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Kidney proteome responses in the teleost fish Paralichthys olivaceus indicate a putative immune response against Streptococcus parauberis
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
Affiliation:Research Institute of Life Science, Gyeongsang National University, Jinju, South Korea.
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.
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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