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In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries
Background: High rates of resistance to third-generation cephalosporins and carbapenems in Enterobacterales have been reported in Latin America. Ceftazidime/avibactam (CZA) is the combination of a third-generation cephalosporin and a non-β-lactam β-lactamase inhibitor, which has shown activity again...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168198/ https://www.ncbi.nlm.nih.gov/pubmed/32033394 http://dx.doi.org/10.3390/antibiotics9020062 |
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author | Appel, Tobias Manuel Mojica, María Fernanda De La Cadena, Elsa Pallares, Christian José Radice, Marcela A. Castañeda-Méndez, Paulo Jaime-Villalón, Diego A. Gales, Ana C. Munita, José M. Villegas, María Virginia |
author_facet | Appel, Tobias Manuel Mojica, María Fernanda De La Cadena, Elsa Pallares, Christian José Radice, Marcela A. Castañeda-Méndez, Paulo Jaime-Villalón, Diego A. Gales, Ana C. Munita, José M. Villegas, María Virginia |
author_sort | Appel, Tobias Manuel |
collection | PubMed |
description | Background: High rates of resistance to third-generation cephalosporins and carbapenems in Enterobacterales have been reported in Latin America. Ceftazidime/avibactam (CZA) is the combination of a third-generation cephalosporin and a non-β-lactam β-lactamase inhibitor, which has shown activity against isolates producing class A, C and D β-lactamases. Herein, we evaluated the activity of CZA and comparators against clinical isolates of Enterobacterales in Latin America. Methods: The activity of CZA and comparators was evaluated against clinical isolates of Enterobacterales from Argentina, Brazil, Chile, Colombia and Mexico that were collected between January 2016 and October 2017. One specific phenotypic subset was evaluated. A carbapenem non-susceptible (CNS) phenotype was defined as any isolate displaying a minimum inhibitory concentration (MIC) ≥1 mg/L for ertapenem. Results: CZA was active against 95.8% of all isolates and 77.5% of CNS isolates. Fosfomycin (FOS) and tigecycline (TGC) were the second most active antibiotics with 93.4% of Enterobacterales being susceptible. Conclusions: The results of this study underline the potential therapeutic role of CZA in Latin America. |
format | Online Article Text |
id | pubmed-7168198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-71681982020-04-21 In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries Appel, Tobias Manuel Mojica, María Fernanda De La Cadena, Elsa Pallares, Christian José Radice, Marcela A. Castañeda-Méndez, Paulo Jaime-Villalón, Diego A. Gales, Ana C. Munita, José M. Villegas, María Virginia Antibiotics (Basel) Brief Report Background: High rates of resistance to third-generation cephalosporins and carbapenems in Enterobacterales have been reported in Latin America. Ceftazidime/avibactam (CZA) is the combination of a third-generation cephalosporin and a non-β-lactam β-lactamase inhibitor, which has shown activity against isolates producing class A, C and D β-lactamases. Herein, we evaluated the activity of CZA and comparators against clinical isolates of Enterobacterales in Latin America. Methods: The activity of CZA and comparators was evaluated against clinical isolates of Enterobacterales from Argentina, Brazil, Chile, Colombia and Mexico that were collected between January 2016 and October 2017. One specific phenotypic subset was evaluated. A carbapenem non-susceptible (CNS) phenotype was defined as any isolate displaying a minimum inhibitory concentration (MIC) ≥1 mg/L for ertapenem. Results: CZA was active against 95.8% of all isolates and 77.5% of CNS isolates. Fosfomycin (FOS) and tigecycline (TGC) were the second most active antibiotics with 93.4% of Enterobacterales being susceptible. Conclusions: The results of this study underline the potential therapeutic role of CZA in Latin America. MDPI 2020-02-05 /pmc/articles/PMC7168198/ /pubmed/32033394 http://dx.doi.org/10.3390/antibiotics9020062 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Brief Report Appel, Tobias Manuel Mojica, María Fernanda De La Cadena, Elsa Pallares, Christian José Radice, Marcela A. Castañeda-Méndez, Paulo Jaime-Villalón, Diego A. Gales, Ana C. Munita, José M. Villegas, María Virginia In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries |
title | In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries |
title_full | In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries |
title_fullStr | In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries |
title_full_unstemmed | In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries |
title_short | In Vitro Susceptibility to Ceftazidime/Avibactam and Comparators in Clinical Isolates of Enterobacterales from Five Latin American Countries |
title_sort | in vitro susceptibility to ceftazidime/avibactam and comparators in clinical isolates of enterobacterales from five latin american countries |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7168198/ https://www.ncbi.nlm.nih.gov/pubmed/32033394 http://dx.doi.org/10.3390/antibiotics9020062 |
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