tetano
Editor, Senior Moderator
Arch Virol
. 2023 Mar 23;168(4):119.
doi: 10.1007/s00705-023-05729-2.
TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
Fateme Zabihi Rizi[SUP] 1 [/SUP], Atousa Ghorbani[SUP] 1 [/SUP], Parnia Zahtab[SUP] 2 [/SUP], Niloufar Naderi Darbaghshahi[SUP] 3 [/SUP], Nioosha Ataee[SUP] 3 [/SUP], Pardis Pourhamzeh[SUP] 4 [/SUP], Behnaz Hamzei[SUP] 5 [/SUP], Nasrin Fatahi Dolatabadi[SUP] 6 7 [/SUP], Atefeh Zamani[SUP] 5 [/SUP], Masoud Hooshmand[SUP] 8 [/SUP]
Affiliations
Abstract
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.
Keywords: ACE2; COVID-19; Genotyping; Predisposition; SNP; TYK2.
. 2023 Mar 23;168(4):119.
doi: 10.1007/s00705-023-05729-2.
TYK2 single-nucleotide variants associated with the severity of COVID-19 disease
Fateme Zabihi Rizi[SUP] 1 [/SUP], Atousa Ghorbani[SUP] 1 [/SUP], Parnia Zahtab[SUP] 2 [/SUP], Niloufar Naderi Darbaghshahi[SUP] 3 [/SUP], Nioosha Ataee[SUP] 3 [/SUP], Pardis Pourhamzeh[SUP] 4 [/SUP], Behnaz Hamzei[SUP] 5 [/SUP], Nasrin Fatahi Dolatabadi[SUP] 6 7 [/SUP], Atefeh Zamani[SUP] 5 [/SUP], Masoud Hooshmand[SUP] 8 [/SUP]
Affiliations
- PMID: 36959416
- DOI: 10.1007/s00705-023-05729-2
Abstract
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.
Keywords: ACE2; COVID-19; Genotyping; Predisposition; SNP; TYK2.