Association of IFIH1 and DDX58 genes polymorphism with susceptibility to COVID-19

Parisa Feizollahi1,2, Mohammad Hossein Zamanian3, Sara Falahi1

  • 1Department of Immunology, School of Medicine, Kermanshah University of Medical Sciences, Daneshgah Street, Shahid Shiroudi Boulevard, PO-Box: 6714869914, Kermanshah, Iran.

Insights

Genetic variations in the DDX58 gene, specifically the rs10813831 polymorphism, are linked to increased COVID-19 susceptibility. This innate immune system study highlights a potential genetic factor influencing disease severity in Iran.

Area of Science:

  • Immunology
  • Genetics
  • Virology

Background:

  • Pattern recognition receptors (RLRs) like RIG-I and MDA5 are crucial for innate immunity and viral detection.
  • Genetic variations in RLRs may influence COVID-19 severity.
  • RLR signaling plays a role in immune responses.

Purpose of the Study:

  • To investigate the association between specific single nucleotide polymorphisms (SNPs) in the IFIH1 and DDX58 genes and COVID-19 susceptibility.
  • To analyze the impact of these genetic variations on disease severity in the Kermanshah population, Iran.

Main Methods:

  • Genotyping of three SNPs (rs1990760 and rs3747517 in IFIH1; rs10813831 in DDX58) using PCR-RFLP.
  • Analysis of genomic DNA from 177 severe and 182 mild COVID-19 patients.
  • Statistical analysis of genotype frequencies and their association with COVID-19 susceptibility.

Main Results:

  • The AA genotype of DDX58 rs10813831 (G>A) was significantly associated with increased COVID-19 susceptibility (p=0.017, OR=2.593).
  • A significant association was also observed in the recessive model for rs10813831 (AA vs. GG+GA, p=0.003, OR=2.901).
  • No significant association was found between IFIH1 gene polymorphisms (rs1990760 and rs3747517) and COVID-19.

Conclusions:

  • The DDX58 rs10813831 polymorphism may be associated with COVID-19 severity in the studied Iranian population.
  • IFIH1 gene polymorphisms do not appear to be associated with COVID-19 susceptibility in this cohort.
  • Further research is warranted to elucidate the role of DDX58 in COVID-19 pathogenesis.

Related Concept Videos

Single Nucleotide Polymorphisms-SNPs01:05

Single Nucleotide Polymorphisms-SNPs

A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
15.3K
Exon Recombination02:32

Exon Recombination

The evolution of new genes is critical for speciation. Exon recombination, also known as exon shuffling or domain shuffling, is an important means of new gene formation. It is observed across vertebrates, invertebrates, and in some plants such as potatoes and sunflowers. During exon recombination, exons from the same or different genes recombine and produce new exon-intron combinations, which might evolve into new genes. 
Exon shuffling follows “splice frame rules.” Each exon...
3.6K
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
13.6K
Genetic Lingo01:11

Genetic Lingo

Overview
103.3K
Human Genetics01:28

Human Genetics

Human genetics provides a profound framework for understanding the interplay between genetic predispositions and human psychology. At the heart of this discipline lies the study of how genes influence physical traits, behaviors, and susceptibility to diseases. Each person carries a unique genetic code that subtly or significantly shapes their psychological and behavioral landscape.
The complex relationship between genetics and psychology is observable through common biological components such...
628