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Genetic interaction between NS4A and NS4B for replication of Japanese encephalitis virus.
Li, Xiao-Dan; Ye, Han-Qing; Deng, Cheng-Lin; Liu, Si-Qing; Zhang, Hong-Lei; Shang, Bao-Di; Shi, Pei-Yong; Yuan, Zhi-Ming; Zhang, Bo.
Afiliación
  • Li XD; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Ye HQ; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Deng CL; Key Laboratory of Agricultural and Environmental Microbiology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Liu SQ; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Zhang HL; Key Laboratory of Agricultural and Environmental Microbiology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Shang BD; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Shi PY; Key Laboratory of Special Pathogens and Biosafety, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, PR China.
  • Yuan ZM; Guizhou Fisheries Research Institute, Guiyang 550025, PR China.
  • Zhang B; Wadsworth Center, New York State Department of Health, Albany, NY, USA.
J Gen Virol ; 96(Pt 6): 1264-1275, 2015 Jun.
Article en En | MEDLINE | ID: mdl-25575708
ABSTRACT
Flavivirus NS4A and NS4B are important membrane proteins for viral replication that are assumed to serve as the scaffold for the formation of replication complexes. We previously demonstrated that a single Lys-to-Arg mutation at position 79 in NS4A (NS4A-K79R) significantly impaired Japanese encephalitis virus (JEV) replication. In this study, the mutant virus was subject to genetic selection to search for the potential interaction between NS4A and other viral components. Sequencing of the recovered viruses revealed that, in addition to an A97E change in NS4A itself, a Y3N compensatory mutation located in NS4B had emerged from independent selections. Mutagenesis analysis, using a genome-length RNA and a replicon of JEV, demonstrated that both adaptive mutations greatly restored the replication defect caused by NS4A-K79R. Our results, for the first time to our knowledge, clearly showed the genetic interaction between NS4A and NS4B, although the mechanism underlying their interaction is unknown.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Replicación Viral / Proteínas no Estructurales Virales / Mapeo de Interacción de Proteínas / Virus de la Encefalitis Japonesa (Especie) Límite: Animals Idioma: En Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Replicación Viral / Proteínas no Estructurales Virales / Mapeo de Interacción de Proteínas / Virus de la Encefalitis Japonesa (Especie) Límite: Animals Idioma: En Año: 2015 Tipo del documento: Article