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Biomedical subjects

C Vermeil

Publications and source records attributed to C Vermeil.

At least 19 recordsLinked to original sources

[Does Boutonneuse fever in France have equivalents outside the Mediterranean area?].

In western of France, outside of mediterranean spotted fever area, several sera from autochthonous patients were positive for the presence of anti-R. conori antibodies by indirect immunofluorescence test. What is it all about: authentic rickettsiosis or paraspecific seroreactions with other microorganisms? We discuss these hypothesis.

Arachnid Vectors

Modulation of antibody synthesis by an anti-tumour alga.

An unicellular alga, Chlorella pyrenoidosa, which had been reported to protect C3H mice against sarcoma BP8, is shown, when injected in Freund's incomplete adjuvant, to modulate the antibody synthesis induced by immunization with a hapten-carrier complex. C. pyrenoidosa appeared to be able to initiate an antigenic competition between hapten and carrier determinants of the antigen molecule during antibody synthesis, and thus it could be speculated that C. pyrenoidosa modulates the immune response at the macrophage level.

Anaphylaxis

[Observation of Schistosoma mansoni by scanning electron microscopy].

The integumental surface of adult Schistosoma mansoni was studied by scanning electron microscopy (SEM) at 220 to 10,000 magnifications. SEM shows certain basic features such as spines in the oral sucker and the acetabulum which may facilitate rasping and attachment of the parasite to stay in the bloodstream of the definitive host. It seems likely that SEM visualization will be a means for differentiation some species of the genus Schistosoma.

Animals

[Autoradiography of the exchanges that can occur between murine sarcoma cells (BP 8) and yeast cells (Saccharomyces cerevisiae, complete or protoplast)].

We can tell after observing the resulting negative that yeasts are able, in our experimental conditions, to collect a sequence of ADN and of ARN proceeding from the cancerous cells. Then, those yeasts could turn their synthesis towards the production of new materials. If those informed yeasts were introduced into a mouse, they would induce at the level of the immunocompetent cells a specific immunizing antitumoral power.

Animals

[Experimental role of the unicellular algae Prototheca and Chlorella (Chlorellaceae) in anti-cancer immunogenesis (murine BP8 sarcoma)].

Bacteria and Yeasts are able to induce, when inoculated into laboratory rodents, a general stimulation of defences by an immune process. We could estimate that unicellular algae would induce the same phenomenon because the chemical compounds of their walls are related to those of the precedings microorganisms specially to bacteria. Indeed, two Chlorellaceae, Prototheca segbwema and Chlorella pyrenoidosa are respectively protecting 78% and 82% CH3 mice against the sarcoma BP8 grafting.

Animals

[Human pulmonary adiaspiromycosis: comment on a new case in Brittany].

Pulmonary and human adiaspiromycosis in Brittany: a new observation. A young woman is operated on for pulmonary abcess. The histological study the pulmonary tissue around and at a distance from the abcess shows numerous adiaspores of Emmonsia crescens Emmons & Jellison (1960). The culture of the fungus were not possible. The authors discuss the relationship between the fungus and the pulmonary lesions observed in the cases of human adiaspiromycosis.

Chrysosporium

[Deviation of the life cycle of Dipetalonema viteae (Filarioidea)].

Dipetalonema viteae is a filarial that can evoluate among hosts zoologically broadly apart (Ixodides and Argasides), but always gathered from meriones burrows. Its evolution is, on the contrary, blocked among most of the other ticks, particularly among Ornithodoros erraticus morphologically very similar to the normal vector. Our work concerns the experimental deviation of the cycle of Dipetalonema viteae, with its possible adaptability in the bosom of an intermediate of fowl tropism and a permanent host, different from a gnawing.

Animals

[Do the eosinophilic granulomas observed in Brittany represent a form of anisakiasis? The larvae of Thynnascaris aduncum do not produce these granulomas experimentally].

To explain the enigmatical origin of gastric eosinophilic granulomas prevailing among patients in Brittany (France), we have tried to experiment with the larvae of Thynnascaris (Thynnascaris aduncum (Rud.)), a Nematode found in the sardine (Sardina pilchardus (Walbaum)), a fish sometimes eaten raw in our country. In a preliminary experiment, larvae of Thynnascaris were observed to penetrate the mucosa of the rabbit stomach in vitro at room temperature. But in vivo, whatever the means, the ways and the experimented mammals of our study, we have failed to experimentally reproduce such tumours. We think that this result belongs to the fact that the larvae of Thynnascaris in the conditions of our experimentation could not perform an evolution in homeothermal animals.

Animals

[Release of "Saccharomyces cerevisiae" protoplasts: scanning electron microscope study (author's transl)].

In a previous study we described the minimal methodology used to obtain protoplasts from ascomycetous yeasts. Using a reducing agent associated with 1,3-beta-glucanase at 26 degrees C, protoplasts were invariably obtained. In the present study we localized the disruption spots of the cell wall using the two same reagents. The observations were made with the scanning electron microscope. The disruption site was always in the subterminal region, and this very simple structure (proteins with disulphide bridges and 1,3-beta-glucans) was opposite the birth-scar. The dissociation of the two reagents showed that a small part of the yeast population was able to release protoplasts with only glucanase. We believe these very sensitive yeasts (2 to 10% population) to be very young cells. These disruption sites seemed very different from budding-sites. They might be identical with elongation-sites, or with the opening in the ascus-wall during germinating ascospore release.

Glucan Endo-1,3-beta-D-Glucosidase