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Autographa Californica Multiple Nucleopolyhedrovirus Enters Host Cells via Clathrin-Mediated Endocytosis and Direct Fusion with the Plasma Membrane

机译:加利福尼亚州的Autographa Californica多核多角体病毒通过网格蛋白介导的内吞作用并与血浆膜直接融合进入宿主细胞

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摘要

The cell entry mechanism of Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is not fully understood. Previous studies showed that AcMNPV entered host cells primarily through clathrin-mediated endocytosis, and could efficiently infect cells via fusion with the plasma membrane after a low-pH trigger. However, whether AcMNPV enters cells via these two pathways simultaneously, and the exact manner in which AcMNPV particles are internalized into cells remains unclear. In this study, using single-virus tracking, we observed that AcMNPV particles were first captured by pre-existing clathrin-coated pits (CCP), and were then delivered to early endosomes. Population-based analysis of single-virus tracking and quantitative electron microscopy demonstrated that the majority of particles were captured by CCPs and internalized via invagination. In contrast, a minority of virus particles were not delivered to CCPs, and were internalized through direct fusion with the plasma membrane without invagination. Quantitative electron microscopy also showed that, while inhibition of CCP assembly significantly impaired viral internalization, inhibition of endosomal acidification blocked virus particles out of vesicles. Collectively, these findings demonstrated that approximately 90% of AcMNPV particles entered cells through clathrin-mediated endocytosis and 10% entered via direct fusion with the plasma membrane. This study will lead toward a better understanding of AcMNPV infection.
机译:加州苜蓿多核多角体病毒(AcMNPV)的细胞进入机制尚未完全了解。先前的研究表明,AcMNPV主要通过网格蛋白介导的内吞作用进入宿主细胞,并且在低pH触发条件下可以通过与质膜融合来有效感染细胞。但是,AcMNPV是否同时通过这两种途径进入细胞,以及将AcMNPV颗粒内化到细胞中的确切方式仍不清楚。在这项研究中,使用单病毒跟踪,我们观察到AcMNPV颗粒首先被预先存在的网格蛋白包膜的凹坑(CCP)捕获,然后被递送至早期的内体。基于人群的单病毒跟踪和定量电子显微镜分析表明,CCP捕获了大多数颗粒,并通过内陷作用被内在化。相反,少数病毒颗粒没有传递到CCP,而是通过与质膜的直接融合而无内陷地被内在化。定量电子显微镜还显示,虽然抑制CCP装配会大大损害病毒的内在化,但抑制内体酸化会阻止病毒颗粒脱离囊泡。总的来说,这些发现表明,大约90%的AcMNPV颗粒通过网格蛋白介导的内吞作用进入细胞,而10%的通过与质膜直接融合进入细胞。这项研究将有助于更好地了解AcMNPV感染。

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