NOD1 Is Associated With the Susceptibility of Pekin Duck Flock to Duck Hepatitis A Virus Genotype 3

Front Immunol. 2021 Oct 20:12:766740. doi: 10.3389/fimmu.2021.766740. eCollection 2021.

Abstract

Duck viral hepatitis (DVH) is an acute, highly lethal infectious disease of ducklings that causes huge losses in the duck industry. Duck hepatitis A virus genotype 3 (DHAV-3) has been one of the most prevalent DVH pathogen in the Asian duck industry in recent years. Here, we investigated the genetic basis of the resistance and susceptibility of ducks to DVH by comparing the genomes and transcriptomes of a resistant Pekin duck flock (Z8) and a susceptible Pekin duck flock (SZ7). Our comparative genomic and transcriptomic analyses suggested that NOD1 showed a strong signal of association with DVH susceptibility in ducks. Then, we found that NOD1 showed a significant expression difference between the livers of susceptible and resistant individuals after infection with DHAV-3, with higher expression in the SZ7 flock. Furthermore, suppression and overexpression experiments showed that the number of DHAV-3 genomic copies in primary duck hepatocytes was influenced by the expression level of NOD1. In addition, in situ RNAscope analysis showed that the localization of NOD1 and DHAV-3 in liver cells was consistent. Altogether, our data suggested that NOD1 was likely associated with DHAV-3 susceptibility in ducks, which provides a target for future investigations of the pathogenesis of DVH.

Keywords: DHAV-3; NOD1; Pekin duck; genome-wide association studies; transcriptome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Aspartate Aminotransferases / blood
  • Avian Proteins / genetics*
  • Avian Proteins / metabolism
  • Cells, Cultured
  • Ducks / blood
  • Ducks / genetics*
  • Ducks / virology
  • Female
  • Genotype
  • Hepatitis Virus, Duck / genetics*
  • Hepatitis Virus, Duck / physiology
  • Hepatitis, Viral, Animal / genetics*
  • Hepatitis, Viral, Animal / virology
  • Hepatocytes / metabolism
  • Hepatocytes / virology
  • In Situ Hybridization / methods
  • Male
  • Nod1 Signaling Adaptor Protein / genetics*
  • Nod1 Signaling Adaptor Protein / metabolism
  • Picornaviridae Infections / genetics*
  • Picornaviridae Infections / veterinary
  • Picornaviridae Infections / virology
  • Poultry Diseases / genetics*
  • Poultry Diseases / virology
  • RNA-Seq / methods
  • Survival Analysis
  • Transcriptome / genetics

Substances

  • Avian Proteins
  • Nod1 Signaling Adaptor Protein
  • Aspartate Aminotransferases
  • Alanine Transaminase