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JAC Advance Access originally published online on August 27, 2009
Journal of Antimicrobial Chemotherapy 2009 64(4):684-693; doi:10.1093/jac/dkp285
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© The Author 2009. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy.
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.


Original research

Population dynamics of methicillin-susceptible and -resistant Staphylococcus aureus in remote communities

F. G. O'Brien1,*, G. W. Coombs1,2, J. W. Pearman1,2, M. Gracey3, F. Moss4, K. J. Christiansen1,2 and W. B. Grubb1

1 Gram-positive Bacteria Typing and Research Unit, Curtin University of Technology, School of Biomedical Sciences, Perth, Western Australia 2 Gram-positive Bacteria Typing and Research Unit, PathWest Laboratory Medicine-WA, Department of Microbiology and Infectious Disease, Royal Perth Hospital, Perth, Western Australia 3 Health Department of Western Australia, Office of Aboriginal Health, Perth, Western Australia 4 Health Department of Western Australia, West Geraldton, Western Australia

Received 7 April 2009; returned 14 May 2009; revised 13 July 2009; accepted 14 July 2009


* Corresponding author. Tel: +61-8-9224-0302; Fax: +61-8-9266-2342; E-mail: f.g.obrien{at}curtin.edu.au

Objectives: Community-associated methicillin-resistant Staphylococcus aureus (CA-MRSA) was first reported in remote regions of Western Australia (WA) in 1992 and is now the predominant MRSA isolated in the State. To gain insights into the emergence of CA-MRSA, 2146 people living in 11 remote WA communities were screened for colonization with S. aureus.

Methods: Antibiogram analysis, contour-clamped homogeneous electric field electrophoresis, multilocus sequence typing, Panton–Valentine leucocidin determinant detection and accessory genetic regulator typing were performed to characterize the isolates. MRSA was further characterized by staphylococcal cassette chromosome mec typing.

Results: The S. aureus population consisted of 13 clonal complexes and two Singleton lineages together with 56 sporadic isolates. Five lineages contained MRSA; however, these were not the predominant methicillin-susceptible S. aureus (MSSA) lineages. There was greater diversity amongst the MSSA while the MRSA appeared to have emerged clonally following acquisition of the staphylococcal cassette chromosome mec. Three MRSA lineages were considered to have been endemic in the communities and have subsequently become predominant lineages of CA-MRSA in the wider WA community. People colonized with MSSA tended to harbour clones of a different genetic lineage at each anatomical site while people colonized with MRSA tended to harbour clones of the same lineage at each site. Overall, the isolates were resistant to few antimicrobials.

Conclusions: Although the evidence suggests that in WA CA-MRSA strains arose in remote communities and have now disseminated into the wider community, there is no evidence that they arose from the predominant MSSA clones in these communities.

Keywords: S. aureus , community methicillin-resistant Staphylococcus aureus , population structure , colonization


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