IN VITRO ACTIVITY OF VANCOMYCIN AND DAPTOMYCIN AGAINST HEALTHCARE-ASSOCIATED METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS ISOLATED FROM CLINICAL SPECIMENS

Authors

  • Jyoti Kumari
  • Shalini Shenoy M
  • Chakrapani M
  • Vidyalakshmi K
  • Gopalkrishna Bhat K Addtional ProfessorDept. of MicrobiologyKasturba Medical CollegeMangalore-575001

Abstract

ABSTRACT
Objective: The present cross-sectional study was conducted to determine minimum inhibitory concentration (MIC) of daptomycin and vancomycin
to clinical isolates of healthcare-associated-methicillin-resistant Staphylococcus aureus (HA-MRSA).
Methods: Centers for Disease Control and Prevention Criteria were used to define HR infections due to MRSA. Antibiotic susceptibility testing was
done by Kirby–Bauer disk diffusion method. MIC of vancomycin and daptomycin was determined by Agar dilution method and E-test, respectively.
Results of antibiotic susceptibility testing and MIC were interpreted as per Clinical Laboratory Standard Institute guidelines.
Results: A total of 110 strains of MRSA were isolated from healthcare-associated infections. All were susceptible to daptomycin, linezolid, and
teicoplanin. A total of 106 isolates were vancomycin susceptible and four were vancomycin-intermediate S. aureus (VISA). MIC
of
vancomycin were 2 µg/ml. All MRSA isolates were susceptible to daptomycin. Four VISA strains had daptomycin MIC 1 µg/ml.
Conclusion: The present study showed the emergence of VISA among HA-MRSA isolates with high MIC
for vancomycin. Although all HA-MRSA
isolates were susceptible to daptomycin, VISA isolates had high daptomycin MIC. This indicates that daptomycin may not be used as an alternative
choice for VISA infections.
Keywords: Healthcare-associated methicillin-resistant Staphylococcus aureus, Vancomycin, Daptomycin.
90

90

and MIC

50

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Published

01-05-2016

How to Cite

Kumari, J., S. Shenoy M, C. M, V. K, and G. Bhat K. “IN VITRO ACTIVITY OF VANCOMYCIN AND DAPTOMYCIN AGAINST HEALTHCARE-ASSOCIATED METHICILLIN-RESISTANT STAPHYLOCOCCUS AUREUS ISOLATED FROM CLINICAL SPECIMENS”. Asian Journal of Pharmaceutical and Clinical Research, vol. 9, no. 3, May 2016, pp. 44-46, https://mail.innovareacademics.in/journals/index.php/ajpcr/article/view/11434.

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