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用于理解抗原变异 RNA 病毒进化动态的无量纲数。

A dimensionless number for understanding the evolutionary dynamics of antigenically variable RNA viruses.

机构信息

Department of Biology, Duke University, PO Box 90338, Durham, NC 27708, USA.

出版信息

Proc Biol Sci. 2011 Dec 22;278(1725):3723-30. doi: 10.1098/rspb.2011.0435. Epub 2011 May 4.

Abstract

Antigenically variable RNA viruses are significant contributors to the burden of infectious disease worldwide. One reason for their ubiquity is their ability to escape herd immunity through rapid antigenic evolution and thereby to reinfect previously infected hosts. However, the ways in which these viruses evolve antigenically are highly diverse. Some have only limited diversity in the long-run, with every emergence of a new antigenic variant coupled with a replacement of the older variant. Other viruses rapidly accumulate antigenic diversity over time. Others still exhibit dynamics that can be considered evolutionary intermediates between these two extremes. Here, we present a theoretical framework that aims to understand these differences in evolutionary patterns by considering a virus's epidemiological dynamics in a given host population. Our framework, based on a dimensionless number, probabilistically anticipates patterns of viral antigenic diversification and thereby quantifies a virus's evolutionary potential. It is therefore similar in spirit to the basic reproduction number, the well-known dimensionless number which quantifies a pathogen's reproductive potential. We further outline how our theoretical framework can be applied to empirical viral systems, using influenza A/H3N2 as a case study. We end with predictions of our framework and work that remains to be done to further integrate viral evolutionary dynamics with disease ecology.

摘要

抗原变异的 RNA 病毒是全球传染病负担的重要贡献者。它们无处不在的一个原因是,它们能够通过快速抗原进化逃避群体免疫,从而重新感染以前感染过的宿主。然而,这些病毒在抗原上进化的方式是高度多样化的。有些病毒在长期内只有有限的多样性,每出现一种新的抗原变异体,就会伴随着旧变异体的取代。其他病毒随着时间的推移会迅速积累抗原多样性。还有一些病毒的动态可以被认为是这两个极端之间的进化中间体。在这里,我们提出了一个理论框架,通过考虑给定宿主群体中病毒的流行病学动态,旨在理解这些进化模式的差异。我们的框架基于一个无量纲数,概率地预测病毒抗原多样化的模式,从而量化病毒的进化潜力。因此,它在精神上类似于基本繁殖数,这是一个众所周知的无量纲数,用于量化病原体的繁殖潜力。我们进一步概述了如何将我们的理论框架应用于流感 A/H3N2 等实证病毒系统,并对该框架的预测进行了总结,同时还指出了进一步将病毒进化动态与疾病生态学相结合所需完成的工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cff1/3203497/bb165c834009/rspb20110435-g1.jpg

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