杨树溃疡病病原的多重PCR检测技术

利用真菌通用引物ITS1/ITS4,EF1-728F/EF1-986R对4种杨树溃疡病病原菌株和环境样本的核糖体DNA内部转录间隔区ITS序列和转录延伸因子EF-1α基因序列分别进行普通和多重PCR检测,再进行测序比对分析。结果表明:退火温度为55.6℃,各引物终浓度为0.2μmol·L-1,可以成功地扩增出菌株和环境样本的目的条带,并通过测序比对鉴定出多种来自培养和环境病害组织中的溃疡病病菌,多重PCR能够检测到1ng的基因组DNA。研究结果将为建立溃疡病病原多重PCR鉴定技术和以环境溃疡病病害样本为直接检测鉴定对象的高通量的基因芯片检测方法奠定基础。     

中药材黄连水浸提液对梨树腐烂病的室内防效评价

梨树腐烂病是危害梨树生产的重要病害之一,为探寻梨树腐烂病(Pear valsa canker)的绿色防治药剂,室内采用菌丝生长速率法和离体枝条打孔接种法,测定了不同浓度的黄连水浸提液对梨树腐烂病菌菌落生长的影响及其在离体梨树枝条上的保护作用。结果表明,不同浓度的黄连水浸提液对梨树腐烂病菌均有不同程度的抑制作用,其中浓度为5.000 0%时抑菌率高达100%;当黄连水浸提液浓度为5.000 0%和10.000 0%时,病疤面积间无显著差异,室内防效分别高达75.8%和78.2%。表明不同浓度的中药材黄连水浸提液对梨树腐烂病均有一定防效,浓度为5.000 0%时对菌丝的抑制作用和离体枝条保护作用最为经济有效。     

周至县核桃溃疡病发生规律及控制方法

调查分析了周至县核桃溃疡病发生规律,提出了包括农业、物理、化学、管理等措施在内的预防和防治方法.     

Isolation and characterisation of phages against Pseudomonas syringae pv. actinidiae

Purpose: Pseudomonas syringae pv. actinidiae causes bacterial canker of kiwifruit and is responsible for severe economic losses and emergence of drug-resistant bacteria. Bacteriophages are viruses that infect target bacterial hosts and may be the best strategy to prevent and control kiwifruit canker disease. The objective of this experiment was to monitor the prevalence of Pseudomonas syringae pv. actinidiae and provide insight for the use of phages in biological control.

Materials and methods: In this study, 52 strains of Pseudomonas syringae pv. actinidiae were isolated from 68 stem samples of kiwi plant (cv. Hongyang & Jinkui). Following polymerase chain reaction (PCR) analysis, 15 isolates belonging to biovar 3 were identified, one of which was named XWY0007 and used as the target strain to isolate the phages. Thirty-six phages were isolated and purified from a total of 51 surface water samples collected in Shanghai. All phages were identified by transmission electron microscopy (TEM) and their host ranges were evaluated. Three phages, designated φXWY0013, φXWY0014 and φXWY0026 were selected and further characterised using one-step growth curve and stability at different temperatures and pH.

Results and conclusions: The isolated phages are promising for use as antimicrobials against bacterial canker in kiwi. This report is regarding Pseudomonas syringae pv. actinidiae and its phages from major areas of kiwifruit cultivation.     

猕猴桃溃疡病菌biovar 3群体MLVA分型技术的建立与应用

 丁香假单胞菌猕猴桃致病变种生物型3(Pseudomonas syringae pv. actinidiae biovar 3,Psa3)是猕猴桃溃疡病菌的世界流行群体,但仅在中国存在复杂的遗传多样性。开发适于Psa3群体分型的MLVA(multilocus variable-number tandem-repeat analysis)技术是探索中国Psa3起源与流行学特性的基础。本研究对7个Psa3菌株进行了全基因组测序,结合已公布的86个全基因组数据,进行比较分析发现,中国Psa3至少存在7个亚群;在各亚群间存在多态性的24个串联重复序列中,其中10个可以通过琼脂糖凝胶电泳区分开且变异指数合适,据此建立了适于Psa3的MLVA技术。采用该技术对分别来自贵州和陕西的62和9个Psa3菌株进行群体分型,分型结果与全基因组分析高度一致,证明该MLVA体系分型准确。MLVA分型结果表明:贵州主产区修文县Psa3有3个MLVA群体,其中亚群4的组内分化明显,代表最早发生的群体;而亚群 1和3的结构单一,且多在新果园发现,是新传入群体。总之,本研究建立了一套可用于Psa3群体分型的MLVA技术,将有助于解析中国各猕猴桃产区Psa3群体结构,以及探索中国Psa3的起源、传播和流行学特征。     

Differentiating A and B groups of Leptosphaeria maculans, causal agent of stem canker (blackleg) of oilseed rape

Stem canker or blackleg of brassicas, caused by Leptosphaeria maculans , is one of the most damaging diseases of winter oilseed rape in the UK. Airborne ascospores, released in autumn and winter, initiate leaf infections which may lead to colonization of the petiole and, later in the season, formation of stem lesions and cankers. Although isolates of the pathogen differ in ability to cause damaging stem cankers, this is not readily apparent from leaf spotting or stem lesion symptoms. However, several cultural, biochemical and genetic characteristics appear to be associated with the ability to form damaging stem cankers and isolates can be assigned to one of two groups, termed A and B, on the basis of differences in these characteristics. To investigate the relationship between leaf spotting symptoms and subsequent stem canker formation, and to improve understanding of the epidemiology of this pathogen, it is desirable to differentiate between the stem canker forming A group and the less damaging B group of L. maculans . Characterization of isolate type is also important in seed testing and crop breeding programs, particularly in countries such as Canada and Poland where the A type is not ubiquitous. This article reviews methods, including plant assays, assessments of growth characteristics in vitro , isozyme analyses, secondary metabolite profiling, serology, and nucleic acid analyses, that can be used to differentiate the A and B groups.     

Interactions Between French Isolates of Phomopsis/Diaporthe Helianthi Munt.-Cvet. et al. and Sunflower (Helianthus annuus L.) Genotypes

Three artificial infection tests measuring the rate of mycelial growth of 7 Phomopsis/Diaporthe helianthi isolates were used on leaves, stems and capitula of 6 sunflower hybrids. Isolates and hybrids were chosen to cover the range of variability and resistance levels known at the present time. Significant genotype and isolate effects and isolate×genotype interactions were shown in all the tests, with some changes in order of hybrids according to the isolate used for infection. Consequences of interactions in breeding for stable resistance to P./D. helianthi are discussed.     

杨树栽植初期体内水分含量变化与大斑型溃疡病关系的研究

由Dothiorella gregaria Sacc.引起的杨树大斑型溃疡病是辽宁、河北、山西等地区杨树上的重要病害。近几年我们对该病的防治措施进行了研究,发现用截头法种植杨树,对减轻发病程度,提高造林成活率及生长量均有显著作用。在研究这种栽培技术的防病原理过程中,我们首先对树体内各部位水分的变化与发病的关系进行了探讨。     

管芯片技术通量检测杨树溃疡病病菌的应用

正基因芯片技术因能对生物样本进行快速、高通量的定性和定量分析,而在植物病害诊断中也得到普遍的应用[1]。树木溃疡病是指引起木本植物树皮上出现溃疡腐烂等症状的病害[2]。引起杨树溃疡病的真菌种类较多,加之其无性型和有性型多样,所以,关于杨树溃疡病病原菌的报道多有不同。另外,受地理位置、寄主植物关系及分类体系的限制,迫切需要发展不依赖于常规分离培养的病原鉴定新技术。     

Current situation and characterization of Pseudomonas syringae pv. actinidiae on kiwifruit in Galicia (northwest Spain)

Bacterial canker of kiwifruit, caused by Pseudomonas syringae pv. actinidiae (Psa), is a disease that is spreading rapidly in several kiwifruit‐producing countries, causing significant economic losses. In 2011, it was detected for the first time in Spain, in the south of Galicia (northwest Spain). Kiwifruit orchards were therefore inspected and sampled in 2011 and 2012 to determine the pathogen distribution, and the isolates obtained were characterized by morphology, fatty acids profile, biochemical tests and molecular techniques. Isolates were obtained from Actinidia deliciosa ‘Hayward’ (from leaves, canes, flower buds, fruits and roots), from A. deliciosa ‘Summer’, from Actinidia chinensis ‘Jin Tao’ (from canes and leaves) and from A. chinensis pollinator ‘Belén’ (from canes). Results of the analysis of the cfl gene (phytotoxin production‐related), the tox–argK gene cluster and phylogenetic analysis of the cts gene demonstrated that all Psa isolates from northwest Spain correspond to the Psa3 population, which includes strains of haplotype 2. This is the first record of Psa3 and haplotype 2 in Spain.