Polypeptide metabolites secreted by the fungal pathogen Eutypa lata participate in Vitis vinifera cell structure damage observed in Eutypa dieback

2006 ◽  
Vol 33 (3) ◽  
pp. 297 ◽  
Author(s):  
Stéphane Octave ◽  
Gabriel Roblin ◽  
Magali Vachaud ◽  
Pierrette Fleurat-Lessard
Keyword(s):  
Vitis Vinifera ◽  
Fungal Pathogen ◽  
Cell Walls ◽  
Cell Structure ◽  
Middle Lamella ◽  
Protective Layer ◽  
Mesophyll Cells ◽  
Artificial Culture ◽  
Eutypa Lata ◽  
Eutypa Dieback

Eutypa dieback is a devastating disease of Vitis vinifera L. caused by the fungal pathogen Eutypa lata. This wood-inhabiting fungus degrades tissues in the trunk and cordons of infected vines and induces symptoms in the foliage. These symptoms have been attributed to the production of toxic metabolites by the pathogen, in particular eutypine. Recently, we have isolated polypeptide compounds secreted by the fungus in artificial culture. The aims of this study were to examine the effects induced in leaves by applying polypeptides and eutypine to detached canes and to compare this to the changes in leaf structure induced by E. lata in the vineyard. In leaves taken from vines infected with E. lata, the changes in mesophyll cells indicate that the fungus has an effect on tissue remote from the infected area. The size of mesophyll cells decreased by more than half, starch content was reduced and tannins were abundant. Plastids, mitochondria and cell walls were highly modified. In leaves taken from healthy canes treated with polypeptides of E. lata, the structure of mesophyll cells was also modified. The cell size did not change, but the tannin content increased and modifications in plastids and mitochondria were similar to those observed in leaves taken from infected vines. The major effect was the complete disorganisation of cell walls. Eutypine had less effect on organelle structure and did not modify the cell wall. In canes treated with polypeptides, vessel-associated cells (VACs) were also damaged. Abundant tannins occurred in the vacuoles of VACs and marked changes were noted in mitochondria, plastids and the protective layer, in particular in the pit at the vessel interface. In these pits, the protective layer, the primary wall and the middle lamella were all highly modified. In contrast, treatment with eutypine induced the development of a large transfer apparatus bordering the unmodified pectocellulose wall. These results illustrate that treatment with polypeptides produced by E. lata may cause changes in mesophyll cells in leaves and VACs in canes, that resemble changes observed in naturally infected vines. Comparatively, the differences with eutypine action were stressed. Both types of toxins may co-operate in vivo to produce the degeneration observed during the disease.

Structural modifications induced by Eutypa lata in the xylem of trunk and canes of Vitis vinifera

2005 ◽  
Vol 32 (6) ◽  
pp. 537 ◽  
Author(s):  
Jérome Rudelle ◽  
Stéphane Octave ◽  
Meriem Kaid-Harche ◽  
Gabriel Roblin ◽  
Pierrette Fleurat-Lessard
Keyword(s):  
Vitis Vinifera ◽  
Protective Layer ◽  
Secretory Activity ◽  
Apical Part ◽  
Xylem Structure ◽  
Structural Modifications ◽  
Eutypa Lata ◽  
Eutypa Dieback ◽  
Foliar Symptoms ◽  
Transfer Apparatus

Eutypa dieback, a devastating disease in grapevines, is caused by the fungal pathogen Eutypa lata, a wood-inhabiting fungus. E. lata acts by degrading wood tissues in the colonisation areas, and produces foliar symptoms. These striking symptoms have been attributed to the production of toxic metabolites by the pathogen, the most widely studied being eutypine. The aims of the study were to compare the effects of E. lata on xylem structure at the site of infection and in remote tissues. In healthy Vitis vinifera, the vessel-associated cells (VACs) in the trunk have a protective layer that covers the entire lignified wall and forms a transfer apparatus in pits located at the VAC / vessel interface. This apparatus occurs similarly in VACs in the basal part of canes but is less developed in the apical part. In the presence of E. lata, which is found only in the trunk and the cordons, the VACs initiated a program of secretory activity that led to the enlargement of the transfer apparatus, which is formed by tightly associated fibrils. This secretory activity was followed by VAC death. Furthermore, the hypertrophy of the transfer apparatus spread according to an acropetal gradient in the canes. Treatment with eutypine also induced the development of the transfer apparatus in VACs of basal and apical parts of canes excised from healthy vines. However, this apparatus was formed by loosely packed fibrils in VACs that were not completely damaged. Therefore, metabolites other than eutypine are expected to be involved in the VAC degeneration observed in infected vines.

Ultrastructure of wilt syndrome caused by Verticillium dahliae. V. Attempted localization of phenolic compounds in the vascular region

1978 ◽  
Vol 56 (20) ◽  
pp. 2594-2612 ◽  
Author(s):  
Jane Robb ◽  
J. D. Brisson ◽  
Lloyd Busch ◽  
B. C. Lu
Keyword(s):  
Phenolic Compounds ◽  
Ferric Chloride ◽  
Verticillium Dahliae ◽  
Cell Walls ◽  
Middle Lamella ◽  
Protective Layer ◽  
Multivesicular Body ◽  
Ferric Ion ◽  
Parenchyma Cells ◽  
Cytoplasmic Structures

Ferric chloride has been used in an attempt to detect phenolic compounds at the ultrastructure level in the petioles of chrysanthemums and sunflowers infected with Verticillium dahliae. The fungus contains two types of cytoplasmic structures which stain very densely with ferric chloride; one is similar to a multivesicular body, the other solid and apparently spherical. In treated chrysanthemums, the ferric ion accumulates mainly in vessel plugs, in laminar arrays or localized diffuse deposits in the secondary walls of vessels, in vasicentric parenchyma cells, and the protective layer of parenchyma cells immediately adjacent to the vessels. In treated sunflowers the ferric ion accumulates mainly in vessel plugs, in the pectinaceous layers of the cell wall (i.e. middle lamella and primary cell walls), and in the vasicentric parenchyma cells. Differences in the pattern of phenolic deposition in the two hosts could account wholly or in part for differences in symptom expression.

scholarly journals Pathogenicity of Diatrypaceous Fungi on Grapevines in Australia

Plant Disease ◽  
2013 ◽  
Vol 97 (6) ◽  
pp. 749-756 ◽  
Author(s):  
Wayne M. Pitt ◽  
Florent P. Trouillas ◽  
Walter D. Gubler ◽  
Sandra Savocchia ◽  
Mark R. Sosnowski
Keyword(s):  
Vitis Vinifera ◽  
Healthy Tissue ◽  
The Other ◽  
Cabernet Sauvignon ◽  
Eutypa Lata ◽  
Pruning Wound ◽  
Eutypa Dieback ◽  
Wound Protection ◽  
Woody Tissues

In addition to Eutypa lata, which causes Eutypa dieback, numerous other fungi in the Diatrypaceae family have been isolated from diseased grapevines (Vitis vinifera) and other woody hosts. Pathogenicity trials comprising 70 strains of diatrypaceous fungi representing nine species in six genera were conducted to determine whether these fungi, collected in Australia, were pathogenic to grapevines. When inoculated into wounded trunks of ‘Cabernet Sauvignon’, eight species, including E. lata, E. leptoplaca, Cryptovalsa ampelina, C. rabenhorstii, Eutypella citricola, E. microtheca, Diatrypella vulgaris, and a Diatrype sp. produced necrotic lesions significantly longer than on controls. In addition, all nine species (including a Cryptosphaeria sp.) were reisolated from the margins of developing lesions and at varying distances above and below the point of inoculation. Diatrypaceous fungi were frequently isolated from asymptomatic or otherwise healthy tissue several centimeters ahead of the disease margin. Methods to control diseases associated with diatrypaceous fungi must take into account their propensity to colonize woody tissues ahead of or in the absence of visible symptoms. Current recommendations for the management of Eutypa dieback using remedial surgery and pruning wound protection appear sufficient for the control of the other diatrypaceous fungi included in this study.

Silicification of wood-cell walls

1994 ◽  
Vol 52 ◽  
pp. 428-429
Author(s):  
S. E. Keckler ◽  
D. M. Dabbs ◽  
N. Yao ◽  
I. A. Aksay
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Cell Walls ◽  
Lignin Content ◽  
Resin Composite ◽  
Middle Lamella ◽  
Cellulose Fibers ◽  
Complex Structures ◽  
Rich Region ◽  
Inorganic Precursors

Cellular organic structures such as wood can be used as scaffolds for the synthesis of complex structures of organic/ceramic nanocomposites. The wood cell is a fiber-reinforced resin composite of cellulose fibers in a lignin matrix. A single cell wall, containing several layers of different fiber orientations and lignin content, is separated from its neighboring wall by the middle lamella, a lignin-rich region. In order to achieve total mineralization, deposition on and in the cell wall must be achieved. Geological fossilization of wood occurs as permineralization (filling the void spaces with mineral) and petrifaction (mineralizing the cell wall as the organic component decays) through infiltration of wood with inorganics after growth. Conversely, living plants can incorporate inorganics into their cells and in some cases into the cell walls during growth. In a recent study, we mimicked geological fossilization by infiltrating inorganic precursors into wood cells in order to enhance the properties of wood. In the current work, we use electron microscopy to examine the structure of silica formed in the cell walls after infiltration of tetraethoxysilane (TEOS).

Isolation and characterization of cell walls from the mesocarp of mature grape berries (Vitis vinifera)

2020 ◽  
Author(s):  
KJ Nunan ◽  
Ian Sims ◽  
A Bacic ◽  
SP Robinson ◽  
GB Fincher
Keyword(s):  
Vitis Vinifera ◽  
Cell Walls ◽  
Vascular Tissue ◽  
Compositional Analysis ◽  
Water Soluble ◽  
Vitis Vinifera L ◽  
Nylon Mesh ◽  
Cytoplasmic Material ◽  
Isolation And Characterization ◽  
Tissue Homogenates

Cell walls have been isolated from the mesocarp of mature grape (Vitis vinifera L.) berries. Tissue homogenates were suspended in 80% (v/v) ethanol to minimise the loss of water-soluble wall components and wet-sieved on nylon mesh to remove cytoplasmic material. The cell wall fragments retained on the sieve were subsequently treated with buffered phenol at pH 7.0, to inactivate any wall-bound enzymes and to dislodge small amounts of cytoplasmic proteins that adhered to the walls. Finally, the wall preparation was washed with chloroform/methanol (1:1, v/v) to remove lipids and dried by solvent exchange. Scanning electron microscopy showed that the wall preparation was essentially free of vascular tissue and adventitious protein of cytoplasmic origin. Compositional analysis showed that the walls consisted of approximately 90% by weight of polysaccharide and less than 10% protein. The protein component of the walls was shown to be rich in arginine and hydroxyproline residues. Cellulose and polygalacturonans were the major constituents, and each accounted for 30-40% by weight of the polysaccharide component of the walls. Substantial varietal differences were observed in the relative abundance of these two polysaccharides. Xyloglucans constituted approximately 10% of the polysaccharide fraction and the remainder was made up of smaller amounts of mannans, heteroxylans, arabinans and galactans.

UV-microscopic analysis of acetylated spruce and birch cell walls

Holzforschung ◽  
2004 ◽  
Vol 58 (5) ◽  
pp. 483-488 ◽  
Author(s):  
Christian Hansmann ◽  
Manfred Schwanninger ◽  
Barbara Stefke ◽  
Barbara Hinterstoisser ◽  
Wolfgang Gindl
Keyword(s):  
Cell Walls ◽  
Middle Lamella ◽  
Microscopic Analysis ◽  
Weight Percent ◽  
Cellular Level ◽  
Uv Spectrum ◽  
Spectral Shifts ◽  
Microscopy Analysis ◽  
Absorbance Peak ◽  
Absorbance Spectra

Abstract Spruce and birch earlywood was acetylated to different weight percent gains using three different acetylation procedures. The absorbance spectra of secondary cell wall and compound cell corner middle lamella were determined by means of UV microscopy. Analysis of the spectra showed that the characteristic lignin absorbance peak in the UV spectrum of wood around 280 nm shifted to shorter wavelengths in acetylated samples. A distinct relationship between achieved weight percent gains after acetylation and observed spectral shifts could be established revealing a certain potential to measure acetylation on a cellular level by means of UV microscopy.

Enzymatic detoxification of eutypine, a toxin from Eutypa lata , by Vitis vinifera cells: partial purification of an NADPH-dependent aldehyde reductase

Planta ◽  
1999 ◽  
Vol 207 (4) ◽  
pp. 544-550 ◽  
Author(s):  
S. Colrat ◽  
C. Deswarte ◽  
A. Latché ◽  
A. Klaébé ◽  
M. Bouzayen ◽  
...  
Keyword(s):  
Vitis Vinifera ◽  
Partial Purification ◽  
Aldehyde Reductase ◽  
Eutypa Lata ◽  
Enzymatic Detoxification

The morphology of grain abscission in Zizania aquatica

1980 ◽  
Vol 58 (21) ◽  
pp. 2269-2273 ◽  
Author(s):  
H. B. Hanten ◽  
G. E. Ahlgren ◽  
J. B. Carlson
Keyword(s):  
Wild Rice ◽  
Cell Walls ◽  
Vascular Tissue ◽  
Embryo Sac ◽  
Middle Lamella ◽  
Abscission Zone ◽  
Rice Grains ◽  
Zizania Aquatica ◽  
Parenchyma Cells ◽  
Anatomical Evidence

The anatomical development of the abscission zone in grains of Zizania aquatica L. was correlated with development of the embryo. The abscission zone is well developed when the embryo sac is mature. Soon after pollination, the first anatomical evidence of abscission appears as plasmolysis of the separation layer parenchyma cells. This is followed by separation of the layers by dissolution of the middle lamella and fragmentation of cell walls. Persistence of intact vascular tissue and presence of a surrounding cone-shaped mass of lignified cells may be involved in abscission of wild rice grains.

scholarly journals Melanin Externalization in Candida albicans Depends on Cell Wall Chitin Structures

2010 ◽  
Vol 9 (9) ◽  
pp. 1329-1342 ◽  
Author(s):  
Claire A. Walker ◽  
Beatriz L. Gómez ◽  
Héctor M. Mora-Montes ◽  
Kevin S. Mackenzie ◽  
Carol A. Munro ◽  
...  
Keyword(s):  
Cell Wall ◽  
Candida Albicans ◽  
Fungal Pathogen ◽  
Cell Walls ◽  
Chitin Synthesis ◽  
Melanin Production ◽  
Content Type ◽  
Encoding Gene ◽  
Chitinase Genes

ABSTRACT The fungal pathogen Candida albicans produces dark-pigmented melanin after 3 to 4 days of incubation in medium containing l-3,4-dihydroxyphenylalanine (l-DOPA) as a substrate. Expression profiling of C. albicans revealed very few genes significantly up- or downregulated by growth in l-DOPA. We were unable to determine a possible role for melanin in the virulence of C. albicans. However, we showed that melanin was externalized from the fungal cells in the form of electron-dense melanosomes that were free or often loosely bound to the cell wall exterior. Melanin production was boosted by the addition of N-acetylglucosamine to the medium, indicating a possible association between melanin production and chitin synthesis. Melanin externalization was blocked in a mutant specifically disrupted in the chitin synthase-encoding gene CHS2. Melanosomes remained within the outermost cell wall layers in chs3Δ and chs2Δ chs3Δ mutants but were fully externalized in chs8Δ and chs2Δ chs8Δ mutants. All the CHS mutants synthesized dark pigment at equivalent rates from mixed membrane fractions in vitro, suggesting it was the form of chitin structure produced by the enzymes, not the enzymes themselves, that was involved in the melanin externalization process. Mutants with single and double disruptions of the chitinase genes CHT2 and CHT3 and the chitin pathway regulator ECM33 also showed impaired melanin externalization. We hypothesize that the chitin product of Chs3 forms a scaffold essential for normal externalization of melanosomes, while the Chs8 chitin product, probably produced in cell walls in greater quantity in the absence of CHS2, impedes externalization.

scholarly journals Eutypa, Eutypella, and Cryptovalsa Species (Diatrypaceae) Associated with Prunus Species in South Africa

Plant Disease ◽  
2018 ◽  
Vol 102 (7) ◽  
pp. 1402-1409 ◽  
Author(s):  
Providence Moyo ◽  
Ulrike Damm ◽  
Lizel Mostert ◽  
Francois Halleen
Keyword(s):  
South Africa ◽  
Phylogenetic Analyses ◽  
Fruit Trees ◽  
Fungal Species ◽  
Stone Fruit ◽  
Prunus Species ◽  
Internal Transcribed Spacer Region ◽  
Eutypa Lata ◽  
Eutypa Dieback ◽  
Prunus Spp

Stone fruit trees (Prunus spp.) are economically important fruit trees cultivated in South Africa. These trees are often grown in close proximity to vineyards and are to a large extent affected by the same trunk disease pathogens as grapevines. The aim of the present study was to determine whether stone fruit trees are inhabited by Diatrypaceae species known from grapevines and whether these trees could act as alternative hosts for these fungal species. Isolations were carried out from symptomatic wood of Prunus species (almond, apricot, cherry, nectarine, peach, and plum) in stone fruit growing areas in South Africa. Identification of isolates was based on phylogenetic analyses of the internal transcribed spacer region and β-tubulin gene. Forty-six Diatrypaceae isolates were obtained from a total of 380 wood samples, from which five species were identified. All five species have also been associated with dieback of grapevine. The highest number of isolates was found on apricot followed by plum. No Diatrypaceae species were isolated from peach and nectarine. Eutypa lata was the dominant species isolated (26 isolates), followed by Cryptovalsa ampelina (7), Eutypa cremea (5), Eutypella citricola (5), and Eutypella microtheca (3). First reports from Prunus spp. are E. cremea, E. citricola, and E. microtheca. Pathogenicity tests conducted on apricot and plum revealed that all these species are pathogenic to these hosts, causing red-brown necrotic lesions like those typical of Eutypa dieback on apricot.

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