Transcriptomic Analysis on Responses of Murine Lungs to Pasteurella multocida Infection

Front Cell Infect Microbiol. 2017 Jun 20:7:251. doi: 10.3389/fcimb.2017.00251. eCollection 2017.

Abstract

Pasteurella multocida infection in cattle causes serious epidemic diseases and leads to great economic losses in livestock industry; however, little is known about the interaction between host and P. multocida in the lungs. To explore a fully insight into the host responses in the lungs during P. multocida infection, a mouse model of Pasteurella pneumonia was established by intraperitoneal infection, and then transcriptomic analysis of infected lungs was performed. P. multocida localized and grew in murine lungs, and induced inflammation in the lungs, as well as mice death. With transcriptomic analysis, approximately 107 clean reads were acquired. 4236 differently expressed genes (DEGs) were detected during P. multocida infection, of which 1924 DEGs were up-regulated. By gene ontology (GO) and Kyoto encyclopedia of genes and genomes (KEGG) enrichments, 5,303 GO enrichments and 116 KEGG pathways were significantly enriched in the context of P. multocida infection. Interestingly, genes related to immune responses, such as pattern recognition receptors (PRRs), chemokines and inflammatory cytokines, were significantly up-regulated, suggesting the key roles of these genes in P. multocida infection. Transcriptomic data showed that IFN-γ/IL-17-related genes were increased, which were validated by qRT-PCR, ELISA, and immunoblotting. Our study characterized the transcriptomic profile of the lungs in mice upon Pasteurella infection, and our findings could provide valuable information with respect to better understanding the responses in mice during P. multocida infection.

Keywords: IFN-γ; IL-17; P. multocida; lung; transcriptomic analysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Bacterial Proteins / genetics
  • Cell Proliferation
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Disease Models, Animal
  • Gene Expression Profiling*
  • Gene Expression Regulation
  • Gene Ontology
  • Genes, Bacterial / genetics
  • Interferon-gamma / genetics
  • Interferon-gamma / metabolism
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism
  • Lung / microbiology*
  • Lung / pathology
  • Mice
  • Pasteurella Infections / immunology
  • Pasteurella Infections / microbiology*
  • Pasteurella Infections / mortality
  • Pasteurella multocida / genetics*
  • Pasteurella multocida / immunology
  • Pasteurella multocida / pathogenicity*
  • RNA, Bacterial
  • Up-Regulation

Substances

  • Bacterial Proteins
  • Chemokines
  • Cytokines
  • IFNG protein, mouse
  • Interleukin-17
  • RNA, Bacterial
  • Interferon-gamma