Frontiers in Immunology (May 2021)

Analysis of Porcine RIG-I Like Receptors Revealed the Positive Regulation of RIG-I and MDA5 by LGP2

  • Shuangjie Li,
  • Shuangjie Li,
  • Shuangjie Li,
  • Shuangjie Li,
  • Jie Yang,
  • Jie Yang,
  • Jie Yang,
  • Jie Yang,
  • Yuanyuan Zhu,
  • Yuanyuan Zhu,
  • Yuanyuan Zhu,
  • Yuanyuan Zhu,
  • Hui Wang,
  • Hui Wang,
  • Hui Wang,
  • Hui Wang,
  • Xingyu Ji,
  • Xingyu Ji,
  • Xingyu Ji,
  • Xingyu Ji,
  • Jia Luo,
  • Jia Luo,
  • Jia Luo,
  • Jia Luo,
  • Qi Shao,
  • Qi Shao,
  • Qi Shao,
  • Qi Shao,
  • Yulin Xu,
  • Yulin Xu,
  • Yulin Xu,
  • Yulin Xu,
  • Xueliang Liu,
  • Xueliang Liu,
  • Xueliang Liu,
  • Xueliang Liu,
  • Wanglong Zheng,
  • Wanglong Zheng,
  • Wanglong Zheng,
  • Wanglong Zheng,
  • François Meurens,
  • François Meurens,
  • Nanhua Chen,
  • Nanhua Chen,
  • Nanhua Chen,
  • Nanhua Chen,
  • Jianzhong Zhu,
  • Jianzhong Zhu,
  • Jianzhong Zhu,
  • Jianzhong Zhu

DOI
https://doi.org/10.3389/fimmu.2021.609543
Journal volume & issue
Vol. 12

Abstract

Read online

The RLRs play critical roles in sensing and fighting viral infections especially RNA virus infections. Despite the extensive studies on RLRs in humans and mice, there is a lack of systemic investigation of livestock animal RLRs. In this study, we characterized the porcine RLR members RIG-I, MDA5 and LGP2. Compared with their human counterparts, porcine RIG-I and MDA5 exhibited similar signaling activity to distinct dsRNA and viruses, via similar and cooperative recognitions. Porcine LGP2, without signaling activity, was found to positively regulate porcine RIG-I and MDA5 in transfected porcine alveolar macrophages (PAMs), gene knockout PAMs and PK-15 cells. Mechanistically, LGP2 interacts with RIG-I and MDA5 upon cell activation, and promotes the binding of dsRNA ligand by MDA5 as well as RIG-I. Accordingly, porcine LGP2 exerted broad antiviral functions. Intriguingly, we found that porcine LGP2 mutants with defects in ATPase and/or dsRNA binding present constitutive activity which are likely through RIG-I and MDA5. Our work provided significant insights into porcine innate immunity, species specificity and immune biology.

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