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Epigallocatechin-3-gallate inhibits the early stages of Japanese encephalitis virus infection.
Wang, Ching-Ying; Hour, Mann-Jen; Lai, Hsueh-Chou; Chen, Chao-Hsien; Chang, Pei-Jung; Huang, Su-Hua; Lin, Cheng-Wen.
Afiliação
  • Wang CY; Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan.
  • Hour MJ; School of Pharmacy, China Medical University, Taichung, Taiwan.
  • Lai HC; School of Chinese Medicine, China Medical University, Taichung, Taiwan; Division of Hepato-gastroenterology, Department of internal medicine, China Medical University Hospital, Taichung, Taiwan.
  • Chen CH; Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan.
  • Chang PJ; Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan.
  • Huang SH; Chinese Medicine Research center, China Medical University, Taichung, Taiwan.
  • Lin CW; Department of Medical Laboratory Science and Biotechnology, China Medical University, Taichung, Taiwan; Chinese Medicine Research center, China Medical University, Taichung, Taiwan; Department of Biotechnology, Asia University, Wufeng, Taichung, Taiwan. Electronic address: cwlin@mail.cmu.edu.tw.
Virus Res ; 253: 140-146, 2018 07 15.
Article em En | MEDLINE | ID: mdl-29958923
ABSTRACT
Epigallocatechin-3-gallate (EGCG), a green tea catechin, shows broad sepectrum antiviral activity against many RNA and DNA viruses. This study investigated the antiviral efficacy of EGCG against Japanese encephalitis virus (JEV), a zoonotic flavivirus in Southeast Asia and the Western Pacific region. EGCG concentration-dependently reduced CPE, sub-G1 phase, and virus yield of infected cells with different JEV strains at different MOIs. The antiviral activity of EGCG against JEV in different assays declined in the following order virus yield (IC50 of 7.0 µM) > virus attachment (IC50 of 7.9 µM) > virus entry (IC50 of 9.4 µM) > receptor binding and post-entry. However, EGCG had no virucidal effect on the infectivity of JEV particles. The results indicated that antiviral mechanism of EGCG against JEV was associated with blocking the early steps of JEV infection. The study suggests EGCG as a lead compound for developing broad-spectrum antiviral agents.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Catequina / Encefalite Japonesa / Vírus da Encefalite Japonesa (Espécie) / Internalização do Vírus Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Antivirais / Catequina / Encefalite Japonesa / Vírus da Encefalite Japonesa (Espécie) / Internalização do Vírus Idioma: En Ano de publicação: 2018 Tipo de documento: Article