角蜡蚧和日本龟蜡蚧蜡泌物的超微结构及化学成分分析

采用扫描电镜和气相色谱/质谱联用技术研究了角蜡Ceroplastes ceriferus (Fabricius) 和日本龟蜡蚧C. japonicus Green蜡泌物的超微结构及化学成分。结果表明,这2种蜡蚧分泌蜡质和形成蜡壳的过程基本相似。在1、2龄期分泌的蜡质为“干蜡”,蜡壳为星芒状,虫体周缘的蜡芒均为2大节,与其2个龄期发育相对应,每一个大节又分为若干小节。同时,虫体背面中央蜡质堆积成帽状,也分为均匀的多层。由此说明泌蜡过程具有节律性。虫体周缘与蜡芒对应的突起区上分布着密集的刻点状腺孔,每一个腺孔分泌1根蜡丝,这在以往玻片标本中是观察不到的。雌性第3龄幼虫和成虫期,虫体分泌“湿蜡”,形成龟背状蜡壳,泌蜡腺孔主要为三格腺和四格腺。在肛突区发现了密集的泌蜡腺孔,排列为纵条纹状。从角蜡蚧蜡泌物甲酯化处理样品中检测到14个组分,从直接测试 (未经甲酯化处理) 样品中检测到14个组分;而从日本龟蜡蚧则分别检测到10个组分和25个组分。它们的主要成分是一系列高级的长链饱和与不饱和的烃、脂肪酸、脂肪醇、酯类、醛类以及杂环、多环或大环状化合物。对它们可能的生物生态学功能进行了讨论。     

不同基质多代培养对蚧虫病原真菌蜡蚧霉致病力的影响

【目的】研究昆虫病原真菌蜡蚧霉Lecanicilliurn lecanii(Zimmermann.)菌株No.V3.4504在不同培养基上继代培养,对菌种的菌落生长特性、胞外酶活力和对蚧虫致病力的影响。【方法】试验菌种蜡蚧霉菌株No.V3.4504是从染病蚧虫上分离的。试验蚧虫是沙里院褐球蚧Rhodococcus sariuoni Borchsenius和日本龟蜡蚧Ceroplastes japonicus Green。采用7种培养基继代培养多代。观察菌落形态特征、测定生长速率、产孢量、胞外蛋白酶和几丁质酶活性及对蚧虫的致死率。【结果】在PDA培养基上,菌落生长速率最快,但产孢量最低,胞外蛋白酶和几丁质酶的活性均呈逐代下降趋势,对两种蚧虫致死率也最低;增加蛋白胨对改善菌种致病力没有明显效果;在增加蚧虫尸体的D、E、F培养基上,菌落生长速率虽然较慢,但产孢量上升为8.83×106-9.13×106孢子/cm2。蛋白酶和几丁质酶的活性平均达到2.16-2.13 U/g和1.01-1.03 U/g,对两种蚧虫的致死率分别在55%-58%和39%-42%;在活蚧虫上连续培养3代,蛋白酶和几丁质酶的活性最高,为3.08-2.92 U/g和1.45-1.42 U/g,是PDA培养基上的1.6倍。对两种蚧虫的致死率也最高,分别达到71.30%和58.89%。蛋白酶和几丁质酶的活性与蚧虫死亡率呈正直线相关关系。【结论】采用PDA培养基连续多代培养会引起菌株No.V3.4504明显退化;在培养基中加入蚧虫尸体,对于保持菌种活力有明显效果;在活蚧虫体上继代培养对复壮菌种,提高菌种毒力的效果最佳。     

异色瓢虫对日本龟蜡蚧虫体挥发物的趋性反应

为明确异色瓢虫Harmonia axyridis(Pallas)在取食日本龟蜡蚧Ceroplastes japonicus Green过程中虫体挥发物的作用,本研究采用Y型嗅觉仪测定了异色瓢虫对日本龟蜡蚧的趋性行为反应,并利用顶空固相微萃取和气质联用(HS-SPME-GC/MS)对日本龟蜡蚧(卵、若虫、成虫)的挥发性气味进行分析鉴定。结果表明:异色瓢虫对日本龟蜡蚧各龄期均有趋性,其中对成虫的趋性达到极显著水平(P0.01)。在日本龟蜡蚧虫体挥发性成分中,共检出10种烷烃类、8种烯烃类、9种醇类等47种组分。选取其中两种含量较大的组份1-辛烯-3-醇和1R-α-蒎烯进行单组份趋性试验,结果表明1-辛烯-3-醇在浓度为10-4g/m L和10-5g/m L、1R-α-蒎烯在浓度为10-5g/m L和10-6g/m L时对异色瓢虫具有明显吸引效应,其中10-4g/m L的1-辛烯-3-醇和10-5g/m L的1R-α-蒎烯引诱率分别达到73.65%和76.41%,差异达到极显著水平(P0.01)。上述结果为进一步研究异色瓢虫的引诱剂奠定了基础。     

日本龟蜡蚧卵期的预测预报研究

日本龟蜡蚧是园林花卉、林木和果树的重要害虫,繁殖量大,除初孵若虫外,体被较厚蜡质,为各种防治增加了难度．准确测报若虫盛孵期,是防治该虫的关键．利用自然变温测定卵期的发育起点温度和有效积温,经测定悬铃木：C=18.02±1.69（℃）,K=142.68±29.21（DD）;大叶黄杨：C=18.54±0.74（℃）．K=129.34±11.93（DD）,桅子花：C=19.97±0.87（℃）,K=106.81±13.92（DD）,这种测定简便易行而又更符合实际,仅计算较为复杂．     

医学昆虫的病原真菌

昆虫病原真菌在自然环境中对害虫数量起着抑制作用,在害虫的微生物防治中也占有独特的地位。长期以来,在应用昆虫病原真菌防治人畜害虫方面研究进展较为缓慢,六十年代以来才有较大的发展。本文介绍了近十年的发展概况,并讨论了影响这个研究领域迅速发展的原因及病原真菌在生物防治中应用的潜力。认为尽管至今对这类真菌了解还较少,但通过今后加强有关方面的研究工作,其应用前景是广阔的。     

蚧虫蜡泌物的化学研究进展

总结了国内外对蚧虫蜡泌物及其化学成分的研究进展 ,内容包括蜡泌物形成介壳的主要类型 ;蜡泌物的化学研究方法及已涉及的种类 ;蜡泌物的主要化学组成 ,并对 5类物质 ,即蜡、烃类、树脂或萜类、色素类、内蜜露作了重点叙述。最后 ,讨论了研究蚧虫蜡泌物的化学成分具有的意义和应用前景 ,包括蜡泌物作为生物资源的利用 ;以蚧虫作为农林、果树和花卉业的重要害虫 ,针对蜡泌物的特点研制相应的新型杀虫剂 ;利用蜡泌物的化学信息素对天敌的诱导作用 ,开展蚧虫生物防治 ;利用蜡泌物作为化学分类性状的应用等。     

康氏粉蚧蜡泌物的扫描电镜观察

采用制作玻片标本和扫描电镜技术研究了康氏粉蚧Pseudococcus comstocki(Kuwana)在不同发育阶段的显微形态特征及蜡泌物的超微形态。结果表明:三格腺是康氏粉蚧最主要的腺体,随着虫体的发育,数量增多,分布变广,每个腺孔分泌一根蜡丝,覆盖体表;管腺只在特定的时期分泌长的空心蜡管构成卵囊;多格腺分泌多棱形卷曲的小蜡丝粘附在卵粒上,防止其相互粘连。     

一株侵染豌豆蚜的昆虫病原真菌的分离及鉴定

【目的】从采集到的自然染菌的豌豆蚜Acyrthosiphon pisum虫尸分离纯化得到一株病原真菌,定名为TF-2。本研究旨在确定该菌株的分类地位,为豌豆蚜生物防治提供真菌资源。【方法】对自然染菌的豌豆蚜虫尸上寄生真菌TF-2进行回接试验,分离纯化出致病菌株TF-2;在显微镜下配制TF-2菌株不同浓度孢子悬浮液,采用浸渍法和离体叶片饲养法测定其对豌豆蚜成虫的毒力;利用光学显微镜观察菌株形态学特征。PCR扩增TF-2的rDNA-ITS序列并测序,构建系统发育树对TF-2菌株进行分子鉴定。【结果】毒力测定结果表明,TF-2菌株对豌豆蚜成虫表现出很强的致病力,1×10⁷孢子/mL处理6 d后豌豆蚜成虫校正死亡率达到100%。TF-2在PDA培养基上菌落呈圆形,白色或淡黄色毡状,菌落背面呈奶油色;菌株孢梗呈瓶状,在菌丝上单生或侧生2～3个,大小为(19-42)μm×(1.1-2.5)μm,基部较粗至尖端逐渐变细,分生孢子长椭圆形,大小为(4.2-11.8)μm×(1.6-2.6)μm。菌丝体产生晶体呈八面体。该菌株的rDNA-ITS序列与长孢蜡蚧菌Lecanicilli...     

六类常见泌蜡昆虫的蜡腺和蜡泌物研究进展

泌蜡昆虫体表除了具有和其他昆虫一样的薄蜡层之外,还具有特殊的蜡腺,在生长发育过程中能够分泌蜡质覆盖于体表,从而有利于昆虫防止体内水分过度蒸发、抵御外界多种不利条件、阻碍病原物入侵和躲避天敌寄生或捕食,对昆虫的生存和繁衍具有重要的保护作用。本文概述了蚧虫、蚜虫、蜡蝉、木虱、粉虱和粉蛉等6类常见泌蜡昆虫的蜡腺和蜡泌物的超微形态结构、蜡泌物的主要化学组成及泌蜡的分子机制等方面的研究进展,以期为今后其在昆虫分类学和系统发育学的研究以及在害虫防治中的应用提供参考。     

利用黄粉虫分离土壤昆虫病原真菌

利用黄粉虫Tenebrio molitorL.作为寄主从土壤中诱感并分离昆虫病原真菌。结果显示,从吉林市的18个土样中分离出球孢白僵菌(Beauveria bassiana)、金龟子绿僵菌(Metarhiziumanisopliae)和玫烟色拟青霉(Paecilomyces fumosoroseus)。土样中的昆虫病原真菌检出率为77.78%。这表明利用黄粉虫分离土壤中的昆虫病原真菌是一种简单、有效的方法。     

Use of a colorimetric system to detect enzymes expressed by germinating conidia of entomopathogenic fungi

An apiZYM system, with 19 substrates, was used to detect enzymes expressed by germinating conidia of Nomuraea rileyi (5 isolates), Nomuraea atypicola, Nomuraea anemonoides, Beauveria bassiana and Metarhizium anisopliae. Similar enzyme profiles were obtained for two of the N. rileyi isolates (Mississippi, Ecuador) regardless of whether culture medium (Sabouraud-maltose-yeast) or cuticle (from larvae of Trichoplusia ni, Heliothis zea or Heliothis virescens) were used as substrates. Centroid-clustering analysis revealed three distinct enzyme profiles.Mention of a proprietary product in this paper does not consitute a recommendation for use by USDA.     

Use of quantitative PCR to understand within-host competition between two entomopathogenic fungi

Interactions between the entomopathogenic fungi Zoophthora radicans and Pandora blunckii infecting larvae of Plutella xylostella were investigated. This is the first report to quantify within-host growth of one fungus in the presence of another competing for the same host resource using quantitative PCR (qPCR) at regular time points during the infection process. In larvae inoculated only with Z. radicans, there was a cumulative increase in the quantity of Z. radicans DNA throughout the time course of infection. However, in dual-inoculated larvae, there was an initial accelerated rate of growth of Z. radicans compared to when it was inoculated alone, but by the time of host death it had been effectively excluded by P. blunckii. The implications of these results for co-existence of these fungal pathogens in the field are discussed.     

Susceptibility of Brevipalpus phoenicis to entomopathogenic fungi

The pathogenicity of 52 isolates from several fungus species was studied for the false spider mite Brevipalpus phoenicis. In addition, the main stages during the course of infection by Hirsutella thompsonii, by far the most virulent pathogen, were studied by means of light and electron microscopy. Adult mites were confined to arenas prepared with citrus leaves in acrylic dishes containing agar–water. Conidial suspensions containing 10⁸ conidia/ml were applied, except for H. thompsonii, where a concentration of 10⁷ conidia/ml was used. The H. thompsonii isolates caused higher mortality, with indices higher than 90%. Observations under the scanning electron microscope (SEM) were performed at 0, 6, 12, 24, 48, 72, and 120 h after application of a H. thompsonii suspension containing 10⁷ conidia/ml. Twenty-four hours after inoculation, H. thompsonii conidia were observed attached to the mite’s integument. The conidia germinated and penetrated through the base of the setae on the hysterosoma. Colonization occurred after 48 h, as evidenced by mortality. Conidiogenesis occurred after 120 h, with the development of mycelium and conidiophores emerging from the posterior and anterior parts of the mite.     

Insecticidal and antifeedant activities of proteins secreted by entomopathogenic fungi against Spodoptera littoralis (Lep., Noctuidae)

Abstract:  Entomopathogenic fungi are a poorly exploited source of insecticidal proteins, which may be used for the development of new natural insecticides and as alternative molecules for transgenic deployment. The crude soluble protein extracts in Adamek's liquid medium of 25 fungal isolates belonging to the fungal species Metarhizum anisopliae , Beauveria bassiana , Beauveria brongniartii and Scopulariopsis brevicaulis were screened by per os toxicity on Spodoptera littoralis larvae. Whilst extracts from two M. anisopliae and two B. bassiana isolates gave significant mortalities when applied either on alfalfa leaf discs or incorporated into artificial diet, the one from M. anisopliae 01/58-Su isolate was the only most toxic that showed promise for S. littoralis control. In leaf disc assays, this extract exhibited strong dose-related toxic and antifeedant activity against the larvae. At 10, 20 and 40  μ g protein/insect, the extract gave 61.3%, 96.6% and 100.0% mortality, respectively, and average survival time of 5.7, 4.3 and 3.1 days respectively. Not only the antifeeding index was dose-related, but it significantly increased over time in a dose-related manner. Longer exposure times led to a dose-related significant increase in larval mortality. The exposure times for 50% mortality were 91.3 h and 62.1 h for 20 and 40  μ g protein/insect respectively. The crude extract when exposed to higher temperature or protease treatment lost toxicity, indicating that toxicity was protein mediated. In addition, the liquid medium composition did not influence its insecticidal activity. The effects of the protein extract on midgut cells of second instar larvae of S. littoralis were investigated by using both light and electron microscopy. A progressive bleeding of the midgut epithelium into the gut lumen was observed along with lysis of the epithelium and deterioration of the microvilli.     

Biochemistry of insect epicuticle degradation by entomopathogenic fungi

The biochemical interaction between fungal pathogens and their insect host epicuticle was studied by examining fungal hydrocarbon degrading ability. As a contact insecticide, entomopathogenic fungi invade their host through the cuticle, covered by an outermost lipid layer mainly composed of highly stable, very long chain structures. Strains of Beauveria bassiana and Metarhizium anisopliae (Deuteromycotina: Hyphomycetes), pathogenic both to the blood-sucking bug Triatoma infestans (Hemiptera: Reduviidae) and the bean-weevil Acanthoscelides obtectus (Coleoptera, Bruchidae), were grown on different carbon sources. Alkane-grown cells showed a lipid pattern different from that of glucose-grown cells, evidenced by a major switch in the triacylglycerol and sterol components. Radiolabelled hydrocarbons were used to investigate the catabolic pathway and the by-product incorporation into fungal cellular components. The first oxidation round is presumably carried out by a cytochrome P450 enzyme system, the metabolites will traverse the peroxisomal membrane, and after successive transformations will eventually provide the appropriate fatty acyl CoA for complete degradation in the peroxisomes, the site of beta-oxidation in fungi. In this review, we will show the relationship between fungal ability to catabolize very long chain hydrocarbons and virulence parameters.     

Responsiveness of entomopathogenic fungi to menadione-induced oxidative stress

Entomopathogenic fungi are predisposed to ROS induced by heat and UV–A radiation when outside the insect host. When inside the host, they are subject to phagocytic cells that generate ROS to eliminate invading pathogens. The oxidative stress tolerance of the entomopathogenic fungi Aschersonia aleyrodis (ARSEF 430 and 10276), Aschersonia placenta (ARSEF 7637), Beauveria bassiana (ARSEF 252), Isaria fumosorosea (ARSEF 3889), Lecanicillium aphanocladii (ARSEF 6433), Metarhizium acridum (ARSEF 324), Metarhizium anisopliae (ARSEF 5749), Metarhizium brunneum (ARSEF 1187 and ARSEF 5626), Metarhizium robertsii (ARSEF 2575), Tolypocladium cylindrosporum (ARSEF 3392), Tolypocladium inflatum (ARSEF 4877), and Simplicillium lanosoniveum (ARSEF 6430 and ARSEF 6651) was studied based on conidial germination on a medium supplemented with menadione. Conidial germination was evaluated 24 h after inoculation on potato dextrose agar (PDA) (control) or PDA supplemented with menadione. The two Aschersonia species (ARSEF 430, 7637, and 10276) were the most susceptible fungi, followed by the two Tolypocladium species (ARSEF 3392 and 4877) and the M. acridum (ARSEF 324). Metarhizium brunneum (ARSEF 5626) and M. anisopliae (ARSEF 5749) were the most tolerant isolates with MIC 0.28 mM. All fungal isolates, except ARSEF 5626 and ARSEF 5749, were not able to germinate at 0.20 mM.     

Effect of entomopathogenic fungi on detoxification enzyme activity in greater wax moth Galleria mellonella L. (Lepidoptera, Pyralidae) and role of detoxification enzymes in development of insect resistance to entomopathogenic fungi

Fungal infection of insects increases total esterase and glutathione S-transferase activities in the hemolymph. Activities of acid and alkaline phosphatases were similar in the infected and intact insects. Fungal infection increased the resistance of greater wax moth caterpillars to organophosphorus insecticide malathion 1.46 times relative to intact caterpillars. Possible involvement of detoxification enzymes in the development of insect resistance to entomopathogenic fungi and development of complex biological products based on entomopathogenic microorganisms and inhibitors of detoxification enzymes are discussed.     

Pathogenesis-related genes of entomopathogenic fungi

All living things on Earth experience various diseases such as those caused by viruses, bacteria, and fungi. Insects are no exception to this rule, and fungi that cause disease in insects are called entomopathogenic fungi. These fungi have been developed as microbial insecticides and are used to control various pests. Generally, the mode of action of entomopathogenic fungi is divided into the attachment of conidia, germination, penetration, growth, and generation of secondary infectious conidia. In each of these steps, that entomopathogenic fungi use genes in a complex manner (specific or diverse) has been shown by gene knock-out and RNA-sequencing analysis. In this review, the information mechanism of entomopathogenic fungi was divided into six steps: (1) attachment of conidia to host, (2) germination and appressorium, (3) penetration, (4) fungal growth in hemolymph, (5) conidia production on host, and (6) transmission and dispersal. The strategy used by the fungi in each step was described at the genetic level. In addition, an approach for studying the mode of action of the fungi is presented.     

The chemical composition of the wax of the white wax scale,Ceroplastes destructor (Newstead)

The wax of the White Wax Scale [Ceroplastes destructor (Newstead)] is shown to consist principally of a mixture of esters formed from the C₂₆ and C₂₈ alcohols and acids, together with these acids and alcohols in an uncombined state. Paraffin hydrocarbons were not detected. There is a similarity in the composition of the wax secreted by the four members of the genus Ceroplastes which have been investigated.     

The ability of soil-borne fungi to degrade organophosphonate carbon-to-phosphorus bonds

The ability of a wide variety of soil-borne fungal strains to degrade four structurally different com pounds containing PC bonds, namely the naturally occurring amino acid ciliatine, the popular herbicide glyphosate, phosphonoacetic acid and 2-amino-3-phosphonopropionic acid, was studied in order to show that soil fungi may play an important role in the biodegradation of organophosphonates. Most of the strains appeared to utilize ciliatine as the sole source of phosphorus for growth. Only a limited number of strains were able to grow on the other phosphonates used in this work. The strains of Trichoderma harzianum, Scopulariopsis sp. and Aspergillus niger chosen for more detailed study show the ability to degrade ciliatine, glyphosate and also amino(3-methoxyphenyl)mehtylphosphonic acid effectively. Received: 14 May 1997 / Received revision: 10 June 1997 / Accepted: 14 June 1997