from the infected ticks that fed on the bacterin recipients,
B. burgdorferi
was not isolated from the skin or joints, and antibody responses associated specifically with canine infection with
B. burgdorferi
were not produced. In contrast,
B. burgdorferi
was recovered from engorged ticks that fed on 13 (87%) placebo-vaccinated dogs (
P
< 0.0001), skin biopsy specimens from 14 (93%) dogs (
P
< 0.0001), and joint tissue specimens from 8 (53%) dogs (
P
= 0.0022). In addition, 14 (93%) dogs developed specific antibody responses against
B. burgdorferi
proteins, including 11 (73%) with C6 peptide antibodies (
P
< 0.0001). Moreover, 10 (67%) dogs developed Lyme disease-associated joint abnormalities (
P
< 0.0001), including 4 (27%) dogs that developed joint stiffness or lameness and 6 (40%) that developed chronic joint inflammation (synovitis). The results therefore confirmed that the bacterin provided a high level of protection against Lyme disease shortly after immunization.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
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