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Protective immune response induced by Leghorn male hepatoma cell-adapted fowl adenovirus-4.
Lee, Rangyeon; Sung, Haan Woo; Cheong, Hee-Tae; Park, Jeongho.
Afiliação
  • Lee R; College of Veterinary Medicine, Kangwon National University, Chuncheon, Republic of Korea.
  • Sung HW; College of Veterinary Medicine, Kangwon National University, Chuncheon, Republic of Korea.
  • Cheong HT; Institute of Veterinary Science, Kangwon National University, Chuncheon, Republic of Korea.
  • Park J; College of Veterinary Medicine, Kangwon National University, Chuncheon, Republic of Korea.
Heliyon ; 10(3): e25366, 2024 Feb 15.
Article em En | MEDLINE | ID: mdl-38356505
ABSTRACT
Fowl adenovirus-4 (FAdV-4) is a highly contagious virus that causes acute and lethal hepatitis. It leads to substantial economic losses in the poultry industry. Among the structural proteins of FAdV-4, hexon and fiber2 are associated with immunopathogenesis. A frameshift mutation was generated in the fiber2 protein by seral passages in the Leghorn male hepatoma (LMH) cell line. Immunization using the attenuated virus (80 times passaged) before the virulent FAdV-4 challenge protected hosts from the infection and cleared the invading virus. In immunized animals, activated CD4+ and CD8+ T cell populations were larger during the FAdV-4 challenge. The change in the B cell population was similar. Myeloid cells were highly increased during FAdV-4 infection after the immunization, but the immunization inhibited the expansion in both liver and spleen. The functional gene expression for immune modulation was strongly associated with immune cell changes in the liver, however, this association was not strong in the spleen. The present findings imply that genetic modification by cellular adaptation regulates immune cell phenotype and function in the target organ. In addition, we suggest the attenuated virus as a protective strategy against the novel FAdV-4 strains.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Heliyon Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Heliyon Ano de publicação: 2024 Tipo de documento: Article