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Construction and characterization of a reverse genetics system of bovine parainfluenza virus type 3c as a tool for rapid screening of antivirals in vitro.
Han, Yu; Lu, Kejia; Zhang, Riteng; Wei, Xi; Guo, Hanwei; Tong, Lina; Wang, Xinglong; Xiao, Sa; Liu, Haijin; Yang, Zengqi.
Afiliação
  • Han Y; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Lu K; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Zhang R; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Wei X; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Guo H; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Tong L; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Wang X; College of Agriculture and Animal Husbandry, Qinghai University, Xining, China.
  • Xiao S; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Liu H; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
  • Yang Z; College of Veterinary Medicine, Northwest A&F University, Yangling, China.
Front Vet Sci ; 11: 1336663, 2024.
Article em En | MEDLINE | ID: mdl-38545559
ABSTRACT
Bovine parainfluenza virus type 3 (BPIV3) is a key pathogen associated with bovine respiratory disease complex (BRDC). However, its specific pathogenesis mechanisms have not been fully elucidated. Reverse genetics provides a useful method for understanding the pathogenic mechanism of BPIV3. To ensure the functionality of the rescue platforms, we first constructed a minigenome (MG) system of BPIV3 utilizing a 5-plasmid system in this investigation. Then, a full-length infection clone of BPIV3 was obtained from the SX-2021 strain, and different methods were employed to identify the rescued virus. Additionally, we recovered a recombinant BPIV3 using the reverse genetics system that could express enhanced green fluorescence protein (eGFP). Through the growth curve assays, the replicate capability of rBPIV3-SX-EGFP was found to be similar to that of the parental virus. Subsequently, the rBPIV3-SX-EGFP was used to determine the antiviral activity of ribavirin. The results showed that ribavirin had an anti-BPIV3 effect in MDBK cells. In conclusion, the successful development of a reverse genetic system for the SX-2021 strain establishes a foundation for future studies on BPIV3, including investigations into its pathogenic mechanism, gene function, and antiviral screening properties.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article