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辛德毕斯病毒糖蛋白变体所呈现的宿主范围表型是由病毒粒子聚集并滞留在蚊子细胞表面所致。

The host range phenotype displayed by a Sindbis virus glycoprotein variant results from virion aggregation and retention on the surface of mosquito cells.

作者信息

Boehme K W, Popov V L, Heidner H W

机构信息

Division of Life Sciences, University of Texas at San Antonio, San Antonio, Texas 78249-0662, USA.

出版信息

J Virol. 2000 Dec;74(23):11398-406. doi: 10.1128/jvi.74.23.11398-11406.2000.

Abstract

The Sindbis virus variant NE2G216 is a PE2-containing host range mutant that is growth restricted in cultured mosquito cells (C6/36) due to inefficient release of virions from this cell type. The maturation defect of NE2G216 has been linked to the structures of N-linked oligosaccharides synthesized by arthropod cells. Analysis of C6/36 cells infected with NE2G216 by transmission electron microscopy revealed the presence of dense virus aggregates within cytoplasmic vacuoles and virus aggregates adhered to the cell surface. The virus aggregation phenotype of NE2G216 was reproduced in vertebrate cells (Pro-5) by the addition of 1-deoxymannojirimycin, an inhibitor of carbohydrate processing which limits the processing of N-linked oligosaccharides to structures that are structurally similar, albeit not identical, to those synthesized in C6/36 cells. We conclude that defective maturation of NE2G216 in mosquito cells is due to virion aggregation and retention on the cell surface and that this phenotype is directly linked to the carbohydrate-processing properties of these cells.

摘要

辛德毕斯病毒变种NE2G216是一种含PE2的宿主范围突变体,由于从这种细胞类型释放病毒粒子的效率低下,其在培养的蚊细胞(C6/36)中生长受限。NE2G216的成熟缺陷与节肢动物细胞合成的N-连接寡糖的结构有关。通过透射电子显微镜分析感染NE2G216的C6/36细胞,发现细胞质空泡内存在密集的病毒聚集体,且病毒聚集体附着在细胞表面。通过添加1-脱氧甘露基野霉素(一种碳水化合物加工抑制剂,可将N-连接寡糖加工限制为与C6/36细胞中合成的结构相似但不完全相同的结构),在脊椎动物细胞(Pro-5)中重现了NE2G216的病毒聚集表型。我们得出结论,蚊细胞中NE2G216的成熟缺陷是由于病毒粒子聚集并保留在细胞表面,并且这种表型与这些细胞的碳水化合物加工特性直接相关。

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