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RNA sequencing analyses of gene expressions in a canine macrophages cell line DH82 infected with canine distemper virus.

Identifieur interne : 000075 ( Main/Exploration ); précédent : 000074; suivant : 000076

RNA sequencing analyses of gene expressions in a canine macrophages cell line DH82 infected with canine distemper virus.

Auteurs : Xuexing Zheng [République populaire de Chine] ; Yelei Zhu [République populaire de Chine] ; Zhongxin Zhao [République populaire de Chine] ; Lina Yan [République populaire de Chine] ; Tong Xu [République populaire de Chine] ; Xianwei Wang [République populaire de Chine] ; Hongbin He [République populaire de Chine] ; Xianzhu Xia [République populaire de Chine] ; Wenwen Zheng [République populaire de Chine] ; Xianghong Xue [République populaire de Chine]

Source :

RBID : pubmed:31982604

Abstract

Virulent morbillivirus infections, including Meals Virus (MeV) and Canine Distemper Virus (CDV), caused severe immune suppression and leukopenia, while attenuated vaccine strains developed protective host immune responses. However, the detailed molecular foundations of host antiviral responses were poorly characterized. In order to better understand the interactions between attenuated vaccine and host antiviral responses, the global gene expression changes in CDV-11-infected DH82 cells, a macrophage-derived cell line from canine, were investigated by transcriptomic analysis, and portions of results were confirmed with quantitative RT-PCR. The results exhibited that 372 genes significantly up-regulated (p < .01) and 119 genes were significantly down-regulated (p < .01) in CDV-infected macrophages DH82 at 48 h p.i.. The enriched functions of the significantly up-regulated (p < .01) genes were closely associated with interferon stimulated genes (ISGs), chemokine genes and pro-inflammatory factor genes. Gene ontology and pathway analysis of differentially expressed genes (DEGs) revealed that the most significantly involved pathways in CDV-infected DH82 cells were NF-κB and TNF signaling pathway, cytokine-cytokine receptor interaction, and pathogen associated molecular patterns (PAMPs), such as Toll-like, RIG-I-like and NOD-like receptor signalings. Thus, the findings indicated that pattern recognition receptors (PRRs) possibly mediated host innate and protective antiviral immune responses in CDV-11 infected DH82 cells.

DOI: 10.1016/j.meegid.2020.104206
PubMed: 31982604


Affiliations:


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<div type="abstract" xml:lang="en">Virulent morbillivirus infections, including Meals Virus (MeV) and Canine Distemper Virus (CDV), caused severe immune suppression and leukopenia, while attenuated vaccine strains developed protective host immune responses. However, the detailed molecular foundations of host antiviral responses were poorly characterized. In order to better understand the interactions between attenuated vaccine and host antiviral responses, the global gene expression changes in CDV-11-infected DH82 cells, a macrophage-derived cell line from canine, were investigated by transcriptomic analysis, and portions of results were confirmed with quantitative RT-PCR. The results exhibited that 372 genes significantly up-regulated (p < .01) and 119 genes were significantly down-regulated (p < .01) in CDV-infected macrophages DH82 at 48 h p.i.. The enriched functions of the significantly up-regulated (p < .01) genes were closely associated with interferon stimulated genes (ISGs), chemokine genes and pro-inflammatory factor genes. Gene ontology and pathway analysis of differentially expressed genes (DEGs) revealed that the most significantly involved pathways in CDV-infected DH82 cells were NF-κB and TNF signaling pathway, cytokine-cytokine receptor interaction, and pathogen associated molecular patterns (PAMPs), such as Toll-like, RIG-I-like and NOD-like receptor signalings. Thus, the findings indicated that pattern recognition receptors (PRRs) possibly mediated host innate and protective antiviral immune responses in CDV-11 infected DH82 cells.</div>
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<name sortKey="Wang, Xianwei" sort="Wang, Xianwei" uniqKey="Wang X" first="Xianwei" last="Wang">Xianwei Wang</name>
<name sortKey="Xia, Xianzhu" sort="Xia, Xianzhu" uniqKey="Xia X" first="Xianzhu" last="Xia">Xianzhu Xia</name>
<name sortKey="Xu, Tong" sort="Xu, Tong" uniqKey="Xu T" first="Tong" last="Xu">Tong Xu</name>
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<name sortKey="Zhao, Zhongxin" sort="Zhao, Zhongxin" uniqKey="Zhao Z" first="Zhongxin" last="Zhao">Zhongxin Zhao</name>
<name sortKey="Zheng, Wenwen" sort="Zheng, Wenwen" uniqKey="Zheng W" first="Wenwen" last="Zheng">Wenwen Zheng</name>
<name sortKey="Zhu, Yelei" sort="Zhu, Yelei" uniqKey="Zhu Y" first="Yelei" last="Zhu">Yelei Zhu</name>
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