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Updated: Feb 6, 2026

Multiplexed Analysis of Retinal Gene Expression and Chromatin Accessibility Using scRNA-Seq and scATAC-Seq
Published on: March 12, 2021
Identification of potential key genes associated with severe pneumonia using mRNA-seq
Cong Feng1, He Huang2, Sai Huang1,3
1Department of Emergency, Chinese PLA General Hospital, Beijing 100853, P.R. China.
Abstract:
This study aimed to identify the potential key genes associated with severe pneumonia using mRNA-seq. Nine peripheral blood samples from patients with severe pneumonia alone (SP group, n=3) and severe pneumonia accompanied with chronic obstructive pulmonary disease (COPD; CSP group, n=3), as well as volunteers without pneumonia (control group, n=3) underwent mRNA-seq. Based on the sequencing data, differentially expressed genes (DEGs) were identified by Limma package. Following the pathway enrichment analysis of DEGs, the genes that were differentially expressed in the SP and CSP groups were selected for pathway enrichment analysis and coexpression analysis. In addition, potential genes related to pneumonia were identified based on the information in the Comparative Toxicogenomics Database. In total, 645 and 528 DEGs were identified in the SP and CSP groups, respectively, compared with the normal controls. Among these DEGs, 88 upregulated genes and 80 downregulated genes were common between the two groups. The functions of the common DEGs were similar to those of the DEGs in the SP group. In the coexpression network, the commonly downregulated genes (including ND1, ND3, ND4L, and ND6) and the commonly upregulated genes (including TSPY6P and CDY10P) exhibited a higher degree. In addition, 131 DEGs (including ND1, ND3, ND6, MIR449A and TAS2R43) were predicted to be potential pneumonia-related genes. In conclusion, the present study demonstrated that the common DEGs may be associated with the progression of severe pneumonia.
Insights
This study identified key genes linked to severe pneumonia progression. Common differentially expressed genes (DEGs) between severe pneumonia and severe pneumonia with COPD patients may play a crucial role.
Area of Science:
- Genomics
- Respiratory Medicine
- Bioinformatics
Background:
- Severe pneumonia is a significant health concern.
- Understanding the genetic basis of severe pneumonia, especially when co-occurring with chronic obstructive pulmonary disease (COPD), is crucial for effective treatment.
- Gene expression profiling offers insights into disease mechanisms.
Purpose of the Study:
- To identify key genes associated with severe pneumonia using mRNA sequencing.
- To investigate gene expression differences in patients with severe pneumonia alone (SP) versus severe pneumonia with COPD (CSP) compared to healthy controls.
- To explore potential pneumonia-related genes through pathway and coexpression analyses.
Main Methods:
- mRNA sequencing (mRNA-seq) was performed on peripheral blood samples from SP, CSP, and control groups.
- Differentially expressed genes (DEGs) were identified using the Limma package.
- Pathway enrichment, coexpression network, and Comparative Toxicogenomics Database analyses were conducted on DEGs.
Main Results:
- 645 DEGs were found in the SP group and 528 DEGs in the CSP group compared to controls.
- 88 upregulated and 80 downregulated genes were common to both SP and CSP groups.
- Commonly downregulated genes (e.g., ND1, ND3, ND6) and upregulated genes (e.g., TSPY6P, CDY10P) showed high network degrees. 131 DEGs were predicted as pneumonia-related.
Conclusions:
- Commonly differentially expressed genes are potentially associated with the progression of severe pneumonia.
- Specific downregulated and upregulated genes identified in this study may serve as biomarkers or therapeutic targets.
- Further research into these key genes could elucidate severe pneumonia pathogenesis.
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