Commentary on: Biofilms in human and veterinary infections: a central link in One Health frameworks

Authors

  • Mohammed Elbediwi Oldenburg University, Germany Author

DOI:

https://doi.org/10.66585/ohmi.2026.2.0033

Keywords:

Biofilms, One Health frameworks, veterinary infections, Surveillance, Evolutionary dimensions, Phage therapy

Abstract

Not applicable

References

1. Schweizer TA. Biofilms in human and veterinary infections: A central link in One Health frameworks. One Health Microbiol. Infect. 2026;2(1):101-109. https://doi.org/10.66585/ohmi.2026.2.0021

2. Jacques M, Malouin F. One Health—One Biofilm. Vet Res. 2022;53(1):51. https://doi.org/10.1186/s13567-022-01067-4

3. Andersson DI, Hughes D. Antibiotic resistance and its cost: Is it possible to reverse resistance? Nat Rev Microbiol. 2010;8(4):260-271. https://doi.org/10.1038/nrmicro2319

4. France MT, Cornea A, Kehlet-Delgado H, Forney LJ. Spatial structure facilitates the accumulation and persistence of antibiotic-resistant mutants in biofilms. Evol Appl. 2019;12(3):498-507. https://doi.org/10.1111/eva.12728

5. Hjort K, Fermér E, Tang PC, Andersson DI. Antibiotic minimal selective concentrations and fitness costs during biofilm and planktonic growth. mBio. 2022;13(3):e01447-22. https://doi.org/10.1128/mbio.01447-22

6. Higazy D, Pham AD, van Hasselt C, Høiby N, Jelsbak L, Moser C, et al. In vivo evolution of antimicrobial resistance in a biofilm model of Pseudomonas aeruginosa lung infection. ISME J. 2024;18(1):wrae036. https://doi.org/10.1093/ismejo/wrae036

7. Gao D, Ji H, Wang L, Li X, Hu D, Zhao J, et al. Fitness trade-offs in phage cocktail-resistant Salmonella enterica serovar Enteritidis result in increased antibiotic susceptibility and reduced virulence. Microbiol Spectr. 2022;10(5):e02914-22. https://doi.org/10.1128/spectrum.02914-22

8. Olsen NS, Riber L. Metagenomics as a transformative tool for antibiotic resistance surveillance: Highlighting the impact of mobile genetic elements with a focus on the complex role of phages. Antibiotics. 2025;14(3):296. https://doi.org/10.3390/antibiotics14030296

9. Trampuz A, Piper KE, Jacobson MJ, Hanssen AD, Unni KK, Osmon DR, et al. Sonication of removed hip and knee prostheses for diagnosis of infection. N Engl J Med. 2007;357(7):654-663. https://doi.org/10.1056/NEJMoa061588

10. Sadia H, Amin A, Ahmed I. Metagenomic and phenotypic insights into biofilm-forming pathogens in patients with nosocomial sepsis. Biomed Res Int. 2026;2026(1):e8989667. https://doi.org/10.1155/bmri/8989667

11. Bellova P, Knop-Hammad V, Königshausen M, Mempel E, Frieler S, Gessmann J, et al. Sonication of retrieved implants improves sensitivity in the diagnosis of periprosthetic joint infection. BMC Musculoskelet Disord. 2019;20(1):623. https://doi.org/10.1186/s12891-019-3006-1

12. Mayorga-Ramos A, Zúñiga-Miranda J, Carrera-Pacheco SE, Barba-Ostria C, Guamán LP. CRISPR-Cas-based antimicrobials: Design, challenges, and bacterial mechanisms of resistance. ACS Infect Dis. 2023;9(7):1283-1302. https://doi.org/10.1021/acsinfecdis.2c00649

13. Koo H, Allan RN, Howlin RP, Stoodley P, Hall-Stoodley L. Targeting microbial biofilms: Current and prospective therapeutic strategies. Nat Rev Microbiol. 2017;15(12):740-755. https://doi.org/10.1038/nrmicro.2017.99

Published

2026-09-24

Issue

Section

Commentary

How to Cite

Elbediwi, M. . (2026). Commentary on: Biofilms in human and veterinary infections: a central link in One Health frameworks. One Health Microbiology & Infection, 2(1), 253-255. https://doi.org/10.66585/ohmi.2026.2.0033

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