Susceptibility and Permissivity of Zebrafish (Danio rerio) Larvae to Cypriniviruses

Author:

Streiff Cindy1,He Bo1ORCID,Morvan Léa1,Zhang Haiyan1,Delrez Natacha1,Fourrier Mickael1,Manfroid Isabelle2ORCID,Suárez Nicolás M.3,Betoulle Stéphane4,Davison Andrew J.3ORCID,Donohoe Owen15ORCID,Vanderplasschen Alain1

Affiliation:

1. Immunology–Vaccinology, Department of Infectious and Parasitic Diseases, Fundamental and Applied Research for Animals & Health (FARAH), Faculty of Veterinary Medicine, University of Liège, B-4000 Liège, Belgium

2. Zebrafish Development and Disease Models Laboratory, GIGA-Molecular Biology of Diseases, University of Liège, B-4000 Liège, Belgium

3. MRC-University of Glasgow Centre for Virus Research, Glasgow G61 1QH, UK

4. UMR-I 02 Stress Environnementaux et BIOsurveillance des Milieux Aquatiques (SEBIO), UFR Sciences Exactes et Naturelles, Université de Reims Champagne-Ardenne, CEDEX 2, 51687 Reims, France

5. Bioscience Research Institute, Technological University of the Shannon, N37 HD68 Athlone, Co. Westmeath, Ireland

Abstract

The zebrafish (Danio rerio) represents an increasingly important model organism in virology. We evaluated its utility in the study of economically important viruses from the genus Cyprinivirus (anguillid herpesvirus 1, cyprinid herpesvirus 2 and cyprinid herpesvirus 3 (CyHV-3)). This revealed that zebrafish larvae were not susceptible to these viruses after immersion in contaminated water, but that infections could be established using artificial infection models in vitro (zebrafish cell lines) and in vivo (microinjection of larvae). However, infections were transient, with rapid viral clearance associated with apoptosis-like death of infected cells. Transcriptomic analysis of CyHV-3-infected larvae revealed upregulation of interferon-stimulated genes, in particular those encoding nucleic acid sensors, mediators of programmed cell death and related genes. It was notable that uncharacterized non-coding RNA genes and retrotransposons were also among those most upregulated. CRISPR/Cas9 knockout of the zebrafish gene encoding protein kinase R (PKR) and a related gene encoding a protein kinase containing Z-DNA binding domains (PKZ) had no impact on CyHV-3 clearance in larvae. Our study strongly supports the importance of innate immunity-virus interactions in the adaptation of cypriniviruses to their natural hosts. It also highlights the potential of the CyHV-3-zebrafish model, versus the CyHV-3-carp model, for study of these interactions.

Funder

University of Liège

FNRS

European Maritime and Fisheries Fund

Welbio

Walloon Region

The Medical Research Council

Publisher

MDPI AG

Subject

Virology,Infectious Diseases

Reference185 articles.

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2. The Zebrafish Reference Genome Sequence and Its Relationship to the Human Genome;Howe;Nature,2013

3. A Systematic Genome-Wide Analysis of Zebrafish Protein-Coding Gene Function;Kettleborough;Nature,2013

4. The Zebrafish as a Model Organism to Study Development of the Immune System;Traver;Adv. Immunol.,2003

5. The Use of Zebrafish to Understand Immunity;Trede;Immunity,2004

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