Differential identification of Chlamydophila abortus live vaccine strain 1B and C. abortus field isolates by PCR-RFLP

Vaccine. 2010 Aug 9;28(35):5653-6. doi: 10.1016/j.vaccine.2010.06.064. Epub 2010 Jun 29.

Abstract

Comparative genomic analysis of a wild-type strain of the ovine pathogen Chlamydophila abortus and its nitrosoguanidine-induced, temperature-sensitive and virulence-attenuated live vaccine derivative identified point mutations unique to the mutant (Burall et al. [1]). Here, we evaluate the capacity of some of these mutations to either create or eliminate restriction sites using the wild-type strain C. abortus S26/3 as a reference. Three of eight genomic sites with confirmed point mutations (CAB153, CAB636 and CAB648) were retained for analysis as each resulted in the loss of a restriction site in the genome sequence of the vaccine strain. PCR-restriction fragment length polymorphism analysis using restriction enzymes chosen to specifically target the three genomic sites was then applied to a large number of C. abortus field isolates and reference strains. Our results indicate that the three mutations are uniquely present in the vaccine strain, and as such provide easy-to-use markers for the differential identification of the vaccine strain and wild-type isolates.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Typing Techniques
  • Bacterial Vaccines / microbiology
  • Chlamydophila / classification
  • Chlamydophila / genetics*
  • Chlamydophila / isolation & purification
  • Comparative Genomic Hybridization*
  • DNA, Bacterial / genetics
  • Point Mutation
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length*

Substances

  • Bacterial Vaccines
  • DNA, Bacterial