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About:
Tauroursodeoxycholic acid (TUDCA) inhibits influenza A viral infection by disrupting viral proton channel M2
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An Entity of Type :
schema:ScholarlyArticle
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wasabi.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
New Facet based on Instances of this Class
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Tauroursodeoxycholic acid (TUDCA) inhibits influenza A viral infection by disrupting viral proton channel M2
Creator
Jiang, Chengyu
Lu, Huijun
Li, Xiao
Jin, Ningyi
Li, Ning
Tian, Mingyao
Zhang, Yanxu
Wang, Hongliang
Li, Zhiqing
Wu, Shuangxiu
Xu, Ruodan
Zhu, Jindong
Source
Elsevier; Medline; PMC
abstract
Influenza is a persistent threat to human health and there is a continuing requirement for updating anti-influenza strategies. Initiated by observations of different endoplasmic reticulum (ER) responses of host to seasonal H1N1 and highly pathogenic avian influenza (HPAI) A H5N1 infections, we identified an alternative antiviral role of tauroursodeoxycholic acid (TUDCA), a clinically available ER stress inhibitor, both in vitro and in vivo. Rather than modulating ER stress in host cells, TUDCA abolished the proton conductivity of viral M2 by disrupting its oligomeric states, which induces inefficient viral infection. We also showed that M2 penetrated cells, whose intracellular uptake depended on its proton channel activity, an effect observed in both TUDCA and M2 inhibitor amantadine. The identification and application of TUDCA as an inhibitor of M2 proton channel will expand our understanding of IAV biology and complement current anti-IAV arsenals.
has issue date
2019-02-15
(
xsd:dateTime
)
bibo:doi
10.1016/j.scib.2018.08.013
bibo:pmid
32288967
has license
no-cc
sha1sum (hex)
2a8a83200b66ae807ce70d4e86ae189d4f3dbcce
schema:url
https://doi.org/10.1016/j.scib.2018.08.013
resource representing a document's title
Tauroursodeoxycholic acid (TUDCA) inhibits influenza A viral infection by disrupting viral proton channel M2
has PubMed Central identifier
PMC7104969
has PubMed identifier
32288967
schema:publication
Sci Bull (Beijing)
resource representing a document's body
covid:2a8a83200b66ae807ce70d4e86ae189d4f3dbcce#body_text
is
schema:about
of
named entity 'highly'
named entity 'complement'
named entity 'amantadine'
named entity 'host'
named entity 'host'
named entity 'vivo'
named entity 'proton'
named entity 'channel'
named entity 'PROTON CHANNEL'
named entity 'PROTON'
named entity 'EXPAND'
named entity 'ROLE'
named entity 'ANTIVIRAL'
named entity 'RESPONSES'
named entity 'PROTON CHANNEL ACTIVITY'
named entity 'INFLUENZA'
named entity 'EFFECT'
named entity 'HIGHLY PATHOGENIC AVIAN INFLUENZA'
named entity 'OBSERVED'
named entity 'UPDATING'
named entity 'HOST CELLS'
named entity 'STRATEGIES'
named entity 'IN VIVO'
named entity 'H1N1'
covid:arg/2a8a83200b66ae807ce70d4e86ae189d4f3dbcce
named entity 'IDENTIFICATION'
named entity 'SEASONAL'
named entity 'RATHER'
named entity 'BIOLOGY'
named entity 'VIRAL INFECTION'
named entity 'INFLUENZA A'
named entity 'TAUROURSODEOXYCHOLIC ACID'
named entity 'VIRAL'
named entity 'IDENTIFIED'
named entity 'INTRACELLULAR UPTAKE'
named entity 'PERSISTENT'
named entity 'CURRENT'
named entity 'THREAT'
named entity 'IN VITRO'
named entity 'OUR'
named entity 'VIRAL'
named entity 'INEFFICIENT'
named entity 'CELLS'
named entity 'UNDERSTANDING'
named entity 'INFECTIONS'
named entity 'TAUROURSODEOXYCHOLIC ACID'
named entity 'PENETRATED'
named entity 'REQUIREMENT'
named entity 'DISRUPTING'
named entity 'ABOLISHED'
named entity 'HOST'
named entity 'ITS'
named entity 'DIFFERENT'
named entity 'CONDUCTIVITY'
named entity 'INHIBITOR'
named entity 'APPLICATION'
named entity 'MODULATING'
named entity 'ALTERNATIVE'
named entity 'HUMAN HEALTH'
named entity 'H5N1'
named entity 'VIRAL INFECTION'
named entity 'OBSERVATIONS'
named entity 'DISRUPTING'
named entity 'IS A'
named entity 'PROTON CHANNEL'
named entity 'COMPLEMENT'
named entity 'ER STRESS'
named entity 'STATES'
named entity 'AVAILABLE'
named entity 'CONTINUING'
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