ISSN: 0973-7510

E-ISSN: 2581-690X

G.K. Mangala1 , P.N.S. Rao1, G. Vishwanath1, K. Suresh1 and V. Vijayanath2
1Department of Microbiology, JJM Medical College, Davangere, India.
2Department of Forensic Medicine & Toxicology S.S.Institute of Medical Sciences & Research Centre, Davangere, India.
J Pure Appl Microbiol. 2012;6(1):407-410
© The Author(s). 2012
Received: 20/03/2011 | Accepted: 09/05/2011 | Published: 31/03/2012
Abstract

Staphylococcus aureus, a common pathogen is well known for its multidrug resistance. Existence of MRSA is further worsened by inducible clindamycin resistance and emerging glycopeptide resistance. Our aim of the study was to detect inducible clindamycin resistance, vancomycin resistance and mupirocin resistance among MRSA isolates.
One hundred non-repetitive isolates were subjected to routine antibiotic susceptibility testing by Kirby Bauer’s disc diffusion method including cefoxitin disc for MRSA.  Inducible clindamycin resistance was detected by D-test, E-test for vancomycin MIC and mupirocin resistance by disc diffusion. Twenty three isolates showed inducible clindamycin resistance, one showed constitutive resistance and three showed MS phenotypes. Inducible clindamycin resistance, constitutive resistance and MS phenotype were found to be higher in MRSA as compared to MSSA. Only one isolate with vancomycin MIC 4µg/ml by E-test was considered as VISA. Forty one isolates were found resistant to mupirocin, which is a cause for concern. Study showed that D-test should be included as routine disc diffusion test to prevent therapeutic failure with clindamycin.

Keywords

Clindamycin resistance, D-test, mupirocin resistance, constitutive MLSB phenotype, inducible MLSB phenotype

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