Characterization of chicken spleen transcriptome after infection with Salmonella enterica serovar Enteritidis

PLoS One. 2012;7(10):e48101. doi: 10.1371/journal.pone.0048101. Epub 2012 Oct 19.

Abstract

In this study we were interested in identification of new markers of chicken response to Salmonella Enteritidis infection. To reach this aim, gene expression in the spleens of naive chickens and those intravenously infected with S. Enteritidis with or without previous oral vaccination was determined by 454 pyrosequencing of splenic mRNA/cDNA. Forty genes with increased expression at the level of transcription were identified. The most inducible genes encoded avidin (AVD), extracellular fatty acid binding protein (EXFABP), immune responsive gene 1 (IRG1), chemokine ah221 (AH221), trappin-6-like protein (TRAP6) and serum amyloid A (SAA). Using cDNA from sorted splenic B-lymphocytes, macrophages, CD4, CD8 and γδ T-lymphocytes, we found that the above mentioned genes were preferentially expressed in macrophages. AVD, EXFABP, IRG1, AH221, TRAP6 and SAA were induced also in the cecum of chickens orally infected with S. Enteritidis on day 1 of life or day 42 of life. Unusual results were obtained for the immunoglobulin encoding transcripts. Prior to the infection, transcripts coding for the constant parts of IgM, IgY, IgA and Ig light chain were detected in B-lymphocytes. However, after the infection, immunoglobulin encoding transcripts were expressed also by T-lymphocytes and macrophages. Expression of AVD, EXFABP, IRG1, AH221, TRAP6, SAA and all immunoglobulin genes can be therefore used for the characterization of the course of S. Enteritidis infection in chickens.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avian Proteins / genetics*
  • Avian Proteins / immunology
  • B-Lymphocytes / immunology
  • B-Lymphocytes / metabolism
  • Cecum / immunology
  • Cecum / metabolism
  • Chickens / genetics*
  • Chickens / immunology
  • Gene Expression Regulation
  • Immunoglobulins / genetics
  • Immunoglobulins / immunology
  • Macrophages / immunology
  • Macrophages / metabolism
  • Organ Specificity
  • Poultry Diseases / genetics*
  • Poultry Diseases / immunology
  • Poultry Diseases / microbiology
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics*
  • Salmonella Infections, Animal / genetics*
  • Salmonella Infections, Animal / immunology
  • Salmonella Infections, Animal / microbiology
  • Salmonella enteritidis / immunology*
  • Salmonella enteritidis / pathogenicity
  • Sequence Analysis, DNA
  • Spleen / immunology
  • Spleen / metabolism*
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism
  • Transcriptome / genetics*
  • Transcriptome / immunology

Substances

  • Avian Proteins
  • Immunoglobulins
  • RNA, Messenger

Grants and funding

This work has been supported by the project MZE0002716202 of the Czech Ministry of Agriculture, AdmireVet project CZ.1.05/2.1.00/01.0006–ED0006/01/01 from the Czech Ministry of Education and Czech Science Foundation project P502/12/0303. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.