海南椰心叶甲病原菌金龟子绿僵菌的分离、鉴定及其生防潜力

椰心叶甲[Brontispa longissima（Gestro）]是椰子的重要害虫,近年来,该虫在海南岛发生普遍,椰子受害严重。由于椰心叶甲受到自然界中某些致病微生物的侵袭,在受害的椰子树心叶上常可发现椰心叶甲僵虫,并发现大部分僵虫表面长出了霉菌,本研究的目的在于从椰心叶甲僵虫表面的霉菌中分离出绿僵菌,并对分离菌株进行鉴定和致病性测定。从僵虫表面刮下孢子或菌丝体,置于绿僵菌选择性培养基（DOA）上培养,挑出真菌菌落,经纯化后,进行生物学特性、菌落生长速率及产孢量的测定,并从PPDA、OMA、VSA和PDA中筛选菌落生长及产孢最适培养基,同时对所分离的菌株进行对椰心叶甲的致病性测定。结果表明,所有分离菌株均鉴定为金龟子绿僵菌[Metarhizium anisopliae（Metschnikoff）],PPDA是菌落生长及产孢的最适培养基,大多数菌株对椰心叶甲有较强的致病力。选取强毒菌株MA4在田间进行防治效果的初步测定,结果表明,该菌株能显著降低椰心叶甲成虫的虫口密度。这些金龟子绿僵菌菌株是首次从海南的椰心叶甲僵虫中分离到的昆虫病原真菌,该菌对海南的椰心叶甲具有很好的生防潜能。     

金龟子绿僵菌固态培养生物变量优化研究

金龟子绿僵菌属于真菌类生物杀虫剂,本文研究了接种量、种龄、菌种代数等生物因素对金龟子绿缰菌生长及产孢量的影响,并对液-固两步发酵工艺进行了研究.经过优化,得到金龟子绿僵菌产孢的最佳生物参数是:接种量为2.5g/100g、种龄为5～6天;采用固体二代种,培养6天,孢子产量可达1.531×1010孢子/g干培养基.     

蔗根土天牛高致病力绿僵菌菌株的生物学特性研究

【目的】明确对蔗根土天牛Dorysthenes granulosus具有良好杀虫活性的金龟子绿僵菌Metarhizium anisopliae JC002菌株生长和产孢所需要的最适营养条件和环境条件。【方法】通过单因素试验,测试了不同培养基、碳源、氮源、温度、pH及紫外线照射不同时间对JC002菌株生长和产孢的影响。【结果】JC002菌株培养基的最佳配方是葡萄糖30 g、蛋白胨15 g、马铃薯200 g、琼脂20 g、水1 000 mL;蔗糖、NaNO3是菌落生长及产孢的最适碳源和氮源;菌株培养的最适温度为25℃,培养基的最适pH值为7.0;紫外光对菌株的生长速率无显著影响,但对产孢量有较大的抑制作用,紫外光照射时间越长,产孢越少。【结论】本研究为JC002菌株的大量培养及其孢子制剂的大量生产和有效利用奠定基础。     

球孢白僵菌和金龟子绿僵菌不同菌株对黑足角胸叶甲成虫的致病力评价

本研究在测定不同球孢白僵菌Beauveria bassiana和金龟子绿僵菌Metarhizium anisopliae菌株的生长速率与产孢量的基础上, 采用孢悬液浸渍法进行了对油茶新害虫--黑足角胸叶甲Basilepta melanopus成虫的生物测定, 旨在筛选出感染该成虫的高致病力菌株, 为防治该虫提供新的生物资源。结果表明： 不同菌株生长速率和产孢量间存在显著差异, MaYTTR-04, BbFZ-17, MaZPTR-01和BbTK-01生长速率和产孢量均显著高于其他菌株。接种后, 叶甲成虫累积死亡率随时间的增加而逐渐增高, 接种白僵菌7 d后, 成虫校正死亡率全部达到100%; 接种MaZPTR-01和MaYTTR-04两个绿僵菌菌株14 d后, 成虫死亡率分别为80.3%和78.8%。而且接种白僵菌后, 叶甲成虫的僵虫率显著较绿僵菌高, 尤其以BbTK-01和BbFZ-17两个菌株较好, 分别达到85.7%和75.8%。BbXJ-01, BbFZ-17和BbTK-01 3个白僵菌菌株的LT₅₀最小, 分别为3.0, 3.3和3.4 d; MaYTTR-04和MaZPTR-01两个绿僵菌的LT₅₀分别为6.0和6.2 d。结果说明, 白僵菌对叶甲成虫的致病力较强, 尤其是BbTK-01和BbFZ-17两个菌株, 不仅致死率高, 且致死速度快, 僵虫率高, 同时这2个菌株生长速度快、 产孢量大, 具有优良的生产特性, 在黑足角胸叶甲的生物防治中将有重要的应用价值。     

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。     

安徽省土壤绿僵菌分离株的分子鉴定

目的进一步验证ITS序列的系统发育分析可为绿僵菌属种的鉴定提供重要的参考依据。方法对分离自安徽土壤的13株绿僵菌菌株的内转录间隔区（ITS）片段进行PCR扩增和序列测定,采用Blast方法将测序结果在GenBank中进行同源搜索,依据邻接法构建获得与其相关菌株的ITS序列系统发育树。结果供试菌株分别位于系统发育树的3个分支上,分支I包括8个菌株和金龟子绿僵菌小孢变种,1个菌株和金龟子绿僵菌鳞鳃金龟变种形成分支III,另外4个菌株和黄绿绿僵菌棉蚜变种聚为分支X。结论结合同源比较的数据,将这8个、4个和1个绿僵菌菌株分别鉴定为金龟子绿僵菌小孢变种、黄绿绿僵菌棉蚜变种和金龟子绿僵菌鳞鳃金龟变种。     

绿僵菌属的三个新种

作者从广东、贵州、北京等地收集的虫生真菌中,发现在我国具有绿僵菌属特征的真菌可分为四个种。根据菌落颜色、分生孢子团块大小、紧密和牢固程度、孢子链连接方式、分生孢子形状等,将我们收集的属于本属的菌株分为四个种。本文报道绿僵菌属三个新种的描述。金龟子绿僵菌Metarhizium anisopliae(Metsch.)Sorokin为最常见的甘蔗金龟子致病菌,是本属的模式种。平沙绿僵菌Metarhizium pingshaense Chen et Guo sp.nov.、柱孢绿僵菌Metarhizium cylindrosporae Chen et Guo sp.nov.和贵州绿僵菌Metarhizium guizhouense Chen et Guo sp.nov.是三个新种。     

mro-miR-33在绿僵菌产孢中的作用

罗伯茨绿僵菌Metarhizium robertsii是一种重要的广谱性杀虫真菌,在害虫的生物防治中应用广泛。研究表明microRNAs在丝状真菌的生长发育中可能发挥重要调控作用。迄今有关miRNAs在绿僵菌产孢过程中的作用还未见研究报道。本文分析了实验室前期鉴定的一个绿僵菌新miRNA(mro-miR-33)在绿僵菌产孢过程中的作用。结果表明,绿僵菌在不同培养条件下mro-miR-33的表达量有显著差异,且在孢子发育过程表达量下降。在野生菌株中过表达mro-miR-33后,绿僵菌的产孢量显著下降,qRT-PCR分析表明孢子发育关键调控基因brl A表达显著下调,而敲除mro-miR-33后,绿僵菌的产孢量显著增加。这些变化表明mro-miR-33在绿僵菌的产孢过程中发挥着重要的作用。     

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。     

从青杨天牛分离的几种致病真菌

从青杨天牛虫尸上分离出枝顶孢霉、球孢白僵菌、金龟子绿僵菌、轮状镰刀菌和尖孢镰刀菌5种病原真菌,其中枝顶孢霉为国内新记录。利用青杨天牛蛹对五种致病真菌进行了生物测定,5种病原菌的致病力顺序为:金龟子绿僵菌>球孢白僵菌>枝顶孢霉>尖孢镰刀菌>轮状镰刀菌。青杨天牛不同虫期对金龟子绿僵菌的易感性顺序为:1龄幼虫>蛹>老熟幼虫。利用金龟子绿僵菌和枝顶孢霉菌液田间防治青杨天牛幼虫,死亡率分别为95.56％及48.72％。     

Compatability of Metarhizium anisopliae var. anisopliae with chemical pesticides

The effects of various insecticides on the mycelial growth, sporulation and conidial germination of Metarhizium anisopliae var. anisopliae isolate E₉ were studied in the laboratory. Chlorpyrifos was the most toxic organophosphate to mycelial growth and sporulation at all concentrations. Temephos, malathion and leptophos were highly toxic to sporulation while malathion was the most inhibitory to germination. The carbamates, carbofuran, methomyl and oxamyl were moderately toxic to mycelial growth and sporulation while oxamyl had an adverse effect on germination. The pyrethroids (pyrethrin, permethrin and resmethrin) and the insect growth regulators (diflubenzuron and methoprene) were not inhibitory to the various developmental stages of isolate E₉. The chlorinated hydrocarbons (chlordane, lindane and toxaphene) were more deleterious than all other insecticide groups tested. Among the fungicides, benomyl and maneb produced the greatest inhibition.     

Genetic diversity of Metarhizium anisopliae var. anisopliae in southwestern British Columbia

The abundance and genetic diversity of the entomopathogenic fungus, Metarhizium anisopliae var. anisopliae, in southwestern British Columbia (BC) and southern Alberta was examined. The fungus was found to be widespread in soil throughout southwestern BC, and was recovered from 56% of 85 sample sites. In contrast to southwestern BC, no M. anisopliae isolates were recovered in southern Alberta. An automated fluorescent amplified fragment length polymorphism (AFLP) method was used to examine genetic diversity. In excess of 200 isolates were characterized. The method identified 211 polymorphic amplicons, ranging in size from ≈92 to 400 base pairs, and it was found to be reproducible with a resolution limit of 86.2% similarity. The AFLP method distinguished Metarhizium from other entomopathogenic fungal genera, and demonstrated considerable genetic diversity (25 genotypes) among the reference strains of M. anisopliae isolates examined (i.e. recovered from various substrates and geographical locations). Although 13 genotypes of M. anisopliae var. anisopliae were recovered from southwestern BC soils, the vast majority of isolates (91%) belonged to one of two closely-related genotypes. Furthermore, these two genotypes predominated in urban, agricultural and forest soils. The reasons for the limited diversity of M. anisopliae var. anisopliae in southwestern BC are uncertain. However, findings of this study are consistent with island biogeography theory, and have significant implications for the development of this fungus for microbial control of pest insects.     

Virulence of mutants and revertants of Metarhizium anisopliae var. anisopliae toward Rhodnius prolixus

The derivation of mutants of Metarhizium anisopliae var. anisopliae which had lost or showed reduced ability to produce extracellular amylases, lipases, and proteases was studied by the enzymatic index. Reversion induced by ultraviolet light was also studied. The virulence of mutants and revertant strains was evaluated in bioassays against third-instar nymphs of Rhodnius prolixus. The mutant strains for amylase and lipase showed enzymatic indices equal to one, but this was not the case for the proteolytic mutants. The revertant strains were phenotypically similar to the parental strains. The virulence of amylolytic and lipolytic mutants was reduced in relation to the parental strain, whereas the proteolytic mutants did not show any significant reduction. Virulence was restored in all revertant strains.     

Laboratory and field evaluation of Metarhizium anisopliae var. anisopliae for controlling subterranean termites

The efficacy of the Metarhizium anisopliae strain ARSEF 6911 was determined in the laboratory and field against two sugarcane pests, Microtermes obesi Holmgren and Odontotermes obesus Rambur (Termitidae: Isoptera). The susceptibility of both termite species to different conidial suspensions (1 × 10(10), 1 × 10(8), 1 × 10(6) and 1 × 10(4) conidia/ml) was determined in laboratory. All conidial suspensions were able to induce mortality. Termite mortality caused by the fungal suspensions was dose dependent. There were no significant differences in the LT50 values between species. Field evaluation of M. anisopliae alone or in combination with diesel oil and thiamethoxam was carried out in two growing seasons (autumn 2005 and spring 2006) at two sites located in Punjab, Pakistan. Dipping the sugarcane setts in these suspensions was tried to determine their effects on germination and percentage of bud damage to sugarcane setts. All treatments significantly reduced termite infestation compared to the untreated control. The combined treatment of M. anisopliae and diesel oil significantly reduced insect damage by attaining higher germination > 55% and lower bud damage < 5.50% at both sites in both seasons. The results suggest that the application of M. anisopliae and diesel oil in combination might be a useful treatment option for the management of termites in sugarcane.     

Differential expression of genes involved in entomopathogenicity of the fungi Metarhizium anisopliae var. anisopliae and M. anisopliae var. acridum (Clavicipitaceae)

Expression analysis of the genes involved in germination, conidiogenisis and pathogenesis of Metarhizium anisopliae during its saprophytic and pathogenic life stages can help plan strategies to increase its efficacy as a biological control agent. We quantified relative expression levels of the nitrogen response regulator gene (nrr1) and a G-protein regulator of genes involved in conidiogenesis (cag8), using an RT-qPCR assay. Comparisons were made between M. anisopliae var. anisopliae and M. anisopliae var. acridum during germination and conidiogenesis and at different stages of pathogenesis. The cag8 gene was repressed during germination and induced during conidial development and the pathogenic phase, and the nrr1 gene was induced during germination, conidiogenesis and the pathogenic phase. Both genes were more expressed in M. anisopliae var. anisopliae, demonstrating that different varieties of M. anisopliae differ in activation of genes linked to virulence for certain environments and hosts. This suggests that differences among these varieties in the ability to adapt could be attributed not only to specific genomic regions and genes, but also to differential gene expression in this fungus, modulating its ability to respond to environmental stimuli.     

FI-1045: A Profile of a Commercially Useful Isolate of Metarhizium anisopliae var. anisopliae

The isolate FI-1045 is the basis of a mycoinsecticide, BioCane TM granules recently registered for the control of greyback canegrub, Dermolepida albohirtum (Coleoptera: Scarabaeidae: Melolonthinae) in Australian sugarcane fields. The isolate was obtained from a naturally infected larva of D. albohirtum collected from Tully in north Queensland. The isolate can be distinguished from others infecting the same insect and also other species of canegrub by means of RAPD patterns and sequence data from the ITS region. A comparison of a stored FI-1045 isolate with three derived isolates which had different histories of host-passage, showed no variation in RAPD pattern. All isolates grew well at temperatures between 20 and 30°C but did not grow at 35°C and grew slowly at 15°C. However, on potato dextrose agar, the original FI-1045 grew more rapidly and did not produce as much pigment as the derived isolates. It is speculated that this difference was due to the storage method used with the original FI-1045 being stored at -70°C and the other isolates being freeze-dried. Bioassays against third instar greyback canegrubs gave a mean LC 50 of 8.7 ×10 4 conidia g -1 peat substrate after 10 weeks. Using Tenebrio molitor as a host, it was found that conidia taken directly from the infected insect were similar in virulence to the cultured FI-1045. Using injection of culture filtrate as the assay method, it was found that FI-1045 produced destruxins. In laboratory host range tests, a dose of 10 6 conidia g -1 peat killed 96% of southern oneyear canegrubs, Antitrogus consanguineius , 85% of Lepidiota picticollis and less than 30% of the other five species of canegrub tested.     

Efficacy of Metarhizium anisopliae microsclerotial granules

The entomopathogenic fungus Metarhizium anisopliae has very recently been shown to produce microsclerotia (MS) – compact, heavily melanised, hyphal aggregates – in liquid media. Soil incorporation bioassays of dried MS preparations of three isolates of M. anisopliae were conducted using third instar Tetanops myopaeformis (sugarbeet root maggot) in clay and/or clay loam field soils as a model system to demonstrate efficacy. At rates as low as 23 mg MS granules/100 g dry soil, the biocontrol efficacy of MS granules of M. anisopliae Strain F52 produced in liquid media with a high carbon concentration (36 g/L) and high C:N ratios (30:1, 50:1) were superior to MS preparations produced in low carbon (8 g carbon/L) media and a high carbon medium with a 10:1 C:N ratio. Bioassays using MS formulations of M. anisopliae strains MA1200 and TM109 produced in high carbon and high C:N ratio media were superior in efficacy to the other MS production media tested. MS preparations of M. anisopliae F52 showed superior efficacy against the sugarbeet root maggot in comparison with more conventional, conidia-covered nutritive (corn grit) granules in a clay and clay soil. The MS granules were also highly efficacious against the sugarbeet root maggot at soil moisture levels as low as 0.983 A _w (?2.33 MPa). Granular preparations incorporating Metarhizium MS can serve as a viable formulation for the use of this fungus against soil insects.     

Variability in esterases of Metarhizium anisopliae

The variability in esterases of the entomogenous fungus Metarhizium anisopliae was determined electrophoretically on 8.5% polyacrylamide gel. Ten isolates from diverse taxonomic groups of insects were analyzed. The electrophoretic analysis showed differences and similarities between these isolates and it was possible to distinguish six different patterns. The results obtained show a great polymorphism for the esterase system of M. anisopliae.     

Chitooligosaccharides enzymatic production by Metarhizium anisopliae

The products of chitosan hydrolysis are chitooligosaccharides and are used mainly for medical applications due to their specific biological activities. The objective of this study was to detect and identify the products of enzymatic hydrolysis of chitosan (dimers to hexamers) using a crude extract of chitosanolytic enzymes produced by the fungus Metarhizium anisopliae. These fungus was able to produce, during 48 h cultivation in a medium containing chitosan, chitooligosaccharides ranging from dimers, trimers, tetramers and pentamers at concentrations 0.2, 0.19, 0.06, 0.04 mg/mL, respectively, and the enzymatic activity was 2.5 U/L. Using the crude enzyme extract for chitosan hydrolysis, we detected the presence of dimers to hexamers at hydrolysis times of 10, 20, 30, 40, 50 and 60 min of enzymatic reaction, but the yields were higher at 10 min (54%). The hexamers was obtained only with 30 min of reaction with concentration of 0.004 mg/mL.     

Transformants of Metarhizium anisopliae sf. anisopliae overexpressing chitinase from Metarhizium anisopliae sf. acridum show early induction of native chitinase but are not altered in pathogenicity to Manduca sexta

Extracellular chitinase activity has been implicated in the pathogenesis of several fungal infections. Following induction with chitin, the insect pathogens Metarhizium anisopliae sf. acridum ARSEF strain 324 and Metarhizium anisopliae sf. anisopliae ARSEF strain 2575 secrete 44-kDa basic and acidic isoforms of endochitinase, respectively. The gene from strain 324 (Chit1) was cloned and inserted into the genome of strain 2575 under the control of Aspergillus regulatory elements such that transgenic 2575 (2575-Chit(+)) expressed CHIT1 in a noninducing medium (i.e., not containing chitin). Isoelectric focusing followed by a zymogram technique revealed that neither wild-type 2575 nor 2575-Chit(+) produced significant amounts of the native 2575 acidic chitinase in a noninducing medium. However, in a chitin-containing medium, 2575-Chit(+) produced the native chitinase earlier than strain 2575, soon after secretion of CHIT1. We hypothesize that this is due to the production of soluble inducers following chitin hydrolysis by CHIT1 and that M. anisopliae uses enzymes expressed at low levels to sense the nature of the polymeric nutrient present in the immediate environment. However, the chitinase overproducers did not show altered virulence to caterpillars (Manduca sexta) compared to the wild-type fungus, suggesting that wild-type levels of chitinase are not limiting for cuticle penetration.