米尔顿姬小蜂rDNA ITS1和ITS2的序列分析及其分子鉴定

本研究测定了米尔顿姬小蜂Anselmella miltoni Girault的rDNA ITS1和ITS2序列,以探讨其分子鉴定方法。米尔顿姬小蜂的ITS1和ITS2侧翼区（18S和5.8S）序列相对稳定,ITS1和ITS2序列存在种间差异。根据18S rDNA部分序列,利用DNAMAN的Maximum Likelihood方法构建了与膜翅目其它科的系统发育树。根据米尔顿姬小蜂ITS1和ITS2序列设计了特异性引物,应用特异性引物对样品进行了PCR扩增,扩增效果理想,采用上述特异性引物可从单头米尔顿姬小蜂稳定地扩增出明显的目的DNA条带。因此,可以采用ITS1和ITS2区的特异性对米尔顿姬小蜂进行快速的分子鉴定。     

含有小檗碱的药用植物DNA条形码鉴定研究

[目的]评价ITS2与psbA-trnH条形码候选序列对含有小檗碱的药用植物的鉴定作用。[方法]对含有小檗碱与不含有小檗碱的药用植物的ITS2与psbA-trnH序列进行PCR扩增和测序,进行种内和种间变异分析,构建NJ进化树评价不同序列的鉴定能力。[结果]ITS2与psbA-trnH序列均能够成功地区分含有小檗碱与不含有小檗碱的药用植物。然而,ITS2在区分含有小檗碱的不同科药用植物的效率优于psbA-trnH序列。[结论]建立了以ITS2序列为主,psbA-trnH序列为辅的鉴定含有小檗碱的药用植物的方法,这为含有小檗碱的药用植物种质资源的整理与标准化,甚至育种都提供了有效的基础数据。     

石斛内生炭角菌DNA提取方法优化及分子鉴定

本文对石斛内生炭角菌DNA提取方法进行优化,并基于ITS序列及其ITS2二级结构对其进行分子鉴定。比较试剂盒法及不同浓度（2%、3%、4%）CTAB法的DNA提取效果并对CTAB法进行优化;进行ITS序列的扩增及ITS2二级结构的预测。结果表明：4%的CTAB提取效果最佳,优化的CTAB法大大缩短了DNA提取时间;ITS序列与炭角菌属3个种的相似度均为99%,ITS2二级结构仅与Xylaria arbuscula的二级结构100%相似。本研究所优化的CTAB法能为后续相关研究提供便利;结合ITS序列及ITS2二级结构能对石斛内生炭角菌进行准确的分子鉴定。     

基于ITS条形码序列的刺桐姬小蜂分子鉴定

【目的】刺桐姬小蜂Quadrastichus erythrinae Kim体型小,传统的形态学鉴定方法难以快速准确识别。【方法】本研究测定了刺桐姬小蜂的rDNA ITS1和ITS2序列,根据18S rDNA部分序列,利用MEGA的最大相似法(Maximum Likehood)构建系统发育树。根据刺桐姬小蜂ITS1和ITS2序列设计了特异引物,应用特异引物对单只刺桐姬小蜂进行PCR扩增,可稳定地扩增出明显的目的DNA条带。【结果】研究表明,基于ITS基因的DNA条形码技术可以用于刺桐姬小蜂的快速准确鉴定。【结论】因此,采用ITS1和ITS2区的特异性引物可对刺桐姬小蜂进行快速分子鉴定。     

基于rDNA ITS1和ITS2序列的褐飞虱、白背飞虱和灰飞虱的分子鉴定

本研究测定了褐飞虱Nilaparvata lugens、白背飞虱Sogatella furcifera和灰飞虱Laodelphax striatellus的rDNA ITS1和ITS2的序列, 以探讨这3种稻飞虱的分子鉴定方法。3种飞虱的ITS1和ITS2侧翼区（18S, 5.8S和28S）序列相对稳定, 但ITS1和ITS2序列在3种飞虱中变异较大。 ITS1在所分析的438个位点中可变位点达294个, ITS2在分析的403个位点中可变位点为177个。根据3种飞虱rDNA的ITS1和ITS2序列设计了特异性引物, 应用特异性引物对样品进行了PCR扩增, 分析发现3种飞虱ITS1区的特异性引物扩增效果不理想, 而ITS2区的特异性引物可以稳定地扩增出明显的目的DNA条带. 因此, 采用ITS2区的特异性引物可以对3种飞虱进行快速的分子鉴定。     

基于rDNA ITSl和ITS2序列的褐飞虱、白背飞虱和灰飞虱的分子鉴定

本研究测定了褐飞虱 Nilaparvata lugens、白背飞虱 Sogatella furcifera 和灰飞虱Laodelphax striatellus 的rDNA ITSl和ITS2的序列,以探讨这3种稻飞虱的分子鉴定方法.3种飞虱的ITSI和ITS2侧翼区(18S,5.8S和28S)序列相对稳定,但ITS1和ITS2序列在3种飞虱中变异较大.ITS1在所分析的438个位点中可变位点达294个,ITS2在分析的403个位点中可变位点为177个.根据3种飞虱rDNA的ITS1和ITS2序列设计了特异性引物,应用特异性引物对样品进行了PCR扩增,分析发现3种飞虱ITS1区的特异性引物扩增效果不理想.而ITS2区的特异性引物可以稳定地扩增出明显的目的DNA条带.因此,采用ITS2区的特异性引物可以对3种飞虱进行快速的分子鉴定.     

基于形态特征和ITS序列对7个鹅膏菌属菌株的分类鉴定

以采自浙江省丽水地区的7个鹅膏菌属菌株作为研究材料,在基于形态特征进行初步鉴定的基础上,对7种鹅膏菌的rDNAITS区段进行克隆测序和序列特征比较分析。进一步对ITS序列进行核酸序列数据库GenBank同源性检索比对,将从GenBank检索获得的9个最相似物种的ITS序列连同7种鹅膏菌的ITS序列一起作系统发育分析。结果表明:基于ITS序列对f6、f9和f493个菌株的分子鉴定支持了基于形态特征的鉴定结果,对f5的分子鉴定不支持形态鉴定的结果,f8为鹅膏菌属内某种,f66为鹅膏菌属内某种,并与Amanitafulva,A.atrofusca,A.orientifulva3种鹅膏菌的亲缘关系较近,f7与另外6种鹅膏菌的亲缘关系相差甚远。研究结果提示基于分子水平上的ITS序列分析不能单方面作为大型真菌分类鉴定的可靠依据,可以作为基于传统形态学分类鉴定的辅助参考依据。     

ITS2序列在植物DNA条形码鉴定中的应用(综述)

DNA条形码技术的迅速发展极大地推动了植物的鉴定工作,随着鉴定工作的不断进行和新序列的不断发现,利用ITS2序列进行鉴定已成为目前较为广泛使用的鉴定技术。本文根据ITS2序列的特点和性质,介绍ITS2序列鉴定的一般过程,并分析其特点和存在问题,以期为植物鉴定方面的研究提供参考。     

ITS鉴定真菌病原:一例司法鉴定研究实例

本研究选择一例疑似空气污染物伤害松树的司法鉴定案作为研究实例,在现场勘察和初步形态鉴定的基础上,应用ITS序列分析鉴定了对疑似空气污染物伤害松树的病原做了分子鉴定。我们对委托鉴定的疑似空气污染物伤害松树的地及周边地区进行了勘查,现场勘查结果并不支持空气污染物伤害松树的看法。为明确松树枯死的原因,对取样病枝上的疑似病原物进行了显微镜观察和培养性状观察,根据显微镜下孢子的形态和病原菌的培养性状,初步判断导致马尾松枯死的病原可能为拟盘多毛孢属(Pestalotipsis)真菌。为进一步确定病原种类,我们应用分子生物学技术对危害马尾松的病原物进行了ITS分子鉴定。测定了疑似真菌的ITS序列,并进行了比对和系统发育分析。研究结果表明,导致松树枯死的病原菌系韦司梅拟盘多毛孢(Pestalotipsis vismiae)。在本研究案例中,利用真菌ITS序列的系统发育分析,快速、准确地鉴定了真正导致松树枯死的病原,为今后类似司法鉴定案件审理提供了证据鉴定的新手段。     

评价ITS、BenA和CaM序列分析在曲霉菌种鉴定方面的应用

目的评价内转录间隔区(ITS)、β-微管蛋白基因(BenA)和钙调蛋白基因(CaM)序列分析技术对曲霉的鉴定能力。方法对169株曲霉临床分离株分别进行ITS、BenA和CaM序列测定,并在Genbank数据库中进行比对分析以获得其菌种鉴定信息。结果 169株曲霉经ITS、BenA和CaM序列分析分别有52.7%、66.3%、97.6%菌株鉴定至种水平,47.3%、33.7%、2.4%菌株鉴定至属水平,3个序列对曲霉均不存在无法鉴定情况。结论 ITS、BenA和CaM均可用于曲霉菌种鉴定,其中以CaM的鉴定能力最强。     

Development of PCR assay based on ITS2 rDNA polymorphism for the detection and differentiation of Fusarium sporotrichioides

A polymerase chain reaction assay was developed for detection of Fusarium sporotrichioides, a plant pathogen in many parts of the world. Based on small nucleotide differences in ITS2 (Internal Transcribed Spacer) rDNA of our local isolate of F. sporotrichioides (Accession No. AY510069) and other isolates found in NCBI/GeneBank database, species specific primer FspITS2K was selected. Primer pair FspITS2K and P28SL amplified a fragment of 288 bp containing a portion of ITS2 and 28S rDNA of all the F. sporotrichioides isolates tested, originated from different hosts and regions of the world but did not amplify any other species of Fusarium and plant's DNA. To use the PCR assay in seed health testing, a protocol was setup for the rapid and effective preparations of fungal DNA from wheat seeds. The method developed may be useful for the rapid detection and identification of F. sporotrichioides both from culture and from plant tissue.     

中药乌头及其近缘种的rDNA—ITS序列分析

运用PCR扩增产物直接测序的方法对云南、安徽的乌头及其近缘种植物的ITS区碱基序列测定。表明核糖体DNA中ITS区的完整序列（包括ITS1,ITS2和5．8s）,4种乌头属植物的ITS1序列长度为249bp,云南鸟头和安徽乌头及黄山鸟头ITS2序列长度为189bp,赣皖乌头ITS2序列长度为217bp。运用Mega2软件进行系统分析得到系统进化树。ITS序列特征是乌头鉴别的有效分子标记。     

亚稀褶黑菇和稀褶黑菇的ITS序列分析

对亚稀褶黑菇和稀褶黑菇的ITS全序列进行了测定和比较,首次报道了亚稀褶黑菇的ITS1和5.8S区域.在ITS区域中,不同采集地的亚稀褶黑菇与稀褶黑菇的5.8S rDNA具有100%的同源性,而两侧ITS之间表现出种内和种间的多态性,种内的差异均不超过5%,种间的差异达10%左右.ITS序列分析方法可以作为两者的鉴定方法.     

亚稀褶黑菇和稀褶黑菇的ITS序列分析

对亚稀褶黑菇和稀褶黑菇的ITS全序列进行了测定和比较,首次报道了亚稀褶黑菇的ITS1和5.8S区域。在ITS区域中,不同采集地的亚稀褶黑菇与稀褶黑菇的5.8S rDNA具有100%的同源性,而两侧ITS之间表现出种内和种间的多态性,种内的差异均不超过5%,种间的差异达10%左右。ITS序列分析方法可以作为两者的鉴定方法。     

Extensive 5.8S nrDNA polymorphism in <Emphasis Type="Italic">Mammillaria</Emphasis> (Cactaceae) with special reference to the identification of pseudogenic internal transcribed spacer regions

The internal transcribed spacer (ITS) region (ITS1, 5.8S rDNA, ITS2) represents the most widely applied nuclear marker in eukaryotic phylogenetics. Although this region has been assumed to evolve in concert, the number of investigations revealing high degrees of intra-individual polymorphism connected with the presence of pseudogenes has risen. The 5.8S rDNA is the most important diagnostic marker for functionality of the ITS region. In Mammillaria, intra-individual 5.8S rDNA polymorphisms of up to 36% and up to nine different types have been found. Twenty-eight of 30 cloned genomic Mammillaria sequences were identified as putative pseudogenes. For the identification of pseudogenic ITS regions, in addition to formal tests based on substitution rates, we attempted to focus on functional features of the 5.8S rDNA (5.8S motif, secondary structure). The importance of functional data for the identification of pseudogenes is outlined and discussed. The identification of pseudogenes is essential, because they may cause erroneous phylogenies and taxonomic problems. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Internal transcribed spacer 2 amplicon as a molecular marker for identification of Peronospora parasitica (crucifer downy mildew)

AIMS: The purpose of the study was to characterize the internal transcribed spacer (ITS) regions of Peronospora parasitica (crucifer downy mildew) in order to evaluate their potential as molecular markers for pathogen identification. METHODS AND RESULTS: PCR amplification of ribosomal RNA gene block (rDNA) spacers (ITS1 and ITS2) performed in 44 P. parasitica isolates from different Brassica oleracea cultivars and distinct geographic origins, revealed no length polymorphisms. ITS restriction analysis with three endonucleases, confirmed by sequencing, showed no fragment length polymorphisms among isolates. Furthermore, ITS amplification with DNA isolated from infected host tissues also allowed the detection of the fungus in incompatible interactions. The combination of the universal ITS4 and ITS5 primers, for amplification of full ITS, with a new specific forward internal primer for ITS2 (PpITS2F), originates a P. parasitica specific amplicon, suitable for diagnosis. CONCLUSIONS: As ITS2 regions of P. parasitica, B. oleracea, other B. oleracea fungal pathogens and other Peronospora species are clearly distinct, a fast and reliable molecular identification method based on multiplex PCR amplification of full ITS and P. parasitica ITS2 is proposed for the diagnosis of crucifer downy mildew. SIGNIFICANCE AND IMPACT OF THE STUDY: The method can be applied to diagnose the disease in the absence of fungal reproductive structures, thus being useful to detect nonsporulating interactions, early stages of infection on seedlings, and infected young leaves packed in sealed plastic bags. Screening of seed stocks in sanitary control is also a major application of this diagnostic method.     

Identification of Taxa in the Genus shape Beta using ITS1 Sequence Information

Sequence variation in the ITS1 locus of the nuclear ribosomal DNA in beets has previously been used to reconstruct phylogeny of the species in the genus Beta. We have developed protocols that allow the identification of Beta taxa by use of taxon-specific primers. Beta sections, species and subspecies can be identified. Differences within the ITS1 region of a single base can be exploited for species identification. The results from this study not only provide effective methods for wild beet identification, but also indicate the potential use of the techniques in other crops.