HIV-1 病毒储库中任务诱发功能基因组网络的可区分拓扑结构。

IF 4.6 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES iScience Pub Date : 2024-10-21 eCollection Date: 2024-11-15 DOI:10.1016/j.isci.2024.111222
Janusz Wiśniewski, Kamil Więcek, Haider Ali, Krzysztof Pyrc, Anna Kula-Păcurar, Marek Wagner, Heng-Chang Chen
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引用次数: 0

摘要

HIV-1 病毒库具有异质性,既有完整的前病毒,也有缺陷的前病毒。为了加深我们对这种异质性 HIV-1 病毒库及其功能影响的理解,我们结合图论的基本概念来描述 HIV-1 病毒库的组成。我们的分析发现,在比较抗逆转录病毒疗法(ART)治疗的HIV-1感染者和精英控制者时,网络中存在明显的拓扑特性,其特点是富含完整和缺陷前病毒基因的免疫学特征。关键变量 "富集因子 "在网络中不同拓扑特性的分类中发挥了关键作用。宿主基因表达加强了精英控制者和抗逆转录病毒疗法治疗患者之间分类的准确性。模拟不同图网络的马尔可夫链建模表明,精英控制者和非精英控制者之间存在内在障碍。总之,我们的研究为利用基因组学方法和数学工具来揭示 HIV-1 病毒库的复杂性提供了一个很好的范例。
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Distinguishable topology of the task-evoked functional genome networks in HIV-1 reservoirs.

HIV-1 reservoirs display a heterogeneous nature, lodging both intact and defective proviruses. To deepen our understanding of such heterogeneous HIV-1 reservoirs and their functional implications, we integrated basic concepts of graph theory to characterize the composition of HIV-1 reservoirs. Our analysis revealed noticeable topological properties in networks, featuring immunologic signatures enriched by genes harboring intact and defective proviruses, when comparing antiretroviral therapy (ART)-treated HIV-1-infected individuals and elite controllers. The key variable, the rich factor, played a pivotal role in classifying distinct topological properties in networks. The host gene expression strengthened the accuracy of classification between elite controllers and ART-treated patients. Markov chain modeling for the simulation of different graph networks demonstrated the presence of an intrinsic barrier between elite controllers and non-elite controllers. Overall, our work provides a prime example of leveraging genomic approaches alongside mathematical tools to unravel the complexities of HIV-1 reservoirs.

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来源期刊
iScience
iScience Multidisciplinary-Multidisciplinary
CiteScore
7.20
自引率
1.70%
发文量
1972
审稿时长
6 weeks
期刊介绍: Science has many big remaining questions. To address them, we will need to work collaboratively and across disciplines. The goal of iScience is to help fuel that type of interdisciplinary thinking. iScience is a new open-access journal from Cell Press that provides a platform for original research in the life, physical, and earth sciences. The primary criterion for publication in iScience is a significant contribution to a relevant field combined with robust results and underlying methodology. The advances appearing in iScience include both fundamental and applied investigations across this interdisciplinary range of topic areas. To support transparency in scientific investigation, we are happy to consider replication studies and papers that describe negative results. We know you want your work to be published quickly and to be widely visible within your community and beyond. With the strong international reputation of Cell Press behind it, publication in iScience will help your work garner the attention and recognition it merits. Like all Cell Press journals, iScience prioritizes rapid publication. Our editorial team pays special attention to high-quality author service and to efficient, clear-cut decisions based on the information available within the manuscript. iScience taps into the expertise across Cell Press journals and selected partners to inform our editorial decisions and help publish your science in a timely and seamless way.
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