Luki N, Lebel P, Boucher M, Doray B, Turgeon J, Brousseau R
Environmental Genetics Group, Biotechnology Research Institute, Montreal, Quebec, Canada.
Eur J Clin Microbiol Infect Dis. 1998 Apr;17(4):255-63. doi: 10.1007/BF01699982.
The polymerase chain reaction (PCR) technique was compared with culture for the detection of Ureaplasma urealyticum, Mycoplasma hominis, and Mycoplasma genitalium in clinical samples (vaginal secretions, throat and endotracheal secretions, and skin swabs) obtained from 47 high-risk pregnant women peripartum and eight newborn infants. Detection using PCR with homologous primers was highly specific, as a product with the expected length was consistently amplified with homologous but not with heterologous species. The limit of detection of the PCR assay was 10 color-changing units (CCU) of Mycoplasma strains. The PCR technique facilitated detection of Ureaplasma urealyticum DNA in 31 of 55 patients studied, of Mycoplasma hominis in seven samples, and of Mycoplasma genitalium in two samples. Four PCR-positive patients yielded culture-negative results. In one case a culture-positive sample was negative by PCR. The results show that PCR is a valuable tool for rapid detection of genital mycoplasmas in clinical samples. It is fast, sensitive, specific, and easy to perform, requiring minimal preparation of the clinical sample.
采用聚合酶链反应(PCR)技术与培养法对47名高危孕妇围产期及8名新生儿的临床样本(阴道分泌物、咽喉及气管分泌物、皮肤拭子)中的解脲脲原体、人型支原体和生殖支原体进行检测并比较。使用同源引物进行PCR检测具有高度特异性,因为预期长度的产物始终能在同源而非异源菌种中扩增出来。PCR检测方法的检测限为支原体菌株的10个颜色变化单位(CCU)。PCR技术有助于在所研究的55名患者中的31名检测到解脲脲原体DNA,7份样本中检测到人型支原体,2份样本中检测到生殖支原体。4例PCR阳性患者培养结果为阴性。1例培养阳性样本PCR检测为阴性。结果表明,PCR是临床样本中快速检测生殖支原体的有价值工具。它快速、灵敏、特异且易于操作,临床样本的预处理要求极低。