Cargando…

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

Background: Early detection of expanded-spectrum cephalosporinase (ESC) hydrolyzing ß-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 ß-la...

Descripción completa

Detalles Bibliográficos
Autores principales: Moguet, Christian, Gonzalez, Camille, Naas, Thierry, Simon, Stéphanie, Volland, Hervé
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775197/
https://www.ncbi.nlm.nih.gov/pubmed/35054357
http://dx.doi.org/10.3390/diagnostics12010190
_version_ 1784636526231027712
author Moguet, Christian
Gonzalez, Camille
Naas, Thierry
Simon, Stéphanie
Volland, Hervé
author_facet Moguet, Christian
Gonzalez, Camille
Naas, Thierry
Simon, Stéphanie
Volland, Hervé
author_sort Moguet, Christian
collection PubMed
description Background: Early detection of expanded-spectrum cephalosporinase (ESC) hydrolyzing ß-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 ß-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 ß-lactamase content. One single colony was resuspended in 150 µL 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 β-lactamase hydrolyzing cefotaxime gave negative results, and all 171 isolates expressing a β-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.
format Online
Article
Text
id pubmed-8775197
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-87751972022-01-21 Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes Moguet, Christian Gonzalez, Camille Naas, Thierry Simon, Stéphanie Volland, Hervé Diagnostics (Basel) Article Background: Early detection of expanded-spectrum cephalosporinase (ESC) hydrolyzing ß-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 ß-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 ß-lactamase content. One single colony was resuspended in 150 µL 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 β-lactamase hydrolyzing cefotaxime gave negative results, and all 171 isolates expressing a β-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. MDPI 2022-01-13 /pmc/articles/PMC8775197/ /pubmed/35054357 http://dx.doi.org/10.3390/diagnostics12010190 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Moguet, Christian
Gonzalez, Camille
Naas, Thierry
Simon, Stéphanie
Volland, Hervé
Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes
title Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes
title_full Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes
title_fullStr Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes
title_full_unstemmed Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes
title_short Multiplex Lateral Flow Immunoassay for the Detection of Expanded-Spectrum Hydrolysis and CTX-M Enzymes
title_sort multiplex lateral flow immunoassay for the detection of expanded-spectrum hydrolysis and ctx-m enzymes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8775197/
https://www.ncbi.nlm.nih.gov/pubmed/35054357
http://dx.doi.org/10.3390/diagnostics12010190
work_keys_str_mv AT moguetchristian multiplexlateralflowimmunoassayforthedetectionofexpandedspectrumhydrolysisandctxmenzymes
AT gonzalezcamille multiplexlateralflowimmunoassayforthedetectionofexpandedspectrumhydrolysisandctxmenzymes
AT naasthierry multiplexlateralflowimmunoassayforthedetectionofexpandedspectrumhydrolysisandctxmenzymes
AT simonstephanie multiplexlateralflowimmunoassayforthedetectionofexpandedspectrumhydrolysisandctxmenzymes
AT vollandherve multiplexlateralflowimmunoassayforthedetectionofexpandedspectrumhydrolysisandctxmenzymes