Sensitive detection of Treponema pallidum by using the polymerase chain reaction

J. M. Burstain, E. Grimprel, S. A. Lukehart, M. V. Norgard, J. D. Radolf

Research output: Contribution to journalArticle

129 Scopus citations

Abstract

We have developed a sensitive assay for Treponema pallidum subsp. pallidum (T. pallidum), the agent of venereal syphilis, based upon the polymerase chain reaction (PCR). A 658-bp portion of the gene encoding the 47-kDa membrane immunogen was amplified, and the PCR products were probed by DNA-DNA hybridization with a 496-bp fragment internal to the amplified DNA. The assay detected approximately 0.01 pg of purified T. pallidum DNA, and positive results were obtained routinely from suspensions of treponemes calculated to contain 10 or more organisms and from some suspensions calculated to contain a single organism. Specific PCR products were obtained for the closely related agent of yaws, Treponema pallidum subsp. pertenue, but not with human DNA or DNAs from other spirochetes (including Borrelia burgdorferi), skin microorganisms, sexually transmitted disease pathogens, and central nervous system pathogens. T. pallidum DNA was detected in serum, cerebrospinal fluids, and amniotic fluids from syphilis patients but not in nonsyphilitic controls. T. pallidum DNA was also amplified from paraffin-embedded tissue. The diagnosis of syphilis by using PCR may become a significant addition to the diagnostic armamentarium and a valuable technique for the investigation of syphilis pathogenesis.

Original languageEnglish (US)
Pages (from-to)62-69
Number of pages8
JournalJournal of clinical microbiology
Volume29
Issue number1
DOIs
StatePublished - 1991

ASJC Scopus subject areas

  • Microbiology (medical)

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