e pathway, we performed a map based pathway analy sis by using th

e pathway, we performed a map based pathway analy sis by using the GenMAPP software package In our study, 4004 Mus musculus homologs were used to create the GenMAPP. Mus mus culus homologs http://www.selleckchem.com/products/Axitinib.html were identified by searching the 8216 unigenes against the zebrafish RefSeq data downloaded from the UCSC website and then the database of HomoloGene at the NCBI. GenMAPP analysis was per formed to identify genes involved in the MAPK pathway. In total, seven genes were identified as highly upregulated upon infection, Casp9, Prkcb1, Hspa5, Radd45a, Dusp7, Rac1, and Casp1. Contrarily, four genes were highly downregulated in response to A. hydrophila infection, Map3k12, Crkl, Jun, and Raf1. We also used GenMAPP to analyze genes involved in TCR signaling.

T cell activa tion, a key event in adaptive immunity, promotes a vari ety of signaling cascades that ultimately lead to cytokine production, cell survival, proliferation, and differentia tion. The resultant map revealed eight remarkably downregulated genes and seven remarkably upregulated genes involved in TCR signaling after A. hydrophila infection. Discussion At present, molecular studies on the immune response to pathogens in the large yellow croaker are still rare. To increase our knowledge of host responses to bacterial infection, we firstly analyzed the transcriptome profile of the fish after A. hydrophila infection. Bioinformatic ana lysis of RNA seq data should involve mapping of short reads to the genome. However, genome and tran scriptome resources for most vertebrate species have not yet been obtained, including the large yellow croaker.

We analyzed the transcriptome of the large yellow croaker in advance and obtained a mass of sequence information. Then quantitative gene expression profile analysis was performed, and the tags were mapped to obtained tran scriptome database. In the set of highly differentially expressed genes, a number of genes were reported to be involved in immunity and signal transduction, encoding receptors, cytokines, innate defense molecules, enzymes, signal transducers, transcription factors, and other func tional proteins. The innate immune system represents an efficient first line of defense against invading microbial pathogens. TLRs signal the presence of pathogens and elicit an innate immune response. This process has been reported in zebrafish infected with Mycobacterium mari num.

Our data Brefeldin_A revealed Dorsomorphin ALK 35 genes involved in TLR cascades in the transcriptome of infected large yel low croaker and 29 differentially expressed genes in expression profiles. TLR1 and TLR2 function together to recognize lipopeptides with a triacylated N terminal cysteine. TLR1 is only mildly expressed in T. nigroviridis tissues and slightly upregulated in the spleens of LPS injected fish. Our data demonstrated that TLR1 was upregulated while TLR2 was downregu lated at 24 h after A. hydrophila infection. This result was partly consistent with that reported by Baoprasertkul et al. in which TLR2 expression

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