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Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening

Hand, foot and mouth disease (HFMD) is a common pediatric illness mainly caused by infection with enterovirus 71 (EV71) and coxsackievirus A16 (CA16). The frequent HFMD outbreaks have become a serious public health problem. Currently, no vaccine or antiviral drug for EV71/CA16 infections has been ap...

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Autores principales: Xu, Lin, Su, Weiheng, Jin, Jun, Chen, Jiawen, Li, Xiaojun, Zhang, Xuyuan, Sun, Meiyan, Sun, Shiyang, Fan, Peihu, An, Dong, Zhang, Huafei, Zhang, Xiguang, Kong, Wei, Ma, Tonghui, Jiang, Chunlai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113793/
https://www.ncbi.nlm.nih.gov/pubmed/25036464
http://dx.doi.org/10.3390/v6072778
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author Xu, Lin
Su, Weiheng
Jin, Jun
Chen, Jiawen
Li, Xiaojun
Zhang, Xuyuan
Sun, Meiyan
Sun, Shiyang
Fan, Peihu
An, Dong
Zhang, Huafei
Zhang, Xiguang
Kong, Wei
Ma, Tonghui
Jiang, Chunlai
author_facet Xu, Lin
Su, Weiheng
Jin, Jun
Chen, Jiawen
Li, Xiaojun
Zhang, Xuyuan
Sun, Meiyan
Sun, Shiyang
Fan, Peihu
An, Dong
Zhang, Huafei
Zhang, Xiguang
Kong, Wei
Ma, Tonghui
Jiang, Chunlai
author_sort Xu, Lin
collection PubMed
description Hand, foot and mouth disease (HFMD) is a common pediatric illness mainly caused by infection with enterovirus 71 (EV71) and coxsackievirus A16 (CA16). The frequent HFMD outbreaks have become a serious public health problem. Currently, no vaccine or antiviral drug for EV71/CA16 infections has been approved. In this study, a two-step screening platform consisting of reporter virus-based assays and cell viability‑based assays was developed to identify potential inhibitors of EV71/CA16 infection. Two types of reporter viruses, a pseudovirus containing luciferase-encoding RNA replicons encapsidated by viral capsid proteins and a full-length reporter virus containing enhanced green fluorescent protein, were used for primary screening of 400 highly purified natural compounds. Thereafter, a cell viability-based secondary screen was performed for the identified hits to confirm their antiviral activities. Three compounds (luteolin, galangin, and quercetin) were identified, among which luteolin exhibited the most potent inhibition of viral infection. In the cell viability assay and plaque reduction assay, luteolin showed similar 50% effective concentration (EC(50)) values of about 10 μM. Luteolin targeted the post-attachment stage of EV71 and CA16 infection by inhibiting viral RNA replication. This study suggests that luteolin may serve as a lead compound to develop potent anti-EV71 and CA16 drugs.
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spelling pubmed-41137932014-07-29 Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening Xu, Lin Su, Weiheng Jin, Jun Chen, Jiawen Li, Xiaojun Zhang, Xuyuan Sun, Meiyan Sun, Shiyang Fan, Peihu An, Dong Zhang, Huafei Zhang, Xiguang Kong, Wei Ma, Tonghui Jiang, Chunlai Viruses Article Hand, foot and mouth disease (HFMD) is a common pediatric illness mainly caused by infection with enterovirus 71 (EV71) and coxsackievirus A16 (CA16). The frequent HFMD outbreaks have become a serious public health problem. Currently, no vaccine or antiviral drug for EV71/CA16 infections has been approved. In this study, a two-step screening platform consisting of reporter virus-based assays and cell viability‑based assays was developed to identify potential inhibitors of EV71/CA16 infection. Two types of reporter viruses, a pseudovirus containing luciferase-encoding RNA replicons encapsidated by viral capsid proteins and a full-length reporter virus containing enhanced green fluorescent protein, were used for primary screening of 400 highly purified natural compounds. Thereafter, a cell viability-based secondary screen was performed for the identified hits to confirm their antiviral activities. Three compounds (luteolin, galangin, and quercetin) were identified, among which luteolin exhibited the most potent inhibition of viral infection. In the cell viability assay and plaque reduction assay, luteolin showed similar 50% effective concentration (EC(50)) values of about 10 μM. Luteolin targeted the post-attachment stage of EV71 and CA16 infection by inhibiting viral RNA replication. This study suggests that luteolin may serve as a lead compound to develop potent anti-EV71 and CA16 drugs. MDPI 2014-07-17 /pmc/articles/PMC4113793/ /pubmed/25036464 http://dx.doi.org/10.3390/v6072778 Text en © 2014 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Xu, Lin
Su, Weiheng
Jin, Jun
Chen, Jiawen
Li, Xiaojun
Zhang, Xuyuan
Sun, Meiyan
Sun, Shiyang
Fan, Peihu
An, Dong
Zhang, Huafei
Zhang, Xiguang
Kong, Wei
Ma, Tonghui
Jiang, Chunlai
Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening
title Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening
title_full Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening
title_fullStr Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening
title_full_unstemmed Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening
title_short Identification of Luteolin as Enterovirus 71 and Coxsackievirus A16 Inhibitors through Reporter Viruses and Cell Viability-Based Screening
title_sort identification of luteolin as enterovirus 71 and coxsackievirus a16 inhibitors through reporter viruses and cell viability-based screening
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4113793/
https://www.ncbi.nlm.nih.gov/pubmed/25036464
http://dx.doi.org/10.3390/v6072778
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