4.4 Article

Analysis of skin and secretions of Dybowski's frogs (Rana dybowskii) exposed to Staphylococcus aureus or Escherichia coli identifies immune response proteins

Journal

VETERINARY JOURNAL
Volume 200, Issue 1, Pages 127-132

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.tvjl.2014.01.011

Keywords

Immune responses; Microbial infection; Proteomic analysis; Rana dybowskii

Funding

  1. National Natural Science Foundation of China [30870301]
  2. Science and Technology Projects of the State General Administration of Quality Supervision, Inspection and Quarantine [2012IK157]
  3. Special Fund of Harbin Science and Technology Innovation Talent [2012RFQYN032]

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The aim of the present study was to investigate responses in Dybowski's frogs (Rana dybowskii) exposed to bacteria, using proteomic and transcriptomic approaches. Staphylococcus aureus and Escherichia coli were used as representative Gram-positive and Gram-negative bacteria, respectively, in an infectious challenge model. Frog skin and skin secretions were collected and protein expression in infected frogs compared to control frogs by two-dimensional gel electrophoresis, silver staining, and image analysis. Proteins that demonstrated differential expression were analysed by mass spectrometry and identified by searching protein databases. More than 180 protein spots demonstrated differential expression in E. coli- or S. aureus-challenged groups and, of these, more than 55 spots were up- or down-regulated at least sixfold, post-infection. Proteins with a potential function in the immune response were identified, such as stathmin la, annexin A1, superoxide dismutase A, C-type lectin, lysozyme, antimicrobial peptides, cofilin-1-B, mannose receptor, histone H4, prohormone convertase 1, carbonyl reductase 1 and some components of the Toll-like receptor (TLR) signalling pathway. These molecules are potential candidates for further investigation of immune mechanisms in R. dybowskii; in particular, TLR-mediated responses, which might be activated in frogs exposed to pathogenic bacteria as part of innate immune defence, but which might also impact on adaptive immunity to infection. (C) 2014 Elsevier Ltd. All rights reserved.

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