Wüstenhagen Elena, Hampe Laura, Boukhallouk Fatima, Schneider Marc A, Spoden Gilles A, Negwer Inka, Koynov Kaloian, Kast W Martin, Florin Luise
Department of Medical Microbiology and Hygiene, University Medical Center of the Johannes Gutenberg University Mainz, Mainz, Germany.
Translational Research Unit, Thoraxklinik at Heidelberg University Hospital, Heidelberg, Germany.
J Virol. 2016 Nov 14;90(23):10629-10641. doi: 10.1128/JVI.01222-16. Print 2016 Dec 1.
The human papillomavirus (HPV) capsid protein L2 is essential for viral entry. To gain a deeper understanding of the role of L2, we searched for novel cellular L2-interacting proteins. A yeast two-hybrid analysis uncovered the actin-depolymerizing factor gelsolin, the membrane glycoprotein dysadherin, the centrosomal protein 68 (Cep68), and the cytoskeletal adaptor protein obscurin-like 1 protein (OBSL1) as putative L2 binding molecules. Pseudovirus (PsV) infection assays identified OBSL1 as a host factor required for gene transduction by three oncogenic human papillomavirus types, HPV16, HPV18, and HPV31. In addition, we detected OBSL1 expression in cervical tissue sections and noted the involvement of OBSL1 during gene transduction of primary keratinocytes by HPV16 PsV. Complex formation of HPV16 L2 with OBSL1 was demonstrated in coimmunofluorescence and coimmunoprecipitation studies after overexpression of L2 or after PsV exposure. We observed a strong colocalization of OBSL1 with HPV16 PsV and tetraspanin CD151 at the plasma membrane, suggesting a role for OBSL1 in viral endocytosis. Indeed, viral entry assays exhibited a reduction of viral endocytosis in OBSL1-depleted cells. Our results suggest OBSL1 as a novel L2-interacting protein and endocytosis factor in HPV infection.
Human papillomaviruses infect mucosal and cutaneous epithelia, and the high-risk HPV types account for 5% of cancer cases worldwide. As recently discovered, HPV entry occurs by a clathrin-, caveolin-, and dynamin-independent endocytosis via tetraspanin-enriched microdomains. At present, the cellular proteins involved in the underlying mechanism of this type of endocytosis are under investigation. In this study, the cytoskeletal adaptor OBSL1 was discovered as a previously unrecognized interaction partner of the minor capsid protein L2 and was identified as a proviral host factor required for HPV16 endocytosis into target cells. The findings of this study advance the understanding of a so far less well-characterized endocytic pathway that is used by oncogenic HPV subtypes.
人乳头瘤病毒(HPV)衣壳蛋白L2对病毒进入至关重要。为了更深入了解L2的作用,我们寻找了与L2相互作用的新型细胞蛋白。酵母双杂交分析发现肌动蛋白解聚因子凝溶胶蛋白、膜糖蛋白失粘连蛋白、中心体蛋白68(Cep68)以及细胞骨架衔接蛋白类 obscurin 样1蛋白(OBSL1)为假定的L2结合分子。伪病毒(PsV)感染试验确定OBSL1是三种致癌性人乳头瘤病毒HPV16、HPV18和HPV31进行基因转导所需的宿主因子。此外,我们在宫颈组织切片中检测到OBSL1的表达,并注意到OBSL1在HPV16 PsV对原代角质形成细胞进行基因转导过程中的作用。在L2过表达后或PsV暴露后,通过共免疫荧光和共免疫沉淀研究证实了HPV16 L2与OBSL1形成复合物。我们观察到OBSL1与HPV16 PsV和四跨膜蛋白CD151在质膜上强烈共定位,表明OBSL1在病毒内吞作用中发挥作用。事实上,病毒进入试验显示在OBSL1缺失的细胞中病毒内吞作用减少。我们的结果表明OBSL1是HPV感染中一种新型的L2相互作用蛋白和内吞作用因子。
人乳头瘤病毒感染黏膜和皮肤上皮,高危型HPV占全球癌症病例的5%。最近发现,HPV通过富含四跨膜蛋白的微结构域以一种不依赖网格蛋白、小窝蛋白和发动蛋白的内吞作用进入细胞。目前,参与这种内吞作用潜在机制的细胞蛋白正在研究中。在本研究中,细胞骨架衔接蛋白OBSL1被发现是次要衣壳蛋白L2之前未被识别的相互作用伙伴,并被确定为HPV16进入靶细胞所需的前病毒宿主因子。本研究结果推进了对致癌性HPV亚型所使用的一种迄今特征较少的内吞途径的理解。