Bankovskiy D, Safonov G, Kurilchuk Y
Pokrov Plant of Biologics, Volginskiy, Vladimir region, Russia.
Dev Biol (Basel). 2008;131:461-6.
The immunogenic properties of ERA G 333 attenuated rabies virus strain in foxes and raccoon dogs by the oral route of administration were examined. This strain is a proposed candidate for oral rabies vaccine in Russia. As was previously demonstrated, the advantage of this virus, provided by the US Centers for Disease Control and Prevention in the framework of the Biotechnology Engagement Program, is apathogenicity for 3-week old and adult mice, as well as for other target and non-target species, even when challenged via the intracerebral route. A group of 12, 7-8 month-old foxes and eight wild captured raccoon dogs were given 2.0 ml of ERA G 333 (titre 107.5 FFU) orally on the tongue. Another three foxes and three raccoon dogs were retained as controls. Blood samples were collected before immunization and on day 60 thereafter. The antibody titres were determined by the fluorescent antibody virus neutralization (FAVN) test. Eight foxes and three raccoon dogs showed seroconversion on day 60 postvaccination. Eleven foxes and four raccoon dogs survived challenge with a virulent rabies virus strain. This study has demonstrated the possibility of using ERA G 333 for the oral vaccination of red foxes and raccoon dogs. Further experiments are needed to determine the effective dose, virus stability, and the strength and duration of immunity.
研究了ERA G 333减毒狂犬病病毒株经口服途径在狐狸和貉体内的免疫原性。该毒株是俄罗斯口服狂犬病疫苗的候选毒株。如先前所示,美国疾病控制与预防中心在生物技术参与计划框架下提供的这种病毒的优势在于,对3周龄和成年小鼠以及其他目标和非目标物种无致病性,即使通过脑内途径进行攻击。给一组12只7 - 8月龄的狐狸和8只野生捕获的貉在舌头上口服2.0毫升ERA G 333(滴度为107.5 FFU)。另外三只狐狸和三只貉作为对照。在免疫前和免疫后第60天采集血样。通过荧光抗体病毒中和(FAVN)试验测定抗体滴度。8只狐狸和3只貉在接种疫苗后第60天出现血清转化。11只狐狸和4只貉在受到强毒狂犬病病毒株攻击后存活。本研究证明了使用ERA G 333对赤狐和貉进行口服疫苗接种的可能性。需要进一步实验来确定有效剂量、病毒稳定性以及免疫强度和持续时间。