Within-host dynamics and evolution

P. Schmid-Hempel
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Abstract

Infections typically spread from a primary site to target organs. Rapid early defences are critical to contain an infection. However, recognition is not error-free and shows a trade-off between specificity and sensitivity. The within-host dynamics of an infection can be studied in various ways, e.g. with target cell-limited models. The disease space can trace within-host infection trajectories and predict the eventual outcome. Also, computational and systems immunology identify important defence elements and predict the course of an infection. Infecting populations evolve within their hosts. Horizontal transfer of genetic elements, recombination, and mutations thereby allow pathogens to escape host defences; examples are escape mutants or antigenic variation. The evolution of antimicrobial resistance is of special concern. Co-infecting parasites, such as bacteria, can cooperate to exploit a host (e.g. by production of siderophores) or compete for access (e.g. by releasing bacteriocins). Multiscale models combine within- and between-host episodes.
宿主内动态和进化
感染通常从原发部位扩散到靶器官。早期的快速防御对于控制感染至关重要。然而,识别并非没有错误,需要在特异性和敏感性之间进行权衡。感染的宿主内动力学可以用各种方法进行研究,例如用靶细胞限制模型。疾病空间可以追踪宿主内感染轨迹并预测最终结果。此外,计算和系统免疫学识别重要的防御因素,并预测感染的过程。感染种群在宿主体内进化。遗传元素的水平转移、重组和突变从而使病原体逃脱宿主的防御;例如逃逸突变或抗原性变异。抗菌素耐药性的演变值得特别关注。共同感染的寄生虫,如细菌,可以合作利用宿主(例如通过产生铁载体)或竞争获取宿主(例如通过释放细菌素)。多尺度模型结合了宿主内部和宿主之间的情节。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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