288 research outputs found
Philippe Cormier, Les irréguliers de l’amour. Une question pour l’Église, Paris, Cerf, 2015
No full textGrellier Isabelle. Philippe Cormier, Les irréguliers de l’amour. Une question pour l’Église, Paris, Cerf, 2015. In: Revue d'histoire et de philosophie religieuses, 96e année n°2, Avril-Juin 2016. pp. 192-193
Streamlined targeting of Amaryllidaceae alkaloids from the bulbs of Crinum scillifolium using spectrometric and taxonomically-informed scoring metabolite annotations
No full textN'Tamon, Amon Diane, Timoth, Aboua, Okpekon, ee, Bony, Nicaise F., Bernadat, Guillaume, Gallard, Jean-François, Tap, Kouam, e, e, S, Blandine, eon-M, eniel, Leblanc, Karine, Rharrabti, Somia, Mouray, Elisabeth, Grellier, Philippe, Ake, Mich`ele, Amin, N'Cho Christophe, Champy, Pierre, Beniddir, Mehdi A., Pogam, Pierre Le (2020): Streamlined targeting of Amaryllidaceae alkaloids from the bulbs of Crinum scillifolium using spectrometric and taxonomically-informed scoring metabolite annotations. Phytochemistry (112485) 179: 1-8, DOI: 10.1016/j.phytochem.2020.112485, URL: http://dx.doi.org/10.1016/j.phytochem.2020.11248
Deconjugated bile salts produced by extracellular bile-salt hydrolase-like activities from the probiotic Lactobacillus johnsonii La1 inhibit Giardia duodenalis in vitro growth
No full textGiardiasis, currently considered a neglected disease, is caused by the intestinal protozoan parasite Giardia duodenalis and is widely spread in human as well as domestic and wild animals. The lack of appropriate medications and the spread of resistant parasite strains urgently call for the development of novel therapeutic strategies. Host microbiota or certain probiotic strains have the capacity to provide some protection against giardiasis. By combining biological and biochemical approaches, we have been able to decipher a molecular mechanism used by the probiotic strain Lactobacillus johnsonii La1 to prevent Giardia growth in vitro. We provide evidence that the supernatant of this strain contains active principle(s) not directly toxic to Giardia but able to convert non-toxic components of bile into components highly toxic to Giardia. By using bile acid profiling, these components were identified as deconjugated bile-salts. A bacterial bile-salt-hydrolase of commercial origin was able to mimic the properties of the supernatant. Mass spectrometric analysis of the bacterial supernatant identified two of the three bile-salt-hydrolases encoded in the genome of this probiotic strain. These observations document a possible mechanism by which L. johnsonii La1, by secreting, or releasing BSH-like activity(ies) in the vicinity of replicating Giardia in an environment where bile is present and abundant, can fight this parasite. This discovery has both fundamental and applied outcomes to fight giardiasis, based on local delivery of deconjugated bile salts, enzyme deconjugation of bile components, or natural or recombinant probiotic strains that secrete or release such deconjugating activities in a compartment where both bile salts and Giardia are present
In vivo study of the potential role of group IIA phospholipase A2 in malaria : Pathophysiological characterization of C57BL/6 group IIA phospholipase A2 transgenic mice infected with Plasmodium chabaudi
No full textLe paludisme est une maladie tropicale causée par un parasite du genre Plasmodium. Chez l’Homme, un niveau élevé de phospholipase A2 sécrétée de groupe IIA humaine (hGIIA) est mesuré dans le plasma des patients impaludés. Cette enzyme est connue pour son rôle antibactérien et pro-inflammatoire. Cependant, son rôle dans le paludisme n’a jamais été exploré. Pour comprendre le rôle in vivo de la hGIIA dans cette pathologie, nous avons entrepris la caractérisation hématologique, histopathologique et immunohistochimique de l’infection de souris C57BL/6, transgéniques (Tg+) pour l’enzyme humaine, par l’espèce murine Plasmodium chabaudi chabaudi 864VD. Ce modèle reproduit un paludisme non létal. Nos résultats ont permis d’établir que les souris Tg+ ont un meilleur contrôle de l’infection au moment du pic de crise parasitaire (J14 post-inoculation), avec une diminution de 27% de la parasitémie, comparé aux souris « littermates » non transgéniques (Tg-). L’injection de hGIIA recombinante aux jours 12, 13 et 14 p.i. (0,125 mg/kg deux fois par jour) à des souris C57BL/6 wild-type (WT) infectées par P. c. chabaudi 864VD provoque une diminution d’environ 19% de la parasitémie à J14 p.i., démontrant un rôle direct de la hGIIA dans la diminution de la population parasitaire. Les données hématologiques montrent que l’infection chez la souris Tg+ provoque une anémie plus durable que chez la souris Tg- et une élévation nettement plus importante du nombre de leucocytes, en particulier des polynucléaires neutrophiles. Chez la souris Tg+ parasitée, on observe aussi l’activation d’un nombre important de lymphocytes et une activation spécifique des monocytes avant le pic de crise. Chez la souris Tg- infectée, les données histologiques mettent en avant une meilleure récupération des lésions histopathologiques du foie et une hyperplasie des lymphocytes B dans la rate, tandis que les souris Tg+ infectées présentent des lésions hépatiques tardives et une hématopoïèse extramédullaire splénique. Les résultats des analyses par RT-qPCR suggèrent que l’ARNm de la hGIIA augmente au pic parasitaire dans le foie des souris Tg+ infectées, mais diminue dans la rate et les cellules sanguines. L’injection de hGIIA recombinante au début de la phase patente est sans effet sur la parasitémie, ce qui laisse supposer que des événements plus tardifs dans l’infection sont nécessaires à l’activité antiparasitaire de l’enzyme. L’étude du rôle des lipoprotéines oxydées comme substrat potentiel de l’activité antiparasitaire de l’enzyme, basée sur des résultats in vitro, est abordée. En conclusion, nos études ont permis de dresser un tableau large de l’infection à Plasmodium chez la souris exprimant la hGIIA, et ouvrent de nouvelles perspectives dans l’analyse du rôle de l’enzyme dans la physiopathologie du paludisme.Malaria is a tropical disease caused by a parasite of the Plasmodium genus. High levels of circulating human group IIA secreted phospholipase A2 (hGIIA) have been reported in malaria patients. The enzyme is well known for its bactericidal and pro-inflammatory actions. However, so far its role in malaria is unknown. In order to address the in vivo role of hGIIA in malaria, we performed a hematological, histopathological and immunohistochemical characterization of C57BL/6 hGIIA transgenic mice (Tg+ mice) infected with P. chabaudi chabaudi (864VD strain), a murine Plasmodium species and strain which causes non-lethal chronic malaria. Infected Tg+ mice present a 27% reduction of parasitaemia at the peak of infection (D14 post-inoculation, p.i.) compared to infected non-transgenic littermates (Tg- mice). Intraperitoneal injection of recombinant hGIIA at D12, D13 and D14 p.i. (0.125 mg/kg twice a day) into P. chabaudi 864VD-infected WT C57BL/6 mice leads to a 19% reduction of the parasitaemia at D14 p.i., demonstrating the direct and acute role of hGIIA in lowering parasite population and presumably ruling out a potential effect linked to chronic overexpression of hGIIA in Tg+ mice. Hematological data show a durable anemia in Tg+ mice compared to Tg- mice during the infection and an important increase of leucocytes, especially of polynuclear neutrophils. The parasitized Tg+ mouse also presents a higher activation of lymphocytes and a specific activation of monocyte cells at the pic of crisis. In the infected Tg- mouse, histological data show a better histopathological recovery in the liver and B cells hyperplasia in the spleen, whereas the infected Tg+ mouse presents late hepatic injuries and splenic extra-medullar hematopoiesis. RT-qPCR analyses suggest that hGIIA mRNA increases at the pic of infection in the liver of infected Tg+ mice, but decreases in spleen and blood. Intraperitoneal injection of recombinant hGIIA at the patent phase is without effect on parasitaemia, which suggests that later infection events are needed for the enzyme antiparasitic activity. Involvement of oxidized-lipoproteins as potential hGIIA substrates, based on in vitro studies, is discussed. In conclusion, our studies allowed us to elaborate a larger picture of the infection of Plasmodium in the mice expressing hGIIA and open new perspectives in the analysis of the role of the enzyme in malaria pathophysiology
La differenciation des merozoietes de Plasmodium falciparum et la phase de reinvasion des globules rouges
No full textSIGLEINIST T 71098 / INIST-CNRS - Institut de l'Information Scientifique et TechniqueFRFranc
Transferts hydriques dans l'enrobage de semences
No full text* INRA, Centre d'Angers Diffusion du document : INRA, Centre d'Angers Diplôme : Dr. d'Universit
Diversity of apostome ciliates, Chromidina spp. (Oligohymenophorea, Opalinopsidae), parasites of cephalopods of the Mediterranean Sea
No full textChromidina spp. are enigmatic apostome ciliates (Oligohymenophorea, Opalinopsidae) that parasitise the renal and pancreatic appendages of cephalopods. Only four species have been described, among which only three have been formally named. No DNA sequence has been reported so far. To investigate Chromidina spp. diversity, we sampled cephalopods in the Mediterranean Sea off Tunis, Tunisia, and identified two distinct Chromidina spp. in two different host species: Loligo vulgaris and Sepia officinalis. From haematoxylin-stained slides, we described morphological traits for these parasitic species and compared them to previous descriptions. We also re-described the morphology of Chromidina elegans (Foettinger, 1881) from Chatton and Lwoff’s original materials and designated a neohapantotype and paraneohapantotypes for this species. We describe a new species, Chromidina chattoni Souidenne, Florent and Grellier n. sp., found in L. vulgaris off Tunisia, and evidence for a probable novel species, found in S. officinalis off Tunisia, although this latter species presents similarities to some morphological stages previously described for Chromidina cortezi Hochberg, 1971. We amplified, for the first time, an 18S rDNA marker for these two Chromidina species. Phylogenetic analysis supports the association of Chromidina within apostome ciliates. Genetic distance analysis between 18S rDNA sequences of representative apostomes indicates Pseudocollinia as the most closely related genus to Chromidina
Harmonic Functions on the Real Hyperbolic Ball II : Hardy and Lipschitz Spaces
No full textIn this paper, we pursue the study of harmonic functions on the real hyperbolic ball started in \cite{Ja3}. Our focus here is on the theory of Hardy-Sobolev and Lipschitz spaces of these functions. We prove here that these spaces admit Fefferman-Stein like characterizations in terms of maximal and square functionals. We further prove that the hyperbolic harmonic extension of Lipschitz functions on the boundary extend into Lipschitz functions on the whole ball. In doing so, we exhibit differences of behaviour of derivatives of harmonic functions depending on the parity of the dimension of the ball and on the parity of the order of derivation
Traits épigénétiques chez Trypanosoma cruzy (modifications de l'ADN et les histones liés à son cycle vitale)
No full textPARIS-BIUSJ-Physique recherche (751052113) / SudocSudocFranceF
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