Grattard F, Pozzetto B, de Barbeyrac B, Renaudin H, Clerc M, Gaudin O G, Bébéar C
Laboratoire de Bactériologie-Virologie, Université de Saint-Etienne, France.
Mol Cell Probes. 1995 Dec;9(6):383-9. doi: 10.1006/mcpr.1995.0060.
Fourteen serotypes are currently recognized in the Ureaplasma urealyticum species. These serotypes have been divided into two genomic clusters or biovars by a large number of typing methods. The parvo-biovar includes strains of serotypes 1, 3, 6 and 14 and the T960-biovar, strains belonging to the ten other serotypes. In this study, arbitrarily primed polymerase chain reaction (AP-PCR) has been applied to the analysis of reference strains of the 14 U. urealyticum serotypes. By using two different sets of 10-mer oligonucleotide primers, the method allowed the clear differentiation between the two known biovars of the species. However, further differentiation within a same biovar was only achieved for a few standard strains of the T960-biovar analysed by using a pairwise combination of primers. The reproducibility of AP-PCR profiles was shown on strains tested after repeated subcultures and with different thermal cyclers. Additional experiments were performed on forty isolates of U. urealyticum recovered from subjects of various origins. They confirmed that AP-PCR was able to identify the strains at the biovar level. With reference to the other typing methods, AP-PCR is easy to perform and can be applied to large numbers of strains for epidemiological purposes.
目前在解脲脲原体物种中已识别出14种血清型。通过大量分型方法,这些血清型已被分为两个基因组簇或生物变种。细小生物变种包括血清型1、3、6和14的菌株,而T960生物变种则包括属于其他十种血清型的菌株。在本研究中,任意引物聚合酶链反应(AP-PCR)已应用于分析14种解脲脲原体血清型的参考菌株。通过使用两组不同的10聚体寡核苷酸引物,该方法能够清晰地区分该物种的两个已知生物变种。然而,仅通过使用引物的成对组合对T960生物变种的少数标准菌株进行分析,才实现了同一生物变种内的进一步区分。在重复传代培养后测试的菌株以及使用不同热循环仪测试的菌株上,显示了AP-PCR图谱的可重复性。对从不同来源的受试者中分离出的40株解脲脲原体进行了额外实验。这些实验证实,AP-PCR能够在生物变种水平上鉴定菌株。与其他分型方法相比,AP-PCR易于操作,可用于大量菌株的流行病学研究。