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Evolution of ColE1-like plasmids across γ-Proteobacteria: From bacteriocin production to antimicrobial resistance

Authors :
Manuel Ares-Arroyo
Eduardo P. C. Rocha
Bruno Gonzalez-Zorn
Universidad Complutense de Madrid = Complutense University of Madrid [Madrid] (UCM)
Génomique évolutive des Microbes / Microbial Evolutionary Genomics
Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
B.G.Z. was supported by grants from the European Joint Program One Health EJP, ARDIG Grant Agreement No 77380
from the European Union’s Horizon 2020 research and innovation program. M.A.A. was supported by the Universidad Complutense de Madrid (Grant ID CT27/16-CT28/16 and EB14/19). E.P.C.R. acknowledges the financial support of Equipe FRM (EQU201903007835) and the Laboratoire d’Excellence IBEID (ANR-10-LABX-62-IBEID).
ANR-10-LABX-0062,IBEID,Integrative Biology of Emerging Infectious Diseases(2010)
European Project: 773830, H2020-SFS-2017-1 ,One Health EJP(2018)
Source :
PLoS Genetics, PLoS Genetics, 2021, 17 (11), pp.e1009919. ⟨10.1371/journal.pgen.1009919⟩
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

Abstract

Antimicrobial resistance is one of the major threats to Public Health worldwide. Understanding the transfer and maintenance of antimicrobial resistance genes mediated by mobile genetic elements is thus urgent. In this work, we focus on the ColE1-like plasmid family, whose distinctive replication and multicopy nature has given rise to key discoveries and tools in molecular biology. Despite being massively used, the hosts, functions, and evolutionary history of these plasmids remain poorly known. Here, we built specific Hidden Markov Model (HMM) profiles to search ColE1 replicons within genomes. We identified 1,035 ColE1 plasmids in five Orders of γ-Proteobacteria, several of which are described here for the first time. The phylogenetic analysis of these replicons and their characteristic MOBP5/HEN relaxases suggest that ColE1 plasmids have diverged apart, with little transfer across orders, but frequent transfer across families. Additionally, ColE1 plasmids show a functional shift over the last decades, losing their characteristic bacteriocin production while gaining several antimicrobial resistance genes, mainly enzymatic determinants and including several extended-spectrum betalactamases and carbapenemases. Furthermore, ColE1 plasmids facilitate the intragenomic mobilization of these determinants, as various replicons were identified co-integrated with large non-ColE1 plasmids, mostly via transposases. These results illustrate how families of plasmids evolve and adapt their gene repertoires to bacterial adaptive requirements.<br />Author summary The extraordinary adaptability of bacteria and the massive prevalence of mobile genetic elements within populations has turned antimicrobial resistance into a growing threat to Public Health. Among all the mobile genetic elements, plasmids have been the focus of attention as these extrachromosomal molecules of DNA are able to mobilize several antimicrobial resistance genes at once through conjugation. However, although small mobilizable and non-conjugative replicons have been traditionally overlooked when analyzing plasmid-mediated antimicrobial resistance, they have recently been described as important carriers of AMR genes. In this work, we have analyzed the ColE1-like plasmid family, whose study has been neglected even if they are one of the main groups of small plasmids in natural populations of Proteobacteria. We observed that these plasmids have evolved for a long time within γ-Proteobacteria acquiring different genetic features in specific hosts, being major players in the spread of antimicrobial resistance determinants.

Subjects

Subjects :
Evolutionary Genetics
Cancer Research
Relaxases
Molecular biology
Markov models
Genome
Biochemistry
Plasmid
Bacteriocins
Mobile Genetic Elements
Medicine and Health Sciences
Replicon
Hidden Markov models
Genetics (clinical)
Phylogeny
Data Management
Genetics
ColE1
Phylogenetic tree
[SDV.BID.EVO]Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE]
Phylogenetic Analysis
Genomics
[SDV.BIBS]Life Sciences [q-bio]/Quantitative Methods [q-bio.QM]
Markov Chains
Enzymes
Anti-Bacterial Agents
Phylogenetics
Nucleic acids
Physical sciences
Gammaproteobacteria
Research Article
Plasmids
Computer and Information Sciences
Forms of DNA
Biology
DNA construction
Microbiology
Evolution, Molecular
Genetic Elements
Bacterial Proteins
Microbial Control
[SDV.BBM.GTP]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Genomics [q-bio.GN]
Drug Resistance, Bacterial
Evolutionary Systematics
Gene
Ecology, Evolution, Behavior and Systematics
Taxonomy
Pharmacology
Evolutionary Biology
Bacterial Evolution
[SDV.GEN.GPO]Life Sciences [q-bio]/Genetics/Populations and Evolution [q-bio.PE]
Human evolutionary genetics
Biology and Life Sciences
Proteins
Probability theory
Bacteriology
DNA
[SDV.MP.BAC]Life Sciences [q-bio]/Microbiology and Parasitology/Bacteriology
Organismal Evolution
Research and analysis methods
Molecular biology techniques
Genes, Bacterial
Plasmid Construction
Microbial Evolution
Enzymology
bacteria
Antimicrobial Resistance
Mobile genetic elements
[INFO.INFO-BI]Computer Science [cs]/Bioinformatics [q-bio.QM]
Mathematics

Details

Language :
English
ISSN :
15537390 and 15537404
Database :
OpenAIRE
Journal :
PLoS Genetics, PLoS Genetics, 2021, 17 (11), pp.e1009919. ⟨10.1371/journal.pgen.1009919⟩
Accession number :
edsair.doi.dedup.....93e59f51af44b0e5fbd1766297d6b77e
Full Text :
https://doi.org/10.1371/journal.pgen.1009919⟩