基因组熵与网络中心性对比:食源性致病菌进化的探索与开发。

IF 2 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Sheryl Le Chang, Carl J E Suster, Rebecca Rockett, Adam Svahn, Oliver Cliff, Alicia Arnott, Qinning Wang, Rady Kim, Basel Suliman, Mailie Gall, Tania Sorrell, Vitali Sintchenko, Mikhail Prokopenko
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引用次数: 0

摘要

模拟食源性病原体的进化对减轻和预防疫情至关重要。我们应用网络理论和信息论方法,通过研究包括几次暴发在内的5年全基因组测序监测数据,追踪澳大利亚新南威尔士州沙门氏菌的进化途径。该研究基于遗传接近性导出了无向和有向基因型网络,并将网络的结构特性(中心性)与其功能特性(患病率)联系起来。无向网络的中心性-流行空间揭示了病原体之间显著的探索-利用区别,并通过规范化香农熵和相应壳基因组的Fisher信息进一步量化。通过在中心性-流行空间中沿着进化路径跟踪概率密度,还分析了这种区别。我们量化了进化路径,并表明病原体在考虑的时期内探索进化搜索空间开始利用其环境(其流行率增加导致爆发),但最终遇到流行病控制措施形成的瓶颈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genome entropy and network centrality contrast exploration and exploitation in evolution of foodborne pathogens.

Modelling evolution of foodborne pathogens is crucial for mitigation and prevention of outbreaks. We apply network-theoretic and information-theoretic methods to trace evolutionary pathways ofSalmonellaTyphimurium in New South Wales, Australia, by studying whole genome sequencing surveillance data over a five-year period which included several outbreaks. The study derives both undirected and directed genotype networks based on genetic proximity, and relates the network's structural property (centrality) to its functional property (prevalence). The centrality-prevalence space derived for the undirected network reveals a salient exploration-exploitation distinction across the pathogens, further quantified by the normalised Shannon entropy and the Fisher information of the corresponding shell genome. This distinction is also analysed by tracing the probability density along evolutionary paths in the centrality-prevalence space. We quantify the evolutionary pathways, and show that pathogens exploring the evolutionary search-space during the considered period begin to exploit their environment (their prevalence increases resulting in outbreaks), but eventually encounter a bottleneck formed by epidemic containment measures.

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来源期刊
Physical biology
Physical biology 生物-生物物理
CiteScore
4.20
自引率
0.00%
发文量
50
审稿时长
3 months
期刊介绍: Physical Biology publishes articles in the broad interdisciplinary field bridging biology with the physical sciences and engineering. This journal focuses on research in which quantitative approaches – experimental, theoretical and modeling – lead to new insights into biological systems at all scales of space and time, and all levels of organizational complexity. Physical Biology accepts contributions from a wide range of biological sub-fields, including topics such as: molecular biophysics, including single molecule studies, protein-protein and protein-DNA interactions subcellular structures, organelle dynamics, membranes, protein assemblies, chromosome structure intracellular processes, e.g. cytoskeleton dynamics, cellular transport, cell division systems biology, e.g. signaling, gene regulation and metabolic networks cells and their microenvironment, e.g. cell mechanics and motility, chemotaxis, extracellular matrix, biofilms cell-material interactions, e.g. biointerfaces, electrical stimulation and sensing, endocytosis cell-cell interactions, cell aggregates, organoids, tissues and organs developmental dynamics, including pattern formation and morphogenesis physical and evolutionary aspects of disease, e.g. cancer progression, amyloid formation neuronal systems, including information processing by networks, memory and learning population dynamics, ecology, and evolution collective action and emergence of collective phenomena.
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