Spiropoulou C F, Goldsmith C S, Shoemaker T R, Peters C J, Compans R W
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, GA 30333, USA.
Virology. 2003 Mar 30;308(1):48-63. doi: 10.1016/s0042-6822(02)00092-2.
Sin Nombre virus (SNV) is a major representative of the New World hantaviruses and the most common cause of hantavirus pulmonary syndrome (HPS) with high mortality in North America. Unlike other members of the family Bunyaviridae which mature in the Golgi complex, New World hantaviruses have been previously reported to mature at the cell surface. For family Bunyaviridae viruses, retention of the viral glycoproteins at the Golgi complex is thought to be responsible for their Golgi maturation. In our studies, the majority of SNV glycoproteins, G1 and G2, was localized in the Golgi complex when expressed from a full-length GPC clone or in SNV-infected cells, in agreement with data for other members of the family Bunyaviridae, including the Old World hantaviruses. However, the SNV glycoproteins could also be detected at the cell surface at advanced posttransfection or postinfection time points. G1 expressed in the absence of G2 did not accumulate in the Golgi, but remained predominantly associated with the endoplasmic reticulum (ER). Overexpressed amounts of apparently misfolded G1 were aggregated in a subcellular compartment likely to represent the aggresome. Unexpectedly, an additional major pool of G1 was detected intracellularly in SNV-infected and GPC-expressing transfected cells, by using a SNV G1-specific Fab antibody. This pool of G1 is predominantly localized in late endosomes-lysosomes.
辛诺柏病毒(SNV)是新大陆汉坦病毒的主要代表,也是北美汉坦病毒肺综合征(HPS)最常见的病因,具有高死亡率。与在高尔基体中成熟的布尼亚病毒科其他成员不同,此前有报道称新大陆汉坦病毒在细胞表面成熟。对于布尼亚病毒科病毒,病毒糖蛋白在高尔基体中的保留被认为是其在高尔基体中成熟的原因。在我们的研究中,当从全长GPC克隆表达或在SNV感染的细胞中时,大多数SNV糖蛋白G1和G2定位于高尔基体,这与包括旧大陆汉坦病毒在内的布尼亚病毒科其他成员的数据一致。然而,在转染后或感染后的晚期时间点,也可以在细胞表面检测到SNV糖蛋白。在没有G2的情况下表达的G1不会在高尔基体中积累,而是主要与内质网(ER)相关。过量表达的明显错误折叠的G1在一个可能代表聚集体的亚细胞区室中聚集。出乎意料的是,通过使用SNV G1特异性Fab抗体,在SNV感染的细胞和表达GPC的转染细胞中,在细胞内检测到了另外一个主要的G1池。这个G1池主要定位于晚期内体-溶酶体。