Abstract
A real-time PCR assay with a Taqman probe was developed that targeted the polA gene of Treponema pallidum. The test was validated using an analytical panel (n = 140) and a clinical panel of genital samples (n = 112) from patients attending a sexually transmitted infections clinic. High sensitivities and specificities of 94-100% were achieved using two real-time PCR platforms, the Rotor-Gene and the iCycler. The assay can be completed within 2 h, enabling reporting in <8 h. This fast and robust assay is suitable for implementation in routine laboratories for diagnosing primary syphilis
Original language | English |
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Pages (from-to) | 1233-1236 |
Journal | Clinical Microbiology and Infection |
Volume | 12 |
Issue number | 12 |
DOIs | |
Publication status | Published - 2006 |