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The rapid detection of cefotaxime-resistant Enterobacteriaceae by HPLC
Andrew M Robinson1, Natalie J Medlicott2, James E Ussher3
1Department of Microbiology & Immunology, University of Otago, Dunedin, New Zealand; Department of Microbiology & Immunology, University of Otago, Dunedin, New Zealand.
Aim:
Antibiotic resistance mediated by extended-spectrum β-lactamases (ESBL) and AmpC β-lactamases is widespread and increasingly common, often rendering empiric antibiotic therapy ineffective. In septicemia, delays in initiating effective antibiotic therapy are associated with worse clinical outcomes. With current phenotypic antimicrobial susceptibility testing methods, there is often a delay of 18-24 h before the susceptibility of an isolate is known.
Results:
Using an HPLC assay, breakdown of the third-generation cephalosporin cefotaxime by ESBL- and AmpC- β-lactamase-producing organisms could be detected within 90 min with 86.4% sensitivity and 100% specificity; sensitivity for ESBL detection was 100%.
Conclusion:
This assay could be readily established in any clinical laboratory with an HPLC to rapidly detect ESBL-producing Enterobacteriaceae.
