Wildlife Zoonoses and Vector-Borne Diseases Research Group, Animal and Plant Health Agency (APHA), Weybridge, London KT15 3NB, UK.
School of Life Sciences, University of Sussex, Falmer, Brighton BN1 9QG, UK.
Viruses. 2021 May 20;13(5):947. doi: 10.3390/v13050947.
Rabies is a fatal encephalitis caused by an important group of viruses within the genus. The prototype virus, rabies virus, is still the most commonly reported lyssavirus and causes approximately 59,000 human fatalities annually. The human and animal burden of the other lyssavirus species is undefined. The original reports for the novel lyssavirus, Kotalahti bat lyssavirus (KBLV), were based on the detection of viral RNA alone. In this report we describe the successful generation of a live recombinant virus, cSN-KBLV; where the full-length genome clone of RABV vaccine strain, SAD-B19, was constructed with the glycoprotein of KBLV. Subsequent in vitro characterisation of cSN-KBLV is described here. In addition, the ability of a human rabies vaccine to confer protective immunity in vivo following challenge with this recombinant virus was assessed. Naïve or vaccinated mice were infected intracerebrally with a dose of 100 focus-forming units/30 µL of cSN-KBLV; all naïve mice and 8% ( = 1/12) of the vaccinated mice succumbed to the challenge, whilst 92% ( = 11/12) of the vaccinated mice survived to the end of the experiment. This report provides strong evidence for cross-neutralisation and cross-protection of cSN-KBLV using purified Vero cell rabies vaccine.
狂犬病是一种由属内一组重要病毒引起的致命脑炎。原型病毒,狂犬病病毒,仍然是最常报告的狂犬病病毒,每年导致约 59000 人死亡。其他狂犬病病毒的人和动物负担尚未确定。新型狂犬病病毒,科塔拉赫蒂蝙蝠狂犬病病毒(KBLV)的最初报告仅基于病毒 RNA 的检测。在本报告中,我们描述了成功生成活重组病毒 cSN-KBLV 的情况;其中 RABV 疫苗株 SAD-B19 的全长基因组克隆与 KBLV 的糖蛋白构建。这里描述了 cSN-KBLV 的随后体外特性。此外,评估了这种重组病毒在体内攻击时人类狂犬病疫苗赋予保护免疫力的能力。用 100 焦点形成单位/30 µL 的 cSN-KBLV 剂量通过脑内感染未接种或接种疫苗的小鼠;所有未接种疫苗的小鼠和 8%(= 1/12)接种疫苗的小鼠屈服于挑战,而 92%(= 11/12)接种疫苗的小鼠存活到实验结束。本报告提供了使用纯化的 Vero 细胞狂犬病疫苗对 cSN-KBLV 进行交叉中和和交叉保护的有力证据。