Reversible mutations in gliding motility and virulence genes: A flexible and efficient phage defence mechanism in Flavobacterium psychrophilum.


Journal

Environmental microbiology
ISSN: 1462-2920
Titre abrégé: Environ Microbiol
Pays: England
ID NLM: 100883692

Informations de publication

Date de publication:
10 2022
Historique:
revised: 27 06 2022
received: 03 05 2022
accepted: 04 07 2022
pubmed: 16 7 2022
medline: 20 10 2022
entrez: 15 7 2022
Statut: ppublish

Résumé

Flavobacteria are among the most important pathogens in freshwater salmonid aquaculture worldwide. Due to concerns regarding development of antibiotic resistance, phage therapy has been proposed as a solution to decrease pathogen load. However, application of phages is challenged by the development of phage resistance, and knowledge of the mechanisms and implications of phage resistance is therefore required. To study this, 27 phage-resistant isolates of F. psychrophilum were genome sequenced and characterized to identify genetic modifications and evaluate changes in phenotypic traits, including virulence against rainbow trout. Phage-resistant isolates showed reduction or loss of gliding motility, proteolytic activity, and adhesion to surfaces, and most isolates were completely non-virulent against rainbow trout fry. Genomic analysis revealed that most phage-resistant isolates had mutations in genes associated with gliding motility and virulence. Reversal of these mutations in a sub-set of isolates led to regained motility, proteolytic activity, virulence and phage susceptibility. Although costly, the fast generation of phage resistance driven by single, reversible mutations likely represents a flexible and efficient phage defence mechanism in F. psychrophilum. The results further suggest that phage administration in aquaculture systems to prevent F. psychrophilum outbreaks selects for non-virulent phage-resistant phenotypes.

Identifiants

pubmed: 35837851
doi: 10.1111/1462-2920.16126
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

4915-4930

Informations de copyright

© 2022 The Authors. Environmental Microbiology published by Society for Applied Microbiology and John Wiley & Sons Ltd.

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Auteurs

Jóhanna Jørgensen (J)

Department of Biology, University of Copenhagen, Helsingør, Denmark.

Krister Sundell (K)

Laboratory of Aquatic Pathobiology, Åbo Akademi University, Turku, Finland.

Daniel Castillo (D)

Department of Biology, University of Copenhagen, Helsingør, Denmark.

Liv S Dramshøj (LS)

Department of Biology, University of Copenhagen, Helsingør, Denmark.

Natasja B Jørgensen (NB)

Department of Biology, University of Copenhagen, Helsingør, Denmark.

Susie B Madsen (SB)

Department of Biology, University of Copenhagen, Helsingør, Denmark.

Lotta Landor (L)

Laboratory of Aquatic Pathobiology, Åbo Akademi University, Turku, Finland.
Department of Biological Sciences, University of Bergen, Bergen, Norway.

Tom Wiklund (T)

Laboratory of Aquatic Pathobiology, Åbo Akademi University, Turku, Finland.

Valentina L Donati (VL)

National Institute of Aquatic Resources, Technical University of Denmark, Kongens Lyngby, Denmark.

Lone Madsen (L)

National Institute of Aquatic Resources, Technical University of Denmark, Kongens Lyngby, Denmark.

Inger Dalsgaard (I)

National Institute of Aquatic Resources, Technical University of Denmark, Kongens Lyngby, Denmark.

Mathias Middelboe (M)

Department of Biology, University of Copenhagen, Helsingør, Denmark.

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