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Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages
Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages
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Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages
Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages

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Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages
Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages
Journal Article

Mechanisms of African swine fever virus pathogenesis and immune evasion inferred from gene expression changes in infected swine macrophages

2019
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Overview
African swine fever (ASF) is a swine disease caused by a large, structurally complex, double-stranded DNA virus, African swine fever virus (ASFV). In domestic pigs, acute infection by highly virulent ASF viruses causes hemorrhagic fever and death. Previous work has suggested that ASFV pathogenesis is primarily mediated by host cytokines produced by infected monocytes and macrophages. To better understand molecular mechanisms mediating virus pathogenesis and immune evasion, we used transcriptome analysis to identify gene expression changes after ASFV infection in ex vivo swine macrophages. Our results suggest that the cytokines of TNF family including FASLG, LTA, LTB, TNF, TNFSF4, TNFSF10, TNFSF13B and TNFSF18 are the major causative cytokine factors in ASF pathogenesis via inducing apoptosis. Other up-regulated proinflammatory cytokines (IL17F and interferons) and down-regulated anti-inflammatory cytokine (IL10) may also significantly contribute to ASF pathogenesis and cause excessive tissue inflammatory responses. The differential expression of genes also indicates that ASFV could evade both the innate and adaptive immune responses by (i) inhibiting MHC Class II antigen processing and presentation, (ii) avoiding CD8+ T effector cells and neutrophil extracellular traps via decreasing expression of neutrophil/CD8+ T effector cell-recruiting chemokines, (iii) suppressing M1 activation of macrophages, (iv) inducing immune suppressive cytokines, and (v) inhibiting the processes of macrophage autophagy and apoptosis. These results provide novel information to further investigate and better understand the mechanism of pathogenesis and immune evasion of this devastating swine disease.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject

Adaptive immunity

/ Adaptive Immunity - genetics

/ African swine fever

/ African Swine Fever - genetics

/ African Swine Fever - immunology

/ African Swine Fever - virology

/ African Swine Fever Virus - immunology

/ African Swine Fever Virus - pathogenicity

/ Analysis

/ Animal diseases

/ Animals

/ Antigen presentation

/ Antigen Presentation - genetics

/ Antigen processing

/ Antigens

/ Apoptosis

/ Asfarviridae

/ Autophagy

/ Autophagy-Related Proteins - genetics

/ Bacterial infections

/ Biochemistry

/ Biology and Life Sciences

/ CD8 antigen

/ Cell activation

/ Cell culture

/ Cells, Cultured

/ Chemokines

/ Chemokines - genetics

/ Cytokines

/ Cytokines - genetics

/ Death

/ Deoxyribonucleic acid

/ DNA

/ Domestic animals

/ Down-Regulation

/ Effector cells

/ Fever

/ Gene expression

/ Gene Expression Profiling

/ Genes

/ Genomes

/ Health aspects

/ Hemorrhage

/ Hemorrhagic fever

/ Hemorrhagic fevers

/ Hog cholera

/ Hogs

/ Immune evasion

/ Immune Evasion - genetics

/ Immune response

/ Immunity, Innate - genetics

/ Infection

/ Infections

/ Inflammation

/ Instrument industry (Equipment)

/ Interferon

/ Interleukin 1

/ Interleukin 10

/ Ligands

/ Livestock

/ Lymphocytes

/ Macrophage Activation - genetics

/ Macrophage Activation - immunology

/ Macrophages

/ Macrophages - immunology

/ Macrophages - virology

/ Major histocompatibility complex

/ Medicine and Health Sciences

/ Molecular modelling

/ Monocytes

/ Pathogenesis

/ Phagocytosis

/ Proteins

/ Receptors, Cytokine - genetics

/ Signal Transduction - genetics

/ Sus scrofa

/ Swine

/ Tumor necrosis factor

/ Up-Regulation

/ Virology

/ Virulence (Microbiology)

/ Viruses