The development and zoospore ultrastructure of a polycentric chytridiomycete gut fungus, Orpinomyces joyonii comb.nov.

1991 ◽  
Vol 69 (3) ◽  
pp. 580-589 ◽  
Author(s):  
Jinliang Li ◽  
I. Brent Heath ◽  
K.-J. Cheng
Keyword(s):  
Electron Microscopy ◽  
Distribution Pattern ◽  
Key Words ◽  
Light And Electron Microscopy ◽  
General Morphology ◽  
Organelle Distribution ◽  
Central Nuclei

Orpinomyces bovis, a polycentric gut fungus isolated from a steer, was examined with both light and electron microscopy and renamed Orpinomyces joyonii comb.nov. on the basis of its general morphology and zoospore ultrastructure. The multinucleate rhizomycelium is extensively branched, and sporangia form exogenously on branched or unbranched sporangiophores. The organelles in the zoospores have a distribution pattern typical of other gut fungi, i.e., anterior ribosomal aggregates, central nuclei, and posterior presumptive hydrogenosomes. The perikinetosomal apparatus in O. joyonii is comparable to that in monocentric gut fungi but with minor variations. New details of the posterior dome are described. It contains highly ordered specialized lamellae, peripheral granules, and megatubules. Microtubules intersect the dome predominantly at approximately right angles to its surface; this differs from monocentric gut fungi, in which microtubules form a posterior fan running parallel to the dome. We suggest that both monocentric and polycentric gut fungi are monophyletic, since both have a similar, distinctive perikinetosomal apparatus, posterior dome, and organelle distribution pattern. Key words: Orpinomyces joyonii, gut fungi, ultrastructure, posterior dome, perikinetosomal apparatus.

Piromyces mae and Piromyces dumbonica, two new species of uniflagellate anaerobic chytridiomycete fungi from the hindgut of the horse and elephant

1990 ◽  
Vol 68 (5) ◽  
pp. 1021-1033 ◽  
Author(s):  
Jinliang Li ◽  
I. Brent Heath ◽  
Tom Bauchop
Keyword(s):  
Electron Microscopy ◽  
New Species ◽  
Key Words ◽  
General Model ◽  
Light And Electron Microscopy ◽  
Limited Range ◽  
Organelle Distribution ◽  
Two New Species

Vegetative thalli, developing sporangia, and zoospores of two new uniflagellate anaerobic chytridiomycete gut fungi, Piromyces mae sp. nov. and Piromyces dumbonica sp.nov., isolated from manure derived from the hindgut of the horse and elephant, respectively, were examined by light and electron microscopy. Piromyces mae differs from Piromyces communis by having papillae-like structures on the sporangium. Piromyces dumbonica differs from P. communis by its C-shaped elongated circumflagellar ring and characteristic organelle distribution in the zoospores. The circumflagellar rings in both new species are tilted at about 10° towards the spur in both prereleased and free zoospores. Three struts in both species connect the circumflagellar ring to the skirt and connective (a newly described perikinetosomal structure) surrounding the kinetosome opposite to the skirt. The connective interconnects the strut, skirt, scoop, kinetosome, and spur. A general model of the kinetosome and perikinetosomal apparatus is proposed for the gut fungi. This model attempts to unify and clarify previous descriptions of the apparatus in these fungi and shows the limited range of variations reported. Key words: gut fungi, Chytridiomycetes, kinetosomes, perikinetosomal apparatus.

Development of wheat (Triticum aestivum) pollen wall before and after effect of a gametocide

1990 ◽  
Vol 68 (11) ◽  
pp. 2509-2516 ◽  
Author(s):  
Gamal A. El-Ghazaly ◽  
William A. Jensen
Keyword(s):  
Electron Microscopy ◽  
Triticum Aestivum ◽  
Key Words ◽  
Light And Electron Microscopy ◽  
Pollen Grains ◽  
Pollen Wall ◽  
Seed Plants ◽  
Before And After ◽  
After Effect

Light and electron microscopy studies show that pollen wall development in plants treated with the gametocide RH0007 and untreated plants was similar until the stage at which sporopollenin is normally deposited on the wall. At this stage, the pollen wall of treated plants is 80% thinner than that of the control. Shortly after this stage, the pollen grains in the treated plants collapse and abort. We conclude that the gametocide clearly acts through the inhibition of sporopollenin formation, which results in pollen death. As sporopollenin is found only in the pollen wall of seed plants and the spores of nonseed plants, harm to other parts of the plant is not expected to occur. Key words: pollen wall development, Triticum aestivum, gametocide.

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.

Vestibular Ganglion of the Squirrel Monkey

1982 ◽  
Vol 91 (1) ◽  
pp. 44-52 ◽  
Author(s):  
César D. Fermin ◽  
Makoto Igarashi
Keyword(s):  
Electron Microscopy ◽  
Squirrel Monkey ◽  
Myelin Sheath ◽  
Ganglion Cells ◽  
Light And Electron Microscopy ◽  
Squirrel Monkeys ◽  
Saimiri Sciureus ◽  
General Morphology ◽  
Outermost Surface ◽  
Large Neurons

The vestibular ganglia of adult squirrel monkeys (Saimiri sciureus) were studied with the aid of light and electron microscopy. The vestibular ganglia are formed by small and large neurons (perikarya). The perikarya's outermost surface is surrounded by 2–20 lamellae of compact myelin. The compact myelin sheath varies its thickness around one perikaryon. The sheath generally thins out in the vicinity of the axon hillock. Occasionally, the compact myelin transforms completely into loose myelin for a length of 2–5 μ. Two to eight lamellae of loose myelin usually face the cytoplasm of the neurons. This myelin arrangement is constant in the majority of the cells examined regardless of shape and/or size. Large myelinated perikarya form the majority of the ganglion cells. There are, however, a few neurons that lack a true compact myelin sheath. Others are surrounded by very few lamellae of loose myelin. The general morphology of the neurons was compared to the available literature on other species. Possible variation on the myelination pattern due to fixation differences, and variation on perikaryal size due to the angle of cut and irregular shape of the cells are also discussed.

The Morphology of Vacuolated Cells in the Liver Following Administration of Vitamin A.

1973 ◽  
Vol 31 ◽  
pp. 408-409
Author(s):  
Odell T. Minick ◽  
Hidejiro Yokoo ◽  
Fawzia Batti
Keyword(s):  
Electron Microscopy ◽  
Body Weight ◽  
Vitamin A ◽  
Light And Electron Microscopy ◽  
Liver Cells ◽  
Prominent Feature ◽  
Vascular Space ◽  
Vacuolated Cell ◽  
Vacuolated Cells ◽  
Vacuolated Cytoplasm

Vacuolated cells in the liver of young rats were studied by light and electron microscopy following the administration of vitamin A (200 units per gram of body weight). Their characteristics were compared with similar cells found in untreated animals.In rats given vitamin A, cells with vacuolated cytoplasm were a prominent feature. These cells were found mostly in a perisinusoidal location, although some appeared to be in between liver cells (Fig. 1). Electron microscopy confirmed their location in Disse's space adjacent to the sinusoid and in recesses between liver cells. Some appeared to be bordering the lumen of the sinusoid, but careful observation usually revealed a tenuous endothelial process separating the vacuolated cell from the vascular space. In appropriate sections, fenestrations in the thin endothelial processes were noted (Fig. 2, arrow).

Control of Autogenous Vein Grafts Prior to Reimplantation, By Electron Microscopy

1972 ◽  
Vol 30 ◽  
pp. 106-107
Author(s):  
John H. L. Watson ◽  
John L. Swedo ◽  
M. Vrandecic
Keyword(s):  
Electron Microscopy ◽  
Light And Electron Microscopy ◽  
Physiological Saline ◽  
Experimental Conditions ◽  
Vein Grafts ◽  
Arterial Blood ◽  
Saphenous Veins ◽  
Autogenous Vein ◽  
Control Of Parameters ◽  
Post Implantation

The ambient temperature and the nature of the storage fluids may well have significant effects upon the post-implantation behavior of venus autografts. A first step in the investigation of such effects is reported here. Experimental conditions have been set which approximate actual operating room procedures. Saphenous veins from dogs have been used as models in the experiments. After removal from the dogs the veins were kept for two hours under four different experimental conditions, viz at either 4°C or 23°C in either physiological saline or whole canine arterial blood. At the end of the two hours they were prepared for light and electron microscopy. Since no obvious changes or damage could be seen in the veins by light microscopy, even with the advantage of tissue specific stains, it was essential that the control of parameters for successful grafts be set by electron microscopy.

Ultrastructure of two neoplasms in culture compared with original biopsies

1984 ◽  
Vol 42 ◽  
pp. 50-51
Author(s):  
Joseph M. Harb ◽  
James T. Casper ◽  
Vlcki Piaskowski
Keyword(s):  
Electron Microscopy ◽  
Tissue Culture ◽  
Biopsy Specimen ◽  
Cultured Cells ◽  
Light And Electron Microscopy ◽  
Human Tumor ◽  
Soft Agar ◽  
Human Tumor Cells ◽  
Morphological Distinction ◽  
Tumor Types

The application of tissue culture and the newer methodologies of direct cloning and colony formation of human tumor cells in soft agar hold promise as valuable modalities for a variety of diagnostic studies, which include morphological distinction between tumor types by electron microscopy (EM). We present here two cases in which cells in culture expressed distinct morphological features not apparent in the original biopsy specimen. Evaluation of the original biopsies by light and electron microscopy indicated both neoplasms to be undifferentiated sarcomas. Colonies of cells propagated in soft agar displayed features of rhabdomyoblasts in one case, and cultured cells of the second biopsy expressed features of Ewing's sarcoma.

The Effect of Vitamin A on the Intermittent Nitrogen Dioxide Gas Exposure in Hamsters

1976 ◽  
Vol 34 ◽  
pp. 176-177
Author(s):  
J.C.S. Kim ◽  
M.G. Jourden ◽  
E.S. Carlisle
Keyword(s):  
Electron Microscopy ◽  
Vitamin A ◽  
Nitrogen Dioxide ◽  
Chronic Exposure ◽  
Light And Electron Microscopy ◽  
Specific Effect ◽  
Deficient Diet ◽  
Intermittent Exposure ◽  
Hypovitaminosis A ◽  
Gas Exposure

Chronic exposure to nitrogen dioxide in rodents has shown that injury reaches a maximum after 24 hours, and a reparative adaptive phase follows (1). Damage occurring in the terminal bronchioles and proximal portions of the alveolar ducts in rats has been extensively studied by both light and electron microscopy (1).The present study was undertaken to compare the response of lung tissue to intermittent exposure to 10 ppm of nitrogen dioxide gas for 4 hours per week, while the hamsters were on a vitamin A deficient diet. Ultrastructural observations made from lung tissues obtained from non-gas exposed, hypovitaminosis A animals and gas exposed animals fed a regular commercially prepared diet have been compared to elucidate the specific effect of vitamin A on nitrogen dioxide gas exposure. The interaction occurring between vitamin A and nitrogen dioxide gas has not previously been investigated.

mRNA localization by Electron microscopic in situ hybridization

1991 ◽  
Vol 49 ◽  
pp. 430-431
Author(s):  
J. A. Pollock ◽  
M. Martone ◽  
T. Deerinck ◽  
M. H. Ellisman
Keyword(s):  
Electron Microscopy ◽  
High Resolution ◽  
Nucleic Acids ◽  
Recombinant Dna ◽  
Light And Electron Microscopy ◽  
Electron Microscopic ◽  
High Voltage Electron Microscopy ◽  
Functional Sites ◽  
Voltage Electron

Localization of specific proteins in cells by both light and electron microscopy has been facilitate by the availability of antibodies that recognize unique features of these proteins. High resolution localization studies conducted over the last 25 years have allowed biologists to study the synthesis, translocation and ultimate functional sites for many important classes of proteins. Recently, recombinant DNA techniques in molecular biology have allowed the production of specific probes for localization of nucleic acids by “in situ” hybridization. The availability of these probes potentially opens a new set of questions to experimental investigation regarding the subcellular distribution of specific DNA's and RNA's. Nucleic acids have a much lower “copy number” per cell than a typical protein, ranging from one copy to perhaps several thousand. Therefore, sensitive, high resolution techniques are required. There are several reasons why Intermediate Voltage Electron Microscopy (IVEM) and High Voltage Electron Microscopy (HVEM) are most useful for localization of nucleic acids in situ.

The Response of Testis Cells to Low Dose X-Irradiation

1981 ◽  
Vol 39 ◽  
pp. 542-543
Author(s):  
D. E. Philpott ◽  
W. Sapp ◽  
C. Williams ◽  
Joann Stevenson ◽  
S. Black
Keyword(s):  
Electron Microscopy ◽  
Stem Cell ◽  
Light Microscopy ◽  
Dose Level ◽  
Cross Sections ◽  
Low Dose ◽  
Light And Electron Microscopy ◽  
Cellular Responses ◽  
Post Irradiation ◽  
X Irradiation

The response of spermatogonial cells to X-irradiation is well documented. It has been shown that there is a radiation resistent stem cell (As) which, after irradiation, replenishes the seminiferous epithelium. Most investigations in this area have dealt with radiation dosages of 100R or more. This study was undertaken to observe cellular responses at doses less than 100R of X-irradiation utilizing a system in which the tissue can be used for light and electron microscopy.Brown B6D2F1 mice aged 16 weeks were exposed to X-irradiation (225KeV; 15mA; filter 0.35 Cu; 50-60 R/min). Four mice were irradiated at each dose level between 1 and 100 rads. Testes were removed 3 days post-irradiation, fixed, and embedded. Sections were cut at 2 microns for light microscopy. After staining, surviving spermatogonia were identified and counted in tubule cross sections. The surviving fraction of spermatogonia compared to control, S/S0, was plotted against dose to give the curve shown in Fig. 1.

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