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About:
Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
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schema:ScholarlyArticle
, within Data Space :
covidontheweb.inria.fr
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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
Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
Creator
Drosten, Christian
Grenfell, Bryan
Wang, Lin-Fa
Chandran, Kartik
Boots, Mike
Ng, Melinda
Brook, Cara
Dobson, Andrew
Graham, Andrea
Haydon, Dan
Mü Ller, Marcel
Van Leeuwen, Anieke
Source
Medline; PMC
abstract
Bats host virulent zoonotic viruses without experiencing disease. A mechanistic understanding of the impact of bats’ virus hosting capacities, including uniquely constitutive immune pathways, on cellular-scale viral dynamics is needed to elucidate zoonotic emergence. We carried out virus infectivity assays on bat cell lines expressing induced and constitutive immune phenotypes, then developed a theoretical model of our in vitro system, which we fit to empirical data. Best fit models recapitulated expected immune phenotypes for representative cell lines, supporting robust antiviral defenses in bat cells that correlated with higher estimates for within-host viral propagation rates. In general, heightened immune responses limit pathogen-induced cellular morbidity, which can facilitate the establishment of rapidly-propagating persistent infections within-host. Rapidly-transmitting viruses that have evolved with bat immune systems will likely cause enhanced virulence following emergence into secondary hosts with immune systems that diverge from those unique to bats.
has issue date
2020-02-03
(
xsd:dateTime
)
bibo:doi
10.7554/elife.48401
bibo:pmid
32011232
has license
cc-by
sha1sum (hex)
f2cc0d63ff2c4aaa127c4caae21d8f3a0067e3d5
schema:url
https://doi.org/10.7554/elife.48401
resource representing a document's title
Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
has PubMed Central identifier
PMC7064339
has PubMed identifier
32011232
schema:publication
eLife
resource representing a document's body
covid:f2cc0d63ff2c4aaa127c4caae21d8f3a0067e3d5#body_text
is
schema:about
of
named entity 'diverge'
named entity 'mechanistic'
named entity 'immune systems'
named entity 'constitutive'
named entity 'constitutive'
named entity 'hosting'
named entity 'zoonotic'
covid:arg/f2cc0d63ff2c4aaa127c4caae21d8f3a0067e3d5
named entity 'emergence'
named entity 'phenotypes'
named entity 'needed'
named entity 'general'
named entity 'zoonotic'
named entity 'virus'
named entity 'persistent infections'
named entity 'viruses'
named entity 'viruses'
named entity 'theoretical model'
named entity 'cell lines'
named entity 'cell lines'
named entity 'immune responses'
named entity 'bat'
named entity 'viral dynamics'
named entity 'microscope'
named entity 'infection'
named entity 'inflammation'
named entity 'molecular biological'
named entity 'RNA'
named entity 'cDNA'
named entity 'rVSV-EBOV'
named entity 'time series'
named entity 'cell lines'
named entity 'cross-species'
named entity 'infection'
named entity 'time series'
named entity 'recombinant'
named entity 'viral infections'
named entity 'viral infection'
named entity 'influenza'
named entity 'qPCR'
named entity 'limit cycles'
named entity 'cell lines'
named entity 'plaque assays'
named entity 'antiviral'
named entity 'reproductive number'
named entity 'stochastic'
named entity 'cell line'
named entity 'viruses'
named entity 'basic reproduction number'
named entity 'long-term'
named entity 'rabies'
named entity 'antiviral'
named entity 'Hoechst'
named entity 'Pteropus alecto'
named entity 'interferon-stimulated genes'
named entity 'eGFP'
named entity 'phenotypes'
named entity 'rVSV-EBOV'
named entity 'Hoechst'
named entity 'cell death'
named entity 'HIV'
named entity 'natural reservoirs'
named entity 'IFN'
named entity 'bat'
named entity 'Invitrogen'
named entity 'streptomycin'
named entity 'antiviral'
named entity 'cell line'
named entity 'evolutionary history'
named entity 'epidemics'
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