Evidence map›Paper›PMID 35995772›Full record

ArticleNature communications2022

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

Sammy Nyongesa, Philipp M Weber, Ève Bernet, Francisco Pulido, Cecilia Nieves, Marta Nieckarz, Marie Delaby, Tobias Viehboeck, Nicole Krause, Alex Rivera-Millot and 7 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Frontiers in cellular and infection microbiology · 2025
    Review
  6. International journal of systematic and evolutionary microbiology · 2024
    Article
  7. Article
  8. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 6 institutions in 5 countries.

Sammy Nyongesa *INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.
Philipp M Weber *Department of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-1577-2690
Ève BernetINRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.ORCID http://orcid.org/0000-0001-9566-6320
Francisco PulidoINRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.
Cecilia NievesINRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.ORCID http://orcid.org/0000-0001-7324-1663
Marta NieckarzDepartment of Molecular Biology and Laboratory for Molecular Infection Medicine Sweden (MIMS), Umeå Centre for Microbial Research (UCMR), Umeå University, Umeå, SE-90187, Sweden.ORCID http://orcid.org/0000-0002-3813-4923
Marie DelabyDépartement de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, Canada.
Tobias ViehboeckDepartment of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0002-7128-3461
Nicole KrauseDepartment of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria.ORCID http://orcid.org/0000-0001-7229-9185
Alex Rivera-MillotINRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.
Arnaldo NakamuraINRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada.ORCID http://orcid.org/0000-0002-0777-7790
Norbert O E VischerBacterial Cell Biology & Physiology, Swammerdam Institute of Life Sciences, Faculty of Science, University of Amsterdam, Science Park 904, 1098, Amsterdam, the Netherlands.
Michael vanNieuwenhzeIndiana University, Bloomington, IN, 47405, USA.ORCID http://orcid.org/0000-0001-6093-5949
Yves V BrunDépartement de microbiologie, infectiologie et immunologie, Université de Montréal, Montréal, QC, Canada.ORCID http://orcid.org/0000-0002-9289-1909
Felipe CavaDepartment 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 *Department of Functional and Evolutionary Ecology, Environmental Cell Biology Group, University of Vienna, Vienna, Djerassiplatz 1, 1030, Vienna, Austria. silvia.bulgheresi@univie.ac.at.ORCID http://orcid.org/0000-0002-1441-7152
Frédéric J Veyrier *INRS-Centre Armand-Frappier Santé Biotechnologie, Bacterial Symbionts Evolution, Laval, QC, H7V 1B7, Canada. frederic.veyrier@inrs.ca.ORCID http://orcid.org/0000-0002-8574-0547
Institut National de la Recherche Scientifique · CAUniversity of Vienna · ATUmeå University · SEUniversité de Montréal · CAIndiana University Bloomington · USUniversity of Amsterdam · NL

Funding

Austrian Science Fund FWF DOC 69Austrian Science Fund FWF P 28593
6 · The paper itself

Abstract

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.

Indexed as

Cell DivisionNeisseriaceaeAnimalsBacterial ProteinsBiological EvolutionCell WallMammalsPeptidoglycanBacterial ProteinsPeptidoglycan

Identifiers

PMID35995772
PMCPMC9395523
OpenAlexW4292603009

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.