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Identification of a Domain within the Human T-Cell Leukemia Virus Type 2 Envelope Required for Syncytium Induction and Replication

机译:识别合胞体诱导和复制所需的人类T细胞白血病病毒2型信封中的域

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摘要

In vitro infection by human T-cell leukemia virus type 1 and 2 (HTLV-1 and HTLV-2) can result in syncytium formation, facilitating viral entry. Using cell lines that were susceptible to HTLV-2-mediated syncytium formation but were nonfusogenic with HTLV-1, we constructed chimeric envelopes between HTLV-1 and -2 and assayed for the ability to induce syncytia in BJAB cells and HeLa cells. We have identified a fusion domain composed of the first 64 amino acids at the amino terminus of the HTLV-2 transmembrane protein, p21, the retention of which was required for syncytium induction. Construction of replication-competent HTLV genomic clones allowed us to correlate the ability of HTLV-2 to induce syncytia with the ability to replicate in BJAB cells. Differences in the ability to induce syncytia were not due to differences in the levels of total or cell membrane-associated envelope or in the formation of multimers. Therefore, we have localized a fusion domain within the amino terminus of the transmembrane protein of HTLV-2 envelope that is necessary for syncytium induction and viral replication.
机译:1型和2型人类T细胞白血病病毒(HTLV-1和HTLV-2)的体外感染可导致合胞体形成,促进病毒进入。使用对HTLV-2介导的合胞体形成敏感但与HTLV-1非融合的细胞系,我们在HTLV-1和-2之间构建了嵌合包膜,并测定了在BJAB细胞和HeLa细胞中诱导合胞体的能力。我们已经确定了一个融合域,由HTLV-2跨膜蛋白p21的氨基末端的前64个氨基酸组成,其融合的诱导是必需的。具有复制能力的HTLV基因组克隆的构建使我们能够将HTLV-2诱导合胞体的能力与在BJAB细胞中复制的能力相关联。诱导合胞体能力的差异不是由于总膜水平或与细胞膜相关的包膜水平或多聚体形成水平的差异。因此,我们已经定位了HTLV-2包膜跨膜蛋白氨基端的融合域,这对于合胞体诱导和病毒复制是必需的。

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