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Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures

Due to the importance of a rapid determination of patients infected by multidrug resistant bacteria, we evaluated two rapid diagnostic tests for the detection of third-generation cephalosporins (3GC)-resistant Enterobacterales directly from positive blood cultures within 1 h: BL-RED(TM) (electrochem...

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Autores principales: Durand, Clarisse, Boudet, Agathe, Lavigne, Jean-Philippe, Pantel, Alix
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516202/
https://www.ncbi.nlm.nih.gov/pubmed/33014900
http://dx.doi.org/10.3389/fcimb.2020.00491
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author Durand, Clarisse
Boudet, Agathe
Lavigne, Jean-Philippe
Pantel, Alix
author_facet Durand, Clarisse
Boudet, Agathe
Lavigne, Jean-Philippe
Pantel, Alix
author_sort Durand, Clarisse
collection PubMed
description Due to the importance of a rapid determination of patients infected by multidrug resistant bacteria, we evaluated two rapid diagnostic tests for the detection of third-generation cephalosporins (3GC)-resistant Enterobacterales directly from positive blood cultures within 1 h: BL-RED(TM) (electrochemical method) and β-LACTA(TM) test (chromogenic method). A panel of 150 clinical strains characterized for their resistance profiles (e.g., penicillinases, extended-spectrum beta-lactamases (ESBLs), overproduction of cephalosporinase, carbapenemases, impermeability) was tested. Approximately 100 CFU of each isolate was spiked into sterile blood culture bottles and incubated in a BD BACTEC(TM) FX automated system (Becton Dickinson, USA). Positive blood cultures were examined to parallel testing using the BL-RED(TM) and β-LACTA(TM) tests and conventional susceptibility method (disc diffusion following EUCAST recommendations). For all phenotypes combined, the sensitivity, specificity, positive predictive value, and negative predictive value in the detection of 3GC resistance were, respectively (i) with BL-RED(TM): 45.7, 100, 100, and 54.2% and (ii) with β-LACTA(TM) test: 52.2, 100, 100, and 56.9%. The positivity of tests allows to adapt antibiotic treatment whereas the negative result requires other tests. Moreover, these tests detect most Ambler class A-producing Enterobacterales (KPC, ESBL, extended-spectrum OXY) with sensitivities and specificities of 87.5 and 99% for BL-RED(TM), respectively and both 100% for β-LACTA(TM) test (47/47 isolates). These two rapid tests failed to detect AmpC overexpressed (sensitivities of 2.7% for BL-RED(TM) and 0% for β-LACTA(TM) test) and Ambler class B-producing Enterobacterales (sensitivities of 40% for both tests) notably strains without ESBLs associated (sensitivities of 0% for both tests). BL-RED(TM) and β-LACTA(TM) tests are easy-to-use and mainly attractive when a positive result is obtained notably to detect most of the Ambler class A-producing Enterobacterales in <1 h after the positivity of the blood culture, allowing a rapid adaptation of the antibiotic therapy in patients.
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spelling pubmed-75162022020-10-02 Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures Durand, Clarisse Boudet, Agathe Lavigne, Jean-Philippe Pantel, Alix Front Cell Infect Microbiol Cellular and Infection Microbiology Due to the importance of a rapid determination of patients infected by multidrug resistant bacteria, we evaluated two rapid diagnostic tests for the detection of third-generation cephalosporins (3GC)-resistant Enterobacterales directly from positive blood cultures within 1 h: BL-RED(TM) (electrochemical method) and β-LACTA(TM) test (chromogenic method). A panel of 150 clinical strains characterized for their resistance profiles (e.g., penicillinases, extended-spectrum beta-lactamases (ESBLs), overproduction of cephalosporinase, carbapenemases, impermeability) was tested. Approximately 100 CFU of each isolate was spiked into sterile blood culture bottles and incubated in a BD BACTEC(TM) FX automated system (Becton Dickinson, USA). Positive blood cultures were examined to parallel testing using the BL-RED(TM) and β-LACTA(TM) tests and conventional susceptibility method (disc diffusion following EUCAST recommendations). For all phenotypes combined, the sensitivity, specificity, positive predictive value, and negative predictive value in the detection of 3GC resistance were, respectively (i) with BL-RED(TM): 45.7, 100, 100, and 54.2% and (ii) with β-LACTA(TM) test: 52.2, 100, 100, and 56.9%. The positivity of tests allows to adapt antibiotic treatment whereas the negative result requires other tests. Moreover, these tests detect most Ambler class A-producing Enterobacterales (KPC, ESBL, extended-spectrum OXY) with sensitivities and specificities of 87.5 and 99% for BL-RED(TM), respectively and both 100% for β-LACTA(TM) test (47/47 isolates). These two rapid tests failed to detect AmpC overexpressed (sensitivities of 2.7% for BL-RED(TM) and 0% for β-LACTA(TM) test) and Ambler class B-producing Enterobacterales (sensitivities of 40% for both tests) notably strains without ESBLs associated (sensitivities of 0% for both tests). BL-RED(TM) and β-LACTA(TM) tests are easy-to-use and mainly attractive when a positive result is obtained notably to detect most of the Ambler class A-producing Enterobacterales in <1 h after the positivity of the blood culture, allowing a rapid adaptation of the antibiotic therapy in patients. Frontiers Media S.A. 2020-09-11 /pmc/articles/PMC7516202/ /pubmed/33014900 http://dx.doi.org/10.3389/fcimb.2020.00491 Text en Copyright © 2020 Durand, Boudet, Lavigne and Pantel. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Durand, Clarisse
Boudet, Agathe
Lavigne, Jean-Philippe
Pantel, Alix
Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures
title Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures
title_full Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures
title_fullStr Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures
title_full_unstemmed Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures
title_short Evaluation of Two Methods for the Detection of Third Generation Cephalosporins Resistant Enterobacterales Directly From Positive Blood Cultures
title_sort evaluation of two methods for the detection of third generation cephalosporins resistant enterobacterales directly from positive blood cultures
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7516202/
https://www.ncbi.nlm.nih.gov/pubmed/33014900
http://dx.doi.org/10.3389/fcimb.2020.00491
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