Molecular cloning and functional characterization of duck nucleotide-binding oligomerization domain 1 (NOD1)

Dev Comp Immunol. 2017 Sep:74:82-89. doi: 10.1016/j.dci.2017.04.012. Epub 2017 Apr 19.

Abstract

Nucleotide-binding oligomerization domain 1 (NOD1) is an imperative cytoplasmic pattern recognition receptor (PRR) and considered as a key member of the NOD-like receptor (NLR) family which plays a critical role in innate immunity through sensing microbial components derived from bacterial peptidoglycan. In the current study, the full-length of duck NOD1 (duNOD1) cDNA from duck embryo fibroblasts (DEFs) was cloned. Multiple sequence alignment and phylogenetic analysis demonstrated that duNOD1 exhibited a strong evolutionary relationship with chicken and rock pigeon NOD1. Tissue-specific expression analysis showed that duNOD1 was widely distributed in various organs, with the highest expression observed in the liver. Furthermore, duNOD1 overexpression induced NF-κB activation in DEFs and the CARD domain is crucial for duNOD1-mediated NF-κB activation. In addition, silencing the duNOD1 decreased the activity of NF-κB in DEFs stimulated by iE-DAP. Overexpression of duNOD1 significantly increased the expression of TNF-α, IL-6, and RANTES in DEFs. These findings highlight the crucial role of duNOD1 as an intracellular sensor in duck innate immune system.

Keywords: Duck; NF-κB; NOD1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avian Proteins / genetics*
  • Avian Proteins / metabolism
  • Biological Evolution
  • Cells, Cultured
  • Cloning, Molecular
  • Cytokines / metabolism
  • Ducks / immunology*
  • Fibroblasts / physiology*
  • Immunity, Innate
  • Inflammation Mediators / metabolism
  • Liver / physiology*
  • NF-kappa B / metabolism
  • Nod1 Signaling Adaptor Protein / genetics*
  • Nod1 Signaling Adaptor Protein / metabolism
  • Peptidoglycan / immunology
  • RNA, Small Interfering / genetics
  • Sequence Alignment
  • Transcriptome

Substances

  • Avian Proteins
  • Cytokines
  • Inflammation Mediators
  • NF-kappa B
  • Nod1 Signaling Adaptor Protein
  • Peptidoglycan
  • RNA, Small Interfering