A Putative Cell Surface Receptor for White Spot Syndrome Virus Is a Member of a Transporter Superfamily

被引:34
|
作者
Huang, Huai-Ting [1 ]
Leu, Jiann-Horng [1 ,2 ]
Huang, Po-Yu [1 ]
Chen, Li-Li [1 ,2 ]
机构
[1] Natl Taiwan Ocean Univ, Inst Marine Biol, Keelung, Taiwan
[2] Natl Taiwan Ocean Univ, Ctr Excellence Marine Bioenvironm & Biotechnol, Keelung, Taiwan
来源
PLOS ONE | 2012年 / 7卷 / 03期
关键词
SHRIMP PENAEUS-MONODON; LEUKEMIA-VIRUS; BACULOVIRUS WSBV; BINDING-PROTEIN; IDENTIFICATION; PATHOGENESIS; ENTRY; WSSV; NUCLEOTIDES; INFECTION;
D O I
10.1371/journal.pone.0033216
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
White spot syndrome virus (WSSV), a large enveloped DNA virus, can cause the most serious viral disease in shrimp and has a wide host range among crustaceans. In this study, we identified a surface protein, named glucose transporter 1 (Glut1), which could also interact with WSSV envelope protein, VP53A. Sequence analysis revealed that Glut1 is a member of a large superfamily of transporters and that it is most closely related to evolutionary branches of this superfamily, branches that function to transport this sugar. Tissue tropism analysis showed that Glut1 was constitutive and highly expressed in almost all organs. Glut1's localization in shrimp cells was further verified and so was its interaction with Penaeus monodon chitin-binding protein (PmCBP), which was itself identified to interact with an envelope protein complex formed by 11 WSSV envelope proteins. In vitro and in vivo neutralization experiments using synthetic peptide contained WSSV binding domain (WBD) showed that the WBD peptide could inhibit WSSV infection in primary cultured hemocytes and delay the mortality in shrimps challenged with WSSV. These findings have important implications for our understanding of WSSV entry.
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页数:10
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