应用UP-PCR进行玉米丝黑穗病菌遗传多样陛研究

本研究探讨了UP-PCR技术在玉米丝黑穗病菌遗传多样性分析中的利用可行性。在13个通用引物中，筛选出9个扩增多态性好且稳定的通用引物，共扩增出113条DNA条带，大小分布于250~2000bp之间，其中多态性条带为95条，为总条带数的84．07％。遗传距离为0．76处时，所有丝黑穗病菌菌株被聚为6个组。利用UP-PCR技术，可以充分展现玉米丝黑穗病菌菌株间的亲缘关系及差异性，可用于玉米丝黑穗病菌遗传多样性研究，为有效地开展玉米丝黑穗病菌的遗传进化甚至探讨病菌致病性的生理分化提供了一个新的技术方法。     

应用UP-PCR进行玉米丝黑穗病菌遗传多样性研究

本研究探讨了UP PCR技术在玉米丝黑穗病菌遗传多样性分析中的利用可行性。在13个通用引物中，筛选出9个扩增多态性好且稳定的通用引物，共扩增出113条DNA条带，大小分布于250～2 000 bp之间，其中多态性条带为95条，为总条带数的84.07%。遗传距离为0.76处时，所有丝黑穗病菌菌株被聚为6个组。利用UP-PCR技术，可以充分展现玉米丝黑穗病菌菌株间的亲缘关系及差异性，可用于玉米丝黑穗病菌遗传多样性研究，为有效地开展玉米丝黑穗病菌的遗传进化甚至探讨病菌致病性的生理分化提供了一个新的技术方法。     

小麦白粉菌ISSR分子标记体系构建及其分离菌株的多样性分析

为了对小麦白粉菌群体的多样性进行研究,构建了其ISSR分子标记体系。以小麦白粉菌基因组DNA为模板,用正交设计和单因素水平优化的方法对ISSR反应程序中的一些重要参数进行摸索和优化,建立了小麦白粉菌ISSR-PCR反应的优化反应体系;对20个ISSR引物的退火温度进行了优化,并筛选出一些多态性较好的ISSR引物。对33个分离菌株的ISSR扩增表明,ISSR标记在我国小麦白粉菌中存在较高的多态性;对ISSR标记揭示的白粉菌的遗传多样性和毒性多样性进行了比较,结果表明两者之间存在一定程度的相关性。     

玉米圆斑病菌(Bipolaris zeicola)遗传多样性ISSR分析

利用简单序列重复间隔区(inter-simple sequence repeats,ISSR)标记对玉米圆斑病菌(Bipolaris zeicola)的遗传多样性进行了分析。筛选出9个扩增多态性好且稳定的通用引物,共扩增出47条DNA条带,大小分布于250~2 000bp之间,其中多态性条带为33条,为总条带数的70.21%。遗传距离为0.91处时,所有菌株被聚为6个组。ISSR标记可以揭示菌株间的亲缘关系及差异性,可用于玉米圆斑病菌遗传多样性研究。此外,通过分子标记划分的类群与利用寄主反应型之间存在一定相关性,但其关系并不密切。     

我国玉米灰斑病菌遗传多样性的ISSR分析

为明确我国发生的玉米灰斑病菌地理差异及遗传结构,利用简单序列重复区间(ISSR)对玉米灰斑病菌遗传多样性进行了分析,并利用尾孢菌特异引物对分离自四川、云南、湖北、贵州等西南地区的16个玉米灰斑病菌菌株进行了分子鉴定。结果显示,通过ISSR标记筛选出10个扩增多态性好且稳定的通用引物,共扩增出81条DNA条带,均为多态性条带,扩增片段大小在200~2 000 bp之间,菌株遗传相似系数为0.19~1.00。在遗传相似系数为0.19时,供试菌株被聚为2大类群,来自西南地区和东北地区的菌株各自聚为一组,在DNA水平上表现出明显差异,认为是2类不同的致病类群。分子鉴定结果显示引起西南各地区玉米灰斑病的主要致病菌均为玉米尾孢菌Cercospora zeina。表明我国玉米灰斑病菌存在丰富的遗传多样性,ISSR标记可揭示出玉米灰斑病菌株间的亲缘关系及遗传差异性,可用于其遗传多样性研究。     

玉米大斑病菌ISSR反应体系的优化和遗传多样性分析

以玉米大斑病菌基因组DNA为模板,采用单因素水平优化的方法对DNA聚合酶的来源及浓度、引物浓度、dNTPs浓度、DNA模板浓度、Tm(退火温度)、PCR反应循环数等重要参数进行摸索和优化,建立了玉米大斑病菌ISSR-PCR优化反应体系,并从40条ISSR引物中筛选出9条多态性较好的ISSR引物。对来自河北、河南、辽宁等玉米主产区的44个菌株进行ISSR分析表明,ISSR标记在我国玉米大斑病菌中存在较高的多态性,多态性条带占40.3%。聚类分析显示,在阈值为0.8时菌株被分为7个类群。对ISSR揭示的玉米大斑病菌的遗传多样性与菌株交配型、地理来源之间的关系进行分析,结果显示菌株的遗传多样性与交配型间的关系密切,而与其地理来源无明显相关性。     

应用ISSR-PCR分析福建水稻纹枯菌的遗传多样性

本研究应用简单序列重复区间(inter-simple sequence repeats,ISSR)标记技术对福建省10个县市100个水稻纹枯病菌菌株的遗传多样性进行了分析。从16个随机引物中筛选出3个重复性好、特异性高的引物对菌株进行ISSR-PCR扩增,共产生41个ISSR分子标记,其中90.2%的片段具有多态性。PopGene分析结果表明,种群的平均多态位点百分率为55.14%,Shannon表型多样性指数I平均为0.2953,具有较高的遗传多样性;种群间存在着明显的遗传分化(Nei′s信息多样性指数h平均值为0.1991,Gst平均值为0.6423),聚类分析可将它们分成5个遗传聚类群。同时还进行了菌株生长速率和致病力的测定。ISSR遗传聚类组群的划分与菌株的地理来源有明显的相关性,但与菌株的致病力和生长速率都没有明显的相关性。以上结果为进一步开展水稻纹枯病菌群体遗传分析和纹枯病防治提供了一定的理论依据。     

我国烟草赤星病菌遗传多样性的ISSR分析

为明确我国烟草赤星病的2种主要致病菌链格孢菌Alternaria alternata和长柄链格孢菌A.longipes的地理差异与遗传结构,采用ISSR标记对分离自9个省市的135株烟草赤星病菌进行遗传多样性分析。结果显示,通过正交优化试验建立的烟草赤星病菌ISSR-PCR最佳反应体系稳定性较好,筛选出17条多态性高且稳定的引物,共扩增出192条谱带,其中有177条具有多态性,多态率为92.19%。UPGMA聚类分析结果显示,链格孢菌和长柄链格孢菌的遗传相似性系数分别在0.67~1.00和0.66~1.00之间,遗传相似性系数为0.83时可使链格孢菌和长柄链格孢菌分别划分为5个和6个亚群,其中前者不同地理种群间表现出地理相关性,后者不同菌株随机分组。烟草赤星病菌种群的基因多态性和遗传多样性丰富,链格孢菌和长柄链格孢菌的群体间遗传分化系数分别为0.36和0.37,均存在遗传分化;群居每代迁移数分别为0.89和0.85,不同地理种群间存在基因交流;2种烟草赤星病菌的遗传分化结构表现出相似性。表明我国烟草赤星病菌中的链格孢菌和长柄链格孢菌均存在丰富的遗传多样性,且二者进化方向相似,ISSR标记能较好地揭示烟草赤星病菌种群间的亲缘关系和遗传差异性,可用于其遗传多样性分析。     

河南省西部山区小麦白粉菌群体遗传多样性分析

为揭示河南省小麦白粉菌群体遗传结构、起源及进化关系,采用简单重复序列区间(inter-simple sequence repeats,ISSR)和扩增片段长度多态性(amplified fragment length polymorphism,AFLP)分子标记技术对河南省西部山区4个小麦产区的35个小麦白粉菌单孢分离菌株进行了群体遗传多样性分析。结果显示:ISSR和AFLP分析均将35个菌株分为3个组,组Ⅰ包括来自卢氏和灵宝的大部分菌株;组Ⅱ包括来自栾川、卢氏和巩义的菌株;组Ⅲ由4个地区的个别菌株组成,同时包含1个闭囊壳释放子囊孢子获得的菌株。ISSR分析出菌株遗传距离分布在0.0139～0.6592之间,扩增多态性比率为64.83%,各菌株间的Shannon指数为0.2749;而AFLP分析所得的各菌株遗传距离变化幅度在0.1257～0.9322之间,扩增多态性比率为82.68%,各菌株间的Shannon指数为0.5100。可见,河南省小麦白粉菌具有丰富的遗传多样性,研究所用的2种方法均可用于遗传多样性分析,其中AFLP分析小麦白粉菌群体表现出更为丰富的遗传多样性。     

黑龙江省水稻纹枯病菌的致病力分化与AFLP分析

为了明确黑龙江省水稻纹枯病菌遗传多样性，为水稻抗病育种和水稻纹枯病的综合防治提供依据。本文对采自13个水稻种植地区的29个水稻纹枯病菌菌株进行了致病力测定和AFLP分析。结果表明9对AFLP引物对供试菌株扩增出396条带，其中多态性带187条，占总扩增带数的47.22%。黑龙江省水稻纹枯病菌的遗传距离变化在0.50~0.92之间，平均为0.71，群体遗传多样性较为丰富。UPGMA法可以将供试菌株分成4个AFLP聚类组群(Ⅰ、Ⅱ、Ⅲ和Ⅳ)，相同地理来源的菌株基本上聚集在同一组群内，表明AFLP类群划分与菌株的地理来源有较强的相关性。黑龙江省水稻纹枯病菌致病性分化较为明显，并且AFLP类群划分与菌株的致病性鉴定之间存在一定相关性。     

Genetic diversity of the annual weed Monochoria vaginalis in southern China detected by random amplified polymorphic DNA and inter-simple sequence repeat analyses

Two molecular genetic screening techniques, RAPD (random amplified polymorphic DNAs) and ISSR (inter-simple sequence repeats), were applied to detect the level and pattern of genetic diversity of Monochoria vaginalis, a common weed of rice fields, in seven populations from southern China. Among these populations, 116 bands were amplified by 18 RAPD primers, of which 34 bands (29.31%) were polymorphic, and 14 ISSR primers produced 111 bands with 87 polymorphic bands (78.38%). Within each population, a relatively low level of genetic diversity was detected by both RAPD and ISSR analyses, with a mean genetic diversity (H) of 0.0348 and 0.0551 respectively. Analysis of molecular variance of the data from the RAPD and ISSR markers detected that the majority of total genetic variation existed among populations (73.50% and 76.70% respectively) and only minor genetic variation within populations (26.50% and 23.30% respectively). Cluster analysis divided the seven populations into two groups, indicating that the genetic relationships among populations have relatively low correlation with their geographical distribution (Mantel test; r = 0.45 and 0.48 respectively). Our results indicated that both RAPD and ISSR markers were effective and reliable for accurately assessing the degree of genetic variation of M. vaginalis. Comparing the two techniques, ISSR markers were more efficient than the RAPD assay. The Mantel test gave r = 0.16, suggesting no correlation between these two molecular markers.     

蔬菜保护地木霉菌rDNA-ITS序列和UP-PCR遗传多样性分析

采用传统形态学分类和ITS序列比对的方法,研究蔬菜保护地土壤中木霉菌种群分布和遗传多样性。木霉菌分离培养结果显示,共获得397株木霉菌,鉴定出11个种,分别为:长枝木霉Trichoderma longibrachiatum、深绿木霉T.atroviride、哈茨木霉T.harzianum、粘绿木霉T.viren、微孢木霉T.minutisporum、拟康木霉T.pseudokoningii、黄绿木霉T.aureoviride、非钩木霉T.inhamatum、棘孢木霉T.asperellum、长孢木霉T.longipile和螺旋木霉T.helicum。经ITS序列建立系统发育树后,将木霉菌分为5个组。用5条通用引物经UP-PCR扩增后,扩增出46条谱带,其中多态性条带43条,占总条带数的93.5%。遗传多样性分析表明,当相似系数为0.80时,可将24个菌株划分为9个组。UP-PCR与ITS序列相比,更能体现木霉菌种间和种内的亲缘关系及遗传差异性,可以作为木霉菌分类的辅助方法。     

陕西省苹果树腐烂病菌基因多态性的ISSR分析

为了从分子水平上揭示苹果树腐烂病菌的群体遗传多样性,采用正交设计对ISSR-PCR体系进行了4因素3水平的筛选,并从47条ISSR引物中筛选出11条多态性较好的引物。对供试的87个分离株进行扩增的结果显示,11条引物在129个位点扩增出稳定的条带,其中多态性位点119个,多态性位点率为92.25%。POPGENE分析显示,病菌种群的遗传多样性和基因多态性丰富,群体间的遗传分化系数(Gst)为0.109,群体内为0.891,群体内多样性大于群体间多样性。两个地理种群间的居群每代迁移数(Nm)为2.046,两者之间存在广泛的基因交流。在遗传相似系数为0.88时,可将21个自然种群划分为9个不同的类群,表明陕西省苹果树腐烂病菌的各个自然种群之间的遗传亲缘关系与其地理来源之间无明显的相关性。     

Characterization of a Fusarium poae world-wide collection by using molecular markers

Fusarium poae has been considered as a minor species among those that cause Fusarium Head Blight (FHB) disease but in recent years several researchers have documented a high frequency of occurrence of this species. In this study, a total of 173 F. poae isolates from Argentina, Belgium, Canada, England, Finland, France, Germany, Hungary, Italy, Luxembourg, Poland, Switzerland and Uruguay were evaluated by using inter simple sequence repeats (ISSR) and amplified fragment length polymorphism (AFLP) to evaluate genetic variability within F. poae and to amplify MAT idiomorphs as a possible mechanism that could explain part of the variability found in this species. The molecular analysis obtained from both molecular markers showed a high intraspecific variability. However, a partial clustering between F. poae isolates and their geographic origin was obtained by ISSR markers while AFLP showed isolates from different geographic locations distributed throughout the dendrogram. Moreover, ISSR grouped all the F. poae isolates into a different cluster from the F. langsethiae and F. sporotrichioides isolates used as outgroups compared with the dendrogram obtained using AFLP markers. Analysis of molecular variance (AMOVA) indicated a high genetic variability in the F. poae collection, with most of the genetic variability resulting from differences within, rather than between, American and European populations by using both molecular markers. Regarding MAT idiomorphs, for most F. poae isolates both MAT-1 and MAT-2 were present from each isolate.     

Population genetic structure of <Emphasis Type="Italic">Rhizoctonia solani</Emphasis> AG1IA from rice field in North India

Rhizoctonia solani AG1IA is an important fungal pathogen causing significant yield and quality losses in rice production. However, little is known about the levels of genetic diversity and structure of this pathogen in North India. Out of 240 samples collected from different rice-growing regions of North India, 112 isolates were identified as R. solani AG1IA subgroups using species-specific primers. All 112 isolates were organized into four groups on the basis of percent disease index (PDI). The majority of the isolates were weakly virulent. Population genetic analysis was performed within and between populations using inter simple sequence repeat (ISSR) markers. A total of 8249 alleles were identified from the 112 isolates of R. solani AG1IA through analysis of the ten inter simple sequence repeat markers. All the ten ISSR markers were polymorphic. The average number of bands per primer was 7.3 which ranged in size from 250 to 1500 bp. Genetic structure of the isolates using inter simple sequence repeat primers showed high degree of polymorphism (PIC ≥0.81). The analysis of molecular variance (AMOVA) indicated that most of the genetic diversity occurred within populations (60%), while the variability among populations and among regions contributed 25 and 15%, respectively. Overall, the present study reveals that a large variation exists among rice-infecting isolates of R. solani AG1IA in North India. Fingerprinting of the isolates using ISSRs along with phenotypic characterization and virulence analysis will help epidemiological studies that can provide new insights into pathogen biology and disease spread.     

内蒙古亚洲小车蝗种群遗传多样性和遗传分化的ISSR分析

亚洲小车蝗Oedaleus asiaticus Bei-Bienko是我国北方草原和农牧交错区的主要害虫。为评价内蒙古地区亚洲小车蝗种群的遗传多样性和遗传分化，应用ISSR标记方法对内蒙古15个亚洲小车蝗种群遗传多样性及遗传分化进行了分析。结果表明，7条引物扩增出85条ISSR条带，均为多态性条带。多态性比例（P）、Nei''s遗传多样性指数（H）和香农多样性指数（I）分别为82.59%、0.2319和0.3421，表明亚洲小车蝗种群具有较高的遗传多样性。基因流（Nm）和基因分化系数（Gst）分别为1.2298和0.3352，表明亚洲小车蝗不同地理种群具有明显的遗传分化。遗传距离与地理距离呈极显著正相关关系。表明地理距离和地形差异可能是形成亚洲小车蝗种群遗传分化的主要原因。     

Genetic diversity and structure of the Fusarium oxysporum f.sp. lini populations on linseed (Linum usitatissimum) in China

The genetic diversity of specific Fusarium oxysporum f.sp. lini from six provinces in China was investigated using molecular markers, inter-simple sequence repeats (ISSR). Based on the morphological features and the internal transcribed spacer (ITS) sequences, 96 isolates were identified as Fusarium oxysporum. The 96 isolates were amplified by PCR with 12 ISSR primers. The number of bands amplified by each primer ranged from 43 to 142, with sizes ranging from 250 to 4,500 bp. A total of 800 bands were observed, out of which 797 were polymorphic (99.62%). The percentage of polymorphic loci varied from 17.25% in Gansu and Inner Mongolia to 33.75% in Sinkiang. Nei’s gene diversity index (h) ranged from 0.0428 in Gansu to 0.0666 in Sinkiang, and Shannon’s information index (I) ranged from 0.0675 in Gansu to 0.1117 in Sinkiang. The genetic identity using the Nei’s genetic identity varied from 0.9643 between the populations from Hebei and Gansu to 0.9844 between the populations from Sinkiang and Shanxi. Unweighted pair group mean analysis (UPGMA) cluster analysis, as indicated by the Nei’s genetic distance, showed the distances ranging from 0.0158 between the populations from Sinkiang and Shanxi to 0.0364 between the populations from Hebei and Gansu. The six populations were clustered into three subgroups. The Gansu population was clustered into one subgroup, the same as the Inner Mongolia population. The four other populations were clustered into the third subgroup. The Nei’s GST (0.2972) and gene flow among populations (Nm =1.1825) revealed large gene exchanges among populations.