Distinctive features of IncRNA and mRNA between severe and mild patients with influenza a (H1N1) virus pneumonia

Dangsheng Xiao1, Jinyou Li1, Xuehui Zhao2

  • 1Zhejiang Provincial Key Laboratory for Diagnosis and Treatment of Aging and Physic-Chemical Injury Diseases, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Abstract

Insights

This study identified 3655 differentially expressed genes (DEGs) in severe versus mild Influenza A virus H1N1 infections. These DEGs, linked to ribosome assembly and MAPK signaling, may serve as biomarkers for disease severity.

Area of Science:

  • Molecular Biology
  • Genomics
  • Infectious Diseases

Background:

  • Influenza A virus H1N1 causes significant respiratory illness with potential for severe complications.
  • Understanding molecular differences between severe and mild H1N1 cases is crucial for identifying pathogenesis insights and therapeutic targets.

Purpose of the Study:

  • To investigate transcriptional differences in mRNA and lncRNA between severe and mild H1N1 infection cases.
  • To identify potential molecular markers associated with H1N1 infection severity.

Main Methods:

  • Transcriptome sequencing of peripheral blood mononuclear cells (PBMCs) from patients with severe and mild H1N1 infection.
  • Analysis of mRNA and lncRNA transcriptional profiles to detect differential gene expression patterns.

Main Results:

  • Identified 3655 differentially expressed genes (DEGs) between severe and mild H1N1 cases, comprising 3147 protein-coding genes and 508 lncRNAs.
  • Associated DEGs with critical cellular functions, including ribosome assembly and the MAPK signaling pathway.

Conclusions:

  • Differentially expressed genes related to ribosome assembly and MAPK signaling may act as potential biomarkers for H1N1 infection severity.
  • Findings provide insights into the transcriptomic features of severe H1N1 pathogenesis, aiding differential diagnosis and therapeutic target identification.