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About:
MicroRNA-based strategy to mitigate the risk of gain-of-function influenza studies
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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
MicroRNA-based strategy to mitigate the risk of gain-of-function influenza studies
Creator
Angel, Matthew
Sutton, Troy
Xu, Kemin
GarcĂa-Sastre, Adolfo
Perez, Daniel
Finch, Courtney
Kimble, Brian
Chua, Mark
Langlois #1, Ryan
Shapiro, Jillian
Silvia Gonzalez-Reiche, Ana
Tenoever, Benjamin
Source
PMC
abstract
Recent gain-of-function studies in influenza A virus H5N1 strains revealed that as few as three amino-acid changes in the hemagglutinin protein confer the capacity for viral transmission between ferrets(1, 2). As transmission between ferrets is considered a surrogate indicator of transmissibility between humans, these studies raised concerns about the risks of gain-of-function influenza A virus research. Here we present an approach to strengthen the biosafety of gain-of-function influenza experiments. We exploit species-specific endogenous small RNAs to restrict influenza A virus tropism. In particular, we found that the microRNA miR-192 was expressed in primary human respiratory tract epithelial cells as well as mouse lungs but absent from the ferret respiratory tract. Incorporation of miR-192 target sites into influenza A virus did not prevent influenza replication and transmissibility in ferrets, but did attenuate influenza pathogenicity in mice. This molecular biocontainment approach should be applicable beyond influenza A virus to minimize the risk of experiments involving other pathogenic viruses.
has issue date
2013-08-11
(
xsd:dateTime
)
bibo:doi
10.1038/nbt.2666
bibo:pmid
23934176
has license
no-cc
sha1sum (hex)
fdc336253485b3b3e895271a27f3457611e826f4
schema:url
https://doi.org/10.1038/nbt.2666
resource representing a document's title
MicroRNA-based strategy to mitigate the risk of gain-of-function influenza studies
has PubMed Central identifier
PMC3808852
has PubMed identifier
23934176
schema:publication
Nat Biotechnol
resource representing a document's body
covid:fdc336253485b3b3e895271a27f3457611e826f4#body_text
is
schema:about
of
named entity 'BASED'
named entity 'SITES'
named entity 'SPECIFIC'
named entity 'PARTICULAR'
named entity 'TARGET'
named entity 'MOLECULAR'
named entity 'FUNCTION'
named entity 'PRESENT'
named entity 'FERRETS'
named entity 'PREVENT'
named entity 'MICE'
named entity 'STRAINS'
named entity 'RECENT'
named entity 'PRIMARY'
named entity 'BEYOND'
named entity 'Incorporation'
named entity 'exploit'
named entity 'molecular'
named entity 'transmission'
named entity 'strategy'
named entity 'HHS'
named entity 'OF-'
named entity 'PUBLIC'
named entity 'MICRORNA'
named entity 'FUNCTION'
named entity 'ATTENUATE'
named entity 'EXPERIMENTS'
named entity 'MITIGATE'
named entity 'RISK OF'
covid:arg/fdc336253485b3b3e895271a27f3457611e826f4
named entity 'MANUSCRIPT'
named entity 'SPECIES'
named entity 'PATHOGENIC'
named entity 'H5N1'
named entity 'HEMAGGLUTININ'
named entity 'THESE'
named entity 'VIRAL TRANSMISSION'
named entity 'CONSIDERED'
named entity 'MIR-192'
named entity 'APPROACH'
named entity 'STRATEGY'
named entity 'STUDIES'
named entity 'GAIN'
named entity 'INFLUENZA'
named entity 'SMALL'
named entity 'INFLUENZA'
named entity 'EXPLOIT'
named entity 'RNAS'
named entity 'DID'
named entity 'VIRUSES'
named entity 'REPLICATION'
named entity 'CAPACITY'
named entity 'RESTRICT'
named entity 'PATHOGENICITY'
named entity 'INFLUENZA A VIRUS'
named entity 'HERE'
named entity 'INVOLVING'
named entity 'CHANGES'
named entity 'TRANSMISSION'
named entity 'EXPRESSED'
named entity 'FERRET'
named entity 'INDICATOR'
named entity 'STUDIES'
named entity 'RISKS'
named entity 'ACCESS'
named entity 'AUTHOR'
named entity 'LUNGS'
named entity 'CONCERNS'
named entity 'VIRUS TROPISM'
named entity 'HUMANS'
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