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자료유형
학술저널
저자정보
Nie Ying (The First Affiliated Hospital Guizhou University of Traditional Chinese Medicine Guiyang 550002 Guizhou Province P.R. ChinaDepartment of Parasitology; Provincial Key Laboratory of Modern Pathogen Biol) Deng Dongqing (Department of Parasitology; Provincial Key Laboratory of Modern Pathogen Biology College of Basic Medical Sciences Guizhou Medical University Guiyang 550025 P.R. China) Mou Lumin (Department of Parasitology; Provincial Key Laboratory of Modern Pathogen Biology College of Basic Medical Sciences Guizhou Medical University Guiyang 550025 P.R. China) Long Qizhou (Department of Parasitology; Provincial Key Laboratory of Modern Pathogen Biology College of Basic Medical Sciences Guizhou Medical University Guiyang 550025 P.R. China) Chen Jinzhi (Department of Parasitology; Provincial Key Laboratory of Modern Pathogen Biology College of Basic Medical Sciences Guizhou Medical University Guiyang 550025 P.R. China) Wu Jiahong (Department of Parasitology; Provincial Key Laboratory of Modern Pathogen Biology College of Basic Medical Sciences Guizhou Medical University Guiyang 550025 P.R. China)
저널정보
한국미생물생명공학회 Journal of Microbiology and Biotechnology Journal of Microbiology and Biotechnology 제33권 제5호
발행연도
2023.5
수록면
600 - 606 (7page)
DOI
10.4014/jmb.2210.10006

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Dengue virus (DENV) is a widespread arbovirus. To efficiently establish infection, DENV evolves multiple strategies to hijack the host innate immune response. Herein, we examined the inhibitory effects of DENV serotype 2 (DENV2) nonstructural proteins on RIG-I-directed antiviral immune response. We found that DENV2 NS2A, NS2B, NS4A, and NS4B significantly inhibited RIG-I-mediated IFN-β promoter activation. The roles of NS2B in RIG-I-directed antiviral immune response are unknown. Our study further showed that NS2B could dose-dependently suppress RIG-I/MAVSinduced activation of IFN-β promoter. Consistently, NS2B significantly decreased RIG-I- and MAVSinduced transcription of IFNB1, ISG15, and ISG56. Mechanistically, NS2B was found to interact with MAVS and IKKε to impair RIG-I-directed antiviral response. Our findings demonstrated a previously uncharacterized function of NS2B in RIG-I-mediated antiviral response, making it a promising drug target for anti-DENV treatments.

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