药剂拌种对春油菜白粉病和茎象甲的防效及对油菜产量的影响

为明确不同药剂拌种对春油菜出苗率、病虫害防效及产量的影响, 本文在3种不同种植密度下, 针对春油菜白粉病、油菜茎象甲, 选择25 g/L咯菌腈FSC、600 g/L吡虫啉SC、30%噻虫嗪SC、600 g/L吡虫啉SC+25 g/L咯菌腈FSC、30%噻虫嗪SC+25 g/L咯菌腈FSC进行了拌种处理试验。结果表明, 各拌种处理对春油菜的出苗有一定的影响, 其中600 g/L吡虫啉SC、30%噻虫嗪SC、600 g/L吡虫啉SC+25 g/L咯菌腈FSC、30% 噻虫嗪SC+25 g/L咯菌腈FSC拌种对春油菜出苗的影响大于25 g/L咯菌腈FSC拌种; 600 g/L吡虫啉SC+25 g/L咯菌腈FSC、30%噻虫嗪SC+25 g/L咯菌腈FSC拌种对白粉病和茎象甲的防效均高于单剂拌种; 600 g/L吡虫啉SC+25 g/L咯菌腈FSC拌种, 对春油菜白粉病的最高防效可达59.3%, 30%噻虫嗪SC+25 g/L咯菌腈FSC拌种对油菜茎象甲最高防效可达69.2%。白粉病病情指数与春油菜种植密度呈正相关, 拌种防效随密度增加而降低, 综合产量分析, 最佳种植密度为28.5万～34.5万株/hm2。     

利用CRISPR/Cas9系统敲除葡萄中VviEDR2提高对白粉病的抗性

利用CRISPR/Cas9系统定点编辑葡萄白粉病感病基因VviEDR2（Enhanced disease resistance 2），在VviEDR2的DUF1336结构域设计靶位点VviEDR2-T1，构建CRISPR/Cas9敲除载体，通过农杆菌介导法转化‘无核白’葡萄胚性愈伤组织。对PCR阳性植株进行靶位点扩增测序，结果表明，共有8个转基因植株在靶位点处发生不同类型的双等位基因突变，编辑效率为32%；突变体植株生长势较弱，叶片较小，茎秆丛生、细弱。进一步对突变体植株进行抗病检测，结果表明，接种葡萄白粉菌（Erysiphe necator Schw.）5 d后，突变体植株叶片上白粉菌孢子仅能萌发出少量较短初级菌丝，表皮细胞产生大量明显的H2O2，而野生型叶片中白粉菌萌发出大量初级菌丝、次级菌丝和吸器，无明显H2O2产生。这些结果表明，可以利用CRISPR/Cas9技术编辑葡萄感病基因VviEDR2，提高葡萄白粉菌抗性。     

刺槐白粉病病原菌鉴定

<正>刺槐(Robinia pseudoacacia L.)又名洋槐,属蝶形花科刺槐属的落叶乔木。原生于北美洲,现被广泛引种到亚洲、欧洲等地。刺槐白粉病是刺槐叶部、嫩枝病害,能降低叶片光合作用,严重的引起叶部畸形、茎尖和枝梢枯死。Braun最早记载中国刺槐白粉病病原菌为Microsphaera subtrichotoma~([1,2])。刺槐白粉病在日本也有报道,引起白粉病的病原菌为Erysiphe     

波叶大黄白粉病病原菌的鉴定

正波叶大黄Rheum rhabarbarum L.隶属于蓼科Polygonaceae大黄属Rheum,是一种重要的药用植物。白粉病多发生在波叶大黄的叶部,会影响其光合作用进而降低其药用价值。据笔者统计,目前关于蓼白粉菌Erysiphe polygoni DC.在世界范围内的报道有很多~([1~9]),但其中关于蓼科Polygonaceae波叶大黄白粉病病原菌的报道较少,目前仅有1个     

周口地区大叶黄杨白粉病菌的鉴定和进化分析

对周口地区的大叶黄杨白粉病菌进行了显微形态、核糖体DNA转录间隔区(ITS)及进化树分析。结果表明:在扫描电子显微镜下病菌分生孢子呈圆柱形或椭圆形,无支链;ITS序列与来自日本和阿根廷的Erysipheeuonymi-japonici的ITS序列聚在一个进化枝上。表明来自河南周口地区的白粉病属于E.euonymi-japonici,与日本和阿根廷的E.euonymi-japonici亲缘关系最近。     

小麦热激蛋白基因TaHSP70克隆及其在植物防卫和抗逆反应中的表达分析

热激蛋白是一类结构非常保守的分子伴侣类型的应激蛋白,在调控动、植物代谢和信号传导等方面发挥重要作用.本研究利用同源克隆法,筛选非亲和条锈菌小种CYR32侵染诱导的cDNA文库,分离获得1个HSP70家族基因的全长cDNA序列TaHSP70.序列分析发现,该cDNA片段包含1个2 412 by开放阅读框,推测其编码包含6...     

Inheritance of the Powdery Mildew Resistance Mlk in Wheat

The inheritance of the Mlk powdery mildew resistance originating from ‘Heine 2174.50’ was analyzed by crossing the Mlk resistant cultivar ‘Ralle’× cv. ‘Amor’ (highly susceptible) and vice versa and by observing the reactions of F₁- and F₂-plants after inoculation with two different Mlk avirulent powdery mildew isolates. In all cases, a 3 (resistant): I (susceptible) segregation was found in F₂. The reactions of the F₂plants against the two powdery mildew isolates were identical in each case. Therefore, it is supposed that one dominant resistant gene is responsible for the resistant reactions against these two isolates. These results support the earlier assumption of Heun and Fischbeck (1987b) that the whole Mlk resistance pattern is controlled by a single gene.     

New molecular markers linked to qualitative and quantitative powdery mildew and scald resistance genes in barley for dry areas

A partial genetic linkage map was constructed on 71 doubled-haploid lines derived from a cross between the barley lines Tadmor and WI2291 with 181 molecular markers. The segregating population was used to detect markers linked to the gene Mlg conferring resistance to powdery mildew (Erysiphe graminis f. sp. hordei) and to genes for quantitative resistance to scald (Rhynchosporium secalis). The gene Mlg on chromosome 4H was flanked by two AFLP markers at a distance of 2.0 and 2.4 cM, respectively. QTLs for resistance to scald were detected on chromosomes 2H and 3H. This association of molecular markers with qualitative and quantitative disease resistance loci represents a valuable starting-point for marker-assisted selection. This revised version was published online in July 2006 with corrections to the Cover Date.     

Genetic analysis of powdery-mildew (Erysiphe graminis f.sp. hordei) resistance derived from wild barley (Hordeum vulgare ssp. spontaneum)

The inheritance of resistance to powdery mildew was investigated in 20 accessions of Hordeum spontaneum and in 20 F₄ lines derived from crosses between the variety ‘Aramir’ and 13 accessions of H. spontaneum. Two resistance genes were detected in 17 accessions, and three resistance genes in one accession. In two accessions, only one resistance gene was present. The 20 breeding lines showed a large variation in infection type and infection level. The genetic relationship between the resistance genes detected was investigated in the seven most resistant F₄ lines. These F₄ lines were divided into three groups which carried different resistance genes. In two lines, the detected resistance gene was shown to be race-specific.     

Effectiveness of Twenty-Four Barley Resistance Genes Against Powdery Mildew (Erysiphe graminis DC f. sp. hordei Em. Marchal) in Spain

Twenty-four near-isogenic barley lines, with a cv.‘Pallas’ background, carrying different mildew resistance genes were subjected in 1987, 1989 and 1990 to natural infection by the pathogen at several different and contrasting Spanish sites in order to study its virulence. The virulence genes proved to be geographically grouped into three regions: western (Valladolid), southern (Sevilla) and northern and northeastern (Navarra, Lleida and Girona). The mildew population of Lleida was more variable when compared with Navarra and Valladolid. Overall, the most effective resistance genes were: Ml-a13 + Ml-(Ru3), mlo and Ml-(1402).