De novo transcriptome analysis of immune response on cobia (Rachycentron canadum) infected with Photobacterium damselae subsp. piscicida revealed inhibition of complement components and involvement of MyD88-independent pathway

Fish Shellfish Immunol. 2018 Jun:77:120-130. doi: 10.1016/j.fsi.2018.03.041. Epub 2018 Mar 23.

Abstract

Cobia, Rachycentron canadum, one of the most important aquatic species in Taiwan, has suffered heavy losses from Photobacterium damselae subsp. piscicida, which is the causal agent of photobacteriosis. In this study, the transcriptomic profiles of livers and spleens from Pdp-infected and non-infected cobia were obtained for the first time by Illumina-based paired-end sequencing method with a focus on immune-related genes. In total, 164,882 high quality unigenes were obtained in four libraries. Following Pdp infection, 7302 differentially expressed unigenes from liver and 8600 differentially expressed unigenes from spleen were identified. Twenty-seven of the differently expressed genes were further validated by RT-qPCR (average correlation coefficient 0.839, p-value <0.01). Results indicated a negative regulation of complement components and increased expression of genes involved in MyD88-independent pathway. Moreover, a remarkable finding was the increased expression of IL-10, implying an inadequacy of immune responses. This study not only characterized several putative immune pathways, but also provided a better understanding of the molecular responses to photobacteriosis in cobia.

Keywords: Immune response; Photobacterium damselae subsp. piscicida; Rachycentron canadum; Transcriptome.

MeSH terms

  • Adaptive Immunity*
  • Animals
  • Complement System Proteins / genetics*
  • Complement System Proteins / immunology
  • Complement System Proteins / metabolism
  • Fish Diseases / immunology*
  • Fish Proteins / genetics
  • Fish Proteins / immunology
  • Fish Proteins / metabolism
  • Gene Expression Profiling*
  • Gram-Negative Bacterial Infections / immunology
  • Immunity, Innate*
  • Myeloid Differentiation Factor 88 / genetics*
  • Myeloid Differentiation Factor 88 / immunology
  • Myeloid Differentiation Factor 88 / metabolism
  • Perciformes / immunology*
  • Photobacterium / physiology
  • Signal Transduction / immunology

Substances

  • Fish Proteins
  • Myeloid Differentiation Factor 88
  • Complement System Proteins