Byeonghwa Jeon
Taradon Luangtongkum
Zhangqi Shen
Catherine M. Logue
Jun Lin- 1Division of Environmental Health Sciences, School of Public Health, University of Minnesota, Minneapolis, MN, United States
- 2Department of Veterinary Public Health, Faculty of Veterinary Science, Chulalongkorn University, Bangkok, Thailand
- 3Beijing Key Laboratory of Detection Technology for Animal-Derived Food Safety, Beijing Laboratory of Food Quality and Safety, College of Veterinary Medicine, China Agricultural University, Beijing, China
- 4Department of Population Health, College of Veterinary Medicine, University of Georgia, Athens, GA, United States
- 5Department of Animal Science, University of Tennessee, Knoxville, Knoxville, TN, United States
Editorial on the Research Topic
Resistance and Tolerance in Food-Borne Pathogens: Mechanisms, Public Health Impact, and Control Measures
Foodborne pathogens are exposed to many stress conditions present in animal hosts and the environment surrounding farms at the stage of primary production and encounter artificial stressors, including disinfectants and non-optimal growth conditions, during food processing, storage, and cooking. Foodborne pathogens can cause foodborne illnesses only when they successfully overcome stress conditions along the farm to fork continuum (Begley and Hill, 2015; Oh et al., 2018; Zhang F. et al.). Most foodborne infections are self-limiting; however, serious cases of illness require antimicrobial chemotherapy. With the increasing prevalence of antibiotic-resistant foodborne pathogens being detected, the efficacy of antimicrobial chemotherapy is significantly compromised, leading to serious patient outcomes. Bacterial tolerance to environmental stress and resistance to antibiotics significantly affect food safety and public health. Although stress tolerance and antibiotic resistance in bacteria may be considered totally different topics, there are some overarching features for both. For instance, oxidative stress is a general tolerance mechanism that affects the lethality of antibiotic treatment (Poole, 2012). Thus, understanding stress tolerance and antibiotic resistance in foodborne pathogens can provide a holistic perspective for food safety from farm to fork and beyond, including clinical treatment of foodborne illnesses. The Research Topic “Resistance and Tolerance in Food-borne Pathogens: Mechanisms, Public Health Impact, and Control Measures” aims to extend our knowledge of how these mechanisms influence food safety and public health.
Two articles about stress tolerance in Listeria monocytogenes were published. Zhang H. et al. reported that L. monocytogenes 1/2b isolates were the predominant strain types isolated from processing facilities of ready-to-eat meat in China irrespective of the observed hygiene levels based on aerobic plate counts and coliform detection. Whole genome sequence analysis suggested that the isolates clonally expanded possibly by forming biofilms, confirming the importance of sanitation procedures for the control of L. monocytogenes. Interestingly, the findings of Li et al. showed that the use of organic acids increases the transcriptional levels of genes associated with acid and bile stress response and virulence. Exposure to acetic acid and lactic acid, both common organic acids used in the food industry, increase the virulence of L. monocytogenes based on testing using the Galleria mellonella infection model. Organic acids are frequently used for the control of Listeria contamination by the food industry. However, organic acids can potentially influence Listeria's stress tolerance and virulence.
With respect to various in vivo stresses encountered by microbes, foodborne pathogens also rely on effective and complex tolerance strategies to survive and establish successful infection in the host. One such study is focused on the resistance of Vibrio vulnificus to nitric oxide (NO), an important antimicrobial effector produced by the host innate immune system to counteract invading pathogens (Choi et al.). The investigators identified a NO-responsive transcriptional regulator NsrR, a strong repressor of hmpA that encodes an NO dioxygenase required for resistance of V. vulnificus to nitrosative stress. Further molecular studies found that NsrR could delicately cooperate with other two regulatory proteins, Lrp and CRP, to tightly control the transcription of hmpA, consequently contributing to the survival of V. vulnificus under host-derived nitrosative stress (Choi et al.).
Several articles in the eCollection ascertained that antibiotic resistance is highly common in the food supply chain worldwide. The article by Lopez-Chavarrias et al. provides a good demonstration of the high prevalence of antibiotic-resistant Campylobacter in healthy livestock in Spain (Lopez-Chavarrias et al.). Approximately 94.5% of Campylobacter coli isolates and 91.1% of Campylobacter jejuni isolates from broilers were resistant to ciprofloxacin, a fluoroquinolone drug of clinical importance in human health, and 66.6% of C. coli from pigs were resistant to erythromycin. Consistently, tetracycline and fluoroquinolone resistance are prevalent in C. jejuni isolates from patients in the United States. Notably, campylobacteriosis associated with fluoroquinolone resistance was significantly associated with international travel (Rodrigues et al.). Barbieri et al. reported that mcr-1 is highly prevalent in Escherichia coli isolates from healthy and sick poultry with colibacillosis in Brazil due to the agricultural application of colistin, a last-resort antibiotic to treat Gram-negative infections (Liu et al., 2016). In addition, multi-drug resistance in Yersinia enterocolitica 4/O:3 derived from fresh pre-washed spinach was found to be the cause of the consecutive foodborne yersiniosis outbreaks in Sweden in 2019. Molecular characterization of the multidrug-resistant Y. enterocolitica outbreak strain revealed that this foodborne pathogen harbored the Tn2670 transposon with resistance determinants against quaternary ammonium compounds, the heavy metal mercury, phenicols, streptomycin, and sulfonamides and an additional plasmid carrying tetracycline resistance gene. Interestingly, neither the Tn2670 transposon nor the tetB resistance plasmid has previously been reported in foodborne Yersinia nor in isolates derived from ready-to-eat products, suggesting that horizontal gene transfer events occurring in the environment, agriculture, or animal husbandry have promoted the selection of Y. enterocolitica carrying multi-antibiotic and metal resistance determinants (Karlsson et al.).
An article included in this collection discussed potential intervention measures to control antibiotic resistance in the food supply chain using bacteriophages (phages). Kim et al. discovered that some phages preferentially infect E. coli based on the phylogenetic group and constructed a highly effective phage cocktail targeting poultry isolates of E. coli producing extended-spectrum β-lactamases (ESBL) that frequently contaminate retail poultry. Although antibiotic-resistant, non-pathogenic E. coli does not develop an infection in animals and humans, antibiotic resistance can be transferred to pathogenic bacteria. The phages strongly inhibited ESBL-producing E. coli on chicken skin at refrigeration temperatures, suggesting that phages have potential application for use in retail raw chicken to reduce antibiotic resistance (Kim et al.).
Humans are continuously exposed to antibiotic-resistant microorganisms through the consumption of food, and the chances of exposure to antibiotic-resistant microorganisms will continue to pose a challenge and potentially increase in prevalence if foodborne pathogenic bacteria can survive stress conditions in the pathway from farm to fork. These articles highlight the concern about food chain contamination as a potential reservoir for transmission and dissemination of antimicrobial resistance, raising concerns for food safety and public health.
Author Contributions
All authors listed have made a substantial, direct and intellectual contribution to the work, and approved it for publication.
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
Begley, M., and Hill, C. (2015). Stress adaptation in foodborne pathogens. Annu. Rev. Food Sci. Technol. 6, 191–210. doi: 10.1146/annurev-food-030713-092350
Liu, Y.-Y., Wang, Y., Walsh, T. R., Yi, L.-X., Zhang, R., Spencer, J., et al. (2016). Emergence of plasmid-mediated colistin resistance mechanism MCR-1 in animals and human beings in China: a microbiological and molecular biological study. Lancet Infect. Dis. 16, 161–168. doi: 10.1016/S1473-3099(15)00424-7
Oh, E., Chui, L., Bae, J., Li, V., Ma, A., Mutschall, S. K., et al. (2018). Frequent implication of multistress-tolerant Campylobacter jejuni in human infections. Emerg. Infect. Dis. 24, 1037–1044. doi: 10.3201/eid2406.171587
Keywords: foodborne pathogens, food safety, public health, antibiotic resistance, stress tolerance
Citation: Jeon B, Luangtongkum T, Shen Z, Logue CM and Lin J (2021) Editorial: Resistance and Tolerance in Food-Borne Pathogens: Mechanisms, Public Health Impact, and Control Measures. Front. Microbiol. 12:769931. doi: 10.3389/fmicb.2021.769931
Received: 02 September 2021; Accepted: 20 September 2021;
Published: 14 October 2021.
Edited by:
Giovanna Suzzi, University of Teramo, ItalyReviewed by:
Pierina Visciano, University of Teramo, ItalyCopyright © 2021 Jeon, Luangtongkum, Shen, Logue and Lin. 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: Byeonghwa Jeon, bjeon@umn.edu