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Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria

The emergence of carbapenem-resistant organisms posed considerable threat to global health while only limited treatment options are available and led to efforts to discover a novel way to treat them. To evaluate in vitro synergistic activity of meropenem plus ertapenem, a total of 203 carbapenem-res...

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Autores principales: Lu, Jiayue, Qing, Yan, Dong, Ning, Liu, Congcong, Zeng, Yu, Sun, Qiaoling, Shentu, Qiao, Huang, Lixing, Wu, Yingqian, Zhou, Hongwei, Shen, Zhangqi, Zhang, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257860/
https://www.ncbi.nlm.nih.gov/pubmed/35812137
http://dx.doi.org/10.1016/j.jsps.2022.03.007
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author Lu, Jiayue
Qing, Yan
Dong, Ning
Liu, Congcong
Zeng, Yu
Sun, Qiaoling
Shentu, Qiao
Huang, Lixing
Wu, Yingqian
Zhou, Hongwei
Shen, Zhangqi
Zhang, Rong
author_facet Lu, Jiayue
Qing, Yan
Dong, Ning
Liu, Congcong
Zeng, Yu
Sun, Qiaoling
Shentu, Qiao
Huang, Lixing
Wu, Yingqian
Zhou, Hongwei
Shen, Zhangqi
Zhang, Rong
author_sort Lu, Jiayue
collection PubMed
description The emergence of carbapenem-resistant organisms posed considerable threat to global health while only limited treatment options are available and led to efforts to discover a novel way to treat them. To evaluate in vitro synergistic activity of meropenem plus ertapenem, a total of 203 carbapenem-resistant strains, collected from 12 provinces and municipalities in China, were examined with a dual carbapenem combination therapy. The statistical software R was used for analysis. Two hundred and one (201) of carbapenem-resistant strains mainly produced four types of carbapenemase: KPC-2 (n = 142, 69.95%), OXA-232 (n = 7, 3.45%), NDM (n = 38, 18.72%; 36 NDM-1, 1 NDM-4, 1 NDM-5), and IMP (n = 15, 7.39%; 1 IMP-26, 10 IMP-30, 4 IMP-4). Fifty-one out of two hundred and three (51/203 or 25.12%) of the examined strains showed a synergistic effect for the meropenem plus ertapenem combination throughout the checkerboard method, while only three isolates showed potential clinically relevant synergy (3/203, 1.48%). An additive effect was observed in 55/203 (27.09%) of the examined strains. Ninety-seven of the examined isolates (47.78%) showed fractional inhibitory concentration (FIC) greater or equal to 2 (indicating antagonism). The synergistic activity of meropenem plus ertapenem combination suggests this combination can be a possible way to treat the infection caused by the carbapenem-resistant organisms, especially for IMP or NDM producer with a lesser minimum inhibitory concentration (MIC) and the infected individual who was not recommended to use colistin or tigecycline.
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spelling pubmed-92578602022-07-07 Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria Lu, Jiayue Qing, Yan Dong, Ning Liu, Congcong Zeng, Yu Sun, Qiaoling Shentu, Qiao Huang, Lixing Wu, Yingqian Zhou, Hongwei Shen, Zhangqi Zhang, Rong Saudi Pharm J Original Article The emergence of carbapenem-resistant organisms posed considerable threat to global health while only limited treatment options are available and led to efforts to discover a novel way to treat them. To evaluate in vitro synergistic activity of meropenem plus ertapenem, a total of 203 carbapenem-resistant strains, collected from 12 provinces and municipalities in China, were examined with a dual carbapenem combination therapy. The statistical software R was used for analysis. Two hundred and one (201) of carbapenem-resistant strains mainly produced four types of carbapenemase: KPC-2 (n = 142, 69.95%), OXA-232 (n = 7, 3.45%), NDM (n = 38, 18.72%; 36 NDM-1, 1 NDM-4, 1 NDM-5), and IMP (n = 15, 7.39%; 1 IMP-26, 10 IMP-30, 4 IMP-4). Fifty-one out of two hundred and three (51/203 or 25.12%) of the examined strains showed a synergistic effect for the meropenem plus ertapenem combination throughout the checkerboard method, while only three isolates showed potential clinically relevant synergy (3/203, 1.48%). An additive effect was observed in 55/203 (27.09%) of the examined strains. Ninety-seven of the examined isolates (47.78%) showed fractional inhibitory concentration (FIC) greater or equal to 2 (indicating antagonism). The synergistic activity of meropenem plus ertapenem combination suggests this combination can be a possible way to treat the infection caused by the carbapenem-resistant organisms, especially for IMP or NDM producer with a lesser minimum inhibitory concentration (MIC) and the infected individual who was not recommended to use colistin or tigecycline. Elsevier 2022-06 2022-03-14 /pmc/articles/PMC9257860/ /pubmed/35812137 http://dx.doi.org/10.1016/j.jsps.2022.03.007 Text en © 2022 The Authors. Published by Elsevier B.V. on behalf of King Saud University. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Lu, Jiayue
Qing, Yan
Dong, Ning
Liu, Congcong
Zeng, Yu
Sun, Qiaoling
Shentu, Qiao
Huang, Lixing
Wu, Yingqian
Zhou, Hongwei
Shen, Zhangqi
Zhang, Rong
Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria
title Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria
title_full Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria
title_fullStr Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria
title_full_unstemmed Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria
title_short Effectiveness of a double-carbapenem combinations against carbapenem-resistant Gram-negative bacteria
title_sort effectiveness of a double-carbapenem combinations against carbapenem-resistant gram-negative bacteria
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257860/
https://www.ncbi.nlm.nih.gov/pubmed/35812137
http://dx.doi.org/10.1016/j.jsps.2022.03.007
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