Differential effects of -mannose and 2-deoxy- -glucose on attempted powdery mildew fungal infection of inappropriate and appropriate ramineae

Barley, oat and wheat were used as both inappropriate hosts (IH) and appropriate hosts (AH) for three formae speciales of the fungus Blumeria graminis, the causal agent of powdery mildew disease. Treatment with either the glucose analog 2-deoxy- -glucose (DDG) or with -mannose dramatically suppressed penetration resistance in IH and to a much lesser extent in AH combinations. Other effects of DDG and -mannose were strikingly dissimilar. DDG greatly reduced localized autofluorescence at fungal attack sites on epidermal cells, and prevented hypersensitive epidermal cell death (HR). -mannose had little effect on autofluorescence or HR. DDG arrested the development of fungal haustoria and apparently prohibited biotrophy leading to secondary hyphae. -mannose allowed haustorial development and functional biotrophy leading to the production of elongating secondary hyphae. This suggests that B. graminis is in some way capable of utilizing -mannose as a carbon substrate. Results with IH combinations paralleled those of known mlo -barley responses to DDG and -mannose. Results are discussed in relation to specific physiological processes known to be influenced by either DDG or by -mannose, or by both compounds.     

单对汰选方法在加速抗高效氯氟氰菊酯棉铃虫品系汰选中的应用

通过设计杂合种群单对杂交方式,研究了加速获得抗性品系的方法。以高效氯氟氰菊酯群体汰选后抗性倍数为4.9倍的棉铃虫种群及其同源对照种群为材料,同时设置常规群体汰选方法与单对汰选方法,研究单对汰选方法在加速抗高效氯氟氰菊酯棉铃虫品系汰选中的作用。结果表明,群体汰选两代后抗性倍数由4.9倍提高到7.4倍, 而单对汰选两代后抗性倍数由4.9倍提高到27.3倍。表明在常规群体汰选中穿插几代单对汰选方法可明显加快棉铃虫种群对高效氯氟氰菊酯的抗性汰选进程。     

水稻白叶枯病菌对噻枯唑的抗药性监测

采用活体寄主法和离体含药平板法 ,测定了 1999年安徽省滁州市田间水稻白叶枯病菌对噻枯唑的抗药性。结果表明 ,在水稻活体上存在噻枯唑抗药突变体 ,其比例为67.65%,比1997、1998年有较大程度升高 ,但是离体含药平板上未能监测到抗药突变体。     

甘薯根腐病抗性在不同环境条件下的表现及遗传趋势

结果表明,甘薯根腐病发病轻重与环境条件有很大关系,表现为干旱少雨的年份发病较重,降雨量较多的年份发病较轻;土壤瘠薄的发病较重,肥力条件较好的则发病较轻;通常情况下,年份间品种的抗性表现较为一致,但遇特殊气候则年份间品种的抗性有一定的差异。对1150份甘薯品种资源及育种材料的根腐病抗性鉴定结果表明,高抗型材料占14.6％,抗病型占15.7％,感病型占26.0％,高感型占43.7％。对754份材料及亲本的抗性分析表明,不同的抗性组合后代中均可分离出高抗至高感类型的材料,杂交后代的抗性强弱随双亲抗性水平的提高而提高。中国自1970年以来采用品种间杂交和种间杂交育种技术,先后育成了一批高产、优质的高抗型优良品种。     

田间菜蛾绒茧蜂对有机磷敏感性监测及毒理机制分析

对甲胺磷敏感性的田间监测结果显示,绒茧蜂存在着抗性演化,毒力生物测定结果与AChE的K_i值的监测结果呈明显的相关性,每年9月至次年2月期间AChE敏感性最低,8月期间敏感性最高。甲胺磷可显著地抑制绒茧蜂AChE、CarE和GSTs的活性。PB和TPP对AChE的活体抑制率极低,但PB可强烈抑制CarE的活性,而TPP仅在高浓度时对CarE有较显著的抑制作用,PB对甲胺磷有显著的增效作用,而TPP对甲胺磷无增效作用。AChE的K_m、V_(max)及K_i值研究结果表明,田间绒茧蜂对有机磷和氨基甲酸酯的抗性与AChE对杀虫剂的不敏感性有关。由此认为,绒茧蜂对有机磷的抗性主要与其最重要的靶标酶AChE的敏感性改变及多功能氧化酶有关。     

一种监测棉铃虫对Bt杀虫晶体蛋白抗性的技术

研究了以诊断试剂盒监测棉铃虫对苏云金杆菌(Bt)杀虫晶体蛋白(ICP)抗性的技术。将1日龄幼虫在含诊断剂量的饲料中(每毫升饲料含Bt ICP0.01mg)取食7天,以生长至3龄以上的个体作为抗性个体的判断指标;筛选出人工饲料中防腐剂剂量的最佳值为每350毫升饲料中含丙酸2.5ml。经对多个棉铃虫不同抗性种群的验证试验,证明诊断试剂盒检测抗性个体频率较为精确且应用简便。     

二点叶螨对氧乐果、甲氰菊酯、四螨嗪及螨嗪菊酯混剂的抗药性

以兰州吐鲁沟公园金花忍冬植物上采集的二点叶螨为敏感种群,在室内盆栽菜豆苗上饲养繁殖后分别用氧乐果、甲氰菊酯、四螨嗪及螨嗪菊酯(甲氰菊酯 四螨嗪)混剂喷雾处理20代,获得二点叶螨抗氧乐果种群(抗性指数RF=35.84倍)、抗甲氰菊酯种群(RF=479.79倍)、抗四螨嗪种群(RF=67.26倍)以及抗混剂螨嗪菊酯种群(RF=26.75倍)。用生化法测定离体酶活性的结果表明,上述四个抗性种群的形成与体内羧酸酯酶、磷酸酯酶、谷胱甘肽转移酶的活力增加及乙酰胆碱酯酶的活性降低有关。4个抗性种群对常用15种供试药剂交互抗性测定结果表明,氧乐果、甲氰菊酯与联苯菊酯、三氟氯氰菊酯、水胺硫磷、久效磷、氰久合剂有交互抗性,甲氰菊酯还与螨蚧克有交互抗性;四螨嗪与三氯杀螨醇(RF=14.15倍)、齐螨素(RF=10.26倍)有交互抗性;螨嗪菊酯与双甲脒、氧乐菊酯有负交互抗性,RF值分别为0.85、0.71倍。     

朱砂叶螨对两种杀螨剂的抗性遗传力及风险评估

在室内抗性培育的基础上,应用数量遗传学中的域性状分析法研究了朱砂叶螨对甲氰菊酯和阿维菌素两种杀螨剂的抗性现实遗传力,并对两种药剂在不同杀死率下,朱砂叶螨抗性发展的速率进行了预测。结果表明,用甲氰菊酯、阿维菌素分别连续汰选16、18代后,朱砂叶螨对两者的抗性分别为28.61和4.36倍,抗性现实遗传力分别为0.2685和0.1385。在室内选择条件下,杀死率为50％～90％时,要获得10倍抗性,甲氰菊酯需要约13～6代,阿维菌素需要约28～13代。生物源农药阿维菌素的抗性风险明显低于菊酯类药剂甲氰菊酯。试验结果为朱砂叶螨抗性治理提供了理论依据。     

Development and fecundity ofSitobion avenae on some wheat cultivars under laboratory conditions

Nymphal development time and fecundity ofSitobion avenae (F.) (Homoptera: Aphididae) were determined on nine widespread wheat varieties cultivated in Tekirdağ Region in Turkey. Tests were carried out in controlled environment chambers (25±1°C, 65±5% r.h.; 16:8, L:D). Development time (±S.E.) ranged from 5.75±0.25 to 7.20±0.20 days. Fecundity per female ofS. avenae was found to be the highest (12.87±1.50) on wheat cv. ‘Sana’. In this investigation cvs. ‘MV-17’, ‘Miryana’, ‘Pehlivan’ and ‘Saraybosna’ were particularly resistant againstS. avenae. http://www.phytoparasitica.org posting July 8, 2002.     

Identification of ALS inhibitor‐resistant Amaranthus biotypes using polymerase chain reaction amplification of specific alleles

Summary Polymerase chain reaction (PCR) amplification of specific alleles (PASA) was adapted as a molecular marker‐based method for the rapid detection of point mutations in Amaranthus retroflexus and Amaranthus rudis leading to ALS inhibitor resistance. Two pairs of primers were designed for the specific amplification of alleles of the ALS gene of susceptible and resistant biotypes. The allele‐specific primer matched the desired allele, but mismatched the different allele at its 3′ end. Differentiation was carried out by comparison of the amplified DNA fragments in gel electrophoresis after PASA‐PCR. In A. rudis, differentiation was possible with one PCR and genomic DNA as probe. A ‘nested’ PCR was necessary for the differentiation of sensitive and resistant A. retroflexus. PASA is useful for the identification of resistant weed biotypes and also as a monitoring tool to map resistance occurrence and distribution. Advantages include the fast and clear separation of those plants with and without mutations at an early stage of development, its easy and consistent performance and quick results compared with existing resistance detection tests. These advantages, when combined with management strategies, enable further activities to reduce herbicide resistance.