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解析病原体脱落和传播中宿主异质性的遗传和性别特异性来源。

Dissecting genetic and sex-specific sources of host heterogeneity in pathogen shedding and spread.

机构信息

Institute of Evolutionary Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.

Centre for Immunity, Infection and Evolution, University of Edinburgh, Edinburgh, United Kingdom.

出版信息

PLoS Pathog. 2021 Jan 19;17(1):e1009196. doi: 10.1371/journal.ppat.1009196. eCollection 2021 Jan.

Abstract

Host heterogeneity in disease transmission is widespread but precisely how different host traits drive this heterogeneity remains poorly understood. Part of the difficulty in linking individual variation to population-scale outcomes is that individual hosts can differ on multiple behavioral, physiological and immunological axes, which will together impact their transmission potential. Moreover, we lack well-characterized, empirical systems that enable the quantification of individual variation in key host traits, while also characterizing genetic or sex-based sources of such variation. Here we used Drosophila melanogaster and Drosophila C Virus as a host-pathogen model system to dissect the genetic and sex-specific sources of variation in multiple host traits that are central to pathogen transmission. Our findings show complex interactions between genetic background, sex, and female mating status accounting for a substantial proportion of variance in lifespan following infection, viral load, virus shedding, and viral load at death. Two notable findings include the interaction between genetic background and sex accounting for nearly 20% of the variance in viral load, and genetic background alone accounting for ~10% of the variance in viral shedding and in lifespan following infection. To understand how variation in these traits could generate heterogeneity in individual pathogen transmission potential, we combined measures of lifespan following infection, virus shedding, and previously published data on fly social aggregation. We found that the interaction between genetic background and sex explained ~12% of the variance in individual transmission potential. Our results highlight the importance of characterising the sources of variation in multiple host traits to understand the drivers of heterogeneity in disease transmission.

摘要

宿主在疾病传播中的异质性很普遍,但确切地说,不同的宿主特征如何驱动这种异质性仍知之甚少。将个体变异与群体水平的结果联系起来的部分困难在于,个体宿主在行为、生理和免疫等多个轴向上可能存在差异,这些差异将共同影响它们的传播潜力。此外,我们缺乏特征明确的、能够量化关键宿主特征个体变异的经验系统,同时也缺乏对这种变异的遗传或性别来源进行特征描述的系统。在这里,我们使用黑腹果蝇和果蝇 C 病毒作为宿主-病原体模型系统,来剖析与病原体传播密切相关的多个宿主特征的遗传和性别特异性变异来源。我们的研究结果表明,遗传背景、性别和雌性交配状态之间存在复杂的相互作用,这些因素共同导致了感染后寿命、病毒载量、病毒脱落和死亡时病毒载量的很大一部分变异。两个值得注意的发现包括遗传背景和性别之间的相互作用,这几乎解释了病毒载量变异的近 20%,而遗传背景本身则解释了病毒脱落和感染后寿命变异的约 10%。为了了解这些特征的变异如何导致个体病原体传播潜力的异质性,我们将感染后寿命、病毒脱落的测量值与之前关于苍蝇社会聚集的数据相结合。我们发现,遗传背景和性别之间的相互作用解释了个体传播潜力变异的约 12%。我们的研究结果强调了对多个宿主特征的变异来源进行特征描述的重要性,以了解疾病传播异质性的驱动因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e014/7846003/fb7d876af7f2/ppat.1009196.g001.jpg

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