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Recombinant live attenuated avian coronavirus vaccines with deletions in the accessory genes 3ab and/or 5ab protect against infectious bronchitis in chickens

机译:重组现场活病毒禽冠状病毒疫苗,缺失在附件基因3ab和/或5ab中免受鸡中的传染性支气管炎

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Avian coronavirus infectious bronchitis virus (IBV) is a respiratory pathogen of chickens, causing severe economic losses in poultry industry worldwide. Live attenuated viruses are widely used in both the broiler and layer industry because of their efficacy and ability to be mass applied. Recently, we established a novel reverse genetics system based on targeted RNA recombination to manipulate the genome of IBV strain H52. Here we explore the possibilities to attenuate IBV in a rational way in order to generate safe and effective vaccines against virulent IBV (van Beurden et al., 2017). To this end, we deleted the nonessential group-specific accessory genes 3 and/or 5 in the IBV genome by targeted RNA recombination and selected the recombinant viruses in embryonated eggs. The resulting recombinant (r) rIBV-Delta 3ab, rIBV-Delta 5ab, and rIBV-Delta 3ab5ab could be rescued and grew to the same virus titer as recombinant and wild type IBV strain H52. Thus, genes 3ab and 5ab are not essential for replication in ovo. When administered to one-day-old chickens, rIBV-Delta 3ab, rIBV-Delta 5ab, and rIBV-Delta 3ab5ab showed reduced ciliostasis as compared to rIBV H52 and wild type H52, indicating that the accessory genes contribute to the pathogenicity of IBV. After homologous challenge with the virulent IBV strain M41, all vaccinated chickens were protected against disease based on reduced loss of ciliary movement in the trachea compared to the non vaccinated but challenged controls. Taken together, deletion of accessory genes 3ab and/or 5ab in IBV resulted in mutant viruses with an attenuated phenotype and the ability to induce protection in chickens. Hence, targeted RNA recombination based on virulent IBV provides opportunities for the development of a next generation of rationally designed live attenuated IBV vaccines. (C) 2018 The Authors. Published by Elsevier Ltd.
机译:禽冠状病病毒感染性支气管炎病毒(IBV)是鸡的呼吸道病原体,在全球家禽业造成严重的经济损失。由于它们的功效和批量施加的能力,Live Agentenation病毒广泛用于肉鸡和层行业。最近,我们建立了基于靶标重组的新型反向遗传系统,以操纵IBV菌株H52的基因组。在这里,我们探讨了以合理的方式衰减IBV的可能性,以便对毒力IBV产生安全有效的疫苗(Van Beurden等,2017)。为此,我们通过靶向的RNA重组将非子性群体特异性辅助基因3和/或5删除在IBV基因组中,并在胚胎卵中选择重组病毒。得到的重组(R)Ribv-delta 3ab,Ribv-delta 5ab和Ribv-delta 3ab5ab可以救出并增长与重组和野生型IBV菌株H52相同的病毒滴度。因此,3ab和5ab基因对OVO中的复制不是必需的。当与Ribv H52和野生型H52相比,饲给单日鸡,Ribv-Delta 3ab,Ribv-Delta 3ab和Ribv-delta 3ab5ab,表明辅助基因有助于IBV的致病性促成降低的Ciliostasis。在与毒性IBV菌株M41的同源攻击之后,与非接种疫苗但挑战对照组的睫状体运动减少,保护所有接种疫苗的疾病免受疾病的影响。连合在一起,在IBV中删除辅助基因和/或5Ab,导致突变病毒具有减毒表型和诱导鸡免受保护的能力。因此,基于毒性IBV的靶向RNA重组为开发下一代合理设计的现场减毒IBV疫苗提供了机会。 (c)2018年作者。 elsevier有限公司出版

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