| Literature DB >> 29950336 |
François Caméléna1,2, Aurélie Cointe1,3, Vincent Mathy3, Claire Hobson1, Catherine Doit1,3, Béatrice Bercot1,2, Dominique Decré4,5, Isabelle Podglajen6,7, Laurent Dortet8,9, Audrey Monjault3, Philippe Bidet1,3, Stéphane Bonacorsi10,3, André Birgy1,3.
Abstract
The dissemination of carbapenemase-producing Enterobacteriaceae (CPE) is a major threat to public health. Rapid and accurate detection of CPE is essential for initiating appropriate antimicrobial treatment and establishing infection control measures. The carbapenem inactivation method (CIM), which has good sensitivity and specificity but a detection time of 20 h, was recently described. In this study, we evaluated the performances of a new version, the CIMplus test, which allows detection of carbapenemases in 8 h and characterization of carbapenemase classes, according to the Ambler classification, in 20 h. A panel of 110 carbapenem-resistant Enterobacteriaceae strains, including 92 CPE strains (with NDM, VIM, IMP, KPC, GES, OXA-48, and OXA-48-like enzymes), was used to evaluate test performance. Carbapenemase activity was detected at 8 h and 20 h. Characterization of carbapenemase classes, using specific inhibitors, was possible in 20 h. The CIMplus test had sensitivities of 95.7% and 97.8% at 8 h and 20 h, respectively, and a specificity of 94.4%, independent of the culture duration. Using a decision algorithm, this test was successful in identifying the carbapenemase class for 98.9% of tested CPE isolates (87/88 isolates). In total, the characterization was correct for 100%, 96.9%, and 100% of Ambler class A, B, and D isolates, respectively. Therefore, this test allows detection of carbapenemase activity in 8 h and characterization of carbapenemase classes, according to the Ambler classification, in 20 h. The CIMplus test represents a simple, affordable, easy-to-read, and accurate tool that can be used without any specific equipment.Entities:
Keywords: EDTA; Enterobacteriaceae; NDM; OXA-48; carbapenemase; carbapenemase inactivation method; mCIM; phenotypic characterization; phenotypic detection; phenylboronic acid
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Year: 2018 PMID: 29950336 PMCID: PMC6113496 DOI: 10.1128/JCM.00137-18
Source DB: PubMed Journal: J Clin Microbiol ISSN: 0095-1137 Impact factor: 5.948