=Paper= {{Paper |id=Vol-3805/ICBO-2022_paper_3333 |storemode=property |title=Ontological Representation and Analysis of the Molecular Interactions Related to COVID-19-associated Acute Kidney Injury |pdfUrl=https://ceur-ws.org/Vol-3805/ICBO-2022_paper_3333.pdf |volume=Vol-3805 |authors=Ghida Arnous,Yongqun He |dblpUrl=https://dblp.org/rec/conf/icbo/ArnousH22 }} ==Ontological Representation and Analysis of the Molecular Interactions Related to COVID-19-associated Acute Kidney Injury== https://ceur-ws.org/Vol-3805/ICBO-2022_paper_3333.pdf
                         Ontological representation and analysis of the molecular
                         interactions related to COVID-19-associated Acute Kidney Injury
                         Ghida Arnous 1, and Yongqun He 1
                         1
                                University of Michigan, Ann Arbor, MI 48109, USA.

                                             Abstract
                                             COVID-19 is related to multiple organ injuries, and its effects on the kidneys is well
                                             demonstrated in the literature. This study aims to expand and ontologically present knowledge
                                             available regarding the relationship between COVID-19 and Acute Kidney Injury (AKI). To
                                             achieve our goal, we conducted literature mining and utilized data available from the
                                             Anatomical structures, Cell Types, Biomarkers (ASCT+B) to determine kidney biomarkers
                                             involved in the process. We utilized BioGRID data to determine SARS-CoV-2 and host
                                             protein/gene interactions implicated in COVID-19 associated AKI. By using the above two
                                             resources, we found 17 biomarkers (out of 146) interacting with 14 SARS-CoV-2 viral proteins,
                                             yielding a total of 36 interactions. In addition to ACE2 being the most significant SARS-CoV-
                                             2 receptor and its implications being well studied, multiple other interactors are discovered and
                                             are presented in our paper. We utilized Reactome for pathway analysis and the Coronavirus
                                             Infectious Disease Ontology (CIDO) as a platform to represent our findings ontologically. Our
                                             CIDO-based ontological representation will provide a systematic and computer-interpretable
                                             logic knowledge representation of the molecular interactions related to COVID-19-associated
                                             AKI mechanisms, leading to the uncovering of many scientific insights. The recently added
                                             protein-protein interactions (PPIs) will further expand on the already existing knowledge
                                             regarding COVID-19 associated AKI PPIs. Our work provides host/virus interaction
                                             information, allowing for discovering potential targets and developing pharmacological
                                             therapies to treat AKI in COVID-19 patients.

                                             Keywords 1
                                             COVID-19, Acute Kidney Injury, Ontology, CIDO, ASCT+B, Protein-protein interaction
                                             BioGRID, Reactome




                         ICBO 2022, September 25-28, 2022, Ann Arbor, MI, USA.
                         EMAIL:        Ghida.arnous@gmail.com         (A.       1);
                         yongqunh@med.umich.edu (A. 2)
                         ORCID: 0000-0003-3403-3719 (A. 1); 0000-0001-9189-9661 (A.
                         2)
                                         ©️ 2020 Copyright for this paper by its authors. Use permitted under Creative
                                         Commons License Attribution 4.0 International (CC BY 4.0).

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