49 research outputs found

    Emergence des nanotechnologies : Vers un nouveau "modĂšle industriel "?

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    Les technologies Ă©mergentes comme la microĂ©lectronique des annĂ©es 70, les biotechnologies des annĂ©es 80-90 ou les nanotechnologies des annĂ©es 2000 s'expriment sous forme de vagues technologiques (Kahane, 2008) qui sont porteuses de promesses scientifiques et techniques (Pautrat, 2002), de nouveaux marchĂ©s, de perspectives de bien-ĂȘtre pour certains (Birraux et al., 2003), de risques, d'incertitudes et d'aliĂ©nation pour d'autres (Dupuy et al., 2004). Alors que le dĂ©veloppement Ă©conomique des nanotechnologies ne fait que commencer, plusieurs schĂ©mas de dĂ©veloppement sont envisageables (Kahane, Mangematin, 2007).Pour plus d'informations consulter le site http://www.nanoeconomics.eu/

    The Phenotypic Analysis of Lactobacillus plantarum shsp Mutants Reveals a Potential Role for hsp1 in Cryotolerance

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    Small heat shock proteins (sHSPs) are ubiquitous, low molecular weight (MW) proteins that share a conserved alpha-crystallin domain. sHSPs oligomers exhibit chaperon-like activities by interacting with unfolded substrates, thereby preventing their aggregation and precipitation. Unlike most lactobacilli, which have single shsp genes, three different sHSP-encoding genes, i.e., hsp1, hsp2, and hsp3, were previously identified in the probiotic Lactobacillus plantarum WCFS1. Early studies, including the characterization of the knock out (KO) mutant for hsp2, indicated a different organization and transcriptional regulation of these genes and suggested that the three L. plantarum sHSPs might accomplish different tasks in stress response. To unravel the role of sHSPs, KO mutants of hsp1 and hsp3 were generated using a Cre-lox based system. Mutation of either genes resulted in impaired growth capacity under normal conditions, heat-stress and stresses typically found during host interactions and food technological process. However, survival to heat shock and the level of thermal stabilization of cytoplasmic proteins were similar between mutants and parental strain. Transcriptional analysis revealed that in the mutant genetic backgrounds there is an upregulated basal expression of the un-mutated mate hsps and other stress-related genes, which may compensate for the loss of HSP function, hence possibly accounting for the lack of a remarkable susceptibility to heat challenge. HSP3 seemed relevant for the induction of thermotolerance, while HSP1 was required for improved cryotolerance. Cell surface properties and plasma membrane fluidity were investigated to ascertain the possible membrane association of sHSP. Intriguingly, the loss of hsp1 was associated to a lower level of maximal membrane fluidity upon heat stress. A role for HSP1 in controlling and improving membrane fluidity is suggested which may pertains its cryoprotective function

    Resveratrol-Induced Xenophagy Promotes Intracellular Bacteria Clearance in Intestinal Epithelial Cells and Macrophages

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    Autophagy is a lysosomal degradation process that contributes to host immunity by eliminating invasive pathogens and the modulating inflammatory response. Several infectious and immune disorders are associated with autophagy defects, suggesting that stimulation of autophagy in these diseases should be beneficial. Here, we show that resveratrol is able to boost xenophagy, a selective form of autophagy that target invasive bacteria. We demonstrated that resveratrol promotes in vitro autophagy-dependent clearance of intracellular bacteria in intestinal epithelial cells and macrophages. These results were validated in vivo using infection in a transgenic GFP-LC3 zebrafish model. We also compared the ability of resveratrol derivatives, designed to improve the bioavailability of the parent molecule, to stimulate autophagy and to induce intracellular bacteria clearance. Together, our data demonstrate the ability of resveratrol to stimulate xenophagy, and thereby enhance the clearance of two invasive bacteria involved life-threatening diseases, Salmonella Typhimurium and Crohn's disease-associated Adherent-Invasive Escherichia coli. These findings encourage the further development of pro-autophagic nutrients to strengthen intestinal homeostasis in basal and infectious states

    RĂŽle du systĂšme de communication AGR dans la formation de biofilm de Listeria monocytogenes (incidence sur sa persistance dans les biofilms)

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    Des mutants de Listeria monocytogenes possĂ©dant des dĂ©lĂ©tions dans le cadre de lecture des gĂšnes codant le rĂ©gulateur transcriptionnel (agrA) et le prĂ©curseur du peptide de signalisation (agrD) ont Ă©tĂ© obtenus au laboratoire. La capacitĂ© de ces souches Ă  se dĂ©velopper sous forme de biofilm sur plusieurs surfaces abiotiques a Ă©tĂ© Ă©valuĂ©e dans diffĂ©rents modĂšles de culture de biofilm (statique et dynamique). Le nombre de cellules adhĂ©rĂ©es est affectĂ© par la dĂ©lĂ©tion de agrA et agrD quel que soit le modĂšle utilisĂ©. Ces rĂ©sultats suggĂšrent que le systĂšme agr de L. monocytogenes est impliquĂ© dans les premiĂšres Ă©tapes de la formation de biofilm. Une nouvelle structure de biofilm composĂ©e d un rĂ©seau complexe de microcolonies reliĂ©es par des chaĂźnettes de cellules a Ă©tĂ© mise en Ă©vidence par microscopie confocale dans le modĂšle de culture dynamique. L expression d agr augmente progressivement pendant la croissance du biofilm et cette expression est principalement localisĂ©e Ă  l extĂ©rieur des microcolonies. Par ailleurs, plusieurs niveaux de rĂ©gulation transcriptionnelle et post-transcriptionnelle ont Ă©tĂ© mis en Ă©vidence pour l expression d agr. La formation de biofilm de L. monocytogenes a aussi Ă©tĂ© caractĂ©risĂ©e en prĂ©sence de l espĂšce bactĂ©rienne Staphylococcus aureus. Une augmentation de la quantitĂ© de cellules de L. monocytogenes dans le biofilm a Ă©tĂ© observĂ©e en prĂ©sence d une souche de S. aureus avec un changement de la morphologie des cellules de L. monocytogenes. Des molĂ©cules de nature peptidique prĂ©sents dans le surnageant de biofilm de S. aureus semblent ĂȘtre impliquĂ©es dans ce phĂ©nomĂšne, ce qui suggĂšre que des mĂ©canismes complexes interviennent dans cette stimulation.AgrA and agrD in frame deletion mutants of Listeria monocytogenes were constructed in the laboratory. Adhesion on abiotic surfaces (glass, polystyrene and stainless steel) and biofilm formation of these mutants were assessed under static and dynamic conditions. The number of adhered cells was affected by the deletion of agrA and agrD whatever the model used. These results suggest the involvement of the agr system of L. monocytogenes during the early stages of biofilm formation. A new structure of L. monocytogenes biofilm consisting in a network of knitted-chains was identified by confocale microscopy in a dynamic growth conditions. agr expression progressively increased during the biofilm growth and this expression was preferentially located in cells outside the knitted-chains structure. Moreover, several levels of transcriptional and post-transcriptional regulation were evidenced for agr expression. The biofilm formation of L. monocytogenes was characterized in presence of Staphylococcus aureus strains. An increase of the quantity of L. monocytogenes cells in the biofilm was noticed in the presence of one out of seven S. aureus strain with a change of the morphology of the L. monocytogenes cells. Peptide molecules within cell-free supernatants from S. aureus could be involved in this phenomenon, it suggests that complex mechanisms are involved in this stimulation.DIJON-BU Sciences Economie (212312102) / SudocSudocFranceF

    Sensitivity to acetic acid, ability to colonize abiotic surfaces and virulence potential of Listeria monocytogenes EGD-e after incubation on parsley leaves.

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    International audienceAbstract Aim: To investigate how the survival of Listeria monocytogenes on parsley leaves may affect its ability to sustain process-related harsh conditions and its virulence. Methods and Results: Parsley seedlings were spot inoculated with stationary phase cells of L. monocytogenes EGD-e and incubated for 15 days. Each day, bacterial cells were harvested and enumerated, and their ability to survive acetic acid challenge (90 min, pH 4.0), to colonize abiotic surfaces and to grow as biofilms was assessed. After a 3-log decrease over the first 48 h, the population stabilized to about 10(6) CFU g(-1) until the sixth day. After the sixth day, L. monocytogenes was no longer detected, even after specific enrichment. Incubation on parsley leaves affected the ability of L. monocytogenes to survive acetic acid challenge (90 min, pH 4.0) and to adhere to stainless steel although the ability to grow as biofilm was preserved. To further investigate these physiological alterations, the mRNA levels of six target genes (bsh, clpC, groEL, inlA, opuC, prfA) was quantified using reverse transcription qPCR after 5 h of incubation on parsley leaves. A decrease was observed in all but one (bsh) target, including groEL and clpC which are involved in resistance to salt and acid. Moreover, the decrease in the levels of inlA, prfA and opuC transcripts after incubation on parsley suggested a repression of some genes involved in pathogenicity. In vitro assessment of mammalian cell adherence and invasion using Caco-2 cells confirmed the repression of the virulence factor InlA; however, the virulence potential in vivo in the chick embryo model was not affected. Conclusion: Listeria monocytogenes did undergo rapid changes to adapt its physiology to the phyllosphere. Significance and Impact of the Study: This study highlights the physiological changes undergone by L. monocytogenes during/after survival on parsley leaves

    ConsĂ©quences de l'Accord Economique et Commercial Global ( AECG/CETA). Les principaux impacts de l’Accord Economique et Commercial Global (AECG/CETA) sur les productions animales europĂ©ennes

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    International audienceNearly 10 years after the launch of the negotiations, the CETA (Comprehensive Economic and Trade Agreement) was ratified by the EU institutions in February 2017. Even though member States of the European Union (EU) still have to ratify it, the bulk of this so-called mixed" agreement (shared powers between the EU and its member states) has been applied since the provisional entry of the agreement at the end of September 2017. Indeed, the implementation of the provisions of Community competence will not wait for the final ratification of the agreement. This is particularly the case for tariff issues that will have an impact on European agriculture, in particular by reducing still significant customs duties. It also offers new opportunities for downward revision of sanitary, phytosanitary and environmental standards.A study published by the Livestock Institute, IFIP and AgroParisTech shows that this agreement could weaken European production of beef and pork, through additional imports of meat at zero customs duty at certain times.PrĂšs de 10 ans aprĂšs le lancement des nĂ©gociations, l’Accord Economique et Commercial Global (AECG) ou « Comprehensive Economic and Trade Agreement » (CETA, acronyme utilisĂ© ci-aprĂšs dans le texte) a Ă©tĂ© ratifiĂ© par les institutions communautaires en fĂ©vrier 2017. Si les Etats membres de l’Union europĂ©enne (UE) doivent encore le ratifier, la majeure partie de cet accord dit « mixte » (compĂ©tences partagĂ©es entre l’UE et ses Etats membres) s’applique depuis l’entrĂ©e provisoire de l’accord fin septembre 2017. En effet, la mise en Ɠuvre des dispositions de compĂ©tence communautaire n’attendra pas la ratification dĂ©finitive de l’accord. C’est notamment le cas des questions tarifaires qui auront un impact sur les agricultures europĂ©ennes, notamment par la baisse de droits de douane encore importants. Il offre Ă©galement de nouvelles possibilitĂ©s de rĂ©vision Ă  la baisse des normes sanitaires, phytosanitaires et environnementales. Une Ă©tude publiĂ©e par l’Institut de l’Elevage, l’IFIP et AgroParisTech montre ainsi que cet accord risque de fragiliser les productions europĂ©ennes de viandebovine et porcine par des imports supplĂ©mentaires de viande Ă  droits de douane nuls Ă  certaines pĂ©riodes
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