Ultrastructural changes associated with induced systemic resistance of cucumber to disease: host response and development of Colletotrichum lagenarium in systemically protected leaves

1988 ◽  
Vol 66 (6) ◽  
pp. 1028-1038 ◽  
Author(s):  
X. L. Xuei ◽  
U. Järlfors ◽  
J. Kuć
Keyword(s):  
Electron Microscopy ◽  
Host Cell ◽  
Host Response ◽  
Structural Changes ◽  
Induced Systemic Resistance ◽  
Light And Electron Microscopy ◽  
Systemic Resistance ◽  
Ultrastructural Changes ◽  
Mesophyll Cells ◽  
Before And After

Systemic resistance to anthracnose caused by Colletotricum lagenarium was induced in cucumber by inoculation with fungal conidia. Control and immunized leaves were examined by both light and electron microscopy before and after subsequent challenge with the fungus. Penetration through the epidermal wall was evident 36 h after challenge and was followed by hyphal proliferation and host-cell destruction in control tissues. Penetration was rarely seen in immunized tissues before 72 h, but at 24 h, invaginations of the appressorial wall were observed, as well as highly electron opaque epidermal walls beneath the appressoria. At 72 h, thin penetration pegs were seen within the dense host wall, and at 96 h, the peg was embedded within the underlying papilla and aggregates of callose-like material. Penetration through the epidermis was rare in immunized tissue, but when it was observed, development appeared to be similar to that in control leaves. Evidence is presented to show that ultra-structural changes in immunized tissues as well as in the fungus occur within 24 h after challenge of the host. There appears to be a correlation between the comparatively few lesions observed macroscopically in immunized leaves and the sparsity of successful penetrations into host mesophyll cells.

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 Redox Mechanism of Azathioprine and Its Interaction with DNA

2021 ◽  
Vol 22 (13) ◽  
pp. 6805
Author(s):  
Mihaela-Cristina Bunea ◽  
Victor-Constantin Diculescu ◽  
Monica Enculescu ◽  
Horia Iovu ◽  
Teodor Adrian Enache
Keyword(s):  
Electron Microscopy ◽  
Mass Spectrometry ◽  
Scanning Electron Microscopy ◽  
Structural Changes ◽  
Differential Pulse ◽  
Immunosuppressive Drug ◽  
Redox Mechanism ◽  
Before And After ◽  
Dna Film ◽  
Scanning Electron

The electrochemical behavior and the interaction of the immunosuppressive drug azathioprine (AZA) with deoxyribonucleic acid (DNA) were investigated using voltammetric techniques, mass spectrometry (MS), and scanning electron microscopy (SEM). The redox mechanism of AZA on glassy carbon (GC) was investigated using cyclic and differential pulse (DP) voltammetry. It was proven that the electroactive center of AZA is the nitro group and its reduction mechanism is a diffusion-controlled process, which occurs in consecutive steps with formation of electroactive products and involves the transfer of electrons and protons. A redox mechanism was proposed and the interaction of AZA with DNA was also investigated. Morphological characterization of the DNA film on the electrode surface before and after interaction with AZA was performed using scanning electron microscopy. An electrochemical DNA biosensor was employed to study the interactions between AZA and DNA with different concentrations, incubation times, and applied potential values. It was shown that the reduction of AZA molecules bound to the DNA layer induces structural changes of the DNA double strands and oxidative damage, which were recognized through the occurrence of the 8-oxo-deoxyguanosine oxidation peak. Mass spectrometry investigation of the DNA film before and after interaction with AZA also demonstrated the formation of AZA adducts with purine bases.

scholarly journals Establishment of an in vitro model for analyzing mitochondrial ultrastructure in PRKN-mutated patient iPSC-derived dopaminergic neurons

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Mutsumi Yokota ◽  
Soichiro Kakuta ◽  
Takahiro Shiga ◽  
Kei-ichi Ishikawa ◽  
Hideyuki Okano ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Dopaminergic Neurons ◽  
Structural Changes ◽  
In Vitro Model ◽  
Induced Pluripotent Stem Cell ◽  
Substantia Nigra Pars Compacta ◽  
Ultrastructural Changes ◽  
Mitochondrial Morphology ◽  
Vitro Model

AbstractMitochondrial structural changes are associated with the regulation of mitochondrial function, apoptosis, and neurodegenerative diseases. PRKN is known to be involved with various mechanisms of mitochondrial quality control including mitochondrial structural changes. Parkinson’s disease (PD) with PRKN mutations is characterized by the preferential degeneration of dopaminergic neurons in the substantia nigra pars compacta, which has been suggested to result from the accumulation of damaged mitochondria. However, ultrastructural changes of mitochondria specifically in dopaminergic neurons derived from iPSC have rarely been analyzed. The main reason for this would be that the dopaminergic neurons cannot be distinguished directly among a mixture of iPSC-derived differentiated cells under electron microscopy. To selectively label dopaminergic neurons and analyze mitochondrial morphology at the ultrastructural level, we generated control and PRKN-mutated patient tyrosine hydroxylase reporter (TH-GFP) induced pluripotent stem cell (iPSC) lines. Correlative light-electron microscopy analysis and live cell imaging of GFP-expressing dopaminergic neurons indicated that iPSC-derived dopaminergic neurons had smaller and less functional mitochondria than those in non-dopaminergic neurons. Furthermore, the formation of spheroid-shaped mitochondria, which was induced in control dopaminergic neurons by a mitochondrial uncoupler, was inhibited in the PRKN-mutated dopaminergic neurons. These results indicate that our established TH-GFP iPSC lines are useful for characterizing mitochondrial morphology, such as spheroid-shaped mitochondria, in dopaminergic neurons among a mixture of various cell types. Our in vitro model would provide insights into the vulnerability of dopaminergic neurons and the processes leading to the preferential loss of dopaminergic neurons in patients with PRKN mutations.

Anatomy of the Unpollinated and Pollinated Watermelon Stigma

1982 ◽  
Vol 54 (1) ◽  
pp. 341-355
Author(s):  
M. SEDGLEY
Keyword(s):  
Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Light And Electron Microscopy ◽  
Freeze Fracture ◽  
Pollen Grain ◽  
Acidic Polysaccharides ◽  
Before And After ◽  
Em Autoradiography ◽  
Pollen Grain Wall ◽  
Stigma Secretion

The structure of the watermelon stigma before and after pollination was studied using light and electron microscopy, freeze-fracture and autoradiography. The wall thickenings of the papilla transfer cells contained callose and their presence prior to pollination was confirmed using EM-autoradiography, freeze-fracture and fixation. No further callose thickenings were produced following pollination. Pollination resulted in a rapid increase in aqueous stigma secretion and localized disruption of the cuticle, which appeared to remain on the surface of the secretion. Autolysis of the papilla cells, which had commenced prior to pollination, was accelerated and appeared to take place via cup-shaped vacuoles developed from distended endoplasmic reticulum. The reaction was localized to the papilla cells adjacent to the pollen tube only. Both pollen-grain wall and stigma secretion contained proteins, carbohydrates, acidic polysaccharides, lipids and phenolics.

Functional medial thickening and folding of the internal elastic lamina in coronary spasm

2011 ◽  
Vol 300 (2) ◽  
pp. H423-H430 ◽  
Author(s):  
Yasumi Uchida ◽  
Yasuto Uchida ◽  
Akimasa Matsuyama ◽  
Atsushi Koga ◽  
Yuko Maezawa ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Structural Changes ◽  
Light And Electron Microscopy ◽  
Coronary Spasm ◽  
Cellular Level ◽  
Internal Elastic Lamina ◽  
Circular Smooth Muscle ◽  
The Media ◽  
Medial Thickening ◽  
Elastic Lamina

Although there are a number of studies on vasospastic angina, the structural changes at the cellular level that occur in the coronary arterial wall during spasm are not well known. Coronary spasm was induced by brushing the coronary adventitia in nine anesthetized beagles, and structural changes in the spastic coronary segments were examined by light and electron microscopy, making comparisons with the adjacent nonspastic segments. The % diameter stenosis of the spastic segments as measured angiographically was 79.4 ± 12% (mean ± SD). Light microscopic changes in the spastic and nonspastic segments were as follows: medial thickness 1,512 vs. 392 μm ( P < 0.0001) and % diameter and % area stenoses of spastic segment 81.0% and 96.5%, respectively, indicating that spasm was induced by medial thickening. Circular smooth muscle cells (SMCs) in the media were arranged in parallel with the internal (IEL) and external (EEL) elastic lamina in nonspastic segments but radially rearranged in spastic segments. SMCs were classified by their patterns of connection to IEL into six types by electron microscopy. Of these, three contracted and pulled the IEL toward the EEL, causing folding of the IEL and waving of EEL resulting in thickening of the media and narrowing of the lumen. We conclude that coronary spasm was elicited by radial rearrangement of the medial SMCs due to their own contraction and resultant medial thickening and folding of IEL, creating a piston effect to narrow the lumen, i.e., spasm.

Phenolic Deposits and Kranz Syndrome in Leaf Tissues of Spotted (Euphorbia maculata) and Prostrate (Euphorbia supina) Spurge

Weed Science ◽  
1983 ◽  
Vol 31 (1) ◽  
pp. 131-136 ◽  
Author(s):  
C. Dennis Elmore ◽  
Rex N. Paul
Keyword(s):  
Electron Microscopy ◽  
Phenolic Compounds ◽  
Light And Electron Microscopy ◽  
Bundle Sheath ◽  
Fixation Technique ◽  
Mesophyll Cells ◽  
Kranz Anatomy ◽  
Bundle Sheath Cells ◽  
Leaf Tissues ◽  
Sheath Cells

Spotted spurge (Euphorbia maculataL.) and prostrate spurge (E. supinaRaf.), both in subgenusChamesyce,were examined by light and electron microscopy using a caffeine - fixation technique to sequester the phenolic pools intercellularly. Both species have typical dicotyledon-type Kranz anatomy. Sequestered phenolic pools were located in vacuoles in epidermal and mesophyll cells. Only in spotted spurge, however, were additional phenolic pools formed in bundle - sheath cells. This study was undertaken because allelopathy has been demonstrated in prostrate spurge and because phenolic compounds have been implicated in allelopathy. These results would indicate that spotted spurge should also be allelopathic.

scholarly journals Trypanosoma congolense in the Microvasculature of the Pituitary Gland of Experimentally Infected Boran Cattle (Bos indicus)

1993 ◽  
Vol 30 (5) ◽  
pp. 401-409 ◽  
Author(s):  
G. Abebe ◽  
M. K. Shaw ◽  
R. M. Eley
Keyword(s):  
Electron Microscopy ◽  
Extracellular Matrix ◽  
Structural Changes ◽  
Bos Indicus ◽  
Light And Electron Microscopy ◽  
Trypanosoma Congolense ◽  
Glossina Morsitans ◽  
Glossina Morsitans Centralis ◽  
Pituitary Glands ◽  
Female Control

The pituitary glands of seven Boran cattle ( Bos indicus), five infected with a clone of Trypanosoma congolense IL 1180 (ILNat 3.1) transmitted by Glossina morsitans centralis and two uninfected controls, were examined by light and electron microscopy 43 (experiment 2) or 56 (experiment 1) days after fly challenge. The three cattle used in the first experiment included a 15-month-old female (No. 1), a 24–month-old female (No. 2), and a 21–month-old male (No. 3) as a control. In the second experiment, four cattle were used: two females (Nos. 4, 5) and one male (No. 6), all between 15 and 24 months of age, and one female control (No. 7) of similar age. In all the infected animals, dilation of both the sinusoids and microvasculature was apparent, as was an increase in the thickness of the extracellular matrix between the pituitary lobules. Trypanosomes were found in the microvasculature of the adenohypophysis and neurohypophysis in all the infected animals. Focal degenerative changes were seen in the adenohypophyseal section of glands from the infected animals euthanatized 56 days post-infection. These degenerative structural changes were confined to the somatotrophs cells. The possible role that trypanosomes in the microvasculature may play in inducing pituitary damage and dysfunction is discussed.

scholarly journals Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease

2007 ◽  
Vol 61 (4) ◽  
pp. 460-466 ◽  
Author(s):  
M Pronicki ◽  
E Matyja ◽  
D Piekutowska-Abramczuk ◽  
T Szymańska-Dębińska ◽  
A Karkucińska-Więckowska ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Lipid Accumulation ◽  
Morphological Changes ◽  
Light And Electron Microscopy ◽  
Gene Mutations ◽  
Leigh Syndrome ◽  
Typical Feature ◽  
Ultrastructural Changes ◽  
Consistent Feature ◽  
Muscle Changes

Aims:Leigh syndrome (LS) is characterised by almost identical brain changes despite considerable causal heterogeneity. SURF1 gene mutations are among the most frequent causes of LS. Although deficiency of cytochrome c oxidase (COX) is a typical feature of the muscle in SURF1-deficient LS, other abnormalities have been rarely described. The aim of the present work is to assess the skeletal muscle morphology coexisting with SURF1 mutations from our own research and in the literature.Methods:Muscle samples from 21 patients who fulfilled the criteria of LS and SURF1 mutations (14 homozygotes and 7 heterozygotes of c.841delCT) were examined by light and electron microscopy.Results:Diffuse decreased activity or total deficit of COX was revealed histochemically in all examined muscles. No ragged red fibres (RRFs) were seen. Lipid accumulation and fibre size variability were found in 14 and 9 specimens, respectively. Ultrastructural assessment showed several mitochondrial abnormalities, lipid deposits, myofibrillar disorganisation and other minor changes. In five cases no ultrastructural changes were found. Apart from slight correlation between lipid accumulation shown by histochemical and ultrastructural techniques, no other correlations were revealed between parameters investigated, especially between severity of morphological changes and the patient’s age at the biopsy.Conclusion:Histological and histochemical features of muscle of genetically homogenous SURF1-deficient LS were reproducible in detection of COX deficit. Minor muscle changes were not commonly present. Also, ultrastructural abnormalities were not a consistent feature. It should be emphasised that SURF1-deficient muscle assessed in the light and electron microscopy panel may be interpreted as normal if COX staining is not employed.

scholarly journals Alterations to the structure of Leishmania major induced by N-arylisoquinolines correlate with compound accumulation and disposition

2010 ◽  
Vol 59 (1) ◽  
pp. 69-75 ◽  
Author(s):  
Alicia Ponte-Sucre ◽  
Tanja Gulder ◽  
Tobias A. M. Gulder ◽  
Gerina Vollmers ◽  
Gerhard Bringmann ◽  
...  
Keyword(s):  
Cell Death ◽  
Host Cell ◽  
Mechanism Of Action ◽  
Structural Changes ◽  
Leishmania Major ◽  
Ultrastructural Changes ◽  
Synthetic Analogues ◽  
Intracellular Compartments ◽  
Intracellular Organelles ◽  
Fluorescent Derivative

Naphthylisoquinoline alkaloids equipped with a N,C-hetero-‘biaryl’ axis, and, in particular, simplified synthetic analogues thereof, kill intracellular Leishmania major at concentrations in the low submicromolar range, while being significantly less toxic to their major host cell, the macrophage, at the same concentrations. To further investigate their mechanism of action we evaluated the morphological and ultrastructural changes induced by specific N-arylisoquinolines in L. major, and the correlation of these changes with compound accumulation and disposition by the parasite. After 24 h of treatment with the synthetic arylisoquinolinium salts 3 or 4, dramatic structural changes and cell death were observed. Furthermore, the auto-fluorescent derivative salt 3 accumulates continually in intracellular compartments. Our results thus suggest that the leishmanicidal effect of arylisoquinolinium salts may involve their ability to accumulate and precipitate in intracellular organelles, form a huge vacuole and eventually promote cell lysis.

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.

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