4.6 Article

Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes

期刊

DIAGNOSTICS
卷 12, 期 1, 页码 -

出版社

MDPI
DOI: 10.3390/diagnostics12010190

关键词

lateral flow immunoassay; fi-lactamase detection; CTX-M enzymes; cephalosporin hydrolysis

资金

  1. Assistance Publique-Hopitaux de Paris (APHP)
  2. University Paris-Saclay
  3. Institut National de la Sante et de la Recherche Medical (INSERM)
  4. French Alternative Energies and Atomic Energy Commission (CEA)
  5. CEA

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A multiplex lateral flow immunoassay (LFIA) was developed to detect cefotaxime-hydrolyzing activity and CTX-M enzymes. The LFIA showed high sensitivity and specificity, making it a rapid and accurate method for routine laboratory work.
Background: Early detection of expanded-spectrum cephalosporinase (ESC) hydrolyzing beta-lactamases is essential for antibiotic stewardship. Here we have developed a multiplex lateral flow immunoassay (LFIA) that detects cefotaxime-hydrolyzing activity as well as the most prevalent ESC-hydrolyzing beta-lactamases: the CTX-M-like. Methods: The Rapid LFIA ESC test was evaluated retrospectively on 188 (139 Enterobacterales, 30 Pseudomonas spp. and 14 Acinetobacter spp.) agar-grown bacterial isolates with well-characterized beta-lactamase content. One single colony was resuspended in 150 mu L extraction buffer containing cefotaxime, incubated at room temperature for 30 min prior to loading on the LFIA for reading within 10 min. Results: Out of the 188 isolates, all 17 that did not express a beta-lactamase hydrolyzing cefotaxime gave negative results, and all 171 isolates expressing a beta-lactamase known to hydrolyze cefotaxime, gave a positive test result. In addition, all 86 isolates expressing a CTX-M-variant belonging to one of the five CTX-M-subgroups were correctly identified. The sensitivity and specificity was 100% for both tests. Conclusions: The results showed that the multiplex LFIA was efficient, fast, low cost and easy to implement in routine laboratory work for the confirmation of ESC hydrolyzing activity and the presence of CTX-M enzymes.

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