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Vaccination with FAdV-8a induces protection against inclusion body hepatitis caused by homologous and heterologous strains.
Steer-Cope, Penelope A; Sandy, Jeanine R; O'Rourke, Denise; Scott, Peter C; Browning, Glenn F; Noormohammadi, Amir H.
Afiliação
  • Steer-Cope PA; Asia-Pacific Centre for Animal Health, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne , Werribee , Australia.
  • Sandy JR; Poultry CRC, University of New England , Armidale , Australia.
  • O'Rourke D; Asia-Pacific Centre for Animal Health, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne , Werribee , Australia.
  • Scott PC; Asia-Pacific Centre for Animal Health, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne , Werribee , Australia.
  • Browning GF; Asia-Pacific Centre for Animal Health, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne , Werribee , Australia.
  • Noormohammadi AH; Asia-Pacific Centre for Animal Health, Faculty of Veterinary and Agricultural Sciences, The University of Melbourne , Werribee , Australia.
Avian Pathol ; 48(5): 396-405, 2019 Oct.
Article em En | MEDLINE | ID: mdl-31042049
Fowl aviadenoviruses (FAdV) are important avian pathogens, responsible for several poultry diseases prevalent worldwide, including inclusion body hepatitis (IBH). FAdV intraspecies cross-protection has been clearly demonstrated, but there is little evidence that any interspecies cross-protection exists. The present study aimed to assess the inter- and intraspecies protection between three FAdV field isolates (FAdV-8a, FAdV-8b, FAdV-11) identified in association with severe IBH outbreaks. Inocula prepared using inactivated plaque-purified virus with adjuvant Montanide™ ISA 71VG, were injected intramuscularly into 3-week-old SPF chickens. At 6-weeks of age, the birds were challenged with 106 TCID50 of homologous or heterologous virus intraperitoneally, and full post mortem examination performed at 4 days post-challenge. Various tissues were examined for gross and histological lesions and assessed for the presence of virus by PCR-HRM. All homologous-type vaccine/challenge groups exhibited protection against IBH lesions with no virus detected in the tissues. Unvaccinated groups challenged with virus showed evidence of FAdV-induced lesions; however, FAdV-8a demonstrated lower pathogenicity compared with FAdV-8b and FAdV-11. In the heterologous-type vaccine/challenge groups, FAdV-8a vaccine was shown to protect against challenge with both FAdV-8b and FAdV-11. FAdV-8a and 8b belong to species E and were therefore anticipated to cross-protect. However, FAdV-11 belongs to species D and therefore cross-protection by FAdV-8a was an uncharacteristic and unique finding of this study. Further research is required to disseminate the molecular basis for the interspecies cross-protection between FAdV-8a and FAdV-11. Nonetheless, the FAdV-8a isolate was shown to have substantial potential as a vaccine candidate in countries where FAdV-8a, 8b or 11 are prevalent.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças das Aves Domésticas / Vacinas Virais / Galinhas / Vacinação / Infecções por Adenoviridae / Aviadenovirus / Hepatite Viral Animal Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Avian Pathol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças das Aves Domésticas / Vacinas Virais / Galinhas / Vacinação / Infecções por Adenoviridae / Aviadenovirus / Hepatite Viral Animal Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Avian Pathol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Austrália País de publicação: Reino Unido