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Production of microsclerotia of the fungal entomopathogen Metarhizium anisopliae and their potential for use as a biocontrol agent for soil-inhabiting insects

机译:真菌性昆虫病原菌小僵菌的小菌核的产生及其作为土壤昆虫的生物防治剂的潜力

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Microsclerotia (MS), overwintering structures produced by many plant pathogenic fungi, have not been described for Metarhizium anisopliae. Three strains of M. anisopliae - F52, TM109, and MA1200 - formed MS in shake flask cultures using media with varying carbon concentrations and carbon-to-nitrogen (C:N) ratios. Under the conditions of this study, all strains produced MS, compact hyphal aggregates that become pigmented with culture age, in addition to more typical blastospores and mycelia. While all strains formed desiccation tolerant MS, highest concentrations (2.7-2.9x10^8L^-^1 liquid medium) were produced in rich media with C:N ratios of 30:1 and 50:1 by strain F52. All three strains of M. anisopliae produced similar biomass concentrations when media and growth time were compared. Strain MA1200 produced higher concentrations of blastospores than the other two strains of M. anisopliae with highest blastospore concentrations (1.6 and 4.2x10^8blastosporesml^-^1 on days 4 and 8, respectively) in media with the highest carbon and nitrogen concentrations. Microsclerotial preparations of M. anisopliae containing diatomaceous earth survived air-drying (to <5 % moisture) with no significant loss in viability. Rehydration and incubation of air-dried MS granules on water agar plates resulted in hyphal germination and sporogenic germination to produce high concentrations of conidia. Bioassays using soil-incorporated, air-dried MS preparations resulted in significant infection and mortality in larvae of the sugar beet root maggot, Tetanops myopaeformis. This is the first report of the production of sclerotial bodies by M. anisopliae and provides a novel approach for the control of soil-dwelling insects with this entomopathogenic fungus.
机译:微菌核(MS),由许多植物病原真菌产生的越冬结构,尚未被描述为Metarhizium anisopliae。使用不同碳浓度和碳氮比(C:N)的培养基,摇瓶培养物中的三株分离的支链支原体菌株F52,TM109和MA1200形成了MS。在这项研究的条件下,除了更典型的芽孢孢子和菌丝体,所有菌株均产生MS,致密的菌丝聚集体,随着培养年龄而变色。尽管所有菌株均形成耐干燥性MS,但菌株F52在C:N比为30:1和50:1的富培养基中产生了最高浓度(2.7-2.9x10 ^ 8L ^-^ 1液体培养基)。当比较培养基和生长时间时,所有三种菌株的分枝杆菌均​​产生相似的生物质浓度。在具有最高碳和氮浓度的培养基中,MA1200菌株产生的孢子浓度高于其他两个菌株的最高芽孢杆菌浓度(在第4和第8天分别为1.6和4.2x10 ^ 8blastosporesml ^-^ 1)。含硅藻土的厌食支原体的微菌制剂在风干下幸存下来(水分含量<5%),生存能力没有明显降低。在水琼脂平板上对风干的MS颗粒进行再水化和孵育会导致菌丝萌发和孢子发芽,从而产生高浓度的分生孢子。使用掺入土壤,风干的MS制剂的生物测定法导致甜菜根(Tetanops myopaeformis)的幼虫感染和死亡。这是关于分枝杆菌产生菌核的第一份报道,并提供了一种利用这种昆虫病原真菌控制土壤昆虫的新方法。

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