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本文引用的文献

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The polyphagous plant pathogenic fungus Botrytis cinerea encompasses host-specialized and generalist populations.多寄主植物病原真菌灰葡萄孢包含寄主专化型和非专化型种群。
Environ Microbiol. 2019 Dec;21(12):4808-4821. doi: 10.1111/1462-2920.14829. Epub 2019 Nov 3.
2
Genetic Structure of Botrytis cinerea Populations from Different Host Plants in California.加利福尼亚不同寄主植物上灰葡萄孢菌种群的遗传结构
Plant Dis. 2005 Oct;89(10):1083-1089. doi: 10.1094/PD-89-1083.
3
Detection and Molecular Characterization of Boscalid-Resistant Botrytis cinerea Isolates from Strawberry.草莓中对啶酰菌胺具有抗性的灰葡萄孢菌株的检测及分子特征分析
Plant Dis. 2011 Oct;95(10):1302-1307. doi: 10.1094/PDIS-04-11-0317.
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Mating-type loci of Ustilago esculenta are essential for mating and development.糙皮侧耳交配型基因座对于交配和发育是必需的。
Fungal Genet Biol. 2019 Apr;125:60-70. doi: 10.1016/j.fgb.2019.01.008. Epub 2019 Jan 24.
5
Prevalence of Botrytis Cryptic Species in Strawberry Nursery Transplants and Strawberry and Blueberry Commercial Fields in the Eastern United States.美国东部草莓苗圃移栽和草莓蓝莓商业田块中葡萄孢隐种的流行情况。
Plant Dis. 2018 Feb;102(2):398-404. doi: 10.1094/PDIS-07-17-1065-RE. Epub 2017 Dec 18.
6
Striking Similarities Between From Non-agricultural and From Agricultural Habitats.来自非农业栖息地和农业栖息地之间的显著相似之处。
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The evolutionary origins of pesticide resistance.抗农药性的进化起源。
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8
How Does Botrytis cinerea Infect Red Raspberry?灰葡萄孢菌如何感染红树莓?
Phytopathology. 2018 Nov;108(11):1287-1298. doi: 10.1094/PHYTO-01-18-0016-R. Epub 2018 Oct 2.
9
Characterization of Botrytis cinerea isolates collected on pepper in Southern Turkey by using molecular markers, fungicide resistance genes and virulence assay.利用分子标记、杀菌剂抗性基因和致病力测定对土耳其南部辣椒上采集的灰葡萄孢菌分离物进行鉴定。
Infect Genet Evol. 2018 Jun;60:151-159. doi: 10.1016/j.meegid.2018.02.019. Epub 2018 Mar 2.
10
Mating-type genes of the anamorphic fungus Ulocladium botrytis affect both asexual sporulation and sexual reproduction.出芽短梗霉的有性型基因影响无性孢子形成和有性生殖。
Sci Rep. 2017 Aug 11;7(1):7932. doi: 10.1038/s41598-017-08471-3.

人为环境中的真菌进化:感染西北太平洋小果宿主的种群迅速适应人为选择压力。

Fungal Evolution in Anthropogenic Environments: Populations Infecting Small Fruit Hosts in the Pacific Northwest Rapidly Adapt to Human-Induced Selection Pressures.

机构信息

Department of Plant Pathology, Washington State University, Pullman, Washington, USA

USDA ARS, Horticultural Crops Research Laboratory, Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, USA.

出版信息

Appl Environ Microbiol. 2020 Apr 17;86(9). doi: 10.1128/AEM.02908-19.

DOI:10.1128/AEM.02908-19
PMID:32086310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7170486/
Abstract

Many fungal pathogens have short generation times, large population sizes, and mixed reproductive systems, providing high potential to adapt to heterogeneous environments of agroecosystems. Such adaptation complicates disease management and threatens food production. A better understanding of pathogen population biology in such environments is important to reveal key aspects of adaptive divergence processes to allow improved disease management. Here, we studied how evolutionary forces shape population structure of , the causal agent of gray mold, in the Pacific Northwest agroecosystems. Populations of from adjacent fields of small fruit hosts were characterized by combining neutral markers (microsatellites) with markers that directly respond to human-induced selection pressures (fungicide resistance). Populations were diverse, without evidence for recombination and association of pathogen genotype with host. Populations were highly localized with limited migration even among adjacent fields within a farm. A fungicide resistance marker revealed strong selection on population structure due to fungicide use. We found no association of resistance allele with genetic background, suggesting development of fungicide resistance and frequent extinction/recolonization events by different genotypes rather than the spread of resistance alleles among fields via migration of a dominant genotype. Overall our results showed that in agroecosystems, populations respond strongly to selection by fungicide use with greater effect on population structure compared to adaptation to host plant species. This knowledge will be used to improve disease management by developing strategies that limit pathogen local adaptation to fungicides and other human-induced selection pressures present in Pacific Northwest agroecosystems and elsewhere. Agroecosystems represent an efficient model for studying fungal adaptation and evolution in anthropogenic environments. In this work, we studied what evolutionary forces shape populations of one of the most important fungal plant pathogens, , in small fruit agroecosystems of the Pacific Northwest. We hypothesized that host, geographic, and anthropogenic factors of agroecosystems structure populations. By combining neutral markers with markers that directly respond to human-induced selection pressures, we show that pathogen populations are highly localized and that selection pressure caused by fungicide use can have a greater effect on population structure than adaptation to host. Our results give a better understanding of population biology and evolution of this important plant pathogen in heterogeneous environments but also provide a practical framework for the development of efficient management strategies by limiting pathogen adaptation to fungicides and other human-induced selection pressures present in agroecosystems of the Pacific Northwest and elsewhere.

摘要

许多真菌病原体具有较短的世代时间、较大的种群规模和混合繁殖系统,这使其具有高度适应农业生态系统中异质环境的潜力。这种适应能力增加了疾病管理的复杂性,并威胁到粮食生产。更好地了解此类环境中病原体的种群生物学对于揭示适应过程的关键方面至关重要,这有助于改善疾病管理。在这里,我们研究了进化力量如何塑造太平洋西北地区农业生态系统中灰霉病病原菌的种群结构。通过结合中性标记(微卫星)和直接响应人类诱导选择压力的标记(杀菌剂抗性),对来自小果宿主相邻田地的 种群进行了特征描述。种群具有多样性,没有证据表明重组和病原体基因型与宿主之间的关联。种群高度本地化,即使在农场内的相邻田地之间,迁移也很有限。杀菌剂抗性标记揭示了由于杀菌剂使用而对种群结构产生的强烈选择。我们没有发现抗性等位基因与遗传背景之间的关联,这表明杀菌剂抗性的发展和不同基因型的频繁灭绝/再定殖事件,而不是通过迁移优势基因型在田间传播抗性等位基因来导致田间间抗性等位基因的传播。总的来说,我们的研究结果表明,在农业生态系统中, 种群对杀菌剂使用的选择反应强烈,对种群结构的影响大于对宿主植物物种的适应。这一知识将用于通过开发策略来改善疾病管理,这些策略限制了病原体对杀菌剂和其他人类诱导的选择压力的局部适应,这些压力存在于太平洋西北地区和其他地区的农业生态系统中。农业生态系统是研究真菌在人为环境中的适应和进化的有效模型。在这项工作中,我们研究了最重要的真菌植物病原体之一的进化力量如何塑造小果农业生态系统中 的种群。我们假设农业生态系统的宿主、地理和人为因素会影响 种群结构。通过将中性标记与直接响应人类诱导选择压力的标记相结合,我们表明病原体种群高度本地化,并且由杀菌剂使用引起的选择压力对种群结构的影响大于对宿主的适应。我们的研究结果更好地了解了这种重要植物病原体在异质环境中的种群生物学和进化,但也为通过限制病原体对杀菌剂和其他人类诱导的选择压力的适应来制定高效管理策略提供了实用框架,这些压力存在于太平洋西北地区和其他地区的农业生态系统中。