Genetic determinants of pOXA-48 plasmid maintenance and propagation in Escherichia coli

Y Yannick Baffert N Nathan Fraikin Y Yasmine Makhloufi J Julie Baltenneck M Marie-Eve Val A Annick Dedieu-Berne J Jonathan Degosserie B Bogdan I. Iorga P Pierre Bogaerts E Erwan Gueguen C Christian Lesterlin (Microbiologie Moléculaire et Biochimie Structurale, Université Lyon 1, CNRS, Inserm) S Sarah Bigot (Microbiologie Moléculaire et Biochimie Structurale, Université Lyon 1, CNRS, Inserm)

Abstract

Abstract Conjugative plasmids are the main drivers of antibiotic resistance dissemination contributing to the emergence and extensive spread of multidrug resistance clinical bacterial pathogens. pOXA-48 plasmids, belonging to the IncL group, emerge as the primary vehicle for carbapenem resistance in Enterobacteriaceae . Despite the problematic prevalence of pOXA-48, most research focus on epidemiology and genomics, leaving gaps in our understanding of the mechanisms behind its propagation. In this study, we use a transposon sequencing approach to identify genetic elements critical for plasmid stability, replication, and conjugative transfer. Our results identify a novel type I toxin-antitoxin system, uncharacterized essential maintenance factors, and components of the type IV secretion system and regulatory elements crucial for conjugation. This study advances our understanding of pOXA-48 biology, providing key insights into the genetic factors underlying its successful maintenance and spread in bacterial populations.

Article Details

Volume / Issue Vol. 16, Issue 1
Published August 19, 2025
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (12)

Y

Yannick Baffert

N

Nathan Fraikin

Y

Yasmine Makhloufi

J

Julie Baltenneck

M

Marie-Eve Val

A

Annick Dedieu-Berne

J

Jonathan Degosserie

B

Bogdan I. Iorga

P

Pierre Bogaerts

E

Erwan Gueguen

C

Christian Lesterlin

Microbiologie Moléculaire et Biochimie Structurale, Université Lyon 1, CNRS, Inserm

S

Sarah Bigot

Microbiologie Moléculaire et Biochimie Structurale, Université Lyon 1, CNRS, Inserm