An electron microscope study of initiation of infection by conidia of Harposporium oxycoracum, an endozoic nematophagous Hyphomycete

1983 ◽  
Vol 61 (3) ◽  
pp. 893-898 ◽  
Author(s):  
Masatoshi Saikawa ◽  
Junko Totsuka ◽  
Chiharu Morikawa
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Electron Microscope ◽  
Electron Microscope Study ◽  
Germ Tube ◽  
Ruthenium Red ◽  
Convex Side ◽  
En Bloc ◽  
Dense Mass ◽  
Ultrathin Sections

Infective conidia of an endozoic nematophagous hyphomycete, Harposporium oxycoracum Drechsler, were examined by means of electron microscopy. Each of the conidia is very narrow and has a sharply pointed distal and slightly swollen basal end. The swollen basal end was shown, in ultrathin sections stained with ruthenium red en bloc, to be an electron-dense mass of fibrils (ca. 2–3 μm in diameter). The fibrils, thought to be derived from the conidial cell wall, were densely aggregated and were surrounded by a network of more sparsely aggregated fibrils spreading from the fibrous mass of the conidial base. The spreading fibrils seemed to correspond to the mucous droplet observed under the light microscope. It was also found in the present study that the conidia of the fungus were swallowed by nematodes into their lower gut. On germination in the lower gut, a narrow germ tube 5–6 μm wide developed from the convex side of the conidium and produced a simple pore septum at the site of penetration to delimit the empty conidium.

An electron microscope study of Meria coniospora, an endozoic nematophagous Hyphomycete

1982 ◽  
Vol 60 (10) ◽  
pp. 2019-2023 ◽  
Author(s):  
Masatoshi Saikawa
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Germ Tube ◽  
Nematophagous Fungus ◽  
Mucous Layer ◽  
Ultrathin Sections

Conidia of Meria coniospora Drechsler, an endozoic nematophagous fungus, were examined by electron microscopy at various stages of infection. The conidia are almost conical in shape and develop a knoblike structure at the apical end. Ultrathin sections show that the knob is always covered with a mucous layer, which is composed of a number of radiating fibrils. Attachment to the nematode's integument is by means of this fibrillose layer. The germ tube from the bud grows between the conidium and nematode and forms a tiny infection bladder in the integument.

scholarly journals THE FINE STRUCTURE OF CHONDROCOCCUS COLUMNARIS

1967 ◽  
Vol 35 (1) ◽  
pp. 37-51 ◽  
Author(s):  
Jack L. Pate ◽  
Erling J. Ordal
Keyword(s):  
Cell Wall ◽  
Plasma Membrane ◽  
Fine Structure ◽  
Electron Microscope ◽  
Outer Membrane ◽  
Electron Microscope Study ◽  
Ruthenium Red ◽  
Gliding Motility ◽  
Dense Layer ◽  
Adhesive Properties

An electron microscope study of the myxobacterium Chondrococcus columnaris has revealed the following structures in the peripheral layers of the cells: (1) a plasma membrane, (2) a single dense layer (probably the mucopeptide component of the cell wall), (3) peripheral fibrils, (4) an outer membrane, and (5) a material coating the surfaces of the cells which could be stained with the dye ruthenium red.The ruthenium red-positive material is probably an acid mucopolysaccharide and may be involved in the adhesive properties of the cells. The outer membrane and plasma membrane both have the appearance of unit membranes: an electron-translucent layer sandwiched between two electron-opaque layers. The peripheral fibrils span the gap between the outer membrane and the mucopeptide layer, a distance of about 100 A, and run parallel to each other along the length of the cell. The fibrils appear to be continuous across the ends of the cells. The location of these fibrillar structures suggests that they may play a role in the gliding motility of these bacteria.

scholarly journals STUDIES ON THE BIOCHEMISTRY AND FINE STRUCTURE OF SILICA SHELL FORMATION IN DIATOMS

1965 ◽  
Vol 24 (1) ◽  
pp. 39-55 ◽  
Author(s):  
B. E. F. Reimann ◽  
Joyce C. Lewin ◽  
B. E. Volcani
Keyword(s):  
Cell Wall ◽  
Organic Material ◽  
Hydrofluoric Acid ◽  
Electron Microscope Study ◽  
Silica Shell ◽  
Ruthenium Red ◽  
Enzyme Treatment ◽  
Shell Formation ◽  
Mechanical Method ◽  
Ultrathin Sections

An electron microscope study on the cell wall of the diatom Cylindrotheca fusiformis was carried out using stereoscopic and sectioning techniques. Material prepared by an enzyme treatment or by a mechanical method showed that the wall consists of two major components: a silica shell and organic material. Vapor of hydrofluoric acid was employed to remove the silica and thereby reveal the arrangement of the organic material. An attempt was made to increase the contrast of the organic component by "staining." Uranylacetate not only increased the electron opacity of the organic material but also apparently decreased the electron opacity of the silica shell. In ultrathin sections of complete cells, the structure as revealed by stereoscopy could be confirmed and extended. Every part of the silica shell is tightly enclosed by organic material. In the valve region the silica enclosed in this way is located between other layers of organic material. The whole cell wall is surrounded by a mucilaginous substance which stains with ruthenium red.

Electron microscopy of an endoparasitic fungus, Gonimochaete pyriforme, infecting nematodes

1985 ◽  
Vol 63 (12) ◽  
pp. 2326-2331 ◽  
Author(s):  
Masatoshi Saikawa ◽  
Takashi Anazawa
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Electron Density ◽  
Germ Tube ◽  
Adhesive Layer ◽  
Ruthenium Red ◽  
Ruthenium Red Staining ◽  
Dense Vesicles

Gonimochaete pyriforme Barron was studied using the electron microscope. Protoplasm in the pyriform-shaped aplanospore is filled with electron-dense vesicles (0.1–0.3 μm) except at the base where it is vacuolated. The globose knob at the apical end of the spore is covered with a very thin adhesive layer (ca. 0.1 μm) whose electron density is slightly enhanced by ruthenium red staining but which does not show a fibrillose appearance. After attachment to the nematode's cuticle, a narrow germ tube (0.15 μm) arises from the globose knob and penetrates through the adhesive layer and the host's cuticle into the nematode body. The adhesive knob of the aplanospore in G. pyriforme is very similar in ultrastructure to the encysted zoospore of Myzocytium humicola Barron and Percy in the Lagenidiales after the cyst has germinated.

Platinum Compounds as Stains for Electron Microscopy

1974 ◽  
Vol 32 ◽  
pp. 230-231
Author(s):  
S. K. Aggarwal ◽  
P. McAllister ◽  
R. W. Wagner ◽  
B. Rosenberg
Keyword(s):  
Electron Microscopy ◽  
Hela Cells ◽  
Uranyl Acetate ◽  
Sarcoma 180 ◽  
Platinum Compounds ◽  
Kb Cells ◽  
En Bloc ◽  
Human Lymphoma ◽  
Ultrathin Sections ◽  
Blue Coloration

Uranyl acetate has been used as an electron stain for en bloc staining as well as for staining ultrathin sections in conjunction with various lead stains (Fig. 1). Present studies reveal that various platinum compounds also show promise as electron stains. Certain platinum compounds have been shown to be effective anti-tumor agents. Of particular interest are the compounds with either uracil or thymine as one of the ligands (cis-Pt(II)-uracil; cis-Pt(II)-thymine). These compounds are amorphous, highly soluble in water and often exhibit an intense blue coloration. These compounds show enough electron density to be used as stains for electron microscopy. Most of the studies are based on various cell lines (human AV, cells, human lymphoma cells, KB cells, Sarcoma-180 ascites cells, chick fibroblasts and HeLa cells) while studies on tissue blocks are in progress.

Electron Microscope Study of RNA's of Paramyxoviruses

1972 ◽  
Vol 30 ◽  
pp. 196-197
Author(s):  
Ruchama Baum ◽  
J.T. Seto
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Electron Microscope Study ◽  
Sendai Virus ◽  
Sodium Dodecyl ◽  
Rna Molecules ◽  
Virus Particles ◽  
Molecular Weights ◽  
Length Measurements

The ribonucleic acid (RNA) of paramyxoviruses has been characterized by biochemical and physiochemical methods. However, paramyxovirus RNA molecules have not been studied by electron microscopy. The molecular weights of these single-stranded viral RNA molecules are not known as yet. Since electron microscopy has been found to be useful for the characterization of single-stranded RNA, this investigation was initiated to examine the morphology and length measurements of paramyxovirus RNA's.Sendai virus Z strain and Newcastle disease virus (NDV), Milano strain, were used. For these studies it was necessary to develop a method of extracting RNA molecules from purified virus particles. Highly purified Sendai virus was treated with pronase (300 μg/ml) at 37°C for 30 minutes and the RNA extracted by the sodium dodecyl sulfate (SDS)-phenol procedure.

scholarly journals An Electron Microscope Study of Basophile Substances of Frozen-Dried Rat Liver

1958 ◽  
Vol 4 (3) ◽  
pp. 291-300 ◽  
Author(s):  
Henry Finck
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Rat Liver ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Freeze Drying ◽  
Light And Electron Microscopy ◽  
Enzyme Treatment ◽  
Dense Granules ◽  
Homogeneous Matrix

Small pieces of liver from rats subjected to different dietary regimes were fixed by freeze-drying, and postfixed by in vacuo heating and denaturation with alcohol. Specimens were digested with ribo- or deoxyribonuclease, and stained with gallocyanin-chromalum, azure II, the Feulgen procedure or alcoholic platinic tetrabromide. Some specimens were reserved as controls of the effects of enzyme treatment. Stained and unstained specimens were embedded in methacrylate and examined by light and electron microscopy. Basophilic and Feulgen-positive substances, after contact with watery reagents, were found by electron microscopy to exist as small dense granules embedded in a less dense homogeneous matrix, forming the walls of submicroscopic vacuoles. These granules were absent after digestion with nucleodepolymerases. In specimens (unstained, or stained with platinic tetrabromide) which had not passed through water, the dense (basophile) substances in nuclei and cytoplasm were found to exist, not as granules, but as ill defined submicroscopic concentrates which blended imperceptibly into the homogeneous matrix of the vacuolar walls. Objections to the use of stains for improving contrast conditions in electron microscopy of tissues are discussed, and it is concluded that the reagents do not necessarily produce the observed increases in contrast by selectively stabilizing certain structures. The concept of microsomes as pre-existing distinct morphological entities in intact (unhomogenized) cells is thought to be inconsistent with the distribution of basophile substances in frozen-dried liver.

scholarly journals ELECTRON MICROSCOPY OF THE NUCLEAR MEMBRANE OF AMOEBA PROTEUS

1956 ◽  
Vol 2 (4) ◽  
pp. 445-448 ◽  
Author(s):  
Marie H. Greider ◽  
Wencel J. Kostir ◽  
Walter J. Frajola
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Nuclear Membrane ◽  
Outer Layer ◽  
Microscope Study ◽  
Electron Microscope Study ◽  
Cell Types ◽  
Amoeba Proteus ◽  
Nuclear Membranes ◽  
Thin Sectioning

An electron microscope study of the nuclear membrane of Amoeba proteus by thin sectioning techniques has revealed an ultrastructure in the outer layer of the membrane that is homologous to the pores and annuli observed in the nuclear membranes of many other cell types studied by these techniques. An inner honeycombed layer apparently unique to Amoeba proteus is also described.

Electron microscopy of the replicative events of A25 bacteriophages in group A streptococci

1972 ◽  
Vol 18 (1) ◽  
pp. 93-96 ◽  
Author(s):  
S. E. Read ◽  
R. W. Reed
Keyword(s):  
Electron Microscopy ◽  
Cell Wall ◽  
Electron Microscope ◽  
Nucleic Acid ◽  
Group A Streptococcus ◽  
Group A Streptococci ◽  
Virulent Phage ◽  
Acid Pool ◽  
Group A ◽  
A Cell

The replicative events of a virulent phage (A25) infection of a group A Streptococcus (T253) were studied using the electron microscope. The first intracellular evidence of phage replication in a cell occurred 30 min after infection with arrest of cell division and increase in the nucleic acid pool. Phage heads were evident in the nucleic acid pool of the cells 45 min after infection. Release of phages occurred by splitting of the cell wall along discrete lines. This appeared to be at sites of active wall synthesis, i.e., near the region of septum formation. Many phage components were released but relatively few complete phages indicating a relatively inefficient replicative system.

scholarly journals AN ELECTRON MICROSCOPE STUDY OF THE EMBRYOLOGY OF THE INTERCALATED DISC IN THE HEART OF THE RABBIT

1957 ◽  
Vol 3 (2) ◽  
pp. 193-202 ◽  
Author(s):  
Alan R. Muir
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Cardiac Muscle ◽  
Microscope Study ◽  
Light Microscope ◽  
Electron Microscope Study ◽  
Muscle Cells ◽  
Intercalated Disc ◽  
Adult Cell ◽  
Embryonic Muscle

Prenatal and postnatal cardiac muscle from rabbits has been studied by electron microscopy, after osmium fixation and methacrylate embedding. The observations showed that 1. Cell membranes divide the muscle into cellular units from the youngest embryo which was studied (9½ days after coitus) until the adult state. 2. The embryonic muscle cells contain only one nucleus, whereas the adult cell may be multinucleated. 3. At all stages of development, wherever a myofibrillar axis crosses a cellular boundary, the myofilaments are interrupted by an intercalated disc. 4. With age, increase in size and complexity of the discs render them recognisable by the light microscope.

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