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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/24111
Title: Proteomic analysis of differentially expressed proteins in Penaeus vannamei hemocytes upon Taura syndrome virus infection
Authors: Phattara Orn Chongsatja
Apichai Bourchookarn
Fang Lo Chu
Visith Thongboonkerd
Chartchai Krittanai
Mahidol University
National Taiwan University
Keywords: Biochemistry, Genetics and Molecular Biology
Issue Date: 1-Oct-2007
Citation: Proteomics. Vol.7, No.19 (2007), 3592-3601
Abstract: To understand molecular responses of crustacean hemocytes to virus infection, we applied 2-DE proteomics approach to investigate altered proteins in hemocytes of Penaeus vannamei during Taura syndrome virus (TSV) infection. At 24 h postinfection, quantitative intensity analysis and nano-LC-ESI-MS/MS revealed 11 forms of 8 proteins that were significantly up-regulated, whereas 9 forms of 5 proteins were significantly down-regulated in the infected shrimps. These altered proteins play important roles in host defense (hemocyanin, catalase, carboxylesterase, transglutaminase, and glutathione transferase), signal transduction (14-3-3 zeta), carbohydrate metabolism (acetylglucosamine pyrophosphorylase), cellular structure and integrity (beta-tubulin, beta-actin, tropomyosin, and myosin), and ER-stress response (protein disulfide isomerase). Semiquantitative RT-PCR and Western blot analysis confirmed the upregulation of 14-3-3 at both mRNA and protein levels. Interestingly, several altered protein spots were identified as fragments of hemocyanin. Mass spectrometric analysis showed that the hemocyanin spots at acidic and basic regions represented the C- and N-terminal hemocyanin fragments, respectively. As three-quarters of C-terminal fragments were up-regulated, whereas two-thirds of N-terminal hemocyanin fragments were down-regulated, we therefore hypothesize that C- and N-terminal hemocyanin fragments may have differential roles in hemocytes. Further investigation of these data may lead to better understanding of the molecular responses of crustacean hemocytes to TSV infection. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=35348964100&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/24111
ISSN: 16159861
16159853
Appears in Collections:Scopus 2006-2010

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