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Molecular Pathogenesis and Immune Evasion of Vesicular Stomatitis New Jersey Virus Inferred from Genes Expression Changes in Infected Porcine Macrophages

Journal Article · · Pathogens
 [1];  [2];  [3];  [3]
  1. US Dept. of Agriculture (USDA), Greenport, NY (United States). ARS-Plum Island Animal Disease Center; Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States); OSTI
  2. US Dept. of Agriculture (USDA), Greenport, NY (United States). ARS-Plum Island Animal Disease Center; Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States)
  3. US Dept. of Agriculture (USDA), Greenport, NY (United States). ARS-Plum Island Animal Disease Center
The molecular mechanisms associated with the pathogenesis of vesicular stomatitis virus (VSV) in livestock remain poorly understood. Several studies have highlighted the relevant role of macrophages in controlling the systemic dissemination of VSV during infection in different animal models, including mice, cattle, and pigs. To gain more insight into the molecular mechanisms used by VSV to impair the immune response in macrophages, we used microarrays to determine the transcriptomic changes produced by VSV infection in primary cultures of porcine macrophages. The results indicated that VSV infection induced the massive expression of multiple anorexic, pyrogenic, proinflammatory, and immunosuppressive genes. Overall, the interferon (IFN) response appeared to be suppressed, leading to the absence of stimulation of interferon-stimulated genes (ISG). Interestingly, VSV infection promoted the expression of several genes known to downregulate the expression of IFNβ. This represents an alternate mechanism for VSV control of the IFN response, beyond the recognized mechanisms mediated by the matrix protein. Although there was no significant differential gene expression in macrophages infected with a highly virulent epidemic strain compared to a less virulent endemic strain, the endemic strain consistently induced higher expression of all upregulated cytokines and chemokines. Collectively, this study provides novel insights into VSV molecular pathogenesis and immune evasion that warrant further investigation.
Research Organization:
Oak Ridge Inst. for Science and Education (ORISE), Oak Ridge, TN (United States)
Sponsoring Organization:
USDA; USDOE Office of Science (SC)
Grant/Contract Number:
SC0014664
OSTI ID:
1904965
Journal Information:
Pathogens, Journal Name: Pathogens Journal Issue: 9 Vol. 10; ISSN 2076-0817
Publisher:
MDPICopyright Statement
Country of Publication:
United States
Language:
English

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  • Shaheen, Zachary R.; Christmann, Benjamin S.; Stafford, Joshua D.
  • American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, Vol. 316, Issue 5 https://doi.org/10.1152/ajpregu.00019.2019
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