Author:
DHAWAN B.,RAO C.,UDO E. E.,GADEPALLI R.,VISHNUBHATLA S.,KAPIL A.
Abstract
SUMMARYTwo-hundred MRSA strains from inpatients with healthcare-associated (HA) and 100 MRSA strains from outpatients with community-associated (CA) skin and soft tissue infections (SSTIs) were tested for antimicrobial susceptibility, staphylococcal cassette chromosome mec (SCCmec) typing, Panton–Valentine leucocidin (PVL) toxin,sehandarcAgenes. Based on SCCmectyping, HA-MRSA isolates were further divided into HA-SCCmecI/II/III MRSA and HA-SCCmecIV/V MRSA, and CA-MRSA isolates into CA-SCCmecI/II/III MRSA and CA-SCCmecIV/V MRSA. SCCmectypes were further characterized by pulsed-field gel electrophoresis,spatyping and multi-locus sequence typing. Seventy-five (37·5%) HA-MRSA isolates and 83/100 CA-MRSA isolates were SCCmecIV/V genotype. HA-SCCmecIV/V MRSA was associated with malignancy (P = 0·03) and bone fractures (P = 0·02) compared to CA-SCCmecIV/V MRSA. HA-SCCmecIV/V MRSA was associated with PVL gene carriage compared to HA-SCCmecI/II/III MRSA (P < 0·001). ST22-MRSA-IV (EMRSA-15), ST772-MRSA-V, and ST36-MRSA-IV and ST239:EMRSA-I:III were the major clones identified. Our study documents the emergence of SCCmecIV and SCCmecV MRSA clones in an Indian hospital.
Publisher
Cambridge University Press (CUP)
Subject
Infectious Diseases,Epidemiology
Cited by
44 articles.
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