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A Chaperone for the Stator Units of a Bacterial Flagellum

The stator units of the flagellum supply power to the flagellar motor via ion transport across the cytoplasmic membrane and generate torque on the rotor for rotation. Flagellar motors across bacterial species have evolved adaptations that impact and enhance stator function to meet the demands of eac...

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Autores principales: Ribardo, Deborah A., Kelley, Brittni R., Johnson, Jeremiah G., Hendrixson, David R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686046/
https://www.ncbi.nlm.nih.gov/pubmed/31387912
http://dx.doi.org/10.1128/mBio.01732-19
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author Ribardo, Deborah A.
Kelley, Brittni R.
Johnson, Jeremiah G.
Hendrixson, David R.
author_facet Ribardo, Deborah A.
Kelley, Brittni R.
Johnson, Jeremiah G.
Hendrixson, David R.
author_sort Ribardo, Deborah A.
collection PubMed
description The stator units of the flagellum supply power to the flagellar motor via ion transport across the cytoplasmic membrane and generate torque on the rotor for rotation. Flagellar motors across bacterial species have evolved adaptations that impact and enhance stator function to meet the demands of each species, including producing stator units using different fuel types or various stator units for different motility modalities. Campylobacter jejuni produces one of the most complex and powerful flagellar motors by positioning 17 stator units at a greater radial distance than in most other bacteria to increase power and torque for high velocity of motility. We report another evolutionary adaptation impacting flagellar stators by identifying FlgX as a chaperone for C. jejuni stator units to ensure sufficient power and torque for flagellar rotation and motility. We discovered that FlgX maintains MotA and MotB stator protein integrity likely through a direct interaction with MotA that prevents their degradation. Suppressor analysis suggested that the physiology of C. jejuni drives the requirement for FlgX to protect stator units from proteolysis by the FtsH protease complex. C. jejuni ΔflgX was strongly attenuated for colonization of the natural avian host, but colonization capacity was greatly restored by a single mutation in MotA. These findings suggest that the likely sole function of FlgX is to preserve stator unit integrity for the motility required for host interactions. Our findings demonstrate another evolved adaptation in motile bacteria to ensure the equipment of the flagellar motor with sufficient power to generate torque for motility.
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spelling pubmed-66860462019-08-13 A Chaperone for the Stator Units of a Bacterial Flagellum Ribardo, Deborah A. Kelley, Brittni R. Johnson, Jeremiah G. Hendrixson, David R. mBio Research Article The stator units of the flagellum supply power to the flagellar motor via ion transport across the cytoplasmic membrane and generate torque on the rotor for rotation. Flagellar motors across bacterial species have evolved adaptations that impact and enhance stator function to meet the demands of each species, including producing stator units using different fuel types or various stator units for different motility modalities. Campylobacter jejuni produces one of the most complex and powerful flagellar motors by positioning 17 stator units at a greater radial distance than in most other bacteria to increase power and torque for high velocity of motility. We report another evolutionary adaptation impacting flagellar stators by identifying FlgX as a chaperone for C. jejuni stator units to ensure sufficient power and torque for flagellar rotation and motility. We discovered that FlgX maintains MotA and MotB stator protein integrity likely through a direct interaction with MotA that prevents their degradation. Suppressor analysis suggested that the physiology of C. jejuni drives the requirement for FlgX to protect stator units from proteolysis by the FtsH protease complex. C. jejuni ΔflgX was strongly attenuated for colonization of the natural avian host, but colonization capacity was greatly restored by a single mutation in MotA. These findings suggest that the likely sole function of FlgX is to preserve stator unit integrity for the motility required for host interactions. Our findings demonstrate another evolved adaptation in motile bacteria to ensure the equipment of the flagellar motor with sufficient power to generate torque for motility. American Society for Microbiology 2019-08-06 /pmc/articles/PMC6686046/ /pubmed/31387912 http://dx.doi.org/10.1128/mBio.01732-19 Text en Copyright © 2019 Ribardo et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Ribardo, Deborah A.
Kelley, Brittni R.
Johnson, Jeremiah G.
Hendrixson, David R.
A Chaperone for the Stator Units of a Bacterial Flagellum
title A Chaperone for the Stator Units of a Bacterial Flagellum
title_full A Chaperone for the Stator Units of a Bacterial Flagellum
title_fullStr A Chaperone for the Stator Units of a Bacterial Flagellum
title_full_unstemmed A Chaperone for the Stator Units of a Bacterial Flagellum
title_short A Chaperone for the Stator Units of a Bacterial Flagellum
title_sort chaperone for the stator units of a bacterial flagellum
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686046/
https://www.ncbi.nlm.nih.gov/pubmed/31387912
http://dx.doi.org/10.1128/mBio.01732-19
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