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SRX4893353: GSM3431861: NA-03-3-SAL-HYP_S3; Taeniopygia guttata; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 27M spots, 1.9G bases, 712.6Mb downloads

Submitted by: NCBI (GEO)
Study: Transcriptomics of the Avian Immune Response in Hypothalamus, Spleen, and Red Blood Cells using RNA-seq
show Abstracthide Abstract
The goal of this research is to better understand the transcriptomic response in peripheral and neural tissue of zebra finch to lipopolysaccharide (LPS) challenge using RNASeq. The acute phase response (APR) is the initial reaction of the immune system to infection, and is triggered by pro-­inflammatory cytokines or exposure to immunogens, such as bacterial LPS. The APR also inhibits reproduction and induces a number of physiological and behavioral symptoms, such as fever and sickness behavior. Through RNAseq, we can better understand the transcriptomic response of genes that are important for response to infection in a wild species such as the Zebra Finch. This has implications for disease surveillance programs that monitor the epidemiology of zoonotic diseases, like avian influenza and West Nile virus. We examine the transcriptomic response in Zebra Finch spleen and hypothalumus to lipopolysaccharide (LPS) challenge; however, unlike mammals, with the exception of the camel, avian species have red blood cells that contain a nucleus, and will have gene regulation depending on the physiological needs of the organism. Therefore, we also took the opportunity to investigate the transcriptomic response of nucleated red blood cells to lipopolysaccharide (LPS) challenge. Overall design: A comparison was made of the transcriptomic response to lipopolysccharide challenge (Escherishia Coli) of Zebra Finch hypothalamus, spleen, and red blood cells using birds injected with saline as experimental controls.
Sample: NA-03-3-SAL-HYP_S3
SAMN10247611 • SRS3940337 • All experiments • All runs
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Birds were euthanized at 2 h post-injection and tissue samples collected. Red blood cells were extracted from the trunk.The density gradient media Polymorphprep (Axis-Shield) was used to separate whole blood into the components of plasma, mononuclear white blood cells, polymorphonuclear white blood cells, and red blood cells. This media allowed the removal of polymorphonuclear white blood cells that would remain within the red blood cell layer by other separation methods. Total RNA was isolated using an RNeasy Kit (Qiagen) with a modified protocol involving Trizol (Life Technologies). Libraries were prepared using the SMART-Seq v4 Ultra Low Input RNA Kit; Clonetech Catalog# 634889 and Nextera XT DNA; Illumina Catalog# FC-131-1024
Experiment attributes:
GEO Accession: GSM3431861
Links:
Runs: 1 run, 27M spots, 1.9G bases, 712.6Mb
Run# of Spots# of BasesSizePublished
SRR806499527,047,8351.9G712.6Mb2019-07-18

ID:
6593842

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