两株椰心叶甲分离物的鉴定及其系统发育分析

采用形态学方法对2株从自然罹病死亡的椰心叶甲虫尸上分离到的致病菌株Dz01和Ma4进行了鉴定,发现2个菌株在菌丝、瓶梗和分生孢子等形态特征上与金龟子绿僵菌小孢变种基本一致,可将2个菌株鉴定为金龟子绿僵菌小孢变种。基于Dz01和Ma4菌株和其它31个代表绿僵菌主要种或变种菌株rDNA上ITS1-5.8S-ITS2区序列构建的最大简约树显示,Dz01和Ma4菌株均聚在金龟子绿僵菌小孢变种所构成的分支中,这为2个菌株形态学鉴定结果提供了分子依据。     

感染水椰八角铁甲的绿僵菌的分子鉴定及致病力测定

在室内饲养的水椰八角铁甲Octodonta nipae(Maulik)种群中,发现有大量甲虫被病原菌感染致死.对死虫体表的病原真菌进行分离鉴定,并依据ITS序列分析鉴定,确定该病原真菌为金龟子绿僵菌小孢变种(Metarhizium anisopliae var.anisopliae).经室内致病力测定,接种浓度分别为1...     

不同寄主及地理来源的16株绿僵菌对桃蚜的毒力比较

害虫生防真菌绿僵菌的不同种及变种被广泛应用于害虫微生物防治,但罕见以蚜虫等同翅目刺吸式害虫作为靶标。从两种绿僵菌的4个变种中精选16个不同寄主及地理来源的菌株,用喷塔接种桃蚜(Myzus persicae)无翅成蚜并在25±1℃和12L∶12D条件下饲养观察,所获生物测定数据进行时间-剂量-死亡率模型模拟分析。结果显示,高接种剂量(~1000个孢子/mm2)下7d内死亡率达67%~100%的10个菌株均为金龟子绿僵菌Metarhiziumanisopliae(Ma)及其金龟子变种M.anisopliaevar.anisopliae(Maa);而高剂量处理下仅感染致死个别或少数蚜虫的菌株包括金龟子绿僵菌及其金龟子变种、大孢变种M.anisopliaevar.majus和蝗变种M.anisopliaevar.acridum以及黄绿绿僵菌小孢变种M.flavoviridevar.minus。杀蚜活性优异的2个菌株分别为Ma 456和Maa 3332,接种后第4天的LC50分别为113和260个孢子/mm2,第5天为32和43个孢子/mm2,第6天为17和26个孢子/mm2,第7天仅11.4和19.9个孢子/mm2。这两个菌株具有用于蚜虫微生物防治的良好开发潜力。     

白星花金龟绿僵菌分离及毒力测定

目的 2008年在山东泰安市黄庄堆肥中发现白星花金龟幼虫被病原菌寄生死亡,病虫体上长满灰绿色霉层,对其进行分离,经纯化获得1株真菌,编号为M-08。通过对幼虫接种,证明其致病性。方法对分离纯化出的菌株M-08,根据菌体形态特征、培养性状,按常规方法鉴定。结果 M-08菌株鉴定结果为金龟子绿僵菌长孢型变种Metarhiziumnaisopliae[Metsch Sorokin Var major（Johnston）Tulloch],毒力测定结果表明,对白星花金龟幼虫致死率高达93.3%~100%。结论金龟子绿僵菌长孢型毒力测定表明具有很高的毒性,今后有良好的应用前景。     

黄绿绿僵菌Ma130821对暗黑鳃金龟幼虫的室内毒力及毒杀作用研究

采用浸渍法测定了黄绿绿僵菌Metarhizium flavoviride菌株Ma130821对暗黑鳃金龟Holotrichia parallela Motschulsky幼虫的毒力,采用室内盆栽拌土法、环施法和穴施法施用黄绿绿僵菌Ma130821分生孢子粉,测定了该菌株对暗黑鳃金龟幼虫的毒杀效果。结果表明:黄绿绿僵菌菌株Ma130821对暗黑鳃金龟3龄幼虫的侵染致病效应可利用"时间—剂量—死亡率"模型进行模拟分析和参数估计分析,侵染效应常数为0. 597。接种后第3天该菌株对暗黑鳃金龟3龄幼虫的致死剂量LC_(50)和LC_(90)的对数值分别为9. 2182±0. 2968和11. 2291±0. 4385。在6. 20×108孢子/m L黄绿绿僵菌菌悬液对暗黑鳃金龟幼虫侵染致病的LT_(50)和LT_(90)分别为1. 5 d和3. 8 d。室内盆栽拌土法、环施法和穴施法施用黄绿绿僵菌菌株Ma130821分生孢子粉对暗黑鳃金龟3龄幼虫均具有良好的毒杀作用,其中拌土法施用后对暗黑鳃金龟幼虫的毒杀效果高于其他两种方法,拌土法、环施法和穴施法施用后对暗黑鳃金龟3龄幼虫的累积死亡率分别为95. 69%、84. 35%和57. 43%,累积僵虫率分别为99. 65%、98. 65%和99. 37%。综合以上结果,黄绿绿僵菌Ma130821对暗黑鳃金龟幼虫具有良好的毒力和毒杀作用,在暗黑鳃金龟的生防制剂开发中具有良好潜力。     

暗黑鳃金龟幼虫生防黄绿绿僵菌Ma130821菌株的室内培养条件的研究

从云南省玉溪市塔甸镇玉米地自然罹病的暗黑鳃金龟幼虫僵虫上分离纯化获得了黄绿绿僵菌Ma130821,为了弄清该菌株培养条件,为蛴螬生物制剂开发应用提供依据,本研究在室内测定了该菌株在PDA和SDAY培养基上的生长繁殖情况及在不同pH、温度、光照条件下培养特征及产孢特性。结果表明:黄绿绿僵菌Ma130821菌株在PDA和SDAY两种培养基上均能生长,但在PDA培养基上产孢时间早于SDAY,其中在PDA和SDAY培养基上分别于第6天和9天开始产孢。在25℃时生长最好,平均直径日增量为0.24 cm/d,第4天时就开始产孢且产孢量最高,为1.091×10~7孢子/cm~2。在16 L∶8 D的光周期条件下菌落生长最快,产孢时间最早,且产孢量最大。pH 6.5最适宜该黄绿绿僵菌菌株的生长及产孢。综合以上结果,PDA培养基可用于黄绿绿僵菌Ma130821菌株的室内培养,最适培养条件为pH 6.5、25℃、16 L∶8 D。该研究结果将为蛴螬生防黄绿绿僵菌Ma130821制剂的开发提供依据。     

绿僵菌素的分离制备及其对蛴螬的毒力

以金龟子绿僵菌金龟子变种Metarhizium anisopliae var. anisopliae菌株MaQ10发酵液为材料,采用萃取、浓缩、制备色谱及重结晶技术,分离纯化出5种绿僵菌素的晶体,经与标准样品以及参考文献相对照,此5种晶体与绿僵菌素A、A2、B、C和E相吻合。进而,采用浸渍法测定了绿僵菌素A和B对大等鳃金龟Exolontha serrulata (Gyllenhall) 和卵圆齿爪鳃金龟Holotrichia ovata Chang 1龄幼虫的触杀毒力。结果表明： 绿僵菌素A和B对大等鳃金龟的触杀活性,在处理后96～120 h内最高,LC₅₀分别为78.1571 mg/L和88.7562 mg/L; 处理浓度为300 mg/L时,LT₅₀分别为13.4159 h和10.5331 h。绿僵菌素A和B对卵圆齿爪鳃金龟的触杀活性,在处理后96 h时最高,LC₅₀分别为66.5308 mg/L和79.4309 mg/L;处理浓度为300 mg/L时,LT₅₀分别是13.6399 h和9.9451 h。     

绿僵菌属的新记录种

<正> 金龟子绿僵菌Metarhizium aunisopliae(Metschn.)Sorokin中的金龟子绿僵菌原变种Metarhizium anntsopliae var.anisopliae寄生范围较广,是一个世界性分布的昆虫病原真菌。而金龟子绿僵菌大孢变种Metarhizium anisopliae var.major.却较稀有。自从Trioderichs(1930)以后的许多工作者都曾报道此菌的主要寄主是独角仙Oryctes。尔后仅仅在Herb IMI收到一个来自蝉的标本(Tulloch 1976)。我们1985年首次从罹病蝉上分离到一个绿僵菌大孢变种。     

不同来源绿僵菌对云斑金龟蛴螬致病力评价

以云斑金龟蛴螬为检测昆虫,检测了不同来源的6株金龟子绿僵菌（Metarhiziumanisopliae）菌株,结果认为,以RAW8菌株对云斑金龟蛴螬的致病力最强。     

几种虫生真菌菌株的培养性状及其对褐飞虱的毒力

从褐飞虱Nilaparvata lugens (St(a)l)罹病虫体上新分离出的一种黄绿绿僵菌菌株Metarhizium flavoviride (Mf82),与实验室保存的黄绿绿僵菌、金龟于绿僵菌和白僵菌3种菌种5个菌株作为对比,研究了在SDAY和PDA培养基上的培养性状,并测定了它们对褐飞虱成虫的毒力.结果表明:...     

柱孢绿僵菌和绿色野村菌分类地位的研究

通过测定柱孢绿僵菌 Metarhizium cylindrospora、绿色野村菌 Nomuraea viridula及莱氏野村菌N. rileyi的ITS1-5.8S-ITS2 rDNA区域序列,为柱孢绿僵菌和绿色野村菌正确归属提供了新的分子依据。依据形态学和分子生物学的证据将绿色野村菌组合到绿僵菌属中,并对野村菌属的存在提出疑议。     

Metarhizium frigidum sp. nov.: a cryptic species of M. anisopliae and a member of the M. flavoviride complex

The anamorph genus Metarhizium is composed of arthropod pathogens, several with broad geographic and host ranges. Members of the genus, including "M. anisopliae var. frigidum" nomen nudum and Metarhizium flavoviride, have been used as biological insecticides. In a recent revision of the genus the variety "M. anisopliae var. frigidum" was suggested to be a synonym of M. flavoviride based largely on ITS sequence phylogenetic analysis. In this study we conducted morphological evaluations and multigene phylogenetic analyses with EF-1alpha, RPB1 and RPB2 for strains of M. flavoviride and "M. anisopliae var. frigidum." Included in these evaluations were the ex-type of M. flavoviride var. flavoviride and what likely would be considered the "ex-type' of the invalidly published taxon "M. anisopliae var. frigidum". Based on morphological and molecular evidence we conclude that "M. anisopliae var. frigidum" is distinct from M. flavoviride and the taxon M. frigidum sp. nov. is described.     

衣藻属的系统发育分析——基于形态形状和nrDNA ITS序列

通过实验分析莱茵衣藻 ( Chlamydomonas reinhardtii) 1个种和互连网获得衣藻属 1 5个种及丝藻属 1个种 ( Ulothrix zonata) ,共 1 7个种的 nr DNA ITS序列 ,并以 U.zonata为外类群 ,采用计算机分析软件包对其进行分析及构建分子系统发育树图。同时以 1 2个传统分类性状 ,对此 1 6种衣藻构建数据矩阵 ;以 U.zonata动孢子的相应性状为外类群原始性状 ,用Wagner法在计算机上对其进行分枝分析 ;然后比较并分析分子系统树和表征性状分支分析树的异同。初步尝试以 ITS分子序列系统发育分析作为传统性状分析的补充来研究衣藻种间的亲缘关系。     

ITS假基因对栎属系统学研究的影响及其对分子系统学研究的启示

核糖体rDNA ITS是被子植物系统发育研究中应用最广泛的分子标记之一。以前人们认为同一物种中的ITS序列因致同进化而使不同拷贝高度一致,在分子系统学研究中常以ITS1-5.8S-ITS2序列作为构建系统进化树的基础。近年来,在对一些被子植物的研究中发现这段序列在同一物种中具有多态性,有些拷贝中的5．8S区不具编码功能,人们把含有不具编码功能5．8S区的ITS1-5．8S-ITS2序列定义为ITS假基因序列,它对同源基因致同进化的假设形成了新的挑战。在诸多应用ITS序列重建系统进化关系的研究中,栎属系统学研究因ITS假基因的发现而倍受关注。本文以栎属为例回顾了ITS假基因的发现过程,分析了其对该属系统学研究的影响,为分子生物学在植物系统进化研究中的应用提供一些新的参考。     

IGS sequence variation,group-I introns and the complete nuclear ribosomal DNA of the entomopathogenic fungus Metarhizium: excellent tools for isolate detection and phylogenetic analysis

The complete nuclear rDNA gene complex of Metarhizium anisopliae var. anisopliae isolate ME1 is 8118bp long and contains the 18S, 5.8S, and 28S rRNA genes as well as the ITS and IGS regions. Variation in the ITS of isolates of M. anisopliae var. anisopliae and one each of Metarhizium anisopliae var. acridum, Metarhizium flavoviride var. flavoviride, and Metarhizium flavoviride var. minus, clustered 39 out of 40 of M. anisopliae var. anisopliae isolates in one clade. Nucleotide sequence variation in the IGS among 21 of M. anisopliae var. anisopliae isolates showing IGS length variation sorted them into three strongly supported clades, which were weakly correlated with insect hosts and were not correlated with geographic location. Two group-I introns, Ma-int4 and Ma-int5, were discovered in the 18S and the 3(') end of the 28S, in M. anisopliae var. anisopliae isolates ITALY-12 and IMBST 9601. The insertion sites and sub-group of these introns correlated with their closest relatives, as judged by phylogenetic analysis of intron nucleotide sequence.     

Molecular phylogeny and evolution of Caricaceae based on rDNA internal transcribed spacers and chloroplast sequence data

This study focused on clarifying phylogenetic relationships and evolution within Caricaceae. Our phylogenetic analysis based on nucleotide sequences from the ITS of the ribosomal DNA and three chloroplast fragments (matK, trnL-trnF, and psbA-trnH) included 29 taxa belonging to five genera: the neotropical genera Carica, Vasconcellea, Jarilla, and Jacaratia and the equatorial African genus Cylicomorpha. Having a relatively low mutation rate, matK, and trnL-trnF were used for estimating relationships at the generic level, while intrageneric evolution within Vasconcellea was studied with the more variable ITS and psbA-trnH sequences. Gaps, coded as binary characters, were added to the sequence alignments before performing Maximum Parsimony and Maximum Likelihood analyses. Monophyly of Caricaceae as well as phylogenetic distance between Carica and Vasconcellea species, previously belonging to the same genus, and monophyly of the resurrected genus Vasconcellea were emphasized. Within Vasconcellea, the largest genus of this family, two well-confirmed evolutionary lineages could be discerned: (1) V.xheilbornii, V. weberbaueri, V. stipulata, and V. parviflora and (2) a clade holding all other taxa of the genus. Incongruence between nuclear ITS and chloroplast psbA-trnH datasets, shown to be significantly caused by some taxa of the genus Vasconcellea, indicated that reticulate events in this genus might be more frequent than previously suspected. Moreover, intra-individual ITS sequence heterogeneity provided further evidence for the hybrid or introgressed origin of different taxa and one presumed hybrid belonging to this genus.     

Re-evaluation of the phylogenetic relationship among species of the genus Tricholoma

The internal transcribed spacer sequences spanning the regions between the 17S and 25S rRNAs (ITS1 and ITS2) and including the complete sequence of the 5.8S rRNA were used for phylogenetic analyses. This approach to define phylogenetic relationships within the genus Tricholoma was tested using different isolates of T. terreum. Fruitbodies identified in nature were analysed in order to allow use of morphology for taxonomy. The isolates from different locations were closely related as could be expected for one species. Thus, the method could be applied to different Tricholoma species. Three clusters within the genus Tricholoma can be distinguished with four additional species not included in any of these clusters. Molecular analyses of two Cortinarius species confirm a phylogenetically distinct genus.     

裸盖菇属的真菌鉴定及分子系统学初探

裸盖菇属(Psilocybe)的许多真菌含有神经致幻型毒素,这些毒素被中国卫生部列为A类管制药品。在药检时,这些真菌样品通常是粉末。因此,仅依靠形态分类鉴定该类真菌非常困难。研究采用ITS序列分析的方法鉴定该类真菌并初步探讨了该属种间的系统发育关系。由系统发育树推断Psilocybe属可能是多源进化的。通过序列分析可以鉴定真菌样品为Psilocybe属。     

The ITS1-5.8S-ITS2 sequence region in the Musaceae: structure, diversity and use in molecular phylogeny

Genes coding for 45S ribosomal RNA are organized in tandem arrays of up to several thousand copies and contain 18S, 5.8S and 26S rRNA units separated by internal transcribed spacers ITS1 and ITS2. While the rRNA units are evolutionary conserved, ITS show high level of interspecific divergence and have been used frequently in genetic diversity and phylogenetic studies. In this work we report on the structure and diversity of the ITS region in 87 representatives of the family Musaceae. We provide the first detailed information on ITS sequence diversity in the genus Musa and describe the presence of more than one type of ITS sequence within individual species. Both Sanger sequencing of amplified ITS regions and whole genome 454 sequencing lead to similar phylogenetic inferences. We show that it is necessary to identify putative pseudogenic ITS sequences, which may have negative effect on phylogenetic reconstruction at lower taxonomic levels. Phylogenetic reconstruction based on ITS sequence showed that the genus Musa is divided into two distinct clades--Callimusa and Australimusa and Eumusa and Rhodochlamys. Most of the intraspecific banana hybrids analyzed contain conserved parental ITS sequences, indicating incomplete concerted evolution of rDNA loci. Independent evolution of parental rDNA in hybrids enables determination of genomic constitution of hybrids using ITS. The observation of only one type of ITS sequence in some of the presumed interspecific hybrid clones warrants further study to confirm their hybrid origin and to unravel processes leading to evolution of their genomes.