The DOI matches its Crossref record; 9 of the 10 references it cites were found in a registry or an index.
Demonstration of the ability of a canine Lyme vaccine to reduce the incidence of histological synovial lesions following experimentally-induced canine Lyme borreliosis
Abstract
Lyme disease in dogs can be effectively prevented by vaccination against antigens expressed by the spirochete Borrelia burgdorferi during transmission by the tick vector Ixodes sp. Lyme vaccine efficacy has traditionally been based on indicators of infection following wild-caught tick challenge whereas most other types of vaccine are required to demonstrate protection from clinical signs of disease. In this vaccination-challenge study we sought to demonstrate the ability of a nonadjuvanted, outer surface protein A (OspA) vaccine to protect from infection and to prevent synovial lesions consistent with Borreliosis. Thirty, purpose-bred beagles were randomly divided into vaccinated and unvaccinated groups. The vaccinated group was administered two subcutaneous doses of a nonadjuvanted, purified, Borrelia burgdorferi OspA vaccine at a 21- day interval. Dogs were challenged by wild-caught, B. burgdorferi-infected ticks (Ixodes scapularis). Clinical signs, serology, Borrelia isolation and PCR evaluated antemortem vaccine efficacy. Postmortem histopathological analysis of synovial tissue was compared to antemortem infection status. Borreliosis was demonstrated by Borrelia isolation from skin biopsies in 13 out of 15 unvaccinated dogs. All unvaccinated dogs' Western blot profiles were consistent with infection. Two of 15 vaccinated dogs had at least one positive spirochete culture which cleared 91days post-challenge, and Western blot profiles were consistent with vaccination alone. No dogs, vaccinated or unvaccinated, exhibited clinical signs consistent with borreliosis. Based on a histopathological cumulative joint scoring system (CJS), all unvaccinated dogs had synovial lesions indicative of Lyme disease. Only one of the vaccinated dogs had a CJS that was greater than the statistical cut off score for the absence of synovial lesions. There was high correlation between clinical histopathology and spirochete isolation. Infection with B burgdorferi may produce inconsistent clinical signs of lameness. Histopathological changes in joints from infected dogs are reliable indicators of borreliosis and correlate well with other indicators of infection. This model provides support that vaccination with a nonadjuvanted, purified OspA vaccine offers protection from Borrelia infection and the resulting synovial lesions that can lead to clinical signs of lameness.
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“Although many experimental studies were classified as a “low” risk of bias for random sequence generation because they stated that dogs were randomly assigned to an intervention group, only 1 study specified the actual method used to randomly assign dogs to an intervention group.38”
From Efficacy of Borrelia burgdorferi vaccine in dogs in North America: A systematic review and meta-analysis (2019) · cites this paper as [38]
Citations
Cites
Experimental Lyme Disease in Dogs Produces Arthritis and Persistent Infection
Appel, M. J. G., Allan, S., Jacobson, R. H., Lauderdale, T. L., Chang, Y., Shin, S. J., Thomford, J. W., Todhunter, R. J., & Summers, B. A. (1993) · The Journal of Infectious Diseases · doi:10.1093/infdis/167.3.651 · Cited by 221
ACVIM small animal consensus statement on Lyme disease in dogs: diagnosis, treatment, and prevention
Littman, M. P., Goldstein, R. E., Labato, M. A., Lappin, M. R., & Moore, G. E. (2006) · Journal of Veterinary Internal Medicine · doi:10.1111/j.1939-1676.2006.tb02880.x · Cited by 143
Levy, S. A., & Magnarelli, L. A. (1992) · Journal of the American Veterinary Medical Association · doi:10.2460/javma.1992.200.03.344 · Cited by 89
Histopathological Studies of Experimental Lyme Disease in the Dog
Summers, B. A., Straubinger, A. F., Jacobson, R. H., Chang, Y., Appel, M. J. G., & Straubinger, R. K. (2005) · Journal of Comparative Pathology · doi:10.1016/j.jcpa.2004.11.006 · Cited by 67
LaFleur, R. L., Dant, J. C., Wasmoen, T. L., Callister, S. M., Jobe, D. A., Lovrich, S. D., WARNER, T. F. C. S., Abdelmagid, O. Y., & Schell, R. F. (2008) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00373-08 · Cited by 48
Töpfer, K., & Straubinger, R. K. (2006) · Vaccine · doi:10.1016/j.vaccine.2006.07.031 · Cited by 47
Synovial Lesions in Experimental Canine Lyme Borreliosis
Susta, L., Uhl, E. W., Grosenbaugh, D. A., & Krimer, P. M. (2011) · Veterinary Pathology · doi:10.1177/0300985811424754 · Cited by 15
Self-citationKrimer, P. M., Miller, A. D., Li, Q., Grosenbaugh, D. A., Susta, L., & Schatzberg, S. J. (2011) · Journal of Veterinary Diagnostic Investigation · doi:10.1177/1040638711408281 · Cited by 13
Self-citationFretwell, B., & Jarecki, M. (2006) · Cited by 13
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ACVIM consensus update on Lyme borreliosis in dogs and cats
Littman, M. P., Gerber, B., Goldstein, R. E., Labato, M. A., Lappin, M. R., & Moore, G. E. (2018) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.15085 · Cited by 152
Borrelia burgdorferi Infection and Lyme Disease in North American Horses: A Consensus Statement
Divers, T. J., Gardner, R. B., Madigan, J. E., Witonsky, S. G., Bertone, J. J., Swinebroad, E. L., Schutzer, S. E., & Johnson, A. L. (2018) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.15042 · Cited by 77
Scurtu, L. G., Jinga, V., & Simionescu, O. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23073550 · Cited by 20
Spirochetal Lipoproteins and Immune Evasion
Christodoulides, A., Boyadjian, A., & Kelesidis, T. (2017) · Frontiers in Immunology · doi:10.3389/fimmu.2017.00364 · Cited by 20
Vogt, N. A., Sargeant, J. M., MacKinnon, M. C., & Versluis, A. M. (2019) · Journal of Veterinary Internal Medicine · doi:10.1111/jvim.15344 · Cited by 16
“Although many experimental studies were classified as a “low” risk of bias for random sequence generation because they stated that dogs were randomly assigned to an intervention group, only 1 study specified the actual method used to randomly assign dogs to an intervention group.(38) For all 3 observational studies, t…”
Method
Metadata
- Authors
- Grosenbaugh, D. A., Rissi, D. R., & Krimer, P. M.
- Affiliations
- University of Georgia (US)
- Corresponding author
- Grosenbaugh, Deborah A.
- Venue
- Veterinary Immunology and Immunopathology
- Publisher
- Elsevier BV
- Published
- 2016-11
- Volume
- 180
- Pages
- 29-33
- ISSN
- 0165-2427 (ISSN-L)
- OpenAlex
- W2511026750
- Cited by
- 12
- References
- 10
- Citations by year
- 2026: 1 · 2022: 4 · 2021: 2 · 2018: 4 · 2017: 1
- FWCI
- 1.72
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Veterinary Immunology and Immunopathology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Merial, Inc
- Topics
- Life Sciences › Immunology and Microbiology › Parasitology › Vector-borne infectious diseases
- Health Sciences › Medicine › Infectious Diseases › Brucella: diagnosis, epidemiology, treatment
- Life Sciences › Immunology and Microbiology › Microbiology › Microbial infections and disease research
- Keywords
- Borrelia burgdorferi, vaccine efficacy, synovial lesions, Ixodes scapularis, tick challenge, joint histopathology, lameness, serology, spirochete isolation, beagle dogs, clinical signs of infection
- MeSH terms
- Animals, Antigens, Surface, Bacterial Outer Membrane Proteins, Bacterial Vaccines, Dog Diseases, Dogs, Female, Lameness, Animal, Lipoproteins, Lyme Disease, Male, Synovial Membrane, Vaccination, Borrelia burgdorferi
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