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Host-Polarized Cell Growth in Animal Symbionts
To determine the fundamentals of cell growth, we must extend cell biological studies to non-model organisms. Here, we investigated the growth modes of the only two rods known to widen instead of elongating, Candidatus Thiosymbion oneisti and Thiosymbion hypermnestrae. These bacteria are attached by...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611161/ https://www.ncbi.nlm.nih.gov/pubmed/29576473 http://dx.doi.org/10.1016/j.cub.2018.02.028 |
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author | Pende, Nika Wang, Jinglan Weber, Philipp M. Verheul, Jolanda Kuru, Erkin Rittmann, Simon K.-M.R. Leisch, Nikolaus VanNieuwenhze, Michael S. Brun, Yves V. den Blaauwen, Tanneke Bulgheresi, Silvia |
author_facet | Pende, Nika Wang, Jinglan Weber, Philipp M. Verheul, Jolanda Kuru, Erkin Rittmann, Simon K.-M.R. Leisch, Nikolaus VanNieuwenhze, Michael S. Brun, Yves V. den Blaauwen, Tanneke Bulgheresi, Silvia |
author_sort | Pende, Nika |
collection | PubMed |
description | To determine the fundamentals of cell growth, we must extend cell biological studies to non-model organisms. Here, we investigated the growth modes of the only two rods known to widen instead of elongating, Candidatus Thiosymbion oneisti and Thiosymbion hypermnestrae. These bacteria are attached by one pole to the surface of their respective nematode hosts. By incubating live Ca. T. oneisti and T. hypermnestrae with a peptidoglycan metabolic probe, we observed that the insertion of new cell wall starts at the poles and proceeds inward, concomitantly with FtsZ-based membrane constriction. Remarkably, in Ca. T. hypermnestrae, the proximal, animal-attached pole grows before the distal, free pole, indicating that the peptidoglycan synthesis machinery is host oriented. Immunostaining of the symbionts with an antibody against the actin homolog MreB revealed that it was arranged medially—that is, parallel to the cell long axis—throughout the symbiont life cycle. Given that depolymerization of MreB abolished newly synthesized peptidoglycan insertion and impaired divisome assembly, we conclude that MreB function is required for symbiont widening and division. In conclusion, our data invoke a reassessment of the localization and function of the bacterial actin homolog. |
format | Online Article Text |
id | pubmed-6611161 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-66111612019-07-05 Host-Polarized Cell Growth in Animal Symbionts Pende, Nika Wang, Jinglan Weber, Philipp M. Verheul, Jolanda Kuru, Erkin Rittmann, Simon K.-M.R. Leisch, Nikolaus VanNieuwenhze, Michael S. Brun, Yves V. den Blaauwen, Tanneke Bulgheresi, Silvia Curr Biol Article To determine the fundamentals of cell growth, we must extend cell biological studies to non-model organisms. Here, we investigated the growth modes of the only two rods known to widen instead of elongating, Candidatus Thiosymbion oneisti and Thiosymbion hypermnestrae. These bacteria are attached by one pole to the surface of their respective nematode hosts. By incubating live Ca. T. oneisti and T. hypermnestrae with a peptidoglycan metabolic probe, we observed that the insertion of new cell wall starts at the poles and proceeds inward, concomitantly with FtsZ-based membrane constriction. Remarkably, in Ca. T. hypermnestrae, the proximal, animal-attached pole grows before the distal, free pole, indicating that the peptidoglycan synthesis machinery is host oriented. Immunostaining of the symbionts with an antibody against the actin homolog MreB revealed that it was arranged medially—that is, parallel to the cell long axis—throughout the symbiont life cycle. Given that depolymerization of MreB abolished newly synthesized peptidoglycan insertion and impaired divisome assembly, we conclude that MreB function is required for symbiont widening and division. In conclusion, our data invoke a reassessment of the localization and function of the bacterial actin homolog. 2018-03-22 2018-04-02 /pmc/articles/PMC6611161/ /pubmed/29576473 http://dx.doi.org/10.1016/j.cub.2018.02.028 Text en This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Article Pende, Nika Wang, Jinglan Weber, Philipp M. Verheul, Jolanda Kuru, Erkin Rittmann, Simon K.-M.R. Leisch, Nikolaus VanNieuwenhze, Michael S. Brun, Yves V. den Blaauwen, Tanneke Bulgheresi, Silvia Host-Polarized Cell Growth in Animal Symbionts |
title | Host-Polarized Cell Growth in Animal Symbionts |
title_full | Host-Polarized Cell Growth in Animal Symbionts |
title_fullStr | Host-Polarized Cell Growth in Animal Symbionts |
title_full_unstemmed | Host-Polarized Cell Growth in Animal Symbionts |
title_short | Host-Polarized Cell Growth in Animal Symbionts |
title_sort | host-polarized cell growth in animal symbionts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6611161/ https://www.ncbi.nlm.nih.gov/pubmed/29576473 http://dx.doi.org/10.1016/j.cub.2018.02.028 |
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