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About:
Antiviral activities of ISG20 in positive-strand RNA virus infections
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An Entity of Type :
schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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document(s)
Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
has title
Antiviral activities of ISG20 in positive-strand RNA virus infections
Creator
Rijnbrand, Rene
Holbrook, Michael
Guo, Ju-Tao
Wei, Lai
Li, Kui
Zhou, Zhi
Wang, Jie
Dong, Qingming
Wang, Nan
Liang, Yuqiong
Lemon, Stanley
Nichols, Joan
Woodson, Sara
Source
Elsevier; Medline; PMC
abstract
Abstract ISG20 is an interferon-inducible 3′–5′ exonuclease that inhibits replication of several human and animal RNA viruses. However, the specificities of ISG20's antiviral action remain poorly defined. Here we determine the impact of ectopic expression of ISG20 on replication of several positive-strand RNA viruses from distinct viral families. ISG20 inhibited infections by cell culture-derived hepatitis C virus (HCV) and a pestivirus, bovine viral diarrhea virus and a picornavirus, hepatitis A virus. Moreover, ISG20 demonstrated cell-type specific antiviral activity against yellow fever virus, a classical flavivirus. Overexpression of ISG20, however, did not inhibit propagation of severe acute respiratory syndrome coronavirus, a highly-pathogenic human coronavirus in Huh7.5 cells. The antiviral effects of ISG20 were all dependent on its exonuclease activity. The closely related cellular exonucleases, ISG20L1 and ISG20L2, did not inhibit HCV replication. Together, these data may help better understand the antiviral specificity and action of ISG20.
has issue date
2011-01-20
(
xsd:dateTime
)
bibo:doi
10.1016/j.virol.2010.10.008
bibo:pmid
21036379
has license
els-covid
sha1sum (hex)
3489ec2ad98743262cdd5d6735b3a3f13878cc62
schema:url
https://doi.org/10.1016/j.virol.2010.10.008
resource representing a document's title
Antiviral activities of ISG20 in positive-strand RNA virus infections
has PubMed Central identifier
PMC3018280
has PubMed identifier
21036379
schema:publication
Virology
resource representing a document's body
covid:3489ec2ad98743262cdd5d6735b3a3f13878cc62#body_text
is
schema:about
of
named entity 'RNA virus'
named entity 'INTERFERON '
named entity 'BOVINE VIRAL DIARRHEA VIRUS'
named entity 'INNATE IMMUNITY'
named entity 'ANTIVIRAL'
named entity 'YELLOW FEVER VIRUS'
named entity 'ISG20L1'
named entity 'ISG20'
named entity 'ACTIVITIES'
named entity 'RNA VIRUS INFECTIONS'
named entity 'ANTIVIRAL'
named entity 'ISG20L2'
named entity 'KEYWORDS'
named entity 'SEVERE ACUTE RESPIRATORY SYNDROME CORONAVIRUS'
named entity 'HEPATITIS A VIRUS'
named entity 'ISG20'
named entity 'VIRUS HEPATITIS'
named entity 'HEPATITIS C VIRUS'
named entity 'POSITIVE-STRAND RNA VIRUS'
covid:arg/3489ec2ad98743262cdd5d6735b3a3f13878cc62
named entity 'virus'
named entity 'Hepatitis C virus'
named entity 'ISG20'
named entity 'Yellow fever virus'
named entity 'ISG20'
named entity 'ISG20'
named entity 'ISG20'
named entity 'IFN'
named entity 'virus'
named entity 'luciferase'
named entity 'hepatitis viruses'
named entity 'viral entry'
named entity 'titrated'
named entity 'coding sequences'
named entity 'encephalomyocarditis virus'
named entity 'YFV'
named entity 'mAb'
named entity 'ISG20'
named entity 'p53'
named entity 'mRNA'
named entity 'TRIzol'
named entity 'SARS-CoV'
named entity 'HEK293 cells'
named entity 'HCV'
named entity 'Huh7'
named entity 'HCV'
named entity '7.5'
named entity 'resistance gene'
named entity '7.5'
named entity '7.5'
named entity 'ISG56'
named entity 'transfection'
named entity 'mutation'
named entity 'Huh7'
named entity 'gene'
named entity 'ISG20'
named entity 'hepatoma'
named entity 'EMCV'
named entity 'Arboviruses'
named entity 'actin'
named entity 'HCV'
named entity 'antiviral'
named entity 'cell lysis'
named entity 'N-terminus'
named entity 'HEK293 cells'
named entity '7.5'
named entity 'RNA replication'
named entity 'PCR analysis'
named entity 'cell types'
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