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Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector

Cyclic diguanosine monophosphate (c-di-GMP) is widely used by bacteria to control biological functions in response to diverse signals or cues. A previous study showed that potential c-di-GMP metabolic enzymes play a role in the regulation of biofilm formation and motility in Acinetobacter baumannii....

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Autores principales: Guo, Quan, Cui, Binbin, Wang, Mingfang, Li, Xia, Tan, Huihui, Song, Shihao, Zhou, Jianuan, Zhang, Lian-Hui, Deng, Yinyue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564936/
https://www.ncbi.nlm.nih.gov/pubmed/36191190
http://dx.doi.org/10.1073/pnas.2209838119
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author Guo, Quan
Cui, Binbin
Wang, Mingfang
Li, Xia
Tan, Huihui
Song, Shihao
Zhou, Jianuan
Zhang, Lian-Hui
Deng, Yinyue
author_facet Guo, Quan
Cui, Binbin
Wang, Mingfang
Li, Xia
Tan, Huihui
Song, Shihao
Zhou, Jianuan
Zhang, Lian-Hui
Deng, Yinyue
author_sort Guo, Quan
collection PubMed
description Cyclic diguanosine monophosphate (c-di-GMP) is widely used by bacteria to control biological functions in response to diverse signals or cues. A previous study showed that potential c-di-GMP metabolic enzymes play a role in the regulation of biofilm formation and motility in Acinetobacter baumannii. However, it was unclear whether and how A. baumannii cells use c-di-GMP signaling to modulate biological functions. Here, we report that c-di-GMP is an important intracellular signal in the modulation of biofilm formation, motility, and virulence in A. baumannii. The intracellular level of c-di-GMP is principally controlled by the diguanylate cyclases (DGCs) A1S_1695, A1S_2506, and A1S_3296 and the phosphodiesterase (PDE) A1S_1254. Intriguingly, we revealed that A1S_2419 (an elongation factor P [EF-P]), is a novel c-di-GMP effector in A. baumannii. Response to a c-di-GMP signal boosted A1S_2419 activity to rescue ribosomes from stalling during synthesis of proteins containing consecutive prolines and thus regulate A. baumannii physiology and pathogenesis. Our study presents a unique and widely conserved effector that controls bacterial physiology and virulence by sensing the second messenger c-di-GMP.
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spelling pubmed-95649362022-10-15 Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector Guo, Quan Cui, Binbin Wang, Mingfang Li, Xia Tan, Huihui Song, Shihao Zhou, Jianuan Zhang, Lian-Hui Deng, Yinyue Proc Natl Acad Sci U S A Biological Sciences Cyclic diguanosine monophosphate (c-di-GMP) is widely used by bacteria to control biological functions in response to diverse signals or cues. A previous study showed that potential c-di-GMP metabolic enzymes play a role in the regulation of biofilm formation and motility in Acinetobacter baumannii. However, it was unclear whether and how A. baumannii cells use c-di-GMP signaling to modulate biological functions. Here, we report that c-di-GMP is an important intracellular signal in the modulation of biofilm formation, motility, and virulence in A. baumannii. The intracellular level of c-di-GMP is principally controlled by the diguanylate cyclases (DGCs) A1S_1695, A1S_2506, and A1S_3296 and the phosphodiesterase (PDE) A1S_1254. Intriguingly, we revealed that A1S_2419 (an elongation factor P [EF-P]), is a novel c-di-GMP effector in A. baumannii. Response to a c-di-GMP signal boosted A1S_2419 activity to rescue ribosomes from stalling during synthesis of proteins containing consecutive prolines and thus regulate A. baumannii physiology and pathogenesis. Our study presents a unique and widely conserved effector that controls bacterial physiology and virulence by sensing the second messenger c-di-GMP. National Academy of Sciences 2022-10-03 2022-10-11 /pmc/articles/PMC9564936/ /pubmed/36191190 http://dx.doi.org/10.1073/pnas.2209838119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Guo, Quan
Cui, Binbin
Wang, Mingfang
Li, Xia
Tan, Huihui
Song, Shihao
Zhou, Jianuan
Zhang, Lian-Hui
Deng, Yinyue
Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
title Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
title_full Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
title_fullStr Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
title_full_unstemmed Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
title_short Elongation factor P modulates Acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
title_sort elongation factor p modulates acinetobacter baumannii physiology and virulence as a cyclic dimeric guanosine monophosphate effector
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9564936/
https://www.ncbi.nlm.nih.gov/pubmed/36191190
http://dx.doi.org/10.1073/pnas.2209838119
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