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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2020
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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. |
format | Online Article Text |
id | pubmed-7064339 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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