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L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake
Acinetobacter baumannii, a Gram-negative opportunistic pathogen, is a leading cause of hospital- and community-acquired infections. Acinetobacter baumannii can rapidly acquire diverse resistance mechanisms and undergo genetic modifications that confer resistance and persistence to all currently used...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144275/ https://www.ncbi.nlm.nih.gov/pubmed/32192413 http://dx.doi.org/10.1080/22221751.2020.1740611 |
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author | Deng, Wanyan Fu, Tiwei Zhang, Zhen Jiang, Xiao Xie, Jianping Sun, Hang Hu, Peng Ren, Hong Zhou, Peifu Liu, Qi Long, Quanxin |
author_facet | Deng, Wanyan Fu, Tiwei Zhang, Zhen Jiang, Xiao Xie, Jianping Sun, Hang Hu, Peng Ren, Hong Zhou, Peifu Liu, Qi Long, Quanxin |
author_sort | Deng, Wanyan |
collection | PubMed |
description | Acinetobacter baumannii, a Gram-negative opportunistic pathogen, is a leading cause of hospital- and community-acquired infections. Acinetobacter baumannii can rapidly acquire diverse resistance mechanisms and undergo genetic modifications that confer resistance and persistence to all currently used clinical antibiotics. In this study, we found exogenous L-lysine sensitizes Acinetobacter baumannii, other Gram-negative bacteria (Escherichia coli and Klebsiella pneumoniae) and a Gram-positive bacterium (Mycobacterium smegmatis) to aminoglycosides. Importantly, the combination of L-lysine with aminoglycosides killed clinically isolated multidrug-resistant Acinetobacter baumannii and persister cells. The exogenous L-lysine can increase proton motive force via transmembrane chemical gradient, resulting in aminoglycoside acumination that further accounts for reactive oxygen species production. The combination of L-lysine and antibiotics highlights a promising strategy against bacterial infection. |
format | Online Article Text |
id | pubmed-7144275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-71442752020-04-13 L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake Deng, Wanyan Fu, Tiwei Zhang, Zhen Jiang, Xiao Xie, Jianping Sun, Hang Hu, Peng Ren, Hong Zhou, Peifu Liu, Qi Long, Quanxin Emerg Microbes Infect Article Acinetobacter baumannii, a Gram-negative opportunistic pathogen, is a leading cause of hospital- and community-acquired infections. Acinetobacter baumannii can rapidly acquire diverse resistance mechanisms and undergo genetic modifications that confer resistance and persistence to all currently used clinical antibiotics. In this study, we found exogenous L-lysine sensitizes Acinetobacter baumannii, other Gram-negative bacteria (Escherichia coli and Klebsiella pneumoniae) and a Gram-positive bacterium (Mycobacterium smegmatis) to aminoglycosides. Importantly, the combination of L-lysine with aminoglycosides killed clinically isolated multidrug-resistant Acinetobacter baumannii and persister cells. The exogenous L-lysine can increase proton motive force via transmembrane chemical gradient, resulting in aminoglycoside acumination that further accounts for reactive oxygen species production. The combination of L-lysine and antibiotics highlights a promising strategy against bacterial infection. Taylor & Francis 2020-03-20 /pmc/articles/PMC7144275/ /pubmed/32192413 http://dx.doi.org/10.1080/22221751.2020.1740611 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Article Deng, Wanyan Fu, Tiwei Zhang, Zhen Jiang, Xiao Xie, Jianping Sun, Hang Hu, Peng Ren, Hong Zhou, Peifu Liu, Qi Long, Quanxin L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
title | L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
title_full | L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
title_fullStr | L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
title_full_unstemmed | L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
title_short | L-lysine potentiates aminoglycosides against Acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
title_sort | l-lysine potentiates aminoglycosides against acinetobacter baumannii via regulation of proton motive force and antibiotics uptake |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7144275/ https://www.ncbi.nlm.nih.gov/pubmed/32192413 http://dx.doi.org/10.1080/22221751.2020.1740611 |
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