The African swine fever virus I10L protein inhibits the NF- κ B signaling pathway by targeting IKK β

Author:

Chen Xing1,Li Lian-Feng2ORCID,Yang Zhong-Yuan1,Li Meilin2,Fan Shuai1,Shi Lan-Fang1,Ren Zi-Yu1,Cao Xue-Jing1,Zhang Yuhang13,Han Shichong13,Wan Bo13ORCID,Qiu Hua-Ji2ORCID,Zhang Gaiping14,He Wen-Rui13ORCID

Affiliation:

1. International Joint Research Center of National Animal Immunology, College of Veterinary Medicine, Henan Agricultural University , Zhengzhou, Henan, China

2. State Key Laboratory for Animal Disease Control and Prevention, National African Swine Fever Para-Reference Laboratory, National High-Containment Facilities for Animal Disease Control and Prevention, Harbin Veterinary Research Institute, Chinese Academy of Agricultural Sciences , Harbin, Heilongjiang, China

3. College of Veterinary Medicine, Henan Agricultural University , Zhengzhou, Henan, China

4. Longhu Laboratory, Henan Agricultural University, Zhengzhou University , Zhengzhou, China

Abstract

ABSTRACT Proinflammatory factors play important roles in the pathogenesis of African swine fever virus (ASFV), which is the causative agent of African swine fever (ASF), a highly contagious and severe hemorrhagic disease. Efforts in the prevention and treatment of ASF have been severely hindered by knowledge gaps in viral proteins responsible for modulating host antiviral responses. In this study, we identified the I10L protein (pI10L) of ASFV as a potential inhibitor of the TNF- α - and IL-1 β -triggered NF- κ B signaling pathway, the most canonical and important part of host inflammatory responses. The ectopically expressed pI10L remarkably suppressed the activation of NF- κ B signaling in HEK293T and PK-15 cells. The ASFV mutant lacking the I10L gene (ASFV ΔI10L ) induced higher levels of proinflammatory cytokines production in primary porcine alveolar macrophages (PAMs) compared with its parental ASFV HLJ/2018 strain (ASFV WT ). Mechanistic studies suggest that pI10L inhibits IKK β phosphorylation by reducing the K63-linked ubiquitination of NEMO, which is necessary for the activation of IKK β . Morever, pI10L interacts with the kinase domain of IKK β through its N-terminus, and consequently blocks the association of IKK β with its substrates I κ B α and p65, leading to reduced phosphorylation. In addition, the nuclear translocation efficiency of p65 was also altered by pI10L. Further biochemical evidence supported that the amino acids 1–102 on pI10L were essential for the pI10L-mediated suppression of the NF- κ B signaling pathway. The present study clarifies the immunosuppressive activity of pI10L, and provides novel insights into the understanding of ASFV pathobiology and the development of vaccines against ASF. IMPORTANCE African swine fever (ASF), caused by the African swine fever virus (ASFV), is now widespread in many countries and severely affects the commercial rearing of swine. To date, few safe and effective vaccines or antiviral strategies have been marketed due to large gaps in knowledge regarding ASFV pathobiology and immune evasion mechanisms. In this study, we deciphered the important role of the ASFV-encoded I10L protein in the TNF- α -/IL-1 β -triggered NF- κ B signaling pathway. This study provides novel insights into the pathogenesis of ASFV and thus contributes to the development of vaccines against ASF.

Funder

MOST | National Natural Science Foundation of China

Publisher

American Society for Microbiology

Subject

Virology,Insect Science,Immunology,Microbiology

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