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. 2014 Mar 24:14:160.
doi: 10.1186/1471-2334-14-160.

The clinical and molecular epidemiology of Staphylococcus aureus infections in Fiji

Affiliations

The clinical and molecular epidemiology of Staphylococcus aureus infections in Fiji

Adam Jenney et al. BMC Infect Dis. .

Abstract

Background: There are few data describing the microbiology and genetic typing of Staphylococcus aureus that cause infections in developing countries.

Methods: In this study we observed S. aureus infections in Pacific Island nation of Fiji in both the community and hospital setting with an emphasis on clonal complex (CC) genotyping and antimicrobial susceptibility.

Results: S. aureus was commonly found in impetigo lesions of school children and was recovered from 57% of impetigo lesions frequently in conjunction with group A streptococcal infection. Methicillin-resistant S. aureus (MRSA) comprised 7% (20/299) of isolates and were all non-multi-resistant and all genotyped as CC1. In contrast, there was a diverse selection of 17 CCs among the 105 genotyped methicillin-susceptible S.aureus (MSSA) strains. Isolates of the rare, phylogenetically divergent and non-pigmented CC75 lineage (also called S. argenteus) were found in Fiji.From hospitalized patients the available 36 MRSA isolates from a 9-month period were represented by five CCs. The most common CCs were CC1 and CC239. CC1 is likely to be a community-acquired strain, reflecting what was found in the school children, whereas the CC239 is the very successful multi-drug resistant MRSA nosocomial lineage. Of 17 MSSA isolates, 59% carried genes for Panton-Valentine leukocidin. The S. aureus bacteraemia incidence rate of 50 per 100,000 population is among the highest reported in the literature and likely reflects the high overall burden of staphylococcal infections in this population.

Conclusions: S. aureus is an important cause of disease in Fiji and there is considerable genotypic diversity in community skin infections in Fijian schoolchildren. Community acquired- (CA)- MRSA is present at a relatively low prevalence (6.7%) and was solely to CC1 (CA-MRSA). The globally successful CC239 is also a significant pathogen in Fiji.

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Figures

Figure 1
Figure 1
Clonal complex types of S.aureus isolated from Fijian schoolchildren’s impetigo lesions. Clonal complexes identified from SNP-typing of Staphylococcus aureus isolates collected from impetigo lesions in school children in Fiji (MSSA: methicillin sensitive Staphylococcus aureus; nmMRSA: non–multidrug-resistant methicillin resistant Staphylococcus aureus; PVL: Panton Valentine Leukocidin).
Figure 2
Figure 2
Clonal complex types of S.aureus isolated from patients at CWMH, Fiji. Clonal complexes identified from SNP typing of Staphylococcus aureus isolates collected from the Colonial War Memorial Hospital, Fiji (MSSA: methicillin sensitive Staphylococcus aureus; nmMRSA: non–multidrug-resistant methicillin resistant Staphylococcus aureus; mMRSA: multidrug-resistant MRSA; PVL: Panton Valentine Leukocidin).
Figure 3
Figure 3
Annualised incidence of S.aureus bacteraemia at CWMH, Fiji. Number of cases and annualised incidence of cases where Staphylococcus aureus was cultured from blood at the Colonial War Memorial Hospital, Central Division, Fiji, May 2006 – September 2007 showing a predominance of cases amongst the iTaukei (Indigenous Fijian) population.

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