NLK suppresses MAVS-mediated signaling in black carp antiviral innate immunity. (September 2021)

• Record Type: Journal Article
• Authors: Chen, Zhaoyuan; Cao, Yingyi; Huang, Jiayi; Tan, Yaqi; Wei, Jing; Xiao, Jun; Zou, Jun; Feng, Hao
• Is Part Of: Developmental and comparative immunology. Volume 122(2021)
• Publication Date: 2021-09
• Subjects: NLK -- MAVS -- Interferon -- SVCV -- Black carp; Immunology -- Periodicals; Developmental immunology -- Periodicals; 616.079
• DOI: 10.1016/j.dci.2021.104105
• Languages: English
• ISSNs: 0145-305X

Abstract

Abstract: Mammalian Nemo-like kinase (NLK) plays important roles in multiple biological processes including immune response; however, the roles of teleost NLK remain largely unknown. In the present study, the NLK homolog (bcNLK) of black carp ( Mylopharyngodon piceus ) has been cloned and characterized. The coding region of bcNLK consists of 1427 nucleotides and encodes 476 amino acid, including two low complexity region (LCR) domains at the N-terminus and a serine/threonine protein kinase catalytic (S-TKc) domain in the middle region. The transcription of bcNLK are promoted after spring viremia of carp virus (SVCV) infection and poly (I:C) stimulation in host cells, but not post LPS treatment. bcNLK exhibits weak impact on the transcription of interferon (IFN) promoter in the reporter assay, however, black carp MAVS (bcMAVS)-mediated IFN promoter transcription is remarkably dampened by bcNLK. The interaction between bcNLK and bcMAVS is detected through the co-immunoprecipitation assay. Accordingly, the plaque assay results show that bcMAVS-mediated antiviral ability is impaired by bcNLK. Moreover, knockdown of bcNLK in host cells leads to the enhanced antiviral ability against SVCV. All these data support the conclusion that black carp NLK associates with MAVS and inhibited MAVS-mediated antiviral signaling. Highlights: bcNLK suppresses bcMAVS-activated IFN production. bcNLK directly binds to bcMAVS and suppresses bcMAVS-mediated antiviral activity. bcNLK deficiency in host cells increased its antiviral ability against SVCV.