Association between -221 X/Y polymorphism of mannose-binding lectin (MBL) gene and susceptibility to HTLV-1 infection among people from an endemic region in the Northeast of Iran

Infect Genet Evol. 2019 Nov:75:104015. doi: 10.1016/j.meegid.2019.104015. Epub 2019 Aug 22.

Abstract

Background: The role of (MBL) gene single nucleotide polymorphisms (SNPs) has been well documented in susceptibility to several infectious diseases. This study aimed to investigate the association between two MBL promoter variants, -550 H/L and -221 X/Y, and susceptibility to HTLV-1 infection.

Methods: A total of 153 subjects infected with HTLV-1 and 169 healthy controls were recruited. SSP-PCR method was applied to genotype -550 H/L and -221 X/Y polymorphisms. Associations between genotypes or alleles and susceptibility to HTLV-1 infection were analyzed by Pearson's Chi-Square. p ≤ .05 was considered statistically significant.

Results: Statistical analysis revealed significant differences between the two groups in the -221 position (χ2 = 19.709; p = .000). The MBL YX genotype was significantly associated with increased susceptibility to HTLV-1 (OR = 2.73, %95 CI = 1.74-4.30). Combined genotype of the two loci showed that the HYHX genotype (OR = 2.20, 95% CI = 1.95-2.48) and LYLX (OR = 1.97, 95% CI = 1.13-3.45) were associated with an increased risk of HTLV-1 infection.

Conclusion: Our results represent the importance of -221 X > Y variants in acquisition of HTLV-1 as this is the case for several other viral and bacterial infections.

Keywords: HTLV-1; Mannose-binding lectin; Promoter polymorphism; rs7096206.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Substitution
  • Case-Control Studies
  • Female
  • Genetic Association Studies
  • Genetic Predisposition to Disease*
  • Genotype
  • HTLV-I Infections / diagnosis
  • HTLV-I Infections / etiology*
  • Human T-lymphotropic virus 1*
  • Humans
  • Iran / epidemiology
  • Male
  • Mannose-Binding Lectin / genetics*
  • Odds Ratio
  • Polymorphism, Single Nucleotide*
  • Promoter Regions, Genetic

Substances

  • MBL2 protein, human
  • Mannose-Binding Lectin