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To Be or Not to Be an OXA-48 Carbapenemase

Since the first description of OXA-48, more than forty variants have been recovered from Enterobacterales isolates. Whereas some OXA-48-related enzymes have been reported as conferring similar resistance patterns, namely, the hydrolysis of carbapenems and penicillins with very weak or almost no acti...

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Autores principales: Dabos, Laura, Oueslati, Saoussen, Bernabeu, Sandrine, Bonnin, Rémy A., Dortet, Laurent, Naas, Thierry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875484/
https://www.ncbi.nlm.nih.gov/pubmed/35208713
http://dx.doi.org/10.3390/microorganisms10020258
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author Dabos, Laura
Oueslati, Saoussen
Bernabeu, Sandrine
Bonnin, Rémy A.
Dortet, Laurent
Naas, Thierry
author_facet Dabos, Laura
Oueslati, Saoussen
Bernabeu, Sandrine
Bonnin, Rémy A.
Dortet, Laurent
Naas, Thierry
author_sort Dabos, Laura
collection PubMed
description Since the first description of OXA-48, more than forty variants have been recovered from Enterobacterales isolates. Whereas some OXA-48-related enzymes have been reported as conferring similar resistance patterns, namely, the hydrolysis of carbapenems and penicillins with very weak or almost no activity against expanded-spectrum cephalosporins, some have reduced carbapenem and temocillin hydrolysis, and others hydrolyze expanded-spectrum cephalosporins and carbapenems only marginally. With such drastic differences in the hydrolytic profile, especially of carbapenems, it becomes urgent to establish hydrolytic cutoffs in order to determine when an OXA-48-like enzyme may be considered as a carbapenemase or not. With this aim, the coefficient of activity for imipenem (k(cat)/K(m)) was determined for a total of 30 enzymes, including OXA-48, OXA-48-like natural variants, and OXA-48 synthetic mutants. In addition, six different methods for the detection of carbapenemase-producers were performed. The coefficients of activity for imipenem for all the different enzymes went from 550 mM(−1)·s(−1) to 0.02 mM(−1)·s(−1). In order to match the coefficient of activity results with the biochemical confirmatory tests, we suggest the value of 0.27 mM(−1)·s(−1) as the cutoff above which an OXA-48 variant may be considered a carbapenem-hydrolyzing enzyme.
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spelling pubmed-88754842022-02-26 To Be or Not to Be an OXA-48 Carbapenemase Dabos, Laura Oueslati, Saoussen Bernabeu, Sandrine Bonnin, Rémy A. Dortet, Laurent Naas, Thierry Microorganisms Communication Since the first description of OXA-48, more than forty variants have been recovered from Enterobacterales isolates. Whereas some OXA-48-related enzymes have been reported as conferring similar resistance patterns, namely, the hydrolysis of carbapenems and penicillins with very weak or almost no activity against expanded-spectrum cephalosporins, some have reduced carbapenem and temocillin hydrolysis, and others hydrolyze expanded-spectrum cephalosporins and carbapenems only marginally. With such drastic differences in the hydrolytic profile, especially of carbapenems, it becomes urgent to establish hydrolytic cutoffs in order to determine when an OXA-48-like enzyme may be considered as a carbapenemase or not. With this aim, the coefficient of activity for imipenem (k(cat)/K(m)) was determined for a total of 30 enzymes, including OXA-48, OXA-48-like natural variants, and OXA-48 synthetic mutants. In addition, six different methods for the detection of carbapenemase-producers were performed. The coefficients of activity for imipenem for all the different enzymes went from 550 mM(−1)·s(−1) to 0.02 mM(−1)·s(−1). In order to match the coefficient of activity results with the biochemical confirmatory tests, we suggest the value of 0.27 mM(−1)·s(−1) as the cutoff above which an OXA-48 variant may be considered a carbapenem-hydrolyzing enzyme. MDPI 2022-01-24 /pmc/articles/PMC8875484/ /pubmed/35208713 http://dx.doi.org/10.3390/microorganisms10020258 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 Communication
Dabos, Laura
Oueslati, Saoussen
Bernabeu, Sandrine
Bonnin, Rémy A.
Dortet, Laurent
Naas, Thierry
To Be or Not to Be an OXA-48 Carbapenemase
title To Be or Not to Be an OXA-48 Carbapenemase
title_full To Be or Not to Be an OXA-48 Carbapenemase
title_fullStr To Be or Not to Be an OXA-48 Carbapenemase
title_full_unstemmed To Be or Not to Be an OXA-48 Carbapenemase
title_short To Be or Not to Be an OXA-48 Carbapenemase
title_sort to be or not to be an oxa-48 carbapenemase
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8875484/
https://www.ncbi.nlm.nih.gov/pubmed/35208713
http://dx.doi.org/10.3390/microorganisms10020258
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