{"title":"ERA g333狂犬病毒株对狐狸和貉的免疫原性研究。","authors":"D Bankovskiy, G Safonov, Y Kurilchuk","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":11190,"journal":{"name":"Developments in biologicals","volume":"131 ","pages":"461-6"},"PeriodicalIF":0.0000,"publicationDate":"2008-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Immunogenicity of the ERA G 333 rabies virus strain in foxes and raccoon dogs.\",\"authors\":\"D Bankovskiy, G Safonov, Y Kurilchuk\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":11190,\"journal\":{\"name\":\"Developments in biologicals\",\"volume\":\"131 \",\"pages\":\"461-6\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2008-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developments in biologicals\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developments in biologicals","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
研究ERA g333减毒狂犬病毒经口服给药对狐狸和貉的免疫原性。该毒株是俄罗斯建议用于口服狂犬病疫苗的候选毒株。如前所述,由美国疾病控制和预防中心在生物技术参与计划框架内提供的这种病毒的优势是对3周龄和成年小鼠以及其他目标和非目标物种具有致病性,即使通过脑内途径受到攻击。选取12只7-8月龄狐狸和8只捕获的野生貉,舌上口服ERA G 333(滴度107.5 FFU) 2.0 ml。另留三只狐狸和三只浣熊作为对照。免疫前和免疫后第60天采集血样。采用荧光抗体病毒中和(FAVN)试验测定抗体滴度。8只狐狸和3只貉在接种后第60天出现血清转化。11只狐狸和4只浣熊在一种致命的狂犬病毒毒株的攻击中幸存下来。本研究证明了ERA g333用于红狐和貉口服疫苗接种的可能性。需要进一步的实验来确定有效剂量、病毒稳定性以及免疫的强度和持续时间。
Immunogenicity of the ERA G 333 rabies virus strain in foxes and raccoon dogs.
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.