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Destruction of the vascular viral receptor in infectious salmon anaemia provides in vivo evidence of homologous attachment interference.
Aamelfot, Maria; Fosse, Johanna Hol; Viljugrein, Hildegunn; Ploss, Frieda Betty; Benestad, Sylvie L; McBeath, Alastair; Christiansen, Debes Hammershaimb; Garver, Kyle; Falk, Knut.
Afiliación
  • Aamelfot M; Norwegian Veterinary Institute, Ås, Norway.
  • Fosse JH; Norwegian Veterinary Institute, Ås, Norway.
  • Viljugrein H; Norwegian Veterinary Institute, Ås, Norway.
  • Ploss FB; Norwegian Veterinary Institute, Ås, Norway.
  • Benestad SL; Norwegian Veterinary Institute, Ås, Norway.
  • McBeath A; Marine Laboratory, Aberdeen, Scotland, United Kingdom.
  • Christiansen DH; Faroese Food and Veterinary Authority, National Reference Laboratory for Fish Diseases, Tórshavn, Faroe Islands.
  • Garver K; Fisheries and Oceans Canada Pacific Biological Station, Nanaimo, British Columbia, Canada.
  • Falk K; Norwegian Veterinary Institute, Ås, Norway.
PLoS Pathog ; 18(10): e1010905, 2022 10.
Article en En | MEDLINE | ID: mdl-36240255
ABSTRACT
Viral interference is a process where infection with one virus prevents a subsequent infection with the same or a different virus. This is believed to limit superinfection, promote viral genome stability, and protect the host from overwhelming infection. Mechanisms of viral interference have been extensively studied in plants, but remain poorly understood in vertebrates. We demonstrate that infection with infectious salmon anaemia virus (ISAV) strongly reduces homologous viral attachment to the Atlantic salmon, Salmo salar L. vascular surface. A generalised loss of ISAV binding was observed after infection with both high-virulent and low-virulent ISAV isolates, but with different kinetics. The loss of ISAV binding was accompanied by an increased susceptibility to sialidase, suggesting a loss of the vascular 4-O-sialyl-acetylation that mediates ISAV attachment and simultaneously protects the sialic acid from cleavage. Moreover, the ISAV binding capacity of cultured cells dramatically declined 3 days after ISAV infection, accompanied by reduced cellular permissiveness to infection with a second antigenically distinct isolate. In contrast, neither infection with infectious haematopoietic necrosis virus nor stimulation with the viral mimetic poly IC restricted subsequent cellular ISAV attachment, revealing an ISAV-specific mechanism rather than a general cellular antiviral response. Our study demonstrates homologous ISAV attachment interference by de-acetylation of sialic acids on the vascular surface. This is the first time the kinetics of viral receptor destruction have been mapped throughout the full course of an infection, and the first report of homologous attachment interference by the loss of a vascular viral receptor. Little is known about the biological functions of vascular O-sialyl-acetylation. Our findings raise the question of whether this vascular surface modulation could be linked to the breakdown of central vascular functions that characterises infectious salmon anaemia.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones por Orthomyxoviridae / Salmo salar / Isavirus / Enfermedades de los Peces / Anemia Límite: Animals Idioma: En Revista: PLoS Pathog Año: 2022 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones por Orthomyxoviridae / Salmo salar / Isavirus / Enfermedades de los Peces / Anemia Límite: Animals Idioma: En Revista: PLoS Pathog Año: 2022 Tipo del documento: Article País de afiliación: Noruega