A helicase-containing module defines a family of pCD630-like plasmids in Clostridium difficile

Wiep Klaas Smits1, J Scott Weese2, Adam P Roberts3

  • 1Department of Medical Microbiology, Leiden University Medical Center, PO Box 9600, 2300RC, Leiden, The Netherlands; Netherlands Centre for One Health, The Netherlands.

Anaerobe
|December 17, 2017
PubMed

Insights

Plasmids are common in Clostridium difficile, a major cause of healthcare-associated infections. This study identifies a novel family of pCD630-like plasmids, revealing two distinct subgroups within this important bacterial species.

Area of Science:

  • Microbiology
  • Genomics
  • Molecular Biology

Background:

  • Clostridium difficile is a significant Gram-positive enteropathogen responsible for healthcare-associated infections.
  • Despite extensive genomic sequencing of C. difficile, plasmids remain poorly characterized.
  • Few plasmids have been previously described in C. difficile literature.

Purpose of the Study:

  • To investigate the prevalence and diversity of plasmids in Clostridium difficile.
  • To characterize a specific family of plasmids related to pCD630.
  • To identify novel plasmid replicons and their compatibility within C. difficile strains.

Main Methods:

  • In silico genomic analyses.
  • Laboratory experiments for plasmid characterization.
  • Comparative analysis of plasmid sequences.

Main Results:

  • Plasmids are common in Clostridium difficile.
  • A novel family of pCD630-like plasmids was identified, characterized by a conserved putative helicase.
  • Two distinct subgroups of pCD630-like plasmids were discovered, differing in size and accessory modules.
  • The identified replicon is compatible with other C. difficile replicons, allowing co-existence.

Conclusions:

  • This study provides the first description of a plasmid family in Clostridium difficile.
  • The findings expand our understanding of C. difficile plasmid biology and mobile genetic elements.
  • The characterization of pCD630-like plasmids offers new insights into C. difficile genomics and potential virulence factors.

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