Subramaniam S, Bergonier D, Poumarat F, Capaul S, Schlatter Y, Nicolet J, Frey J
Institute for Veterinary Bacteriology, University of Berne, Switzerland.
Mol Cell Probes. 1998 Jun;12(3):161-9. doi: 10.1006/mcpr.1998.0160.
The DNA repair genes uvrC from Mycoplasma bovis and Mycoplasma agalactiae type strains were cloned and their nucleotide sequences were established. These sequences were used to design polymerase chain reaction (PCR) primer pairs for M. bovis and M. agalactiae. Each primer pair amplified a 1-6 kb fragment of the uvrC gene in the respective species. The specificity of the primer pairs for the two species was demonstrated through the lack of cross-amplifications in heterologous PCR reactions and in reactions using DNA from other mycoplasma species. Subsequent restriction enzyme analysis of the amplified uvrC gene segments from type and field strains of M. bovis and M. agalactiae showed that the uvrC genes are well conserved in both species but differ significantly between the two species. The diagnostic PCR assay enabled unambiguous identification of M. bovis and M. agalactiae strains isolated from geographically diverse places, even in cases where 16S rRNA gene sequence analysis was unable to discriminate between the two species.
克隆了来自牛支原体和无乳支原体模式菌株的DNA修复基因uvrC,并确定了它们的核苷酸序列。这些序列被用于设计针对牛支原体和无乳支原体的聚合酶链反应(PCR)引物对。每对引物在各自物种中扩增出一段1 - 6 kb的uvrC基因片段。通过在异源PCR反应以及使用其他支原体物种DNA的反应中缺乏交叉扩增,证明了这两对引物对这两个物种的特异性。随后对来自牛支原体和无乳支原体模式菌株及田间菌株的扩增uvrC基因片段进行限制性酶切分析,结果表明uvrC基因在这两个物种中都高度保守,但两个物种之间存在显著差异。这种诊断性PCR检测方法能够明确鉴定从不同地理位置分离出的牛支原体和无乳支原体菌株,即使在16S rRNA基因序列分析无法区分这两个物种的情况下也是如此。