Genetic differences in Chlamydia pecorum between neighbouring sub-populations of koalas (Phascolarctos cinereus).

Vet Microbiol

Sydney School of Veterinary Science, The University of Sydney, Sydney, 2006, NSW, Australia; Marie Bashir Institute for Emerging Infectious diseases and Biosecurity, The University of Sydney, 176 Hawkesbury road, 2145, Westmead, NSW, Australia. Electronic address:

Published: April 2019

AI Article Synopsis

  • - Chlamydiosis, caused by Chlamydia pecorum, poses a significant threat to koala populations, with the severity of infection varying across different geographical areas due to strain diversity and pathogenicity.
  • - A study conducted on koalas in Liverpool Plains, NSW, utilized Multi-Locus Sequence Typing (MLST) to analyze genetic diversity and found a strong link between sequence type ST 69 and clinical disease, though this type was also seen in subclinical cases.
  • - The research highlights that sequence variations such as ST 73 and ST 69 are found in koalas across various regions, suggesting multiple introductions of strains and limitations of MLST in determining the relationship between pathogen types and disease severity.

Article Abstract

Chlamydiosis, caused by Chlamydia pecorum, is regarded as an important threat to koala populations. Across the koala's geographical range, disease severity associated with C. pecorum infection varies, with pathogen diversity and strain pathogenicity being likely important factors. To examine C. pecorum diversity on a sub-population level a Multi-Locus Sequence Typing (MLST) scheme, containing the housekeeping genes; gatA, oppA_3, hflX, gidA, enoA, hemN and fumC, was used to type strains from two sub-populations of koalas from the Liverpool Plains, NSW, Australia, with different disease expressions. Typing of samples from 2015 to 2017, revealed a significant association between sequence type ST 69 and clinical disease and a significant difference in sequence type frequencies between sub-populations. Sequence type ST 69 has previously been identified in both subclinical and clinically diseased koalas indicating that these markers alone are not illustrative of pathogenicity. However, recent emergence of this sequence type in a naïve population may explain the differing disease expressions. Sequence types ST 73 and ST 69 have been described in koalas across a broad geographic range, indicating multiple introduction events and/or a limited veracity of the MLST loci to explore fine scale epidemiological investigations, particularly those examining the interface between pathogenic strain and disease outcome.

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Source
http://dx.doi.org/10.1016/j.vetmic.2019.02.020DOI Listing

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