Skip to main content
Clinical and Diagnostic Laboratory Immunology logoLink to Clinical and Diagnostic Laboratory Immunology
. 1997 May;4(3):321–327. doi: 10.1128/cdli.4.3.321-327.1997

Protection of rats against Mycoplasma arthritidis-induced arthritis by active and passive immunizations with two surface antigens.

L R Washburn 1, E J Weaver 1
PMCID: PMC170526  PMID: 9144371

Abstract

We previously identified two surface-exposed Mycoplasma arthritidis protein antigens, designated MAA1 and MAA2, that may be involved in cytadherence. Since adherence to host tissues is an important first step in most bacterial infections, we suggest that MAA1 and MAA2 may be virulence factors for M. arthritidis. In order to provide evidence for such a role, we conducted a series of experiments in which rats were actively immunized with each of these proteins purified from sodium dodecyl sulfate-polyacrylamide gels or passively immunized with poly- or monoclonal antibodies against MAA1 and MAA2. In each case, immunity against MAA1 and MAA2 conferred at least partial protection against M. arthritidis-induced disease. The greatest protection was achieved by passive immunization with monoclonal antibody A9a, directed against a surface-exposed epitope of putative adhesin MAA1. Because protective immunity in most bacterial infections is directed against major virulence factors, these results suggest that MAA1 and MAA2 may play a role in the pathogenesis of M. arthritidis-induced arthritis of rats, possibly by mediating initial colonization of joint tissues.

Full Text

The Full Text of this article is available as a PDF (734.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bordier C. Phase separation of integral membrane proteins in Triton X-114 solution. J Biol Chem. 1981 Feb 25;256(4):1604–1607. [PubMed] [Google Scholar]
  2. Cole B. C., Atkin C. L. The Mycoplasma arthritidis T-cell mitogen, MAM: a model superantigen. Immunol Today. 1991 Aug;12(8):271–276. doi: 10.1016/0167-5699(91)90125-D. [DOI] [PubMed] [Google Scholar]
  3. Cole B. C., Cahill J. F., Wiley B. B., Ward J. R. Immunological responses of the rat to Mycoplasma arthritidis. J Bacteriol. 1969 Jun;98(3):930–937. doi: 10.1128/jb.98.3.930-937.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cole B. C., Golightly-Rowland L., Ward J. R., Wiley B. B. Immunological response of rodents to murine mycoplasmas. Infect Immun. 1970 Oct;2(4):419–425. doi: 10.1128/iai.2.4.419-425.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Cole B. C., Thorpe R. N., Hassell L. A., Washburn L. R., Ward J. R. Toxicity but not arthritogenicity of Mycoplasma arthritidis for mice associates with the haplotype expressed at the major histocompatibility complex. Infect Immun. 1983 Sep;41(3):1010–1015. doi: 10.1128/iai.41.3.1010-1015.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Cole B. C., Ward J. R. Fate of intravenously injected Mycoplasma arthritidis in rodents and effect of vaccines. Infect Immun. 1973 Mar;7(3):416–425. doi: 10.1128/iai.7.3.416-425.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Cole B. C., Ward J. R. Interaction of Mycoplasma arthritidis and other mycoplasmas with murine peritoneal macrophages. Infect Immun. 1973 May;7(5):691–699. doi: 10.1128/iai.7.5.691-699.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Cole B. C., Ward J. R., Jones R. S., Cahill J. F. Chronic proliferative arthritis of mice induced by Mycoplasma arthritidis. I. Induction of disease and histopathological characteristics. Infect Immun. 1971 Oct;4(4):344–355. doi: 10.1128/iai.4.4.344-355.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Hannan P. C., Hughes B. O. Reproducible polyarthritis in rats caused by Mycoplasma arthritidis. Ann Rheum Dis. 1971 May;30(3):316–321. doi: 10.1136/ard.30.3.316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Lee C., Levin A., Branton D. Copper staining: a five-minute protein stain for sodium dodecyl sulfate-polyacrylamide gels. Anal Biochem. 1987 Nov 1;166(2):308–312. doi: 10.1016/0003-2697(87)90579-3. [DOI] [PubMed] [Google Scholar]
  11. Voelker L. L., Weaver K. E., Ehle L. J., Washburn L. R. Association of lysogenic bacteriophage MAV1 with virulence of Mycoplasma arthritidis. Infect Immun. 1995 Oct;63(10):4016–4023. doi: 10.1128/iai.63.10.4016-4023.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Washburn L. R., Cole B. C., Gelman M. I., Ward J. R. Chronic arthritis of rabbits induced by mycoplasmas. I. Clinical microbiologic, and histologic features. Arthritis Rheum. 1980 Jul;23(7):825–836. doi: 10.1002/art.1780230709. [DOI] [PubMed] [Google Scholar]
  13. Washburn L. R., Cole B. C., Ward J. R. Chronic arthritis of rabbits induced by mycoplasmas. II. Antibody response and the deposition of immune complexes. Arthritis Rheum. 1980 Jul;23(7):837–845. doi: 10.1002/art.1780230710. [DOI] [PubMed] [Google Scholar]
  14. Washburn L. R., Hirsch S. Comparison of four Mycoplasma arthritidis strains by enzyme immunoassay, metabolism inhibition, one- and two-dimensional electrophoresis, and immunoblotting. J Clin Microbiol. 1990 Sep;28(9):1974–1981. doi: 10.1128/jcm.28.9.1974-1981.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Washburn L. R., Hirsch S., McKenzie M., Voelker L. L. Vaccination of Lewis rats against Mycoplasma arthritidis-induced arthritis. Am J Vet Res. 1992 Jan;53(1):52–58. [PubMed] [Google Scholar]
  16. Washburn L. R., Hirsch S., Voelker L. L. Mechanisms of attachment of Mycoplasma arthritidis to host cells in vitro. Infect Immun. 1993 Jun;61(6):2670–2680. doi: 10.1128/iai.61.6.2670-2680.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Washburn L. R., Ramsay J. R., Andrews M. B. Recognition of Mycoplasma arthritidis membrane antigens by rats and rabbits: comparison by immunoblotting and radioimmunoprecipitation. Vet Microbiol. 1988 May;17(1):45–57. doi: 10.1016/0378-1135(88)90078-8. [DOI] [PubMed] [Google Scholar]
  18. Washburn L. R., Ramsay J. R. Experimental induction of arthritis in LEW rats and antibody response to four Mycoplasma arthritidis strains. Vet Microbiol. 1989 Nov;21(1):41–55. doi: 10.1016/0378-1135(89)90017-5. [DOI] [PubMed] [Google Scholar]
  19. Washburn L. R., Ramsay J. R., Roberts L. K. Characterization of the metabolism inhibition antigen of Mycoplasma arthritidis. Infect Immun. 1985 Aug;49(2):357–364. doi: 10.1128/iai.49.2.357-364.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Washburn L. R. Spectrophotometric method for determining titers of antimycoplasma metabolism inhibition antibody. Appl Environ Microbiol. 1983 Jan;45(1):343–346. doi: 10.1128/aem.45.1.343-346.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Washburn L. R., Voelker L. L., Ehle L. J., Hirsch S., Dutenhofer C., Olson K., Beck B. Comparison of Mycoplasma arthritidis strains by enzyme-linked immunosorbent assay, immunoblotting, and DNA restriction analysis. J Clin Microbiol. 1995 Sep;33(9):2271–2279. doi: 10.1128/jcm.33.9.2271-2279.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Clinical and Diagnostic Laboratory Immunology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES