» Articles » PMID: 33498243

Animal Models in the Evaluation of the Effectiveness of Phage Therapy for Infections Caused by Gram-Negative Bacteria from the ESKAPE Group and the Reliability of Its Use in Humans

Overview
Journal Microorganisms
Specialty Microbiology
Date 2021 Jan 27
PMID 33498243
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

The authors emphasize how extremely important it is to highlight the role played by animal models in an attempt to determine possible phage interactions with the organism into which it was introduced as well as to determine the safety and effectiveness of phage therapy in vivo taking into account the individual conditions of a given organism and its physiology. Animal models in which phages are used make it possible, among other things, to evaluate the effective therapeutic dose and to choose the possible route of phage administration depending on the type of infection developed. These results cannot be applied in detail to the human body, but the knowledge gained from animal experiments is invaluable and very helpful. We would like to highlight how useful animal models may be for the possible effectiveness evaluation of phage therapy in the case of infections caused by gram-negative bacteria from the ESKAPE (, , , , , species) group of pathogens. In this review, we focus specifically on the data from the last few years.

Citing Articles

Mucosal-adapted bacteriophages as a preventive strategy for a lethal Pseudomonas aeruginosa challenge in mice.

Coelho L, de Souza Terceti M, Neto S, Amaral R, Dos Santos A, Gozzi W Commun Biol. 2025; 8(1):13.

PMID: 39762450 PMC: 11704353. DOI: 10.1038/s42003-024-07269-0.


Pharmacokinetics and pharmacodynamics of bacteriophage therapy: a review with a focus on multidrug-resistant Gram-negative bacterial infections.

Siopi M, Skliros D, Paranos P, Koumasi N, Flemetakis E, Pournaras S Clin Microbiol Rev. 2024; 37(3):e0004424.

PMID: 39072666 PMC: 11391690. DOI: 10.1128/cmr.00044-24.


Navigating ESKAPE Pathogens: Considerations and Caveats for Animal Infection Models Development.

Yu H, Xu Y, Imani S, Zhao Z, Ullah S, Wang Q ACS Infect Dis. 2024; 10(7):2336-2355.

PMID: 38866389 PMC: 11249778. DOI: 10.1021/acsinfecdis.4c00007.


Disrupting quorum sensing as a strategy to inhibit bacterial virulence in human, animal, and plant pathogens.

Gonzales M, Kergaravat B, Jacquet P, Billot R, Grizard D, Chabriere E Pathog Dis. 2024; 82.

PMID: 38724459 PMC: 11110857. DOI: 10.1093/femspd/ftae009.


Controlling the bacterial load of Salmonella Typhi in an experimental mouse model by a lytic Salmonella phage STWB21: a phage therapy approach.

Mondal P, Halder P, Mallick B, Bhaumik S, Koley H, Dutta S BMC Microbiol. 2023; 23(1):324.

PMID: 37924001 PMC: 10623789. DOI: 10.1186/s12866-023-03040-3.


References
1.
Vazquez R, Garcia E, Garcia P . Phage Lysins for Fighting Bacterial Respiratory Infections: A New Generation of Antimicrobials. Front Immunol. 2018; 9:2252. PMC: 6232686. DOI: 10.3389/fimmu.2018.02252. View

2.
Fukuda K, Ishida W, Uchiyama J, Rashel M, Kato S, Morita T . Pseudomonas aeruginosa keratitis in mice: effects of topical bacteriophage KPP12 administration. PLoS One. 2012; 7(10):e47742. PMC: 3474789. DOI: 10.1371/journal.pone.0047742. View

3.
Davin-Regli A, Lavigne J, Pages J . spp.: Update on Taxonomy, Clinical Aspects, and Emerging Antimicrobial Resistance. Clin Microbiol Rev. 2019; 32(4). PMC: 6750132. DOI: 10.1128/CMR.00002-19. View

4.
Wintachai P, Naknaen A, Thammaphet J, Pomwised R, Phaonakrop N, Roytrakul S . Characterization of extended-spectrum-β-lactamase producing Klebsiella pneumoniae phage KP1801 and evaluation of therapeutic efficacy in vitro and in vivo. Sci Rep. 2020; 10(1):11803. PMC: 7367294. DOI: 10.1038/s41598-020-68702-y. View

5.
Britt N, Ritchie D, Kollef M, Burnham C, Durkin M, Hampton N . Importance of Site of Infection and Antibiotic Selection in the Treatment of Carbapenem-Resistant Pseudomonas aeruginosa Sepsis. Antimicrob Agents Chemother. 2018; 62(4). PMC: 5913923. DOI: 10.1128/AAC.02400-17. View