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Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence

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...

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Autores principales: Brook, Cara E, Boots, Mike, Chandran, Kartik, Dobson, Andrew P, Drosten, Christian, Graham, Andrea L, Grenfell, Bryan T, Müller, Marcel A, Ng, Melinda, Wang, Lin-Fa, van Leeuwen, Anieke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064339/
https://www.ncbi.nlm.nih.gov/pubmed/32011232
http://dx.doi.org/10.7554/eLife.48401
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author Brook, Cara E
Boots, Mike
Chandran, Kartik
Dobson, Andrew P
Drosten, Christian
Graham, Andrea L
Grenfell, Bryan T
Müller, Marcel A
Ng, Melinda
Wang, Lin-Fa
van Leeuwen, Anieke
author_facet Brook, Cara E
Boots, Mike
Chandran, Kartik
Dobson, Andrew P
Drosten, Christian
Graham, Andrea L
Grenfell, Bryan T
Müller, Marcel A
Ng, Melinda
Wang, Lin-Fa
van Leeuwen, Anieke
author_sort Brook, Cara E
collection PubMed
description 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.
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spelling pubmed-70643392020-03-11 Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence Brook, Cara E Boots, Mike Chandran, Kartik Dobson, Andrew P Drosten, Christian Graham, Andrea L Grenfell, Bryan T Müller, Marcel A Ng, Melinda Wang, Lin-Fa van Leeuwen, Anieke eLife Ecology 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. eLife Sciences Publications, Ltd 2020-02-03 /pmc/articles/PMC7064339/ /pubmed/32011232 http://dx.doi.org/10.7554/eLife.48401 Text en © 2020, Brook et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Ecology
Brook, Cara E
Boots, Mike
Chandran, Kartik
Dobson, Andrew P
Drosten, Christian
Graham, Andrea L
Grenfell, Bryan T
Müller, Marcel A
Ng, Melinda
Wang, Lin-Fa
van Leeuwen, Anieke
Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
title Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
title_full Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
title_fullStr Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
title_full_unstemmed Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
title_short Accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
title_sort accelerated viral dynamics in bat cell lines, with implications for zoonotic emergence
topic Ecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7064339/
https://www.ncbi.nlm.nih.gov/pubmed/32011232
http://dx.doi.org/10.7554/eLife.48401
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