Abstract

Bacteria can evolve rapidly by acquiring new traits such as virulence, metabolic properties, and most importantly, antimicrobial resistance, through horizontal gene transfer (HGT). Multidrug resistance in bacteria, especially in Gram-negative organisms, has become a global public health threat often through the spread of mobile genetic elements. Conjugation represents a major form of HGT and involves the transfer of DNA from a donor bacterium to a recipient by direct contact. Conjugative plasmids, a major vehicle for the dissemination of antimicrobial resistance, are selfish elements capable of mediating their own transmission through conjugation. To spread to and survive in a new bacterial host, conjugative plasmids have evolved mechanisms to circumvent both host defense systems and compete with co-resident plasmids. Such mechanisms have mostly been studied in model plasmids such as the F plasmid, rather than in conjugative plasmids that confer antimicrobial resistance (AMR) in important human pathogens. A better understanding of these mechanisms is crucial for predicting the flow of antimicrobial resistance-conferring conjugative plasmids among bacterial populations and guiding the rational design of strategies to halt the spread of antimicrobial resistance. Here, we review mechanisms employed by conjugative plasmids that promote their transmission and establishment in Gram-negative bacteria, by following the life cycle of conjugative plasmids.

Highlights

  • Bacteria can evolve rapidly by acquiring new traits such as virulence, metabolic properties, and most importantly, antimicrobial resistance, through horizontal gene transfer (HGT)

  • Shen et al Military Medical Research (2022) 9:3 such as carbapenems and amikacin, a few of them have developed extensive resistance to the action of antibiotics. Among these multi-resistant bacteria, “the ESKAPE pathogens”, which consist of Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae (K. pneumoniae), Acinetobacter baumannii (A. baumannii), Pseudomonas aeruginosa (P. aeruginosa), and Enterobacter species, constitute the biggest threat to human health as they are responsible for the majority of nosocomial infections [8, 9]

  • This review aims to focus on two mechanisms by which conjugative plasmids (CPs) employ to enhance their evolutionary fitness by manipulating subsequent conjugation events in their new hosts: entry exclusion and fertility inhibition

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Summary

Introduction

Bacteria can evolve rapidly by acquiring new traits such as virulence, metabolic properties, and most importantly, antimicrobial resistance, through horizontal gene transfer (HGT). To spread to and survive in a new bacte‐ rial host, conjugative plasmids have evolved mechanisms to circumvent both host defense systems and compete with co-resident plasmids Such mechanisms have mostly been studied in model plasmids such as the F plasmid, rather than in conjugative plasmids that confer antimicrobial resistance (AMR) in important human pathogens. Shen et al Military Medical Research (2022) 9:3 such as carbapenems and amikacin, a few of them have developed extensive resistance to the action of antibiotics Among these multi-resistant bacteria, “the ESKAPE pathogens”, which consist of Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae (K. pneumoniae), Acinetobacter baumannii (A. baumannii), Pseudomonas aeruginosa (P. aeruginosa), and Enterobacter species, constitute the biggest threat to human health as they are responsible for the majority of nosocomial infections [8, 9]. Many ESKAPE pathogens, especially K. pneumoniae and Enterobacter species, acquire AMR mainly through the process of conjugation, which involves the concerted action of a mating pair formation (MPF) system and a matching DNA processing system, resulting in the transfer of one strand of DNA (the T-strand) from a donor cell to a recipient in which the complementary DNA strand is synthesized subsequently [10–12]

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