Eifart Patricia, Ludwig Kai, Böttcher Christoph, de Haan Cornelis A M, Rottier Peter J M, Korte Thomas, Herrmann Andreas
Institut für Biologie/Biophysik, Humboldt-Universität zu Berlin, Invalidenstr. 42, D-10115 Berlin, Germany.
J Virol. 2007 Oct;81(19):10758-68. doi: 10.1128/JVI.00725-07. Epub 2007 Jul 11.
Infection by the coronavirus mouse hepatitis virus strain A59 (MHV-A59) requires the release of the viral genome by fusion with the respective target membrane of the host cell. Fusion is mediated by the viral S protein. Here, the entry pathway of MHV-A59 into murine fibroblast cells was studied by independent approaches. Infection of cells assessed by plaque reduction assay was strongly inhibited by lysosomotropic compounds and substances that interfere with clathrin-dependent endocytosis, suggesting that MHV-A59 is taken up via endocytosis and delivered to acidic endosomal compartments. Infection was only slightly reduced in the presence of substances inhibiting proteases of endosomal compartments, precluding that the endocytic uptake is required to activate the fusion potential of the S protein by its cleavage. Fluorescence confocal microscopy of labeled MHV-A59 confirmed that virus is taken up via endocytosis. Bright labeling of intracellular compartments suggests their fusion with the viral envelope. No fusion with the plasma membrane was observed at neutral pH conditions. However, when virus was bound to cells and the pH was lowered to 5.0, we observed a strong labeling of the plasma membrane. Electron microscopy revealed low pH triggered conformational alterations of the S ectodomain. Very likely, these alterations are irreversible because low-pH treatment of viruses in the absence of target membranes caused an irreversible loss of the fusion activity. The results imply that endocytosis plays a major role in MHV-A59 infection and the acidic pH of the endosomal compartment triggers a conformational change of the S protein mediating fusion.
冠状病毒小鼠肝炎病毒A59株(MHV - A59)的感染需要通过与宿主细胞的相应靶膜融合来释放病毒基因组。融合由病毒S蛋白介导。在此,通过独立的方法研究了MHV - A59进入小鼠成纤维细胞的途径。通过噬斑减少试验评估的细胞感染受到溶酶体亲和性化合物和干扰网格蛋白依赖性内吞作用的物质的强烈抑制,这表明MHV - A59通过内吞作用被摄取并传递到酸性内体区室。在存在抑制内体区室蛋白酶的物质时,感染仅略有降低,这排除了内吞摄取是通过其裂解激活S蛋白融合潜能所必需的。标记的MHV - A59的荧光共聚焦显微镜检查证实病毒通过内吞作用被摄取。细胞内区室的明亮标记表明它们与病毒包膜融合。在中性pH条件下未观察到与质膜的融合。然而,当病毒与细胞结合且pH降低至5.0时,我们观察到质膜有强烈的标记。电子显微镜显示低pH触发了S胞外域的构象改变。很可能这些改变是不可逆的,因为在没有靶膜的情况下对病毒进行低pH处理会导致融合活性的不可逆丧失。结果表明内吞作用在MHV - A59感染中起主要作用,内体区室的酸性pH触发介导融合的S蛋白的构象变化。