Please use this identifier to cite or link to this item:
https://ir.swu.ac.th/jspui/handle/123456789/13082
Title: | Characterization of PmSpӓtzle 1 from the black tiger shrimp Peneaus monodon |
Authors: | Boonrawd S. Mani R. Ponprateep S. Supungul P. Masrinoul P. Tassanakajon A. Rimphanitchayakit V. |
Keywords: | ALFPm3 protein complementary DNA crustinPm1 protein crustinPm7 protein DNA fragment isoprotein penaeidin3 protein penaeidin5 protein pmspatzle 1 protein toll like receptor unclassified drug antimicrobial cationic peptide arthropod protein complementary DNA isoprotein amino acid sequence animal cell animal tissue Article blood cell comparative study controlled study eye tissue Fenneropenaeus chinensis gene expression heart tissue hemolymph hepatopancreas ichthyophthiriasis intestine tissue lymphoid tissue muscle tissue nonhuman nucleotide sequence Penaeus monodon protein analysis signal transduction stomach tissue upregulation Western blotting White spot syndrome virus animal chemistry gene expression genetics immunology innate immunity metabolism molecular cloning Penaeidae physiology sequence alignment virology Amino Acid Sequence Animals Antimicrobial Cationic Peptides Arthropod Proteins Base Sequence Cloning, Molecular DNA, Complementary Gene Expression Hemocytes Immunity, Innate Penaeidae Protein Isoforms Sequence Alignment White spot syndrome virus 1 |
Issue Date: | 2017 |
Abstract: | Spätzle is a signaling ligand in innate immune response that signals pathogenic infection via Toll receptor and Toll pathway into the cells for the synthesis of antimicrobial proteins. Herein, three PmSpӓtzle isoforms were identified in Penaeus monodon, namely PmSpz1, 2 and 3. The PmSpz1 was chosen for detailed study. The PmSpz1 gene was expressed in all nine tissues tested including the hemocytes, stomach, hepatopancreas, gill, lymphoid tissue, eyestalk, muscle, intestine and heart. Its expression was up-regulated upon white spot syndrome virus (WSSV) infection. Western blot analysis of hemolymph showed that the PmSpz1 mostly existed as a cleaved active form awaiting to activate the Toll pathway. Injection of a recombinant PmSpz1 rendered the shrimp less susceptible to the WSSV infection. Injection of a recombinant active form of PmSpz1 into a normal shrimp activated the synthesis of crustinPm1, crustinPm7, ALFPm3, penaeidin3 but not penaeidin5 indicating that the expression of all antimicrobial proteins but not penaeidin5 was under the regulation of Toll pathway. © 2017 Elsevier Ltd |
URI: | https://ir.swu.ac.th/jspui/handle/123456789/13082 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85017449346&doi=10.1016%2fj.fsi.2017.04.005&partnerID=40&md5=6e8a109052eabdc84ea47ec277170f54 |
ISSN: | 10504648 |
Appears in Collections: | Scopus 1983-2021 |
Files in This Item:
There are no files associated with this item.
Items in SWU repository are protected by copyright, with all rights reserved, unless otherwise indicated.