Laboratory diagnosis of Treponema pallidum infection in patients with early syphilis and neurosyphilis through a PCR-based test

被引:0
|
作者
Garcia C, Patricia [1 ]
Grassi C, Bruno [6 ]
Fich S, Felix [2 ]
Salvo L, Aurelio [9 ]
Araya C, Luis [7 ]
Abarzua C, Fernando [3 ]
Soto M, Julia [4 ]
Poggi M, Helena [4 ]
Lagos L, Marcela [4 ]
Vasquez T, Patricia [8 ]
Leon C, Eugenia P. [1 ]
Perez C, Carlos [1 ]
Wozniak B, Aniela [5 ]
机构
[1] Pontificia Univ Catolica Chile, Dept Lab Clin, Microbiol Lab, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Unidad Docente Apoyo Dermatol, Santiago, Chile
[3] Pontificia Univ Catolica Chile, Div Ginecol & Obstet, Santiago, Chile
[4] Pontificia Univ Catolica Chile, Mol Biol Lab, Santiago, Chile
[5] Pontificia Univ Catolica Chile, Dept Med Interna, Santiago, Chile
[6] Pontificia Univ Catolica Chile, Escuela Med, Santiago, Chile
[7] Hosp San Juan Dios, Serv Neurol, Santiago, Chile
[8] Hosp San Juan Dios, Unidad Infectol, Santiago, Chile
[9] Hosp Sotero Del Rio, Serv Dermatol, Santiago, Chile
来源
REVISTA CHILENA DE INFECTOLOGIA | 2011年 / 28卷 / 04期
关键词
Treponema pallidum; syphilis; polymerase chain reaction; diagnosis; CLINICAL SPECIMENS; FLUID;
D O I
10.4067/S0716-10182011000500002
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Syphilis is a sexually transmitted disease caused by Treponema pallidum. The diagnosis is based mainly in clinical presentation and non-specific assays. PCR-based diagnosis has been suggested as an attractive alternative method. The aim of this study was the validation of a PCR-based test for the diagnosis of early syphilis (ES) and neurosyphilis (NS). Clinical samples of mucocutaneous lesions and cerebrospinal fluid (CSF) specimens from patients previously diagnosed for ES and NS respectively using an enlarged gold standard, were tested by PCR. The reaction was done using primers targeting the tpN47gene. Twenty out of 21 mucocutaneous samples from patients diagnosed with ES were positive by PCR, with a clinical sensitivity of 95%. Four out of 8 CSF samples from patients previously diagnosed with NS were positive by PCR, with a clinical sensitivity of 50%. The clinical specificity for both ES and NS was 100%. The PCR sensitivity and specificity for mucocutaneous samples allowed us to implement this assay in our laboratory for routine diagnosis. Although the sensitivity of the PCR in CSF was low, it may be useful to support clinical diagnosis.
引用
收藏
页码:310 / 315
页数:6
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