Some coronaviruses (CoVs) have an extra furin cleavage site (RRKR/S, furin-S2' site) upstream of the fusion peptide in the spike protein, which plays roles in virion adsorption and fusion. Mutation of the S2' site of QX genotype (QX-type) infectious bronchitis virus (IBV) spike protein (S) in a recombinant virus background results in higher pathogenicity, pronounced neural symptoms and neurotropism when compared with conditions in wild-type IBV (WT-IBV) infected chickens. In this study, we present evidence suggesting that recombinant IBV with a mutant S2' site (furin-S2' site) leads to higher mortality. Infection with mutant IBV induces severe encephalitis and breaks the blood-brain barrier. The results of a neutralization test and immunoprotection experiment show that an original serum and vaccine can still provide effective protection in vivo and in vitro. This is the first demonstration of IBV-induced neural symptoms in chickens with encephalitis and the furin-S2' site as a determinant of neurotropism.

译文

:某些冠状病毒(CoV)在穗蛋白中的融合肽上游具有额外的弗林蛋白酶切割位点(RRKR / S,弗林蛋白酶S2'位点),在病毒体吸附和融合中发挥作用。与野生型IBV的条件相比,重组病毒背景中QX基因型(QX型)传染性支气管炎病毒(IBV)刺突蛋白(S)的S2'位点突变导致更高的致病性,明显的神经症状和嗜神经性( WT-IBV)感染的鸡。在这项研究中,我们提供证据表明具有突变S2'位点(弗林蛋白酶S2'位点)的重组IBV导致更高的死亡率。突变型IBV感染会引起严重的脑炎并打破血脑屏障。中和试验和免疫保护实验的结果表明,原始的血清和疫苗仍然可以在体内和体外提供有效的保护。这是IBV诱发的脑炎鸡的神经症状的首次证明,弗林蛋白酶-S2'位点是神经嗜性的决定因素。

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