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通过实时聚合酶链反应对尿道炎男性和无症状男性的首段尿液进行生殖支原体定量检测。

Quantitative detection of Mycoplasma genitalium from first-pass urine of men with urethritis and asymptomatic men by real-time PCR.

作者信息

Yoshida Takashi, Deguchi Takashi, Ito Masayasu, Maeda Shin-Ichi, Tamaki Masayoshi, Ishiko Hiroaki

机构信息

Research and Development Department, Mitsubishi Kagaku Bio-Clinical Laboratories, Inc., Tokyo 174-8555, Japan.

出版信息

J Clin Microbiol. 2002 Apr;40(4):1451-5. doi: 10.1128/JCM.40.4.1451-1455.2002.

Abstract

We developed a TaqMan-based real-time PCR assay for quantifying Mycoplasma genitalium. This assay is able to specifically quantify concentrations of the M. genitalium 16S rRNA gene ranging from 10(7) to 10 copies/reaction. Using the TaqMan assay, we quantified the M. genitalium 16S rRNA gene in first-pass urine of men with urethritis and asymptomatic men who were positive for M. genitalium by PCR- and phylogeny-based assay. Of 130 men with gonococcal urethritis (GU), five were positive for M. genitalium. The mycoplasma load for each specimen was <5 x 10 copies/ml. Of 84 men with chlamydial non-GU (CNGU), seven were positive for M. genitalium. One man had an M. genitalium load of <5 x 10 copies/ml, and six men had loads ranging from 1.1 x 10(7) to 2.7 x 10(2) copies/ml. Of 86 men with nonchlamydial NGU (NCNGU), 17 were positive for M. genitalium. The mycoplasma loads for these men ranged from 3.3 x 10(6) to 2.3 x 10(2) copies/ml. Of 76 asymptomatic men, only two were positive for M. genitalium. For these men, the loads were 2 x 10(2) and <5 x 10 copies/ml. The patients with NGU had significantly higher concentrations of M. genitalium in their first-pass urine than did men with GU (P < 0.01) or asymptomatic men (P < 0.05). In addition, M. genitalium loads were significantly higher in men with NCNGU than those in asymptomatic men (P < 0.05). The quantitative assessment of M. genitalium loads by the TaqMan assay will provide useful information for understanding the pathogenicity of this mycoplasma in the urogenital tract.

摘要

我们开发了一种基于TaqMan的实时PCR检测方法来定量检测生殖支原体。该检测方法能够特异性地定量生殖支原体16S rRNA基因的浓度,范围为10(7)至10拷贝/反应。使用TaqMan检测方法,我们对尿道炎男性和通过基于PCR和系统发育分析检测为生殖支原体阳性的无症状男性的首段尿液中的生殖支原体16S rRNA基因进行了定量。在130例淋菌性尿道炎(GU)男性中,5例生殖支原体呈阳性。每个标本的支原体载量<5×10拷贝/毫升。在84例衣原体非淋菌性尿道炎(CNGU)男性中,7例生殖支原体呈阳性。1例男性的生殖支原体载量<5×10拷贝/毫升,6例男性的载量范围为1.1×10(7)至2.7×10(2)拷贝/毫升。在86例非衣原体非淋菌性尿道炎(NCNGU)男性中,17例生殖支原体呈阳性。这些男性的支原体载量范围为3.3×10(6)至2.3×10(2)拷贝/毫升。在76例无症状男性中,只有2例生殖支原体呈阳性。对于这些男性,载量分别为2×10(2)和<5×10拷贝/毫升。NGU患者首段尿液中的生殖支原体浓度显著高于GU患者(P<0.01)或无症状男性(P<0.05)。此外,NCNGU男性的生殖支原体载量显著高于无症状男性(P<0.05)。通过TaqMan检测方法对生殖支原体载量进行定量评估将为了解该支原体在泌尿生殖道中的致病性提供有用信息。

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本文引用的文献

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Update on sexually transmitted mycoplasmas.性传播支原体的最新进展。
Lancet. 1998;351 Suppl 3:12-5. doi: 10.1016/s0140-6736(98)90004-6.

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