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Series GSE267021 Query DataSets for GSE267021
Status Public on May 21, 2024
Title Upregulation of inflammatory genes and pathways links obesity to severe COVID-19
Organisms Homo sapiens; Mus musculus
Experiment type Expression profiling by high throughput sequencing
Summary Obesity is a risk factor for developing severe COVID-19. However, the mechanism underlying obesity-accelerated COVID-19 remains unclear. Here, we report results from a study in which K18-hACE2 mice were fed an obesity-inducing western diet (WD) for over 3 months before intranasal infection with SARS-CoV2. After infection, the WD-fed K18-hACE2 mice lost more body weight and had more severe lung inflammation than normal chow (NC)-fed mice. Bulk RNAseq analysis of lungs and adipose tissue revealed that a diverse landscape of various immune cells, inflammatory markers, and pathways are upregulated in obese COVID-19 patients or the WD-fed K18-hACE2 mice when compared with their respective control groups. When compared with infected NC-fed mice in the lung, the infected WD-fed mice had upregulation of IL-6, a well-established marker for severe COVID-19. These results indicate that obesity-accelerated severe COVID-19 caused by SARS-CoV-2 infection in the K18-hACE2 mouse model can be used for dissecting the cellular and molecular mechanisms underlying pathogenesis. Furthermore, in the transcriptome analysis of the lung and adipose tissue obtained from deceased COVID-19 patients, we found upregulation of an array of genes and pathways associated with Inflammation. Both the K18-hACE2 mouse model and human COVID-19 patient data support a link between inflammation and an obesity-accelerated COVID-19 disease phenotype.
 
Overall design Comparitive gene expression analysis was done using bulk RNA-seq data comparing NC (normal chow) and WD (western diet to induce obesity) fed K18-hACE2 mice (adipose tissue and lung tissue) infected with SARS-CoV-2 (WA).
 
Contributor(s) Currey J, Qin X, Kolls JK, Shamima Khatun M
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Submission date May 08, 2024
Last update date May 21, 2024
Contact name Jay Kolls
Organization name Tulane University
Department Medicine
Lab Center for Translational Research in Infection and Inflammation
Street address 1430 Tulane Ave
City New Orleans
State/province LA
ZIP/Postal code 70112
Country USA
 
Platforms (2)
GPL30172 NextSeq 2000 (Mus musculus)
GPL30173 NextSeq 2000 (Homo sapiens)
Samples (24)
GSM8258593 3845 NC control l
GSM8258594 3846 NC control l
GSM8258595 3850 NC control l
Relations
BioProject PRJNA1109355

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE267021_Human_adipose.fpkm.txt.gz 602.8 Kb (ftp)(http) TXT
GSE267021_Human_adipose_cuffdiff.txt.gz 9.0 Kb (ftp)(http) TXT
GSE267021_Mouse_adipose.fpkm.txt.gz 612.1 Kb (ftp)(http) TXT
GSE267021_Mouse_adipose_cuffdiff.txt.gz 1.2 Kb (ftp)(http) TXT
GSE267021_Mouse_lung.fpkm.txt.gz 634.2 Kb (ftp)(http) TXT
GSE267021_Mouse_lung_cuffdiff.txt.gz 2.0 Kb (ftp)(http) TXT
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