Increased ATP generation in the host cell is required for efficient vaccinia virus production

被引:41
作者
Chang, Chia-Wei [1 ]
Li, Hui-Chun [1 ,2 ]
Hsu, Che-Fang [3 ]
Chang, Chiao-Yen [3 ]
Lo, Shih-Yen [1 ,2 ,3 ,4 ]
机构
[1] Tzu Chi Univ, Grad Inst Mol & Cellular Biol, Hualien, Taiwan
[2] Tzu Chi Univ, Grad Inst Med Sci, Hualien, Taiwan
[3] Tzu Chi Univ, Grad Inst Med Biotechnol, Hualien, Taiwan
[4] Buddhist Tzu Chi Gen Hosp, Dept Lab Med, Hualien, Taiwan
关键词
HUMAN HELA-CELLS; MESSENGER-RNA; GENE-EXPRESSION; PROTEIN-KINASE; INFECTION; INHIBITION; BCL-2; DNA; MULTIPLICATION; TRANSCRIPTION;
D O I
10.1186/1423-0127-16-80
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
To search for cellular genes up-regulated by vaccinia virus (VV) infection, differential display-reverse transcription-polymerase chain reaction (ddRT-PCR) assays were used to examine the expression of mRNAs from mock-infected and VV-infected HeLa cells. Two mitochondrial genes for proteins that are part of the electron transport chain that generates ATP, ND4 and CO II, were up-regulated after VV infection. Up-regulation of ND4 level by VV infection was confirmed by Western blotting analysis. Up-regulation of ND4 was reduced by the MAPK inhibitor, apigenin, which has been demonstrated elsewhere to inhibit VV replication. The induction of ND4 expression occurred after viral DNA replication since ara C, an inhibitor of poxviral DNA replication, could block this induction. ATP production was increased in the host cells after VV infection. Moreover, 4.5 mu M oligomycin, an inhibitor of ATP production, reduced the ATP level 13 hr after virus infection to that of mock-infected cells and inhibited viral protein expression and virus production, suggesting that increased ATP production is required for efficient VV production. Our results further suggest that induction of ND4 expression is through a Bcl-2 independent pathway.
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页数:10
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