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Presence of long-term stable quasispecies of human immunodeficiency virus type 1 inferred using a quasi-steady-state multiscale model

机译:使用准稳态多尺度模型推断出人类免疫缺陷病毒的长期稳定Quaspecies的存在

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Mathematical modeling studies are useful for an improved understanding of the dynamics of human immunodeficiency virus type 1 (HIV-1) infection dynamics. Mutations are considered to facilitate the escape of HIV-1 from the immune system and anti-HIV-1 drugs. Thus, quasispecies, populations of closely related virus variants, are important in HIV-1 infection. Recently, a multiscale model incorporating both intracellular viral genome replication and extracellular viral infection was developed to study viral dynamics. A multiscale model has also been developed for analyzing HIV-1 infection. However, the multiscale model could not reveal high quasispecies diversity. Herein, I present a new quasi-steady-state multiscale model of HIV-1 infection that incorporates a quasi-steady state among the virion, uninfected cell, and virion–uninfected cell complex similar to that among the enzyme, substrate, and enzyme–substrate complex in enzyme kinetics. This new model can reveal stable quasispecies better than the previously described multiscale model. The model and the strategy to calculate the model might be useful in the field of demographics where multiscale models are used. For HIV-1 infection, the model might be useful for analyzing and predicting the breakthrough of drug-resistant mutants in the future.
机译:数学建模研究可用于改善对人免疫缺陷病毒类型1(HIV-1)感染动态的动态的理解。突变被认为是促进免疫系统和抗HIV-1药物的HIV-1逃逸。因此,Quaspecies,密切相关的病毒变异的群体在HIV-1感染中是重要的。最近,开发了一种包含细胞内病毒基因组复制和细胞外病毒感染的多尺度模型以研究病毒动力学。也开发了多尺度模型来分析HIV-1感染。但是,多尺度模型无法揭示高Quasispecies多样性。在此,我介绍了一种新的拟稳态多尺度模型的HIV-1感染,其含有类似于酶,底物和酶中的病毒群岛,未感染的细胞和维病 - 未感染的细胞复合物中的准稳态。酶动力学中的底物复合物。这个新模型可以比先前描述的多尺度模型更好地揭示稳定的Quasispecies。计算模型的模型和策略可能在使用多尺度模型的人口统计领域中有用。对于HIV-1感染,该模型可能用于分析和预测未来耐药突变体的突破。

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