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


Journal

Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases
ISSN: 1567-7257
Titre abrégé: Infect Genet Evol
Pays: Netherlands
ID NLM: 101084138

Informations de publication

Date de publication:
06 2020
Historique:
received: 15 10 2019
revised: 18 01 2020
accepted: 22 01 2020
pubmed: 27 1 2020
medline: 17 6 2021
entrez: 27 1 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31982604
pii: S1567-1348(20)30038-1
doi: 10.1016/j.meegid.2020.104206
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

104206

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest No conflict of interest.

Auteurs

Xuexing Zheng (X)

Department of Virology, School of Public Health, Shandong University, Jinan 250012, China. Electronic address: zhengxx2513@163.com.

Yelei Zhu (Y)

Department of Virology, School of Public Health, Shandong University, Jinan 250012, China; Zhejiang Provincial Center for Disease Control and Prevention, Hangzhou 310051, China.

Zhongxin Zhao (Z)

Department of Virology, School of Public Health, Shandong University, Jinan 250012, China.

Lina Yan (L)

Department of Virology, School of Public Health, Shandong University, Jinan 250012, China.

Tong Xu (T)

Department of Virology, School of Public Health, Shandong University, Jinan 250012, China.

Xianwei Wang (X)

College of Life Sciences, Shandong University, Qingdao 266237, China.

Hongbin He (H)

College of Life Sciences, Shandong Normal University, Jinan 250014, China.

Xianzhu Xia (X)

Institute of Military Veterinary, Academy of Military Medical Sciences, Changchun 130122, China.

Wenwen Zheng (W)

Department of Virology, School of Public Health, Shandong University, Jinan 250012, China.

Xianghong Xue (X)

Division of Infectious Diseases of Special Animal, Institute of Special Animal and Plant Sciences, The Chinese Academy of Agricultural Sciences, Changchun 130122, China. Electronic address: red99.smile@163.com.

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Classifications MeSH