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本文引用的文献

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First Report of Melampsora larici-populina on Populus spp. in Eastern North America.北美东部杨树山杨栅锈菌的首次报道
Plant Dis. 2004 Jan;88(1):85. doi: 10.1094/PDIS.2004.88.1.85B.
2
Histological Aspects of a Hypersensitive Response in Poplar to Melampsora larici-populina.杨树对黄杨栅锈菌过敏反应的组织学观察。
Phytopathology. 1999 Mar;89(3):233-8. doi: 10.1094/PHYTO.1999.89.3.233.
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Expression of Endochitinase from Trichoderma harzianum in Transgenic Apple Increases Resistance to Apple Scab and Reduces Vigor.哈茨木霉内切几丁质酶在转基因苹果中的表达增加了对苹果黑星病的抗性并降低了活力。
Phytopathology. 2000 Jan;90(1):72-7. doi: 10.1094/PHYTO.2000.90.1.72.
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Use of solid-phase extraction to determine ergosterol concentrations in plant tissue colonized by fungi.使用固相萃取法测定真菌定殖植物组织中的麦角固醇浓度。
Appl Environ Microbiol. 1996 Feb;62(2):415-9. doi: 10.1128/aem.62.2.415-419.1996.
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In vivo study of trichoderma-pathogen-plant interactions, using constitutive and inducible green fluorescent protein reporter systems.利用组成型和诱导型绿色荧光蛋白报告系统对木霉-病原菌-植物相互作用进行的体内研究。
Appl Environ Microbiol. 2004 May;70(5):3073-81. doi: 10.1128/AEM.70.5.3073-3081.2004.
6
Nonhost resistance: how much do we know?非宿主抗性:我们了解多少?
Trends Plant Sci. 2004 Feb;9(2):97-104. doi: 10.1016/j.tplants.2003.12.005.
7
Organization of genetic variation in individuals of arbuscular mycorrhizal fungi.丛枝菌根真菌个体的遗传变异组织
Nature. 2004 Feb 19;427(6976):733-7. doi: 10.1038/nature02290.
8
Seasonal dynamics of previously unknown fungal lineages in tundra soils.苔原土壤中先前未知真菌谱系的季节动态。
Science. 2003 Sep 5;301(5638):1359-61. doi: 10.1126/science.1086940.
9
Branching is coordinated with mitosis in growing hyphae of Aspergillus nidulans.在构巢曲霉生长的菌丝中,分支与有丝分裂相互协调。
Fungal Genet Biol. 2003 Oct;40(1):15-24. doi: 10.1016/s1087-1845(03)00053-7.
10
Mathematics of quantitative kinetic PCR and the application of standard curves.定量动力学PCR的数学原理及标准曲线的应用
Nucleic Acids Res. 2003 Aug 15;31(16):e93. doi: 10.1093/nar/gng093.

通过实时定量聚合酶链反应对活体中专性活体营养型病原菌生长进行监测

In vivo monitoring of obligate biotrophic pathogen growth by kinetic PCR.

作者信息

Boyle Brian, Hamelin Richard C, Séguin Armand

机构信息

Natural Resources Canada, Canadian Forest Service, Laurentian Forestry Centre, 1055 du PEPS, PO Box 3800, Sainte-Foy, Quebec, Canada G1V 4C7.

出版信息

Appl Environ Microbiol. 2005 Mar;71(3):1546-52. doi: 10.1128/AEM.71.3.1546-1552.2005.

DOI:10.1128/AEM.71.3.1546-1552.2005
PMID:15746359
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1065157/
Abstract

The plant kingdom is constantly challenged by a battery of evolving pathogens. New species or races of pathogens are discovered on crops that were initially bred for disease resistance, and globalization is facilitating the movement of exotic pests. Among these pests, obligate biotrophic parasites make up some of the most damaging groups and have been particularly challenging to study. Here we demonstrate the utility of kinetic PCR (kPCR) (real-time PCR, quantitative PCR) to assess the growth of poplar rust, caused by Melampsora species, by quantification of pathogen DNA. kPCR allowed the construction of reliable growth curves from inoculation through the final stages of uredinial maturation, as well as pathogen monitoring before symptoms become visible. Growth parameters, such as latency period, generation time in logarithmic growth, and the increase in DNA mass at saturation, were compared in compatible, incompatible, and nonhost interactions. Pathogen growth was monitored in different applications dealing with plant pathology, such as host and pathogen diversity and transgenic crop improvement. Finally, the capacity of kPCR to differentiate pathogens in the same sample has broad molecular ecology applications for dynamically monitoring the growth of fungi in their environments or in mixed populations or to measure the efficacy of pest control strategies.

摘要

植物王国不断受到一系列不断进化的病原体的挑战。在最初为抗病性而培育的作物上发现了新的病原体物种或小种,全球化也促进了外来害虫的传播。在这些害虫中,专性活体寄生菌构成了一些最具破坏性的群体,并且一直是研究的特别挑战。在这里,我们展示了动力学PCR(kPCR)(实时PCR、定量PCR)通过对病原体DNA进行定量来评估由栅锈菌属物种引起的杨树锈病生长的实用性。kPCR能够构建从接种到夏孢子堆成熟最后阶段的可靠生长曲线,以及在症状出现之前进行病原体监测。在亲和、不亲和和非寄主相互作用中比较了生长参数,如潜伏期、对数生长期的世代时间以及饱和时DNA量的增加。在处理植物病理学的不同应用中监测病原体生长,如寄主和病原体多样性以及转基因作物改良。最后,kPCR区分同一样本中病原体的能力在广泛的分子生态学应用中,可用于动态监测真菌在其环境中或混合群体中的生长,或测量害虫控制策略的效果。