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Title: Gene expression analysis of whole blood RNA from pigs infected with low and high pathogenic African swine fever viruses

Abstract

African swine fever virus (ASFV) is a macrophage-tropic virus responsible for ASF, a transboundary disease that threatens swine production world-wide. Since there are no vaccines available to control ASF after an outbreak, obtaining an understanding of the virus-host interaction is important for developing new intervention strategies. In this study, a whole transcriptomic RNA-Seq method was used to characterize differentially expressed genes in pigs infected with a low pathogenic ASFV isolate, OUR T88/3 (OURT), or the highly pathogenic Georgia 2007/1 (GRG). After infection, pigs infected with OURT showed no or few clinical signs; whereas, GRG produced clinical signs consistent with acute ASF. RNA-Seq detected the expression of ASFV genes from the whole blood of the GRG, but not the OURT pigs, consistent with the pathotypes of these strains and the replication of GRG in circulating monocytes. Even though GRG and OURT possess different pathogenic properties, there was significant overlap in the most upregulated host genes. A small number of differentially expressed microRNAs were also detected in GRG and OURT pigs. These data confirm previous studies describing the response of macrophages and lymphocytes to ASFV infection, as well as reveal unique gene pathways upregulated in response to infection with GRG.

Authors:
 [1];  [2];  [3];  [4];  [1];  [4];  [4];  [4];  [4];  [4];  [2];  [4]
  1. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Physical & Life Sciences Directorate
  2. Kansas State Univ., Manhattan, KS (United States). Department of Diagnostic Medicine and Pathobiology
  3. Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Computation Directorate
  4. CSIRO Australian Animal Health Laboratory, Geelong, Victoria (Australia)
Publication Date:
Research Org.:
Lawrence Livermore National Laboratory (LLNL), Livermore, CA (United States)
Sponsoring Org.:
USDOE
OSTI Identifier:
1395491
Grant/Contract Number:  
AC52-07NA27344
Resource Type:
Accepted Manuscript
Journal Name:
Scientific Reports
Additional Journal Information:
Journal Volume: 7; Journal Issue: 1; Journal ID: ISSN 2045-2322
Publisher:
Nature Publishing Group
Country of Publication:
United States
Language:
English
Subject:
59 BASIC BIOLOGICAL SCIENCES; 60 APPLIED LIFE SCIENCES; Gene expression; Infectious-diesease diagnostics; Virology

Citation Formats

Jaing, Crystal, Rowland, Raymond R. R., Allen, Jonathan E., Certoma, Andrea, Thissen, James B., Bingham, John, Rowe, Brenton, White, John R., Wynne, James W., Johnson, Dayna, Gaudreault, Natasha N., and Williams, David T. Gene expression analysis of whole blood RNA from pigs infected with low and high pathogenic African swine fever viruses. United States: N. p., 2017. Web. doi:10.1038/s41598-017-10186-4.
Jaing, Crystal, Rowland, Raymond R. R., Allen, Jonathan E., Certoma, Andrea, Thissen, James B., Bingham, John, Rowe, Brenton, White, John R., Wynne, James W., Johnson, Dayna, Gaudreault, Natasha N., & Williams, David T. Gene expression analysis of whole blood RNA from pigs infected with low and high pathogenic African swine fever viruses. United States. https://doi.org/10.1038/s41598-017-10186-4
Jaing, Crystal, Rowland, Raymond R. R., Allen, Jonathan E., Certoma, Andrea, Thissen, James B., Bingham, John, Rowe, Brenton, White, John R., Wynne, James W., Johnson, Dayna, Gaudreault, Natasha N., and Williams, David T. Thu . "Gene expression analysis of whole blood RNA from pigs infected with low and high pathogenic African swine fever viruses". United States. https://doi.org/10.1038/s41598-017-10186-4. https://www.osti.gov/servlets/purl/1395491.
@article{osti_1395491,
title = {Gene expression analysis of whole blood RNA from pigs infected with low and high pathogenic African swine fever viruses},
author = {Jaing, Crystal and Rowland, Raymond R. R. and Allen, Jonathan E. and Certoma, Andrea and Thissen, James B. and Bingham, John and Rowe, Brenton and White, John R. and Wynne, James W. and Johnson, Dayna and Gaudreault, Natasha N. and Williams, David T.},
abstractNote = {African swine fever virus (ASFV) is a macrophage-tropic virus responsible for ASF, a transboundary disease that threatens swine production world-wide. Since there are no vaccines available to control ASF after an outbreak, obtaining an understanding of the virus-host interaction is important for developing new intervention strategies. In this study, a whole transcriptomic RNA-Seq method was used to characterize differentially expressed genes in pigs infected with a low pathogenic ASFV isolate, OUR T88/3 (OURT), or the highly pathogenic Georgia 2007/1 (GRG). After infection, pigs infected with OURT showed no or few clinical signs; whereas, GRG produced clinical signs consistent with acute ASF. RNA-Seq detected the expression of ASFV genes from the whole blood of the GRG, but not the OURT pigs, consistent with the pathotypes of these strains and the replication of GRG in circulating monocytes. Even though GRG and OURT possess different pathogenic properties, there was significant overlap in the most upregulated host genes. A small number of differentially expressed microRNAs were also detected in GRG and OURT pigs. These data confirm previous studies describing the response of macrophages and lymphocytes to ASFV infection, as well as reveal unique gene pathways upregulated in response to infection with GRG.},
doi = {10.1038/s41598-017-10186-4},
journal = {Scientific Reports},
number = 1,
volume = 7,
place = {United States},
year = {Thu Aug 31 00:00:00 EDT 2017},
month = {Thu Aug 31 00:00:00 EDT 2017}
}

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55
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journal, March 2001

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CDRK and DRK1 K+ channels have contrasting localizations in sensory systems
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journal, November 2014


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RNA-seq reveals downregulated osteochondral genes potentially related to tibia bacterial chondronecrosis with osteomyelitis in broilers
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Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages
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