Chen Dong, Zhang Jiayi, Liu Yusha, Zhu Jiayang, Chen Jie, Ni Hongxia, Wen Jinsheng
School of Basic Medical Sciences, Health Science Center, Ningbo University, Ningbo, China.
Wenzhou Central Blood Station, Wenzhou, China.
Front Microbiol. 2024 Dec 23;15:1508923. doi: 10.3389/fmicb.2024.1508923. eCollection 2024.
Japanese encephalitis virus (JEV) and Zika virus (ZIKV) are prevalent in over 80 countries or territories worldwide, causing hundreds of thousands of cases annually. But currently there is a lack of specific antiviral agents and effective vaccines.
In the present study, to identify human neutralizing monoclonal antibody (mAb) against JEV or/and ZIKV, we isolated ZIKV-E protein-binding B cells from the peripheral venous blood of a healthy volunteer who had received the JEV live-attenuated vaccine and performed 10× Genomics transcriptome sequencing and BCR sequencing analysis, we then obtained the V region amino acid sequences of a novel mAb LZY3412. We expressed mAb LZY3412 and evaluated its ability to bind to E proteins of dengue virus, JEV and ZIKV, neutralize JEV and ZIKV infections , protect mice against lethal JEV or ZIKV attack. The epitopes on E proteins of JEV/ZIKV recognized by mAb LZY3412 were analyzed using molecular docking and constructing E protein mutants.
Our results show that recombinant mAb LZY3412 has high-affinity with the E proteins of three viruses, with the kinetically derived binding affinity (KD) values of 440 and 482.5 nM against JEV-E protein and ZIKV-E protein, respectively; recombinant mAb LZY3412 can efficiently neutralize JEV and ZIKV infections , with the NT values of 19.9 ng/mL and 631 ng/mL, respectively; application of recombinant mAb LZY3412 can significantly improve the percentage survival and reduce the serum viral loads of neonatal mice infected with JEV or ZIKV. Finally, two amino acid residues (Ala399 and Gly400) located in EDIII of JEV-E protein were potentially recognized by LZY3412 whereas two amino acid residues (Met15 and Thr406) out of EDIII of ZIKV-E proteins were recognized by LZY3412.
Considering mAb LZY3412 has neutralizing effects on various flaviviruses, this mAb is expected to be developed as therapeutic or preventive drug for these flaviviruses, and can also be used to guide the development of vaccines against these flaviviruses.
日本脑炎病毒(JEV)和寨卡病毒(ZIKV)在全球80多个国家或地区流行,每年导致数十万病例。但目前缺乏特异性抗病毒药物和有效疫苗。
在本研究中,为鉴定针对JEV或/和ZIKV的人中和单克隆抗体(mAb),我们从一名接种过JEV减毒活疫苗的健康志愿者外周静脉血中分离出ZIKV-E蛋白结合B细胞,并进行10×基因组转录组测序和BCR测序分析,然后获得一种新型mAb LZY3412的V区氨基酸序列。我们表达了mAb LZY3412,并评估其与登革病毒、JEV和ZIKV的E蛋白结合的能力、中和JEV和ZIKV感染的能力、保护小鼠免受致死性JEV或ZIKV攻击的能力。使用分子对接和构建E蛋白突变体分析mAb LZY3412识别的JEV/ZIKV E蛋白上的表位。
我们的结果表明,重组mAb LZY3412与三种病毒的E蛋白具有高亲和力,对JEV-E蛋白和ZIKV-E蛋白的动力学衍生结合亲和力(KD)值分别为440和482.5 nM;重组mAb LZY3412可有效中和JEV和ZIKV感染,NT值分别为19.9 ng/mL和631 ng/mL;应用重组mAb LZY3412可显著提高感染JEV或ZIKV的新生小鼠的存活率并降低血清病毒载量。最后,JEV-E蛋白EDIII中的两个氨基酸残基(Ala399和Gly400)可能被LZY3412识别,而ZIKV-E蛋白EDIII外的两个氨基酸残基(Met15和Thr406)被LZY3412识别。
鉴于mAb LZY3412对多种黄病毒具有中和作用,该mAb有望开发为针对这些黄病毒的治疗或预防药物,也可用于指导针对这些黄病毒的疫苗开发。