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Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19

Genes functionally associated with SARS-CoV-2 infection and genes functionally related to the COVID-19 disease can be different, whose distinction will become the first essential step for successfully fighting against the COVID-19 pandemic. Unfortunately, this first step has not been completed in al...

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Autor principal: Zhang, Zhengjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608907/
https://www.ncbi.nlm.nih.gov/pubmed/36298522
http://dx.doi.org/10.3390/vaccines10101657
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author Zhang, Zhengjun
author_facet Zhang, Zhengjun
author_sort Zhang, Zhengjun
collection PubMed
description Genes functionally associated with SARS-CoV-2 infection and genes functionally related to the COVID-19 disease can be different, whose distinction will become the first essential step for successfully fighting against the COVID-19 pandemic. Unfortunately, this first step has not been completed in all biological and medical research. Using a newly developed max-competing logistic classifier, two genes, ATP6V1B2 and IFI27, stand out to be critical in the transcriptional response to SARS-CoV-2 infection with differential expressions derived from NP/OP swab PCR. This finding is evidenced by combining these two genes with another gene in predicting disease status to achieve better-indicating accuracy than existing classifiers with the same number of genes. In addition, combining these two genes with three other genes to form a five-gene classifier outperforms existing classifiers with ten or more genes. These two genes can be critical in fighting against the COVID-19 pandemic as a new focus and direction with their exceptional predicting accuracy. Comparing the functional effects of these genes with a five-gene classifier with 100% accuracy identified and tested from blood samples in our earlier work, the genes and their transcriptional response and functional effects on SARS-CoV-2 infection, and the genes and their functional signature patterns on COVID-19 antibodies, are significantly different. We will use a total of fourteen cohort studies (including breakthrough infections and omicron variants) with 1481 samples to justify our results. Such significant findings can help explore the causal and pathological links between SARS-CoV-2 infection and the COVID-19 disease, and fight against the disease with more targeted genes, vaccines, antiviral drugs, and therapies.
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spelling pubmed-96089072022-10-28 Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19 Zhang, Zhengjun Vaccines (Basel) Article Genes functionally associated with SARS-CoV-2 infection and genes functionally related to the COVID-19 disease can be different, whose distinction will become the first essential step for successfully fighting against the COVID-19 pandemic. Unfortunately, this first step has not been completed in all biological and medical research. Using a newly developed max-competing logistic classifier, two genes, ATP6V1B2 and IFI27, stand out to be critical in the transcriptional response to SARS-CoV-2 infection with differential expressions derived from NP/OP swab PCR. This finding is evidenced by combining these two genes with another gene in predicting disease status to achieve better-indicating accuracy than existing classifiers with the same number of genes. In addition, combining these two genes with three other genes to form a five-gene classifier outperforms existing classifiers with ten or more genes. These two genes can be critical in fighting against the COVID-19 pandemic as a new focus and direction with their exceptional predicting accuracy. Comparing the functional effects of these genes with a five-gene classifier with 100% accuracy identified and tested from blood samples in our earlier work, the genes and their transcriptional response and functional effects on SARS-CoV-2 infection, and the genes and their functional signature patterns on COVID-19 antibodies, are significantly different. We will use a total of fourteen cohort studies (including breakthrough infections and omicron variants) with 1481 samples to justify our results. Such significant findings can help explore the causal and pathological links between SARS-CoV-2 infection and the COVID-19 disease, and fight against the disease with more targeted genes, vaccines, antiviral drugs, and therapies. MDPI 2022-10-02 /pmc/articles/PMC9608907/ /pubmed/36298522 http://dx.doi.org/10.3390/vaccines10101657 Text en © 2022 by the author. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zhang, Zhengjun
Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19
title Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19
title_full Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19
title_fullStr Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19
title_full_unstemmed Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19
title_short Genomic Biomarker Heterogeneities between SARS-CoV-2 and COVID-19
title_sort genomic biomarker heterogeneities between sars-cov-2 and covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9608907/
https://www.ncbi.nlm.nih.gov/pubmed/36298522
http://dx.doi.org/10.3390/vaccines10101657
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