Investigation of MBL2 and NOS3 functional gene variants in suspected COVID-19 PCR (-) patients

Pathog Glob Health. 2022 May;116(3):178-184. doi: 10.1080/20477724.2021.1984726. Epub 2021 Sep 27.

Abstract

For COVID-19 (Coronavirus Disease-2019) cases, detecting host-based factors that predispose to infection is a very important research area. In this study, the aim is to investigate the MBL2 and NOS3 gene polymorphisms in COVID-19 patients with lung involvement, whose first nasopharyngeal PCR results were negative. Seventy-nine patients diagnosed with COVID-19 between April-June 2020 who were admitted to a university hospital, and 100 healthy controls were included. In the first statistical analysis performed between PCR-positive, CT-negative and PCR-negative, CT-positive patients; the AB of MBL2 genotype was significantly higher in the first group (p = 0.049). The B allele was also significantly higher in the same subgroup (p = 0.001). The absence of the AB genotype was found to increase the risk of CT positivity by 6.9 times. The AB genotype of MBL2 was higher in healthy controls (p = 0.006). The absence of the AB genotype was found to increase the risk of CT positivity; also, it can be used for early detection and isolation of patients with typical lung involvement who had enough viral loads, but whose initial PCR results were negative.

Keywords: COVID-19; CT; PCR; endothelial nitric oxide synthase (eNOS); mannose-binding lectin 2 (MBL2).

MeSH terms

  • COVID-19* / diagnosis
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Mannose-Binding Lectin* / genetics
  • Nitric Oxide Synthase Type III / genetics
  • Polymerase Chain Reaction / methods

Substances

  • MBL2 protein, human
  • Mannose-Binding Lectin
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III

Grants and funding

The author(s) reported there is no funding associated with the work featured in this article.