Infection studies with canine distemper virus in harbour seals

Arch Virol. 1993;131(3-4):349-59. doi: 10.1007/BF01378637.

Abstract

Infection studies in harbour seal (Phoca vitulina) were conducted with the Snyder-Hill strain of canine distemper virus (CDV) that is virulent for dog and mink. The inoculated seals showed clinical symptoms which were to some degree similar to those observed in CDV infections of sensitive species of carnivores. Viral replication in lymphoid cells was followed by an extended period of immunosuppression. The results did not provide conclusive evidence for viral replication in surface epithelia of seals, and accordingly no spread of the infection to contact seals and mink was demonstrated. The pathogenicity of the infection did not increase upon a second viral passage in seal. The serological data showed that CDV-infected seals mounted an early virus specific antibody response. Overall, the results indicated that the harbour seal was not especially sensitive to CDV infection. The differences in the in vivo biological properties of CDV and PDV add to the distinction between these viruses at the genomic and antigenic levels.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies, Viral / biosynthesis
  • Antigens, Viral / biosynthesis
  • Cells, Cultured
  • Cytopathogenic Effect, Viral
  • Distemper / immunology
  • Distemper / microbiology*
  • Distemper / transmission
  • Distemper Virus, Canine / pathogenicity*
  • Distemper Virus, Canine / physiology
  • Immunoglobulin G / biosynthesis
  • Immunoglobulin M / biosynthesis
  • Leukocytes / microbiology
  • Lymphocytes / immunology
  • Lymphoid Tissue / microbiology
  • Lymphoid Tissue / pathology
  • Mink / immunology
  • Mink / microbiology
  • Neutralization Tests
  • Seals, Earless / immunology
  • Seals, Earless / microbiology*
  • Time Factors
  • Vero Cells
  • Viremia / immunology
  • Viremia / microbiology
  • Virus Replication

Substances

  • Antibodies, Viral
  • Antigens, Viral
  • Immunoglobulin G
  • Immunoglobulin M