Transcriptomic analyses suggest that mucopolysaccharidosis patients may be less susceptible to COVID-19

FEBS Lett. 2020 Oct;594(20):3363-3370. doi: 10.1002/1873-3468.13908. Epub 2020 Sep 6.

Abstract

We used transcriptomic (RNA-seq) analyses to determine whether patients suffering from all types and subtypes of mucopolysaccharidosis (MPS), a severe inherited metabolic disease, may be more susceptible to coronavirus disease 2019 (COVID-19). The expression levels of genes encoding proteins potentially involved in SARS-CoV-2 development were estimated in MPS cell lines. Four genes (GTF2F2, RAB18, TMEM97, PDE4DIP) coding for proteins potentially facilitating virus development were down-regulated, while two genes (FBN1, MFGE8), the products of which potentially interfere with virus propagation, were up-regulated in most MPS types. Although narrowing of respiratory tract and occurrence of thick mucus, characteristic of MPS, are risk factors for COVID-19, transcriptomic analyses suggest that MPS cells might be less, rather than more, susceptible to SARS-CoV-2 infection.

Keywords: COVID-19; mucopolysaccharidosis; transcriptomic analyses.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Angiotensin-Converting Enzyme 2 / genetics
  • Angiotensin-Converting Enzyme 2 / metabolism
  • COVID-19 / genetics*
  • COVID-19 / metabolism
  • COVID-19 / pathology
  • COVID-19 / prevention & control
  • Cells, Cultured
  • Fibroblasts / metabolism
  • Fibroblasts / pathology
  • Fibroblasts / virology
  • Gene Expression Profiling
  • Genetic Predisposition to Disease
  • Humans
  • Mucopolysaccharidoses / genetics*
  • Mucopolysaccharidoses / metabolism
  • Mucopolysaccharidoses / pathology
  • Mucopolysaccharidoses / virology
  • SARS-CoV-2 / pathogenicity
  • SARS-CoV-2 / physiology*
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Transcriptome
  • Virus Internalization*

Substances

  • ACE2 protein, human
  • Angiotensin-Converting Enzyme 2
  • Serine Endopeptidases
  • TMPRSS2 protein, human