Cargando…
Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection
Bat cells and tissue have elevated basal expression levels of antiviral genes commonly associated with interferon alpha (IFNα) signaling. Here, we show Interferon Regulatory Factor 1 (IRF1), 3, and 7 levels are elevated in most bat tissues and that, basally, IRFs contribute to the expression of type...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Author(s).
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755441/ https://www.ncbi.nlm.nih.gov/pubmed/33147460 http://dx.doi.org/10.1016/j.celrep.2020.108345 |
_version_ | 1784632382394990592 |
---|---|
author | Irving, Aaron T. Zhang, Qian Kong, Pui-San Luko, Katarina Rozario, Pritisha Wen, Ming Zhu, Feng Zhou, Peng Ng, Justin H.J. Sobota, Radoslaw M. Wang, Lin-Fa |
author_facet | Irving, Aaron T. Zhang, Qian Kong, Pui-San Luko, Katarina Rozario, Pritisha Wen, Ming Zhu, Feng Zhou, Peng Ng, Justin H.J. Sobota, Radoslaw M. Wang, Lin-Fa |
author_sort | Irving, Aaron T. |
collection | PubMed |
description | Bat cells and tissue have elevated basal expression levels of antiviral genes commonly associated with interferon alpha (IFNα) signaling. Here, we show Interferon Regulatory Factor 1 (IRF1), 3, and 7 levels are elevated in most bat tissues and that, basally, IRFs contribute to the expression of type I IFN ligands and high expression of interferon regulated genes (IRGs). CRISPR knockout (KO) of IRF 1/3/7 in cells reveals distinct subsets of genes affected by each IRF in an IFN-ligand signaling-dependent and largely independent manner. As the master regulators of innate immunity, the IRFs control the kinetics and maintenance of the IRG response and play essential roles in response to influenza A virus (IAV), herpes simplex virus 1 (HSV-1), Melaka virus/Pteropine orthoreovirus 3 Melaka (PRV3M), and Middle East respiratory syndrome-related coronavirus (MERS-CoV) infection. With its differential expression in bats compared to that in humans, this highlights a critical role for basal IRF expression in viral responses and potentially immune cell development in bats with relevance for IRF function in human biology. |
format | Online Article Text |
id | pubmed-8755441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Author(s). |
record_format | MEDLINE/PubMed |
spelling | pubmed-87554412022-01-13 Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection Irving, Aaron T. Zhang, Qian Kong, Pui-San Luko, Katarina Rozario, Pritisha Wen, Ming Zhu, Feng Zhou, Peng Ng, Justin H.J. Sobota, Radoslaw M. Wang, Lin-Fa Cell Rep Article Bat cells and tissue have elevated basal expression levels of antiviral genes commonly associated with interferon alpha (IFNα) signaling. Here, we show Interferon Regulatory Factor 1 (IRF1), 3, and 7 levels are elevated in most bat tissues and that, basally, IRFs contribute to the expression of type I IFN ligands and high expression of interferon regulated genes (IRGs). CRISPR knockout (KO) of IRF 1/3/7 in cells reveals distinct subsets of genes affected by each IRF in an IFN-ligand signaling-dependent and largely independent manner. As the master regulators of innate immunity, the IRFs control the kinetics and maintenance of the IRG response and play essential roles in response to influenza A virus (IAV), herpes simplex virus 1 (HSV-1), Melaka virus/Pteropine orthoreovirus 3 Melaka (PRV3M), and Middle East respiratory syndrome-related coronavirus (MERS-CoV) infection. With its differential expression in bats compared to that in humans, this highlights a critical role for basal IRF expression in viral responses and potentially immune cell development in bats with relevance for IRF function in human biology. The Author(s). 2020-11-03 2020-11-03 /pmc/articles/PMC8755441/ /pubmed/33147460 http://dx.doi.org/10.1016/j.celrep.2020.108345 Text en © 2020 The Author(s) Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Irving, Aaron T. Zhang, Qian Kong, Pui-San Luko, Katarina Rozario, Pritisha Wen, Ming Zhu, Feng Zhou, Peng Ng, Justin H.J. Sobota, Radoslaw M. Wang, Lin-Fa Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection |
title | Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection |
title_full | Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection |
title_fullStr | Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection |
title_full_unstemmed | Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection |
title_short | Interferon Regulatory Factors IRF1 and IRF7 Directly Regulate Gene Expression in Bats in Response to Viral Infection |
title_sort | interferon regulatory factors irf1 and irf7 directly regulate gene expression in bats in response to viral infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755441/ https://www.ncbi.nlm.nih.gov/pubmed/33147460 http://dx.doi.org/10.1016/j.celrep.2020.108345 |
work_keys_str_mv | AT irvingaaront interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT zhangqian interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT kongpuisan interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT lukokatarina interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT rozariopritisha interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT wenming interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT zhufeng interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT zhoupeng interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT ngjustinhj interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT sobotaradoslawm interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection AT wanglinfa interferonregulatoryfactorsirf1andirf7directlyregulategeneexpressioninbatsinresponsetoviralinfection |