O'Donnell Vivian, LaRocco Michael, Duque Hernando, Baxt Barry
Department of Pathobiology and Veterinary Science, University of Connecticut at Storrs, 06269, USA.
J Virol. 2005 Jul;79(13):8506-18. doi: 10.1128/JVI.79.13.8506-8518.2005.
It has been demonstrated that foot-and-mouth disease virus (FMDV) can utilize at least four members of the alpha(V) subgroup of the integrin family of receptors in vitro. The virus interacts with these receptors via a highly conserved arginine-glycine-aspartic acid amino acid sequence motif located within the betaG-betaH loop of VP1. While there have been extensive studies of virus-receptor interactions at the cell surface, our understanding of the events during viral entry into the infected cell is still not clear. We have utilized confocal microscopy to analyze the entry of two FMDV serotypes (types A and O) after interaction with integrin receptors at the cell surface. In cell cultures expressing both the alphaVbeta3 and alphaVbeta6 integrins, virus adsorbed to the cells at 4 degrees C appears to colocalize almost exclusively with the alphaVbeta6 integrin. Upon shifting the infected cells to 37 degrees C, FMDV capsid proteins were detected within 15 min after the temperature shift, in association with the integrin in vesicular structures that were positive for a marker of clathrin-mediated endocytosis. In contrast, virus did not colocalize with a marker for caveola-mediated endocytosis. Virus remained associated with the integrin until about 1 h after the temperature shift, when viral proteins appeared around the perinuclear region of the cell. By 15 min after the temperature shift, viral proteins were seen colocalizing with a marker for early endosomes, while no colocalization with late endosomal markers was observed. In the presence of monensin, which raises the pH of endocytic vesicles and has been shown to inhibit FMDV replication, viral proteins were not released from the recycling endosome structures. Viral proteins were not observed associated with the endoplasmic reticulum or the Golgi. These data indicate that FMDV utilizes the clathrin-mediated endocytosis pathway to infect the cells and that viral replication begins due to acidification of endocytic vesicles, causing the breakdown of the viral capsid structure and release of the genome by an as-yet-unidentified mechanism.
已经证明口蹄疫病毒(FMDV)在体外可利用整联蛋白受体家族α(V)亚组的至少四个成员。该病毒通过位于VP1的βG-βH环内的高度保守的精氨酸-甘氨酸-天冬氨酸氨基酸序列基序与这些受体相互作用。虽然已经对细胞表面的病毒-受体相互作用进行了广泛研究,但我们对病毒进入受感染细胞过程中发生的事件仍不清楚。我们利用共聚焦显微镜分析了两种FMDV血清型(A 型和 O 型)在细胞表面与整联蛋白受体相互作用后的进入情况。在同时表达αVβ3和αVβ6整联蛋白的细胞培养物中,4℃吸附到细胞上的病毒似乎几乎完全与αVβ6整联蛋白共定位。将感染细胞转移到37℃后,在温度转移后15分钟内检测到FMDV衣壳蛋白,其与网格蛋白介导的内吞作用标记物呈阳性的囊泡结构中的整联蛋白相关。相比之下,病毒与小窝介导的内吞作用标记物不共定位。病毒在温度转移后约1小时内一直与整联蛋白结合,此时病毒蛋白出现在细胞的核周区域周围。温度转移后15分钟,可见病毒蛋白与早期内体标记物共定位,而未观察到与晚期内体标记物的共定位。在莫能菌素存在下,莫能菌素可提高内吞囊泡的pH值并已证明可抑制FMDV复制,病毒蛋白未从再循环内体结构中释放。未观察到病毒蛋白与内质网或高尔基体相关。这些数据表明FMDV利用网格蛋白介导的内吞作用途径感染细胞,并且病毒复制由于内吞囊泡的酸化而开始,导致病毒衣壳结构的破坏并通过一种尚未确定的机制释放基因组。