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Volume 65, Issue 4, Pages 351-357 (December 2009)

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Panton–Valentine leukocidin (PVL)-positive methicillin-susceptible and resistant Staphylococcus aureus in Taiwan: identification of oxacillin-susceptible mecA-positive methicillin-resistant S. aureus

Feng-Jui Chena, Keiichi Hiramatsub, I-Wen Huanga, Chen-Her Wanga, Tsai-Ling Yang LauderdaleaCorresponding Author Informationemail address

Received 10 May 2009; accepted 30 July 2009. published online 22 September 2009.

Abstract 

Methicillin-resistant Staphylococcus aureus (MRSA) arises when methicillin-susceptible S. aureus (MSSA) acquires the staphylococcal cassette chromosome mec (SCCmec). Most pvl-positive MRSA in Taiwan belong to ST59 lineage and carry SCCmec V. The genetic profiles of 51 MSSA were compared with those of 80 MRSA from the same hospitals. Nine pvl-positive MSSA (oxacillin MIC ≤2 μg/mL) shared >80% similarity in pulsed field gel electrophoresis pattern with 17 pvl-positive SCCmec V MRSA. Further investigation found that 5 of these 9 isolates were MRSA by cefoxitin and carried SCCmec V. All 26 pvl-positive isolates had very similar genetic profile (ST59, protein A clonal complex [spa-CC] c2:441/437, and agr group I). The success of the ST59:SCCmec V MRSA may be due in part to its heterogeneous and borderline resistance to methicillin, which may be missed by testing only oxacillin, with subsequent exposure to β-lactams causing the emergence of more resistant subpopulations.

a Division of Infectious Diseases, National Health Research Institutes, Zhunan Town, Miaoli County 350, Taiwan, ROC

b Department of Bacteriology, School of Medicine, Juntendo University, Tokyo 113-8421, Japan

Corresponding Author InformationCorresponding author. Tel.: +1-886-37-246-166; fax: +1-886-37-586-457.

 Part of the results of the MRSA used for comparison with MSSA in the present study has been previously published. These are clearly stated and referenced (Emerg Infect Dis 11[2005]1761–1763) at appropriate places in the manuscript.

PII: S0732-8893(09)00330-7

doi:10.1016/j.diagmicrobio.2009.07.024

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