首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >African swine fever virus Georgia isolate harboring deletions of 9GL and MGF360/505 genes is highly attenuated in swine but does not confer protection against parental virus challenge
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African swine fever virus Georgia isolate harboring deletions of 9GL and MGF360/505 genes is highly attenuated in swine but does not confer protection against parental virus challenge

机译:带有9GL和MGF360 / 505基因缺失的非洲猪瘟病毒佐治亚分离株在猪中高度减毒,但不能抵抗亲代病毒攻击

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African swine fever virus (ASFV) produces a contagious disease of domestic pigs that results in severe economic consequences to the swine industry. Control of the disease has been hampered by the unavailability of vaccines. We recently reported the development of two experimental vaccine strains (ASFV-G-Delta 9GL and ASFV-G-Delta MGF) based on the attenuation of the highly virulent and epidemiologically relevant Georgia2007 isolate. Deletion of the 9GL gene or six genes of the MGF360/505 group produced two attenuated ASFV strains which were able to confer protection to animals when challenged with the virulent parental virus. Both viruses, although efficient in inducing protection, present concerns regarding their safety. In an attempt to solve this problem we developed a novel virus strain, ASFV-G-Delta 9GL/Delta MGF, based on the deletion of all genes deleted in ASFV-G-Delta 9GL and ASFV-G-Delta MGF. ASFV-G-Delta 9GL/Delta MGF is the first derivative of a highly virulent ASFV field strain subjected to a double round of recombination events seeking to sequentially delete specific genes. ASFV-G-Delta 9GL/Delta MGF showed a decreased ability to replicate in primary swine macrophage cultures relative to that of ASFV-G and ASFV-G-Delta MGF but similar to that of ASFV-G-Delta 9GL. ASFV-G-Delta 9GL/Delta MGF was attenuated when intramuscularly inoculated into swine, even at doses as high as 10(6) HAD(50). Animals infected with doses ranging from 10(2) to 10(6) HAD(50) did not present detectable levels of virus in blood at any time post-infection and they did not develop detectable levels of anti-ASFV antibodies. Importantly, ASFV-G-Delta 9GL/Delta MGF does not induce protection against challenge with the virulent parental ASFV-G isolate. Results presented here suggest caution towards approaches involving genomic manipulations when developing rationally designed ASFV vaccine strains. Published by Elsevier B.V.
机译:非洲猪瘟病毒(ASFV)会引起家猪的传染性疾病,给养猪业带来严重的经济后果。疫苗的缺乏已经阻碍了对疾病的控制。我们最近报告了基于高毒力和流行病学相关的Georgia2007分离株的减毒,开发了两种实验疫苗菌株(ASFV-G-Delta 9GL和ASFV-G-Delta MGF)。 MGF360 / 505组的9GL基因或6个基因的缺失产生了2株ASFV减毒株,它们在受到有毒的亲代病毒攻击时能够对动物提供保护。两种病毒虽然都可以有效地诱导保护作用,但它们的安全性令人担忧。为了解决这个问题,我们基于删除在ASFV-G-Delta 9GL和ASFV-G-Delta MGF中删除的所有基因,开发了一种新型病毒株ASFV-G-Delta 9GL / Delta MGF。 ASFV-G-Delta 9GL / Delta MGF是高毒力ASFV田间菌株的一阶衍生物,该菌株经历了两次轮回重组事件,试图顺序删除特定基因。与ASFV-G和ASFV-G-Delta MGF相比,ASFV-G-Delta 9GL / Delta MGF在原代猪巨噬细胞培养物中的复制能力降低,但与ASFV-G-Delta 9GL相似。肌内接种猪后,即使在高达10(6)HAD(50)的剂量下,ASFV-G-Delta 9GL / Delta MGF也会减弱。感染后10到10(2)到10(6)HAD(50)范围内的动物感染的血液中均未检测到病毒水平,并且抗ASFV抗体的水平也未检测到。重要的是,ASFV-G-Delta 9GL / Delta MGF不会诱导针对有毒的亲代ASFV-G分离株的攻击。本文介绍的结果表明,在开发合理设计的ASFV疫苗株时,应谨慎对待涉及基因组操作的方法。由Elsevier B.V.发布

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