Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Deng, Wanyan, Fu, Tiwei, Zhang, Zhen, Jiang, Xiao, Xie, Jianping, Sun, Hang, Hu, Peng, Ren, Hong, Zhou, Peifu, Liu, Qi, Long, Quanxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
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
_version_ 1783519806215946240
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
work_keys_str_mv AT dengwanyan llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT futiwei llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT zhangzhen llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT jiangxiao llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT xiejianping llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT sunhang llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT hupeng llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT renhong llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT zhoupeifu llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT liuqi llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake
AT longquanxin llysinepotentiatesaminoglycosidesagainstacinetobacterbaumanniiviaregulationofprotonmotiveforceandantibioticsuptake