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No evidence of a death-like function for species B1 human adenovirus type 3 E3-9K during A549 cell line infection

机译:在A549细胞株感染期间没有证据表明3型B3人类E3-9K B1型人类腺病毒具有类似死亡的功能

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摘要

BackgroundSubspecies B1 human adenoviruses (HAdV-B1) are prevalent respiratory pathogens. Compared to their species C (HAdV-C) counterparts, relatively little work has been devoted to the characterization of their unique molecular biology. The early region 3 (E3) transcription unit is an interesting target for future efforts because of its species-specific diversity in genetic content among adenoviruses. This diversity is particularly significant for the subset of E3-encoded products that are membrane glycoproteins and may account for the distinct pathobiology of the different human adenovirus species. In order to understand the role of HAdV-B-specific genes in viral pathogenesis, we initiated the characterization of unique E3 genes. As a continuation of our efforts to define the function encoded in the highly polymorphic ORF E3-10.9K and testing the hypothesis that the E3-10.9K protein orthologs with a hydrophobic domain contribute to the efficient release of viral progeny, we generated HAdV-3 mutant viruses unable to express E3-10.9K ortholog E3-9K and examined their ability to grow, disseminate, and egress in cell culture.
机译:背景亚种B1人类腺病毒(HAdV-B1)是流行的呼吸道病原体。与它们的物种C(HAdV-C)对应物相比,有关其独特分子生物学特性的研究工作相对较少。早期区域3(E3)转录单位是未来工作的一个有趣目标,因为它在腺病毒之间的遗传含量具有特定物种的多样性。这种多样性对于以E3编码的膜糖蛋白产物的子集尤其重要,并且可以解释不同人类腺病毒物种的独特病理生物学特性。为了了解HAdV-B特异性基因在病毒发病机制中的作用,我们启动了独特E3基因的表征。为了继续努力定义高度多态的ORF E3-10.9K中编码的功能,并验证具有疏水域的E3-10.9K蛋白质直系同源物有助于有效释放病毒后代的假设,我们产生了HAdV-3突变病毒无法表达E3-10.9K直系同源E3-9K,并且无法检测其在细胞培养中的生长,传播和流出能力。

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