Lentiviral Resistance to Tetherin

描述（由申请人提供）：Tetherin （BST-2或CD317）是一种干扰素诱导的跨膜蛋白，可抑制病毒从感染细胞中释放。尽管大多数猿类免疫缺陷病毒（siv）在非人灵长类宿主中使用Nef来克服拴链蛋白的限制，但HIV-1的Vpu蛋白和HIV-2的Env蛋白已经进化到在人类中发挥这一功能，因为人类拴链蛋白的细胞质结构域中缺乏赋予Nef易感性的序列。我们最近在恒河猴中发现了gp41尾部的代偿性变化，该变化在一种网络缺失的SIV毒株中恢复了对tetherin的抗性，该毒株在恒河猴中恢复了致病表型。这些观察结果类似于HIV-2 Env对人类tetherin的拮抗的适应性，并暗示对tetherin的抗性对慢病毒的发病机制很重要。我们现在已经确定了HIV-1 Nef等位基因能够

DESCRIPTION (provided by applicant): Tetherin (BST-2 or CD317) is an interferon-inducible transmembrane protein that inhibits virus release from infected cells. Whereas most simian immunodeficiency viruses (SIVs) use Nef to overcome restriction by tetherin in their non-human primate hosts, the Vpu protein of HIV-1 and the Env protein of HIV-2 have evolved to serve this function in humans due to the absence of sequences in the cytoplasmic domain of human tetherin that confer susceptibility to Nef. We recently identified compensatory changes in the gp41 tail that restore resistance to tetherin in a nef-deleted strain of SIV that regained a pathogenic phenotype in rhesus macaques. These observations are analogous to the adaptation of HIV-2 Env for antagonism of human tetherin and imply that resistance to tetherin is important for lentiviral pathogenesis. We have now identified HIV-1 Nef alleles that are able to counteract restriction by human tetherin, further underscoring the extraordinary plasticity of the primate lentiviruses in adapting to the tetherin proteins of their respective hosts and revealing a previously unappreciated role for Nef in HIV-1 infection. The studies outlined in this proposal seek to advance our understanding of the mechanisms of lentiviral resistance to tetherin and their role in immunodeficiency virus infection. The first objective of this proposal (Aim 1) is to define the molecular interactions and cellular trafficking pathways involved in SIV Nef antagonism of rhesus tetherin. This aim will build on work by our group identifying Nef as the viral gene product of SIV that antagonizes restriction by tetherin to determinie the nature of the molecular interactions between Nef and tetherin and the fate of tetherin in SIV-infected cells. Our second objective (Aim 2) is define the genetic changes associated with the gain of anti-tetherin activity by HIV-1 Nef and the mechanism by which HIV-1 Nef counteracts human tetherin. These studies are important for determining how widespread this activity of Nef is among primary HIV-1 isolates, the circumstances that lead to tetherin antagonism by HIV-1 Nef, and the mechanistic differences in tetherin antagonism by HIV-1 Nef versus SIV Nef. Our third objective (Aim 3) is to assess the natural variation in anti-tetherin activity for primary HIV-2 En proteins and to define the sequences in Env required for this activity. These studies will reveal the prevalence/range of anti-tetherin activity for primary HIV-2 Env proteins and the molecular adaptations in Env that contribute to this activity. By comparing the activity of Env alleles derived from individuals with progressive courses of HIV-2 infection to Env alleles derived from asymptomatic individuals who contain virus replication, these studies may also reveal whether differences in tetherin antagonism are related to differences in HIV-2 pathogenesis.