Kidney proteome responses in the teleost fish Paralichthys olivaceus indicate a putative immune response against Streptococcus parauberis |
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Authors: | Cha In-Seok Kwon Joseph Park Seong-Hwa Nho Seong-Won Jang Ho-Bin Park Seong-Bin del Castillo Carmelo S Hikima Jun-ichi Aoki Takashi Jung Tae-Sung |
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Affiliation: | Research Institute of Life Science, Gyeongsang National University, Jinju, South Korea. |
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Abstract: | The proteomic response to bacterial infection in a teleost fish (Paralichthys olivaceus) infected with Streptococcus parauberis was analyzed using label-free protein quantitation coupled with LC-MS(E) tandem mass spectrometry. A total of 82 proteins from whole kidney, a major lymphoid organ in this fish, were found to be differentially expressed between healthy and diseased fish analyzed 6, 24, 72 and 120 h post-infection. Among the differentially expressed proteins, those involved in mediating immune responses (e.g., heat shock proteins, cathepsins, goose-type lysozyme and complement components) were most significantly up-regulated by infection. In addition, cell division cycle 48 (CDC48) and calreticulin, which are associated with cellular recovery and glycoprotein synthesis, were up-regulated in the universal protein group, whereas the other proteins in that group were down-regulated. There was continuous activation of expression of immune-associated proteins during infection, but there was also loss of expression of proteins not involved in immune function. We expect that our findings regarding immune response at the protein level would offer new insight into the systemic response to bacterial infection of a major immune organ in teleost fish. |
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Keywords: | LC, liquid chromatography MS, mass spectrometry UPLC, ultra performance liquid chromatography CDC48, cell division cycle 48 EST, expressed sequence tag iTRAQ, isobaric tag for relative and absolute quantitation SILAC, stable isotope labeling by amino acids in cell culture ICAT, isotope-code affinity tags emPAI, exponentially modified protein abundance index SRM, selected reaction monitoring MRM, multiple reaction monitoring TSA, tryptone soya agar TSB, tryptone soya broth PBS, phosphate buffered saline TCA, trichloroacetic acid SDS-PAGE, sodium dodecyl sulfate polyacrylamide gel electrophoresis ABC, ammonium bicarbonate CAN, acetonitrile DTT, dithiothreitol IAA, iodoacetamide PLGS, ProteinLynx Global Server IPA, Ingenuity Pathway Analysis PICR, Protein Identifier Cross-Reference HSP, heat shock protein LMP7, low molecular mass polypeptide 7 TLR, toll-like receptor MHC, major histocompatibility complex NAM, N-acetylmuramic acid NAG, N-acetylglucosamine IgM, immunoglobulin M APCs, antigen presenting cells ISG, interferon-stimulation gene 15 ER, endoplasmic reticulum GLUT-1, glucose transporter l (GLUT-l) AAA ATPase, ATPases associated with various cellular activities. |
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