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首页> 外文期刊>Virology >Variable infectivity and conserved engagement in cell-to-cell viral transfer by HIV-1 Env from Clade B transmitted founder clones
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Variable infectivity and conserved engagement in cell-to-cell viral transfer by HIV-1 Env from Clade B transmitted founder clones

机译:来自CLADE B的HIV-1 ENV传输的创始克隆,可变感染性和守恒的细胞对细胞病毒转移的参与

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摘要

HIV-1 transmission is usually initiated by a single viral strain called transmitted/ founder (T/F) virus. In in vitro models, HIV-1 can efficiently spread via cell-free and virological synapse (VS)-mediated cell-to-cell infection. Both modes of infection require the viral glycoprotein Envelope (Env). The efficiency with which T/F Envs initiate VS and mediate cell-to-cell infection has not been well characterized. Here we tested a panel of isogenic HIV-1 molecular clones that carry different Clade B T/F Envs. We found that despite variable infectivity among different Env clones in the two modes of infection, T/F Envs generally mediated efficient VS formation and subsequent cell-to-cell transfer. In contrast, in vitro infectivity of the T/F Env clones was more variable and strongly correlated with intrinsic fusogenicity of various Envs. We speculate that the conservation of cell-to-cell transfer by T/F Env is indicative of a biologically important function of Env.
机译:HIV-1传输通常由称为传输/创始人(T / F)病毒的单一病毒菌株引发。 在体外模型中,HIV-1可以通过无细胞和病毒学突触(VS)介导的细胞对细胞感染有效地传播。 两种感染模式都需要病毒糖蛋白包膜(ENV)。 T / F EVEN引发VS和介导细胞对细胞感染的效率并未得到很好的表征。 在这里,我们测试了一种携带不同的疏水性的Isogenic HIV-1分子克隆的面板。 我们发现,尽管在两种感染模式中不同的ENV克隆之间的可变感染性,但是T / F通常介导的有效vs形成和随后的细胞对细胞转移。 相反,T / F EVEN克隆的体外感染性更可变,与各种envs的内在熔体性强烈相关。 我们推测,T / F ENV的细胞对细胞传递的保护表明ENV的生物学重要功能。

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