TL;DR: All human treponematoses share remarkable similarities in pathogenesis and clinical manifestations, consistent with the high genetic and antigenic relatedness of their etiological agents.
Abstract: The agents of human treponematoses include four closely related members of the genus Treponema: three subspecies of Treponema pallidum plus Treponema carateum. T. pallidum subsp. pallidum causes venereal syphilis, while T. pallidum subsp. pertenue, T. pallidum subsp. endemicum, and T. carateum are the agents of the endemic treponematoses yaws, bejel (or endemic syphilis), and pinta, respectively. All human treponematoses share remarkable similarities in pathogenesis and clinical manifestations, consistent with the high genetic and antigenic relatedness of their etiological agents. Distinctive features have been identified in terms of age of acquisition, most common mode of transmission, and capacity for invasion of the central nervous system and fetus, although the accuracy of these purported differences is debated among investigators and no biological basis for these differences has been identified to date. In 2012, the World Health Organization (WHO) officially set a goal for yaws eradication by 2020. This challenging but potentially feasible endeavor is favored by the adoption of oral azithromycin for mass treatment and the currently focused distribution of yaws and endemic treponematoses and has revived global interest in these fascinating diseases and their causative agents.
TL;DR: This review summarizes genome structure of uncultivable pathogenic treponemes including genetically variable regions and identifies molecular differences at several different chromosomal loci identified among TPA strains or isolates.
TL;DR: An enzyme-linked immunosorbent assay (ELISA) for syphilis has been developed that detects IgG antibody to purified recombinant Treponema pallidum surface antigen 4D, indicating that a 4D antigen-like molecule also exists in the closely related pathogenic treponemes Trep onema pertenue and TrepOnema carateum.
Abstract: An enzyme-linked immunosorbent assay (ELISA) for syphilis has been developed that detects IgG antibody to purified recombinant Treponema pallidum surface antigen 4D. The 4D ELISA was capable of detecting 25 ng of 4D antigen-specific antibody. Neither 172 nonsyphilitic sera nor 20 false-positive sera in the Venereal Disease Research Laboratory test reacted in the 4D ELISA. The sensitivity of the 4D ELISA was comparable to that of the adsorbed fluorescent treponemal antibody test in primary, secondary, and latent disease. Most sera from patients with yaws or pinta were also reactive, a result indicating that a 4D antigen-like molecule also exists in the closely related pathogenic treponemes Treponema pertenue and Treponema carateum.
TL;DR: The development of antibody reactivity to the full spectrum of T. pallidum antigens during the course of infection demonstrates the high degree of antigenic relatedness of Rheumatoid arthritis and is similar to the development of humoral responsiveness during syphilis infection.
Abstract: Inhabitants of a remote Panamanian village were examined for clinical and serological evidence of pinta infection. Of 104 persons examined, 21 (20^o) had clinical evidence of active or inactive pinta, and 54 (52^0) were seropositive. Sera were evaluated for antibody to individual Treponema pallidum antigens. Sera from all four patients with active pinta contained antibody to the 47-48-kilodalton major antigen; the intensity of reactivity and the number of antigens recognized increased with age and, presumably, duration of infection. Sera from six children with inactive pinta reacted strongly with multiple T. pallidum antigens, whereas adults with inactive pinta had less intense reactivity against fewer molecules. Seronegative controls demonstrated only weak reactivity to fewer than five molecules. The development of antibody reactivity to the full spectrum of T. pallidum antigens during the course of infection demonstrates the high degree of antigenic relatedness of T. pallidum and Treponema carateum and is similar to the development of humoral responsiveness during syphilis infection.
TL;DR: Methods of laboratory identification of both Treponema and Brachyspira include direct detection methods such as dark-field microscopy, immunohistochemistry, and PCR, but syphilis diagnosis is highly dependent on serologic testing since T. pallidum can only be isolated by inoculation of rabbits (rabbit infectivity testing).
Abstract: Treponema and Brachyspira represent two clusters of the phylum Spirochetes that are either pathogenic or human host associated. Treponema pallidum subsp. pallidum, endemicum, and pertenue are the agents of venereal syphilis, endemic syphilis, and yaws, respectively, while Treponema carateum causes pinta. Numerous treponemal phylotypes in the oral cavity cause gingivitis or periodontitis. Brachyspira aalborgi, Brachyspira pilosicoli, and Brachyspira hominis cause human intestinal spirochetosis. T. pallidum subsp. pallidum is the only treponeme transmitted by sexual contact and vertically from a pregnant woman to her fetus; it is alsoe only pathogenic treponeme that regularly breaches the blood-brain barrier. Venereal syphilis remains a significant public health problem worldwide. Methods of laboratory identification of both Treponema and Brachyspira include direct detection methods such as dark-field microscopy, immunohistochemistry, and PCR. However, while Brachyspira can be cultured, syphilis diagnosis is highly dependent on serologic testing since T. pallidum can only be isolated by inoculation of rabbits (rabbit infectivity testing). Serologic testing for syphilis involves nontreponemal tests that detect antibodies directed against lipoidal antigens and treponemal tests that detect IgM and IgG antibodies directed against T. pallidum protein antigens. Newer treponemal assays now include enzyme immunoassays, point-of-care tests, chemiluminescence assays, immunoblots, and multiplex flow immunoassays, the majority of which use recombinant T. pallidum antigens. In-depth knowledge of these assays and their performance, as well as the application of the reverse syphilis screening algorithm, is critical for both laboratory and clinical practice.