ANTIMICROBIAL SUSCEPTIBILITY PATTERN OF STAPHYLOCOCCUS AUREUS ON CLINICAL ISOLATES AND EFFICACY OF LABORATORY TESTS TO DIAGNOSE MRSA: A MULTI-CENTRE STUDY

Authors

  • Syed Zahid Bukhari
  • Safia Ahmed
  • Naheed Zia

Abstract

Background: The global problem of increasing trend in antimicrobial resistance is particularly pressingin the developing countries, where the Methicillin-Resistant Staphylococcus aureus (MRSA) is often thesevere casual agent in hospital-acquired infections. Methods: This multi-centre surveillance prospectivestudy was planned to define the magnitude of problem of MRSA among clinical isolates from fourteaching hospitals of Lahore Pakistan; Mayo, Services, Jinnah and Shaikh Zayed Hospitals during April2006–March 2008. Identification of organisms was done by the standard Microbiology methods. MRSAisolates identified on Kirby-Bauer disc diffusion were further evaluated by minimum inhibitoryconcentration on BD PhoenixTM system and detection of mecA gene by pulsed-field gel electrophoresis(PFGE) PCR. Results: Of the total 1,102 S. aureus isolates, oxacillin resistance was found in 462 on discdiffusion and 420 on MIC while mecA gene was detected from 307 strains. The prevalence of MRSAamong S. aureus isolates was 41.9%, 38.1% and 27.9% on disc diffusion, MIC, and mecA genedetection respectively. Hospital acquired-MRSA strains were multi drug resistant while communityacquired-MRSA showed susceptibility to clindamycin (63%), ciprofloxacin (24.2%) and SMZ/TMP(3.9%). In diagnosing MRSA, the sensitivity and specificity rates of disc diffusion test were 100% and83.7% while MIC 96.2% and 93.3% respectively. Conclusion: There is an increasing trend inemergence MRSA and the conventional method of antimicrobial susceptibility testing showed falsepositive tests. This is the reason of misuse of vancomycin by physicians which may further increaseMRSA in Pakistan. Therefore, molecular diagnostic facilities are recommended to avoid falsesusceptibleresults.Keywords: S. aureus, MRSA, mecA gene, MIC

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Published

2011-03-01