Skip to main content

EDITORIAL article

Front. Microbiol., 23 June 2023
Sec. Antimicrobials, Resistance and Chemotherapy
This article is part of the Research Topic Horizontal Gene Transfer Mediated Bacterial Antibiotic Resistance, Vol II View all 11 articles

Editorial: Horizontal gene transfer mediated bacterial antibiotic resistance, volume II

  • 1College of Biotechnology and Bioengineering, Zhejiang University of Technology, Hangzhou, China
  • 2Department of Molecular Medicine, Morsani College of Medicine, University of South Florida, Tampa, FL, United States
  • 3State Key Laboratory of Animal Nutrition, College of Animal Science and Technology, China Agricultural University, Beijing, China
  • 4Université Paris-Saclay, CEA, CNRS, Institute for Integrative Biology of the Cell (I2BC), Gif-sur-Yvette, France

The issue of bacterial antibiotic resistance (BAR) has reached an alarming level in recent years. In 2019 alone, BAR was responsible for the deaths of approximately five million people globally, making it the third leading cause of death (Antimicrobial Resistance Collaborators, 2022). This figure surpasses the previous estimation (WHO, 2014), highlighting the severity of the situation. Bacteria can easily transfer antibiotic resistance genes (ARGs) through horizontal gene transfer (HGT), which can promote the development and spread of resistance within the bacterial population (Sun et al., 2019). Ten publications have recently been published on the topic of “Horizontal Gene Transfer Mediated Bacterial Antibiotic Resistance II,” presenting the latest findings and advancements in this field. These publications could serve as new reference points to tackle BAR in the future.

In this Research Topic, three reports (Xin et al.; Zhang S. et al.; Yang et al.) demonstrated the high prevalence of ARGs in different regions of China, revealing the serious challenge of BAR in the country. By evaluating 4, 414 strains of enterococci from hospitals in 26 provinces in China, Xin et al. demonstrated the wide distribution of the fosfomycin resistance gene fosX in E. faecium, a human pathogen responsible for gastrointestinal tract infections. ARGs tet(X), bla, and mcr threaten the efficacy of tigecycline, carbapenems, and colistin, which represent the three last-resort antibiotics. Zhang S. et al. summarized the distribution of tet(X) genes in China and demonstrated the presence of tet(X) genes in 24 provinces. Remarkably, tet(X) genes were identified not only in humans, livestocks, poultries and aquatic animals but also in wild animals and the environment, reflecting the fast spread of this ARG in the wild in China. Yang et al. reported not only the presence of blaNDM − 5 and mcr-8.1 in an animal breeding area in eastern China but also the clonal transfer of the two ARGs and their potential dissemination through horizontal gene transfer. These studies highlight the urgency of taking action to combat BAR in China.

Although observational studies have manifested the present situation of BAR, our understanding of this issue largely relies on retrospective analysis. A review article in this Research Topic summarized the recent progress of in silico, in vitro, and in vivo modeling of HGT, providing new perspectives and directions on understanding the plasmid-mediated transfer of ARGs in the gut of animals (Ott and Mellata). In nature, ARGs are often disseminated by vehicles (e.g., plasmid) and mobile genetic elements (MGEs). Guzman-Otazo et al. found that IncN plasmids can transmit ARGs via conjugation from environmental waterborne bacteria to Escherichia coli, which colonizes in the intestine of terrestrial animals, enabling the spread of ARGs across aquatic and terrestrial environments. Integrative and conjugative elements (ICEs) and integrons are MGEs that mediate the dissemination of ARGs. Two studies in this Research Topic investigated the roles of ICEs and integrons in facilitating the spread of ARGs. Through whole-genome analysis of 27 multidrug-resistant (MDR) Proteus strains, Li Y. et al. revealed that nine ICEs shared a common backbone structure, implicating the dissemination of ICEs in Proteus strains from livestocks and poultries and humans. Their study also revealed that ARGs were carried by MGEs of genetic diversity, highlighting the necessity of continuous monitoring. Bitar et al. analyzed 32 VIM metallo-β-lactamase producing Enterobacterales from Czech hospitals, and sequenced 19 isolates. Their work revealed that the spread of VIM-encoding integron In110 was more prevalent than other VIM-encoding integrons and that many new ARGs-carrying MGEs could be evolving.

Compared with that in non-pathogenic bacteria, the transfer of ARGs in pathogens is more threatening. Two studies in this Research Topic showed that the impact of HGT on the evolution of pathogens could be species-specific. Li P. et al. reported that outer membrane vesicles were able to incorporate DNA and deliver both virulence and antimicrobial-resistant plasmids. Their work provides new evidence supporting that HGT plays an important role in facilitating the evolution of carbapenem-resistant hypervirulent Klebsiella pneumonia. Whereas, Kandinov et al. discovered that the plasmid expressing blaTEM − 20 reduced the viability of Neisseria gonorrhoeae. This could result from the expression of extended-spectrum β-lactamase, which may affect the structure of the peptidoglycan layer, providing an explanation for the absence of clinical isolates of extensive spectrum beta-lactamase-producing N. gonorrhoeae. Investigation of the transfer of ARGs in pathogens would not only explain co-evolutionary relationships between resistance and virulence but also provide guidance for the clinical use of antibiotics.

To be stably inherited, horizontally transferred ARGs need to be maintained in either a plasmid or the genome of the recipient bacteria through genetic recombination. Zhang G. et al. characterized an integrase of genomic island GIsul2, which mediated the integration of MGEs through site-specific recombination in Shigella flexneri. They found that GIsul2 can excise and integrate GIsul2 and the ISCR-related element CR2-sul2 unit by site-specific recombination between the host chromosomal attachment sites, suggesting a potential role of GIsul2 integrase homologs in the dissemination of GIsul2 units.

In summary, articles of this Research Topic demonstrated the prevalence of ARGs, diverse mechanisms of transfer of ARGs under different settings, and novel ways of integration of MGEs carrying ARGs. Although remarkable advances in the knowledge of the dissemination of ARGs have been made in recent years, we still know little about associations between environmental cues and the HGT-driven spread of ARGs under different environmental conditions. More importantly, despite the severity of BAR being more serious than estimated, there is a lack of effective strategies to tackle this problem. To address this global crisis, collaboration among different fields from countries all over the world remains in high demand.

We would like to acknowledge all participating authors for their contributions, reviewers for their constructive comments, and our editorial team members for their great efforts.

Author contributions

All authors participated in editing manuscripts in this Research Topic, reviewed, and approved the final version of the editorial.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Antimicrobial Resistance Collaborators. (2022). Antimicrobial resistance, global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet. 399, 629–655. doi: 10.1016/S0140-6736(21)02724-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, D., Jeannot, K., Xiao, Y., and Knapp, C. W. (2019). Editorial: horizontal gene transfer mediated bacterial antibiotic resistance. Front. Microbiol. 10:1933. doi: 10.3389/fmicb.2019.01933

PubMed Abstract | CrossRef Full Text | Google Scholar

WHO (2014). Antimicrobial Resistance Global Report on Surveillance. World Health Organization. Available online at: https://www.who.int/publications-detail-redirect/9789241564748

Google Scholar

Keywords: horizontal gene transfer (HGT), bacterial antibiotic resistance, antibiotic resistance genes (ARGs), plasmid, bacterial conjugation, mobile genetic elements (MGEs)

Citation: Sun D, Sun X, Hu Y and Yamaichi Y (2023) Editorial: Horizontal gene transfer mediated bacterial antibiotic resistance, volume II. Front. Microbiol. 14:1221606. doi: 10.3389/fmicb.2023.1221606

Received: 12 May 2023; Accepted: 30 May 2023;
Published: 23 June 2023.

Edited and reviewed by: Rustam Aminov, University of Aberdeen, United Kingdom

Copyright © 2023 Sun, Sun, Hu and Yamaichi. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Dongchang Sun, sundch@zjut.edu.cn; Xingmin Sun, sun5@usf.edu; Yongfei Hu, huyongfei@cau.edu.cn; Yoshiharu Yamaichi, yoshiharu.yamaichi@i2bc.paris-saclay.fr

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.