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Gewählte Publikation:

Zoechling, N; Schluepen, EM; Soyer, HP; Kerl, H; Volkenandt, M.
Molecular detection of Treponema pallidum in secondary and tertiary syphilis.
Br J Dermatol. 1997; 136(5):683-686 Doi: 10.1046%2Fj.1365-2133.1997.6561614.x
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Co-Autor*innen der Med Uni Graz
Kerl Helmut
Soyer Hans Peter
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Abstract:
Treponema pallidum can be detected by conventional techniques such as dark-field microscopy, immunofluorescence or the rabbit infectivity test, in large numbers in the skin lesions of primary and early secondary syphilis. In the skin lesions of late secondary and tertiary syphilis, conventional techniques fail to detect spirochaetes in general, perhaps due to increasing degeneration and the disappearance of treponemal spirochaetes in late syphilitic skin lesions. We used the highly sensitive technique of polymerase chain reaction (PCR) to prove the presence of Treponema pallidum-specific DNA in six lesions of late secondary syphilis and seven lesions of tertiary syphilis, including one syphilitic gumma. A Whartin-Starry stain was carried out in all 13 specimens and did not reveal any treponemal structures. Treponema pallidum-specific DNA was amplified by PCR in four of six cases of secondary syphilis and in the syphilitic gumma. These results are in favour of a direct cell-mediated immune reaction directed against treponemal antigen rather than the concept of an Id-reaction. Beside the usefulness of a PCR-based assay for understanding the aetiology of lesions of late syphilis, the assay described can be of clinical importance in various situations where traditional methods fail to detect Treponema pallidum because of lack of sensitivity.
Find related publications in this database (using NLM MeSH Indexing)
DNA, Bacterial - analysis
Humans - analysis
Polymerase Chain Reaction - methods
Skin - microbiology
Syphilis, Cutaneous - microbiology
Treponema pallidum - isolation and purification

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