Hossain Md Shakhawat, Vogt Megan B, Hawks Seth A, Coutermarsh-Ott Sheryl L, Duggal Nisha K
Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA.
Department of Biomedical Sciences and Pathobiology, Virginia-Maryland College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg, VA, 24061, USA.
Virology. 2025 Jul;608:110555. doi: 10.1016/j.virol.2025.110555. Epub 2025 Apr 18.
West Nile virus (WNV), Usutu virus (USUV), and Saint Louis encephalitis virus (SLEV) are emerging mosquito-borne flaviviruses within the Japanese encephalitis virus serocomplex. They share a similar transmission cycle between passerine birds and Culex spp. mosquitoes, and their spillover can cause neuroinvasive diseases among humans and animals. Individuals might be exposed to more than one of these viruses during their lifetime. Previously, we found that WNV vaccination protected mice from USUV disease, and sera collected from the WNV vaccinated mice cross-neutralized USUV in vitro. However, whether WNV convalescent (post-recovery) plasma cross-protects against heterologous SLEV or USUV infection is unknown. In this study, in vivo experiments were conducted to assess whether WNV human convalescent plasma and/or mouse convalescent serum afforded protection to mice against SLEV and USUV infection and neuroinvasion. First, we found that human and mouse WNV convalescent samples cross-neutralized USUV and SLEV in vitro. We then passively transferred human or mouse WNV convalescent samples into mice and challenged them with WNV, USUV, or SLEV. Both human and mouse WNV convalescent samples reduced WNV neuroinvasion and SLEV and USUV viremia during acute infection. Mouse WNV convalescent serum significantly reduced SLEV titers in the brain and showed a trend towards resulting in less inflammation in the brain. These findings helped to better understand the potential cross-protection among WNV, SLEV, and USUV, and identified cross-neutralizing antibodies as potential correlates of protection for individuals exposed to multiple flaviviruses, though protection was incomplete.
西尼罗河病毒(WNV)、乌苏图病毒(USUV)和圣路易斯脑炎病毒(SLEV)是日本脑炎病毒血清复合体中新兴的蚊媒黄病毒。它们在雀形目鸟类和库蚊属蚊子之间具有相似的传播循环,其溢出传播可导致人类和动物发生神经侵袭性疾病。个体在其一生中可能会接触到不止一种这些病毒。此前,我们发现WNV疫苗接种可保护小鼠免受USUV疾病侵害,并且从接种WNV疫苗的小鼠中收集的血清在体外可交叉中和USUV。然而,WNV恢复期(康复后)血浆是否能交叉保护免受异源SLEV或USUV感染尚不清楚。在本研究中,进行了体内实验,以评估WNV人类恢复期血浆和/或小鼠恢复期血清是否能保护小鼠免受SLEV和USUV感染及神经侵袭。首先,我们发现人类和小鼠WNV恢复期样本在体外可交叉中和USUV和SLEV。然后,我们将人类或小鼠WNV恢复期样本被动转移到小鼠体内,并用WNV、USUV或SLEV对它们进行攻击。人类和小鼠WNV恢复期样本均降低了急性感染期间WNV的神经侵袭以及SLEV和USUV的病毒血症。小鼠WNV恢复期血清显著降低了大脑中的SLEV滴度,并显示出导致大脑炎症减轻的趋势。这些发现有助于更好地理解WNV、SLEV和USUV之间潜在的交叉保护作用,并确定交叉中和抗体是暴露于多种黄病毒的个体潜在的保护相关因素,尽管保护并不完全。