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Pseudotyping of vesicular stomatitis virus with the envelope glycoproteins of highly pathogenic avian influenza viruses

机译:用高致病性禽流感病毒的包膜糖蛋白对水疱性口炎病毒进行假分型

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摘要

Pseudotype viruses are useful for studying the envelope proteins of harmful viruses. This work describes the pseudotyping of vesicular stomatitis virus (VSV) with the envelope glycoproteins of highly pathogenic avian influenza viruses. VSV lacking the homotypic glycoprotein (G) gene (VSVΔG) was used to express haemagglutinin (HA), neuraminidase (NA) or the combination of both. Propagation-competent pseudotype viruses were only obtained when HA and NA were expressed from the same vector genome. Pseudotype viruses containing HA from different H5 clades were neutralized specifically by immune sera directed against the corresponding clade. Fast and sensitive reading of test results was achieved by vector-mediated expression of GFP. Pseudotype viruses expressing a mutant VSV matrix protein showed restricted spread in IFN-competent cells. This pseudotype system will facilitate the detection of neutralizing antibodies against virulent influenza viruses, circumventing the need for high-level biosafety containment.
机译:伪型病毒可用于研究有害病毒的包膜蛋白。这项工作描述了高致病性禽流感病毒的包膜糖蛋白对水泡性口炎病毒(VSV)的假型化。缺乏同型糖蛋白(G)基因(VSVΔG)的VSV用于表达血凝素(HA),神经氨酸酶(NA)或两者的组合。仅当从同一载体基因组表达HA和NA时,才能获得具有繁殖能力的假型病毒。含有来自不同H5进化枝的HA的假型病毒被针对相应进化枝的免疫血清特异性中和。通过载体介导的GFP表达,可以快速而敏感地读取测试结果。表达突变型VSV基质蛋白的假型病毒在具有IFN的细胞中显示出有限的扩散。该假型系统将有助于检测针对强力流感病毒的中和抗体,从而避免了对高水平生物安全性围堵的需求。

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