Department of Urology of Tangdu Hospital, The Fourth Military Medical University, Xian 710032, China.
J Biotechnol. 2010 Oct 1;150(1):41-3. doi: 10.1016/j.jbiotec.2010.07.024. Epub 2010 Jul 29.
A simple and practical method for simultaneous detection of Ureaplasma urealyticum (U. urealyticum), Ureaplasma parvum (U. parvum), Mycoplasma hominis (M. hominis) and Mycoplasma genitalium (M. genitalium) by fluorescence polarization (FP) assay has been developed. DNA of the 16S rRNA gene of U. urealyticum, U. parvum, M. genitalium and M. hominis was amplified using a forward primer and two reverse primers in an asymmetric PCR. Four probes labeled with different fluorophores were specific for U. urealyticum, U. parvum, M. hominis and M. genitalium, respectively. The probes hybridized with their target PCR products, and the hybridization increased the fluorescence polarization (FP) values. The pathogens were identified by the increased FP values. DNA extracted from 757 urethral samples was detected by the FP assay and the sequence method. The FP assay could detect co-infection more effectively than the sequence method did. The method presented in this study was expected to be extremely useful in clinic.
建立了一种荧光偏振(FP)检测法,可同时检测解脲脲原体(U. urealyticum)、微小脲原体(U. parvum)、人型支原体(M. hominis)和生殖支原体(M. genitalium)。采用不对称 PCR 技术,用正向引物和两个反向引物扩增 16S rRNA 基因的 DNA。四种探针分别用不同的荧光染料标记,特异性地针对 U. urealyticum、U. parvum、M. hominis 和 M. genitalium。探针与目标 PCR 产物杂交,增加荧光偏振(FP)值。通过增加的 FP 值来鉴定病原体。用 FP 检测法和序列法检测了 757 例尿道样本中的 DNA。FP 检测法比序列法更能有效地检测混合感染。本研究提出的方法有望在临床上非常有用。