Nagashima Shigeo, Primadharsini Putu Prathiwi, Takahashi Masaharu, Nishiyama Takashi, Murata Kazumoto, Okamoto Hiroaki
Division of Virology, Department of Infection and Immunity, Jichi Medical University School of Medicine, 3311-1 Yakushiji, Shimotsuke-shi 329-0498, Tochigi, Japan.
Pathogens. 2024 Dec 20;13(12):1130. doi: 10.3390/pathogens13121130.
Hepatitis E virus (HEV) exists in two distinct forms: a non-enveloped form (neHEV), which is present in feces and bile, and a quasi-enveloped form (eHEV), found in circulating blood and culture supernatants. This study aimed to elucidate the roles of Ras-associated binding 13 (Rab13) and protein kinase A (PKA) in the entry mechanisms of both eHEV and neHEV, utilizing small interfering RNA (siRNA) and chemical inhibitors. The results demonstrated that the entry of both viral forms is dependent on Rab13 and PKA. Further investigation into the involvement of tight junction (TJ) proteins revealed that the targeted knockdown of zonula occludens-1 (ZO-1) significantly impaired the entry of both eHEV and neHEV. In addition, in ZO-1 knockout (KO) cells inoculated with either viral form, HEV RNA levels in culture supernatants did not increase, even up to 16 days post-inoculation. Notably, the absence of ZO-1 did not affect the adsorption efficiency of eHEV or neHEV, nor did it influence HEV RNA replication. In cell-to-cell spread assays, ZO-1 KO cells inoculated with eHEV showed a lack of expression of HEV ORF2 and ORF3 proteins. In contrast, neHEV-infected ZO-1 KO cells showed markedly reduced ORF2 and ORF3 protein expression within virus-infected foci, compared to non-targeting knockout (NC KO) cells. These findings underscore the crucial role of ZO-1 in facilitating eHEV entry and mediating the cell-to-cell spread of neHEV in infected cells.
戊型肝炎病毒(HEV)以两种不同形式存在:一种是非包膜形式(neHEV),存在于粪便和胆汁中;另一种是准包膜形式(eHEV),存在于循环血液和培养上清液中。本研究旨在利用小干扰RNA(siRNA)和化学抑制剂阐明Ras相关结合蛋白13(Rab13)和蛋白激酶A(PKA)在eHEV和neHEV进入机制中的作用。结果表明,两种病毒形式的进入均依赖于Rab13和PKA。对紧密连接(TJ)蛋白参与情况的进一步研究表明,靶向敲除闭合蛋白-1(ZO-1)显著损害了eHEV和neHEV的进入。此外,在用任何一种病毒形式接种的ZO-1基因敲除(KO)细胞中,培养上清液中的HEV RNA水平即使在接种后16天也没有增加。值得注意的是,ZO-1的缺失不影响eHEV或neHEV的吸附效率,也不影响HEV RNA复制。在细胞间传播试验中,接种eHEV的ZO-1 KO细胞显示缺乏HEV ORF2和ORF3蛋白的表达。相比之下,与非靶向敲除(NC KO)细胞相比,感染neHEV的ZO-1 KO细胞在病毒感染灶内的ORF2和ORF3蛋白表达明显降低。这些发现强调了ZO-1在促进eHEV进入以及介导neHEV在感染细胞中的细胞间传播方面的关键作用。