Evolution of longitudinal division in multicellular bacteria of the Neisseriaceae family.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
22 08 2022
Historique:
received: 10 01 2022
accepted: 25 07 2022
entrez: 22 8 2022
pubmed: 23 8 2022
medline: 25 8 2022
Statut: epublish

Résumé

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.

Identifiants

pubmed: 35995772
doi: 10.1038/s41467-022-32260-w
pii: 10.1038/s41467-022-32260-w
pmc: PMC9395523
doi:

Substances chimiques

Bacterial Proteins 0
Peptidoglycan 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4853

Informations de copyright

© 2022. The Author(s).

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Auteurs

Sammy Nyongesa (S)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.

Philipp M Weber (PM)

Department of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria.
University of Vienna, Vienna Doctoral School of Ecology and Evolution, Vienna, Austria.

Ève Bernet (È)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.

Francisco Pulido (F)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.

Cecilia Nieves (C)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.

Marta Nieckarz (M)

Department of Molecular Biology and Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå Centre for Microbial Research (UCMR), Umeå University, Umeå, SE-90187, Sweden.

Marie Delaby (M)

Département de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, Canada.

Tobias Viehboeck (T)

Department of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria.
University of Vienna, Vienna Doctoral School of Ecology and Evolution, Vienna, Austria.
Division of Microbial Ecology, Center for Microbiology and Environmental Systems Science, , University of Vienna, Djerassiplatz 1, 1030, Vienna, Austria.

Nicole Krause (N)

Department of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria.
University of Vienna, Vienna Doctoral School of Ecology and Evolution, Vienna, Austria.

Alex Rivera-Millot (A)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.

Arnaldo Nakamura (A)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.

Norbert O E Vischer (NOE)

Bacterial Cell Biology & Physiology, Swammerdam Institute of Life Sciences, Faculty of Science, University of Amsterdam, Science Park 904, 1098, Amsterdam, the Netherlands.

Michael vanNieuwenhze (M)

Indiana University, Bloomington, IN, 47405, USA.

Yves V Brun (YV)

Département de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, Canada.

Felipe Cava (F)

Department of Molecular Biology and Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå Centre for Microbial Research (UCMR), Umeå University, Umeå, SE-90187, Sweden.

Silvia Bulgheresi (S)

Department of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria. silvia.bulgheresi@univie.ac.at.

Frédéric J Veyrier (FJ)

INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada. frederic.veyrier@inrs.ca.

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Classifications MeSH