Ultrastructure of penetration of Phaseolus spp. by Sclerotinia sclerotiorum

1986 ◽  
Vol 64 (12) ◽  
pp. 2909-2915 ◽  
Author(s):  
V. N. Tariq ◽  
P. Jeffries
Keyword(s):  
Electron Microscopy ◽  
Epidermal Cell ◽  
Sclerotinia Sclerotiorum ◽  
Cell Walls ◽  
Intact Plant ◽  
Plant Surface ◽  
Cellular Necrosis ◽  
Hyphal Tip ◽  
Electron Lucent

The infection of leaf and stem tissues of Phaseolus by Sclerotinia sclerotiorum was studied using electron microscopy. Direct entry of the intact plant surface was achieved by hyphae from simple or compound appressoria. A closely appressed hyphal tip developed an electron-lucent region at the apex, in which a plasmalemmal invagination formed. This invagination surrounded a region of extracytoplasmic vesicular material which penetrated the cuticle during invasion. Penetration occurred by a narrow infection peg which passed through the cuticle via a narrow pore and caused little change in cuticle integrity. Once the cuticle was breached, a walled subcuticular vesicle developed from which infection hyphae spread laterally. Destruction of the epidermal cell walls was both rapid and extensive. Leaf and stem colonization occurred by intercellular growth of undifferentiated hyphae accompanied by cellular necrosis in advance of the mycelial front.

Ectodesmata as Revealed By Freeze-Etch Preparations of Plant Epidermal Cell Walls

1973 ◽  
Vol 31 ◽  
pp. 468-469
Author(s):  
N.C. Lyon ◽  
W. C. Mueller
Keyword(s):  
Electron Microscopy ◽  
Acetic Acid ◽  
Nitric Acid ◽  
Oxalic Acid ◽  
Light Microscopy ◽  
Epidermal Cell ◽  
Cell Walls ◽  
Plant Viruses ◽  
Plant Leaves ◽  
Thin Sections

Schumacher and Halbsguth first demonstrated ectodesmata as pores or channels in the epidermal cell walls in haustoria of Cuscuta odorata L. by light microscopy in tissues fixed in a sublimate fixative (30% ethyl alcohol, 30 ml:glacial acetic acid, 10 ml: 65% nitric acid, 1 ml: 40% formaldehyde, 5 ml: oxalic acid, 2 g: mecuric chloride to saturation 2-3 g). Other workers have published electron micrographs of structures transversing the outer epidermal cell in thin sections of plant leaves that have been interpreted as ectodesmata. Such structures are evident following treatment with Hg++ or Ag+ salts and are only rarely observed by electron microscopy. If ectodesmata exist without such treatment, and are not artefacts, they would afford natural pathways of entry for applied foliar solutions and plant viruses.

Ultrastructure of hyperparasitism of Coniothyrium minitans on sclerotia of Sclerotinia sclerotiorum

1987 ◽  
Vol 65 (12) ◽  
pp. 2483-2489 ◽  
Author(s):  
H. C. Huang ◽  
E. G. Kokko
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Cell Wall ◽  
Sclerotinia Sclerotiorum ◽  
Cell Walls ◽  
Chemical Activity ◽  
Coniothyrium Minitans ◽  
Medullary Tissue ◽  
Transmission Electron

Transmission electron microscopy revealed that hyphae of the hyperparasite Coniothyrium minitans invade sclerotia of Sclerotinia sclerotiorum, resulting in the destruction and disintegration of the sclerotium tissues. The dark-pigmented rind tissue is more resistant to invasion by the hyperparasite than the unpigmented cortical and medullary tissues. Evidence from cell wall etching at the penetration site suggests that chemical activity is required for hyphae of C. minitans to penetrate the thick, melanized rind walls. The medullary tissue infected by C. minitans shows signs of plasmolysis, aggregation, and vacuolization of cytoplasm and dissolution of the cell walls. While most of the hyphal cells of C. minitans in the infected sclerotium tissue are normal, some younger hyphal cells in the rind tissue were lysed and devoid of normal contents.

Ultrastructural studies on infection of sclerotia of Sclerotinia sclerotiorum by Talaromyces flavus

1989 ◽  
Vol 67 (7) ◽  
pp. 2199-2205 ◽  
Author(s):  
D. L. McLaren ◽  
H. C. Huang ◽  
S. R. Rimmer ◽  
E. G. Kokko
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Sclerotinia Sclerotiorum ◽  
Cell Walls ◽  
Ultrastructural Studies ◽  
Transmission Electron ◽  
Talaromyces Flavus

Talaromyces flavus is a destructive hyperparasite capable of infecting sclerotia of Sclerotinia sclerotiorum. Examinations of sclerotia by transmission electron microscopy at 3, 7, and 12 days after inoculation revealed that hyphae of T. flavus penetrated the rind cell walls directly. Etching of the cell walls at the penetration site was evident. This suggests that wall-lysing enzymes may be involved in the process of infection. Hyphae of T. flavus grew both intercellularly and intracellularly throughout the rind, cortical, and medullary tissues. Ramification of the hyperparasite in the sclerotium resulted in destruction and collapse of sclerotial tissues.

Penetration of Zea mays by Helminthosporium carbonum

1975 ◽  
Vol 53 (23) ◽  
pp. 2872-2883 ◽  
Author(s):  
Gordon M. Murray ◽  
Douglas P. Maxwell
Keyword(s):  
Electron Microscopy ◽  
Epidermal Cell ◽  
Cell Walls ◽  
Epidermal Cells ◽  
Cell Cytoplasm ◽  
Mesophyll Cells ◽  
Fibrillar Material ◽  
Transmission Electron ◽  
Corn Plants ◽  
Resistant Genotypes

Light microscopy showed that on corn leaves, 81–93% of appressoria of Helminthosporium carbonum races I and II are formed over junctions of epidermal cells. During the early stages of penetration of corn plants resistant and susceptible to race I, 63–83% of appressoria have an epidermal cell nucleus within 10 μm. Transmission electron microscopy of race II on inbred W187R showed that appressoria are attached to the cuticle by fibrillar material. Vesicles are present in the appressorium at the site of cuticle penetration and initial cuticle penetration appears to be enzymic; subsequent rupture may be mechanical as the penetration peg widens. A septum forms between the appressorium and the subcuticular hyphae. Epidermal cell cytoplasm is thicker beneath penetration sites than elsewhere under the epidermal wall. Changes in epidermal cytoplasm were observed 8 h after inoculation; by 18 h epidermal cells beneath subcuticular hyphae have electron-opaque contents. Hyphae are mainly subcuticular up to 48 h after inoculation, and underlying epidermal and mesophyll cells are frequently collapsed. Results indicate that H. carbonum races I and II have similar initial reactions on susceptible and resistant genotypes and that penetration occurs by degradation of the cuticle and host cell walls.

Vesicular system associated with spermiogenesis of bullfrog

1987 ◽  
Vol 45 ◽  
pp. 818-819
Author(s):  
K. C. Liu ◽  
S. F. Tsay
Keyword(s):  
Electron Microscopy ◽  
Microscopic Study ◽  
Electron Microscopic Study ◽  
Reproductive System ◽  
Seminiferous Tubule ◽  
Rana Catesbeiana ◽  
Routine Procedure ◽  
Electron Microscopic ◽  
Twisted Tubules ◽  
Electron Lucent

In the histologic and electron microscopic study of the male reproductive system of bullfrog, Rana catesbeiana, a vesicular system associated with spermiogenesis was observed. It appeared in the lumenal space of the seminiferous tubule (Fig. 1), in the heads of spermatids (Fig. 2), associated with the chromatins of the spermatid (Fig. 4). As deduced from sections, this vesicular system consisted of vesicles of various size or a large group of waving and twisted tubules (Fig. 3), After routine procedure of treatment for electron microscopy, the lumens of both of the vesicles and tubules were electron lucent.In human, vesicles and vesicular system associated with reproductive cell and tissue were reported. In abnormal spermiogenesis, flower-like body, actually vesicles, and giant vesicle associated with the head of spermatid were observed. In both cases the number of vesicle was limited from a single one to a few.

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).

Actinomycetes in discolored wood of living silver maple

1981 ◽  
Vol 59 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Robert A. Blanchette ◽  
John B. Sutherland ◽  
Don L. Crawford
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Carbon Source ◽  
Cell Walls ◽  
Hydroxybenzoic Acid ◽  
Liquid Media ◽  
Streptomyces Strain ◽  
Culture Techniques ◽  
Silver Maple ◽  
Scanning Electron

The greenish-brown margin of discolored wood in three living silver maple trees, Acer saccharinum L., was examined by scanning electron microscopy and microbiological culture techniques. Micrographs of xylem vessels revealed filamentous structures; some of them appeared to be actinomycetous hyphae. Actinomycetes identified as Streptomyces parvullus Waksman & Gregory, S. sparsogenes Owen, Dietz & Camiener, and a third Streptomyces strain were isolated repeatedly from discolored wood of each tree. These isolates grew in liquid media in the presence of 0.1% (w/v) concentrations of several phenols. Although other phenols included in the test were not substantially degraded, p-hydroxybenzoic acid was utilized as a carbon source by S. parvullus. All three actinomycetes inhibited growth of selected wood-inhabiting fungi when paired on malt agar. When inoculated on sterilized sapwood and discolored wood from silver maple, the actinomycetes colonized vessel walls and occlusions, but were not observed to decay cell walls.

scholarly journals THE INCORPORATION OF RADIOACTIVE PROLINE INTO CULTURED CELLS

1968 ◽  
Vol 39 (3) ◽  
pp. 698-715 ◽  
Author(s):  
H. W. Israel ◽  
M. M. Salpeter ◽  
F. C. Steward
Keyword(s):  
Electron Microscopy ◽  
Cell Walls ◽  
Plant Cell Wall ◽  
Cultured Cells ◽  
Initial Period ◽  
Special Problem ◽  
General Concept ◽  
Cell Wall Protein ◽  
Quiescent Cells ◽  
Growth Induction

Cultured carrot explants, stimulated to grow rapidly in a medium containing coconut milk, were labeled with radioactive proline. After an initial period of absorption (8 hr for proline-3H; 24 hr for proline-14C) the tissue was allowed to grow for a further period of 6 days in a similar medium free from the radioactivity. Samples were prepared for electron microscopy and radioautography at the end of the absorption period and also after the further growth. The distribution of the products from the radioactive proline in the cells is shown by high-resolution radioautography and is rendered quantitative for the different regions of the cells. The results show that the combined label, which was present in the form of proline and the hydroxyproline derived from it, was all in the protoplasm, not in the cell walls. Any combined label that appeared to be over the cell walls is shown to be due to scatter from adjacent cytoplasmic sites. Initially the radioactivity was concentrated in nuclei, even more so in nucleoli, but it subsequently appeared throughout the ground cytoplasm and was also concentrated in the plastids. The significance of these observations for the general concept of a plant cell wall protein and for the special problem of growth induction in otherwise quiescent cells is discussed.

scholarly journals Co-operative action by endo- and exo-β-(1→3)-glucanases from parasitic fungi in the degradation of cell-wall glucans of Sclerotinia sclerotiorum (Lib.) de Bary

1974 ◽  
Vol 140 (1) ◽  
pp. 47-55 ◽  
Author(s):  
David Jones ◽  
Alex. H. Gordon ◽  
John S. D. Bacon
Keyword(s):  
Cell Wall ◽  
Sclerotinia Sclerotiorum ◽  
Culture Filtrate ◽  
Cell Walls ◽  
Trichoderma Viride ◽  
Major Constituent ◽  
Coniothyrium Minitans ◽  
Parasitic Fungi ◽  
Complete Breakdown

1. Two fungi, Coniothyrium minitans Campbell and Trichoderma viride Pers. ex Fr., were grown on autoclaved crushed sclerotia of the species Sclerotinia sclerotiorum, which they parasitize. 2. in vitro the crude culture filtrates would lyse walls isolated from hyphal cells or the inner pseudoparenchymatous cells of the sclerotia, in which a branched β-(1→3)-β-(1→6)-glucan, sclerotan, is a major constituent. 3. Chromatographic fractionation of the enzymes in each culture filtrate revealed the presence of several laminarinases, the most active being an exo-β-(1→3)-glucanase, known from previous studies to attack sclerotan. Acting alone this brought about a limited degradation of the glucan, but the addition of fractions containing an endo-β-(1→3)-glucanase led to almost complete breakdown. A similar synergism between the two enzymes was found in their lytic action on cell walls. 4. When acting alone the endo-β-(1→3)-glucanase had a restricted action, the products including a trisaccharide, tentatively identified as 62-β-glucosyl-laminaribiose. 5. These results are discussed in relation to the structure of the cell walls and of their glucan constituents.

Review — The Orientation of Cellulose Microfibrils in the cell walls of Tracheids in Conifers

IAWA Journal ◽  
2005 ◽  
Vol 26 (2) ◽  
pp. 161-174 ◽  
Author(s):  
Hisashi Abe ◽  
Ryo Funada
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Outer Layer ◽  
Cell Walls ◽  
Secondary Wall ◽  
Middle Layer ◽  
Cellulose Microfibrils ◽  
Conifer Species ◽  
Predominant Orientation ◽  
Scanning Electron

We examined the orientation of cellulose microfibrils (Mfs) in the cell walls of tracheids in some conifer species by field emission-scanning electron microscopy (FE-SEM) and developed a model on the basis of our observations. Mfs depositing on the primary walls in differentiating tracheids were not well-ordered. The predominant orientation of the Mfs changed from longitudinal to transverse, as the differentiation of tracheids proceeded. The first Mfs to be deposited in the outer layer of the secondary wall (S1 layer) were arranged as an S-helix. Then the orientation of Mfs changed gradually, with rotation in the clockwise direction as viewed from the lumen side of tracheids, from the outermost to the innermost S1 layer. Mfs in the middle layer of the secondary wall (S2 layer) were oriented in a steep Z-helix with a deviation of less than 15° within the layer. The orientation of Mfs in the inner layer of the secondary wall (S3 layer) changed, with rotation in a counterclockwise direction as viewed from the lumen side, from the outermost to the innermost S3 layer. The angle of orientation of Mfs that were deposited on the innermost S3 layer varied among tracheids from 40° in a Z-helix to 20° in an S-helix.

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