Author
Listed:
- Patiyan Andersson
(Menzies School of Health Research, Charles Darwin University)
- Simon R. Harris
(Pathogen Variation Programme, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus)
- Helena M. B. Seth Smith
(Pathogen Variation Programme, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus
Functional Genomics Centre Zürich, University of Zurich
Institute for Veterinary Pathology, Vetsuisse Faculty, University of Zurich)
- James Hadfield
(Pathogen Variation Programme, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus)
- Colette O’Neill
(Molecular Microbiology Group, University Medical School, Southampton General Hospital)
- Lesley T. Cutcliffe
(Molecular Microbiology Group, University Medical School, Southampton General Hospital)
- Fiona P. Douglas
(Menzies School of Health Research, Charles Darwin University)
- L. Valerie Asche
(Menzies School of Health Research, Charles Darwin University)
- John D. Mathews
(Menzies School of Health Research, Charles Darwin University
School of Population and Global Health, University of Melbourne)
- Susan I. Hutton
(Menzies School of Health Research, Charles Darwin University)
- Derek S. Sarovich
(Menzies School of Health Research, Charles Darwin University)
- Steven Y. C. Tong
(Menzies School of Health Research, Charles Darwin University)
- Ian N. Clarke
(Molecular Microbiology Group, University Medical School, Southampton General Hospital)
- Nicholas R. Thomson
(Pathogen Variation Programme, The Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus
London School of Hygiene and Tropical Medicine)
- Philip M. Giffard
(Menzies School of Health Research, Charles Darwin University
School of Psychological and Clinical Sciences, Charles Darwin University)
Abstract
Chlamydia trachomatis causes sexually transmitted infections and the blinding disease trachoma. Current data on C. trachomatis phylogeny show that there is only a single trachoma-causing clade, which is distinct from the lineages causing urogenital tract (UGT) and lymphogranuloma venerum diseases. Here we report the whole-genome sequences of ocular C. trachomatis isolates obtained from young children with clinical signs of trachoma in a trachoma endemic region of northern Australia. The isolates form two lineages that fall outside the classical trachoma lineage, instead being placed within UGT clades of the C. trachomatis phylogenetic tree. The Australian trachoma isolates appear to be recombinants with UGT C. trachomatis genome backbones, in which loci that encode immunodominant surface proteins (ompA and pmpEFGH) have been replaced by those characteristic of classical ocular isolates. This suggests that ocular tropism and association with trachoma are functionally associated with some sequence variants of ompA and pmpEFGH.
Suggested Citation
Patiyan Andersson & Simon R. Harris & Helena M. B. Seth Smith & James Hadfield & Colette O’Neill & Lesley T. Cutcliffe & Fiona P. Douglas & L. Valerie Asche & John D. Mathews & Susan I. Hutton & Derek, 2016.
"Chlamydia trachomatis from Australian Aboriginal people with trachoma are polyphyletic composed of multiple distinctive lineages,"
Nature Communications, Nature, vol. 7(1), pages 1-11, April.
Handle:
RePEc:nat:natcom:v:7:y:2016:i:1:d:10.1038_ncomms10688
DOI: 10.1038/ncomms10688
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