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SRX15285291: GSM6153670: 24h_Vneg_IFNb_M3 [15]; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 35.2M spots, 3.6G bases, 1.2Gb downloads

External Id: GSM6153670_r1
Submitted by: Department of Biochemistry, University of Lausanne
Study: Macrophage response towards infection by the Leishmania-viral endosymbiont duo
show Abstracthide Abstract
Leishmania RNA virus 1 (LRV1) is a double stranded RNA (dsRNA) virus found in some strains of the human protozoan parasite Leishmania, the causative agent of leishmaniasis, a neglected tropical disease. Interestingly, the presence of LRV1 inside Leishmania constitutes an important virulence factor which worsens leishmaniasis outcome in a type I interferon (type I IFN) dependent manner and contributes to treatment failure. Understanding how macrophages respond towards Leishmania alone or in combination with LRV1 as well as the role that type I IFNs may play during infection is fundamental to oversee new therapeutic strategies. In order to dissect the macrophage response towards infection, RNA Sequencing (RNA-Seq) was performed on murine wild-type (WT) bone marrow derived macrophages infected with Leishmania guyanensis (Lgy) devoid or not of LRV1 (LgyLRV1- and LgyLRV1+ respectively) or co-infected with LgyLRV1- and Lymphocytic choriomeningitis virus (LCMV) for 8 and 24 hours. Additionally, macrophages were treated with type I IFN (IFNa or IFNß) after 6 hours of infection. Overall design: Transcriptomic analysis of WT bone marrow derived macrophages (BMDMs) under 5 different conditions and 2 time points. Total number of samples 30, each condition was done in triplicates.
Sample: 24h_Vneg_IFNb_M3 [15]
SAMN28448329 • SRS13015107 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM6153670
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: BMDMs were cleared out of supernatants and lysed with 350 µl RLT buffer (Qiagen) supplemented with 40 mM DTT (Dithiotreitol) for RNA extraction. Plates were then frozen at -80°C until the RNA purification. The RNA samples were purified with the RNeasy Plus Mini Kit (Qiagen) following the manufacturer's instructions. Purified RNA was eluted with 30 µl RNase-free water (Qiagen). Library preparation and sequencing were performed at the Lausanne Genomic Technologies Facility (GTF), University of Lausanne (UNIL), Switzerland
Runs: 1 run, 35.2M spots, 3.6G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR1922139235,164,4263.6G1.2Gb2022-05-19

ID:
21816616

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