Interactions hôte–parasite lors de l'infection par Cercosporella herpotrichoides, agent du piétin-verse : morphologie du parasite et ultrastructure des parois d'hôtes sensibles et résistants

1985 ◽  
Vol 63 (5) ◽  
pp. 851-858 ◽  
Author(s):  
Marie-Christine Soulie ◽  
Brigitte Vian ◽  
Thérèse Guillot-Salomon

Segments of seedlings of susceptible and resistant lines of Triticineae were infected in vitro by a virulent strain of Cercosporella herpotrichoides Fron. Samples were taken 4 days after inoculation and examined using scanning electron microscopy. In susceptible lines, a strong adhesion and an important development of the mycelium occurred in contact with the coleoptile. Simultaneously, a massive sporulation was observed. Conversely, in resistant lines, the hyphal stroma remained loose and poorly developed and failed to sporulate. A cytochemical and ultrastructural study of the walls of host cells showed changes in texture and an important deposition of strongly reactive compounds. These components could not be extracted by the usual solvents of matrix constituents of both cellulosic and lignified cell walls. An enhanced synthesis of such substances could prevent the action of the parasite glycolytic enzymes and therefore stop the fungal invasion. The wall, or at least some of its components, seems to be implicated both in the recognition of the pathogen by the host and in the triggering of a response leading to sequestration of the latter and arrest in its development.

1987 ◽  
Vol 65 (1) ◽  
pp. 124-130 ◽  
Author(s):  
James A. Traquair ◽  
Denis A. Gaudet ◽  
Eric G. Kokko

The effects of temperature on the production of sclerotia by the snow mold basidiomycete, Coprinus psychromorbidus, are described for the first time. Numbers of sclerotia produced and the optimum temperature for sclerotium production were variable for isolates observed. In general, the influence of temperature on sclerotium production was independent of its influence on colony growth. Optimal temperatures for production of sclerotia were higher than those for radial growth of colonies. Scanning electron microscopy revealed a centripetal pattern of differentiation in developing sclerotia. Distinctive rind, cortex, and medulla were evident after 8 to 10 weeks. Rind and cortex were multilayered. Thick-walled cells were cemented together by an amorphous intercellular matrix. Melanin was located in the rind cell walls for the first time by scanning electron microscopy and backscattered electron imaging of silver-stained sections. With the transmission electron microscope, melanin granules were observed only in the intercellular matrix and outer layers of rind cell walls. Inflated medullary cells were predominantly thin walled and contained vacuolate cytoplasm.


Author(s):  
William J. Lamoreaux ◽  
David L. Smalley ◽  
Larry M. Baddour ◽  
Alfred P. Kraus

Infections associated with the use of intravascular devices have been documented and have been reported to be related to duration of catheter usage. Recently, Eaton et al. reported that Staphylococcus epidermidis may attach to silastic catheters used in continuous ambulatory peritoneal dialysis (CAPD) treatment. The following study presents findings using scanning electron microscopy (SEM) of S. epidermidis adherence to silastic catheters in an in vitro model. In addition, sections of polyvinyl chloride (PVC) dialysis bags were also evaluated by SEM.The S. epidermidis strain RP62A which had been obtained in a previous outbreak of coagulase-negative staphylococcal sepsis at local hospitals was used in these experiments. The strain produced surface slime on exposure to glucose, whereas a nonadherent variant RP62A-NA, which was also used in these studies, failed to produce slime. Strains were grown overnight on blood agar plates at 37°C, harvested from the surface and resuspended in sterile saline (0.85%), centrifuged (3,000 rpm for 10 minutes) and then washed twice in 0.1 M phosphate-buffered saline at pH 7.0. Organisms were resuspended at a concentration of ca. 106 CFU/ml in: a) sterile unused dianeal at 4.25% dextrose, b) sterile unused dianeal at 1.5% dextrose, c) sterile used dialysate previously containing 4.25% dextrose taken from a CAPD patient, and d) sterile used dialysate previously containing 1.5% dextrose taken from a CAPD patient.


1984 ◽  
Vol 52 (02) ◽  
pp. 102-104 ◽  
Author(s):  
L J Nicholson ◽  
J M F Clarke ◽  
R M Pittilo ◽  
S J Machin ◽  
N Woolf

SummaryA technique for harvesting mesothelial cells is described. This entails collagenase digestion of omentum after which the cells can be cultured. The technique has been developed using the rat, but has also been successfully applied to human tissue. Cultured rat mesothelial cells obtained in this way have been examined by scanning electron microscopy. Rat mesothelial cells grown on plastic film have been exposed to blood in an in vitro system using a Baumgartner chamber and have been demonstrated to support blood flow. No adhering platelets were observed on the mesothelial cell surface. Fibroblasts similarily exposed to blood as a control were washed off the plastic.


2017 ◽  
Vol 68 (6) ◽  
pp. 1188-1192
Author(s):  
Daniela Avram ◽  
Nicolae Angelescu ◽  
Dan Nicolae Ungureanu ◽  
Ionica Ionita ◽  
Iulian Bancuta ◽  
...  

The study in vitro of the glass powders bioactivity was performed by soaking them in simulated body fluid for 3 to 21 days at a temperature of 37�C and pH = 7.20. The synthesis de novo of hydroxyapatite, post soaking was confirmed by Fourier Transform Infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The study of the antimicrobial activity was performed by microbiological examination on two strains of pathogenic bacteria involved in postoperative nosocomial infections.


2021 ◽  
Vol 22 (11) ◽  
pp. 5730
Author(s):  
Jomarien García-Couce ◽  
Marioly Vernhes ◽  
Nancy Bada ◽  
Lissette Agüero ◽  
Oscar Valdés ◽  
...  

Hydrogels obtained from combining different polymers are an interesting strategy for developing controlled release system platforms and tissue engineering scaffolds. In this study, the applicability of sodium alginate-g-(QCL-co-HEMA) hydrogels for these biomedical applications was evaluated. Hydrogels were synthesized by free-radical polymerization using a different concentration of the components. The hydrogels were characterized by Fourier transform-infrared spectroscopy, scanning electron microscopy, and a swelling degree. Betamethasone release as well as the in vitro cytocompatibility with chondrocytes and fibroblast cells were also evaluated. Scanning electron microscopy confirmed the porous surface morphology of the hydrogels in all cases. The swelling percent was determined at a different pH and was observed to be pH-sensitive. The controlled release behavior of betamethasone from the matrices was investigated in PBS media (pH = 7.4) and the drug was released in a controlled manner for up to 8 h. Human chondrocytes and fibroblasts were cultured on the hydrogels. The MTS assay showed that almost all hydrogels are cytocompatibles and an increase of proliferation in both cell types after one week of incubation was observed by the Live/Dead® assay. These results demonstrate that these hydrogels are attractive materials for pharmaceutical and biomedical applications due to their characteristics, their release kinetics, and biocompatibility.


1981 ◽  
Vol 59 (1) ◽  
pp. 1-7 ◽  
Author(s):  
Robert A. Blanchette ◽  
John B. Sutherland ◽  
Don L. Crawford

The greenish-brown margin of discolored wood in three living silver maple trees, Acer saccharinum L., was examined by scanning electron microscopy and microbiological culture techniques. Micrographs of xylem vessels revealed filamentous structures; some of them appeared to be actinomycetous hyphae. Actinomycetes identified as Streptomyces parvullus Waksman & Gregory, S. sparsogenes Owen, Dietz & Camiener, and a third Streptomyces strain were isolated repeatedly from discolored wood of each tree. These isolates grew in liquid media in the presence of 0.1% (w/v) concentrations of several phenols. Although other phenols included in the test were not substantially degraded, p-hydroxybenzoic acid was utilized as a carbon source by S. parvullus. All three actinomycetes inhibited growth of selected wood-inhabiting fungi when paired on malt agar. When inoculated on sterilized sapwood and discolored wood from silver maple, the actinomycetes colonized vessel walls and occlusions, but were not observed to decay cell walls.


1987 ◽  
Vol 16 (1) ◽  
pp. 48-52
Author(s):  
C. A. Chamorro ◽  
P. de Paz ◽  
J. G. Fernandez ◽  
M. Fernandez ◽  
J. M. Villar

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