A multiplex lateral flow immunoassay for the rapid identification of NDM-, KPC-, IMP-and VIM-type and OXA-48-like carbapenemase-producing Enterobacteriaceae
H Boutal, A Vogel, S Bernabeu… - Journal of …, 2018 - academic.oup.com
H Boutal, A Vogel, S Bernabeu, K Devilliers, E Creton, G Cotellon, M Plaisance, S Oueslati…
Journal of Antimicrobial Chemotherapy, 2018•academic.oup.comObjectives The global spread of carbapenemase-producing Enterobacteriaceae represents
a substantial challenge in clinical practice and rapid and reliable detection of these
organisms is essential. The aim of this study was to develop and validate a lateral flow
immunoassay (Carba5) for the detection of the five main carbapenemases (KPC-, NDM-,
VIM-and IMP-type and OXA-48-like). Methods Carba5 was retrospectively and prospectively
evaluated using 296 enterobacterial isolates from agar culture. An isolated colony was …
a substantial challenge in clinical practice and rapid and reliable detection of these
organisms is essential. The aim of this study was to develop and validate a lateral flow
immunoassay (Carba5) for the detection of the five main carbapenemases (KPC-, NDM-,
VIM-and IMP-type and OXA-48-like). Methods Carba5 was retrospectively and prospectively
evaluated using 296 enterobacterial isolates from agar culture. An isolated colony was …
Objectives
The global spread of carbapenemase-producing Enterobacteriaceae represents a substantial challenge in clinical practice and rapid and reliable detection of these organisms is essential. The aim of this study was to develop and validate a lateral flow immunoassay (Carba5) for the detection of the five main carbapenemases (KPC-, NDM-, VIM- and IMP-type and OXA-48-like).
Methods
Carba5 was retrospectively and prospectively evaluated using 296 enterobacterial isolates from agar culture. An isolated colony was suspended in extraction buffer and then loaded on the manufactured Carba5.
Results
All 185 isolates expressing a carbapenemase related to one of the Carba5 targets were correctly and unambiguously detected in <15 min. All other isolates gave negative results except those producing OXA-163 and OXA-405, which are considered low-activity carbapenemases. No cross-reaction was observed with non-targeted carbapenemases, ESBLs, AmpCs or oxacillinases (OXA-1, -2, -9 and -10). Overall, this assay reached 100% sensitivity and 95.3% (retrospectively) to 100% (prospectively) specificity.
Conclusions
Carba5 is efficient, rapid and easy to implement in the routine workflow of a clinical microbiology laboratory for confirmation of the five main carbapenemases encountered in Enterobacteriaceae.
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