Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease

Enterovirus (EV) infections are a major threat to global public health, and are responsible for mild respiratory illness, hand, foot, and mouth disease (HFMD), acute hemorrhagic conjunctivitis, aseptic meningitis, myocarditis, severe neonatal sepsis-like disease, and acute flaccid paralysis epidemic...

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Main Authors: Yuefei Jin, Rongguang Zhang, Weidong Wu, Guangcai Duan
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-10-01
Series:Frontiers in Microbiology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fmicb.2018.02422/full
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spelling doaj-bc7bd23cd6584630a628c37f256624d82020-11-25T01:49:17ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2018-10-01910.3389/fmicb.2018.02422390864Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth DiseaseYuefei Jin0Rongguang Zhang1Weidong Wu2Guangcai Duan3Department of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, ChinaDepartment of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, ChinaDepartment of Occupational and Environmental Health, School of Public Health, Xinxiang Medical University, Xinxiang, ChinaDepartment of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, ChinaEnterovirus (EV) infections are a major threat to global public health, and are responsible for mild respiratory illness, hand, foot, and mouth disease (HFMD), acute hemorrhagic conjunctivitis, aseptic meningitis, myocarditis, severe neonatal sepsis-like disease, and acute flaccid paralysis epidemic. Among them, HFMD is a common pediatric infectious disease caused by EVs of the family Picornaviridae including EV-A71, coxsackieviruses (CV)-A2, CV-A6, CV-A10, and CV-A16. Due to lack of vaccines and specific antiviral therapeutics, millions of children still suffer from HFMD. Innate immune system detects foreign invaders by means of a relatively limited number of sensors, such as pattern recognition receptors (PRRs) [e.g., retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs), Toll-like receptors (TLRs), and NOD-like receptors (NLRs)] and even some secreted functional proteins. However, a range of research, highlighted in this review, suggest that EV-associated with HFMD have evolved different strategies to avoid detection by innate immunity via different proteases (e.g., 2A, 3C, 2C, and 3D). Ongoing efforts to better understand virus–host interactions that control innate immunity and then distill how that influences HFMD development promises to have real-world significance. In this review, we address this complex topic in nine sections including multiple proteins associated with PRR and type I interferon (IFN) signaling. Recognizing how EVs linked to HFMD evade host innate immune system, we also describe the interactions between them and, finally, suggest future directions to better inform drug development and public health.https://www.frontiersin.org/article/10.3389/fmicb.2018.02422/fullinnate immunity evasionenterovirusescoxsackieviruseshand-foot-mouth diseasetype I IFN signaling
collection DOAJ
language English
format Article
sources DOAJ
author Yuefei Jin
Rongguang Zhang
Weidong Wu
Guangcai Duan
spellingShingle Yuefei Jin
Rongguang Zhang
Weidong Wu
Guangcai Duan
Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease
Frontiers in Microbiology
innate immunity evasion
enteroviruses
coxsackieviruses
hand-foot-mouth disease
type I IFN signaling
author_facet Yuefei Jin
Rongguang Zhang
Weidong Wu
Guangcai Duan
author_sort Yuefei Jin
title Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease
title_short Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease
title_full Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease
title_fullStr Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease
title_full_unstemmed Innate Immunity Evasion by Enteroviruses Linked to Epidemic Hand-Foot-Mouth Disease
title_sort innate immunity evasion by enteroviruses linked to epidemic hand-foot-mouth disease
publisher Frontiers Media S.A.
series Frontiers in Microbiology
issn 1664-302X
publishDate 2018-10-01
description Enterovirus (EV) infections are a major threat to global public health, and are responsible for mild respiratory illness, hand, foot, and mouth disease (HFMD), acute hemorrhagic conjunctivitis, aseptic meningitis, myocarditis, severe neonatal sepsis-like disease, and acute flaccid paralysis epidemic. Among them, HFMD is a common pediatric infectious disease caused by EVs of the family Picornaviridae including EV-A71, coxsackieviruses (CV)-A2, CV-A6, CV-A10, and CV-A16. Due to lack of vaccines and specific antiviral therapeutics, millions of children still suffer from HFMD. Innate immune system detects foreign invaders by means of a relatively limited number of sensors, such as pattern recognition receptors (PRRs) [e.g., retinoic acid-inducible gene I (RIG-I)-like receptors (RLRs), Toll-like receptors (TLRs), and NOD-like receptors (NLRs)] and even some secreted functional proteins. However, a range of research, highlighted in this review, suggest that EV-associated with HFMD have evolved different strategies to avoid detection by innate immunity via different proteases (e.g., 2A, 3C, 2C, and 3D). Ongoing efforts to better understand virus–host interactions that control innate immunity and then distill how that influences HFMD development promises to have real-world significance. In this review, we address this complex topic in nine sections including multiple proteins associated with PRR and type I interferon (IFN) signaling. Recognizing how EVs linked to HFMD evade host innate immune system, we also describe the interactions between them and, finally, suggest future directions to better inform drug development and public health.
topic innate immunity evasion
enteroviruses
coxsackieviruses
hand-foot-mouth disease
type I IFN signaling
url https://www.frontiersin.org/article/10.3389/fmicb.2018.02422/full
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