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RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation

Bacterial persisters are phenotypic variants that tolerate exposure to lethal antibiotics. These dormant cells are responsible for chronic and recurrent infections. Multiple mechanisms have been linked to persister formation. Here, we report that a complex, consisting of an extracellular poly(dC) an...

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Autores principales: Chen, Xu, Li, Gen, Liao, Xuewei, Fang, Jie, Li, Bo, Yu, Shanshan, Sun, Mingming, Wu, Jun, Zhang, Lihao, Hu, Yi, Jiao, Jiaguo, Liu, Ting, Xu, Li, Chen, Xiaoyun, Liu, Manqiang, Li, Huixin, Hu, Feng, Sun, Kouhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318315/
https://www.ncbi.nlm.nih.gov/pubmed/30604752
http://dx.doi.org/10.1038/s41467-018-07861-z
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author Chen, Xu
Li, Gen
Liao, Xuewei
Fang, Jie
Li, Bo
Yu, Shanshan
Sun, Mingming
Wu, Jun
Zhang, Lihao
Hu, Yi
Jiao, Jiaguo
Liu, Ting
Xu, Li
Chen, Xiaoyun
Liu, Manqiang
Li, Huixin
Hu, Feng
Sun, Kouhong
author_facet Chen, Xu
Li, Gen
Liao, Xuewei
Fang, Jie
Li, Bo
Yu, Shanshan
Sun, Mingming
Wu, Jun
Zhang, Lihao
Hu, Yi
Jiao, Jiaguo
Liu, Ting
Xu, Li
Chen, Xiaoyun
Liu, Manqiang
Li, Huixin
Hu, Feng
Sun, Kouhong
author_sort Chen, Xu
collection PubMed
description Bacterial persisters are phenotypic variants that tolerate exposure to lethal antibiotics. These dormant cells are responsible for chronic and recurrent infections. Multiple mechanisms have been linked to persister formation. Here, we report that a complex, consisting of an extracellular poly(dC) and its membrane-associated binding protein RmlB, appears to be associated with persistence of the opportunistic pathogen Pseudomonas aeruginosa. Environmental stimuli triggers a switch in the complex physiological state (from poly(dC)/RmlB to P-poly(dC)/RmlB or RmlB). In response to the switch, bacteria decrease proton motive force and intracellular ATP levels, forming dormant cells. This alteration in complex status is linked to a (p)ppGpp-controlled signaling pathway that includes inorganic polyphosphate, Lon protease, exonuclease VII (XseA/XseB), and the type III secretion system. The persistence might be also an adaptive response to the lethal action of the dTDP-l-rhamnose pathway shutdown, which occurs due to switching of poly(dC)/RmlB.
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spelling pubmed-63183152019-01-07 RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation Chen, Xu Li, Gen Liao, Xuewei Fang, Jie Li, Bo Yu, Shanshan Sun, Mingming Wu, Jun Zhang, Lihao Hu, Yi Jiao, Jiaguo Liu, Ting Xu, Li Chen, Xiaoyun Liu, Manqiang Li, Huixin Hu, Feng Sun, Kouhong Nat Commun Article Bacterial persisters are phenotypic variants that tolerate exposure to lethal antibiotics. These dormant cells are responsible for chronic and recurrent infections. Multiple mechanisms have been linked to persister formation. Here, we report that a complex, consisting of an extracellular poly(dC) and its membrane-associated binding protein RmlB, appears to be associated with persistence of the opportunistic pathogen Pseudomonas aeruginosa. Environmental stimuli triggers a switch in the complex physiological state (from poly(dC)/RmlB to P-poly(dC)/RmlB or RmlB). In response to the switch, bacteria decrease proton motive force and intracellular ATP levels, forming dormant cells. This alteration in complex status is linked to a (p)ppGpp-controlled signaling pathway that includes inorganic polyphosphate, Lon protease, exonuclease VII (XseA/XseB), and the type III secretion system. The persistence might be also an adaptive response to the lethal action of the dTDP-l-rhamnose pathway shutdown, which occurs due to switching of poly(dC)/RmlB. Nature Publishing Group UK 2019-01-03 /pmc/articles/PMC6318315/ /pubmed/30604752 http://dx.doi.org/10.1038/s41467-018-07861-z Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Xu
Li, Gen
Liao, Xuewei
Fang, Jie
Li, Bo
Yu, Shanshan
Sun, Mingming
Wu, Jun
Zhang, Lihao
Hu, Yi
Jiao, Jiaguo
Liu, Ting
Xu, Li
Chen, Xiaoyun
Liu, Manqiang
Li, Huixin
Hu, Feng
Sun, Kouhong
RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation
title RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation
title_full RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation
title_fullStr RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation
title_full_unstemmed RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation
title_short RETRACTED ARTICLE: A switch in the poly(dC)/RmlB complex regulates bacterial persister formation
title_sort retracted article: a switch in the poly(dc)/rmlb complex regulates bacterial persister formation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318315/
https://www.ncbi.nlm.nih.gov/pubmed/30604752
http://dx.doi.org/10.1038/s41467-018-07861-z
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