Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA.
Department of Microbiology and Immunology, Penn State College of Medicine, Hershey, Pennsylvania, USA
J Virol. 2018 Mar 28;92(8). doi: 10.1128/JVI.01993-17. Print 2018 Apr 15.
Superinfection exclusion is a common phenomenon whereby a single cell is unable to be infected by two types of the same pathogen. Superinfection exclusion has been described for various viruses, including vaccinia virus, measles virus, hepatitis C virus, influenza A virus, and human immunodeficiency virus. Additionally, the mechanism of exclusion has been observed at various steps of the viral life cycle, including attachment, entry, viral genomic replication, transcription, and exocytosis. Human papillomavirus (HPV) is the causative agent of cervical cancer. Recent epidemiological studies indicate that up to 50% women who are HPV positive (HPV) are infected with more than one HPV type. However, no mechanism of superinfection exclusion has ever been identified for HPV. Here, we show that superinfection exclusion exists during a HPV coinfection and that it occurs on the cell surface during the attachment/entry phase of the viral life cycle. Additionally, we are able to show that the minor capsid protein L2 plays a role in this exclusion. This study shows, for the first time, that superinfection exclusion occurs during HPV coinfections and describes a potential molecular mechanism through which it occurs. Superinfection exclusion is a phenomenon whereby one cell is unable to be infected by multiple related pathogens. This phenomenon has been described for many viruses and has been shown to occur at various points in the viral life cycle. HPV is the causative agent of cervical cancer and is involved in other anogenital and oropharyngeal cancers. Recent epidemiological research has shown that up to 50% of HPV-positive individuals harbor more than one type of HPV. We investigated the interaction between two high-risk HPV types, HPV16 and HPV18, during a coinfection. We present data showing that HPV16 is able to block or exclude HPV18 on the cell surface during a coinfection. This exclusion is due in part to differences in the HPV minor capsid protein L2. This report provides, for the first time, evidence of superinfection exclusion for HPV and leads to a better understanding of the complex interactions between multiple HPV types during coinfections.
病毒的超级感染排除是一种常见的现象,即单一细胞无法被两种相同病原体同时感染。这种超级感染排除现象已经在各种病毒中得到了描述,包括牛痘病毒、麻疹病毒、丙型肝炎病毒、甲型流感病毒和人类免疫缺陷病毒。此外,在病毒生命周期的各个步骤中都观察到了排除机制,包括附着、进入、病毒基因组复制、转录和胞吐。人乳头瘤病毒(HPV)是宫颈癌的致病因子。最近的流行病学研究表明,高达 50%的 HPV 阳性(HPV)女性感染了一种以上的 HPV 类型。然而,HPV 从未被发现有超级感染排除机制。在这里,我们证明了 HPV 合并感染中存在超级感染排除现象,并且它发生在病毒生命周期的附着/进入阶段的细胞表面。此外,我们能够证明次要衣壳蛋白 L2 在这种排除中起作用。这项研究首次表明,超级感染排除现象发生在 HPV 合并感染中,并描述了它发生的潜在分子机制。超级感染排除是一种现象,即一个细胞无法被多种相关病原体感染。这种现象已经在许多病毒中得到描述,并已证明在病毒生命周期的各个阶段发生。HPV 是宫颈癌的致病因子,与其他肛门生殖器和口咽癌有关。最近的流行病学研究表明,高达 50%的 HPV 阳性个体携带一种以上的 HPV 类型。我们研究了两种高危 HPV 类型 HPV16 和 HPV18 在合并感染中的相互作用。我们提供的数据表明,在合并感染中,HPV16 能够在细胞表面阻止或排除 HPV18。这种排除部分归因于 HPV 次要衣壳蛋白 L2 的差异。本报告首次提供了 HPV 超级感染排除的证据,并加深了对多种 HPV 类型在合并感染中复杂相互作用的理解。