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一种用于宿主内病毒系统发育的非参数分析框架以及HIV-1奠基者多样性测试。

A non-parametric analytic framework for within-host viral phylogenies and a test for HIV-1 founder multiplicity.

作者信息

Lewitus Eric, Rolland Morgane

机构信息

U.S. Military HIV Research Program (MHRP), WRAIR, 503 Robert Grant Avenue, Silver Spring, MD, USA.

Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., 6720A Rockledge Dr, Bethesda, MD, USA.

出版信息

Virus Evol. 2019 Nov 4;5(2):vez044. doi: 10.1093/ve/vez044. eCollection 2019 Jul.

DOI:10.1093/ve/vez044
PMID:31700680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6826062/
Abstract

Phylogenetics is a powerful tool for understanding the diversification dynamics of viral pathogens. Here we present an extension of the spectral density profile of the modified graph Laplacian, which facilitates the characterization of within-host molecular evolution of viruses and the direct comparison of diversification dynamics between hosts. This approach is non-parametric and therefore fast and model-free. We used simulations of within-host evolutionary scenarios to evaluate the efficiency of our approach and to demonstrate the significance of interpreting a viral phylogeny by its spectral density profile in terms of diversification dynamics. The key features that are captured by the profile are positive selection on the viral gene (or genome), temporal changes in substitution rates, mutational fitness, and time between sampling. Using sequences from individuals infected with HIV-1, we showed the utility of this approach for characterizing within-host diversification dynamics, for comparing dynamics between hosts, and for charting disease progression in infected individuals sampled over multiple years. We furthermore propose a heuristic test for assessing founder heterogeneity, which allows us to classify infections with single and multiple HIV-1 founder viruses. This non-parametric approach can be a valuable complement to existing parametric approaches.

摘要

系统发育学是理解病毒病原体多样化动态的有力工具。在此,我们展示了修正图拉普拉斯算子谱密度分布的一种扩展,它有助于刻画病毒在宿主体内的分子进化,并能直接比较不同宿主间的多样化动态。这种方法是非参数的,因此快速且无需模型。我们使用宿主体内进化情景的模拟来评估我们方法的效率,并证明从多样化动态角度通过病毒系统发育的谱密度分布来解释病毒进化的重要性。该分布所捕捉到的关键特征包括病毒基因(或基因组)上的正选择、替换率的时间变化、突变适应性以及采样间隔时间。利用感染HIV - 1个体的序列,我们展示了这种方法在刻画宿主体内多样化动态、比较不同宿主间动态以及描绘多年来采样的感染个体疾病进展方面的实用性。我们还提出了一种用于评估奠基者异质性的启发式检验方法,它能让我们对由单一和多种HIV - 1奠基者病毒引起的感染进行分类。这种非参数方法可以成为现有参数方法的有价值补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/686bb569d101/vez044f8.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/e87ed543cd81/vez044f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/527443cb4983/vez044f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/c4152de82e90/vez044f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/df27ec88870a/vez044f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/2a4ff74efc6a/vez044f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/686bb569d101/vez044f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/5dec55f2da6c/vez044f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/485ef585e7dd/vez044f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/e87ed543cd81/vez044f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/527443cb4983/vez044f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/c4152de82e90/vez044f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/df27ec88870a/vez044f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/2a4ff74efc6a/vez044f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b6c9/6826062/686bb569d101/vez044f8.jpg

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