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Beta interferons from the extant camelids: Unique among eutherian mammals
The COVID-19 pandemic is a wake-up call on the zoonotic viral spillover events and the need to be prepared for future outbreaks. Zoonotic RNA viruses like the Middle East respiratory syndrome coronavirus (MERS-CoV) are potential pathogens that could trigger the next pandemic. Dromedary camels are th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095258/ https://www.ncbi.nlm.nih.gov/pubmed/35568245 http://dx.doi.org/10.1016/j.dci.2022.104443 |
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author | Premraj, Avinash Aleyas, Abi George Nautiyal, Binita Rasool, Thaha Jamal |
author_facet | Premraj, Avinash Aleyas, Abi George Nautiyal, Binita Rasool, Thaha Jamal |
author_sort | Premraj, Avinash |
collection | PubMed |
description | The COVID-19 pandemic is a wake-up call on the zoonotic viral spillover events and the need to be prepared for future outbreaks. Zoonotic RNA viruses like the Middle East respiratory syndrome coronavirus (MERS-CoV) are potential pathogens that could trigger the next pandemic. Dromedary camels are the only known animal source of MERS-CoV zoonotic infections, but little is known about the molecular antiviral response in this species. IFN-β and other type-I interferons provide the first line of defense against invading pathogens in the host immune response. We identified the IFNB gene of the dromedary camel and all extant members of the family Camelidae. Camelid IFN-β is unique with an even number of cysteines in the mature protein compared to other eutherian mammals with an odd number of cysteines. The viral mimetic poly(I:C) strongly induced IFN-β expression in camel kidney cells. Induction of IFN-β expression upon infection with camelpox virus was late and subdued when compared to poly(I:C) treatment. Prokaryotically expressed recombinant dromedary IFN-β induced expression of IFN-responsive genes in camel kidney cells. Further, recombinant IFN-β conferred antiviral resistance to camel kidney cells against the cytopathic effects of the camelpox virus, an endemic zoonotic pathogen. IFN-β from this unique group of mammals will offer insights into antiviral immune mechanisms and aid in the development of specific antivirals against pathogens that have the potential to be the next zoonotic pandemic. |
format | Online Article Text |
id | pubmed-9095258 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90952582022-05-12 Beta interferons from the extant camelids: Unique among eutherian mammals Premraj, Avinash Aleyas, Abi George Nautiyal, Binita Rasool, Thaha Jamal Dev Comp Immunol Article The COVID-19 pandemic is a wake-up call on the zoonotic viral spillover events and the need to be prepared for future outbreaks. Zoonotic RNA viruses like the Middle East respiratory syndrome coronavirus (MERS-CoV) are potential pathogens that could trigger the next pandemic. Dromedary camels are the only known animal source of MERS-CoV zoonotic infections, but little is known about the molecular antiviral response in this species. IFN-β and other type-I interferons provide the first line of defense against invading pathogens in the host immune response. We identified the IFNB gene of the dromedary camel and all extant members of the family Camelidae. Camelid IFN-β is unique with an even number of cysteines in the mature protein compared to other eutherian mammals with an odd number of cysteines. The viral mimetic poly(I:C) strongly induced IFN-β expression in camel kidney cells. Induction of IFN-β expression upon infection with camelpox virus was late and subdued when compared to poly(I:C) treatment. Prokaryotically expressed recombinant dromedary IFN-β induced expression of IFN-responsive genes in camel kidney cells. Further, recombinant IFN-β conferred antiviral resistance to camel kidney cells against the cytopathic effects of the camelpox virus, an endemic zoonotic pathogen. IFN-β from this unique group of mammals will offer insights into antiviral immune mechanisms and aid in the development of specific antivirals against pathogens that have the potential to be the next zoonotic pandemic. Elsevier Ltd. 2022-08 2022-05-12 /pmc/articles/PMC9095258/ /pubmed/35568245 http://dx.doi.org/10.1016/j.dci.2022.104443 Text en © 2022 Elsevier Ltd. All rights reserved. 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 Premraj, Avinash Aleyas, Abi George Nautiyal, Binita Rasool, Thaha Jamal Beta interferons from the extant camelids: Unique among eutherian mammals |
title | Beta interferons from the extant camelids: Unique among eutherian mammals |
title_full | Beta interferons from the extant camelids: Unique among eutherian mammals |
title_fullStr | Beta interferons from the extant camelids: Unique among eutherian mammals |
title_full_unstemmed | Beta interferons from the extant camelids: Unique among eutherian mammals |
title_short | Beta interferons from the extant camelids: Unique among eutherian mammals |
title_sort | beta interferons from the extant camelids: unique among eutherian mammals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095258/ https://www.ncbi.nlm.nih.gov/pubmed/35568245 http://dx.doi.org/10.1016/j.dci.2022.104443 |
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