home > bioproject > PRJEB15047
identifier PRJEB15047
type bioproject
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title RNA-SEQ BASED TRANSCRIPTOME ANALYSIS OF THE INTERFERON HOST RESPONSE UPON VACCINIA VIRUS INFECTION.
description Evasion of interferon (IFN)-mediated antiviral immunity is critical for a successful virus infection. So poxviruses have evolved diverse molecular strategies to counteract IFN host response activity at different levels. In the case of VACV, one of these is to encode a soluble IFN-α/β binding protein (IFNBP) which located at cell surface binds type-I IFN molecules with high affinity, preventing their interaction with the host cell receptor. In the present work, we have dissected by RNA-Seq the viral modulation of the IFN-based host response at the transcriptional level. RNA from VACV-WR infected murine L929 cells was extracted at 0, 4 and 9 h post-infection in the absence or presence of IFN-alpha and/or recombinant purified IFNBP. To examine the immunomodulatory activity of the IFNBP, the transcriptome analysis from cells infected with a VACV-WR deletion mutant lacking the IFNBP was included. RNA libraries were prepared and paired-end sequencing performed using the Illumina HiSeq system. After removal of low quality reads, over 100M high quality reads per sample were obtained, which could be mapped either to the VACV or mus musculus strain C57/BL6 reference genomes. Then, analysis of differential gene expression and GO pathway enrichment analysis were performed to reveal the molecular mechanisms of action. We could validate the experiment identifying the expected transcriptional changes after IFN-induced signalling in the transcriptome from IFN-treated cells. The addition of recombinant IFNBP to cells prior to IFN completely reverted these IFN-induced changes to basal levels found in untreated cells. The addition of recombinant IFNBP to cell cultures did not result in significant activation of any cellular pathway, in spite of the IFNBP attaching to the cell surface. Finally, to detect and analyze those changes in host gene expression after viral infection of cultures, treated or not with IFN, analysis of differential gene expression and GO pathway enrichment analysis were performed and will be discussed.
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dbXrefs
sra-run  ERR1577163ERR1577164ERR1577165ERR1577166ERR1577167ERR1577168ERR1577169ERR1577170ERR1577171ERR1577172 More
sra-submission  ERA688124
biosample  SAMEA4368837SAMEA4368836SAMEA4368838SAMEA4368828SAMEA4368840SAMEA4368839SAMEA4368833SAMEA4368829SAMEA4368830SAMEA4368832 More
sra-study  ERP016737
sra-sample  ERS1280286ERS1280285ERS1280287ERS1280277ERS1280289ERS1280288ERS1280282ERS1280278ERS1280279ERS1280281 More
sra-experiment  ERX1647919ERX1647920ERX1647921ERX1647922ERX1647923ERX1647924ERX1647925ERX1647926ERX1647927ERX1647928 More
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status public
visibility unrestricted-access
dateCreated 2017-05-06T00:00:00Z
dateModified 2017-05-06T00:00:00Z
datePublished