Literature DB >> 9664578

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

S Subramaniam1, D Bergonier, F Poumarat, S Capaul, Y Schlatter, J Nicolet, J Frey.   

Abstract

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.

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Year:  1998        PMID: 9664578     DOI: 10.1006/mcpr.1998.0160

Source DB:  PubMed          Journal:  Mol Cell Probes        ISSN: 0890-8508            Impact factor:   2.365


  23 in total

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9.  First steps towards the genetic manipulation of Mycoplasma agalactiae and Mycoplasma bovis using the transposon Tn4001mod.

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10.  VNTR analysis reveals unexpected genetic diversity within Mycoplasma agalactiae, the main causative agent of contagious agalactia.

Authors:  Laura McAuliffe; Colin P Churchward; Joanna R Lawes; Guido Loria; Roger D Ayling; Robin Aj Nicholas
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