Saman E, Breugelmans K, Heyndrickx L, Merregaert J
N.V. Innogenetics Research Laboratories, Antwerp, Belgium.
J Virol. 1990 Dec;64(12):6319-24. doi: 10.1128/JVI.64.12.6319-6324.1990.
The genome of equine infectious anemia virus (EIAV) contains several small open reading frames (ORFs), the importance of which in the development of the virus is not clear. We investigated the possibility that the largest of these ORFs (ORF S3) is expressed during the course of the viral infection. The ORF S3 information was expressed in Escherichia coli, and the antigen was used to raise monospecific antiserum. A 20-kDa protein expressed in cells producing EIAV was identified as the gene product of ORF S3. Furthermore, sera from EIAV-infected animals specifically recognized this protein, indicating that the ORF S3 antigen is expressed in vivo as well. A model for the expression of this new viral antigen is presented. The proposed splicing pattern is similar to that of the VEP-1 protein of maedi-visna-virus, which tempts us to speculate that ORF S3 defines the second exon of the EIAV Rev protein.
马传染性贫血病毒(EIAV)的基因组包含几个小的开放阅读框(ORF),但其在病毒发育中的重要性尚不清楚。我们研究了这些ORF中最大的一个(ORF S3)在病毒感染过程中是否表达的可能性。将ORF S3信息在大肠杆菌中表达,并用该抗原制备单特异性抗血清。在产生EIAV的细胞中表达的一种20 kDa蛋白被鉴定为ORF S3的基因产物。此外,来自EIAV感染动物的血清能特异性识别该蛋白,表明ORF S3抗原在体内也有表达。本文提出了这种新病毒抗原的表达模型。所提出的剪接模式与梅迪-维斯纳病毒的VEP-1蛋白相似,这促使我们推测ORF S3定义了EIAV Rev蛋白的第二个外显子。