Comparison of two methods to detect carbapenemase & metallo-β-lactamase production in clinical isolates

Mary V. Jesudason, A. J. Kandathil, V. Balaji

Research output: Contribution to journalArticlepeer-review

43 Scopus citations

Abstract

Background & objectives: Bacterial resistance has greatly hampered effective treatment of patients in clinical settings. Non-fermenting Gram-negative bacilli (NFGNB) are common nosocomial pathogens. In this study we attempted to develop a convenient test for early detection of carbapenemase and metallo-β-lactamase (MβL) production in NFGNB. Lack of sufficient reports from India in this area indicated the need for this study. Methods: A total of 50 imipenem resistant NFGNB were speciated, and their resistance reconfirmed by disk diffusion and minimum inhibitory concentration (MIC) determination by agar dilution. Two different methods namely modified Hodge and EDTA disk synergy tests were evaluated for carbapenemase and metallo-β-lactamase (MβL) production. Results: Of the 50 imipenem resistant NFGNB, 48 and two respectively fell in the resistant and intermediate range in MIC using agar dilution. Majority of these were Pseudomonas aeruginosa (n=28), followed by Burkholderia cepacia (n=9). The modified Hodge test could detect 28 strains as carbapenemase and MβL producers, while the EDTA disk synergy test was able to detect an additional 8 strains producing MβL and carbapenemase. Interpretation & conclusion: Pseudomonas aeruginosa was found to be the predominant NFGNB in our hospital setting and EDTA disk synergy could detect more carbapenemase and metallo-β-lactamase producers compared to modified Hodge test.

Original languageEnglish (US)
Pages (from-to)780-783
Number of pages4
JournalIndian Journal of Medical Research
Volume121
Issue number6
StatePublished - Jun 2005
Externally publishedYes

Keywords

  • Disc synergy tests
  • Metallo-β-lactamases
  • Modified Hodge test EDTA
  • Non-fermenting Gram-negative bacili

ASJC Scopus subject areas

  • General Biochemistry, Genetics and Molecular Biology

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