2019
DOI: 10.4049/jimmunol.1900956
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Binding of the Duck Tembusu Virus Protease to STING Is Mediated by NS2B and Is Crucial for STING Cleavage and for Impaired Induction of IFN-β

Abstract: This information is current as β Impaired Induction of IFN-Crucial for STING Cleavage and for to STING Is Mediated by NS2B and Is Binding of the Duck Tembusu Virus Protease

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Cited by 50 publications
(55 citation statements)
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“…The amino acid residues at 164, 167, and 361 in STING were important for NS2A binding with STING [145]. However, NS2B3 polyproteins inhibited IFN induction by hydrolyzing duck STING, and further mapping analysis showed the scissile bond located between the R84 and G85 residues of STING [146]. It is suggested by the immune evasion strategies employed by DTMUV via targeting MAVS and STING were critical for host innate immune responses to DTMUV infection.…”
Section: Inhibition Of Ifn Production By Targeting Important Adaptor mentioning
confidence: 99%
“…The amino acid residues at 164, 167, and 361 in STING were important for NS2A binding with STING [145]. However, NS2B3 polyproteins inhibited IFN induction by hydrolyzing duck STING, and further mapping analysis showed the scissile bond located between the R84 and G85 residues of STING [146]. It is suggested by the immune evasion strategies employed by DTMUV via targeting MAVS and STING were critical for host innate immune responses to DTMUV infection.…”
Section: Inhibition Of Ifn Production By Targeting Important Adaptor mentioning
confidence: 99%
“…Although the focus of this review is on the mammalian cytosolic DNA sensory system and the flaviviral strategies on regulation and modulation of those pathways, the authors believe it is noteworthy to mention some elucidating new research coming from the field of avian flavivirus (duck Tembusu virus, or DTMUV) [88,89,137].…”
Section: Duck Tembusu Virusmentioning
confidence: 99%
“…This single ORF encodes one polyprotein precursor that is subsequently cleaved by viral and cellular proteases into three structural proteins, the capsid (C), precursor membrane (prM) and envelope (E), and seven non-structural proteins (NSs), NS1, NS2A, NS2B, NS3, NS4A, 2KNS4B, and NS5 (Tang et al, 2015;Zhu et al, 2015). In addition to their essential functions in the viral life cycles, both structural and non-structural proteins are probably involved in regulating the innate and adaptive immunity of host cells (Wu et al, 2019).…”
Section: Introductionmentioning
confidence: 99%