共查询到19条相似文献，搜索用时 125 毫秒
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植物对病原菌的防卫反应ＣｈｒｉｓＢｏｗｌｅｒ等植物与病原菌之间有亲和和不亲和两种类型的关系。不亲和关系（抗病寄主，无毒病原菌）常常表现过敏反应（在病原菌穿透位点局部植物细胞坏死），这种过敏反应可以阻止病原菌进一步扩展到其他细胞。在亲和反应（感病寄主，... 相似文献
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在高等植物的生活环境中,微生物与植物的关系是错综复杂的,在植物病原学的研究发展过程中,人们不仅对主效病原菌(major pathogen)的研究不断深入,而且微效病原菌(minor pathogen)也日益引起更多为学者的关注。目前关于根际和叶面此类病原菌的研究报道较多,但植物体内是否也存在有此作用的微效病原菌? 相似文献
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水稻-稻瘟菌(Magnaporthe grisea)相互作用的细胞生物学研究 总被引：2，自引：0，他引：2
在植物一病原菌非亲和性互作中,病菌感染后寄主细胞中会发生一系列与植物抗病性相关的事件。这些事件在时间和空间上与寄主细胞坏死和病原菌的受抑制密切相关,因而人们推测这些事件在植物抗病性中具有重要的意义。 相似文献
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植物病害分子流行学概述 总被引：5，自引：1，他引：4
本文概要地介绍了植物病理学新研究领域——植物病害分子流行学的基本概念、进展和在几个主要方面的研究实例。分子生物技术在病原鉴定方面得到了广泛应用;定量的分子生物技术在测定病菌初侵染源方面显示出特有的快速、准确的优势;分子流行学应用分子生物技术监测病害和病原菌群体的动态,克服了传统流行学方法的弱点;作为有力的补充,分子生物技术正在用于探讨和推测病原菌远距离传播的路径,并注重研究病原菌群体的时、空动态变化,病原菌的长期进化,以及与病害发展的关系;病原群体的竞争将得到更深入的研究以揭示其变化是如何导致植物病害大流行;应用分子流行学手段,植物抗病性的鉴定将大大加速和简化;病害防治策略的制定将具有更科学的依据。宏观与微观研究手段的结合将越来越显示其在植物病害流行学研究中的巨大潜力。 相似文献
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以植物病原细菌黄单胞菌的avrXa7基因和ahpC基因的2个突变体及其野生型菌株为研究对象,探讨植物病原细菌内源过氧化氢水平与菌株毒性的联系。AR/HRP法分析病原菌的过氧化氢清除力,组织化学法对细胞内过氧化氢进行定量和定位分析。结果表明,avrXa7基因的突变诱导病原菌毒性的显著降低,并引起病原菌内源过氧化氢积累水平显著下降;ahpC基因的突变诱导病原菌内源过氧化氢水平显著降低,但未能引起病原菌毒性产生显著的变化。研究结果说明,在植物病原细菌黄单胞病菌的致病机制中,病原菌内源过氧化氢的积累水平并不能直接决定菌株的毒性,而是处在avrXa7基因的下游,受到avrXa7或者更多毒性相关基因的调控,参与病原菌的致病过程。 相似文献
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基于PCR技术的植物病原菌分子定量检测技术研究进展 总被引：2，自引：0，他引：2
植物病原菌的菌源量是病害发生和流行的重要因子之一,对其精准的定量测定或检测可大大提高植物病害预测的准确性,本文对实时荧光定量PCR (qPCR)与数字PCR在植物病原菌定量检测、以及基于RNA水平的real-time PCR和基于核酸染料(EMA/PMA)与qPCR相结合的技术在植物病原菌活体定量检测中的应用进行了综述,并展望其在植物病害流行和预测中的应用前景。 相似文献
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我国几种植物病害抗药性监测情况 总被引：3，自引：0，他引：3
病害和虫害一样可造成农作物毁灭性危害。目前,采用化学农药防治植物病害已成为我国保证农作物高产稳产的重要措施。然而,一些重要植物病原物极易产生抗药性,常常在部分地区导致杀菌剂防治效果下降或完全失效。因此,对病原菌的抗药群体动态进行监测和检测,是预测和治... 相似文献
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植物细胞培养技术与杀菌剂生物测定的结合是一个新的研究领域。通过植物细胞培养技术，在植物细胞水平上建立病原菌／植物悬浮细胞体系筛选系统、快速、准确和高效地筛选杀菌剂。本文讨论病原菌／植物悬浮细胞体系，作为一种新型杀菌剂筛选体系的可行性与特点。 相似文献
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Kang S Blair JE Geiser DM Khang CH Park SY Gahegan M O'Donnell K Luster DG Kim SH Ivors KL Lee YH Lee YW Grünwald NJ Martin FM Coffey MD Veeraraghavan N Makalowska I 《Phytopathology》2006,96(9):920-925
ABSTRACT Plant pathogen culture collections are essential resources in our fight against plant disease and for connecting discoveries of the present with established knowledge of the past. However, available infrastructure in support of culture collections is in serious need of improvement, and we continually face the risk of losing many of these collections. As novel and reemerging plant pathogens threaten agriculture, their timely identification and monitoring depends on rapid access to cultures representing the known diversity of plant pathogens along with genotypic, phenotypic, and epidemiological data associated with them. Archiving such data in a format that can be easily accessed and searched is essential for rapid assessment of potential risk and can help track the change and movement of pathogens. The underexplored pathogen diversity in nature further underscores the importance of cataloguing pathogen cultures. Realizing the potential of pathogen genomics as a foundation for developing effective disease control also hinges on how effectively we use the sequenced isolate as a reference to understand the genetic and phenotypic diversity within a pathogen species. In this letter, we propose a number of measures for improving pathogen culture collections. 相似文献
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Water used for the irrigation of plants has the potential to harbour and spread plant pathogens yet little research is conducted within this field. This review was undertaken to critically review current understanding of waterborne fungal and oomycete plant pathogens in open irrigation systems, particularly in the context of plant biosecurity. It was determined that very limited data exists on these plant pathogens, with the majority of previous studies only recording pathogen presence. There are significant gaps in current knowledge of pathogen survival and spread, and very limited information on their ability to cause disease when contaminated irrigation water is applied to crops. This review highlights the need for new research on the epidemiology and pathogenicity of putative plant pathogens isolated from water, in order to determine their risk to crops. The importance of regular monitoring of irrigation systems for the early detection of plant pathogens is also discussed. 相似文献
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马铃薯是重要的粮食作物, 由致病疫霉侵染引发的晚疫病长期严重制约马铃薯产业的健康发展, 因此, 国内外均将马铃薯晚疫病列为重大病害。目前, 抗病品种选育栽培、晚疫病预测预报和化学防治等相结合的晚疫病综合防治手段已得到普遍推广, 但晚疫病局部大流行在全世界范围内仍时有发生, 给粮食安全和生态安全带来巨大挑战。本文回顾了我国晚疫病的部分研究历史, 集中关注致病疫霉与寄主的互作机制领域, 梳理了近年来关于致病疫霉侵入机理、效应蛋白毒力功能、病原菌变异规律、马铃薯抗病机理等方面的重要研究结果并展望未来主要的研究方向, 以期为晚疫病基础研究和防治技术革新提供参考。 相似文献
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冬生疫霉(Phytophthora hibernalis)的快速分子检测 总被引：4，自引：1，他引：3
由冬生疫霉(Phytophthora hibernalis)引起的疫病是一类植物检疫性病害。为建立该病原菌的快速检测技术,本文比较分析了冬生疫霉和其它疫霉的ITS序列,在此基础上设计了一对检测冬生疫霉的特异性引物751F/752R,该对引物从冬生疫霉中扩增得到一条616bp的条带,而其它19种疫霉和其它真菌菌株均无扩增条带,表明该对引物对冬生疫霉具有特异性。在25μL PCR反应体系中,引物751F/752R检测灵敏度为10龟基因组DNA;而以卵菌ITS区通用引物ITS1/ITS4和751F/752R进行套式PCR扩增,能够检测到10ag的基因组DNA,使检测灵敏度提高了1000倍。该检测体系对灭菌水中游动孢子的检测灵敏度可达0.5个游动孢子。结合快速碱裂解法提取发病组织的DNA,采用该PCR检测技术,在1个工作日内即可从人工接种发病的植物组织中特异性的检测到该病原菌。表明本研究建立的检测方法可用于冬生疫霉的快速分子检测。 相似文献
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土壤中烟草根黑腐病菌的实时定量PCR检测技术研究 总被引：1，自引：0，他引：1
Thielaviopsis basicola is a soil-borne plant pathogen which causes root rot disease in tobacco plants. Detection and monitoring of T. basicolain soil is of great significance to control this disease. Based on the differences in internal transcribed spacer (ITS) sequences of T. basicola and other fungal pathogens, a specific primer pair Tb1/Tb2 for T. basicolawas developed. The results showed that the primer pair gave a single amplicon of 330 bp from T. basicola and revealed no undesirable cross-reaction with other seven soil-borne pathogen isolates and three tobacco rhizosphere dominant fungi isolates. With a series of 10-fold genomic DNA dilutions of T. basicola, the detection limit of 1 pg/μL in conventional PCRand100 fg/μL in real-time quantitative PCR was achieved. With DNA from the soil inoculated with different numbers of T. basicola conidia, the detection limit was 10 conidia per reaction in conventional PCR and 0.4 conidia per reaction in real-time quantitative PCR. 相似文献
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Crop loss due to plant pathogens has provoked renewed interest in bacteriophages as a feasible biocontrol strategy of plant diseases. Phage cocktails in particular present a viable option for broadening the phage host range, limiting the emergence of bacterial resistance while maintaining the lytic activity of the phages. It is therefore important that the design used to formulate a phage cocktail should result in the most effective cocktail against the pathogen. It is also critical that certain factors are considered during the formulation and application of a phage cocktail: their stability, the production time and cost of complex cocktails, the potential impact on untargeted bacteria, the timing of phage application, and the persistence in the plant environment. Continuous monitoring is required to ensure that the efficacy of a cocktail is sustained due to the dynamic nature of phages. Although phage cocktails are considered as a plausible biocontrol strategy of phytobacteria, more research needs to be done to understand the complex interaction between phages and bacteria in the plant environment, and to overcome the technical obstacles. © 2019 Society of Chemical Industry 相似文献
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Molecular detection of Phytophthora capsici in infected plant tissues, soil and water 总被引：2，自引：0，他引：2
A species-specific PCR assay was developed for rapid and accurate detection of the pathogenic oomycete Phytophthora capsici in diseased plant tissues, soil and artificially infested irrigation water. Based on differences in internal transcribed spacer (ITS) sequences of Phytophthora spp. and other oomycetes, one pair of species-specific primers, PC-1/PC-2, was synthesized. After screening 15 isolates of P. capsici and 77 isolates from the Ascomycota, Basidiomycota, Deuteromycota and Oomycota, the PC-1/PC-2 primers amplified only a single PCR band of c . 560 bp from P. capsici . The detection sensitivity with primers PC-1/PC-2 was 1 pg genomic DNA (equivalent to half the genomic DNA of a single zoospore) per 25- µ L PCR reaction volume; traditional PCR could detect P. capsici in naturally infected plant tissues, diseased field soil and artificially inoculated irrigation water. Using ITS1/ITS4 as the first-round primers and PC-1/PC-2 in the second round, nested PCR procedures were developed, increasing detection sensitivity to 1 fg per 25- µ L reaction volume. The results suggested that the assay detected the pathogen more rapidly and accurately than standard isolation methods. The PCR-based methods developed here could simplify both plant disease diagnosis and pathogen monitoring, as well as guiding plant disease management. 相似文献
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Albert H. Ellingboe 《European journal of plant pathology / European Foundation for Plant Pathology》2001,107(1):79-84
The interactions between plants and pathogens can be shifted to favor either plant of pathogen by small changes in the environment, primarily temperature and plant nutrition, and it leaves a quandary as to whether the plant on pathogen is most affected by the change in the environment. The stage of development of a plant can affect the resistance or susceptibility to a pathogen. A plant may be susceptible to a given pathogen a one stage of development but resistant at another stage of development. The view of the gene-for-gene hypotheses as a one-for-one relationship is not supported by experiments that ask whether avirulence genes and resistance genes function alone. The term genomics has been intemreted several different ways, but its most useful impact on studies of host-pathogen interactions will, most likely, be to find all the pieces to the puzzle of how plants and pathogens communicate. 相似文献
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中国马铃薯晚疫病监测预警系统“China-blight”的组建及运行 总被引：4，自引：0，他引：4
马铃薯晚疫病是严重威胁世界马铃薯生产和粮食安全的重要病害之一,同时也是植物病害中流行速度最快的病害之一。由于品种多不抗病,目前国内外主要依靠化学防治控制该病害。为了提高用药的时效性,将信息技术与植物病害流行学原理相结合,设计并组建了中国马铃薯晚疫病监测预警系统"China-blight"(www.china-blight.net)。该系统由"中国晚疫病实时分布"、"未来48小时不同区域晚疫病菌侵染危险性预测"和"晚疫病化学防治决策支持系统"等子系统构成,此外还包括"晚疫病防治方法"、"品种抗病性"、"化学药剂库"、"其他病虫害"、"问题与经验交流"和"用户田间管理电子档案"等知识信息与服务功能。通过对2009年我国北方马铃薯一作区6-7月份病害侵染时段出现次数与晚疫病实际发生情况进行比较,预测信息与病害实际发生程度相符,该系统可以用于对马铃薯晚疫病田间防治的指导。 相似文献