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EDITORIAL article

Front. Microbiol., 04 July 2023
Sec. Food Microbiology
This article is part of the Research Topic Food Pathogens and Antimicrobial Resistance View all 11 articles

Editorial: Food pathogens and antimicrobial resistance

  • 1College of Animal Science and Technology, Henan University of Science and Technology, Luoyang, China
  • 2College of Veterinary Medicine, South China Agricultural University, Guangzhou, China
  • 3College of Animal Science and Technology, Huazhong Agriculture University, Wuhan, China
  • 4College of Veterinary Medicine, Iowa State University, Ames, IA, United States

Editorial on the Research Topic
Food pathogens and antimicrobial resistance

The issue of antimicrobial resistance (AMR) of microorganisms is prevalent worldwide (Neely and Holder, 1999). The overuse of antimicrobials in agricultural animals for food production has been proposed as the leading cause of the proliferation of antimicrobial-resistant pathogens (Minarini et al., 2020). Raw meat, cooked food products, and raw milk are often contaminated by food-borne pathogens, many of which are resistant to a variety of antimicrobials (Chao et al., 2007). The exchange of genetic information among food-borne pathogens is a major factor in the development of antimicrobial resistance. Therefore, monitoring antimicrobial-resistant at different nodes in the food chain is particularly important to understand the spread of antimicrobial-resistant (Di Ciccio, 2021).

In this Research Topic, nine original research articles and one review have been published. Hu et al. comprehensively reviewed the characteristics, epidemiology, pathogenic mechanisms, zoonotic potential, antimicrobial resistance, diagnosis, alternative control measures, and vaccine development of avian pathogenic E. coli (APEC).

Research has shown that intestinal microbiota plays a critical role in maintaining the integrity of gut barrier, and specific microorganisms in digestive tracts can aid in the treatment of gastrointestinal diseases, thereby reducing the reliance of antimicrobials and other drugs (Gresse et al., 2017). Using a model of Porcine epidemic diarrhea virus (PEDV)-infected LC and Large-white piglets established by Li et al., the authors analyzed differences in intestinal microbial diversity, community composition, and intestinal metabolites between PEDV-infected and healthy control piglets. This study offers a theoretical foundation for utilizing intestinal core microorganisms in the digestive system of PEDV-infected pigs, to address the issue of piglet diarrhea that arises from PEDV infection.

Bacterial AMR is usually regulated by genes. The research conducted by Tang et al. demonstrated that the plasmid-borne cfr gene facilitates multidrug resistance (MDR), which subsequently leads to cfr-positive E. coli exhibiting MDR. Moreover, the study revealed that cfr can form a circular intermediate of IS26-cfr during transmission, confirming IS26's significant role in the dissemination of the multidrug resistance gene cfr.

In the study of Chen et al., the genes that play a key role in multiple drug resistance in Bacillus cereus are hblA, hblC, hblD, nheA, and nheB. Lai et al.'s research indicate that the AMR of Salmonella is primarily attributed to the significant impact of the plasmid-mediated quinolone resistance gene pmqr, the β-lactam resistance gene blaTm, and the mutation of the quinolone resistance-determination region (QRDR) that contains the pmqr gene.

Ji et al. sequenced the complete genome of 322 Listeria monocytogenes strains isolated from food and discovered that these strains carry the drug resistance genes aacA4, etM, Tets, and dfrG. Furthermore, the researchers discovered a novel premature stop codon in the inlA gene, leading to a better comprehension of the genomic diversity of Listeria monocytogenes.

Buberg et al. studied the survival rate, colonization characteristics and conjugation ability of ESC-resistant E. coli isolates through a static in vitro digestion model (INFOGEST). The findings demonstrate that the strains are capable of surviving and reproducing within the in vitro digestion model. Furthermore, the strains exhibit the capability to adhere to and invade colon cells post-digestion, with a higher degree of adhesion to colon cells observed than cell invasion. This study demonstrated the survival and colonization ability of E. coli strains resistant to spectrum cephalosporin-resistant.

Krüger et al. discovered that the presence of mobile genetic elements encoding resistance and virulence genes results in variations in gene expression. Multiple drug resistance may be related to the existence of mobile genetic elements. Salmonella Infantis and Salmonella Heidelberg serotypes showing multiple drug resistance have been found to carry the blaTEM−Ib and blaCTX−M−65 genes, which are related to mobile genetic elements.

The research conducted by Ma et al. investigated the prevalence of Arcobacter spp. in Shenzhen, China, as well as identifying its virulence and AMR through whole genome sequencing (WGS). This study discovered that antimicrobial resistant gene counts varied between different strains, and certain strains carried multiple drug resistance genes. Additionally, it was found that corresponding drug-resistant strains exhibited specific drug-resistance genes.

Finally, the results of Wang et al.'s study showed that the phage PaVOA effectively kills Pseudomonas aeruginosa within a short period using a rabbit skin infection model from New Zealand. Therefore, phage cocktail therapy represents a new approach to treating traumatic skin infections caused by MDR Pseudomonas aeruginosa.

In summary, this article Research Topic provides valuable insights into the epidemiological distribution and antimicrobial resistance of foodborne pathogens across various nodes of the food supply chain, aiding readers in understanding this important topic. This Research Topic of articles has garnered considerable attention from the appropriate practitioners, with over 11,000 views and a total of 2,315 downloads.

Author contributions

YW wrote the initial draft of the manuscript while JZ, ZP, XW, and PP provided substantial critical feedback and editing. All authors contributed to the article and approved the submitted version.

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

Chao, G., Zhou, X., Jiao, X., Qian, X., and Xu, L. (2007). Prevalence and antimicrobial resistance of foodborne pathogens isolated from food products in China. Foodborne Pathog. Dis. 4, 277–284. doi: 10.1089/fpd.2007.0088

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Di Ciccio, P. A. (2021). Antimicrobial-resistance of food-borne pathogens. Antibiotics. 10, 372. doi: 10.3390/antibiotics10040372

PubMed Abstract | CrossRef Full Text | Google Scholar

Gresse, R., Chaucheyras-Durand, F., Fleury, M. A., Van de Wiele, T., Forano, E., Blanquet-Diot, S., et al. (2017). Gut microbiota dysbiosis in postweaning piglets: understanding the keys to health. Trends Microbiol. 25, 851–873. doi: 10.1016/j.tim.2017.05.004

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Minarini, L. A. D. R., de Andrade, L. N., De Gregorio, E., Grosso, F., Naas, T., Zarrilli, R., et al. (2020). Editorial: antimicrobial resistance as a global public health problem: how can we address it? Front. Public Health. 8, 612844. doi: 10.3389/fpubh.2020.612844

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Neely, A. N., and Holder, I. A. (1999). Antimicrobial resistance. Burns. 25, 17–24. doi: 10.1016/S0305-4179(98)00134-X

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Keywords: antimicrobial resistance, foodborne pathogens, microorganisms, resistance gene, genetic information

Citation: Wang Y, Zhang J, Peng Z, Wang X and Plummer P (2023) Editorial: Food pathogens and antimicrobial resistance. Front. Microbiol. 14:1243769. doi: 10.3389/fmicb.2023.1243769

Received: 21 June 2023; Accepted: 26 June 2023;
Published: 04 July 2023.

Edited and reviewed by: Aldo Corsetti, University of Teramo, Italy

Copyright © 2023 Wang, Zhang, Peng, Wang and Plummer. 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: Yang Wang, d2FuZ3lvY2VhbiYjeDAwMDQwOzE2My5jb20=

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.