Previous Article | Next Article ![]()
Journal of Virology, January 2006, p. 262-269, Vol. 80, No. 1
0022-538X/06/$08.00+0 doi:10.1128/JVI.80.1.262-269.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Duncan R. Smith,1* and
Sakol Panyim1,2
Institute of Molecular Biology and Genetics,1 Department of Biochemistry, Faculty of Science, Mahidol University, Nakorn Pathom, Thailand2
Received 24 September 2005/ Accepted 5 October 2005
The yellow head virus is a positive-sense, single-stranded RNA virus that causes significant mortality in farmed penaeid shrimp. This study sought to isolate and characterize the receptor protein used by the virus to gain entry into Penaeus monodon Oka (lymphoid) organ cells, a primary target of yellow head virus infections. Virus overlay protein binding assay on Oka organ membrane preparations identified a 65-kDa protein, and antibodies raised against this protein inhibited virus entry in primary Oka cell cultures by approximately 80%. N-terminal sequence analysis of the 65-kDa protein generated a 17-amino acid peptide fragment which was used to design degenerate primers that amplified a 1.5-kbp product from Oka organ total RNA, which was cloned and sequenced. Northern analysis and PCR were used to confirm a single RNA transcript that was expressed in most tissues. Subsequently, the mature cDNA was recloned and the expressed protein shown to cross-react with the antibody raised against the original virus binding band. Down regulation of the message through double-stranded RNA-mediated RNA interference silencing resulted in the complete inhibition of virus entry. While the identity of the clone remains unknown, it nevertheless represents the first invertebrate Nidovirus receptor isolated to date.
Present address: Department of Microbiology, Faculty of Science, Chulalongkorn University, Bangkok, Thailand.
This article has been cited by other articles:
| J. Bacteriol. | Mol. Cell. Biol. | Microbiol. Mol. Biol. Rev. |
|---|
| Clin. Vaccine Immunol. | ALL ASM JOURNALS |
|---|