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首页> 外文期刊>Journal of Translational Medicine >Selective transmission of R5 HIV-1 variants: where is the gatekeeper?
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Selective transmission of R5 HIV-1 variants: where is the gatekeeper?

机译:R5 HIV-1变体的选择性传播:看门人在哪里?

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To enter target cells HIV-1 uses CD4 and a coreceptor. In vivo the coreceptor function is provided either by CCR5 (for R5) or CXCR4 (for X4 HIV-1). Although both R5 and X4 HIV-1 variants are present in body fluids (semen, blood, cervicovaginal and rectal secretions), R5 HIV-1 appears to transmit infection and dominates early stages of HIV disease. Moreover, recent sequence analysis of virus in acute infection shows that, in the majority of cases of transmission, infection is initiated by a single virus. Therefore, the existence of a “gatekeeper” that selects R5 over X4 HIV-1 and that operates among R5 HIV-1 variants has been suggested. In the present review we consider various routes of HIV-transmission and discuss potential gatekeeping mechanisms associated with each of these routes. Although many mechanisms have been identified none of them explains the almost perfect selection of R5 over X4 in HIV-1 transmission. We suggest that instead of one strong gatekeeper there are multiple functional gatekeepers and that their superimposition is sufficient to protect against X4 HIV-1 infection and potentially select among R5 HIV-1 variants. In conclusion, we propose that the principle of multiple barriers is more general and not restricted to protection against X4 HIV-1 but rather can be applied to other phenomena when one factor has a selective advantage over the other(s). In the case of gatekeepers for HIV-1 transmission, the task is to identify them and to decipher their molecular mechanisms. Knowledge of the gatekeepers‘ localization and function may enable us to enhance existing barriers against R5 transmission and to erect the new ones against all HIV-1 variants.
机译:为了进入靶细胞,HIV-1使用CD4和一个共受体。在体内,CCR5(对于R5)或CXCR4(对于X4 HIV-1)提供共受体功能。尽管R5和X4 HIV-1变体都存在于体液(精液,血液,宫颈阴道和直肠分泌物)中,但R5 HIV-1似乎可以传播感染并在HIV疾病的早期占主导地位。此外,最近对急性感染中病毒的序列分析表明,在大多数传播病例中,感染是由单一病毒引发的。因此,已经提出了选择“ R5”而不是“ X4 HIV-1”的“守门人”,并且在“ R5 HIV-1”变体中起作用。在当前的审查中,我们考虑了艾滋病毒传播的各种途径,并讨论了与这些途径相关的潜在关守机制。尽管已经确定了许多机制,但没有一个机制可以解释在HIV-1传播中R5优于X4的完美选择。我们建议,而不是一个强大的网守,而是多个功能的网守,并且它们的叠加足以防止X4 HIV-1感染,并有可能在R5 HIV-1变体中进行选择。总之,我们认为多重障碍的原则更为笼统,不限于针对X4 HIV-1的保护,而是当一个因素比其他因素具有选择优势时,可以应用于其他现象。对于HIV-1传播的看门人,任务是识别他们并破译其分子机制。对网守的本地化和功能的了解可能使我们能够增强针对R5传播的现有障碍,并为所有HIV-1变体建立新的障碍。

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