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分子定年和病毒载量增长率表明,在东非和泰国的 HIV-1 感染者中,日食阶段持续了大约一周。

Molecular dating and viral load growth rates suggested that the eclipse phase lasted about a week in HIV-1 infected adults in East Africa and Thailand.

机构信息

U.S. Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD, United States of America.

Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD, United States of America.

出版信息

PLoS Pathog. 2020 Feb 6;16(2):e1008179. doi: 10.1371/journal.ppat.1008179. eCollection 2020 Feb.

DOI:10.1371/journal.ppat.1008179
PMID:32027734
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7004303/
Abstract

Most HIV-1 infected individuals do not know their infection dates. Precise infection timing is crucial information for studies that document transmission networks or drug levels at infection. To improve infection timing, we used the prospective RV217 cohort where the window when plasma viremia becomes detectable is narrow: the last negative visit occurred a median of four days before the first detectable HIV-1 viremia with an RNA test, referred below as diagnosis. We sequenced 1,280 HIV-1 genomes from 39 participants at a median of 4, 32 and 170 days post-diagnosis. HIV-1 infections were dated by using sequence-based methods and a viral load regression method. Bayesian coalescent and viral load regression estimated that infections occurred a median of 6 days prior to diagnosis (IQR: 9-3 and 11-4 days prior, respectively). Poisson-Fitter, which analyzes the distribution of hamming distances among sequences, estimated a median of 7 days prior to diagnosis (IQR: 15-4 days) based on sequences sampled 4 days post-diagnosis, but it did not yield plausible results using sequences sampled at 32 days. Fourteen participants reported a high-risk exposure event at a median of 8 days prior to diagnosis (IQR: 12 to 6 days prior). These different methods concurred that HIV-1 infection occurred about a week before detectable viremia, corresponding to 20 days (IQR: 34-15 days) before peak viral load. Together, our methods comparison helps define a framework for future dating studies in early HIV-1 infection.

摘要

大多数 HIV-1 感染者并不知道自己的感染日期。确切的感染时间对于记录传播网络或感染时药物水平的研究至关重要。为了提高感染时间的准确性,我们使用前瞻性 RV217 队列,其中血浆病毒血症可检测到的窗口期很窄:最后一次阴性就诊发生在首次可检测到 HIV-1 病毒血症的前中位数为四天,下文称为诊断。我们对 39 名参与者的中位数为 4、32 和 170 天的 1280 个 HIV-1 基因组进行了测序。使用基于序列的方法和病毒载量回归方法对 HIV-1 感染进行了日期标记。贝叶斯合并和病毒载量回归估计感染发生在中位数 6 天前诊断(IQR:9-3 和 11-4 天前)。Poisson-Fitter 分析序列之间汉明距离的分布,根据诊断后 4 天采样的序列估计中位数为 7 天前诊断(IQR:15-4 天),但使用 32 天采样的序列没有产生合理的结果。14 名参与者报告在中位数 8 天前诊断(IQR:12-6 天前)有高风险暴露事件。这些不同的方法都表明,HIV-1 感染发生在可检测到病毒血症前一周左右,相当于峰值病毒载量前 20 天(IQR:34-15 天)。总的来说,我们的方法比较有助于确定未来早期 HIV-1 感染研究的框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/1aed7cbe1f99/ppat.1008179.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/3bd9e519e5c2/ppat.1008179.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/3f3d55614b06/ppat.1008179.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/11fa21631a76/ppat.1008179.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/edc792d40b26/ppat.1008179.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/7bb849fec689/ppat.1008179.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/1aed7cbe1f99/ppat.1008179.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/3bd9e519e5c2/ppat.1008179.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/3f3d55614b06/ppat.1008179.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/11fa21631a76/ppat.1008179.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/edc792d40b26/ppat.1008179.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/7bb849fec689/ppat.1008179.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c895/7004303/1aed7cbe1f99/ppat.1008179.g006.jpg

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