An analysis of two open reading frames (ORF3 and ORF4) of rat hepatitis E virus genome using its infectious cDNA clones with mutations in ORF3 or ORF4

作者：Tanggis; Kobayashi, Tominari; Takahashi, Masaharu; Jirintai, Suljid; Nishizawa, Tsutomu; Nagashima, Shigeo; Nishiyama, Takashi; Kunita, Satoshi; Hayama, Emiko; Tanaka, Takeshi; Mulyanto; Okamoto, Hiroaki^*

来源：Virus Research, 2018, 249: 16-30.

DOI：10.1016/j.virusres.2018.02.014

• Rat hepatitis E virus
• Infectious cDNA clone
• Mutagenesis
• ORF3
• ORF4
• Proline-rich sequence

Rat hepatitis E virus (ratHEV) genome has four open reading frames (ORFs: ORF1, ORF2, ORF3 and ORF4). The functions of ORF3 and ORF4 are unknown. An infectious cDNA clone (pUC-ratELOMB-131L_wt, wt) and its derivatives including ORF3-defective (Delta ORF3) and ORF4-defective (Delta ORF4) mutants, were constructed and their full-length RNA transcripts transfected into PLC/PRF/5 cells. Delta ORF3 replicated as efficiently as wt in cells. However, <= 1/1000 of the number of progenies were detectable in the culture supernatant of Delta ORF3-infected cells compared with wt-infected cells. ORF4 protein was not detectable in ratHEV-infected cells or in the liver tissues of ratHEV-infected rats. No marked differences were noted between wt and Delta ORF4 regarding the viral replication and protein expression. ORF3 mutants with proline-to-leucine mutations at amino acids (aa) 93, 96 and/or 98 in ORF3 were constructed and transfected into PLC/PRF/5 cells. Wt and an ORF3 mutant with leucine at aa 98 (ORF3-L98) replicated efficiently (density 1.15-1.16 g/cm(3)), while ORF3-L93 + L96 exhibited a decreased viral release and banded at 1.26-1.27 g/cm(3), similar to Delta ORF3. In conclusion, the ORF3 protein, especially its proline residues at aa 93 and 96, is essential for the release of membrane-associated ratHEV particles, and ORF4 is unnecessary for the replication of ratHEV.

• 出版日期2018-4-2
• 单位内蒙古农业大学