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Defining early SIV replication and dissemination dynamics following vaginal transmission

机译:定义阴道传播后的早期SIV复制和传播动力学

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Understanding HIV transmission is critical to guide the development of prophylactic interventions to prevent infection. We used a nonhuman primate (NHP) model with a synthetic swarm of sequence-tagged variants of SIVmac239 (“SIVmac239X”) and scheduled necropsy during primary infection (days 3 to 14 after challenge) to study viral dynamics and host responses to the establishment and dissemination of infection following vaginal challenge. We demonstrate that local replication was initiated at multiple sites within the female genital tract (FGT), with each site having multiple viral variants. Local replication and spread in the FGT preceded lymphatic dissemination. Innate viral restriction factors were observed but appeared to follow viral replication and were ineffective at blocking initial viral establishment and dissemination. However, major delays were observed in time to dissemination in animals and among different viral variants within the same animal. It will be important to assess how phenotypic differences affect early viral dynamics.
机译:了解艾滋病毒的传播对于指导预防感染预防措施的发展至关重要。我们使用非人类灵长类动物(NHP)模型和SIVmac239(“ SIVmac239X”)序列标签变体的合成群以及原发感染期间(感染后3到14天)的计划性尸检来研究病毒动力学和宿主对建立和感染的反应阴道感染后传播感染。我们证明了在女性生殖道(FGT)内的多个位点启动了局部复制,每个位点都具有多个病毒变体。 FGT中的局部复制和扩散先于淋巴传播。观察到先天性病毒限制因子,但似乎遵循病毒复制,并且不能有效阻断最初的病毒建立和传播。然而,在动物中以及在同一动物中的​​不同病毒变体之间的传播时间上观察到主要的延迟。评估表型差异如何影响早期病毒动力学将很重要。

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