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药物敏感和耐药病原体模型共存的系统比较。

Systematic comparison of coexistence in models of drug-sensitive and drug-resistant pathogen strains.

机构信息

Department of Mathematics, Simon Fraser University, Canada.

Department of Mathematics, Simon Fraser University, Canada.

出版信息

Theor Popul Biol. 2020 Jun;133:150-158. doi: 10.1016/j.tpb.2019.12.001. Epub 2019 Dec 28.

Abstract

A number of mathematical models have recently been proposed to explain empirical trends of pathogen diversity. In particular, long-term coexistence of both drug-sensitive and drug-resistant variants of a single pathogen is something of a mystery, given that simple models of pathogens competing for the same ecological niche predict competitive exclusion, and more complex models admitting coexistence require assumptions that may not be justified. Coinfection is among the candidate mechanisms to generate coexistence, as it occurs in many pathogens and provides the opportunity for strains to interact directly. Recently, coinfection and competitive release have been described as creating a form of negative frequency-dependent selection that promotes coexistence, and a range of models containing coinfection have been proposed as having generic stable coexistence of multiple strains. This abundance of new models presents the challenge of comparison and interpretation. To this end, we describe a dimensionless quantity that can be used to compare the amount of coexistence generated by different models. We focus on models that include coinfection, although this framework could be generalized to a larger class of structured models.

摘要

近来提出了许多数学模型来解释病原体多样性的经验趋势。特别是,鉴于竞争同一生态位的病原体的简单模型预测竞争排除,而允许共存的更复杂模型需要的假设可能没有依据,因此单一病原体的耐药和敏感变体长期共存是一个谜。合并感染是产生共存的候选机制之一,因为它发生在许多病原体中,并为菌株提供了直接相互作用的机会。最近,合并感染和竞争释放被描述为创造了一种负频率依赖性选择,促进了共存,并且提出了一系列包含合并感染的模型,作为多种菌株的通用稳定共存。大量新模型提出了比较和解释的挑战。为此,我们描述了一个无量纲量,可以用来比较不同模型产生的共存数量。我们专注于包含合并感染的模型,尽管该框架可以推广到更大类别的结构模型。

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