A 10-kDa structural protein of porcine reproductive and respiratory syndrome virus encoded by ORF2b

被引:307
作者
Wu, WH
Fang, Y
Farwell, R
Steffen-Bien, M
Rowland, RRR
Christopher-Hennings, J
Nelson, EA
机构
[1] S Dakota State Univ, Dept Vet Sci, Brookings, SD 57007 USA
[2] S Dakota State Univ, Dept Biol Microbiol, Brookings, SD 57007 USA
关键词
arteriviruses; Nidovirales; open reading frame 2 (ORF2); porcine reproductive and respiratory syndrome virus (PRRSV); structural proteins; recombinant protein;
D O I
10.1006/viro.2001.1034
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The major structural proteins of porcine reproductive and respiratory syndrome virus (PRRSV) are derived from ORFs 5, 6, and 7. Western blots of sucrose gradient-purified virions and PRRSV-infected MARC-145 cells, probed with immune pig serum, showed the presence of an additional 10-kDa protein. Nucleotide sequence analysis of North American PRRSV isolate SDSU-23983 revealed a small ORF within ORF2, named ORF2b, which, when translated, produced a 73-amino-acid nonglycosylated protein. Recombinant 2b protein expressed by a baculovirus clone, AcVR2, comigrated with the 10-kDa virus-associated protein. The loss of 10-kDa protein immunoreactivity after absorption of immune sera with lysates from AcVR2-infected insect cells demonstrated that the 2b and 10-kDa proteins are immunologically similar. Immunoblots were also used for the detection of anti-2b activity in serum samples from experimentally infected adult pigs. Antibodies against PRRSV were apparent by 14 days postinfection, followed by anti-2b activity and serum neutralizing activity. The putative ORF2b start codon is only 6 nucleotides downstream of the adenine of the ORF2a start codon. The expression of ORF2a and 2b as enhanced green fluorescent fusion proteins showed that both proteins were translated; however, the ORF2b was preferentially expressed. These results suggest that the 2b protein is virion associated and the principal product of ORF2. (C) 2001 Academic Press.
引用
收藏
页码:183 / 191
页数:9
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