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Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2

The COVID-19 outbreak has become a global health risk, and understanding the response of the host to the SARS-CoV-2 virus will help to combat the disease. RNA editing by host deaminases is an innate restriction process to counter virus infection, but it is not yet known whether this process operates...

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Autores principales: Di Giorgio, Salvatore, Martignano, Filippo, Torcia, Maria Gabriella, Mattiuz, Giorgio, Conticello, Silvestro G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299625/
https://www.ncbi.nlm.nih.gov/pubmed/32596474
http://dx.doi.org/10.1126/sciadv.abb5813
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author Di Giorgio, Salvatore
Martignano, Filippo
Torcia, Maria Gabriella
Mattiuz, Giorgio
Conticello, Silvestro G.
author_facet Di Giorgio, Salvatore
Martignano, Filippo
Torcia, Maria Gabriella
Mattiuz, Giorgio
Conticello, Silvestro G.
author_sort Di Giorgio, Salvatore
collection PubMed
description The COVID-19 outbreak has become a global health risk, and understanding the response of the host to the SARS-CoV-2 virus will help to combat the disease. RNA editing by host deaminases is an innate restriction process to counter virus infection, but it is not yet known whether this process operates against coronaviruses. Here, we analyze RNA sequences from bronchoalveolar lavage fluids obtained from coronavirus-infected patients. We identify nucleotide changes that may be signatures of RNA editing: adenosine-to-inosine changes from ADAR deaminases and cytosine-to-uracil changes from APOBEC deaminases. Mutational analysis of genomes from different strains of Coronaviridae from human hosts reveals mutational patterns consistent with those observed in the transcriptomic data. However, the reduced ADAR signature in these data raises the possibility that ADARs might be more effective than APOBECs in restricting viral propagation. Our results thus suggest that both APOBECs and ADARs are involved in coronavirus genome editing, a process that may shape the fate of both virus and patient.
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spelling pubmed-72996252020-06-25 Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2 Di Giorgio, Salvatore Martignano, Filippo Torcia, Maria Gabriella Mattiuz, Giorgio Conticello, Silvestro G. Sci Adv Research Articles The COVID-19 outbreak has become a global health risk, and understanding the response of the host to the SARS-CoV-2 virus will help to combat the disease. RNA editing by host deaminases is an innate restriction process to counter virus infection, but it is not yet known whether this process operates against coronaviruses. Here, we analyze RNA sequences from bronchoalveolar lavage fluids obtained from coronavirus-infected patients. We identify nucleotide changes that may be signatures of RNA editing: adenosine-to-inosine changes from ADAR deaminases and cytosine-to-uracil changes from APOBEC deaminases. Mutational analysis of genomes from different strains of Coronaviridae from human hosts reveals mutational patterns consistent with those observed in the transcriptomic data. However, the reduced ADAR signature in these data raises the possibility that ADARs might be more effective than APOBECs in restricting viral propagation. Our results thus suggest that both APOBECs and ADARs are involved in coronavirus genome editing, a process that may shape the fate of both virus and patient. American Association for the Advancement of Science 2020-06-17 /pmc/articles/PMC7299625/ /pubmed/32596474 http://dx.doi.org/10.1126/sciadv.abb5813 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). http://creativecommons.org/licenses/by-nc/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (http://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Di Giorgio, Salvatore
Martignano, Filippo
Torcia, Maria Gabriella
Mattiuz, Giorgio
Conticello, Silvestro G.
Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2
title Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2
title_full Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2
title_fullStr Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2
title_full_unstemmed Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2
title_short Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2
title_sort evidence for host-dependent rna editing in the transcriptome of sars-cov-2
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7299625/
https://www.ncbi.nlm.nih.gov/pubmed/32596474
http://dx.doi.org/10.1126/sciadv.abb5813
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