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TYK2 single-nucleotide variants associated with the severity of COVID-19 disease

Coronavirus disease 2019 (COVID-19) is a lethal disease caused by the coronavirus SARS-CoV-2, which can result in a broad clinical spectrum of respiratory symptoms. While many clinical risk factors such as concomitant chronic diseases play roles in the pathophysiology of COVID-19, genetic predisposi...

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Autores principales: Zabihi Rizi, Fateme, Ghorbani, Atousa, Zahtab, Parnia, Darbaghshahi, Niloufar Naderi, Ataee, Nioosha, Pourhamzeh, Pardis, Hamzei, Behnaz, Dolatabadi, Nasrin Fatahi, Zamani, Atefeh, Hooshmand, Masoud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Vienna 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10035968/
https://www.ncbi.nlm.nih.gov/pubmed/36959416
http://dx.doi.org/10.1007/s00705-023-05729-2
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author Zabihi Rizi, Fateme
Ghorbani, Atousa
Zahtab, Parnia
Darbaghshahi, Niloufar Naderi
Ataee, Nioosha
Pourhamzeh, Pardis
Hamzei, Behnaz
Dolatabadi, Nasrin Fatahi
Zamani, Atefeh
Hooshmand, Masoud
author_facet Zabihi Rizi, Fateme
Ghorbani, Atousa
Zahtab, Parnia
Darbaghshahi, Niloufar Naderi
Ataee, Nioosha
Pourhamzeh, Pardis
Hamzei, Behnaz
Dolatabadi, Nasrin Fatahi
Zamani, Atefeh
Hooshmand, Masoud
author_sort Zabihi Rizi, Fateme
collection PubMed
description Coronavirus disease 2019 (COVID-19) is a lethal disease caused by the coronavirus SARS-CoV-2, which can result in a broad clinical spectrum of respiratory symptoms. While many clinical risk factors such as concomitant chronic diseases play roles in the pathophysiology of COVID-19, genetic predisposition factors have not been widely studied. The aim of this study was, therefore, to evaluate the relationship between some singlenucleotide polymorphisms (SNPs) of the human genes TYK2 and ACE2 and the severity of SARS-CoV-2 infection. Genomic DNA was isolated from 200 SARS-CoV-2-infected individuals with severe (n = 100) or mild (n = 100) disease. Owing to the importance of ACE2 and TYK2 genes in regulating the immune response to SARS-CoV-2 infection, TYK2 gene SNPs, i.e. rs2304255, rs2304256, rs12720270, and rs12720354 and ACE2 rs382746 variants, were genotyped in the samples. To confirm the results, the expression of different TYK2 genotypes was investigated using real-time PCR. The presence of the nucleotide T at the locus rs2304255 was shown to be a risk factor linked to disease severity (OR [95% CI] = 3.2485 [2.1554–4.8961]). Similarly, the presence of A at the locus rs12720354 increased the risk of severity (OR [95% CI]) = 3.9721 [2.6075–6.0509]). In contrast, the presence of A at the loci rs2304256 and rs12720270 was observed to reduce the severity risk (OR [95% CI] = 0.2495 [0.1642–0.3793] and 0.1668 [0.1083–0.2569], respectively). Real-time PCR results also demonstrated that the expression level of TYK2 in samples with the TT genotype of rs2304255 and the AA genotype of rs12720354 and in samples with the GG genotype of rs12720207 was significantly lower than in those with other genotypes. The results of this study suggest that TYK2 SNPs might be utilized to identify individuals who are at risk for severe COVID-19, in order to better manage their health care. It is predicted that the presence of some alleles (T in rs2304255, A in rs12720354, and G in rs12720207) of TYK2 can affect COVID-19 severity by reducing TYK2 expression and thereby affecting the regulatory role of TYK2 in the immune response.
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spelling pubmed-100359682023-03-24 TYK2 single-nucleotide variants associated with the severity of COVID-19 disease Zabihi Rizi, Fateme Ghorbani, Atousa Zahtab, Parnia Darbaghshahi, Niloufar Naderi Ataee, Nioosha Pourhamzeh, Pardis Hamzei, Behnaz Dolatabadi, Nasrin Fatahi Zamani, Atefeh Hooshmand, Masoud Arch Virol Original Article Coronavirus disease 2019 (COVID-19) is a lethal disease caused by the coronavirus SARS-CoV-2, which can result in a broad clinical spectrum of respiratory symptoms. While many clinical risk factors such as concomitant chronic diseases play roles in the pathophysiology of COVID-19, genetic predisposition factors have not been widely studied. The aim of this study was, therefore, to evaluate the relationship between some singlenucleotide polymorphisms (SNPs) of the human genes TYK2 and ACE2 and the severity of SARS-CoV-2 infection. Genomic DNA was isolated from 200 SARS-CoV-2-infected individuals with severe (n = 100) or mild (n = 100) disease. Owing to the importance of ACE2 and TYK2 genes in regulating the immune response to SARS-CoV-2 infection, TYK2 gene SNPs, i.e. rs2304255, rs2304256, rs12720270, and rs12720354 and ACE2 rs382746 variants, were genotyped in the samples. To confirm the results, the expression of different TYK2 genotypes was investigated using real-time PCR. The presence of the nucleotide T at the locus rs2304255 was shown to be a risk factor linked to disease severity (OR [95% CI] = 3.2485 [2.1554–4.8961]). Similarly, the presence of A at the locus rs12720354 increased the risk of severity (OR [95% CI]) = 3.9721 [2.6075–6.0509]). In contrast, the presence of A at the loci rs2304256 and rs12720270 was observed to reduce the severity risk (OR [95% CI] = 0.2495 [0.1642–0.3793] and 0.1668 [0.1083–0.2569], respectively). Real-time PCR results also demonstrated that the expression level of TYK2 in samples with the TT genotype of rs2304255 and the AA genotype of rs12720354 and in samples with the GG genotype of rs12720207 was significantly lower than in those with other genotypes. The results of this study suggest that TYK2 SNPs might be utilized to identify individuals who are at risk for severe COVID-19, in order to better manage their health care. It is predicted that the presence of some alleles (T in rs2304255, A in rs12720354, and G in rs12720207) of TYK2 can affect COVID-19 severity by reducing TYK2 expression and thereby affecting the regulatory role of TYK2 in the immune response. Springer Vienna 2023-03-23 2023 /pmc/articles/PMC10035968/ /pubmed/36959416 http://dx.doi.org/10.1007/s00705-023-05729-2 Text en © The Author(s), under exclusive licence to Springer-Verlag GmbH Austria, part of Springer Nature 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Zabihi Rizi, Fateme
Ghorbani, Atousa
Zahtab, Parnia
Darbaghshahi, Niloufar Naderi
Ataee, Nioosha
Pourhamzeh, Pardis
Hamzei, Behnaz
Dolatabadi, Nasrin Fatahi
Zamani, Atefeh
Hooshmand, Masoud
TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
title TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
title_full TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
title_fullStr TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
title_full_unstemmed TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
title_short TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
title_sort tyk2 single-nucleotide variants associated with the severity of covid-19 disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10035968/
https://www.ncbi.nlm.nih.gov/pubmed/36959416
http://dx.doi.org/10.1007/s00705-023-05729-2
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