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Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii

PURPOSE: To evaluate in vitro activities of β-lactam antibiotics alone and in combination with sulbactam at different ratios against Acinetobacter baumannii clinical strains from China. METHODS: A total of 300 clinical isolates of A. baumannii were collected from 29 hospitals across China in 2018. S...

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Detalles Bibliográficos
Autores principales: Wang, Leilei, Chen, Yuancheng, Han, Renru, Huang, Zhiwei, Zhang, Xuefei, Hu, Fupin, Yang, Fan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487265/
https://www.ncbi.nlm.nih.gov/pubmed/34611414
http://dx.doi.org/10.2147/IDR.S332160
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author Wang, Leilei
Chen, Yuancheng
Han, Renru
Huang, Zhiwei
Zhang, Xuefei
Hu, Fupin
Yang, Fan
author_facet Wang, Leilei
Chen, Yuancheng
Han, Renru
Huang, Zhiwei
Zhang, Xuefei
Hu, Fupin
Yang, Fan
author_sort Wang, Leilei
collection PubMed
description PURPOSE: To evaluate in vitro activities of β-lactam antibiotics alone and in combination with sulbactam at different ratios against Acinetobacter baumannii clinical strains from China. METHODS: A total of 300 clinical isolates of A. baumannii were collected from 29 hospitals across China in 2018. Susceptibility to common antibiotics was assessed, and β-lactamase genes were detected. In vitro activity of ampicillin, cefoperazone and imipenem was tested alone and in combination with sulbactam at the ratios of 2:1, 1:1, 1:1.5, 1:2, 1:2.5 and 1:3. RESULTS: High resistant rates for common antibiotics were observed except tigecycline and polymyxin B. Among carbapenem-resistant A. baumannii, 97.3% isolates harbored bla(OXA-23). MIC(50) and MIC(90) values for sulbactam were 32 mg/L and 64 mg/L, respectively. High resistant rates for ampicillin, cefoperazone and imipenem were observed (92.3%, 93% and 85.3%, respectively). A stepwise increase in the ratio of sulbactam to partner β-lactam antibiotics led to a stepwise decrease in the MICs and a stepwise increase in the susceptible rates. The susceptible rates for imipenem-sulbactam 1:3, ampicillin-sulbactam 1:3 and cefoperazone-sulbactam 1:3 reached 16.3%, 58.3% and 91%, respectively. CONCLUSION: The increasing proportion of sulbactam could enhance antimicrobial activities of imipenem-sulbactam, ampicillin-sulbactam and cefoperazone-sulbactam combinations against A. baumannii clinical strains in China, with cefoperazone-sulbactam as the most potent compound.
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spelling pubmed-84872652021-10-04 Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii Wang, Leilei Chen, Yuancheng Han, Renru Huang, Zhiwei Zhang, Xuefei Hu, Fupin Yang, Fan Infect Drug Resist Original Research PURPOSE: To evaluate in vitro activities of β-lactam antibiotics alone and in combination with sulbactam at different ratios against Acinetobacter baumannii clinical strains from China. METHODS: A total of 300 clinical isolates of A. baumannii were collected from 29 hospitals across China in 2018. Susceptibility to common antibiotics was assessed, and β-lactamase genes were detected. In vitro activity of ampicillin, cefoperazone and imipenem was tested alone and in combination with sulbactam at the ratios of 2:1, 1:1, 1:1.5, 1:2, 1:2.5 and 1:3. RESULTS: High resistant rates for common antibiotics were observed except tigecycline and polymyxin B. Among carbapenem-resistant A. baumannii, 97.3% isolates harbored bla(OXA-23). MIC(50) and MIC(90) values for sulbactam were 32 mg/L and 64 mg/L, respectively. High resistant rates for ampicillin, cefoperazone and imipenem were observed (92.3%, 93% and 85.3%, respectively). A stepwise increase in the ratio of sulbactam to partner β-lactam antibiotics led to a stepwise decrease in the MICs and a stepwise increase in the susceptible rates. The susceptible rates for imipenem-sulbactam 1:3, ampicillin-sulbactam 1:3 and cefoperazone-sulbactam 1:3 reached 16.3%, 58.3% and 91%, respectively. CONCLUSION: The increasing proportion of sulbactam could enhance antimicrobial activities of imipenem-sulbactam, ampicillin-sulbactam and cefoperazone-sulbactam combinations against A. baumannii clinical strains in China, with cefoperazone-sulbactam as the most potent compound. Dove 2021-09-28 /pmc/articles/PMC8487265/ /pubmed/34611414 http://dx.doi.org/10.2147/IDR.S332160 Text en © 2021 Wang et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Leilei
Chen, Yuancheng
Han, Renru
Huang, Zhiwei
Zhang, Xuefei
Hu, Fupin
Yang, Fan
Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
title Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
title_full Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
title_fullStr Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
title_full_unstemmed Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
title_short Sulbactam Enhances in vitro Activity of β-Lactam Antibiotics Against Acinetobacter baumannii
title_sort sulbactam enhances in vitro activity of β-lactam antibiotics against acinetobacter baumannii
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487265/
https://www.ncbi.nlm.nih.gov/pubmed/34611414
http://dx.doi.org/10.2147/IDR.S332160
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