Chalker Victoria J, Jordan Karen, Ali Tahir, Ison Cathy
Sexually Transmitted Bacteria Reference Laboratory, Health Protection Agency Centre for Infections, 61 Colindale Avenue, London NW9 5EQ, UK.
Microbiology Laboratory, Northampton General Hospital Trust, Billing Road, Northampton NN1 5BD, UK.
J Med Microbiol. 2009 Jul;58(Pt 7):895-899. doi: 10.1099/jmm.0.009977-0. Epub 2009 Jun 5.
Real-time PCR was employed to detect a region of the Mycoplasma genitalium mg219 gene, a gene of unknown function, in clinical samples. Amplification of DNA and signal production from 15 other species of human mycoplasmas and 14 other bacteria and viruses did not occur. Using a panel of 208 genital and rectal samples, the sensitivity when compared to the modified mgpa gene (encoding the major surface protein MgPa) real-time PCR assay was found to be 100% and the specificity of the assay 99.5% with a positive predictive value of 80% and a negative predictive value of 100%. The mg219 gene was found to be in all strains of M. genitalium and was highly conserved. M. genitalium was detected in 3.9% (11/280, 95% CI 2.1-6.9) of all male specimens, in 7.7% (10/130, 95% CI 4.1-13.7) of patients with non-gonococcal urethritis (NGU) and in 0.7% (1/150, 95% CI <0.01-4.1) of patients without urethritis. The presence of M. genitalium was significantly associated with NGU (P < or =0.01; 95% Cl 0.88-0.98) and non-chlamydial-non-gonococcal urethritis (P=0.0005; 95% Cl 0.84-0.97).
采用实时荧光定量聚合酶链反应(Real-time PCR)检测临床样本中生殖支原体mg219基因的一个区域,该基因功能未知。对另外15种人型支原体以及14种其他细菌和病毒的DNA进行扩增及信号检测均未成功。使用208份生殖器和直肠样本组成的样本组,与改良的mgpa基因(编码主要表面蛋白MgPa)实时荧光定量聚合酶链反应检测法相比,该检测法的灵敏度为100%,特异性为99.5%,阳性预测值为80%,阴性预测值为100%。发现mg219基因存在于所有生殖支原体菌株中,且高度保守。在所有男性样本中,生殖支原体的检出率为3.9%(11/280,95%可信区间2.1 - 6.9);在非淋菌性尿道炎(NGU)患者中为7.7%(10/130,95%可信区间4.1 - 13.7);在无尿道炎患者中为0.7%(1/150,95%可信区间<0.01 - 4.1)。生殖支原体的存在与非淋菌性尿道炎(P≤0.01;95%可信区间0.88 - 0.98)以及非衣原体非淋菌性尿道炎(P = 0.0005;95%可信区间0.84 - 0.97)显著相关。