scholarly journals Transcriptome analysis of duck embryo fibroblasts for the dynamic response to duck tembusu virus infection and dual regulation of apoptosis genes

Aging ◽  
2020 ◽  
Vol 12 (17) ◽  
pp. 17503-17527
Author(s):  
Yuhong Pan ◽  
Anchun Cheng ◽  
Xingcui Zhang ◽  
Mingshu Wang ◽  
Shun Chen ◽  
...  

2018 ◽  
Vol 19 (8) ◽  
pp. 2328 ◽  
Author(s):  
Guanliu Yu ◽  
Yun Lin ◽  
Yi Tang ◽  
Youxiang Diao

Duck is a major waterfowl species in China, providing high-economic benefit with a population of up to 20–30 billion per year. Ducks are commonly affected by severe diseases, including egg-drop syndrome caused by duck Tembusu virus (DTMUV). The immune mechanisms against DTMUV invasion and infection remain poorly understood. In this study, duck embryo fibroblasts (DEFs) were infected with DTMUV and harvested at 12 and 24 h post-infection (hpi), and their genomes were sequenced. In total, 911 (764 upregulated and 147 downregulated genes) and 3008 (1791 upregulated and 1217 downregulated) differentially expressed genes (DEGs) were identified at 12 and 24 hpi, respectively. Kyoto Encyclopedia of Genes and Genomes enrichment analysis revealed that DEGs were considerably enriched in immune-relevant pathways, including Toll-like receptor signaling pathway, Cytosolic DNA-sensing pathway, RIG-I-like receptor signaling pathway, Chemokine signaling pathway, NOD-like receptor signaling pathway, and Hematopoietic cell lineage at both time points. The key DEGs in immune system included those of the cytokines (IFN α2, IL-6, IL-8L, IL-12B, CCR7, CCL19, and CCL20), transcription factors or signaling molecules (IRF7, NF-κB, STAT1, TMEM173, and TNFAIP3), pattern recognition receptors (RIG-I and MDA5), and antigen-presenting proteins (CD44 and CD70). This suggests DTMUV infection induces strong proinflammatory/antiviral effects with enormous production of cytokines. However, these cytokines could not protect DEFs against viral attack. Our data revealed valuable transcriptional information regarding DTMUV-infected DEFs, thereby broadening our understanding of the immune response against DTMUV infection; this information might contribute in developing strategies for controlling the prevalence of DTMUV infection.



2021 ◽  
Vol 12 ◽  
Author(s):  
Peng Zhou ◽  
Lei Ma ◽  
Zaixiao Rao ◽  
Yaqian Li ◽  
Huijun Zheng ◽  
...  

Duck Tembusu virus (DTMUV) is an emerging pathogenic flavivirus that has caused a substantial drop in egg production and severe neurological disorders in domestic waterfowl. Several studies have revealed that viral proteins encoded by DTMUV antagonize host IFN-mediated antiviral responses to facilitate virus replication. However, the role of host gene expression regulated by DTMUV in innate immune evasion remains largely unknown. Here, we utilized a stable isotope labeling with amino acids in cell culture (SILAC)-based proteomics analysis of DTMUV-infected duck embryo fibroblasts (DEFs) to comprehensively investigate host proteins involved in DTMUV replication and innate immune response. A total of 250 differentially expressed proteins were identified from 2697 quantified cellular proteins, among which duck interferon-induced protein 35 (duIFI35) was dramatically up-regulated due to DTMUV infection in DEFs. Next, we demonstrated that duIFI35 expression promoted DTMUV replication and impaired Sendai virus-induced IFN-β production. Moreover, duIFI35 was able to impede duck RIG-I (duRIG-I)-induced IFN-β promoter activity, rather than IFN-β transcription mediated by MDA5, MAVS, TBK1, IKKϵ, and IRF7. Importantly, we found that because of the specific interaction with duIFI35, the capacity of duRIG-I to recognize double-stranded RNA was significantly impaired, resulting in the decline of duRIG-I-induced IFN-β production. Taken together, our data revealed that duIFI35 expression stimulated by DTMUV infection disrupted duRIG-I-mediated host antiviral response, elucidating a distinct function of duIFI35 from human IFI35, by which DTMUV escapes host innate immune response, and providing information for the design of antiviral drug.



2015 ◽  
Vol 160 (3) ◽  
pp. 757-764 ◽  
Author(s):  
Xiaofei Bai ◽  
Wulin Shaozhou ◽  
Qingshan Zhang ◽  
Chenxi Li ◽  
Na Qiu ◽  
...  




Author(s):  
Zhiqiang Hu ◽  
Yuhong Pan ◽  
Anchun Cheng ◽  
Xingcui Zhang ◽  
Mingshu Wang ◽  
...  


2019 ◽  
Vol 66 (2) ◽  
pp. 1098-1099
Author(s):  
Wikanda Tunterak ◽  
Duangduean Prakairungnamthip ◽  
Patchareeporn Ninvilai ◽  
Supanat Bunyapisitsopa ◽  
Kanisak Oraveerakul ◽  
...  


Author(s):  
Zhiqiang Hu ◽  
Yuhong Pan ◽  
Anchun Cheng ◽  
Xingcui Zhang ◽  
Mingshu Wang ◽  
...  


2020 ◽  
Vol 51 (1) ◽  
Author(s):  
Ning Li ◽  
Jun Zhao ◽  
Yudong Yang ◽  
Yongqing Zeng ◽  
Sidang Liu


2018 ◽  
Vol 65 (6) ◽  
pp. 1943-1950 ◽  
Author(s):  
Wikanda Tunterak ◽  
Duangduean Prakairungnamthip ◽  
Patchareeporn Ninvilai ◽  
Supanat Bunyapisitsopa ◽  
Kanisak Oraveerakul ◽  
...  


2019 ◽  
Vol 66 (2) ◽  
pp. 1097-1097
Author(s):  
L.‐F. Zhao ◽  
J.‐L. Yang ◽  
F.‐M. Miao ◽  
T. Chen ◽  
J.‐H. Zhao


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