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Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection

Bacterial small RNAs (sRNAs) posttranscriptionally regulate gene expressions involved in various biological processes, including pathogenicity. Our previous study identified sRNAs, the expression of which was up-regulated in Bordetella pertussis, the causative agent of whooping cough, upon tracheal...

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Autores principales: Hiramatsu, Yukihiro, Nishida, Takashi, Nugraha, Dendi Krisna, Osada-Oka, Mayuko, Nakane, Daisuke, Imada, Katsumi, Horiguchi, Yasuhiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9770993/
https://www.ncbi.nlm.nih.gov/pubmed/36542710
http://dx.doi.org/10.1126/sciadv.ade8971
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author Hiramatsu, Yukihiro
Nishida, Takashi
Nugraha, Dendi Krisna
Osada-Oka, Mayuko
Nakane, Daisuke
Imada, Katsumi
Horiguchi, Yasuhiko
author_facet Hiramatsu, Yukihiro
Nishida, Takashi
Nugraha, Dendi Krisna
Osada-Oka, Mayuko
Nakane, Daisuke
Imada, Katsumi
Horiguchi, Yasuhiko
author_sort Hiramatsu, Yukihiro
collection PubMed
description Bacterial small RNAs (sRNAs) posttranscriptionally regulate gene expressions involved in various biological processes, including pathogenicity. Our previous study identified sRNAs, the expression of which was up-regulated in Bordetella pertussis, the causative agent of whooping cough, upon tracheal colonization of the bacteria; however, their roles in bacterial infection remain unknown. Here, we found that one sRNA, Bpr4, contributes to B. pertussis infection by posttranscriptionally up-regulating filamentous hemagglutinin (FHA), a major adhesin of the bacteria. Bpr4 bound to the 5′ untranslated region of fhaB mRNA encoding FHA and inhibited its degradation mediated by RNaseE. Our results demonstrated that Bpr4 up-regulation was triggered by the interference of flagellar rotation, which caused the disengagement of MotA, a flagellar stator. Subsequently, MotA activated a diguanylate cyclase to generate cyclic di-GMP, which plays a role in Bpr4 up-regulation through the RisK/RisA two-component system. Our findings indicate that a flagellum-triggered sensory system contributes to B. pertussis infection.
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spelling pubmed-97709932022-12-28 Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection Hiramatsu, Yukihiro Nishida, Takashi Nugraha, Dendi Krisna Osada-Oka, Mayuko Nakane, Daisuke Imada, Katsumi Horiguchi, Yasuhiko Sci Adv Biomedicine and Life Sciences Bacterial small RNAs (sRNAs) posttranscriptionally regulate gene expressions involved in various biological processes, including pathogenicity. Our previous study identified sRNAs, the expression of which was up-regulated in Bordetella pertussis, the causative agent of whooping cough, upon tracheal colonization of the bacteria; however, their roles in bacterial infection remain unknown. Here, we found that one sRNA, Bpr4, contributes to B. pertussis infection by posttranscriptionally up-regulating filamentous hemagglutinin (FHA), a major adhesin of the bacteria. Bpr4 bound to the 5′ untranslated region of fhaB mRNA encoding FHA and inhibited its degradation mediated by RNaseE. Our results demonstrated that Bpr4 up-regulation was triggered by the interference of flagellar rotation, which caused the disengagement of MotA, a flagellar stator. Subsequently, MotA activated a diguanylate cyclase to generate cyclic di-GMP, which plays a role in Bpr4 up-regulation through the RisK/RisA two-component system. Our findings indicate that a flagellum-triggered sensory system contributes to B. pertussis infection. American Association for the Advancement of Science 2022-12-21 /pmc/articles/PMC9770993/ /pubmed/36542710 http://dx.doi.org/10.1126/sciadv.ade8971 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (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 Biomedicine and Life Sciences
Hiramatsu, Yukihiro
Nishida, Takashi
Nugraha, Dendi Krisna
Osada-Oka, Mayuko
Nakane, Daisuke
Imada, Katsumi
Horiguchi, Yasuhiko
Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection
title Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection
title_full Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection
title_fullStr Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection
title_full_unstemmed Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection
title_short Interference of flagellar rotation up-regulates the expression of small RNA contributing to Bordetella pertussis infection
title_sort interference of flagellar rotation up-regulates the expression of small rna contributing to bordetella pertussis infection
topic Biomedicine and Life Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9770993/
https://www.ncbi.nlm.nih.gov/pubmed/36542710
http://dx.doi.org/10.1126/sciadv.ade8971
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