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Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family

Rod-shaped bacteria typically elongate and divide by transverse fission. However, several bacterial species can form rod-shaped cells that divide longitudinally. Here, we study the evolution of cell shape and division mode within the family Neisseriaceae, which includes Gram-negative coccoid and rod...

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Autores principales: Nyongesa, Sammy, Weber, Philipp M., Bernet, Ève, Pulido, Francisco, Nieves, Cecilia, Nieckarz, Marta, Delaby, Marie, Viehboeck, Tobias, Krause, Nicole, Rivera-Millot, Alex, Nakamura, Arnaldo, Vischer, Norbert O. E., vanNieuwenhze, Michael, Brun, Yves V., Cava, Felipe, Bulgheresi, Silvia, Veyrier, Frédéric J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395523/
https://www.ncbi.nlm.nih.gov/pubmed/35995772
http://dx.doi.org/10.1038/s41467-022-32260-w
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author Nyongesa, Sammy
Weber, Philipp M.
Bernet, Ève
Pulido, Francisco
Nieves, Cecilia
Nieckarz, Marta
Delaby, Marie
Viehboeck, Tobias
Krause, Nicole
Rivera-Millot, Alex
Nakamura, Arnaldo
Vischer, Norbert O. E.
vanNieuwenhze, Michael
Brun, Yves V.
Cava, Felipe
Bulgheresi, Silvia
Veyrier, Frédéric J.
author_facet Nyongesa, Sammy
Weber, Philipp M.
Bernet, Ève
Pulido, Francisco
Nieves, Cecilia
Nieckarz, Marta
Delaby, Marie
Viehboeck, Tobias
Krause, Nicole
Rivera-Millot, Alex
Nakamura, Arnaldo
Vischer, Norbert O. E.
vanNieuwenhze, Michael
Brun, Yves V.
Cava, Felipe
Bulgheresi, Silvia
Veyrier, Frédéric J.
author_sort Nyongesa, Sammy
collection PubMed
description Rod-shaped bacteria typically elongate and divide by transverse fission. However, several bacterial species can form rod-shaped cells that divide longitudinally. Here, we study the evolution of cell shape and division mode within the family Neisseriaceae, which includes Gram-negative coccoid and rod-shaped species. In particular, bacteria of the genera Alysiella, Simonsiella and Conchiformibius, which can be found in the oral cavity of mammals, are multicellular and divide longitudinally. We use comparative genomics and ultrastructural microscopy to infer that longitudinal division within Neisseriaceae evolved from a rod-shaped ancestor. In multicellular longitudinally-dividing species, neighbouring cells within multicellular filaments are attached by their lateral peptidoglycan. In these bacteria, peptidoglycan insertion does not appear concentric, i.e. from the cell periphery to its centre, but as a medial sheet guillotining each cell. Finally, we identify genes and alleles associated with multicellularity and longitudinal division, including the acquisition of amidase-encoding gene amiC2, and amino acid changes in proteins including MreB and FtsA. Introduction of amiC2 and allelic substitution of mreB in a rod-shaped species that divides by transverse fission results in shorter cells with longer septa. Our work sheds light on the evolution of multicellularity and longitudinal division in bacteria, and suggests that members of the Neisseriaceae family may be good models to study these processes due to their morphological plasticity and genetic tractability.
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spelling pubmed-93955232022-08-24 Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family Nyongesa, Sammy Weber, Philipp M. Bernet, Ève Pulido, Francisco Nieves, Cecilia Nieckarz, Marta Delaby, Marie Viehboeck, Tobias Krause, Nicole Rivera-Millot, Alex Nakamura, Arnaldo Vischer, Norbert O. E. vanNieuwenhze, Michael Brun, Yves V. Cava, Felipe Bulgheresi, Silvia Veyrier, Frédéric J. Nat Commun Article Rod-shaped bacteria typically elongate and divide by transverse fission. However, several bacterial species can form rod-shaped cells that divide longitudinally. Here, we study the evolution of cell shape and division mode within the family Neisseriaceae, which includes Gram-negative coccoid and rod-shaped species. In particular, bacteria of the genera Alysiella, Simonsiella and Conchiformibius, which can be found in the oral cavity of mammals, are multicellular and divide longitudinally. We use comparative genomics and ultrastructural microscopy to infer that longitudinal division within Neisseriaceae evolved from a rod-shaped ancestor. In multicellular longitudinally-dividing species, neighbouring cells within multicellular filaments are attached by their lateral peptidoglycan. In these bacteria, peptidoglycan insertion does not appear concentric, i.e. from the cell periphery to its centre, but as a medial sheet guillotining each cell. Finally, we identify genes and alleles associated with multicellularity and longitudinal division, including the acquisition of amidase-encoding gene amiC2, and amino acid changes in proteins including MreB and FtsA. Introduction of amiC2 and allelic substitution of mreB in a rod-shaped species that divides by transverse fission results in shorter cells with longer septa. Our work sheds light on the evolution of multicellularity and longitudinal division in bacteria, and suggests that members of the Neisseriaceae family may be good models to study these processes due to their morphological plasticity and genetic tractability. Nature Publishing Group UK 2022-08-22 /pmc/articles/PMC9395523/ /pubmed/35995772 http://dx.doi.org/10.1038/s41467-022-32260-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nyongesa, Sammy
Weber, Philipp M.
Bernet, Ève
Pulido, Francisco
Nieves, Cecilia
Nieckarz, Marta
Delaby, Marie
Viehboeck, Tobias
Krause, Nicole
Rivera-Millot, Alex
Nakamura, Arnaldo
Vischer, Norbert O. E.
vanNieuwenhze, Michael
Brun, Yves V.
Cava, Felipe
Bulgheresi, Silvia
Veyrier, Frédéric J.
Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family
title Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family
title_full Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family
title_fullStr Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family
title_full_unstemmed Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family
title_short Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family
title_sort evolution of longitudinal division in multicellular bacteria of the neisseriaceae family
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9395523/
https://www.ncbi.nlm.nih.gov/pubmed/35995772
http://dx.doi.org/10.1038/s41467-022-32260-w
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