Species identification of Mycoplasma bovis and Mycoplasma agalactiae based on the uvrC genes by PCR

被引:138
作者
Subramaniam, S
Bergonier, D
Poumarat, F
Capaul, S
Schlatter, Y
Nicolet, J
Frey, J
机构
[1] Univ Berne, Inst Vet Bacteriol, CH-3012 Bern, Switzerland
[2] Ecole Natl Vet, Dept Elevage & Prod, F-31076 Toulouse, France
[3] CNEVA, Lab Pathol Bovine, F-69342 Lyon, France
关键词
DNA repair; agalactia; diagnosis; genetic differentiation; taxonomy;
D O I
10.1006/mcpr.1998.0160
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 1998 Academic Press.
引用
收藏
页码:161 / 169
页数:9
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