Antiviral activity and possible mechanisms of action of pentagalloylglucose (PGG) against influenza A virus

被引:67
作者
Liu, Ge [1 ]
Xiong, Sheng [1 ,2 ]
Xiang, Yang-Fei [2 ]
Guo, Chao-Wan [1 ]
Ge, Feng [1 ]
Yang, Chong-Ren [3 ]
Zhang, Ying-Jun [3 ]
Wang, Yi-Fei [2 ]
Kitazato, Kaio [1 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Div Mol Pharmacol Infect agents, Dept Mol Microbiol & Immunol, Nagasaki 8528521, Japan
[2] Jinan Univ, Biomed R&D Ctr, Natl Engn Res Ctr Genet Med, Guangdong Prov Key Lab Bioengn Med, Guangzhou 510632, Guangdong, Peoples R China
[3] Chinese Acad Sci, Kunming Inst Bot, Kunming 650204, Yunnan, Peoples R China
基金
美国国家科学基金会;
关键词
H1N1; VIRUS; INHIBITION; INFECTION; PLANT; H5N1; 1,2,3,4,6-PENTA-O-GALLOYL-BETA-D-GLUCOSE; PROPAGATION; EXPRESSION; EMERGENCE; EFFICACY;
D O I
10.1007/s00705-011-0989-9
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Influenza A virus (IAV) infection is a major public health threat leading to significant morbidity and mortality. The emergence of drug-resistant virus strains highlights the urgent need to develop novel antiviral drugs with alternative modes of action. Pentagalloylglucose (PGG), a naturally occurring polyphenolic compound, possesses a broad spectrum of biological activities. In this study, we found that PGG has anti-influenza-virus activity, and investigated its possible mechanism(s) of action in vitro. Both pre-incubation of virus prior to infection and post-exposure of infected cells with PGG significantly inhibited virus yields. Influenza-virus-induced hemagglutination of chicken red blood cells was inhibited by PGG treatment, suggesting that PGG can inhibit IAV infection by interacting with the viral hemagglutinin. PGG did not affect viral protein synthesis or nuclear transport of viral nucleoprotein (NP) but greatly reduced plasma membrane accumulation of NP protein at the late stage of the replication cycle. Furthermore, PGG significantly reduced virus budding and progeny virus release from infected cells. This study revealed for the first time that PGG can inhibit IAV replication with a dual mode of action and offers new insights into its underlying mechanisms of antiviral action.
引用
收藏
页码:1359 / 1369
页数:11
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