Genetic interaction between NS4A and NS4B for replication of Japanese encephalitis virus
Author(s) -
Xiaodan Li,
HanQing Ye,
Cheng-Lin Deng,
Si-Qing Liu,
Honglei Zhang,
Bao-Di Shang,
PeiYong Shi,
Zhiming Yuan,
Bo Zhang
Publication year - 2015
Publication title -
journal of general virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.55
H-Index - 167
eISSN - 1465-2099
pISSN - 0022-1317
DOI - 10.1099/vir.0.000044
Subject(s) - biology , replicon , virology , viral replication , virus , flavivirus , mutation , mutant , mutagenesis , genetics , japanese encephalitis , replication factor c , replication (statistics) , genome , gene , dna replication , control of chromosome duplication , encephalitis
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.
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