水稻与稻瘟病菌非亲和性互作中重要防御酶活性变化规律研究

 选以CO39为背景的水稻抗稻瘟病近等基因系,与稻瘟菌生理小种ZC₁₃(菌株97-151a)组成的3类典型非亲和性互作,以亲和性互作为对照,对各互作中过氧化物酶(POD)、苯丙氨酸解氨酶(PAL)、几丁质酶及β-1,3-葡聚糖酶的活性变化规律进行了系统研究。完全非亲和性互作C101A51/97-151a、高度非亲和性互作C101L AC/97-151a及中度非亲和性互作C104 PKT/97-151a,POD比活性接种后即开始明显升高,48h前达到高峰,升高趋势一直持续到7d完全显症时,幅度基本与各互作非亲和程度呈正相关;亲和性互作CO39/97-151a接种后40 h POD比活性才开始升高,4~6 d达到高峰,峰值也较大。3类非亲和性互作PAL比活性在接种后0 h或16 h开始较明显升高,整个互作中形成3~4个较明显的峰;亲和性互作中PAL比活性一直明显下降。3类非亲和性互作外切几丁质酶比活性接种后即开始升高,基本一直保持升高趋势,在40 h前幅度较大,并形成1~3个较高的峰;亲和性互作外切几丁质酶比活性接种后即开始大幅度升高直至完全显症,48h后幅度远高于非亲和性互作。3类非亲和性互作β-1,3-葡聚糖酶比活性在24 h内开始较明显升高,在48h前形成2~3个较明显的峰;亲和性互作在接种后β-1,3-葡聚糖酶比活性即开始升高,在48h后显著高于非亲和性互作。讨论了POD、PAL、几丁质酶及β-1,3-葡聚糖酶参与水稻抗稻瘟病的可能性。     

离体条件下水稻种衣剂对串珠镰刀菌生长及形态毒理影响

 检测了黑龙江水稻主产区4个当地主栽品种的种子内部镰刀菌寄藏情况,测定了20%克福甲和20%克多甲种衣剂对种子带菌消毒处理效果及对水稻串珠镰刀菌(Fusarium moniliforme)的抑菌作用和联合毒力,并借助扫描电镜观察了上述2种混配种衣剂对串珠镰刀菌的形态毒理影响。结果表明,种子内部镰刀菌的分离频率高达56.7%~96.0%,其中串珠镰刀菌的分离频率为32.6%~48.2%,2种种衣剂对带菌种子具有显著的消毒处理效果。20%克福甲和20%克多甲种衣剂对镰刀菌F.moniliforme的毒力指数分别为457.11和802.04,增效倍数分别为6.53和0.13。20%克多甲种衣剂(多菌灵:甲基立枯磷为5:5,W/W)对串珠镰刀菌的抑菌作用优于20%克福甲种衣剂(福美双:甲基立枯磷为8:6,W/W),增效作用低于20%克福甲种衣剂。电镜观察表明,种衣剂低浓度至高浓度处理下均可引起串珠镰刀菌菌丝不同程度的异常生长,表现为主菌丝局部膨大或形成菌丝束,菌丝顶端异常膨大、缢缩或形成穗状和花絮状分枝。     

两系稻制种穗期病害发生较重的原因及防治措施

调查分析稻粒黑粉病、穗颈稻瘟等两系杂交稻制种穗期主要病害的发生原因,提出了清除菌源、轮换制种、健身栽培、对口药剂防治等防治措施。     

南方灭鼠应用稻谷与大米毒饵的比较

生物测定法测得谷壳对复方88-1灭鼠剂的阻滞率为54．3％，光谱分析法测得其对敌鼠钠盐的阻滞率在47．43％—57．00％之间。相同条件下，褐家鼠Rattus norvegicus取食敌鼠钠盐稻谷毒饵量为大米毒饵的2倍多。在南方潮湿的环境下，大米毒饵更易松散、霉变，使其适口性更低。综合考虑认为南方灭鼠使用稻谷毒饵更为合适。     

广东优质籼稻抗稻瘟病育种研究进展

通过对广东优质籼稻品种抗瘟性研究、抗病品种的系谱分析以及抗病育种实践的回顾，综述了广东优质稻抗性育种历史及现状，剖析了优质稻抗瘟育种存在的问题及相应对策。提出开发利用不同稻作系统的抗病资源，构建遗传多样性丰富的抗病优质种质，延长品种抗性寿命及解决品种优质与抗病的矛盾。     

微管、微丝特异性抑制剂处理对水稻抗病性的影响

 微管特异性抑制剂oryzalin、微丝特异性抑制剂细胞松弛素A (cytochalasin A,CA)和细胞松弛素D (cytochalasin D,CD)的试验表明:oryzalin在5~50μmol/L、CA在0.5~1.0μg/mL、CD在1~20μg/mL的浓度范围内,对稻瘟病菌孢子的萌发和附着胞的形成基本上没有影响。采用以上几种细胞骨架特异性抑制剂处理水稻叶鞘都可以不同程度地抑制寄主细胞抗病菌扩展的能力。在抑制剂处理的水稻叶鞘细胞中,病菌扩展的速度加快。进一步的观察发现,抑制剂处理抑制水稻细胞抗病菌的扩展能力与水稻的抗病防卫反应如原生质颗粒化、多酚类物质的积累和HR发生的延迟是相关的。     

转基因水稻对稻瘟病的抗性研究

 采用苗期初筛、复筛、抗谱测定和田间自然诱发试验等不同鉴定方法,对经分子检测证明已整合有碱性几丁质酶基因和β-1,3-葡聚精酶基因的22个转化系的转基因水稻植株进行稻瘟病抗性鉴定研究,筛选出对稻瘟病的抗性比原种对照七丝软占有明显提高的一系列转基因水稻品系,其中表现高抗的有来自F4-9转化株系的7个品系。高抗材料的R7代品系,经室内抗谱测定及田间病圃试验结果,仍然表现高抗稻瘟病。本研究通过转基因技术,成功地将优质感病品种改良成高抗品系,研究结果证明了利用基因工程手段培育抗病水稻新品种是一个非常有希望的育种途径。     

哈茨木霉几丁质酶诱导及其对水稻纹枯病菌的拮抗作用

 在实验室条件下分别以几丁质和水稻纹枯病菌(Rhizoctonia solani)细胞壁作唯一碳源诱导哈茨木霉(Trichoderma harzianum)菌株NF9、TC3和P1产生几丁质酶,用硫酸铵沉淀法制备几丁质酶粗提液。上述木霉菌株内切几丁质酶活性(对胶体几丁质浑浊度的减少率)分别为79.8%、74.4%和76.0%,均显著高于非诱导的阳性对照。培养第5 d几丁质诱导的木霉菌株NF9和TC3内切几丁质酶活性显著高于由水稻纹枯病菌细胞壁诱导的酶活性。体外测定表明,通过诱导的木霉菌株TC3、NF9和P1几丁质酶粗提液对水稻纹枯病病菌的拮抗圈直径可达38、21和23 mm,与非诱导的阳性对照比较有显著性差异。对木霉几丁质酶拮抗作用的特点及生防应用进行了讨论。     

Leafhopper and planthopper vectors of rice viruses and their management in Nepal

Research on insect pests (including leafhoppers and planthoppers) in Nepal was initiated in 1956 by the Entomology Division and Plant Protection Units of the Department of Agriculture. More systematic work began after the establishment of a Rice Improvement Programme in 1972. Because of poor documentation and publication of research findings, it is difficult to assess the research efforts and achievements to date. The available research reports are mostly published in the proceedings of national seminars/workshops. They are used here to assess the current status of research on the occurrence and damage caused, distribution and composition, relative abundance, biology and management through chemicals. Much of past research has focused on insect surveys by light traps and sweep nets and the evaluation of insecticides and, since early 1990, some research on rice green leafhoppers (Nephotettix virescens and Nephotettix nigropictus) has begun to determine their relative abundance and population characteristics in relation to their potential as vectors of rice viruses. The challenges to pest management in general and some suggestions for future research needs are discussed, based on the present standing of agricultural research in the country     

Phylogenetic relationships between rice dwarf phytoreovirus isolates from five countries

Rice dwarf virus isolates were collected from several locations in Japan, the Philippines, China, Nepal and Korea. Genomic dsRNA segment profiles in polyacrylamide gel electrophoresis differed among the isolates. There were less differences in the profiles between isolates from Japan and Korea than in those between these two Countries and others. Nucleic acid hybridization was used to examine the extent of genomic variation. Full-length cDNAs to all genomic segments encoding non-structural proteins (S4, S6, S9, S10, S11 and S12) were synthesized from two Japanese isolates, and were used for dot-blot hybridization. Hybridizations using probes generated from the full-length cDNA clones failed to differentiate isolates from different geographical areas. However, cDNA probes covering a variable region of S12 were able to distinguish Japanese and Korean isolates from those of other countries. Phylogenetic tree analysis based on the amino acid sequence of P12 encoded by S12 grouped Japanese and Korean isolates together. The Chinese isolates from two different locations (Yunnan and Fujian) were closely related to each other, and were the most distantly related to Japanese and Korean isolates.