Anderson D E, Torres J V
Department of Medical Microbiology and Immunology, School of Medicine, University of California, Davis 95616, USA.
Viral Immunol. 1999;12(1):47-56. doi: 10.1089/vim.1999.12.47.
Type D simian retroviruses (SRV) cause an acquired immunodeficiency syndrome (AIDS) in monkeys. Results of infection with SRV range from complete recovery with absence of viremia to a viremic state, which produces AIDS-like symptoms and culminates in death. These varied outcomes render the interaction of the host and SRV an attractive model for the study of immunosuppressive retrovirus resulting in different pathologic consequences. We describe here the isolation and determination of the molecular weight of the receptor for SRV. We demonstrate that a cell receptor with the same molecular weight is bound by the envelope protein of all five serotypes of SRV. We also show that the receptor recognizes a region containing amino acids 142-167 of the envelope protein of SRV serotype 1 (SRV-1). In addition, we show that a different region of SRV serotype 2 (SRV-2) envelope protein containing amino acids 93-106, interacts with a cell receptor of identical molecular weight. Furthermore, polyclonal and monoclonal antibodies that are directed to envelope epitopes 142-167 of SRV-1 or to 93-106 of SRV-2, specifically neutralize only the respective viral serotype. Our results indicate that the neutralization of SRV infectivity by antibodies is achieved through blocking the interaction between the virus and its cell receptor.
D型猿猴逆转录病毒(SRV)可导致猴子患上获得性免疫缺陷综合征(AIDS)。感染SRV的结果从无病毒血症的完全康复到病毒血症状态不等,后者会产生类似AIDS的症状并最终导致死亡。这些不同的结果使得宿主与SRV之间的相互作用成为研究导致不同病理后果的免疫抑制逆转录病毒的一个有吸引力的模型。我们在此描述了SRV受体的分离及其分子量的测定。我们证明,所有五种血清型的SRV包膜蛋白都能结合具有相同分子量的细胞受体。我们还表明,该受体识别SRV 1型(SRV-1)包膜蛋白中包含氨基酸142-167的区域。此外,我们表明,SRV 2型(SRV-2)包膜蛋白中包含氨基酸93-106的不同区域与相同分子量的细胞受体相互作用。此外,针对SRV-1包膜表位142-167或SRV-2的93-106的多克隆和单克隆抗体,仅能特异性中和各自的病毒血清型。我们的结果表明,抗体对SRV感染性的中和是通过阻断病毒与其细胞受体之间的相互作用来实现的。