诊断引物应用于我国三种重要赤眼蜂分子鉴定的研究

本研究根据螟黄赤眼蜂rDNA-ITS2序列设计了螟黄赤眼蜂Trichogramma chilonis Ishii特异引物,同时采用文献中发表的松毛虫赤眼蜂Trichogramma dendrolimi Matsumura 和玉米螟赤眼蜂Trichogramma ostriniae Pang et Chen的特异引物以及赤眼蜂属Trichogramma 特异引物对赤眼蜂成虫和寄主卵样品进行了PCR特异扩增分析。结果表明,采用上述特异引物可从单头蜂稳定地扩增出明显的目的DNA条带,并且分子鉴定结果与形态学鉴定结果完全吻合。因此,采用上述3对特异引物可以实现对我国3种重要赤眼蜂种,即松毛虫赤眼蜂、螟黄赤眼蜂和玉米螟赤眼蜂的分子鉴定。     

几种化学因子对三种赤眼蜂离体酚氧化酶活性的影响

为比较不同赤眼蜂酚氧化酶（PO）活性的大小, 明确赤眼蜂种间免疫防御能力强弱, 本研究通过研磨、离心提取松毛虫赤眼蜂Trichogramma dendrolimi、螟黄赤眼蜂T. chilonis、玉米螟赤眼蜂T. ostriniae匀浆液, 首次测定了几种化学因子（Ca²⁺、昆布多糖、纤维素、右旋糖酐、脂多糖和丝氨酸蛋白酶抑制剂）对3种供试赤眼蜂匀浆液中酚氧化酶原激活系统（proPO-AS）的激活程度。结果表明: 玉米螟赤眼蜂匀浆液PO活性最高, 螟黄赤眼蜂次之, 松毛虫赤眼蜂最低。Ca²⁺是激活供试赤眼蜂proPO的必需因子, 且在0.03 mol/L浓度下激活作用最强; 昆布多糖和脂多糖也能有效激活proPO, 0.01及0.05 mg/mL昆布多糖能强烈激活PO活性; 纤维素和右旋糖酐对PO活性存在显著抑制作用。结果证明了赤眼蜂种间存在明显的免疫能力差异。本研究建立了小型昆虫proPO-AS研究体系, 为研究Wolbachia-小型昆虫的免疫互作体系奠定了基础。     

基于诊断引物的赤眼蜂鉴定和检测技术

通过对松毛虫赤眼蜂Tichogramma dendrolimi Matsumura和玉米螟赤眼蜂T.ostriniae Pang et Chen（膜翅目：赤眼蜂科）核内可转录第二间隔区（简称：ITS2）的克隆、测序,并获取和分析了GenBank中已登录的同源序列,然后设计了松毛虫赤蜂的特异引物以用于该蜂的分子鉴定和检测,经过反复筛选发现：采用鉴定引物通过PCR扩增不仅可以区分鑫头样品,单头样品（雌蜂或雄峰）,而且可鉴定幼期虫和卵,这用传统方法是无法办到的。该鉴定技术比基于形态学鉴定检测技术用来鉴定了从中国大陆不同地域和寄主上采集到的12个样品,结果表明：该方法可用于赤眼蜂田间分子监测和实验室拟寄生行为研究。     

松毛虫赤眼蜂和螟黄赤眼蜂羧酸酯酶性质比较研究

该文对松毛虫赤眼蜂Trichogramma dendrolimi和螟黄赤眼蜂T.Chilonis羧酸酯酶的毒理学和生物化学性质进行了初步研究。由时间进程曲线确定了赤眼蜂羧酸酯酶活性测定中的最适反应时间为40min。对两种赤眼蜂单头羧酸酯酶活性的测定表明,松毛虫赤眼蜂羧酸酯酶活性主要分布在0—1OD/(mg·min)之间,而螟黄赤眼蜂羧酸酯酶活性主要分布在1-4OD/(mg·min)之间。比较两种赤眼蜂羧酸酯酶米氏常数(K_m)值,螟黄赤眼蜂羧酸酯酶对底物的亲和力比松毛虫赤眼蜂羧酸酯酶对底物的亲和力高。对氧磷对螟黄赤眼蜂和松毛虫赤眼蜂羧酸酯酶的抑制作用没有明显差异,而对氧磷对松毛虫赤眼蜂羧酸酯酶的抑制作用明显强于磷酸三苯酯(TPP)。该文还将棉铃虫Helicoverpa armigera (Hubner)羧酸酯酶部分性质与两种赤眼蜂作了比较。     

繁殖寄主对赤眼蜂羧酸酯酶和乙酰胆碱酯酶的影响

通过测定赤眼蜂Trichogramma羧酸酯酶和乙酰胆碱酯酶的活性、对底物的亲和力以及对抑制剂的敏感度研究了繁殖寄主对松毛虫赤眼蜂T.dendrolimi和螟黄赤眼蜂T.chilonis的影响。柞蚕卵和米蛾卵繁殖的赤眼蜂羧酸酯酶对底物的亲和力有不同程度的影响,柞蚕卵繁殖的赤眼蜂羧酸酯酶对α-乙酸萘酯或β-乙酸萘酯的亲和力最高是米蛾卵的2倍以上。繁殖寄主对乙酰胆碱酯酶对底物亲和力没有明显的影响。米蛾卵繁殖的松毛虫赤眼蜂羧酸酯酶活性明显高于柞蚕卵繁殖的种群,而米蛾卵繁殖的螟黄赤眼蜂种群羧酸酯酶的活性明显低于柞蚕卵繁殖的种群。用柞蚕卵繁殖的松毛虫赤眼蜂种群对对氧磷的敏感度明显低于米蛾卵繁殖的种群,而增效磷则正好相反。繁殖寄主对松毛虫赤眼蜂吉林种群乙酰胆碱酯酶对DDVP和毒扁豆碱的敏感度没有明显的影响,而在松毛虫赤眼蜂广东种群和螟黄赤眼蜂中,柞蚕卵繁殖的种群乙酰胆碱酯酶对DDVP和毒扁豆碱的敏感度明显低于米蛾卵繁殖的种群。     

米蛾对三种赤眼蜂的适合性及被寄生后卵内游离氨基酸含量的变化

寄生发生前寄生蜂的寄生行为及寄生发生后寄生蜂的生长发育情况能够反映出寄主对寄生蜂的适合性,而寄生蜂对寄主营养物质的吸收和利用是寄生蜂完成发育的生理基础。为了从寄生蜂利用寄主营养能力的角度探讨寄主对不同种赤眼蜂适合性变化的原因,本文观察了以米蛾Corcyra cephalonica Stainton卵为寄主时拟澳洲赤眼蜂Trichogramma confusumViggiani、松毛虫赤眼蜂T. dendrolimi Matsumura和玉米螟赤眼蜂T. ostriniae Pang et Chen的寄生行为及发育和存活情况,测定了被寄生米蛾卵内游离氨基酸的含量 。结果发现,玉米螟赤眼蜂的产卵时间为84.9 s,显著长于拟澳洲赤眼蜂和松毛虫赤眼蜂的产卵时间。拟澳洲赤眼蜂检测寄主所需时间为30.8 s,显著长于玉米螟赤眼蜂和松毛虫赤眼蜂所需时间,但从每寄主卵中羽化出的拟澳洲赤眼蜂数量显著高于松毛虫赤眼蜂及玉米螟赤眼蜂寄生的结果。3种赤眼蜂卵+幼虫的发育历期间不存在显著差异,但卵成虫的发育历期间存在显著差异。玉米螟赤眼蜂幼虫期和预蛹期的死亡率均显著高于拟澳洲赤眼蜂和松毛虫赤眼蜂相应虫期的死亡率。这些结果表明：米蛾卵对松毛虫赤眼蜂及拟澳洲赤眼蜂的适合性高于对玉米螟赤眼蜂的适合性。未被寄生的米蛾卵内游离氨基酸的总量在24～96 h时间段内从开始的2.194 mg/mL逐渐下降到1.565 mg/mL,而被寄生的米蛾卵内游离氨基酸总量均出现先升高后下降的现象。被松毛虫赤眼蜂和拟澳洲赤眼蜂寄生的米蛾卵内游离氨基酸总量在48 h达到最高值,分别为4.239 mg/mL和3.222 mg/mL,被玉米螟赤眼蜂寄生的米蛾在72 h达到最高值,为4 .323 mg/mL,显示同玉米螟赤眼蜂相比,松毛虫赤眼蜂和拟澳洲赤眼蜂能够更快地分解利用寄主营养。这些结果提示,3种赤眼蜂利用米蛾卵内营养物质能力的不同导致了米蛾卵对3种蜂适合性的不同。     

Wolbachia在玉米螟赤眼蜂内的三重感染

Wolbachia是一类广泛存在于节肢动物体内的共生菌。玉米螟赤眼蜂Trichogramma ostriniae是我国玉米田间的优势赤眼蜂种, 据报道, 赤眼蜂种内有Wolbachia感染。本文利用Wolbachia的16s rDNA和wsp基因引物通过PCR方法对玉米螟赤眼蜂的野生种群进行了调查, 发现以wsp基因为鉴定依据, 检测的所有个体都感染了3种Wolbachia ［wOstGDAa (GenBank accession no. EU157103), wOstGDAb (GenBank accession no. EU157104) 和 wOstGDB (GenBank accession no. EU157105)］。本文首次报道了野生赤眼蜂种群内Wolbachia的三重感染率几乎为100%。根据本研究的结果, 可以推测当不同种赤眼蜂寄生同一寄主时, Wolbachia可能会在不同赤眼蜂种间进行横向传播。     

四种松毛虫不同地理种群遗传多样性的等位酶分析

【目的】采用等位酶电泳技术对中国松毛虫属Dendrolimus 4种共9个地理种群进行遗传多样性和遗传分化研究。【方法】对6种等位酶系统乳酸脱氢酶（LDH）、苹果酸脱氢酶（MDH）、苹果酸酶（ME）、乙醇脱氢酶（ADH）、甲酸脱氢酶（FDH）、谷氨酸脱氢酶（GDH）进行聚丙烯酰胺凝胶电泳分析。【结果】在4种松毛虫9个地理居群中共检测到10个基因位点,其中4个位点为多态位点,检测到17个等位基因; 种群总体水平多态位点比率P=40%,平均有效基因数A=1.700,平均期望杂合度He=0.151,种群平均遗传距离为0.001～0.285; 其中马尾松毛虫指名亚种Dendrolimu punctatus Walker 6个居群的遗传分化度Fst=0.265,基因流Nm=0.692。4种松毛虫之间遗传关系最近的是落叶松毛虫D. superans Butler和马尾松毛虫的地理亚种赤松毛虫D. punctatus spectabilis Butler,遗传关系最远的是落叶松毛虫D. superans Butler和云南松毛虫D. houi Lajonquiere。【结论】 马尾松毛虫居群间遗传分化程度较大,基因交流较少,遗传漂变已经成为导致该物种种群分化的主要原因之一;遗传距离与地理距离存在一定相关性。     

中国长斑蚜属研究及新种记述(同翅目：斑蚜科)

该文系统研究了中国长斑蚜属Tinocallis Matsumura的15种蚜虫,其中包括:1个新种,短节长斑蚜T. microtylodes sp.nov.和2个中国新记录种,斑长斑蚜T.platani(Kaltenbach,1943)和木兰长斑蚜T. magnoliae Ghosh & Raychaudhuri,1972。同时提供了该属中国分布种类的检索表,每种提供有详细的寄主植物和地理分布资料,新种还提供了重要的形态特征图。所有标本包括模式标本均保存在中国科学院动物研究所。     

几种赤眼蜂对灰白蚕蛾寄生能力的影响

通过室内功能反应试验,测定松毛虫赤眼蜂T.dendrolimiMatsumura、短管赤眼蜂T.pretiosumRiley、暗黑赤眼蜂T.pintoiVoegele、玉米螟赤眼蜂T.ostriniaePangetChen、卷蛾分索赤眼蜂Trichogrammatoidea bactraeNagaraja、拟澳洲赤眼蜂T.confusumViggiani、舟蛾赤眼蜂T.closteraePangetChen、广赤眼蜂T.evanescensWestwood对广州地区重要园林害虫灰白蚕蛾的寄生能力。结果表明,除卷蛾分索赤眼蜂外,其它7种赤眼蜂对灰白蚕蛾的寄生作用均能用HollingⅡ型功能反应模型拟合。松毛虫赤眼蜂对灰白蚕蛾的寄生能力为最强,短管赤眼蜂和暗黑赤眼蜂次之,最大寄生卵量分别为25.8粒/雌、19.0粒/雌和18.6粒/雌,且在灰白蚕蛾卵内都能发育成功和正常羽化,可进一步进行筛选。虽然玉米螟赤眼蜂和舟蛾赤眼蜂对灰白蚕蛾有较强的寄生能力,但其后代雌蜂率都较低,且玉米螟赤眼蜂不能正常羽化,因此不适宜用来防治灰白蚕蛾。卷蛾分索赤眼蜂、广赤眼蜂和拟澳洲赤眼蜂的最大寄生量都较低,均不超过15.0粒,对灰白蚕蛾卵的寄生潜能不大。     

Molecular-genetics study of entomophages of the genus Trichogramma Westw.

Studies of the genetic structure of the internal noncoding transcribed spacer region 2 (ITS2) of the ribosomal DNA of five entomophage species of the genus Trichogramma, i.e., T. pintoi Voeg., T. evanescens Westw., T. dendrolimi Mats., T. cacoeciae Meyer, and T. semblidis Auriv., are performed. A PCR analysis with subsequent determination of the nucleotide sequence of the ITS2 regions made it possible to identify essential inter-species differences. The data may be used for the identification of the species T. pintoi, T. dendrolini, and T. semblidis.     

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。     

Evidence of Three Subspecies in Trifolium nigrescens Viv.

Germplasm accessions of Trifolium nigrescens Viv. were foundto belong to three distinct taxa which differed in morphology,hybrid seed-set in crosses among themselves and with white clover(T. repens L.), chromosomal distribution of rDNA genes, andrDNA internally transcribed spacer (ITS) region sequences. Thesetaxonomic groups correspond with T. nigrescens ssp. nigrescens,T. nigrescens ssp. petrisavii var.petrisavii and var. meneghinianum.The existence of var. meneghinianum has been rejected or ignoredin recent taxonomic treatments. The present study indicatesthat it is very distinctive and warrants at least subspeciesstatus. Phylogenetic analysis based on ITS sequences and podmorphology placed ssp. nigrescens as progenitor to the others.ITS sequences placed white clover closer to ssp. petrisaviibut neither DNA sequences nor rDNA chromosome locations clearlyshowed whether var. petrisavii or var. meneghinianum was closerto white clover. In contrast, results of hybridization studiesshowed that ssp. nigrescens gave full seed-set when pollinatedwith T. repens whereas both ssp. petrisavii var. petrisaviiand ssp. petrisavii var. meneghinianum gave poor seed-set. Allthree taxa showed close relationships with white clover andnone can clearly be shown to be a direct ancestor of T. repens.Copyright 2001 Annals of Botany Company Fabaceae, Trifolium nigrescens, Trifolium repens, internal transcribed spacer region (ITS), nuclear ribosomal DNA, interspecific hybridization     

Phylogenetic relationships of coffee-tree species (Coffea L.) as inferred from ITS sequences of nuclear ribosomal DNA

 Phylogenetic relationships of Coffea species were estimated from the sequences of the internal transcribed spacer (ITS 2) region of nuclear ribosomal DNA. The ITS 2 region of 37 accessions belonging to 26 Coffea taxa and to three Psilanthus species was directly sequenced from polymerase chain reaction (PCR)-amplified DNA fragments. The level of variation was high enough to make the ITS 2 a useful tool for phylogenetic reconstruction. However, an unusual level of intraspecific variation was observed leading to some difficulty in interpreting rDNA sequence divergences. Sequences were analysed using Wagner parsimony as well as the neighbour-joining distance method. Coffea taxa were divided into several major groups which present a strong geographical correspondence (i.e. Madagascar, East Africa, Central Africa and West Africa). This organisation is well supported by cytogenetic evidence. On the other hand, the results were in contradiction with the present classification of coffee-tree taxa into two genera, namely Coffea and Psilanthus. Furthermore, additivity of parental rDNA types was not observed in the allotetraploid species C. arabica. Received: 25 July 1996 / Accepted: 18 October 1996     

Molecular Variation and Distribution of Anopheles fluviatilis (Diptera: Culicidae) Complex in Iran

Anopheles fluviatilis James (Diptera: Culicidae) is one of the known malaria vectors in south and southeastern Iran. Earlier ITS2 sequences analysis of specimens from Iran demonstrated only a single genotype that was identical to species Y in India, which is also the same as species T. We identified 2 haplotypes in the An. fluviatilis populations of Iran based on differences in nucleotide sequences of D3 domain of the 28S locus of ribosomal DNA (rDNA). Comparison of sequence data from 44 Iranian specimens with those publicly available in the Genbank database showed that all of the 28S-D3 sequences from Kazeroun and Khesht regions in Fars Province were identical to the database entry representing species U in India. In other regions, all the individuals showed heterozygosity at the single nucleotide position, which identifies species U and T. It is argued that the 2 species may co-occur in some regions and hybridize; however, the heterozygosity in the 28S-D3 locus was not reflected in ITS2 sequences and this locus for all individuals was identical to species T. This study shows that in a newly diverged species, like members of An. fluviatilis complex, a single molecular marker may not be sufficiently discriminatory to identify all the taxa over a vast geographical area. In addition, other molecular markers may provide more reliable information for species discrimination.     

PCR-BASED TECHNIQUE FOR IDENTIFICATION AND DETECTION OF TRICHOGRAMMA SPP. (HYMENOPTERA: TRICHOGRAMMATIDAE) WITH SPECIFIC PRIMERS

Abstract The rDNA-ITS2 regions of T. dendrolimi Matsumura and T. ostriniae Pang et Chen (Hymenoptera: Trichogrammatidae) were cloned and sequenced. The homologous sequences available in GenBank were retrieved and analyzed, and then specific primers were designed for molecular identification and detection of T. dendrolimi . Repeated screening showed that PCR amplification by the diagnostic primers enabled the differentiation of not only bulk samples and single adult (male or female), but also eggs and juveniles, which was not possible by conventional methods. The advantage of this system over morphology-based systems is that non-specialists are able to identify individuals or trace specimens efficiently. The derived molecular detection technique was then used to identify 12 specimens collected from different localities on the Chinese mainland; the results showed that this protocol could be applied to molecular monitoring of Trichogramma species in the field. Finally, 1132s of 6 geographical populations of T. dendrolimi (TdCHA, TDJL, TdXZ, TdKH, TdCZ and TdYBL) were cloned and sequenced. The multialignment analysis of intraspecific ITS2 sequences showed that the diagnostic primers have their own theoretical bases.     

USE OF RIBOSOMAL DNA INTERNAL TRANSCRIBED SPACERS FOR PHYLOGENETIC STUDIES IN DIATOMS1

Sequence variation of ribosomal DNA internal transcribed spacers (ITS) among populations, species, and genera of the diatom genus Stephanodiscus was investigated. ITS 1 and ITS 2, including the 5.8S gene, were sequenced from geographically distant and nearby populations of S. niagarae Ehrenberg. In addition, repeats from S. hantzschii Grunow and Cyclotella meneghiniana Kützing were sequenced to determine the taxonomic range over which the ITS region could be used for diatom systematics. The morphologically distinct S. yellowstonensis Theriot & Stoermer, thought to have evolved from S. niagarae in Yellowstone Lake between 12,000 and 8000 years ago, also was sequenced to assess its relationship to nearby S. niagarae populations. The organization and relative sizes of ITS 1 and ITS 2 in Stephanodiscus species were similar to those reported for other eukaryotes. In general, ITS 2 was slightly larger and more variable than ITS 1. Cladistic analysis of ITS sequences did not resolve relationships of nearby S. niagarae and S. yellowstonensis populations. However, central North American S. niagarae populations were in a clade supported by two nucleotide changes. For Cyclotella, much of the ITS region was not alignable with that for Stephanodiscus species; therefore, generic-level comparison within the Thalassiosiraceae may not be possible. The variation (95–96% similarity) between S. hantzschii and other Stephanodiscus species suggests that interspecific relationships could be assessed with ITS sequences. Although S. yellowstonensis is morphologically distinct from S. niagarae, no autapomorphic nucleotide sites were identified. Two S. niagarae populations (Heart and Lewis Lakes), however, did possess autapomorphic ITS sites.     

Phylogenetic Analysis and Karyotype Evolution in the Genus Clivia(Amaryllidaceae)

Phylogenetic relationships of five taxa of Clivia, one probablenew species plus four recognized species, and three outgroupspecies were studied using sequences of the nuclear ribosomal5S non-transcribed spacer and the internal transcribed spacer(ITS) of 45S rDNA. Analysis of the data sets separately generatedsome well-supported groupings and congruent phylogenies. Cliviaminiata and C. gardenii are closely related. ‘Robust Gardenii’,the putative new species, is a sister clade of this group. Clivianobilis is distantly related to these three taxa and C. caulescensoccupies an intermediate position between the two groups. Chromosomelocations and distribution patterns of the 5S nuclear ribosomalgene in the species of Clivia were investigated using fluorescenceinsitu hybridization (FISH). In all species, only one pair of5S rDNA signals was observed. These were located on the shortarm of chromosome 8, at the position of the interstitial C-bands.The phylogenies obtained from the DNA sequences together withthe chromosome data accumulated here and previously publishedinformation on the location of the 45S rDNA sites have beenused to postulate evolutionary trends in Clivia chromosomes.Copyright 2001 Annals of Botany Company Clivia, chromosome evolution, 45S and 5S rDNA, ITS, FISH, molecular phylogeny