中国葡萄野生种对葡萄根癌病的抗性

通过田间接种鉴定，系统研究了中国葡萄属１３个种和变种的２６个株系对葡萄根癌病的抗性，筛选出高抗株系１０个。其中燕山葡萄（♀）因扦插容易生根，可用自根苗作为抗葡萄根癌病砧木进行嫁接试验，其余可用作抗葡萄根癌病的育种资源     

农作物抗旱性鉴定仪的研制和应用

依据陈毓荃等首次提出的连续升温电导法，研制了ＮＫＪ－１型农作物抗旱性鉴定仪，对１４种小麦抗旱性的鉴定结果与田间观测结果一致，也适于果树抗热性鉴定。     

J172等5个柳树良种育苗试验

通过对5个柳树良种在不同类型区的扦插育苗试验,分析苗木生长量、生长季土壤含水量、土壤温度,结果表明:①各参试因素对生长量影响的程度依次为品种(系)>类型区>覆膜>扦插方法,因此在柳树壮苗培育中,应首先考虑优良品种的选择。②在不同类型区内,影响树木生长的主导生态因子亦不同。在高寒湿润区,热量是影响生长量的主导生态因子,故其覆用地膜的效果十分显著,其生长量较对照提高28.6%;在川塬区,土壤水肥是影响生长量的主导生态因子,故其覆用地膜的效果不太显著,应着重加强土壤水肥管理。     

鹅细小病毒HG5/82株的分离鉴定及生物学特性的研究

本研究通过对1982年黑龙江某鹅场发生的鹅细小病毒病疑似病例的肝病变组织病毒分离,进行回顾性研究.将肝脏加PBS研磨后,-70℃/37℃反复冻融三次,除菌过滤后接种12日龄鹅胚.发现病毒对鹅胚的致死时间为5～6 d,胚体体表有轻微出血点.鹅胚尿囊液经磷钨酸染色,可见具有典型特征的细小病毒粒子.将该病毒尿囊液在12日龄鹅胚中连续传16代,随着传代次数的增加,胚体多集中在3～4 d死亡.病毒传至第三代时死亡胚体头、颈、背部出现较为严重的出血点,体表有水肿.第五代病毒尿囊液(命名为HG5/82)对12日龄鹅胚的ELD50为10-5.92/0.1 mL.将20只12日龄雏鹅分为三个试验组和一个阴性对照组,各组分别接种鹅胚尿囊液104.92ELDso、103.92ELD50、102.92ELD50及生理盐水,发现雏鹅接种HG5/82后4 d出现轻微腹泻,随后恢复正常.用套式PCR检测雏鹅肛拭子病毒的体外排放情况.发现三个试验组在接种病毒后1～20 d用套式PCR均可检测到病毒.对照组及试验组接种后20～56d没有检测到病毒.将套式PCR产物进行序列测定并于参考毒株进行比较,表明该序列具有GPV相应区域的共同分子特征,与GPV参考毒株B的相应序列同源性达93.6%.本研究结果表明,该分离毒株为典型的鹅细小病毒(Goose Parvovirus,GPV),对雏鹅的致病力较弱.     

2型猪链球菌的血清学鉴定

本试验首次证实了２型猪链球菌在我国的存在，采用玻片凝集、琼脂扩散及毛细管沉淀等３项试验，对１９９０年以来广东某猪场断奶仔猪暴发流行的败血症、脑膜炎及关节炎病猪中分离的１５株链球菌进行了血清学鉴定。结果表明：１５株链球菌均为２型猪链球菌；用高压法提取抗原进行沉淀反应，其结果比酸热法提取抗原具有简便、敏感、特异性强的特点。     

酥梨采后灰霉病生防菌株的鉴定及抑菌作用

以微生物拮抗病原菌是防治病害安全高效的可行手段。通过对果实表面微生物进行筛选鉴定,以期得到一株可以有效抑制灰霉病的生物防治菌株。对拮抗菌株H-1进行形态学特征、生理生化特性分析,结合16S rDNA序列分析和gyrB 基因序列分析构建系统发育树;采用平板对峙法结合果实伤口试验考察拮抗菌H-1在体外及梨果表面的抑菌作用。结果表明：经鉴定H-I菌株为贝莱斯芽孢杆菌（Bacillus velezensis）;B. velezensis H-1在体外条件下可显著抑制灰葡萄孢霉（Botrytis cinerea）、细极链格孢（Alternaria tenuissima）和串珠镰孢菌（Fusarium verticillioides）的菌丝生长,其中对灰葡萄孢霉菌丝的抑制作用最强;果实伤口试验表明,1×1011 CFU/mL的B. velezensis H-1可完全抑制梨果表面灰霉菌生长。由此可见,B. velezensis H-1可以有效抑制梨果采后灰霉病的发生。     

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。     

New genes for disease resistances through somatic hybridization

Somatic hybridization, a process of combining protoplasts from different plants, can provide new sources of disease resistances for plants. In the case of wild and cultivatedSolanum species, the hybrids express resistances from each partner in the fusion and can often be crossed with cultivars to improve agronomic characteristics of the tubers. Restriction fragment length polymorphism (RFLP) analyses can provide a means for determining that the plants being investigated are actually hybrids as well as a means for following the introgression of DNA into progeny lines. These points are addressed in this paper with specific reference to somatic hybrids betweenSolanum brevidens and potato.     

Detection of squash mosaic virus in seeds of melon (Cucumis melo) by enzyme-linked immunosorbent assay (ELISA)

Squash mosaic virus (SqMV, comovirus) is seed-transmitted in severalCucurbitaceae. Therefore, the use of virus-free seed is important to prevent establishment of this virus in the Netherlands and to avoid spread to other countries.This study was undertaken to develop an enzyme-linked immunosorbent assay (ELISA) for the detection of SqMV in melon seeds. An antiserum was produced to a serotype 1 isolate from melon. Two ELISA variants were investigated viz. an ELISA variant with simultaneous incubation of sample and enzyme conjugate (ELISA 1) and an ELISA variant with successive incubation of sample and enzyme conjugate (ELISA 2). The sensitivity of ELISA was tested by mixing fluor of ground infected and non-infected seeds in different proportions. SqMV was detected by both ELISA variants at dilutions of 1 160 (1 part of infected flour mixed with 159 parts of non-infected flour) or higher after a substrate incubation period of 4 h. However, ELISA 1 gave relatively higher absorbance values than ELISA 2 for nearly all dilutions. Since ELISA 1 is also faster than ELISA 2, ELISA 1 is advised for routine testing. In these test, using subsamples of 100 melon seeds SqMV is detected reliably. ELISA 1 is now used in the Netherlands for routine-indexing of melon seed lots for SqMV.Samenvatting Het pompoenemozaïekvirus gaat over met het zaad van verscheideneCucurbitaceae. Het gebruik van virusvrij zaad is belangrijk om te voorkomen dat het virus zijn intrede doet in Nederland en zich naar andere landen verspreidt.Een antiserum werd geproduceerd tegen een serotype 1 isolaat van meloen. Met behulp van dit antiserum werd een ELISA ontwikkeld om pompoenemozaïekvirus in zaden van meloen aan te tonen. Twee varianten van ELISA werden vergeleken, namelijk een variant waarbij monster en enzymconjugaat gelijktijdig geïncubeerd werden (ELISA 1) en een variant waarbij monster en enzymconjugaat na elkaar geïncubeerd werden (ELISA 2). De gevoeligheid van de ELISA varianten werd uitgetoetst door meel van zieke zaden in verschillende verhoudingen te mengen met meel van gezonde zaden. Het pompoenemozaïekvirus werd met beide ELISA varianten aangetoond in verdunningen van 1 160 (1 deel meel van zieke zaden gemengd met 159 delen meel van gezonde zaden) of hoger na 4 uur incubatie met substraat. ELISA 1 gaf doorgaans hogere extinctiewaarden dan ELISA 2 voor bijna alle verdunningen. Omdat ELISA 1 ook nog sneller is dan ELISA 2, wordt ELISA 1 aanbevolen voor routinematig gebruik. Wanneer voor routinematig gebruik 100 meloenezaden per submonster getoetst worden, kan het pompoenemozaïek virus betrouwbaar worden aangetoond. In Nederland worden momenteel per zaadpartij 20 submonsters van 100 zaden getoetst.