4.6 Article

Cloning of Litopenaeus vannamei CD63 and it's role in white spot syndrome virus infection

Journal

DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY
Volume 60, Issue -, Pages 209-217

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dci.2016.03.004

Keywords

Litopenaeus vannamei; CD63; Cloning; WSSV; Interaction

Funding

  1. National Basic Research Program (973 program) of China [2012CB114401]
  2. Modern Agro-industry Technology Research System [nycytx-46]
  3. National Natural Science Foundation of China [31302233]
  4. special foundation under the construction programme for 'Taishan Scholarship' of Shandong Province of China
  5. Programme for Chinese Outstanding Talents in Agriculture Scientific Research

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White Spot Syndrome Virus (WSSV) is currently the most serious shrimp pathogen, which has brought huge losses to shrimp industry worldwide. CD63 of shrimp belongs to the tetraspanin superfamily, which plays an important role in signal transduction and immune process. In this paper, CD63 cDNA sequence of Litopenaeus vannamei was cloned using RACE method. The amplified sequence is 1472 bp, with its ORF 744 bp, encoding 247 amino acids. Bioinformatics analysis showed that the sequence of LvCD63 has 93% similarity with Penaeus monodon and 92% similarity with Fenneropenaeus chinensis. Real-time PCR analysis showed that the mRNA levels of LvCD63 expressed in the tissues of hemocytes, gill, epithelial tissue, heart, lymphoid, hepatopancreas, stomach, intestines, muscle and nerve. Among these tissues the highest expression level was showed in the tissue of haemolymph, followed by epithelial tissue, hepatopancreas, and nerve. The lowest expression level of LvCD63 was appeared in the muscle tissue. After WSSV challenge, the expression levels of LvCD63 were both up-regulated in the tissues of gill and epithelial. However the expression level of LvCD63 in hepatopancreas was down-regulated. Far-western blot analysis showed that LvCD63 interacts with VP28, and both VP28N and VP28C fragments interact with LvCD63. Flow cytometry analysis showed that LvCD63 was present on the surface of hemocytes and it is required for binding of WSSV virions. Neutral experiments in vivo showed that LvCD63LEL delayed WSSV infection in shrimp. (C) 2016 Elsevier Ltd. All rights reserved.

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