Ultrastructure of Ascodichaena rugosa on beech bark

Ascodichaena rugosa Butin is a corkinhabiting fungus, found frequently on the bark of Fagus sylvatica L. The hyphae of the fungus are distributed solely in the phellem cells, stopping their growth in the last-formed cork cell layer. The cell to cell invasion is effected by penetration hyphae, causing no extensive dissolution of the cork wall. Electron microscopical observations revealed fine structural details of the fruit bodies and of the intracellular hyphae. Of special interest were the finger-like hyaline hyphae in the last-formed layer of cork cells, which are interpreted as haustoria on the basis of the fine structure both of hyphae and host cells. This situation is considered as reflecting a parasitic relationship of Ascodichaena to beech bark. The activity of the fungus led also to the increased production of cork cells, perhaps related to the nutrient supply of the fungus.     

Effects of population density on alienicolae of Aphis fabae Scop.: The expression of migratory urge among alatae in the field

Inspection of naturally or artificially infected Hevea roots showed that Forms lignosus can penetrate undamaged roots directly, but does so more readily through wounds or natural openings like lenticels, or through the bases of lateral roots and bark scales. Therefore, Pomes-infected trees should be identified by leaf symptoms rather than by uncovering and inspecting roots, as this generally leads to root injury, which facilitates fungal penetration. Initial fungal entry into host tissue appears to be by mechanical pressure alone, but deeper penetration is through the action of extracellular enzymes. The fungus remains intercellular in the cortex but is intracellular in the woody tissue. Ray cell walls are penetrated mechanically, but the xylem through pits. The time taken for various stages of infection to occur is assessed. The amount of damage done by the fungus to roots and the blocking of xylem vessels by tyloses suggest that yellowing, curling and buckling of leaves on infected trees are drought symptoms and not a reaction to fungal toxins. The host reacts to the invasion of the cortex by forming a cork cambium and to the invasion of the woody tissue by blocking individual cells with phenols and resins, which could be important when breeding disease resistant Hevea root stocks.     

Effect of root-rot fungus (Macrophomina phaseolina) on the life cycle of root-knot nematode (Meloidogyne javanica) Race-2 on balsam

The penetration of second stage juveniles of Meloidogyne javanica started within 12 hours after inoculation and the rate of penetration gradually increased with the passage of time up to the fifth day in the plants inoculated with root-knot nematode alone and up to the sixth day when plants were infected with root-knot nematode and root-rot fungus. Mostly, the penetration of second stage juveniles of Meloidogyne javanica took place in the meristematic region but in some cases the juveniles also penetrated into the root tips and oriented themselves near the stellar region almost parallel to the longitudinal axis of the roots. The life cycle of Meloidogyne javanica on balsam was completed within 25 days, whereas the duration of the life cycle and fecundity of females was adversely affected in the presence of fungus (Macrophomina phaseolina) and it took about 33 days to complete the life cycle, i.e. the presence of Macrophomina phaseolina delayed the life cycle of the root-knot nematode (Meloidogyne javanica) by eight days.     

An electron-microscopical analysis of capture and initial stages of penetration of nematodes byArthrobotrys oligospora

A detailed analysis was made of the capture and subsequent penetration of nematodes by the nematophagous fungusArthrobotrys oligospora using different electron-microscopical techniques. Capture of nematodes by this fungus occurred on complex hyphal structures (traps) and was effectuated by an adhesive coating, present on these trap cells. The adhesive layer was largely fibrillar in nature and was absent on cells of normal hyphae. Following capture, penetration hyphae were formed at those sites where the trap cell wall was anchored to the nematode cuticle by the adhesive. New walls of these hyphae were formed underneath the original trap cell walls, which were partly hydrolysed to allow growth and development of the penetration tubes through the adhesive coating towards the cuticle. Our observations indicated that the cuticle of the nematode was subsequently penetrated by the penetration tubes by mechanical means. After penetration a large infection bulb was formed from which trophic hyphae arose. Cytochemical experiments indicated that the sites of penetration of the cuticle were intensely stained for acid phosphatase activity. At later stages of infection activity of this enzyme was present throughout the nematode contents; the enzyme was most probably secreted by complex membranous structures associated with the cytoplasmic membrane of the infection bulb and the trophic hyphae.     

Root Browning in Pinus banksiana Lamb. and Eucalyptus pilularis Sm. 2. Anatomy and Permeability of the Cork Zone

The periderm in roots of Pinus banksiana Lamb. and the polyderm in roots of Eucalyptus pilularis Sm. originate from the pericycle. This occurs after the roots have turned brown due to deposition of tannins in the walls of cells external to the endodermis. In both species, cork cells form a continuous sheath around the vascular tissues. The cork cell walls are modified by the presence of suberin, lignin and tannin and it is the latter which imparts a brown colour to the tissue. The first layer of cork cells in both species constitutes an apoplastic barrier which prevents the fluorescent dye, berberine, from entering the vascular tissues, despite the absence of an identifiable Casparian band in the cells. Because the roots are still covered with the cortex and epidermis during early stages of periderm and polyderm formation, it is not possible to tell from the external aspect of the root when it makes a transition from the tannin zone to the cork zone.     

Effect of fungal colonization on mechanical performance of cork

The industrialization of traditional processes relies on the scientific ability to understand the empirical evidence associated with traditional knowledge. Cork manufacturing includes one operation known as stabilization, where humid cork slabs are extensively colonized by fungi. The implications of fungal growth on the chemical quality of cork through the analysis of putative fungal metabolites have already been investigated. However, the effect of fungal growth on the mechanical properties of cork remains unexplored. This study investigated the effect of cork colonization on the integrity of the cork cell walls and their mechanical performance. Fungal colonization of cork by Chrysonilia sitophila, Mucor plumbeus Penicillium glabrum, P. olsonii, and Trichoderma longibrachiatum was investigated by microscopy. Growth occurred primarily on the surface of the cork pieces, but mycelium extended deeper into the cork layers, mostly via lenticular channels and by hyphal penetration of the cork cell wall.In this first report on cork decay in which specific correlation between fungal colonization and mechanical proprieties of the cork has been investigated, all colonizing fungi except C. sitophila, reduced cork strength, markedly altering its viscoelastic behaviour and reducing its Young's modulus.     

Probing the cell wall heterogeneity of micro-dissected wheat caryopsis using both active and inactive forms of a GH11 xylanase

The external envelope of wheat grain (Triticum aestivum L. cv. Isengrain) is a natural composite whose tissular and cellular heterogeneity constitute a significant barrier for enzymatic cell wall disassembly. To better understand the way in which the cell wall network and tissular organization hamper enzyme penetration, we have devised a strategy based on in situ visualization of an active and an inactive form of a xylanase in whole-wheat bran and in three micro-dissected layers (the outer bran, the inner bran and the aleurone layer). The main aims of this study were to (1) evaluate the role of cuticular layers as obstacles to enzyme diffusion, (2) assess the impact of the cell wall network on xylanase penetration, (3) highlight wall heterogeneity. To conduct this study, we created by in vitro mutagenesis a hydrolytically inactive xylanase that displayed full substrate binding ability, as demonstrated by the calculation of dissociation constants (K_d) using fluorescence titration. To examine enzyme penetration and action, immunocytochemical localization of the xylanases and of feebly substituted arabinoxylans (AXs) was performed following incubation of the bran layers, or whole bran with active and inactive isoforms of the enzyme for different time periods. The data obtained showed that the micro-dissected layers provided an increased accessible surface for the xylanase and that the enzyme-targeted cell walls were penetrated more quickly than those in intact bran. Examination of immunolabelling of xylanase indicated that the cuticle layers constitute a barrier for enzyme penetration in bran. Moreover, our data indicated that the cell wall network by itself physically restricts enzyme penetration. Inactive xylanase penetration was much lower than that of the active form, whose penetration was facilitated by the concomitant depletion of AXs in enzyme-sensitive cell walls.     

The Effect of Chitinase on Didymella applanata, the Causal Agent of Raspberry Cane Spur light

In vitro and in vivo studies were conducted to assess the efficacy of the two microbial chitinases Chi I (from Streptomyces sp.) and Chi II (from Serratia marcescens) on Didymella applanata (Niessl.) Sacc., the fungus which causes spur blight of raspberry (Rubus idaeus L.). D. applanata was isolated from canes of diseased raspberries in a plantation in Novosibirsk, Russia. In vitro, the effective concentration of Chi I that reduced the growth of D. applanata was 0.4 U/ml (p = 0.05), but Chi II had no influence on the growth of the fungus in medium. In inoculation experiments on raspberry canes, both chitinases at the rate 0.5 U/ml reduced fungal development. In plantation where canes were inoculated after spraying with chitinase, fruiting bodies of fungus failed to form in all enzyme treatments, whereas a significant number of these fungal fruiting bodies (12.8 per cm²) developed in control treatments lacking chitinases spraying. The chitinases reduced the size of lesions and limited the infection of internal tissues of canes. Field testing of Chi I under natural conditions showed a significant suppression of the independent spur blight. These studies form the basis for further evaluation of ecologically benign control measures for raspberry spur blight.     

Screening the ability of rice roots to overcome the mechanical impedance of wax layers: importance of test conditions and measurement criteria

The development of a wax layer method for screening the ability of rice (Oryza sativa L.) roots to overcome mechanical impedance is described. Wax layers (3 mm thick) made of mixtures of white soft paraffin and paraffin wax were installed 50 mm deep in tubes of sand. The sand was watered with nutrient solution and planted with 3-d old rice seedlings. The numbers of root axes per plant that had penetrated the wax layers 24 d after planting were counted. The ratio of penetrated to total root axes per plant gave a misleading measure of root penetration ability, as rice varieties differed in the ratio of penetrated to total axes in a low impedance (3% wax) control. In non-flooded conditions, a 60% wax layer decreased root penetration (number of roots penetrating the wax layer per plant) to a mean of 74% of the low impedance control, whereas an 80% wax layer decreased mean root penetration to 31% of the control. The best measure of root penetration in non-flooded conditions was the number of axes penetrating an 80% wax layer. Flooding decreased root penetration of a 60% wax layer to a mean of 26% of the low impedance control. The best measure of root penetration in flooded conditions was the number of axes penetrating a 60% wax layer.     

濒危植物海南风吹楠营养器官解剖结构特征

该研究采用石蜡切片和光学显微技术,对海南风吹楠营养器官的解剖结构及其对环境的适应性进行了探讨。结果表明:海南风吹楠为典型异面叶,叶片中脉发达,中部分化出髓,上表皮外侧具角质层,内侧具1层内皮层,下表皮外侧无角质层,有气孔器分布,气孔器为双环型,略下陷;栅栏组织3~4层细胞,海绵组织4~6层细胞。茎的初生结构中表皮轻微角质化,维管束为外韧型,8~10个初生维管束围绕髓排列为1轮;茎的次生结构中,表皮外部角质层加厚,维管柱紧密排列连成环状,次生韧皮部和次生木质部发达,形成层细胞3~5层。根的初生结构中表皮细胞外壁加厚,外皮层细胞体积大,形状不规则,内侧具1层形成层,内皮层具凯氏带,初生木质部为多原型,呈辐射状排列。根的次生结构中木栓层细胞5~6层,木栓层内侧具1层木栓形成层,栓内层细胞3层。海南风吹楠营养器官具有一定耐阴和耐旱结构特征,同时与其生活的热带雨林沟谷中高温荫湿的环境相适应。     

The life cycle of the insect pathogenic fungus Metarhizium anisopliae in the termite Nasutitermes exitiosus

In in vitro and in vivo studies the mode of penetration from Metarhizium anisopliae through the termite integument is elucidated. Serial sections and haemolymph studies elucidate the infective cycle within the host.Conidia germinate and penetrate the cuticle after a not-obligate formation of one or more appressoria. A penetration plate or hyphal bodies between cuticle layers form the base for the invasion of the body cavity, where the haemolymph distributes the multiplicating hyphal bodies. After the death of the insect due to various fungal toxins, organs and tissues are penetrated. Before the gut is invaded, the fungus breaks through to the outside and grows with a special air mycelium, which forms the conidiophores. From these structures the conidia, which stick together in bunches of chains, develope. These conidia can infect the nest mates.     

Impact of the exodermis on infection of roots byFusarium culmorum

Patterns of infection withFusarium culmorum (W G Smith) Saccardo were observed in seedling roots of barley (Hordeum vulgare L.), wheat (Triticum aestivum L.), maize (Zea mays L.) and asparagus (Asparagus officinalis L). Apical regions of the main roots were not infected. Since penetration into the root occurred several days after inoculation and the roots were growing during the experiment, these regions had apparently not been in existence long enough to be infected. In older regions of barley, wheat and asparagus, hyphae entered through the tips of lateral roots. In barley and wheat, which had not developed any suberin lamellae in their subepidermal layer, infection occurred randomly over the remainder of the root. In maize, the fungus penetrated the epidermis at many sites but did not breach the exodermis in which all cells possessed both Casparian bands and suberin lamellae. Maize roots, therefore, sustained only minimal infections. In asparagus, the fungus grew through the short (passage) cells but never the long cells of the exodermis. In doing so, it penetrated cells possessing Casparian bands but lacking suberin lamellae. The results support the hypothesis that suberin lamellae provide effective barriers to the growth ofF. culmorum hyphae.     

Colonization of Fusarium Wilt‐Resistant and Susceptible Watermelon Roots by a Green‐Fluorescent‐Protein‐tagged Isolate of Fusarium oxysporum f.sp. niveum

Interactions between watermelon and a green fluorescent protein (GFP)‐tagged isolate of Fusarium oxysporum f.sp. niveum race 1 (Fon‐1) were studied to determine the differences in infection and colonization of watermelon roots in cultivars resistant to and susceptible to Fusarium wilt. The roots of watermelon seedlings were inoculated with a conidial suspension of the GFP‐tagged isolate, and confocal laser scanning microscopy was used to visualize colonization, infection and disease development. The initial infection stages were similar in both the resistant and susceptible cultivars, but the resistant cultivar responded differentially after the pathogen had penetrated the root. The pathogen penetrated and colonized resistant watermelon roots, but further fungal advance appeared to be halted, and the fungus did not enter the taproot, suggesting that resistance is initiated postpenetration. However, the tertiary and secondary lateral roots of resistant watermelon also were colonized, although not as extensively as susceptible roots, and the hyphae had penetrated into the central cylinder of lateral roots forming a dense hyphal mat, which was followed by a subsequent collapse of the lateral roots. The initial infection zone for both the wilt‐susceptible and wilt‐resistant watermelon roots appeared to be the epidermal cells within the root hair zone, which the fungus penetrated directly after forming appressoria. Areas where secondary roots emerged and wounded root tissue also were penetrated preferentially.     

The effect of cane management techniques on raspberry yellow rust (Phragmidium rubi-idaei)

The effects of various cane removal treatments on the epidemiology of Phragmidium rubi-idaei were studied in four experiments in infected raspberry plantations in Wales and Scotland. In 1981, removal of 15 cm high young canes either by cutting or by spraying dinoseb-in-oil reduced infection of a second flush of canes (replacement canes) compared to that of the first flush of canes on untreated plots of cv. Mailing Delight in Wales and of cv. Glen Clova in Scotland. In 1982, removal of 20 cm high young canes reduced infection of cv. Mailing Delight in Wales but in Scotland only removal of 60 cm high canes by cutting reduced infection of replacement canes. Removal of all fruiting canes and old cane stubs reduced rust infection of young canes, but removal of successive flushes of replacement canes did not reduce infection of lateral shoots on the fruiting canes. Dinoseb-in-oil applied to the bases of fruiting canes before emergence of young canes had no effect on infection of young canes in Wales or Scotland. The production of basidiospores was inhibited in vitro by dinoseb-in-oil at concentrations over 1.0 μg a.i./ml.     

Microscopic Observation on the Development of Puccinia striiformis in the Spike and Stem of Wheat

The majority of germ tubes of the pathotype CYR32 of Puccinia striiformis f.sp. tritici formed on the surface of spike organs of the susceptible wheat cv. Suwon 11 penetrated through the stomatal pore, only a few germ tubes formed small appressoria over the stomata. In the lemma, palea and glume, the stripe rust fungus spread between the parenchyma cells close to the inner epidermal layer, but the fungus did not develop between the thick‐walled cells near the outer epidermal layer of these organs. In the awn and stem, spread of the stripe rust was confined to the intercellular spaces of the chlorophyll parenchyma, beneath the invaded stomatal pore of the epidermis and the urediniospores to be released disrupted the epidermis. In the caryopsis, the spread of hyphae was restricted to the intercellular spaces of the pericarp cells.     

Vigour control, an integrated approach to cane, pest and disease management in red raspberry (Rubus idaeus)

The first flush of young canes of red raspberry (Rubus idaeus) was removed at different dates in spring, using the contact herbicide dinoseb. In comparison with untreated plots, cane removal increased fruit yield, controlled excessive cane vigour, and improved the health status of vegetative canes in a plantation infested by raspberry cane midge (Resseliella theobaldi). At the end of the growing season vegetative canes on treated plots were shorter and thinner, and sustained less physical injury than those on untreated plots. Access to the fruit at harvest was also improved. Reduced competition between fruiting and vegetative canes increased yield in the year of treatment by an average of 35%. Yield was not affected by date of cane removal, but growth of replacement cane was reduced below optimum when first flush cane was removed after mid-May. The later the canes were removed, the less was the incidence of pest and diseases. Cankers and lobate vascular lesions (‘patches’) resulting, respectively, from the feeding of first and second generation midge larvae (with associated fungi) affected fewer canes in treated than in untreated plots. Significantly fewer live larvae of R. theobaldi were recovered in the following winter from soil in plots treated on or after 11 May than from untreated plots. The main effect of vigour control on R. theobaldi and midge blight was that replacement canes provided fewer egg-laying sites (natural splits) than did the first flush canes on untreated plots. The incidence of spreading vascular lesions (‘stripes’) attributed to Leptosphaeria coniothyrium infecting either physical wounds (cane blight) or midge feeding wounds (midge blight) was substantially less in treated than untreated plots. Cane botrytis (Botrytis cinerea) and spur blight (Didymella applanata) were also less common in treated plots. Interactions between vigour control and pest and disease incidence are discussed in relation to the efficient management of cv. Glen Clova in eastern Scotland.     

Ultrastructure of the penetration of the crayfish integument by the fungal parasite, Aphanomyces astaci, Oomycetes

In the crayfish, Astacus astacus, susceptible to the crayfish plague fungus, penetration of the cuticle by the parasite occurred in the soft cuticle. The zoospore lysed the surface lipid layer, tore it away, and formed an infection peg (germ tube) that penetrated through the epicuticle. A septum was formed in the infection peg, and a hypha was formed below the inner epicuticular surface. In the endocuticle, hyphae grew preferrentially parallel to the surface, occassionally perpendicular to it. Growth direction in relation to cuticle architecture is discussed. Subsequently, some hyphae started to penetrate out through the epicuticle. This process was preceded by the swelling of the hyphal tip touching the inner side of the epicuticle. The hypha penetrating out through the epicuticle was much thicker than the infection peg. Histolytic activity, combined with mechanical penetration, seems to be evident in all stages and levels except in the outward penetration of the epicuticular lipid surface layer, where only mechanical rupture could be seen. Differences in the protoplasmic ultrastructure were found between the spore and the penetrant hyphae. Penetration of the cuticle of a resistant crayfish was essentially identical to that in susceptible ones. However, inward penetration of intact epicuticle was too scarce to allow for ultrastructural studies.     

Colonization of Corn, Zea mays, by the Entomopathogenic Fungus Beauveria bassiana

Light and electron microscopy were used to describe the mode of penetration by the entomopathogenic fungus Beauveria bassiana (Balsamo) Vuillemin into corn, Zea mays L. After inoculation with a foliar spray of conidia, germinating hyphae grew randomly across the leaf surface. Often a germ tube formed from a conidium and elongated only a short distance before terminating its growth. Not all developing hyphae on the leaf surface penetrated the cuticle. However, when penetration did occur, the penetration site(s) was randomly located, indicating that B. bassiana does not require specific topographic signals at an appropriate entry site as do some phytopathogenic fungi. Long hyphal structures were observed to follow the leaf apoplast in any direction from the point of penetration. A few hyphae were observed within xylem elements. Because vascular bundles are interconnected throughout the corn plant, this may explain how B. bassiana travels within the plant and ultimately provides overall insecticidal protection. Virulency bioassays demonstrate that B. bassiana does not lose virulence toward the European corn borer, Ostrinia nubilalis (Hübner), once it colonizes corn. This endophytic relationship between an entomopathogenic fungus and a plant suggests possibilities for biological control, including the use of indigenous fungal inocula as insecticides.     

Hyperparasitischer Angriff von Epicoccum purpurascens auf den biotrophen Kontakt-Mykoparasiten Gonatobotrys simplex

Hyperparasitic attack of Epicoccum purpurascens on the biotrophic contact mycoparasite Gonatobotrys simplex The in vivo- and in vitro-hyperparazitation of Gonatobotrys simplex (Gs) by Epicoccum purpurascens (Ep) is presented. Ep, showing positive tropism, grows toward the host fungus Gs. After contact Ep penetrates especially the Gs-conidia, more rarely germ tubes and the mycelium. Two types of penetration can be distinguished: 1) direct penetration and 2) penetration after previous formation of appressoria. On this attack Gs reacts with local cell wall appositions (papillae), which mostly can be pierced by the hyperparasite. At the advanced state of parasitism the host fungus finally dies.     

Infection and colonization of tissues of the aphid Myzus persicae and cassava mealybug Phenacoccus manihoti by the fungus Beauveria bassiana

Histopathogenesis of living insects of Myzus persicae Sulzer (Hemiptera: Aphididae) and Phenacoccus manihoti Matile‐Ferrero (Hemiptera: Pseudococcidae) by Beauveria bassiana (Balsamo) Vuillemin (Ascomycota: Hypocreales) was monitored from penetration through insect death. Important events in aphids included fungal penetration of the integument of the less-resistant leg intersegmental membrane and invasion of natural openings, formation of hyphal bodies in live aphids by three days post-inoculation (PI), and extensive hyphal colonization of the two leg segments closest to the insect body at death of the aphids. Confocal microscopy of green fluorescent protein-labeled B. bassiana in live mealybugs indicated the fungus penetrated the host through the legs and mouthparts. The fungus was scarce in live mealybugs at 1–5 days PI, formed hyphal bodies by six days PI, and growth was limited to parts of dead hosts at 6–7 days PI. In dead mealybugs, hyphal bodies were near solid tissue. Blastospores were in the hemolymph.