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Duckling short beak and dwarfism syndrome virus infection activates host innate immune response involving both DNA and RNA sensors

Duckling short beak and dwarfism syndrome virus (SBDSV), a newly identified goose parvovirus, causes devastating disease in domestic waterfowl and considerable economic losses to Chinese waterfowl industry. The molecular pathogenesis of SBDSV infection, nature and dynamics of host immune responses a...

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Published in:Microbial pathogenesis 2020-01, Vol.138, p.103816-103816, Article 103816
Main Authors: Chen, Shilong, Fang, Tiehui, Xiao, Shifeng, Lin, Fengqiang, Cheng, Xiaoxia, Wang, Shao, Zhu, Xiaoli, Chen, Xiuqin, Zheng, Min, Munir, Muhammad, Huang, Meiqing, Yu, Fusong, Chen, Shaoying
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container_title Microbial pathogenesis
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creator Chen, Shilong
Fang, Tiehui
Xiao, Shifeng
Lin, Fengqiang
Cheng, Xiaoxia
Wang, Shao
Zhu, Xiaoli
Chen, Xiuqin
Zheng, Min
Munir, Muhammad
Huang, Meiqing
Yu, Fusong
Chen, Shaoying
description Duckling short beak and dwarfism syndrome virus (SBDSV), a newly identified goose parvovirus, causes devastating disease in domestic waterfowl and considerable economic losses to Chinese waterfowl industry. The molecular pathogenesis of SBDSV infection, nature and dynamics of host immune responses against SBDSV infection remained elusive. In this study, we systematically explored the relative mRNA expression profiles of major innate immune-related genes in SBDSV infected duck embryo fibroblasts. We found that SBDSV infection effectively activated host innate immune responses and resulted in significant up-regulation of IFN-β and several vital IFN-stimulated genes (ISGs). These up-regulation responses were mainly attributed to viral genomic DNA and dsRNA replication intermediates. Importantly, the expression of cGAS was significantly induced, whereas the expression of other DNA receptors including DDX41, STING, ZBP1, LSM14A and LRRFIP1 have no significant change. Furthermore, SBDSV infection also activates the up-regulation of TLR3 and inhibited the expression of TLR2 and TLR4; however, no effect was observed on the expression of TLR1, TLR5, TLR7, TLR15 and TLR21. Intriguingly, SBDSV infection significantly up-regulated the expression of RNA sensors such as MDA5 and LGP2, and resulted in a delayed but significant up-regulation of RIG-I gene. Taken together, these data indicate that host multiple sensors including DNA sensor (cGAS) and RNA sensors (TLR3, MDA5 and LGP2) are involved in recognizing a variety of different pathogen associated molecular patterns (PAMPs) including viral genomic ssDNA and dsRNA replication intermediates, which trigger an effective antiviral innate immune response. •SBDSV, a new number of goose parvovirus, causes devastating disease in domestic waterfowl.•The relative mRNA expression profiles of innate immune-related genes in SBDSV infected DEFs were systematically explored.•SBDSV infection activates host innate immune responses and results in significant up-regulation of IFN-β and vital ISGs.•Host multiple sensors are involved in recognizing pathogen associated molecular patterns (PAMPs).
doi_str_mv 10.1016/j.micpath.2019.103816
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The molecular pathogenesis of SBDSV infection, nature and dynamics of host immune responses against SBDSV infection remained elusive. In this study, we systematically explored the relative mRNA expression profiles of major innate immune-related genes in SBDSV infected duck embryo fibroblasts. We found that SBDSV infection effectively activated host innate immune responses and resulted in significant up-regulation of IFN-β and several vital IFN-stimulated genes (ISGs). These up-regulation responses were mainly attributed to viral genomic DNA and dsRNA replication intermediates. Importantly, the expression of cGAS was significantly induced, whereas the expression of other DNA receptors including DDX41, STING, ZBP1, LSM14A and LRRFIP1 have no significant change. Furthermore, SBDSV infection also activates the up-regulation of TLR3 and inhibited the expression of TLR2 and TLR4; however, no effect was observed on the expression of TLR1, TLR5, TLR7, TLR15 and TLR21. Intriguingly, SBDSV infection significantly up-regulated the expression of RNA sensors such as MDA5 and LGP2, and resulted in a delayed but significant up-regulation of RIG-I gene. Taken together, these data indicate that host multiple sensors including DNA sensor (cGAS) and RNA sensors (TLR3, MDA5 and LGP2) are involved in recognizing a variety of different pathogen associated molecular patterns (PAMPs) including viral genomic ssDNA and dsRNA replication intermediates, which trigger an effective antiviral innate immune response. •SBDSV, a new number of goose parvovirus, causes devastating disease in domestic waterfowl.•The relative mRNA expression profiles of innate immune-related genes in SBDSV infected DEFs were systematically explored.•SBDSV infection activates host innate immune responses and results in significant up-regulation of IFN-β and vital ISGs.•Host multiple sensors are involved in recognizing pathogen associated molecular patterns (PAMPs).</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31655218</pmid><doi>10.1016/j.micpath.2019.103816</doi><tpages>1</tpages></addata></record>
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subjects Duck embryo fibroblast
Duckling short beak and dwarfism syndrome virus (SBDSV)
Goose parvovirus
Innate immune response
Pattern recognition receptors
title Duckling short beak and dwarfism syndrome virus infection activates host innate immune response involving both DNA and RNA sensors
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