青岛地区茄白粉病的病原菌鉴定

在青岛地区的保护地和露地发现茄白粉病,通过形态学和分子生物学进行鉴定以及致病性测定。结果将青岛地区茄白粉病的病原鉴定为Podosphaera xanthii,本文为该菌在我国茄子上的首次报道。     

菊苣根提取物的抑菌活性研究

采用离体的试验方法测定了菊苣根的石油醚、乙酸乙酯和乙醇提取物对7种植物病原真菌和3种细菌的抑制活性。采用盆栽试验方法测定了菊苣根提取物对小麦白粉病的防治效果。结果表明,乙醇和乙酸乙酯提取物均有一定的抑制植物病原真菌和细菌活性。且乙酸乙酯提取物效果更佳。在10 g.L-1浓度下,乙酸乙酯提取物能显著抑制小麦赤霉病菌、玉米大斑病菌和烟草赤星病菌3种病原真菌菌丝的生长,抑制率均在85%以上;对小麦根腐病菌、玉米大斑病菌和烟草赤星病菌的孢子萌发抑制率也均在80%以上;对枯草芽孢杆菌和金黄色葡萄球菌的抑菌圈直径达21.01 mm和17.23 mm;对盆栽小麦白粉病的预防和治疗作用分别为50.93%和65.82%。     

烟草白粉病抗性基因的遗传分析

以烟草抗白粉病品种台烟7号为母本,感病品种NC89为父本,构建6个世代的群体,利用主基因 多基因混合遗传模型的分离分析方法,研究烟草白粉病的抗性遗传规律。结果表明,烟草白粉病抗性的遗传是由两对加性-显性-上位性主基因 加性-显性-上位性多基因（E-0模型）控制的。B1、B2和F2世代主基因的遗传率分别为88.05%、32.62%、84.43%,主基因遗传率很大,说明可以在抗病育种早期进行选择;B1、F2世代多基因遗传率均为0.00%,说明烟草白粉病的发生受一定环境影响。     

烟草苗期病原微生物病害发生及综合防治

烟草苗期主要病原微生物病害(如炭疽病、猝倒病、立枯病和根黑腐病)的发生流行对我国烟草生产的影响逐渐加剧,研究烟草苗期病害的防治措施变得尤为重要.探索烟草苗期主要病原微生物病害的发生规律和流行趋势,以及当前的防治手段,可以保障烟草生产的质量和数量.基于此,本文对烟草病原微生物苗期病害的防治方法进行了概述,为烟苗病害的研究提供了参考和思路.     

芽胞杆菌防治烟草病虫害的研究进展

烟草病虫害严重影响烟草产业的可持续发展,更为安全的生物防治方法已成为烟草病虫害防治研究的热点领域。芽胞杆菌属(Bacillus)是一类比较理想的生防微生物,在植病生物防治领域显示出了广阔的应用前景。本文论述了芽胞杆菌属细菌的生物学特性及其在烟草黑胫病、赤星病、青枯病、炭疽病、根黑腐病、花叶病、白粉病、烟草斜纹夜蛾和甲虫等烟草病虫害防治中的应用。     

吉林省香菜一新病害——白粉病

通过病害症状和病原形态学特征对吉林省香菜种植区白粉病病原菌进行鉴定,结果为该病由独活白粉菌（Erysiphe heraclei DC．）引起。香菜白粉病为吉林省香菜一新病害,且芫荽属为东北地区白粉菌属级新记录寄主。     

将水稻壳质酶基因导入烟草确认抗白粉病特性

农林水产省的农业生物资源研究所规划调整部规划科科长日比忠明和该研究所机能开发部微生物机能利用研究室西泽洋子等将从水稻分离的壳质酶基因导入烟草,烟草就获得白粉病抗性。打算明年开始封闭式温室实验。     

杆状病毒p35基因诱导烟草产生广谱抗病机理分析

来源于昆虫病毒和动物的抗细胞凋亡基因能够诱导植物对生物或者非生物胁迫产生抗性.但其抗性机理有不同甚至相反的报道.本研究将来源于苜蓿银纹夜蛾核多角体病毒的p35基因转化烟草,T1代转化烟草Western blotting检测P35蛋白的表达,转化烟草接种烟草花叶病毒(Tobacco mosaic virus,TMV)抗病效果增强.进一步的抗病机理研究表明,转化和野生型烟草感染TMV后诱导过氧化氢积累无明显区别,野生型烟草感染24 h后出现DNA Laddering而转化烟草则没有;Western blotting结果显示PR-1蛋白表达没有显著差异.但接种另外一种病原真菌核盘茵(Sclerotiniasclerotiorum)后的RT-PCR分析结果表明,表达P35蛋白的烟草可增强感染核盘菌后PR-1基因的转录.而且表达时间提前.以上结果说明p35基因介导的广谱抗病反应的机理与接种的不同病原有关,对不同病原物的抗病机理存在差异,除抑制细胞凋亡外,还可能通过激活PR基因的表达提高对病原物的抗病能力.     

植物抗白粉病的分子机理

随着分子生物学与其相关技术的飞速发展 ,已克隆到了一系列的植物抗病基因和防御基因 ,加深了对植物与病原微生物相互作用分子机制的了解 ,促进了植物抗病分子机理的研究。国内外许多学者对大麦抗白粉病的分子机制进行了较系统的研究 ,在拟南芥菜中也找到了许多抗白粉病基因 ,这些结果对研究其它植物抗白粉病机制提供了线索。本文就该方面的研究进展加以阐述 ,并讨论了抗病机理在抗病育种工作中的应用前景。     

2008～2009年青岛地区手足口病病原学的调查分析

本研究对2008～2009年青岛地区手足口病的病原学进行调查研究。首先对HFMD病例的咽拭子标本直接进行病毒核酸的提取,然后采用多重荧光逆转录-聚合酶链反应(RT-PCR)方法对总肠道病毒(Enterovirus,EV)、肠道病毒71型(Enterovirus Type 71,EV71)和柯萨奇病毒A组16型(Coxsackievirus Group A 16,CVA16)进行检测,对EV阳性而EV71和CVA16均阴性的标本采用半巢式反转录PCR进行肠道病毒VP1基因部分序列的扩增和序列分析以鉴定其血清型别。结果提示2008～2009年青岛地区手足口病的主要病原为EV71和CVA16,无论轻症和重症病例,EV71的比例都大于CVA16。2008年共获得5个(8株)其它血清型,分别是柯萨奇病毒(Cox-sackievirus,CV)的A5、A6、A10、A12及埃可病毒9(Echovirus 9,E9),血清型分布比较分散、均匀。2009年共获得3个其它血清型(13株),分别是CVA9、CVA12及CVB2,CVA12所占比例较大(11/13),分布比较集中。CVA12成为2009年青岛地区HFMD病原中除EV71和CVA16外,新的较为流行的病原。     

Recent advances in the study of Kaposi's sarcoma-associated herpesvirus replication and pathogenesis

It has now been over twenty years since a novel herpesviral genome was identified in Kaposi's sarcoma biopsies. Since then, the cumulative research effort by molecular biologists, virologists, clinicians, and epidemiologists alike has led to the extensive characterization of this tumor virus, Kaposi's sarcoma-associated herpesvirus(KSHV; also known as human herpesvirus 8(HHV-8)), and its associated diseases. Here we review the current knowledge of KSHV biology and pathogenesis, with a particular emphasis on new and exciting advances in the field of epigenetics. We also discuss the development and practicality of various cell culture and animal model systems to study KSHV replication and pathogenesis.     

The structure, reproduction and taxonomy of Vidalia and Osmundaria (Rhodophyta, Rhodomelaceae)

Comprises species occurring mostly in subtidal habitats in tropical, subtropical and warm-temperate areas of the world. An analysis of the type species, V. spiralis (Sonder) Lamouroux ex J. Agardh, a species from Australia, establishes basic characters for distinguishing species in the genus. These characters are (1) branching patterns of thalli, (2) flat blades that may be spiralled on their axis, (3) width of the blade, (4) primary or secondary derivation of sterile and fertile branchlets and (5) position of sterile and fertile branchlets on the thalli. Application of the latter two characters provides an important basic method for separation of species into three major groups. Osmundaria , a genus known only in southern Australia, was studied in relation to Vidalia , and its separation from the Vidalia assemblage is not accepted. Species of Vidalia therefore are transferred to the older genus name, Osmundaria. Two new species, Osmundaria papenfussii and Osmundaria oliveae are described from Natal. Confusion in the usage of the epithet, Vidalia fimbriala Brown ex Turner has been clarified, and Vidalia gregaria Falkenberg, described as an epiphyte on Osmundaria pro/ifera Lamouroux, is revealed to be young branches of the host, Osmundaria prolifera.     

New or rare chromosome counts in Artemisia L. (Asteraceae, Anthemideae) and related genera from Kazakhstan

Fifteen chromosome counts of six Artemisia taxa and one species of each of the genera Brachanthemum, Hippolytia, Kaschgaria, Lepidolopsis and Turaniphytum are reported from Kazakhstan. Three of them are new reports, two are not consistent with previous counts and the remainder are confirmations of very scarce (one to four) earlier records. All the populations studied have the same basic chromosome number, x = 9, with ploidy levels ranging from 2x to 6x. Some correlations between ploidy level, morphological characters and distribution are noted.     

肝癌中HBV和HCV基因和抗原的分布及意义

采用原位分子杂交方法检测HCV RNA及HBV X基因;采用免疫组织化学方法研究HCV核心抗原,非结构区C33c抗原及HBxAg在肝细胞肝癌中的定位及分布.结果表明(1)HCV RNA、HBV X基因在肝细胞肝癌组织检出率分别为40%(55/136)和82%(112/136).HCV RNA定位于癌细胞的胞浆内,阳性细胞呈散在、灶状及弥漫分布三种形式;HBV X基因在肝癌细胞中的分布呈胞浆型、核型及核浆型,阳性细胞也呈上述三种分布形式;(2)HCV C33c抗原、核心抗原在肝细胞肝癌中的阳性率为81%(133/164)及86%(141/164).C33c抗原定位于癌细胞及肝细胞的胞浆内;核心抗原既定位于癌细胞核中,又可定位于胞浆中.C33c抗原阳性细胞以灶状分布为主;而核心抗原阳性细     

Selection with two alleles and complete dominance

For a plant selection model with frequency-independent viabilities, fertilities and selfing rates, it is shown that apart from global fixation, for certain parameter combinations a protected polymorphism and facultative fixation (either allele may become fixed according to initial frequencies) may both occur. Facultative fixation requires different selling rates for the dominant and recessive type. Protection of the polymorphism requires resource allocation for male and female function. In this connection the problem of purely genetically caused population extinction is discussed.
For general frequency dependence and regular segregation, the chances for establishment of a completely recessive gene are compared to those of a completely dominant gene. It is proven that the process of establishment of the recessive gene, despite a fitness advantage, may be considerably endangered by drift effects if random mating prevails. The recessive gene may reach the same effectivity in establishment as a dominant gene, only if the recessive homozygote mates exclusively with its own type during the period of establishment.