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. 1985 Apr;61(2):75-81.
doi: 10.1136/sti.61.2.75.

Experimental infection of inbred guinea pigs with Treponema pallidum: development of lesions and formation of antibodies

Experimental infection of inbred guinea pigs with Treponema pallidum: development of lesions and formation of antibodies

C S Pavia et al. Genitourin Med. 1985 Apr.

Abstract

Inbred strain 2 and strain 13 guinea pigs were infected intradermally in the hind legs with different numbers of the virulent Nichols strain of Treponema pallidum. About 91% of the animals developed clearly visible lesions after being injected with 5 X 10(6) to 10 X 10(6) treponemes. T pallidum organisms could be isolated from skin lesions at various stages after infection. Infected animals were monitored for the production of specific treponemal and non-specific cardiolipin antibodies by the fluorescent treponemal antibody (FTA) and microhaemagglutination (MHA-TP) tests and the rapid plasma reagin (RPR) card test. Low levels of specific antibodies could be detected by both FTA and MHA-TP tests from three to four weeks after infection. Maximum titres of treponemal antibody generally occurred after week 6 and persisted for several more months. These peak titres ranged from 1/40 to 1/80 in the FTA test and 1/160 to 1/320 in the MHA-TP test. During the same period infected guinea pigs, unlike rabbits with syphilis, did not produce detectable quantities of antibodies against cardiolipin.

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References

    1. Infect Immun. 1982 Apr;36(1):437-9 - PubMed
    1. Infect Immun. 1980 Jun;28(3):909-13 - PubMed
    1. Ann Dermatol Syphiligr (Paris). 1955 Sep-Oct;82(5):481-3 - PubMed
    1. Scand J Immunol. 1983 Sep;18(3):201-6 - PubMed
    1. Br J Vener Dis. 1983 Jun;59(3):157-68 - PubMed

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