Infectious salmon anaemia virus (ISAV) mucosal infection in Atlantic salmon

International audience AbstractAll viruses infecting fish must cross the surface mucosal barrier to successfully enter a host. Infectious salmon anaemia virus (ISAV), the causative agent of the economically important infectious salmon anaemia (ISA) in Atlantic salmon, Salmo salar L., has been shown...

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Bibliographic Details
Published in:Veterinary Research
Main Authors: Aamelfot, Maria, McBeath, Alastair, Christiansen, Debes H., Matejusova, Iveta, Falk, Knut
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 2015
Subjects:
Online Access:https://hal.archives-ouvertes.fr/hal-01341431
https://hal.archives-ouvertes.fr/hal-01341431/document
https://hal.archives-ouvertes.fr/hal-01341431/file/13567_2015_Article_265.pdf
https://doi.org/10.1186/s13567-015-0265-1
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Summary:International audience AbstractAll viruses infecting fish must cross the surface mucosal barrier to successfully enter a host. Infectious salmon anaemia virus (ISAV), the causative agent of the economically important infectious salmon anaemia (ISA) in Atlantic salmon, Salmo salar L., has been shown to use the gills as its entry point. However, other entry ports have not been investigated despite the expression of virus receptors on the surface of epithelial cells in the skin, the gastrointestinal (GI) tract and the conjunctiva. Here we investigate the ISAV mucosal infection in Atlantic salmon after experimental immersion (bath) challenge and in farmed fish collected from a confirmed outbreak of ISA in Norway. We show for the first time evidence of early replication in several mucosal surfaces in addition to the gills, including the pectoral fin, skin and GI tract suggesting several potential entry points for the virus. Initially, the infection is localized and primarily infecting epithelial cells, however at later stages it becomes systemic, infecting the endothelial cells lining the circulatory system. Viruses of low and high virulence used in the challenge revealed possible variation in virus progression during infection at the mucosal surfaces.