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Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus

The predatory bacterium Bdellovibrio bacteriovorus swims rapidly by rotation of a single, polar flagellum comprised of a helical filament of flagellin monomers, contained within a membrane sheath and powered by a basal motor complex. Bdellovibrio collides with, enters and replicates within bacterial...

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Detalles Bibliográficos
Autores principales: Lambert, Carey, Evans, Katy J, Till, Rob, Hobley, Laura, Capeness, Michael, Rendulic, Snjezana, Schuster, Stephan C, Aizawa, Shin-Ichi, Sockett, R Elizabeth
Formato: Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1453311/
https://www.ncbi.nlm.nih.gov/pubmed/16573680
http://dx.doi.org/10.1111/j.1365-2958.2006.05081.x
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author Lambert, Carey
Evans, Katy J
Till, Rob
Hobley, Laura
Capeness, Michael
Rendulic, Snjezana
Schuster, Stephan C
Aizawa, Shin-Ichi
Sockett, R Elizabeth
author_facet Lambert, Carey
Evans, Katy J
Till, Rob
Hobley, Laura
Capeness, Michael
Rendulic, Snjezana
Schuster, Stephan C
Aizawa, Shin-Ichi
Sockett, R Elizabeth
author_sort Lambert, Carey
collection PubMed
description The predatory bacterium Bdellovibrio bacteriovorus swims rapidly by rotation of a single, polar flagellum comprised of a helical filament of flagellin monomers, contained within a membrane sheath and powered by a basal motor complex. Bdellovibrio collides with, enters and replicates within bacterial prey, a process previously suggested to firstly require flagellar motility and then flagellar shedding upon prey entry. Here we show that flagella are not always shed upon prey entry and we study the six fliC flagellin genes of B. bacteriovorus, finding them all conserved and expressed in genome strain HD100 and the widely studied lab strain 109J. Individual inactivation of five of the fliC genes gave mutant Bdellovibrio that still made flagella, and which were motile and predatory. Inactivation of the sixth fliC gene abolished normal flagellar synthesis and motility, but a disordered flagellar sheath was still seen. We find that this non-motile mutant was still able to predate when directly applied to lawns of YFP-labelled prey bacteria, showing that flagellar motility is not essential for prey entry but important for efficient encounters with prey in liquid environments.
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spelling pubmed-14533112006-05-01 Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus Lambert, Carey Evans, Katy J Till, Rob Hobley, Laura Capeness, Michael Rendulic, Snjezana Schuster, Stephan C Aizawa, Shin-Ichi Sockett, R Elizabeth Mol Microbiol Research Articles The predatory bacterium Bdellovibrio bacteriovorus swims rapidly by rotation of a single, polar flagellum comprised of a helical filament of flagellin monomers, contained within a membrane sheath and powered by a basal motor complex. Bdellovibrio collides with, enters and replicates within bacterial prey, a process previously suggested to firstly require flagellar motility and then flagellar shedding upon prey entry. Here we show that flagella are not always shed upon prey entry and we study the six fliC flagellin genes of B. bacteriovorus, finding them all conserved and expressed in genome strain HD100 and the widely studied lab strain 109J. Individual inactivation of five of the fliC genes gave mutant Bdellovibrio that still made flagella, and which were motile and predatory. Inactivation of the sixth fliC gene abolished normal flagellar synthesis and motility, but a disordered flagellar sheath was still seen. We find that this non-motile mutant was still able to predate when directly applied to lawns of YFP-labelled prey bacteria, showing that flagellar motility is not essential for prey entry but important for efficient encounters with prey in liquid environments. Blackwell Publishing Ltd 2006-04 2006-03-03 /pmc/articles/PMC1453311/ /pubmed/16573680 http://dx.doi.org/10.1111/j.1365-2958.2006.05081.x Text en © 2006 The Authors Journal compilation © 2006 Blackwell Publishing Ltd
spellingShingle Research Articles
Lambert, Carey
Evans, Katy J
Till, Rob
Hobley, Laura
Capeness, Michael
Rendulic, Snjezana
Schuster, Stephan C
Aizawa, Shin-Ichi
Sockett, R Elizabeth
Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus
title Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus
title_full Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus
title_fullStr Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus
title_full_unstemmed Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus
title_short Characterizing the flagellar filament and the role of motility in bacterial prey-penetration by Bdellovibrio bacteriovorus
title_sort characterizing the flagellar filament and the role of motility in bacterial prey-penetration by bdellovibrio bacteriovorus
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1453311/
https://www.ncbi.nlm.nih.gov/pubmed/16573680
http://dx.doi.org/10.1111/j.1365-2958.2006.05081.x
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