根际微生物多样性与棉花品种对黄萎病抗性的关系研究 II.不同抗性品种根际真菌区系分析及其对棉花黄萎病菌的抑制作用

对棉花抗黄萎病品种（春矮早和８６－ ６）和感病品种（中棉１７和豫棉１２）的根际真菌区系进行了分析。结果表明每个品种都有自己独特的根际微生物区系,抗病品种根际微生物种数多于感病品种,区系组成更为复杂。抗病品种根际真菌优势种主要是漆斑菌 （Ｍｙｒｏｔｈｅｃｉｕｍ ）、粘帚霉（Ｇｌｉｏｃｌａｄｉｕｍ ）、曲霉（Ａｓｐｅｒｇｉｌｌｕｓ）和青霉（Ｐｅｎｉｃｉｌｌｉｕｍ ）等,感病品种则多为头孢霉（Ｃｅｐ ｈａｌｏｓｐｏｒｉｕｍ ）、镰刀菌（Ｆｕｓａｒｉｕｍ ）、矛束孢（Ｄｏｒａｔｏｍｙｃｅｓ）、粘帚霉（Ｇｌｉｏｃｌａｄｉｕｍ ）和漆斑菌（Ｍｙｒｏｔｈｅｃｉｕｍ ）等。采用平板对峙培养法测定了不同抗性棉花品种根际真菌区系各成员对棉花黄萎病菌的抑制作用,发现抗病品种根际真菌区系中对黄萎病菌具有抑制作用的真菌种数和比率都高于感病品种,而且抗病品种根际真菌的优势种对棉花黄萎病菌的抑制作用较强。这种差异在苗期和现蕾期更为明显,花铃期则显著减小。研究结果表明棉花品种对棉花黄萎病的抗性与根际真菌区系组成及其对黄萎病菌的抑制能力有一定关系。     

向日葵菌核病接种方法及品种抗病性鉴定

为建立有效的向日葵菌核病田间接种鉴定方法,以核盘菌菌丝体悬浮液和孢子悬浮液作为接种物,分别对抗、感向日葵品种在现蕾期、始花期和盛花期进行人工接种,并对接种后保湿材料和保湿时间进行比较。试验结果表明:两种接种物均可使向日葵抗、感品种产生盘腐症状。用菌丝体悬浮液和孢子悬浮液接种时,浓度分别为10.0~15.0g/L和200~500个/mL,始花期接种,牛皮纸袋保湿2~4d,即可区分出向日葵品种间抗感性差异。用此方法鉴定出13个对盘腐型菌核病表现抗病的向日葵品种。     

病原菌诱导后黄瓜叶片中脂氧合酶活性与茉莉酸积累的关系

通过酶活性测定和高效液相色谱分析,研究经病原菌诱导后黄瓜叶片中脂氧合酶(LOX)活性与茉莉酸(JA)积累量的关系。结果表明,黄瓜经褐斑菌诱导后,叶片中茉莉酸(JA)大量积累,同时脂氧合酶(LOX)活性上升,接种叶片的上位叶中LOX活性和JA含量于诱导接种褐斑菌12h后开始升高,并于诱导接种24h后达到峰值,接种叶片的下位叶中LOX活性和JA含量在诱导接种12h后变化不大,但在24h后显著升高,并于48h达到峰值,此后逐渐平稳下降。相关分析表明,LOX与JA呈显著正相关,相关系数r为0.92。同时通过喷施脂氧合酶抑制剂(NDGA)和添加茉莉酸的试验证实LOX是JA合成的关键酶。     

AtEDR1介导拟南芥对稻瘟菌的抗性(英文)

 稻瘟菌(Magnaporthe oryzae)是一种半腐生病原菌,该病原菌可以侵染水稻,产生稻瘟病。对于水稻与稻瘟菌的互作机制,人们已经进行了大量的研究。然而,鉴于水稻基因组相对较大且稻瘟菌生理小种众多,致使研究进展缓慢。本研究通过将稻瘟菌生理小种Y34侵染拟南芥生态型Col-0,发现Y34可以感染Col-0,从而建立Y34-拟南芥互作模型,用以探究Y34与抗白粉突变体edr1的关系。结果显示,edr1比Col-0对于稻瘟菌更敏感。之前有研究表明,降低SA含量的突变体(pad4,sid2,nim1)均可抑制edr1相关表型。接种Y34于edr1与pad4、sid2、nim1形成的双基因突变体发现,所有双突变体的感病性比edr1单突均明显降低。推测EDR1可能在拟南芥抗稻瘟菌方面起一定正调控作用,且其作用依赖于SA途径的相关基因。     

Neurospora crassa对三唑醇的抗药性分子机制研究

 通过紫外光诱变获得Neurospora crassa对三唑醇杀菌剂抗性突变体"Nc70"。用2.5μg/ml三唑醇处理,突变体内甲基甾醇与脱甲基甾醇比例变化幅度远远小于亲本敏感菌株"STA"。突变体对三唑醇的吸收能力与敏感菌株相似,但药剂在体细胞内积累较少。三唑醇处理N.crassa 2 h后,药剂在菌体内的含量趋向稳定,突变体内的药量较敏感菌体低56.1%,而麦角甾醇合成量则高于敏感菌株53.7%。     

西花蓟马抗药性研究进展

西花蓟马是世界范围内蔬菜和花卉上的重要害虫之一,使用化学药剂是防治西花蓟马的主要手段,目前西花蓟马已对有机氯、有机磷、氨基甲酸酯、拟除虫菊酯、阿维菌素和多杀菌素等多种杀虫剂产生了抗药性。本文从抗药性现状、抗性机制和抗性治理等几个方面介绍了国内外有关西花蓟马抗药性的研究进展。     

Selection of virulent populations of Meloidogyne javanica by repeated cultivation of Mi resistance gene tomato rootstocks under field conditions

Field trials were conducted in a plastic house artificially infested with an avirulent population of Meloidogyne javanica to determine the durability of the resistance mediated by the Mi gene in tomato rootstocks after repeated cultivation for three consecutive years. Treatments included an experimental rootstock cv. PG76 ( Solanum lycopersicum  ×  Solanum sp.), a commercial rootstock cv. Brigeor ( S. lycopersicum  ×  S. habrochaites ), a resistant tomato cv. Monika ( S. lycopersicum ), and a susceptible cv. Durinta ( S. lycopersicum ). Based on the reproduction index (RI: number of eggs per g root on the resistant cultivar divided by number of eggs per g root on the susceptible cultivar × 100), rootstock cv. PG76 responded as highly resistant (RI = 7%) after the first cropping cycle (3·4 nematode generations), showed intermediated resistance (RI = 33%) after the second cropping cycle (3·3 generations), and was fully susceptible (RI = 94%) after the third cycle (3·3 generations). In contrast, rootstock cv. Brigeor and resistant cv. Monika retained intermediate resistance levels (RI = 41 and 25%, respectively) after the third cropping cycle. Virulent nematode populations were rapidly selected from an avirulent one after repeated cultivation of resistant tomatoes under field conditions. Bioassays conducted under controlled conditions confirmed that selection for virulence occurred more rapidly in plots with cv. PG76 followed by Brigeor and Monika. The nematode population in the field not exposed to Mi resistance remained avirulent to Mi genotypes. The genetic background of the resistant rootstocks and the frequency of cropping were critical factors for the appearance of virulent nematode populations. Irrespective of nematode infection, all resistant tomatoes yielded more than the susceptible cultivar.     

Assessment of the impact of resistant and susceptible canola on Plasmodiophora brassicae inoculum potential

The impact on clubroot severity of growing susceptible canola or mixtures of resistant and susceptible canola genotypes was examined. Bioassays revealed greater clubroot severity and incidence, and reduced plant height, where 100% of a susceptible cultivar had been grown. A higher proportion of susceptible plants within a resistant canola crop increased root hair and secondary infections. Regression analysis of root hair infection and the amount of Plasmodiophora brassicae DNA (as determined by quantitative PCR) revealed strong linear relationships between the two parameters. The linear relationships between root hair infection and P. brassicae DNA were stronger for the resistant cultivar than for the susceptible cultivar when regression analysis was conducted by cultivar over the sampling dates. In conclusion, the cropping of a resistant cultivar reduced clubroot severity, while the presence of susceptible volunteer canola increased inoculum potential. Quantitative PCR was a reliable tool for the quantification of root hair infection.