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FtsZ-Dependent Elongation of a Coccoid Bacterium

A mechanistic understanding of the determination and maintenance of the simplest bacterial cell shape, a sphere, remains elusive compared with that of more complex shapes. Cocci seem to lack a dedicated elongation machinery, and a spherical shape has been considered an evolutionary dead-end morpholo...

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Autores principales: Pereira, Ana R., Hsin, Jen, Król, Ewa, Tavares, Andreia C., Flores, Pierre, Hoiczyk, Egbert, Ng, Natalie, Dajkovic, Alex, Brun, Yves V., VanNieuwenhze, Michael S., Roemer, Terry, Carballido-Lopez, Rut, Scheffers, Dirk-Jan, Huang, Kerwyn Casey, Pinho, Mariana G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013293/
https://www.ncbi.nlm.nih.gov/pubmed/27601570
http://dx.doi.org/10.1128/mBio.00908-16
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author Pereira, Ana R.
Hsin, Jen
Król, Ewa
Tavares, Andreia C.
Flores, Pierre
Hoiczyk, Egbert
Ng, Natalie
Dajkovic, Alex
Brun, Yves V.
VanNieuwenhze, Michael S.
Roemer, Terry
Carballido-Lopez, Rut
Scheffers, Dirk-Jan
Huang, Kerwyn Casey
Pinho, Mariana G.
author_facet Pereira, Ana R.
Hsin, Jen
Król, Ewa
Tavares, Andreia C.
Flores, Pierre
Hoiczyk, Egbert
Ng, Natalie
Dajkovic, Alex
Brun, Yves V.
VanNieuwenhze, Michael S.
Roemer, Terry
Carballido-Lopez, Rut
Scheffers, Dirk-Jan
Huang, Kerwyn Casey
Pinho, Mariana G.
author_sort Pereira, Ana R.
collection PubMed
description A mechanistic understanding of the determination and maintenance of the simplest bacterial cell shape, a sphere, remains elusive compared with that of more complex shapes. Cocci seem to lack a dedicated elongation machinery, and a spherical shape has been considered an evolutionary dead-end morphology, as a transition from a spherical to a rod-like shape has never been observed in bacteria. Here we show that a Staphylococcus aureus mutant (M5) expressing the ftsZ(G193D) allele exhibits elongated cells. Molecular dynamics simulations and in vitro studies indicate that FtsZ(G193D) filaments are more twisted and shorter than wild-type filaments. In vivo, M5 cell wall deposition is initiated asymmetrically, only on one side of the cell, and progresses into a helical pattern rather than into a constricting ring as in wild-type cells. This helical pattern of wall insertion leads to elongation, as in rod-shaped cells. Thus, structural flexibility of FtsZ filaments can result in an FtsZ-dependent mechanism for generating elongated cells from cocci.
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spelling pubmed-50132932016-09-16 FtsZ-Dependent Elongation of a Coccoid Bacterium Pereira, Ana R. Hsin, Jen Król, Ewa Tavares, Andreia C. Flores, Pierre Hoiczyk, Egbert Ng, Natalie Dajkovic, Alex Brun, Yves V. VanNieuwenhze, Michael S. Roemer, Terry Carballido-Lopez, Rut Scheffers, Dirk-Jan Huang, Kerwyn Casey Pinho, Mariana G. mBio Research Article A mechanistic understanding of the determination and maintenance of the simplest bacterial cell shape, a sphere, remains elusive compared with that of more complex shapes. Cocci seem to lack a dedicated elongation machinery, and a spherical shape has been considered an evolutionary dead-end morphology, as a transition from a spherical to a rod-like shape has never been observed in bacteria. Here we show that a Staphylococcus aureus mutant (M5) expressing the ftsZ(G193D) allele exhibits elongated cells. Molecular dynamics simulations and in vitro studies indicate that FtsZ(G193D) filaments are more twisted and shorter than wild-type filaments. In vivo, M5 cell wall deposition is initiated asymmetrically, only on one side of the cell, and progresses into a helical pattern rather than into a constricting ring as in wild-type cells. This helical pattern of wall insertion leads to elongation, as in rod-shaped cells. Thus, structural flexibility of FtsZ filaments can result in an FtsZ-dependent mechanism for generating elongated cells from cocci. American Society for Microbiology 2016-09-06 /pmc/articles/PMC5013293/ /pubmed/27601570 http://dx.doi.org/10.1128/mBio.00908-16 Text en Copyright © 2016 Pereira et al. http://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 (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Pereira, Ana R.
Hsin, Jen
Król, Ewa
Tavares, Andreia C.
Flores, Pierre
Hoiczyk, Egbert
Ng, Natalie
Dajkovic, Alex
Brun, Yves V.
VanNieuwenhze, Michael S.
Roemer, Terry
Carballido-Lopez, Rut
Scheffers, Dirk-Jan
Huang, Kerwyn Casey
Pinho, Mariana G.
FtsZ-Dependent Elongation of a Coccoid Bacterium
title FtsZ-Dependent Elongation of a Coccoid Bacterium
title_full FtsZ-Dependent Elongation of a Coccoid Bacterium
title_fullStr FtsZ-Dependent Elongation of a Coccoid Bacterium
title_full_unstemmed FtsZ-Dependent Elongation of a Coccoid Bacterium
title_short FtsZ-Dependent Elongation of a Coccoid Bacterium
title_sort ftsz-dependent elongation of a coccoid bacterium
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5013293/
https://www.ncbi.nlm.nih.gov/pubmed/27601570
http://dx.doi.org/10.1128/mBio.00908-16
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