Studies on the ontogeny and ultrastructure of the sclerotium of Botrytis cinerea Pers. ex Nocca & Balbis

1982 ◽  
Vol 28 (12) ◽  
pp. 1347-1354 ◽  
Author(s):  
H. J. Willetts ◽  
Suzanne Bullock
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Botrytis Cinerea ◽  
Transmission Electron ◽  
Polyphosphate Bodies ◽  
Vacuolated Cells

The ontogeny and ultrastructure of sclerotia of the fungus Botrytis cinerea Pers. ex Nocca & Balbis were studied by light, scanning, and transmission electron microscopy. Exudation droplets of various sizes and colour accumulated on sclerotial surfaces during development and eventually disappeared. A surface hyphal weft was present over sclerotia at maturity, forming a dense covering which often obscured the underlying rind. The rind consisted of highly vacuolated cells with thick, pigmented walls that remained intact even in old sclerotia. The cortex was poorly defined and usually consisted of only one layer of cells. The prosenchymatous medulla constituted the main volume of mature sclerotia. The ultrastructure of young sclerotial hyphae was similar to that of actively growing vegetative hyphae. Hyphae of mature sclerotia contained fewer nuclei and profiles of mitochondria and endoplasmic reticulum than young sclerotial hyphae. Electron-dense structures, tentatively identified as protein and polyphosphate bodies, were observed in hyphae of the cortex and medulla. Sclerotia of B. cinerea were structurally similar to those of Sclerotinia spp.

scholarly journals Pollen, Tapetum, and Orbicule Development inColletia paradoxaandDiscaria americana(Rhamnaceae)

2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
M. Gotelli ◽  
B. Galati ◽  
D. Medan
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Pollen Grains ◽  
Pollen Grain ◽  
Ultrastructural Changes ◽  
Transmission Electron ◽  
The Family ◽  
Tapetal Cells ◽  
Grain Formation

Tapetum, orbicule, and pollen grain ontogeny inColletia paradoxaandDiscaria americanawere studied with transmission electron microscopy (TEM). The ultrastructural changes observed during the different stages of development in the tapetal cells and related to orbicule and pollen grain formation are described. The proorbicules have the appearance of lipid globule, and their formation is related to the endoplasmic reticulum of rough type (ERr). This is the first report on the presence of orbicules in the family Rhamnaceae. Pollen grains are shed at the bicellular stage.

scholarly journals Enigmatic origin of the poxvirus membrane from the endoplasmic reticulum shown by 3D imaging of vaccinia virus assembly mutants

2017 ◽  
Vol 114 (51) ◽  
pp. E11001-E11009 ◽  
Author(s):  
Andrea S. Weisberg ◽  
Liliana Maruri-Avidal ◽  
Himani Bisht ◽  
Bryan T. Hansen ◽  
Cindi L. Schwartz ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Vaccinia Virus ◽  
Virus Assembly ◽  
Transmembrane Protein ◽  
Membrane Dynamics ◽  
Deletion Mutants ◽  
Viral Membrane ◽  
Transmission Electron

The long-standing inability to visualize connections between poxvirus membranes and cellular organelles has led to uncertainty regarding the origin of the viral membrane. Indeed, there has been speculation that viral membranes form de novo in cytoplasmic factories. Another possibility, that the connections are too short-lived to be captured by microscopy during a normal infection, motivated us to identify and characterize virus mutants that are arrested in assembly. Five conserved vaccinia virus proteins, referred to as Viral Membrane Assembly Proteins (VMAPs), that are necessary for formation of immature virions were found. Transmission electron microscopy studies of two VMAP deletion mutants had suggested retention of connections between viral membranes and the endoplasmic reticulum (ER). We now analyzed cells infected with each of the five VMAP deletion mutants by electron tomography, which is necessary to validate membrane continuity, in addition to conventional transmission electron microscopy. In all cases, connections between the ER and viral membranes were demonstrated by 3D reconstructions, supporting a role for the VMAPs in creating and/or stabilizing membrane scissions. Furthermore, coexpression of the viral reticulon-like transmembrane protein A17 and the capsid-like scaffold protein D13 was sufficient to form similar ER-associated viral structures in the absence of other major virion proteins. Determination of the mechanism of ER disruption during a normal VACV infection and the likely participation of both viral and cell proteins in this process may provide important insights into membrane dynamics.

scholarly journals Effects of ubiquitin C-terminal hydrolase L1 deficiency on mouse ova

Reproduction ◽  
2012 ◽  
Vol 143 (3) ◽  
pp. 271-279 ◽  
Author(s):  
Sayaka Koyanagi ◽  
Hiroko Hamasaki ◽  
Satoshi Sekiguchi ◽  
Kenshiro Hara ◽  
Yoshiyuki Ishii ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Proteomic Analysis ◽  
Ubiquitin Proteasome System ◽  
Underlying Mechanism ◽  
Wild Type ◽  
Transmission Electron ◽  
Ubiquitin Proteasome

Maternal proteins are rapidly degraded by the ubiquitin–proteasome system during oocyte maturation in mice. Ubiquitin C-terminal hydrolase L1 (UCHL1) is highly and specifically expressed in mouse ova and is involved in the polyspermy block. However, the role of UCHL1 in the underlying mechanism of polyspermy block is poorly understood. To address this issue, we performed a comprehensive proteomic analysis to identify maternal proteins that were relevant to the role of UCHL1 in mouse ova using UCHL1-deficientgad. Furthermore, we assessed morphological features ingadmouse ova using transmission electron microscopy. NACHT, LRR, and PYD domain-containing (NALP) family proteins and endoplasmic reticulum (ER) chaperones were identified by proteomic analysis. We also found that the ‘maternal antigen that embryos require’ (NLRP5 (MATER)) protein level increased significantly ingadmouse ova compared with that in wild-type mice. In an ultrastructural study,gadmouse ova contained less ER in the cortex than in wild-type mice. These results provide new insights into the role of UCHL1 in the mechanism of polyspermy block in mouse ova.

Molecular and atomic analysis of uranium complexes formed by three eco-types of Acidithiobacillus ferrooxidans

2002 ◽  
Vol 30 (4) ◽  
pp. 669-672 ◽  
Author(s):  
M. Merroun ◽  
C. Hennig ◽  
A. Rossberg ◽  
G. Geipel ◽  
T. Reich ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Acidithiobacillus Ferrooxidans ◽  
Energy Dispersive ◽  
Bacterial Cells ◽  
X Ray ◽  
Uranium Complexes ◽  
Transmission Electron ◽  
Polyphosphate Bodies ◽  
Atomic Analysis

A combination of EXAFS, transmission electron microscopy and energy-dispersive X-ray was used to conduct a molecular and atomic analysis of the uranium complexes formed by Acidithiobacillus ferrooxidans. The results demonstrate that this bacterium accumulates uranium as phosphate compounds. We suggest that at toxic levels when the uranium enters the bacterial cells, A. ferrooxidans can detoxify and efflux this metal by a process in which its polyphosphate bodies are involved.

Interrelations between the Parasitophorous Vacuole ofToxoplasma gondiiand Host Cell Organelles

2005 ◽  
Vol 11 (2) ◽  
pp. 166-174 ◽  
Author(s):  
Rodrigo Cardoso Magno ◽  
Lorian Cobra Straker ◽  
Wanderley de Souza ◽  
Marcia Attias
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Host Cell ◽  
Fluorescent Probes ◽  
Parasitophorous Vacuole ◽  
Laser Scanning Microscopy ◽  
Cell Organelles ◽  
Apical Side ◽  
Transmission Electron

Toxoplasma gondii, the causative agent of toxoplasmosis, is capable of actively penetrating and multiplying in any nucleated cell of warm-blooded animals. Its survival strategies include escape from fusion of the parasitophorous vacuole with host cell lysosomes and rearrangement of host cell organelles in relation to the parasitophorous vacuole. In this article we report the rearrangement of host cell organelles and elements of the cytoskeleton of LLCMK2 cells, a lineage derived from green monkey kidney epithelial cells, in response to infection byT. gondiitachyzoites. Transmission electron microscopy made on flat embedded monolayers cut horizontally to the apical side of the cells or field emission scanning electron microscopy of monolayers scraped with scotch tape before sputtering showed that association of mitochondria to the vacuole is much less frequent than previously described. On the other hand, all parasitophorous vacuoles were surrounded by elements of the endoplasmic reticulum. These data were complemented by observations by laser scanning microscopy using fluorescent probes from mitochondria and endoplasmic reticulum and reinforced by three-dimensional reconstruction from serial sections observed by transmission electron microscopy and labeling of mitochondria and endoplasmic reticulum by fluorescent probes.

scholarly journals Resveratrol Oxidation in Botrytis cinerea Conidia

1998 ◽  
Vol 88 (5) ◽  
pp. 472-476 ◽  
Author(s):  
Marielle Adrian ◽  
Homa Rajaei ◽  
Philippe Jeandet ◽  
Jérôme Veneau ◽  
Roger Bessis
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Sulfur Dioxide ◽  
Light Microscopy ◽  
Granular Material ◽  
Botrytis Cinerea ◽  
Sodium Diethyldithiocarbamate ◽  
Transmission Electron ◽  
Spherical Vesicles ◽  
Mediated Oxidation

Observations using light microscopy showed that approximately 30% of Botrytis cinerea conidia treated with semi-lethal concentrations (i.e., 60 μg/ml) of the grapevine phytoalexin resveratrol possessed intracellular brown coloration. This coloration was never observed in the absence of resveratrol or in conidia treated with resveratrol together with sulfur dioxide (antioxidant compound) or sodium diethyldithiocarbamate (inhibitor of laccase action), suggesting that discoloration resulted from the laccase-mediated oxidation of resveratrol. Further studies using transmission electron microscopy enabled the observation of particular intravacuolar spherical vesicles and of granular material deposits along the tonoplast. These observations are likely to be related to the oxidation of resveratrol by an intracellular laccase-like stilbene oxidase of B. cinerea.

Effect of Endoplasmic Reticulum Stress on Resveratrol-Induced Cardioprotection

2014 ◽  
Vol 651-653 ◽  
pp. 227-230
Author(s):  
Hammayun Ayub ◽  
Shakir Ahmed ◽  
Ayesha Yasin ◽  
Yi Dong Zhang ◽  
Zhuo Wang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Endoplasmic Reticulum Stress ◽  
Western Blotting ◽  
Mitochondrial Permeability Transition ◽  
Permeability Transition Pore ◽  
Permeability Transition ◽  
Mptp Opening ◽  
Transmission Electron

To investigate if resveratrol prevent the mitochondrial permeability transition pore (mPTP) opening through inhibition of endoplasmic reticulum stress (ERS). Methods: Rat heart tissue-derived cardiac H9c2 myoblast cell line was cultured. Fluorescence images of mitochondrial membrane potential were obtained with confocal microscopy. Western blotting analyzes the ERS marker protein GRP78 expression. Transmission electron microscopy detects the subcellular structure. Results: Exposure of cardiac H9c2 cells to 100 μM 2-DG, the ERS inducer, for 20 min caused a marked decrease in mitochondrial specific tetramethylrhodamine ethyl ester (TMRE) fluorescence. Resveratrol significantly prevented the loss of TMRE fluorescence. Western blotting revealed that resveratrol decreased GRP78 expression. Experiments with transmission electron microscopy revealed that resveratrol prevented 2-DG-induced swelling of endoplasmic reticulum and mitochondrial damages. Conclusions: These data suggest that inhibition of ERS leads to the prevention of mPTP opening. Resveratrol prevents the mPTP opening through inhibition of ERS.

The role of endoplasmic reticulum during gametogenesis in the aquatic fungus Allomyces macrogynus

1991 ◽  
Vol 69 (2) ◽  
pp. 336-341 ◽  
Author(s):  
Tommy C. Sewall ◽  
Jeffrey C. Pommerville
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Osmium Tetroxide ◽  
Cleavage Furrow ◽  
Aquatic Fungus ◽  
Transmission Electron ◽  
Allomyces Macrogynus ◽  
Zinc Iodide

The Chytridiomycete Allomyces macrogynus generates new membranes for cleavage furrow and nuclear-cap formation during gametogenesis and zoosporogenesis. Transmission electron microscopy after impregnation with a mixture of zinc iodide and osmium tetroxide clearly demonstrated changes in the endoplasmic reticulum. Endoplasmic reticulum was intensely stained but did not appear to contribute to the formation of the unstained flagellar membranes or cleavage furrows. However, the relative cytoplasmic volume of endoplasmic reticulum decreased as positively stained nuclear-cap membrane formed. These observations are consistent with the hypothesis that flagellar membranes and cleavage furrows are derived from trans-Golgi equivalents, whereas the nuclear-cap membrane is derived from the endoplasmic reticulum. Key words: Allomyces macrogynus, Chytridiomycetes, endoplasmic reticulum, gametogenesis, zoosporogenesis.

Autophagy is associated with male sterility in pistillate flowers of Maytenus obtusifolia (Celastraceae)

2018 ◽  
Vol 66 (2) ◽  
pp. 108 ◽  
Author(s):  
Isabella Veríssimo Nader Haddad ◽  
Lygia Dolores Ribeiro de Santiago-Fernandes ◽  
Silvia Rodrigues Machado
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Endoplasmic Reticulum ◽  
Male Sterility ◽  
Reproductive Development ◽  
Vital Role ◽  
Terminal Deoxynucleotidyl Transferase ◽  
Anatomical Analysis ◽  
Transmission Electron

Programmed cell death (PCD) is defined as a sequence of genetically regulated events leading to controlled and organised cellular degradation. It plays a vital role in plant development; however, little is known about the role of PCD in reproductive development. Sterility in pistillate flowers of Maytenus obtusifolia Mart. has been shown to be related to cytoplasmic male sterility (CMS) based on reproductive biology and anatomical analysis. The recurrent PCD led us to investigate changes in the tapetum and sporogenic tissue during the establishment of male sterility using light and transmission electron microscopy combined with the use of TUNEL (terminal deoxynucleotidyl transferase mediated dUDP end-labelling) assay. The interruption of pollen development in pistillate flowers is a result of premature PCD in the tapetum and consequently in the sporogenic cells. Autophagy, via macroautophagy, occurs in the sporogenic cells and involves the formation of autophagosomes, through rough endoplasmic reticulum, and of complex macroautophagic structures. In the final stage of PCD, massive autophagy takes place. Male sterility in female individuals is thus reasonably interpreted as sporophytic CMS associated to autophagy.

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