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SRX9215329: GSM4809814: D152_FV; Equus caballus; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 40.6M spots, 3.1G bases, 1.1Gb downloads

Submitted by: NCBI (GEO)
Study: Pathogenesis, miR-122 gene-regulation, and protective immune responses after acute infection of horses with equine hepacivirus
show Abstracthide Abstract
Equine hepacivirus (EqHV) is the closest genetic relative of hepatitis C virus (HCV) and shares features of genome organization, hepatotropism, persistent infection, and the ability to cause liver disease. As such, EqHV studies are important both in order to understand equine liver disease, and as an outbred animal model for HCV pathogenesis and immune responses. Here, we characterize the natural history and immune response to EqHV infection. Seven horses were experimentally inoculated with EqHV, monitored for 6 months, and challenge inoculated with the same, and subsequently a divergent EqHV inoculum. Clearance was the primary outcome (6 of 7) and was associated with subclinical hepatitis characterized by lymphocytic infiltrate and individual hepatocyte necrosis. Seroconversion was delayed and antibody titers waned slowly. Resolving horses developed non-sterilizing immunity resulting in short duration of infection upon challenge. Unlike those observed in acutely HCV-infected patients, peripheral blood mononuclear cell responses in horses were minimal, although EqHV specific T-cells were identified. In contrast, an interferon stimulated gene signature was detected in the liver during EqHV infection, which is similar to acute HCV in humans. EqHV, similarly to HCV, is stimulated by direct binding of the liver-specific microRNA, miR-122. Surprisingly, we found that EqHV infection sequesters enough miR-122 to functionally affect gene regulation in the liver. This RNA-based mechanism thus could have consequences for pathology. Conclusion: EqHV infection in horses typically has an acute resolving course, and the immune response attenuates subsequent infections lasting for at least a year. This could have important implications to achieve the first goal of an HCV vaccine; to prevent chronicity while accepting acute resolving infection after challenge. Overall design: Seven horses were experimentally infected with equine hepacivirus (EqHV). RNA-Seq on PBMC and liver biopsies was performed pre-inoculation (PRE), during early acute infection (ACUTE), near seroconversion (SC), during falling viremia (FV), and at week 26 (POST). Six horses cleared the infection within the 26 weeks, and these were challenged with homologous serum (week 26) and heterologous serum (week 30-32). Additional challenge time points were included for horses that became positive during challenge and where sampling was possible (horses A, P, R for liver, horses A, N, P, R for PBMCs). One replicate was processed per horse per time point. PBMC libraries were poly-A selected; liver biopsy libraries were total RNA-seq (ribo-depletion).
Sample: D152_FV
SAMN16292904 • SRS7449229 • All experiments • All runs
Organism: Equus caballus
Library:
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Liver biopsies (~10 mg) fixed in RNA later were transferred into a MagNA Lyser Green Beads tube containing 1 mL cold TRIzol. Liver tissue was homogenized using a MagNA Lyser instrument (Roche) at 6500 rpm for 100 s with continuous cooling on ice every 20 s. PBMCs were directly lysed in TRIzol Reagent (Thermo Fisher Scientific). After addition of chloroform and centrifugation, the aqueous phase was mixed with 450 μL anhydrous ethanol and transferred to an RNA Clean & Concentrator-5 column (Zymo Research) for downstream RNA purification and concentration. The integrity of extracted RNA was analyzed on a 2100 bioanalyzer instrument using an RNA 6000 nano assay kit (Agilent Technologies). The standard Illumina TrueSeq stranded mRNA library preparation protocol was followed for PBMC mRNA library preparation, starting from 500 ng input RNA. For the liver samples, total RNA-Seq was prioritized over poly(A) selection in order to recover viral reads. Depletion of ribosomal RNA from 500 ng input RNA was achieved using the Ribo-off rRNA depletion kit (Vazyme) for which horse rRNA removal has been validated. Following purification of rRNA-depleted total RNA using VAHTS RNA clean beads (Vazyme), the RNA was eluted into elution buffer ELB (Illumina) for subsequent TrueSeq stranded mRNA library preparation, starting from the mRNA fragmentation step. Quality of DNA libraries was checked using a 2100 bioanalyzer instrument. The Qubit dsDNA High-Sensitivity Assay Kit (Thermo Fisher Scientific) was used to quantify DNA libraries in order to pool these in equimolar concentrations prior to denaturation. Pooled libraries were loaded on a NextSeq 500/550 v2.5 75 cycle flow-cell, and sequencing performed on a NextSeq benchtop sequencer (Illumina) at the Department of Clinical Microbiology (Hvidovre Hospital, Copenhagen). Data derived from two (PBMCs) or three (liver) independent deep-sequencing runs were pooled to ensure sufficient depth of sequencing coverage.
Experiment attributes:
GEO Accession: GSM4809814
Links:
Runs: 1 run, 40.6M spots, 3.1G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR1274287340,603,4373.1G1.1Gb2020-10-02

ID:
12002374

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