Diversification of division mechanisms in endospore-forming bacteria revealed by analyses of peptidoglycan synthesis in Clostridioides difficile.


Journal

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

Informations de publication

Date de publication:
02 Dec 2023
Historique:
received: 21 08 2023
accepted: 14 11 2023
medline: 4 12 2023
pubmed: 3 12 2023
entrez: 2 12 2023
Statut: epublish

Résumé

The bacterial enzymes FtsW and FtsI, encoded in the highly conserved dcw gene cluster, are considered to be universally essential for the synthesis of septal peptidoglycan (PG) during cell division. Here, we show that the pathogen Clostridioides difficile lacks a canonical FtsW/FtsI pair, and its dcw-encoded PG synthases have undergone a specialization to fulfill sporulation-specific roles, including synthesizing septal PG during the sporulation-specific mode of cell division. Although these enzymes are directly regulated by canonical divisome components during this process, dcw-encoded PG synthases and their divisome regulators are dispensable for cell division during normal growth. Instead, C. difficile uses a bifunctional class A penicillin-binding protein as the core divisome PG synthase, revealing a previously unreported role for this class of enzymes. Our findings support that the emergence of endosporulation in the Firmicutes phylum facilitated the functional repurposing of cell division factors. Moreover, they indicate that C. difficile, and likely other clostridia, assemble a distinct divisome that therefore may represent a unique target for therapeutic interventions.

Identifiants

pubmed: 38042849
doi: 10.1038/s41467-023-43595-3
pii: 10.1038/s41467-023-43595-3
pmc: PMC10693644
doi:

Substances chimiques

Bacterial Proteins 0
Peptidoglycan 0
Membrane Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7975

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI122232
Pays : United States

Commentaires et corrections

Type : UpdateOf

Informations de copyright

© 2023. The Author(s).

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Auteurs

Shailab Shrestha (S)

Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA, USA.
Program in Molecular Microbiology, Tufts University Graduate School of Biomedical Sciences, Boston, MA, USA.

Najwa Taib (N)

Institut Pasteur, Université Paris Cité, Evolutionary Biology of the Microbial Cell Unit, Paris, France.
Institut Pasteur, Université Paris Cité, Bioinformatics and Biostatistics Hub, F-75015, Paris, France.

Simonetta Gribaldo (S)

Institut Pasteur, Université Paris Cité, Evolutionary Biology of the Microbial Cell Unit, Paris, France.

Aimee Shen (A)

Department of Molecular Biology and Microbiology, Tufts University School of Medicine, Boston, MA, USA. aimee.shen@tufts.edu.

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Classifications MeSH