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Acyclovir inhibits channel catfish virus replication and protects channel catfish ovary cells from apoptosis.
Hao, Kai; Yuan, Sheng; Yu, Fei; Chen, Xiao Hui; Bian, Wen Ji; Feng, Yong Hui; Zhao, Zhe.
Afiliação
  • Hao K; College of Oceanography, Hohai University, Nanjing, 210098, China. Electronic address: haokai87@hhu.edu.cn.
  • Yuan S; Jiangsu Agri-animal Husbandry Vocational College, China.
  • Yu F; College of Oceanography, Hohai University, Nanjing, 210098, China.
  • Chen XH; Freshwater Fisheries Research Institute of Jiangsu Province, Nanjing, 210017, China.
  • Bian WJ; Freshwater Fisheries Research Institute of Jiangsu Province, Nanjing, 210017, China.
  • Feng YH; Aquatic science research Institute of xinjiang Uygur autonomous region, China.
  • Zhao Z; College of Oceanography, Hohai University, Nanjing, 210098, China. Electronic address: zhezhao@hhu.edu.cn.
Virus Res ; 292: 198249, 2021 01 15.
Article em En | MEDLINE | ID: mdl-33253717
ABSTRACT
The channel catfish virus (CCV) can cause lethal hemorrhagic infection in channel catfish, resulting in significant economic losses in the fish industry. Effective drugs for the virus are still lacking. Acyclovir is known as a potent antiviral agent against human herpes viruses and some animal DNA viruses. The present study was undertaken to explore the antiviral response and mechanism of acyclovir against CCV in channel catfish ovary (CCO) cells. Acyclovir was able to significantly inhibit the expression of viral genes related to CCV viral DNA synthesis and suppress viral replication at a safe concentration. Furthermore, acyclovir blocked the cytopathic effects and apoptosis induced by CCV, thereby maintaining the normal cellular morphological structure, as shown by the protection of CCO cells from the formation of apoptotic bodies or nuclear fragmentation. Moreover, reverse transcript quantitative polymerase chain reaction (RT-qPCR) demonstrated that acyclovir suppressed the expression of caspase 3, caspase 8 and caspase 9, while there was no significant impact on the expression of the apoptosis-inhibiting gene bcl-2 in CCV-infected cells. In addition, acyclovir did not promote the expression of immune-related genes such as MyD88, Mx1, IRF3, IRF7, IFN-I, NF-kB and IL-1ß, suggesting that the antiviral activity of acyclovir to CCV infection is not achieved by facilitating the expression of immune-related genes in CCO cells. Taken together, the results from this study suggest that acyclovir could effectively regulate CCV-induced infection, and thus is a promising therapeutic agent against CCV. Our results will aid our understanding of the pharmacological mechanisms of antiviral agents.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Ovário / Replicação Viral / Peixes-Gato / Aciclovir / Ictalurivirus / Doenças dos Peixes Limite: Animals Idioma: En Revista: Virus Res Assunto da revista: VIROLOGIA Ano de publicação: 2021 Tipo de documento: Article País de publicação: HOLANDA / HOLLAND / NETHERLANDS / NL / PAISES BAJOS / THE NETHERLANDS

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Antivirais / Ovário / Replicação Viral / Peixes-Gato / Aciclovir / Ictalurivirus / Doenças dos Peixes Limite: Animals Idioma: En Revista: Virus Res Assunto da revista: VIROLOGIA Ano de publicação: 2021 Tipo de documento: Article País de publicação: HOLANDA / HOLLAND / NETHERLANDS / NL / PAISES BAJOS / THE NETHERLANDS