Efficacy assessment of PEV2 phage on Galleria mellonella larvae infected with a Pseudomonas aeruginosa dog otitis isolate.


Journal

Research in veterinary science
ISSN: 1532-2661
Titre abrégé: Res Vet Sci
Pays: England
ID NLM: 0401300

Informations de publication

Date de publication:
May 2021
Historique:
received: 29 12 2020
revised: 29 03 2021
accepted: 12 04 2021
pubmed: 26 4 2021
medline: 16 6 2021
entrez: 25 4 2021
Statut: ppublish

Résumé

Pseudomonas (P.) aeruginosa is the most frequently isolated Gram-negative bacteria in dog otitis. Antimicrobial resistance is particularly prevalent in P. aeruginosa and phage therapy represents a promising alternative therapeutic strategy. The aim of this study was to assess the efficacy of the PEV2 phage against a clinical P. aeruginosa isolate from a canine otitis using a Galleria (G.) mellonella larvae model. The genomic DNA of PAV237 P. aeruginosa isolate was sequenced and analysed. In a first main experiment, the efficacy of PEV2 phage against PAV237 was assessed at different multiplicities of infection (MOI) (50,000, 5000, 500, 50) by analyzing the larvae survival rate during 4 days. In a second experiment, the bacterial and phage titer evolutions were assessed depending on two MOIs (50,000, 5000). No significant survival increase was observed with PEV2 therapy in the infected larvae groups. The generated Kaplan-Meier curves showed that the rate of alive larvae was significantly higher in the non-infected larvae compared to the infected-treated ones irrespective of phage MOIs. An increase of the phage titer was observed at 24 and 48 h post-inoculation (HPI) with both MOIs and the P. aeruginosa titers were lower with MOI 50,000 and 5000 compared to the infectivity control at 24 and 48 HPI. Even if an ineffectiveness of the PEV2 phage was observed on the larvae survival, PEV2 is active against P. aeruginosa in this model and PEV2 replication is correlated with a lower bacterial proliferation in the phage treated larvae.

Identifiants

pubmed: 33895568
pii: S0034-5288(21)00109-0
doi: 10.1016/j.rvsc.2021.04.010
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

598-601

Informations de copyright

Copyright © 2021 Elsevier Ltd. All rights reserved.

Auteurs

C Antoine (C)

Bacteriology, Department of Infectious and Parasitic Diseases, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium; Food Science Department, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium.

F Laforêt (F)

Bacteriology, Department of Infectious and Parasitic Diseases, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium; Food Science Department, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium.

B Blasdel (B)

Vésale Bioscience, Vésale Pharmaceutica, 5310, Noville sur Mehaigne, Belgium.

T Glonti (T)

Laboratory for Molecular and Cellular Technology (LabMCT), Queen Astrid Military Hospital, Neder-over-Heembeek, Belgium.

E Kutter (E)

Evergreen Phage Lab, The Evergreen State College, Olympia, WA, USA.

J P Pirnay (JP)

Laboratory for Molecular and Cellular Technology (LabMCT), Queen Astrid Military Hospital, Neder-over-Heembeek, Belgium.

J Mainil (J)

Bacteriology, Department of Infectious and Parasitic Diseases, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium.

V Delcenserie (V)

Food Science Department, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium.

D Thiry (D)

Bacteriology, Department of Infectious and Parasitic Diseases, FARAH and Faculty of Veterinary Medicine, ULiège, 4000 Liège, Belgium. Electronic address: damien.thiry@uliege.be.

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Classifications MeSH