球根鸢尾的病毒鉴定及试管脱毒成球技术

对上海地区球根鸢尾进行了病毒病害调查。经检测初步确定球根鸢尾普遍存在鸢尾重花叶病毒、鸢尾轻花叶病毒、水仙潜隐病毒３种病毒的复合侵染。对带毒种球进行茎尖组培脱毒,得出了茎尖诱导成芽、芽成球及小球生根的培养基配方。将组培苗在试管苗、成球苗、移栽苗等不同时期进行病毒检测,结果表明,小于１．０ｍｍ的茎尖诱导的幼苗可脱去上述３种病毒。     

RAPD及其在果树上的应用

就RAPD的特点、操作及其在果树品种鉴定、遗传多样性检测、系谱解析和遗传图谱构建等方面的应用和进展进行了简要的阐述。     

应用种子蛋白电泳图谱对高羊茅品种进行鉴别与聚类研究

利用种子贮藏蛋白进行二二烷其磺酸钠－聚丙烯酰胺凝脉电泳,对２３个高羊茅品种进行了 分析。表明该方法成本低,效率高,重复性好,能有效地反应高羊茅品种的遗传差异和亲缘关系。电泳谱带聚类分析所得到的类群,能代表生产上,饲用,草坪用类型以及两种用途中的主要生态类型。     

北方棉区棉花黄萎病菌落叶型菌系鉴定

 采用RAPD扩增与温室致病性测定2种方法,以黄萎病菌Verticillium dahliae的5个落叶型、7个非落叶型菌系和V.albo-atrum的2个菌系为对照,对采自北方棉区6省(自治区)的34个棉花黄萎病菌菌系进行致病型鉴定。94.1%的菌系在2种鉴定结果中表现一致,与对照菌系相比较,确定其中26个菌系为落叶型菌系,6个菌系为非落叶型菌系。从而证实了黄萎病菌落叶型菌系在北方棉区河北、河南、山东3省的存在,并发现所确定的26个北方落叶型菌系中的22个与来自美国的对照落叶型菌系T₉、V₄₄的关系比与来自江苏的对照落叶型菌系V_B、V₉₉₁的关系更近。本实验还初步筛选到2条用于鉴别V.dahliae落叶型与非落叶型菌系的RAPD特异条带OPB-19₉₆₆和OPM-20₁₆₉₁,将它们用于对34个北方菌系的RAPD扩增鉴定,则与温室致病性测定结果的一致性分别为88.2%和94.1%,证明这2条特异条带在鉴定棉花黄萎病菌落叶型菌系上具有一定的实用价值,并为进一步制作特异探针以形成一套简便、准确、规范化的鉴定技术奠定了基础。     

Erwinia pyrifoliae, an Erwinia species different from Erwinia amylovora, causes a necrotic disease of Asian pear trees

Bacteria from necrotic branches of Asian pear trees ( Pyrus pyrifolia ) in Korea were consistently isolated as white colonies on nutrient agar and formed mucoid, slightly yellow colonies on a minimal medium with copper sulphate. Isolates with this colony morphology were studied in a series of microbiological, molecular and pathological tests. Most isolates allowed the verification of Koch's postulate on P. pyrifolia seedlings and on slices from immature pear ( Pyrus communis ) fruits and were also positive in hypersensitivity tests on tobacco leaves. They showed characteristics common to species in the genus Erwinia , but were different from Erwinia amylovora , the agent of fire blight. A relationship between the novel pathogen and E. amylovora was found in microbiological and serological tests. Both organisms had similar but not identical protein patterns in 2-D gel electrophoresis, and in growth morphology the new pathogen produced colonies on MM2 Cu medium that were mucoid and slightly yellow, compared with the clearly yellow colonies of E. amylovora . No similarity was found in the plasmid profiles, and consequently no PCR signal was obtained with primers from the E. amylovora plasmid pEA29. REP-PCR also produced bands differing for the two organisms.     

海南省1株甲属虫媒病毒的分离鉴定及其血清抗体调查

1995 年,从海南省捕获的蚊虫标本中,分离到1 株病毒,编号为HYM1。该病毒以脑内感染的方式感染2～3 日龄乳鼠及3 周龄小鼠,感染后2～4 d 规律致死。在Vero-E6 细胞组织培养中可增殖,并可产生明显的病变。经理化和生物学鉴定,该病毒对酸、乙醚均敏感,抵抗5-氟脱氧尿苷和胰酶,属RNA 病毒。血清学鉴定表明,该病毒与马雅罗病毒(MAY)抗原性关系密切。从当地人血清中检到了HYM1 病毒抗体,其阳性率为3.99% 。     

Leek Proliferation: A New Phytoplasma Disease in the Czech Republic and Italy

During the summer 1996, twelve of twenty-eight leek plants located in a garden near eské Budjovice, South Bohemia exhibited symptoms typical of diseases associated with phytoplasmas. In summer 1998 similar symptoms were detected in leek plants in a field used for seed production located in Romagna, North Italy. In both cases the plants were established in the spring of the previous year. Plants showed flower abnormalities: stamen elongation, anther sterility, pistil proliferation, as well as poor, if any, seed production. Phytoplasma-like structures were detected by scanning and transmission electron microscopy in phloem sieve elements in the Czech diseased plants, but not in healthy ones. Nested-PCR amplifications of extracted DNA with phytoplasma-specific oligonucleotide primer pairs confirmed the presence of phytoplasmas in these plants at low concentrations. Restriction fragment length polymorphism analyses of amplified ribosomal sequences allowed the identification of detected phytoplasmas: all the samples from the Czech Republic contained aster yellows related phytoplasmas (16SrI-B) while in the Italian samples aster yellows related phytoplasmas (16SrI-B) together with stolbur related phytoplasmas (16SrXII-A) were identified. This is the first report of detection and identification of a phytoplasma disease of leek in the Czech Republic and Italy.     

非自然越夏区小麦白粉病模拟鉴定病圃

作者于1990～1995年根据陕西省关中麦区小麦白粉病侵染循环特点,人工模拟自然发病条件,在非自然越夏区杨陵(省农科院试验地)成功地建立起白粉病菌可周年存活,且秋、春季均能充分诱发感染的混合菌系病圃,宜对小麦种质材料进行全生育期抗白粉病鉴定。利用该病圃已对陕西省1000余份小麦品种(系)及部分国内外抗源亲本材料做了抗病性鉴定和利用评价。     

菜豆象检验鉴定及处理研究

本文就菜豆象的生物学特性、适生性及检验处理技术进行了研究，认为菜豆象在北纬４１°～４４°地域，每年可发生４代，论证了菜豆象在延边地区的适生能力；采用了５种除害处理方法进行灭虫处理研究。     

Studies on amoebae and cysts associated with the isolation of Spongospora subterranea f.sp. subterranea in vitro

New evidence is presented to support the contention that the amoeba/cyst colonies isolated from surface-sterilized Spongospora subterranea f.sp. subterranea -infected potato tubers and spore balls have a saprophytic phase but are contaminants and not S. subterranea. Amoebae isolated from infected tissues and spore balls formed colonies associated with bacteria on 1% water agar at 18°C and encysted after 5–7 days. These cysts were morphologically distinct from the resting spores of S. subterranea and were formed singly or in a layer, unlike the spore ball (cystosorus) of S. subterranea . Amoebae, cysts and mixtures of amoebae and cysts in primary, secondary and tertiary subcultures failed to infect tomato roots. PCR amplification of DNA from amoebae, cysts and spore balls using the S. subterranea -specific primer pair SsF/R generated a 434-bp product from S. subterranea spore balls only and not from amoebae or cysts. When an amoeba/cyst-specific primer pair AmF/R was designed and used for PCR amplification, a single 411-bp product was generated from DNA of amoebae and cysts, but not from DNA of S. subterranea spore balls. These results are discussed in relation to earlier reports claiming the successful isolation of S. subterranea and other plasmodiophorids in vitro .