Dinesh Subedi
Tang Fang
Ram Prasad Bhusal
Mark Willcox- 1School of Biological Sciences, Monash University, Clayton, VIC, Australia
- 2College of Veterinary Medicine, Nanjing Agricultural University, Nanjing, China
- 3Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, VIC, Australia
- 4School of Optometry and Vision Science, University of New South Wales, Sydney, NSW, Australia
Editorial on the Research Topic
Bacteriophages to treat infections with multidrug resistant pathogens
This Research Topic was designed by us in response to the growing threat of antibiotic resistance of bacterial infections worldwide. The use of bacteriophages (phages) as alternatives or adjunct agents to treat infections is gaining wider use. Indeed, phage therapy has been successfully used to treat patients across a broad range of pathologies, with substantial clinical improvement and bacterial eradication (1). However, we noted that only a few clinical requests for phage therapy have been fulfilled successfully due to a lack of understanding of the biology of phage-host interactions and resistance development (2), the human immune response to phage particles (3), the right phage dosage and pharmacokinetics (4). Bacterial defenses such as, restriction-modification and CRISPR-Cas system, also contribute to abortive infections by modifying phage DNA (5).
At the conclusion of the Research Topic, 12 articles have been published that address critical and interesting issues. There were six original or brief research reports, five reviews or mini reviews and one case report. There were reviews of phage therapy; studies on phages active against Shigella spp., Salmonella strains, Escherichia coli, and Clostridioides difficile; use of phage endolysin or tail proteins; the effect of mucous or dopamine on phages; a salutary case report of phage therapy failure; use of machine learning and simulations to test phage therapy; and a review of regulatory hurdles for the use of phage.
Phages are versatile agents that can be used for various purposes, from food safety to human health. However, lack of comprehensive guidelines and regulations in many countries hinders their widespread applications. Karn et al. reviewed the use of phages in a variety of situations such as veterinary science, agriculture, food preservation and of course human health (for example bacteremia, gastrointestinal tract infections and respiratory tract infections) due to their high specificity, low toxicity and ability to adapt to bacterial mutations. However, their use has challenges such as their pharmacokinetics and pharmacodynamics and delivery. This paper also includes information on FDA-approved bacteriophage-based product, commercial phage product, and global list of companies using phages for therapeutic purposes. Whilst Karn et al. touched upon the regulatory challenges of phage therapy, this was discussed more in the review of Yang et al.. In Russia and Georgia, phage therapies can be purchased without prescription partly because they have been used frequently and for a long time in these countries. Phage therapy was classified as a medicinal product by European Medicines Agency, but different European countries regulate its use in different ways, with Belgium having “an established, innovative, and distinctive regulatory framework.” China, as many other countries, is developing regulatory systems as the importance of phage therapy is being recognized as a rapidly growing and important technology.
Two papers reviewed the potential and challenges of phage therapy for chronic airways disease, a condition characterized by persistent bacterial infections and neutrophilic inflammation. Phage therapy may help phagocytes of our innate immune system control chronic airways disease, although the Laucirica et al. concluded that the exact mechanisms underlining this require further investigation. As well, phages can adhere to the mucous, helping them remain in lungs, although whether this helps or hinders productive infection was considered by Ling et al. to be relatively understudied.
Phage therapy is a promising, but two original research papers highlighted the challenges it encountered. The study by Zhang et al. demonstrated that dopamine could change the structure of phages preventing them from infecting their host cells. This may have important implications especially as dopamine is being used to bind various moieties including antimicrobials to medical devices (6). Whilst these antimicrobial surfaces are designed to reduce medical device-associated infections, should infections occur, albeit more rarely, phage therapy for infections of such devices could fail. This deserves further research. The case report of Blasco et al. provided a reminder that phage therapy may not always progress as hoped. A patient with a recurring prosthetic vascular graft infection caused by Pseudomonas aeruginosa was treated with a phage cocktail initially alone and subsequently in combination with ceftazidime-avibactam. Another blood stream infection occurred after the phage therapy, although interestingly the P. aeruginosa isolated at that time had reverted to being susceptible to ß-lactams and quinolones, highlighting the beneficial trade-off effects of phage therapy, which could increase the susceptibility of bacteria to antibiotics (7).
Plunder et al. describes how in silico simulations may help tailor future therapeutic choices. The paper developed and tested a novel method that uses machine learning and multi-criterial optimization to find the optimal viral dose and administration time for phage therapy against bacterial infections.
Three Research Topic demonstrated the characteristics and applications of different phages and phage products for bacterial infections. Ahamed et al. characterized two lytic phages that targeted Shigella flexneri, Shigella dysenteriae, and Shigella sonnei. The phages individually or as a cocktail could reduce the numbers Shigella on raw chicken, indicating their potential use in the food industry, and as therapeutics for Shigella infection. However, there are many regulations, dose and stability issues that need to be addressed before phage therapy can be widely applied in the food industry. Jo et al. characterized a new jumbo phage that was active against antimicrobial resistant strains of E. coli. The phage, EJP2, was active against resistant and pathogenic strains of E. coli, as well as biofilms and had synergistic activity with cefotaxime (Jo et al.). Not all bacterial infections are immediately amenable to phage therapy. For example, Umansky and Fortier describe phages of C. difficile as usually being not lytic and so need to be engineered. Studies on the mechanism of action of phage products demonstrated that the tailspike proteins of epsilon 34 phage disrupted the membrane of the Salmonella Typhimurium and Salmonella Newington as well as causing reductions in the bacteria's dehydrogenase activity (Ibrahim et al.). Stevens et al. demonstrated that phage endolysin helped to treat a chronic Enterococcus faecalis prostate infection that was causing severe chronic pelvic pain syndrome associated with bacterial prostatitis.
While phages exhibit promising potential as alternatives for treating drug-resistant bacterial infections and have shown success in various pathologies, the limited fulfillment of clinical requests underscores challenges in comprehending phage biology, host interactions, and the necessity for standardized regulations to fully exploit the benefits of phage therapy.
Author contributions
DS: Writing—review & editing. TF: Writing—review & editing. RB: Writing—review & editing. MW: Writing—original draft, Writing—review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
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
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References
1. Uyttebroek S, Chen B, Onsea J, Ruythooren F, Debaveye Y, Devolder D, et al. Safety and efficacy of phage therapy in difficult-to-treat infections: a systematic review. Lancet Infect Dis. (2022) 22:e208–20. doi: 10.1016/S1473-3099(21)00612-5
2. Stone E, Campbell K, Grant I, McAuliffe O. Understanding and exploiting phage–host interactions. Viruses. (2019) 11:567. doi: 10.3390/v11060567
3. Van Belleghem JD, Dabrowska K, Vaneechoutte M, Barr JJ, Bollyky PL. Interactions between bacteriophage, bacteria, and the mammalian immune system. Viruses. (2018) 11:10. doi: 10.3390/v11010010
4. Nang SC, Lin YW, Petrovic Fabijan A, Chang RYK, Rao GG, Iredell J, et al. Pharmacokinetics/pharmacodynamics of phage therapy: a major hurdle to clinical translation. Clin Microbiol Infect. (2023) 29:702–9. doi: 10.1016/j.cmi.2023.01.021
5. Abedon ST. Bacterial ‘immunity' against bacteriophages. Bacteriophage. (2012) 2:50–4. doi: 10.4161/bact.18609
6. Browne K, Kuppusamy R, Chen R, Willcox MDP, Walsh WR, Black DSC, et al. Bioinspired polydopamine coatings facilitate attachment of antimicrobial peptidomimetics with broad-spectrum antibacterial activity. Int J Mol Sci. (2022) 23:2952. doi: 10.3390/ijms23062952
Keywords: bacteriophage (phage), phage therapy, antimicrobial resistance (AMR), bacteria, infections
Citation: Subedi D, Fang T, Bhusal RP and Willcox M (2024) Editorial: Bacteriophages to treat infections with multidrug resistant pathogens. Front. Med. 10:1348463. doi: 10.3389/fmed.2023.1348463
Received: 02 December 2023; Accepted: 18 December 2023;
Published: 05 January 2024.
Edited and reviewed by: Shisan Bao, The University of Sydney, Australia
Copyright © 2024 Subedi, Fang, Bhusal and Willcox. 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: Mark Willcox, m.willcox@unsw.edu.au