Assessing the effects of quantitative host resistance on the life-history traits of sporulating parasites with growing lesions.

IF 2.2 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Journal of Atmospheric and Solar-Terrestrial Physics Pub Date : 2019-10-09 Epub Date: 2019-10-02 DOI:10.1098/rspb.2019.1244
Melen Leclerc, Julie A J Clément, Didier Andrivon, Frédéric M Hamelin
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Abstract

Assessing life-history traits of parasites on resistant hosts is crucial in evolutionary ecology. In the particular case of sporulating pathogens with growing lesions, phenotyping is difficult because one needs to disentangle properly pathogen spread from sporulation. By considering Phytophthora infestans on potato, we use mathematical modelling to tackle this issue and refine the assessment of pathogen response to quantitative host resistance. We elaborate a parsimonious leaf-scale model by convolving a lesion growth model and a sporulation function, after a latency period. This model is fitted to data obtained on two isolates inoculated on three cultivars with contrasted resistance level. Our results confirm a significant host-pathogen interaction on the various estimated traits, and a reduction of both pathogen spread and spore production, induced by host resistance. Most interestingly, we highlight that quantitative resistance also changes the sporulation function, the mode of which is significantly time-lagged. This alteration of the infectious period distribution on resistant hosts may have strong impacts on the dynamics of parasite populations, and should be considered when assessing the durability of disease control tactics based on plant resistance management. This inter-disciplinary work also supports the relevance of mechanistic models for analysing phenotypic data of plant-pathogen interactions.

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评估宿主定量抗性对有生长病变的孢子寄生虫生活史特征的影响。
评估寄生虫在抗性宿主上的生活史特征在进化生态学中至关重要。在有孢子的病原体有生长性病变的特殊情况下,表型分析是很困难的,因为我们需要将病原体的传播与孢子的产生适当地分开。通过考虑马铃薯上的 Phytophthora infestans,我们利用数学建模来解决这一问题,并完善病原体对宿主抗性定量反应的评估。在潜伏期之后,我们通过病害生长模型和孢子生成函数的卷积,建立了一个简明的叶片尺度模型。该模型适用于接种在三种抗性水平不同的栽培品种上的两个分离株的数据。我们的研究结果证实,在各种估计性状上,宿主与病原体之间存在明显的相互作用,宿主抗性会降低病原体的传播和孢子的产生。最有趣的是,我们强调定量抗性也会改变孢子功能,其模式具有明显的时滞性。抗性宿主感染期分布的这种变化可能会对寄生虫种群的动态产生重大影响,在评估基于植物抗性管理的疾病控制策略的持久性时应加以考虑。这项跨学科工作还证明了机理模型对分析植物与病原体相互作用表型数据的意义。
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来源期刊
Journal of Atmospheric and Solar-Terrestrial Physics
Journal of Atmospheric and Solar-Terrestrial Physics 地学-地球化学与地球物理
CiteScore
4.10
自引率
5.30%
发文量
95
审稿时长
6 months
期刊介绍: The Journal of Atmospheric and Solar-Terrestrial Physics (JASTP) is an international journal concerned with the inter-disciplinary science of the Earth''s atmospheric and space environment, especially the highly varied and highly variable physical phenomena that occur in this natural laboratory and the processes that couple them. The journal covers the physical processes operating in the troposphere, stratosphere, mesosphere, thermosphere, ionosphere, magnetosphere, the Sun, interplanetary medium, and heliosphere. Phenomena occurring in other "spheres", solar influences on climate, and supporting laboratory measurements are also considered. The journal deals especially with the coupling between the different regions. Solar flares, coronal mass ejections, and other energetic events on the Sun create interesting and important perturbations in the near-Earth space environment. The physics of such "space weather" is central to the Journal of Atmospheric and Solar-Terrestrial Physics and the journal welcomes papers that lead in the direction of a predictive understanding of the coupled system. Regarding the upper atmosphere, the subjects of aeronomy, geomagnetism and geoelectricity, auroral phenomena, radio wave propagation, and plasma instabilities, are examples within the broad field of solar-terrestrial physics which emphasise the energy exchange between the solar wind, the magnetospheric and ionospheric plasmas, and the neutral gas. In the lower atmosphere, topics covered range from mesoscale to global scale dynamics, to atmospheric electricity, lightning and its effects, and to anthropogenic changes.
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