Dipartimento di Scienze Agrarie e Ambientali, Università degli Studi di Milano, Milan, Italy.
Ordine dei Dottori Agronomi e dei Dottori Forestali di Milano, Milan, Italy.
Appl Environ Microbiol. 2022 Nov 8;88(21):e0101022. doi: 10.1128/aem.01010-22. Epub 2022 Oct 17.
, the oomycete causing grapevine downy mildew, is one of the most important pathogens in viticulture. is a polycyclic pathogen, able to carry out numerous secondary cycles of infection during a single vegetative grapevine season, by producing asexual spores (zoospores) within sporangia. The extent of these infections is strongly influenced by both the quantity (density) and quality (infectivity) of the inoculum produced by the pathogen. To date, the protocols for evaluating all these characteristics are quite limited and time-consuming and do not allow all the information to be obtained in a single run. In this study, a protocol combining flow cytometry (FCM) and fluorescence-activated cell sorting (FACS) was developed to investigate the composition, the infection efficiency and the dynamics of the inoculum produced by for secondary infection cycles. In our analyses, we identified different structures within the inoculum, including degenerated and intact sporangia. The latter have been sorted, and single sporangia were directly inoculated on grapevine leaf discs, thus allowing a thorough investigation of the infection dynamics and efficiency. In detail, we determined that, in our conditions, 8% of sporangia were able to infect the leaves and that on a susceptible variety, the time required by the pathogen to reach 50% of total infection is about 10 days. The analytical approach developed in this study could open a new perspective to shed light on the biology and epidemiology of this important pathogen. secondary infections contribute significantly to the epidemiology of this important plant pathogen. However, the infection dynamics of asexual spores produced by this organism are still poorly investigated. The main challenges in dissecting the grapevine- interaction are attributable to the biotrophic adaptation of the pathogen. This work provides new insights into the infection efficiency and dynamics imputable to sporangia, contributing useful information on grapevine downy mildew epidemiology. Moreover, future applications of the sorting protocol developed in this work could yield a significant and positive impact in the study of , providing unmatched resolution, precision, and accuracy compared with the traditional techniques.
疫霉菌是引起葡萄霜霉病的卵菌,是葡萄栽培中最重要的病原体之一。疫霉菌是一种多循环病原体,能够在单个营养期内通过在孢子囊中产生无性孢子(游动孢子)进行多次次级感染循环。这些感染的程度受到病原体产生的接种体数量(密度)和质量(感染力)的强烈影响。迄今为止,评估所有这些特征的方案相当有限且耗时,并且不能在单个运行中获得所有信息。在这项研究中,开发了一种结合流式细胞术(FCM)和荧光激活细胞分选(FACS)的方案,以研究 疫霉菌产生的次级感染循环接种体的组成、感染效率和动态。在我们的分析中,我们在接种体中鉴定了不同的结构,包括退化和完整的孢子囊。后者已被分选,并且单个孢子囊被直接接种在葡萄叶片圆盘上,从而可以彻底研究感染动态和效率。具体而言,我们确定在我们的条件下,8%的孢子囊能够感染叶片,并且在易感品种上,病原体达到 50%总感染所需的时间约为 10 天。本研究中开发的分析方法可以为该重要病原体的生物学和流行病学提供新的视角。疫霉菌次级感染对这种重要植物病原体的流行病学有重大贡献。然而,该生物体产生的无性孢子的感染动态仍未得到充分研究。剖析病原体生物营养适应性的主要挑战归因于 疫霉菌与葡萄的相互作用。这项工作提供了对 疫霉菌孢子囊感染效率和动态的新见解,为葡萄霜霉病流行病学提供了有用的信息。此外,本工作中开发的分选方案的未来应用可能会对 的研究产生重大而积极的影响,与传统技术相比,提供无与伦比的分辨率、精度和准确性。