Cellular autophagy machinery is not required for vaccinia virus replication and maturation

被引:44
作者
Zhang, Haiyan
Monken, Claude E.
Zhang, Yong
Lenard, John
Mizushima, Noboru
Lattime, Edmund C.
Jin, Shengkan
机构
[1] UMDNJ, Robert Wood Johnson Med Sch, Dept Pharmacol, Piscataway, NJ 08854 USA
[2] UMDNJ, Robert Wood Johnson Med Sch, Inst Canc, Piscataway, NJ 08854 USA
[3] UMDNJ, Robert Wood Johnson Med Sch, Dept Surg & Mol Genet Microbiol & Immunol, Piscataway, NJ 08854 USA
[4] UMDNJ, Robert Wood Johnson Med Sch, Dept Physiol & Biophys, Piscataway, NJ 08854 USA
[5] Tokyo Metropolitan Inst Med Sci, Dept Bioregulat & Metab, Tokyo 113, Japan
关键词
autophagy; Vaccinia virus; Beclin1; Atg5; electron microscopy; plaque assay;
D O I
10.4161/auto.2.2.2297
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The origin of the primary membrane of the vaccinia virus, a double-membrane structure that surrounds the immature virions (IV), is not fully understood. Here we investigated whether the primary membrane originates from the autophagic membrane. Morphologic studies by electron microscopy (EM) showed no apparent difference in viral maturation in the autophagy-deficient cell lines, the otg5(-/-) mouse embryonic fibroblasts (MEFs) and the beclin1(-/-) embryonic stem (ES) cells, compared to their isogenic wild-type counterparts. Moreover, viral growth curves demonstrated that vaccinia viruses replicate and mature in the autophagy-deficient cell lines as efficiently as they do in their isogenic wild type counterpart cells. This study indicates that the cellular autophagy machinery is not required for the life-cycle of vaccinia virus, suggesting that the primary vaccinia viral membrane does not originate from the autophagic membrane.
引用
收藏
页码:91 / 95
页数:5
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