Characterisation of Australian ovine adenovirus isolates

Vet Microbiol. 1994 Aug 1;41(3):281-91. doi: 10.1016/0378-1135(94)90108-2.

Abstract

We have characterised two groups of adenoviruses isolated from sheep in Australia. Restriction endonuclease maps for enzymes BamHI, ClaI, SalI, SmaI and SphI have been determined for the genome of ovine adenoviruses related to bovine adenovirus serotype 7 (BAV 7) from sheep in Western Australia. Although previously serotyped as BAV 7 these isolates are different from bovine isolates of BAV 7 based on comparison with published restriction endonuclease profiles and maps of BAV 7 cattle isolates. Additional adenovirus isolates obtained from Victorian sheep have been serotyped as ovine adenovirus type 5 (OAV 5). On the basis of restriction endonuclease analysis these viruses are different from the sheep BAV 7 isolates. Following infection of sheep with ovine BAV 7 and OAV 5 isolates, virus was recovered from nasal and rectal swabs for several days. Antibodies detected by ELISA and serum neutralisation tests (SN) developed by 15 days after infection. Virus also spread from the infected sheep to an incontact control and one of ten sheep purchased for infection studies had SN antibodies to BAV 7 suggesting that BAV 7-like viruses naturally infect sheep in Victoria and Western Australia. With further development, these ovine adenoviruses may be suitable as vectors for the delivery of vaccine antigens to sheep and cattle.

MeSH terms

  • Adenoviridae / classification
  • Adenoviridae / genetics*
  • Adenoviridae / growth & development
  • Adenoviridae Infections / immunology
  • Adenoviridae Infections / veterinary*
  • Adenoviridae Infections / virology
  • Animals
  • Antibodies, Viral / analysis
  • Australia
  • DNA Restriction Enzymes / analysis
  • DNA, Viral
  • Genome, Viral*
  • Restriction Mapping
  • Serotyping / veterinary
  • Sheep / virology*
  • Sheep Diseases / immunology
  • Sheep Diseases / virology*

Substances

  • Antibodies, Viral
  • DNA, Viral
  • DNA Restriction Enzymes