Shaoying Chen

Dr. Shaoying Chen


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 June 2016 in Archives of Virology
Verified
Journal Article
Closed access
PDF file
SCShilong Chen
Shilong Chen
SWShao Wang
Shao Wang
XCXiaoxia Cheng
Xiaoxia Cheng
SXShifeng Xiao
Shifeng Xiao
XZXiaoli Zhu
Xiaoli Zhu
FYFusong Yu
Fusong Yu

3 December 2013 in Archives of Virology
Verified
Journal Article
Closed access
PDF file
SCShilong Chen
Shilong Chen
SWShao Wang
Shao Wang
ZLZhaolong Li
Zhaolong Li
FLFengqiang Lin
Fengqiang Lin
XCXiaoxia Cheng
Xiaoxia Cheng
MZMin Zheng
Min Zheng

1 May 2017 in Veterinary Microbiology
Verified
Journal Article
Closed access
SXShifeng Xiao
Shifeng Xiao
SCShilong Chen
Shilong Chen
XCXiaoxia Cheng
Xiaoxia Cheng
FLFengqiang Lin
Fengqiang Lin
SWShao Wang
Shao Wang
FYFusong Yu
Fusong Yu

22 July 2016 in Veterinary Research
Verified
Journal Article
Open access
PDF file
SCShilong Chen
Shilong Chen
GLGuifeng Luo
Guifeng Luo
ZYZhou Yang
Zhou Yang
SLShuncheng Lin
Shuncheng Lin
SCShaoying Chen
Shaoying Chen
JCJi-Long Chen
Ji-Long Chen
Avian Tembusu virus (ATMUV) is a newly emerged flavivirus that belongs to the Ntaya virus group. ATMUV is a highly pathogenic virus causing significant economic loss to the Chinese poultry industry. However, little is known about the role of host innate immune mechanism in defending against ATMUV infection. In this study, we found that ATMUV infection significantly up-regulated the expression of type I and type III interferons (IFN) and some critical IFN-stimulated genes (ISG) in vivo and in vitro. This innate immune response was induced by genomic RNA of ATMUV. Furthermore, we observed that ATMUV infection triggered IFN response mainly through MDA5 and TLR3-dependent signaling pathways. Strikingly, shRNA-based disruption of IPS-1, IRF3 or IRF7 expression significantly reduced the production of IFN in the 293T cell model. Moreover, NF-κB was shown to be activated in both chicken and human cells during the ATMUV infection. Inhibition of NF-κB signaling also resulted in a clear decrease in expression of IFN. Importantly, experiments revealed that treatment with IFN significantly impaired ATMUV replication in the chicken cell. Consistently, type I IFN also exhibited promising antiviral activity against ATMUV replication in the human cell. Together, these data indicate that ATMUV infection triggers host innate immune response through MDA5 and TLR3-dependent signaling that controls IFN production, and thereby induces an effective antiviral immunity.

1 January 2013 in Journal of Veterinary Medical Science
Verified
Journal Article
Open access
PDF file
SWShao Wang
Shao Wang
XCXiao-Xia Cheng
Xiao-Xia Cheng
SCShaoying Chen
Shaoying Chen
XZXiao-Li Zhu
Xiao-Li Zhu
SCShi-Long Chen
Shi-Long Chen
ZLZhao-Long Li
Zhao-Long Li
We report a novel goose parvovirus (MDGPV/PT) isolated from an affected Muscovy duck in Fujian Province, China. In this study, the NS1 sequence analyses indicated a close genetic relationship between MDGPV/PT and Muscovy duck parvovirus (MDPV) strains, although MDGPV/DY, which was isolated from a Muscovy duck in 2006 in Sichuan Province, could be divided into GPV-related groups. Phylogenetic analysis showed that except for differences in the NS1 gene, MDGPV strains PT and DY are closely related to a parvovirus that infects domestic waterfowls. This is the first demonstration of recombination between goose and Muscovy duck parvoviruses in nature, and MDGPV/PT might have led to the generation of a novel waterfowl parvovirus strain circulating in Muscovy duck flocks in China.

1 December 2019 in Microbial Pathogenesis
Verified
Journal Article
Closed access
XCXiuqin Chen
Xiuqin Chen
MZMin Zheng
Min Zheng
FLFengqiang Lin
Fengqiang Lin
XCXiaoxia Cheng
Xiaoxia Cheng
SXShifeng Xiao
Shifeng Xiao
SCShilong Chen
Shilong Chen