Specific immunofluorescent staining of pathogenic treponemes with a monoclonal antibody

Author:

Ito F1,Hunter E F1,George R W1,Pope V1,Larsen S A1

Affiliation:

1. Department of Dermatology, Second Hospital of Nippon Medical School, Kanagawa, Japan.

Abstract

Two hybrid cell lines which produced mouse monoclonal antibody to the DAL-1 street strain of Treponema pallidum subsp. pallidum were established. These monoclonal antibodies strongly reacted with T. pallidum subsp. pallidum (Nichols strain, DAL-1, and two other street strains, strains MN-1 and MN-3) and T. pallidum subsp. pertenue by indirect microimmunofluorescent antibody and enzyme-linked immunosorbent assay techniques, but they did not react with normal rabbit testicular tissue. These monoclonal antibodies did not react with nonpathogenic treponemes, such as T. phagedenis Reiter, T. denticola MRB, T. refringens Noguchi, or other spirochetes, such as Borrelia burgdorferi and Leptospira interrogans serovar pomona in microimmunofluorescent antibody smear slides or in Western blots (immunoblots). While unlabeled antibodies are useful for investigating the antigenic structures of T. pallidum, we labeled these monoclonal antibodies with fluorescein isothiocyanate and used them for diagnosing syphilis by direct staining of lesion exudate or T. pallidum subsp. pallidum in formalin-fixed tissues from patients suspected of having syphilis. Both monoclonal antibodies were directed against antigens of T. pallidum subsp. pallidum with a molecular weight of 37,000 as determined by the Western blotting technique.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference40 articles.

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4. Isolation of a cultivatable spirochete from bcodes ricinus ticks of;Barbour A. G.;Switzerland. Curr. Microbiol.,1983

5. Center for Disease Control. 1969. Manual of tests for syphilis p. 17-20. Public Health Service publication no. 411. United States Department of Health Education and Welfare Washington D.C.

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