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Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection

Our systematic literature collection and annotation identified 106 chemical drugs and 31 antibodies effective against the infection of at least one human coronavirus (including SARS-CoV, SAR-CoV-2, and MERS-CoV) in vitro or in vivo in an experimental or clinical setting. A total of 163 drug protein...

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Autores principales: Liu, Yingtong, Hur, Junguk, Chan, Wallace K. B., Wang, Zhigang, Xie, Jiangan, Sun, Duxin, Handelman, Samuel, Sexton, Jonathan, Yu, Hong, He, Yongqun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806933/
https://www.ncbi.nlm.nih.gov/pubmed/33441564
http://dx.doi.org/10.1038/s41597-021-00799-w
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author Liu, Yingtong
Hur, Junguk
Chan, Wallace K. B.
Wang, Zhigang
Xie, Jiangan
Sun, Duxin
Handelman, Samuel
Sexton, Jonathan
Yu, Hong
He, Yongqun
author_facet Liu, Yingtong
Hur, Junguk
Chan, Wallace K. B.
Wang, Zhigang
Xie, Jiangan
Sun, Duxin
Handelman, Samuel
Sexton, Jonathan
Yu, Hong
He, Yongqun
author_sort Liu, Yingtong
collection PubMed
description Our systematic literature collection and annotation identified 106 chemical drugs and 31 antibodies effective against the infection of at least one human coronavirus (including SARS-CoV, SAR-CoV-2, and MERS-CoV) in vitro or in vivo in an experimental or clinical setting. A total of 163 drug protein targets were identified, and 125 biological processes involving the drug targets were significantly enriched based on a Gene Ontology (GO) enrichment analysis. The Coronavirus Infectious Disease Ontology (CIDO) was used as an ontological platform to represent the anti-coronaviral drugs, chemical compounds, drug targets, biological processes, viruses, and the relations among these entities. In addition to new term generation, CIDO also adopted various terms from existing ontologies and developed new relations and axioms to semantically represent our annotated knowledge. The CIDO knowledgebase was systematically analyzed for scientific insights. To support rational drug design, a “Host-coronavirus interaction (HCI) checkpoint cocktail” strategy was proposed to interrupt the important checkpoints in the dynamic HCI network, and ontologies would greatly support the design process with interoperable knowledge representation and reasoning.
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spelling pubmed-78069332021-01-21 Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection Liu, Yingtong Hur, Junguk Chan, Wallace K. B. Wang, Zhigang Xie, Jiangan Sun, Duxin Handelman, Samuel Sexton, Jonathan Yu, Hong He, Yongqun Sci Data Analysis Our systematic literature collection and annotation identified 106 chemical drugs and 31 antibodies effective against the infection of at least one human coronavirus (including SARS-CoV, SAR-CoV-2, and MERS-CoV) in vitro or in vivo in an experimental or clinical setting. A total of 163 drug protein targets were identified, and 125 biological processes involving the drug targets were significantly enriched based on a Gene Ontology (GO) enrichment analysis. The Coronavirus Infectious Disease Ontology (CIDO) was used as an ontological platform to represent the anti-coronaviral drugs, chemical compounds, drug targets, biological processes, viruses, and the relations among these entities. In addition to new term generation, CIDO also adopted various terms from existing ontologies and developed new relations and axioms to semantically represent our annotated knowledge. The CIDO knowledgebase was systematically analyzed for scientific insights. To support rational drug design, a “Host-coronavirus interaction (HCI) checkpoint cocktail” strategy was proposed to interrupt the important checkpoints in the dynamic HCI network, and ontologies would greatly support the design process with interoperable knowledge representation and reasoning. Nature Publishing Group UK 2021-01-13 /pmc/articles/PMC7806933/ /pubmed/33441564 http://dx.doi.org/10.1038/s41597-021-00799-w Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Analysis
Liu, Yingtong
Hur, Junguk
Chan, Wallace K. B.
Wang, Zhigang
Xie, Jiangan
Sun, Duxin
Handelman, Samuel
Sexton, Jonathan
Yu, Hong
He, Yongqun
Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
title Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
title_full Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
title_fullStr Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
title_full_unstemmed Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
title_short Ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
title_sort ontological modeling and analysis of experimentally or clinically verified drugs against coronavirus infection
topic Analysis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806933/
https://www.ncbi.nlm.nih.gov/pubmed/33441564
http://dx.doi.org/10.1038/s41597-021-00799-w
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