Cargando…

Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways

Bats host a range of disease-causing viruses without displaying clinical symptoms. The mechanisms behind this are a continuous source of interest. Here, we studied the antiviral response in the Egyptian fruit bat and Kuhl’s pipistrelle, representing two subordinal clades. We profiled the antiviral r...

Descripción completa

Detalles Bibliográficos
Autores principales: Schneor, Lilach, Kaltenbach, Stefan, Friedman, Sivan, Tussia-Cohen, Dafna, Nissan, Yomiran, Shuler, Gal, Fraimovitch, Evgeny, Kolodziejczyk, Aleksandra A., Weinberg, Maya, Donati, Giacomo, Teeling, Emma C., Yovel, Yossi, Hagai, Tzachi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415932/
https://www.ncbi.nlm.nih.gov/pubmed/37575178
http://dx.doi.org/10.1016/j.isci.2023.107435
_version_ 1785087657909420032
author Schneor, Lilach
Kaltenbach, Stefan
Friedman, Sivan
Tussia-Cohen, Dafna
Nissan, Yomiran
Shuler, Gal
Fraimovitch, Evgeny
Kolodziejczyk, Aleksandra A.
Weinberg, Maya
Donati, Giacomo
Teeling, Emma C.
Yovel, Yossi
Hagai, Tzachi
author_facet Schneor, Lilach
Kaltenbach, Stefan
Friedman, Sivan
Tussia-Cohen, Dafna
Nissan, Yomiran
Shuler, Gal
Fraimovitch, Evgeny
Kolodziejczyk, Aleksandra A.
Weinberg, Maya
Donati, Giacomo
Teeling, Emma C.
Yovel, Yossi
Hagai, Tzachi
author_sort Schneor, Lilach
collection PubMed
description Bats host a range of disease-causing viruses without displaying clinical symptoms. The mechanisms behind this are a continuous source of interest. Here, we studied the antiviral response in the Egyptian fruit bat and Kuhl’s pipistrelle, representing two subordinal clades. We profiled the antiviral response in fibroblasts using RNA sequencing and compared bat with primate and rodent responses. Both bats upregulate similar genes; however, a subset of these genes is transcriptionally divergent between them. These divergent genes also evolve rapidly in sequence, have specific promoter architectures, and are associated with programs underlying tolerance and resistance. Finally, we characterized antiviral genes that expanded in bats, with duplicates diverging in sequence and expression. Our study reveals a largely conserved antiviral program across bats and points to a set of genes that rapidly evolve through multiple mechanisms. These can contribute to bat adaptation to viral infection and provide directions to understanding the mechanisms behind it.
format Online
Article
Text
id pubmed-10415932
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-104159322023-08-12 Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways Schneor, Lilach Kaltenbach, Stefan Friedman, Sivan Tussia-Cohen, Dafna Nissan, Yomiran Shuler, Gal Fraimovitch, Evgeny Kolodziejczyk, Aleksandra A. Weinberg, Maya Donati, Giacomo Teeling, Emma C. Yovel, Yossi Hagai, Tzachi iScience Article Bats host a range of disease-causing viruses without displaying clinical symptoms. The mechanisms behind this are a continuous source of interest. Here, we studied the antiviral response in the Egyptian fruit bat and Kuhl’s pipistrelle, representing two subordinal clades. We profiled the antiviral response in fibroblasts using RNA sequencing and compared bat with primate and rodent responses. Both bats upregulate similar genes; however, a subset of these genes is transcriptionally divergent between them. These divergent genes also evolve rapidly in sequence, have specific promoter architectures, and are associated with programs underlying tolerance and resistance. Finally, we characterized antiviral genes that expanded in bats, with duplicates diverging in sequence and expression. Our study reveals a largely conserved antiviral program across bats and points to a set of genes that rapidly evolve through multiple mechanisms. These can contribute to bat adaptation to viral infection and provide directions to understanding the mechanisms behind it. Elsevier 2023-07-20 /pmc/articles/PMC10415932/ /pubmed/37575178 http://dx.doi.org/10.1016/j.isci.2023.107435 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Schneor, Lilach
Kaltenbach, Stefan
Friedman, Sivan
Tussia-Cohen, Dafna
Nissan, Yomiran
Shuler, Gal
Fraimovitch, Evgeny
Kolodziejczyk, Aleksandra A.
Weinberg, Maya
Donati, Giacomo
Teeling, Emma C.
Yovel, Yossi
Hagai, Tzachi
Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
title Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
title_full Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
title_fullStr Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
title_full_unstemmed Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
title_short Comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
title_sort comparison of antiviral responses in two bat species reveals conserved and divergent innate immune pathways
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415932/
https://www.ncbi.nlm.nih.gov/pubmed/37575178
http://dx.doi.org/10.1016/j.isci.2023.107435
work_keys_str_mv AT schneorlilach comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT kaltenbachstefan comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT friedmansivan comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT tussiacohendafna comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT nissanyomiran comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT shulergal comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT fraimovitchevgeny comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT kolodziejczykaleksandraa comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT weinbergmaya comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT donatigiacomo comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT teelingemmac comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT yovelyossi comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways
AT hagaitzachi comparisonofantiviralresponsesintwobatspeciesrevealsconservedanddivergentinnateimmunepathways