Electron microscopy of vesicular-arbuscular mycorrhizae of yellow poplar. III. Host–endophyte interactions during arbuscular development

1975 ◽  
Vol 21 (12) ◽  
pp. 1930-1939 ◽  
Author(s):  
Darrell A. Kinden ◽  
Merton F. Brown
Keyword(s):  
Electron Microscopy ◽  
Arbuscular Mycorrhizae ◽  
Fungal Endophyte ◽  
Host Cells ◽  
Wall Material ◽  
Yellow Poplar ◽  
Transmission Electron ◽  
Abundant Cytoplasm ◽  
Mycorrhizal Roots ◽  
Infected Cells

Scanning- and transmission-electron microscopy were used to examine developing and mature functional arbuscules in mycorrhizal roots of yellow poplar. Arbuscules developed from intracellular hyphae which branched repeatedly upon penetration into the host cells. Intermediate and late stages of development were characterized by the production of numerous, short, bifurcate hyphae throughout the arbuscule. Mature arbuscules exhibited a coralloid morphology which resulted in a considerable increase in the surface area of the endophyte exposed within the host cells. Distinctive ultrastructural features of arbuscular hyphae included osmiophilic walls, nuclei, abundant cytoplasm, glycogen, and numerous small vacuoles. All arbuscular components were enclosed by host wall material and cytoplasm during development and at maturity. In infected cells, host nuclei were enlarged and the cytoplasm associated with the arbuscular branches typically contained abundant mitochondria, endoplasmic reticulum, and proplastids. Ultrastructural observations suggested that nutrient transfer may be predominantly directed toward the fungal endophyte during arbuscular development and while mature arbuscules remain functional.

Electron microscopy of vesicular-arbuscular mycorrhizae of yellow poplar. II. Intracellular hyphae and vesicles

1975 ◽  
Vol 21 (11) ◽  
pp. 1768-1780 ◽  
Author(s):  
Darrell A. Kinden ◽  
Merton F. Brown
Keyword(s):  
Electron Microscopy ◽  
Lipid Droplets ◽  
Arbuscular Mycorrhizae ◽  
Wall Material ◽  
Yellow Poplar ◽  
Cortical Cells ◽  
Dense Bodies ◽  
Vesicular Arbuscular ◽  
Abundant Cytoplasm ◽  
Mycorrhizal Roots

Intracellular hyphae and vesicles in mycorrhizal roots of yellow poplar were examined by electron microscopy. An investing layer of host wall material and cytoplasm enclosed the endophyte within the cells. Young developing hyphae contained abundant cytoplasm and few vacuoles. As hyphae matured, they became highly vacuolated and accumulated carbohydrate (glycogen) and lipid reserves. Mature vesicles were engorged with lipid droplets, possessed a trilaminate wall, and were also enclosed by host wall material and cytoplasm. Compared with uninfected cells, infected cortical cells showed an increase in cytoplasmic volume, enlarged nuclei, and a reduction of starch reserves. Host nuclei were always proximal to the hyphae during hyphal development and deterioration. While other cytoplasmic components of infected and uninfected cells were comparable, large electron-dense bodies occurred in vacuoles of most cells containing hyphae. Deterioration of intracellular hyphae occurred throughout the samples examined. Septa separated functional and degenerating portions of the hyphae. Hyphal deterioration involved degeneration and ultimate disappearance of fungal cytoplasm as well as collapse of hyphal walls. Based on these observations, the authors hypothesize that deterioration of the endophyte may release significant quantities of mineral nutrients, via hyphal contents, which are absorbed by the host.

Electron microscopy of vesicular-arbuscular mycorrhizae of yellow poplar. IV. Host–endophyte interactions during arbuscular deterioration

1976 ◽  
Vol 22 (1) ◽  
pp. 64-75 ◽  
Author(s):  
Darrell A. Kinden ◽  
Merton F. Brown
Keyword(s):  
Electron Microscopy ◽  
Arbuscular Mycorrhizae ◽  
Mineral Nutrients ◽  
Wall Material ◽  
Yellow Poplar ◽  
Cortical Cells ◽  
Morphological Alterations ◽  
Transmission Electron ◽  
Vesicular Arbuscular ◽  
Scanning Electron

Scanning electron stereoscopy and transmission electron microscopy were used to correlate morphological alterations and cytological phenomena associated with deterioration of arbuscules in yellow poplar mycorrhizae. Arbuscular degradation was initiated at the tips of the finest branches and progressed basipetally. Cytoplasm in arbuscular hyphae progressively deteriorated and was followed by collapse of the fungal walls. Degraded portions of the arbuscules aggregated into clumps comprised of host wall material and the distorted fungal walls. Host nuclei, abundant mitochondria, and proplastids were closely associated with arbuscular branches undergoing cytoplasmic deterioration and with clumped portions of the arbuscule which contained degraded hyphal branches. Most of the arbuscules observed had deteriorated to the clumped stage. Some cortical cells contained several clumped arbuscules and nearly mature, intact arbuscules which indicated that reinfection occurs even as degradative phenomena are in progress. It is suggested that substantial quantities of mineral nutrients may be made available to the host via degradation of fungal cytoplasm in the arbuscular hyphae preceding aggregation of degraded hyphae into discrete clumps.

A light and electron microscope study of the fungal endophytes in the sporophyte and gametophyte of Lycopodium cernuum with observations on the gametophyte–sporophyte junction

1992 ◽  
Vol 70 (1) ◽  
pp. 58-72 ◽  
Author(s):  
Jeffrey G. Duckett ◽  
Roberto Ligrone
Keyword(s):  
Root Nodules ◽  
Fungal Endophytes ◽  
Fungal Endophyte ◽  
Peninsular Malaysia ◽  
Epidermal Cells ◽  
Host Cells ◽  
Wall Material ◽  
Intercellular Spaces ◽  
Host Cytoplasm ◽  
Fungal Associations

The ventral epidermal cells of the photosynthetic, surface-living gametophytes of Lycopodium cernuum, collected from moist shaded banks in Peninsular Malaysia, contain an aseptate fungus. In some cells the hyphae are thick walled and form coils encapsulated by a thin layer of host wall material. In others the fungus is thin walled and shows limited differentiation into larger trunk hyphae and arbuscules. The adjacent host cytoplasm, separated from the fungus by a granular interfacial matrix, contains numerous chloroplasts, mitochondria, and microtubules. The hyphae contact the substratum via the ventral walls of the epidermal cells and the rhizoids are free from infection. In the protocorm and root nodules, aseptate hyphae initially colonize mucilage-filled schizogenous intercellular spaces. Subsequent invasion of the host cells is associated with the development of massive overgrowths of host wall material. The fungal associations in L. cernuum share a mixture of attributes otherwise found in different angiosperm mycorrhizae and in mycotrophic relationships in liverworts. Wall ingrowths are present in both the gametophyte and sporophyte cells in the placenta of L. cernuum. The very limited development of the placenta, compared with L. appressum, certain bryophytes and ferns, the diminutive size, and early senescence of the gametophytes of L. cernuum are all linked to the presence of the protocorm. This massive absorptive organ, homologous to a foot, in terms of its position in sporophyte ontogeny, but external to the parent gametophyte, derives its nutrition partly from photosynthesis and partly from its fungal endophyte. Key words: chloroplasts, Lycopodium, mycorrhiza, pteridophytes, root nodules, symbiosis, transfer cells.

Ultrastructure of eastern cottonwood clones susceptible or resistant to leaf rust

1987 ◽  
Vol 65 (8) ◽  
pp. 1586-1598 ◽  
Author(s):  
L. Shain ◽  
U. Järlfors
Keyword(s):  
Electron Microscopy ◽  
Leaf Rust ◽  
Light And Electron Microscopy ◽  
Infection Process ◽  
The Other ◽  
Host Cells ◽  
Eastern Cottonwood ◽  
Melampsora Medusae ◽  
Wall Appositions ◽  
Infected Cells

The infection process in four clones of eastern cottonwood susceptible or resistant to leaf rust caused by Melampsora medusae was studied by light and electron microscopy. Infection was initiated by stomatal rather than direct entry. Typical dikaryotic haustoria were observed in all clones within 1 day of inoculation. Some healthy-appearing haustoria were observed in susceptible clones throughout the duration of the study, which was terminated during the initiation of uredial production. Incompatibility was expressed differently in the two resistant clones. In clone St 75, most haustoria and invaded host cells that were observed appeared necrotic within 2 days of inoculation. Cell wall appositions appeared during this time in cells adjoining necrotic host cells. Some infected cells disintegrated within 4 days of inoculation. Affected host cells of clone St 92, on the other hand, plasmolyzed during the first 2 to 3 days after inoculation. Necrotic host cells were not observed in this clone until the 4th day after inoculation. Hyphal ramification and host plasmolysis were extensive at 6 days after inoculation.

Morphology of infection of onion leaves by Alternaria porri

1994 ◽  
Vol 72 (8) ◽  
pp. 1164-1170 ◽  
Author(s):  
Theresa A. S. Aveling ◽  
Heidi G. Snyman ◽  
F. H. J. Rijkenberg
Keyword(s):  
Electron Microscopy ◽  
Epidermal Cell ◽  
Leaf Surface ◽  
Infection Process ◽  
Mesophyll Cells ◽  
Transmission Electron ◽  
Close Proximity ◽  
Alternaria Porri ◽  
Infected Cells ◽  
Germ Tubes

Conidial germination of Alternaria porri, formation of prepenetration structures, penetration of the onion leaf surface, and the postpenetration processes were studied using light, scanning electron, and transmission electron microscopy. Ninety-six percent of conidia germinated at 25 °C within 24 h of inoculation. Each conidium formed several germ tubes that grew in any direction across the leaf surface. Each germ tube usually terminated in a bulbous appressorium formed directly on the epidermal cell (52.4% of appressoria) or on a stoma (48.6% of appressoria). Following direct penetration of the outer epidermal cell wall or the stoma, bulbous primary hyphae developed below the appressoria. Secondary hyphae developed from the primary hyphae within 48 h after inoculation and grew within the intercellular spaces penetrating mesophyll cells. The changes in ultrastructure of cells in close proximity to hyphae and of infected cells are described. Key words: Allium cepa, electron microscopy, infection process, purple blotch.

Plasmodium falciparum: regional differences in lectin and cationized ferritin binding to the surface of the malaria-infected human erythrocyte

Parasitology ◽  
1986 ◽  
Vol 93 (1) ◽  
pp. 17-32 ◽  
Author(s):  
I. W. Sherman ◽  
Jane R. T. Greenan
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Plasmodium Falciparum ◽  
Uniform Distribution ◽  
Lectin Binding ◽  
Red Cells ◽  
Cationized Ferritin ◽  
Transmission Electron ◽  
Erythrocyte Surface ◽  
Infected Cells

SUMMARYThe distribution of anionic residues on the surface of erythrocytes infected withPlasmodium falciparumwas studied using cationized ferritin (CF) and transmission electron microscopy. CF staining of uninfected erythrocytes or erythrocytes infected with a knobless variant resulted in a dense and uniform distribution of ferritin particles; however, when red cells infected with a knob-inducing variant were exposed to CF, aggregates of ferritin particles were observed in the region of membrane elevation. Lectin binding to the erythrocyte surface was visualized by transmission electron microscopy using ferritin-conjugated lectins and lectin-fetuin-gold. No differences were observed in the lectin-binding patterns of malaria-infected or uninfected erythrocytes using WGA (wheat-germ agglutinin), RCA (ricin), andLimax flavuslectin. In distinct contrast to the uniform distribution of ferritin particles seen with these lectins was the appearance of clusters of ferritin-ConA over the knobby regions. Localized aggregates of ConA were not seen in knob-free areas or on the surface of red cells infected with a knobless variant. No significant differences were found in the agglutination reactions of normal and infected cells with theCancer antennariuslectin specific forO-acylated sialic acids.

The effect of praziquantel on the ultrastructure of Schistosoma margrebowiei

1991 ◽  
Vol 65 (2) ◽  
pp. 79-88 ◽  
Author(s):  
A. H. H. Awad ◽  
A. J. Probert
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Immune System ◽  
Neck Region ◽  
Basal Membrane ◽  
Host Cells ◽  
Time Intervals ◽  
Entire Surface ◽  
Transmission Electron ◽  
Severe Erosion

ABSTRACTThe effect of various concentrations of praziquantel at different time intervals post-treatment on the ultrastructure of Schistosoma margrebowiei using scanning and transmission electron microscopy has been examined. The major changes involved blebbing of the entire surface tegument of both sexes (although more marked in males) together with vacuolation of the basal membrane accompanied by the development of membraneous whorls. These effects were progressively more marked with increased concentration and time of exposure resulting in severe erosion of the tubercles and collapse of the sensory organelles. Exposure of the underlying tegumental tissue resulted and paralysis and contraction of the suckers and neck region was apparent. Disruption of the subtegumental musculature and the appearance of vacuolation and membraneous whorl formation were seen. The gastrodermis was similarly affected and the S4 cells of the vitelline gland showed protein disruption of the vitelline droplets. Host cells were seen adhering to the surface of the worms following drug treatment and the synergism between PZQ and the action of the hosts immune system has been discussed.

scholarly journals Effects of miltefosine treatment in fibroblast cell cultures and in mice experimentally infected withNeospora caninumtachyzoites

Parasitology ◽  
2012 ◽  
Vol 139 (7) ◽  
pp. 934-944 ◽  
Author(s):  
KARIM DEBACHE ◽  
ANDREW HEMPHILL
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Treatment Group ◽  
Neospora Caninum ◽  
Fibroblast Cell ◽  
Time Span ◽  
Human Foreskin Fibroblasts ◽  
Transmission Electron ◽  
Infected Cells

SUMMARYMiltefosine was investigated for its activity againstNeospora caninumtachyzoitesin vitro,and was shown to inhibit the proliferation ofN. caninumtachyzoites cultured in human foreskin fibroblasts (HFF) with an IC50of 5·2μM. Treatment of infected cells with 25μM miltefosine for a period of 10 h had only a parasitostatic effect, while after 20 h of treatment parasiticidal effects were observed. This was confirmed by transmission electron microscopy ofN. caninum-infected and miltefosine-treated HFF. Administration of miltefosine toN. caninum-infected Balb/c female mice at 40 mg/kg/day for 14 days resulted in 6 out of 10 mice exhibiting weight loss, ruffled coat and apathy between days 7 and 13 post-infection. In the group that received placebo, only 2 out of 8 mice succumbed to infection, but the cerebral burden was significantly higher compared to the miltefosine treatment group. In a second experiment, the time-span of treatment was reduced to 5 days, and mice were maintained without further treatment for 4 weeks. Only 2 out of 9 mice in the miltefosine treatment group exhibited signs of disease, while 8 out of 10 mice succumbed to infection in the placebo group. These results showed that miltefosine hampered the dissemination of parasites into the CNS during experimentalN. caninuminfection in mice.

Schizophyllum commune Fr. as a destructive mycoparasite

1978 ◽  
Vol 24 (7) ◽  
pp. 780-784 ◽  
Author(s):  
S. S. Tzean ◽  
R. H. Estey
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Host Cell ◽  
Cell Walls ◽  
Schizophyllum Commune ◽  
Host Cells ◽  
Transmission Electron ◽  
Reaction Region

Schizophyllum commune Fr. was shown, by light, scanning, and transmission electron microscopy, to be a destructive mycoparasite on several phytopathogenic and nematode-trapping fungi. The hyphae of S. commune coiled around host hyphae and fruiting structures and penetrated them by means of either unspecialized hyphae or by penetration pegs that developed from terminal appressoria. The host cell walls were usually chemically degraded after which the parasite grew through an electron-dense, papillate, reaction region and its underlying membrane(s) to produce trophic hyphae inside the host cells.

scholarly journals Arrabidaea chicaHexanic Extract Induces Mitochondrion Damage and Peptidase Inhibition onLeishmaniaspp.

2014 ◽  
Vol 2014 ◽  
pp. 1-7 ◽  
Author(s):  
Igor A. Rodrigues ◽  
Mariana M. B. Azevedo ◽  
Francisco C. M. Chaves ◽  
Celuta S. Alviano ◽  
Daniela S. Alviano ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Minimum Inhibitory Concentration ◽  
Inhibitory Concentration ◽  
Host Cells ◽  
Peptidase Activity ◽  
Active Fraction ◽  
Transmission Electron ◽  
Arrabidaea Chica

Currently available leishmaniasis treatments are limited due to severe side effects.Arrabidaea chicais a medicinal plant used in Brazil against several diseases. In this study, we investigated the effects of 5 fractions obtained from the crude hexanic extract ofA. chicaagainstLeishmania amazonensisandL. infantum, as well as on the interaction of these parasites with host cells. Promastigotes were treated with several concentrations of the fractions obtained fromA. chicafor determination of their minimum inhibitory concentration (MIC). In addition, the effect of the most active fraction (B2) on parasite’s ultrastructure was analyzed by transmission electron microscopy. To evaluate the inhibitory activity of B2 fraction onLeishmaniapeptidases, parasites lysates were treated with the inhibitory and subinhibitory concentrations of the B2 fraction. The minimum inhibitory concentration of B2 fraction was 37.2 and 18.6 μg/mL forL. amazonensisandL. infantum, respectively. Important ultrastructural alterations as mitochondrial swelling with loss of matrix content and the presence of vesicles inside this organelle were observed in treated parasites. Moreover, B2 fraction was able to completely inhibit the peptidase activity of promastigotes at pH 5.5. The results presented here further support the use ofA. chicaas an interesting source of antileishmanial agents.

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