Chen Yiyang, Wang Xueting, Zhang Meimei, Li Jinyao, Gao Xueyan, Nan Yuchen, Zhao Qin, Zhou En-Min, Liu Baoyuan
Department of Preventive Veterinary Medicine, College of Veterinary Medicine, Northwest A&F University, Xianyang, China.
Front Microbiol. 2022 Nov 23;13:1048180. doi: 10.3389/fmicb.2022.1048180. eCollection 2022.
Hepatitis E virus (HEV) is thought to be a zoonotic pathogen that causes serious economic loss and threatens human health. However, there is a lack of efficient antiviral strategies. As a more promising tool for antiviral therapy, nanobodies (also named single-domain antibodies, sdAbs) exhibit higher specificity and affinity than traditional antibodies. In this study, nanobody anti-genotype four HEV open reading frame 2 (ORF2) was screened using phage display technology, and two nanobodies (nb14 and nb53) with high affinity were prokaryotically expressed. They were identified to block HEV ORF2 virus like particle (VLP) sp239 (aa 368-606) absorbing HepG2 cells . With the previously built animal model, the detection indicators of fecal shedding, viremia, seroconversion, alanine aminotransferase (ALT) levels, and liver lesions showed that nb14 could completely protect rabbits from swine HEV infection, and nb53 partially blocked swine HEV infection in rabbits. Collectively, these results revealed that nb14, with its anti-HEV neutralizing activity, may be developed as an antiviral drug for HEV.
戊型肝炎病毒(HEV)被认为是一种人畜共患病原体,可导致严重的经济损失并威胁人类健康。然而,目前缺乏有效的抗病毒策略。作为一种更有前景的抗病毒治疗工具,纳米抗体(也称为单域抗体,sdAbs)比传统抗体具有更高的特异性和亲和力。在本研究中,利用噬菌体展示技术筛选出抗4型戊型肝炎病毒开放阅读框2(ORF2)的纳米抗体,并对两种具有高亲和力的纳米抗体(nb14和nb53)进行了原核表达。经鉴定,它们可阻断HEV ORF2病毒样颗粒(VLP)sp239(氨基酸368 - 606)吸附HepG2细胞。利用先前建立的动物模型,粪便排毒、病毒血症、血清转化、丙氨酸转氨酶(ALT)水平和肝脏病变等检测指标表明,nb14可完全保护兔子免受猪戊型肝炎病毒感染,而nb53可部分阻断兔子感染猪戊型肝炎病毒。总体而言,这些结果表明,具有抗HEV中和活性的nb14有望开发成为一种抗戊型肝炎病毒的药物。