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

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.

Publication types

  • Evaluation Study

MeSH terms

  • DNA, Bacterial / analysis
  • Genes, rRNA*
  • Humans
  • Male
  • Mycoplasma / genetics
  • Mycoplasma / isolation & purification*
  • Mycoplasma / pathogenicity
  • Mycoplasma Infections / microbiology
  • Phylogeny
  • Polymerase Chain Reaction / methods*
  • RNA, Ribosomal, 16S / genetics
  • Taq Polymerase / metabolism
  • Urethritis / microbiology*
  • Urine / microbiology*

Substances

  • DNA, Bacterial
  • RNA, Ribosomal, 16S
  • Taq Polymerase