Light and electron microscopy studies on the infection of tomato fruits by Botrytis cinerea

1980 ◽  
Vol 58 (12) ◽  
pp. 1394-1404 ◽  
Author(s):  
F.H. J. Rijkenberg ◽  
G. T. N. De Leeuw ◽  
K. Verhoeff
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Host Cell ◽  
Botrytis Cinerea ◽  
Light And Electron Microscopy ◽  
Microscopy Study ◽  
Wall Material ◽  
Wall Thickening ◽  
Cell Organelles ◽  
Tomato Fruits

A light microscopy study of the host–parasite relationship of Botrytis cinerea on immature tomato fruits was combined with an electron microscopy examination. Both techniques indicate that the cuticle is dissolved enzymatically rather than ruptured mechanically. Inter- and intracellular hyphae have no apparent effect on the cuticle, but do break down wall material. If the penetration tube development is arrested after emerging from the cuticle into the wall, wall discolouration and wall thickening become evident and a considerable increase in host cell organelles below the penetration site is observed. A papilla is also apposited. At successful penetration, when the hypha emerges from the cell wall into the host cell, little cell wall discolouration at the infection site is evident, but the cytoplasm becomes degenerate. Further hyphal extension then occurs in the epidermis, killing more epidermal cells, and leading to collapse, but not penetration, of underlying tissue.

Light and electron microscopy of the host–fungus interaction in the achlorophyllous gametophyte of Botrychium lunaria

1994 ◽  
Vol 72 (2) ◽  
pp. 182-188 ◽  
Author(s):  
E. Schmid ◽  
F. Oberwinkler
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Key Words ◽  
Host Cell ◽  
Matrix Material ◽  
Light And Electron Microscopy ◽  
Thick Layer ◽  
Fungal Endophyte ◽  
Host Fungus ◽  
Translucent Material

The host–fungus interaction between the achlorophyllous gametophyte of Botrychium lunaria and its fungal endophyte was studied by means of light and electron microscopy. Aseptate hyphae with a multilayered cell wall formed intracellular coils. The interface consisted of a thick layer of fibrillar matrix material, an electron-translucent zone, and the host plasmalemma. Several vesicles that show different stages of development and degeneration occurred within one host cell. Degenerating vesicles were encased by large amounts of an electron-translucent material. Arbuscules were not observed. The fungus did not infect the young sporophyte but degenerated within intact gametophyte cells. Key words: Botrychium lunaria, gametophyte, mycorrhiza, ultrastructure.

A cytological study of the development of Erysiphe graminis in its host barley, as influenced by the two fungicides ethirimol and propiconazole

1990 ◽  
Vol 68 (12) ◽  
pp. 2618-2628 ◽  
Author(s):  
Annerose Heller ◽  
Friedrich Grossmann ◽  
Burkhard Frenzel ◽  
Sigrun Hippe
Keyword(s):  
Electron Microscopy ◽  
Host Cell ◽  
Light And Electron Microscopy ◽  
Unknown Origin ◽  
Erysiphe Graminis ◽  
Dense Material ◽  
Ultrastructural Changes ◽  
Wall Thickening ◽  
Electron Dense Material ◽  
Host Parasite

Light and electron microscopy of barley epidermal cells treated with ethirimol or propiconazole and then inoculated with Erysiphe graminis f. sp. hordei showed the complex reaction of this host–parasite system to fungicides. The completely different biochemical modes of action of the two fungicides were reflected in the ultrastructural changes observed. Specific fungicidal effects could be distinguished from degenerative processes associated with senescence of untreated plants. For ethirimol, the first changes to be observed in the nucleus were blebbing of the outer nuclear membrane, invaginations into the nucleoplasm, and loss of the dark-staining material of nuclear pores. Later on, large areas of the cytoplasm were devoid of ribosomes. Moreover, electron-dense material was found in the perinuclear space and in cisternae of the endoplasmic reticulum. Round bodies, containing electron-dense material of unknown origin, appeared in the cytoplasm. Propiconazole, on the other hand, caused severe malformations of haustoria, host cell wall appositions, and wall thickening. The sheaths surrounding the haustoria were significantly enlarged, and vesicular and multivesicular bodies appeared in the extrahaustorial matrix. In later stages, degenerated haustoria were partially encapsulated by the host cell. Large, rectangular, electron-opaque structures, termed Fibrosinkörper, were observed in secondary hyphae. Both fungicides tested caused swelling of secondary hyphae. Key words: Erysiphe graminis f.sp. hordei, ethirimol, propiconazole, host–parasite system, cytology, electron microscopy.

scholarly journals Light and electron microscopy study of late embryonic development in the land snail Limicolaria flammea (Müller) (Pulmonata, Achatinidae)

2007 ◽  
Vol 24 (2) ◽  
pp. 436-441 ◽  
Author(s):  
Rosemary I. Egonmwan
Keyword(s):  
Electron Microscopy ◽  
Embryonic Development ◽  
Light And Electron Microscopy ◽  
Microscopy Study ◽  
Land Snail ◽  
Electron Microscopy Study ◽  
Advanced Embryo ◽  
Embryonic Shell ◽  
Advanced Stages ◽  
Late Stages

The late stages of embryogenesis in the achatinid land snail Limicolariaflammea (Müller, 1774) were described using light and electron microscopy. Embryos at various stages of development were present in the eggs during the first hour after they were laid, from 4-cell blastulae to morulae and fairly advanced stages. The advanced embryo which was fully developed on the second day bears a long cephalic sac, first to be developed, attached to the embryo and a podocyst which is attached to the foot of the embryo. Both of these structures are reduced in size as embryogenesis progresses until they finally disappear at about the 7th day after the egg was deposited. The embryonic shell was apparent on the second day and spiral coiling was apparent at about day 5. The spiral shell had one whorl when formed and more spirals were added so that at hatching the young snails had three whorls.

Meningiomas. A Light and Electron Microscopy Study

1981 ◽  
pp. 122-125 ◽  
Author(s):  
Filomeno Tedeschi ◽  
R. Brizzi ◽  
A. Lechi ◽  
G. Trabattoni ◽  
C. Ferrari ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Microscopy Study ◽  
Electron Microscopy Study

Fine structure of Metchnikovella incurvata Caullery and Mesnil 1914 (microsporidia), a hyperparasite of gregarines Polyrhabdina sp. from the polychaete Pygospio elegans

Parasitology ◽  
2013 ◽  
Vol 140 (7) ◽  
pp. 855-867 ◽  
Author(s):  
Y. Y. SOKOLOVA ◽  
G. G. PASKEROVA ◽  
Y. M. ROTARI ◽  
E. S. NASSONOVA ◽  
A. V. SMIRNOV
Keyword(s):  
Electron Microscopy ◽  
Marine Invertebrates ◽  
Light And Electron Microscopy ◽  
Microscopy Study ◽  
Electron Microscopy Study ◽  
Life Cycles ◽  
Single Family ◽  
Host Cytoplasm ◽  
History Of ◽  
Multinuclear Cells

SUMMARYClass Rudimicrosporea Sprague 1977, with its single family Metchnikovellidae, comprises hyperparasites of gregarines from the guts of marine invertebrates. Metchnikovellids remain poorly studied in spite of their significance to the evolutionary history of microsporidia; their ultrastructure and life cycles require further investigation. Here we present results of the light- and electron-microscopy study of Metchnikovella incurvata Caulleri and Mesnil 1914, isolated from lecudinid gregarines, parasitizing polychaetes Pygospio elegans in the White Sea littoral zone, and yet described only on the light-microscopic level. The life cycle of this microsporidium includes 2 sporogonies: free (FS) and sac-bound (SBS). In FS, sporonts develop into multinuclear cells (sporogonial plasmodia), which generate sporoblasts and free spores residing in direct contact with the host cytoplasm. Electron microscopy revealed their metchnikovellidean structure: a horseshoe-shaped nucleus, short manubrium perpendicular to the long axis of the spore, and a polar cap in a separate membrane container. Merogony was not observed. The earliest stages of SBS were chains of binucleate cells. They underwent a series of nuclear and cell divisions, produced extracellular envelopes, and split into boomerang-shaped spore sacs, containing up to 16 spores each. Ultrastructure and sizes of sac-bounded spores were similar to those of free-living ones. An amended diagnosis of M. incurvata is provided.

Fine structure of tissue bordering lesions induced by wounding and virus infection

1978 ◽  
Vol 56 (23) ◽  
pp. 2990-2999 ◽  
Author(s):  
G. Faulkner ◽  
Warwick C. Kimmins
Keyword(s):  
Cell Wall ◽  
Fine Structure ◽  
Secondary Cell Wall ◽  
Wall Material ◽  
Wall Thickening ◽  
Pinto Bean ◽  
Local Lesions ◽  
Virus Localization ◽  
Similar Appearance ◽  
Secondary Cell Wall Thickening

Tissue in Phaseolus vulgaris L. cv. Pinto bean bordering local lesions induced by tobacco mosaic virus showed cell wall deposition associated with paramural body formation in a narrow ring of viable cells extending one to three cell diameters around the lesions. Deposition, which led to secondary cell wall thickening, was greatest 3–4 days after inoculation, the time when the lesion stopped expanding. Secondary cell wall thickening, of similar appearance but less pronounced, was seen in tissue bordering local lesions which continued to expand; no significant secondary cell wall thickening was observed in leaves with a nonlocalized infection. Cells bordering mechanical lesions differed markedly in fine structure from cells bordering virus and chemical lesions. It is suggested that the deposition of extra cell wall material in the wall regions of cells bordering fully expanded local lesions is associated with virus localization.

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