Discrimination between Mycoplasma mycoides subsp. capri and Mycoplasma capricolum subsp. capricolum using PCR-RFLP and PCR

Vet J. 2015 Sep;205(3):421-3. doi: 10.1016/j.tvjl.2015.05.013. Epub 2015 May 21.

Abstract

In this study, the dihydrolipoyl dehydrogenase (lpdA) gene was used to distinguish Mycoplasma mycoides subsp. capri (Mmc) from Mycoplasma capricolum subsp. capricolum (Mcc), two of four Mycoplasma species that cause contagious agalactia in sheep and goats. After alignment of nucleotide sequences of both species, specific primer sets were designed from unchanging and variable gene segments. The first primer set LPD-C1-F/LPD-C1-R was used to amplify a 911 bp fragment that was subsequently co-digested with FastDigest PstI, SspI, EcoRI and ClaI enzymes. The PCR-RFLP profiles differentiated the two mycoplasma species. The second primer set was used to distinguish Mmc from Mcc by single tube PCR. Both methods were further applied to identify 54 isolates collected from dairy herds from different provinces in Sardinia. The results of this study showed that PCR-RFLP and PCR could be used in routine diagnosis for rapid and specific simultaneous discrimination of Mmc and Mcc.

Keywords: Contagious agalactia; Dihydrolipoyl dehydrogenase; Mycoplasma capricolum subsp. capricolum; Mycoplasma mycoides subsp. capri; PCR; PCR-RFLP.

Publication types

  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cattle
  • Cattle Diseases / microbiology
  • Genes, Bacterial
  • Mycoplasma / classification
  • Mycoplasma / genetics
  • Mycoplasma Infections / microbiology
  • Mycoplasma Infections / veterinary
  • Mycoplasma capricolum / classification*
  • Mycoplasma capricolum / genetics
  • Mycoplasma mycoides / classification*
  • Mycoplasma mycoides / genetics
  • Polymerase Chain Reaction / veterinary*
  • Polymorphism, Restriction Fragment Length*
  • Species Specificity