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Infection and Propagation of Human Rhinovirus C in Human Airway Epithelial Cells

机译:人鼻病毒C在人气道上皮细胞中的感染和繁殖

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摘要

Human rhinovirus species C (HRV-C) was recently discovered using molecular diagnostic techniques and is associated with lower respiratory tract disease, particularly in children. HRV-C cannot be propagated in immortalized cell lines, and currently sinus organ culture is the only system described that is permissive to HRV-C infection ex vivo. However, the utility of organ culture for studying HRV-C biology is limited. Here, we report that a previously described HRV-C derived from an infectious cDNA, HRV-C15, infects and propagates in fully differentiated human airway epithelial cells but not in undifferentiated cells. We demonstrate that this differentiated epithelial cell culture system supports infection and replication of a second virus generated from a cDNA clone, HRV-C11. We show that HRV-C15 virions preferentially bind fully differentiated airway epithelial cells, suggesting that the block to replication in undifferentiated cells is at the step of viral entry. Consistent with previous reports, HRV-C15 utilizes a cellular receptor other than ICAM-1 or LDLR for infection of differentiated epithelial cells. Furthermore, we demonstrate that HRV-C15 replication can be inhibited by an HRV 3C protease inhibitor (rupintrivir) but not an HRV capsid inhibitor previously under clinical development (pleconaril). The HRV-C cell culture system described here provides a powerful tool for studying the biology of HRV-C and the discovery and development of HRV-C inhibitors.
机译:最近使用分子诊断技术发现了人类鼻病毒C(HRV-C),它与下呼吸道疾病有关,尤其是在儿童中。 HRV-C不能在永生化细胞系中繁殖,目前所描述的鼻窦器官培养是唯一允许离体HRV-C感染的系统。但是,器官培养在研究HRV-C生物学中的用途是有限的。在这里,我们报道先前描述的HRV-C源自感染性cDNA HRV-C15,它在完全分化的人气道上皮细胞中而不在未分化的细胞中感染和繁殖。我们证明,这种分化的上皮细胞培养系统支持从cDNA克隆HRV-C11产生的第二种病毒的感染和复制。我们显示,HRV-C15病毒粒子优先结合完全分化的气道上皮细胞,这表明在未分化细胞中复制的阻滞处于病毒进入的步骤。与以前的报道一致,HRV-C15利用ICAM-1或LDLR以外的其他细胞受体感染分化的上皮细胞。此外,我们证明了HRV 3C蛋白酶抑制剂(rupintrivir)可以抑制HRV-C15复制,而先前在临床开发中的HRV衣壳抑制剂(pleconaril)则不能。这里描述的HRV-C细胞培养系统为研究HRV-C的生物学以及HRV-C抑制剂的发现和开发提供了强大的工具。

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