Effet inhibiteur à la longues chaînes et de dérivés thiazolés sur la corrosion du laiton Amirauté.optimale des petites stations d'épuration à boues activées

Dans cette étude, des mesures électrochimiques ont été réalisées pour caractériser le comportement du laiton Amirauté dans une solution de chlorure de sodium 0,5 M en l'absence d'inhibiteur et en présence d'un mélange d'amines à longue chaîne et de dérivés thiazolés. Cette formulation est utilisée pour le traitement des eaux des circuits de refroidissement. Les courbes courant-tension stationnaires et les diagrammes d'impédance électrochimique ont été obtenus avec une electrode tournante.La première partie de cette étude présente les résultats obtenus pour deux concentrations du mélange et deux temps d'immersion préalable au potentiel de corrosion. Les essais électrochimiques montrent que l'effet inhibiteur est d'autant plus marqué que la concentration augmente. Une légère diminution de la protection de la surface du laiton Amirauté est observée avec l'augmentation du temps de maintien au potentiel de corrosion.La deuxième partie de l'étude compare les effets inhibiteurs de chacun des constituants du mélange, d'une part, pour les valeurs de concentration utilisées lors du traitement des eaux des circuits de refroidissement (0,1 mg/l de solution contenant les dérivés thiazolés et 1 mg/l de solution contenant les alkylamines) et, d'autre part, pour des valeurs de concentration comparables (5 mg/l).Pour la concentration de 0,1 mg/l l'action inhibitrice des dérivés thiazolés n'a pas été clairement mise en évidence. Ainsi, la protection contre la corrosion des circuits de refroidissement en laiton Amirauté avec le mélange est apportée principalement par les alkylamines. Celles-ci forment un film compact très protecteur à la surface de l'électrode.Pour des valeurs de concentration plus importantes, l'addition de 0,5 mg/l de dérivés thiazolés à 5 mg/l d'alkylamines améliore la protection du matériau.In this study, electrochemical measurements were carriet out to characterize the behaviour of Admiralty Brass in a 0.5 M sodium chloride solution in the absence of inhibitors and in the presence of a mixture of alkylamines and thiazol-derived products. This formulation is employed for water treatment in cooling circuits.The steady-state current voltage curves and the impedance diagrams were obtained with a rotating disc electrode in order to control the hydrodynamic conditions.The first part of this study deals with the results obtained for two concentrations of the mixture and for two immersion times at the corrosion potential. It has been shown that the inhibitive effect is more marked when the concentration increases from 10 to 50 mg/l. A slight decrease of the protection of the brass surface is observed when the immersion time increasesThe second part of this study is a comparison of the inhibitive effects of each compound of the mixture, on one hand, for concentration values used in the water treatment (0.1 mg/l of tbe solution containing the thiazol-derived products and 1 mg/l of the solution containing the alkylamines) and on the other hand, for identical concentration values (5 mg/l ). For 0.1 mg/l, no inhibitive action of thiazol-derived products could be detected. Thus, the corrosion protection of cooling circuits in Admiralty brass is attributed essentially to the alkylamines. They form a thick, protective film at the electrode surface. For higher concentration values, the addition of 0.5 mg/l of thiazol-derived products to 5 mg/l of alkylamines improves the corrosion resistance of brass

Burkholderia pseudomallei Capsular Polysaccharide Recognition by a Monoclonal Antibody Reveals Key Details toward a Biodefense Vaccine and Diagnostics against Melioidosis.

Burkholderia pseudomallei is the bacterium responsible for melioidosis, an infectious disease with high mortality rates. Since melioidosis is a significant public health concern in endemic regions and the organism is currently classified as a potential biothreat agent, the development of effective vaccines and rapid diagnostics is a priority. The capsular polysaccharide (CPS) expressed by B. pseudomallei is a highly conserved virulence factor and a protective antigen. Because of this, CPS is considered an attractive antigen for use in the development of both vaccines and diagnostics. In the present study, we describe the interactions of CPS with the murine monoclonal antibody (mAb) 4C4 using a multidisciplinary approach including organic synthesis, molecular biology techniques, surface plasmon resonance, and nuclear magnetic spectroscopy. Using these methods, we determined the mode of binding between mAb 4C4 and native CPS or ad hoc synthesized capsular polysaccharide fragments. Interestingly, we demonstrated that the O-acetyl moiety of CPS is essential for the interaction of the CPS epitope with mAb 4C4. Collectively, our results provide important insights into the structural features of B. pseudomallei CPS that enable antibody recognition that may help the rational design of CPS-based vaccine candidates. In addition, our findings confirm that the mAb 4C4 is suitable for use in an antibody-based detection assay for diagnosis of B. pseudomallei infections

Macrophage origin limits functional plasticity in helminth-bacterial co-infection

Rapid reprogramming of the macrophage activation phenotype is considered important in the defense against consecutive infection with diverse infectious agents. However, in the setting of persistent, chronic infection the functional importance of macrophage-intrinsic adaptation to changing environments vs. recruitment of new macrophages remains unclear. Here we show that resident peritoneal macrophages expanded by infection with the nematode Heligmosomoides polygyrus bakeri altered their activation phenotype in response to infection with Salmonella enterica ser. Typhimurium in vitro and in vivo. The nematode-expanded resident F4/80high macrophages efficiently upregulated bacterial induced effector molecules (e.g. MHC-II, NOS2) similarly to newly recruited monocyte-derived macrophages. Nonetheless, recruitment of blood monocyte-derived macrophages to Salmonella infection occurred with equal magnitude in co-infected animals and caused displacement of the nematode-expanded, tissue resident-derived macrophages from the peritoneal cavity. Global gene expression analysis revealed that although nematode-expanded resident F4/80high macrophages made an anti-bacterial response, this was muted as compared to newly recruited F4/80low macrophages. However, the F4/80high macrophages adopted unique functional characteristics that included enhanced neutrophil-stimulating chemokine production. Thus, our data provide important evidence that plastic adaptation of MΦ activation does occur in vivo, but that cellular plasticity is outweighed by functional capabilities specific to the tissue origin of the cell

Combined systems approaches reveal highly plastic responses to antimicrobial peptide challenge in Escherichia coli

Obtaining an in-depth understanding of the arms races between peptides comprising the innate immune response and bacterial pathogens is of fundamental interest and will inform the development of new antibacterial therapeutics. We investigated whether a whole organism view of antimicrobial peptide (AMP) challenge on Escherichia coli would provide a suitably sophisticated bacterial perspective on AMP mechanism of action. Selecting structurally and physically related AMPs but with expected differences in bactericidal strategy, we monitored changes in bacterial metabolomes, morphological features and gene expression following AMP challenge at sub-lethal concentrations. For each technique, the vast majority of changes were specific to each AMP, with such a plastic response indicating E. coli is highly capable of discriminating between specific antibiotic challenges. Analysis of the ontological profiles generated from the transcriptomic analyses suggests this approach can accurately predict the antibacterial mode of action, providing a fresh, novel perspective for previous functional and biophysical studies

Barrier Tissue Macrophages: Functional Adaptation to Environmental Challenges

Macrophages are found throughout the body, where they have crucial roles in tissue development, homeostasis and remodeling, as well as being sentinels of the innate immune system that can contribute to protective immunity and inflammation. Barrier tissues, such as the intestine, lung, skin and liver, are exposed constantly to the outside world, which places special demands on resident cell populations such as macrophages. Here we review the mounting evidence that although macrophages in different barrier tissues may be derived from distinct progenitors, their highly specific properties are shaped by the local environment, which allows them to adapt precisely to the needs of their anatomical niche. We discuss the properties of macrophages in steady-state barrier tissues, outline the factors that shape their differentiation and behavior and describe how macrophages change during protective immunity and inflammation

Stereoselective Access to Iminosugar C, C-Glycosides from 6-Azidoketopyranoses

International audienceWe report the synthesis of iminosugar C,C-glycosides starting from 6-azidoketopyranoses. Their Staudinger-azaWittig-mediated cyclization provided bicyclic N,O-acetals, which were stereoselectively opened with AllMgBr to afford β-hydroxyazepanes with a quaternary carbon α to the nitrogen. Their ring contraction via a β-aminoalcohol rearrangement produced the six-membered l-iminosugars with two functional handles at the pseudoanomeric position. Inversion of the free OH at the azepane level furnished the d-iminosugars

Dysregulation of in vitro cytokine production by monocytes during sepsis.

The production by monocytes of interleukin-1 alpha (IL-1 alpha), interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and tumor necrosis factor alpha (TNF alpha) in intensive care unit (ICU) patients with sepsis syndrome (n = 23) or noninfectious shock (n = 6) is reported. Plasma cytokines, cell-associated cytokines within freshly isolated monocytes and LPS-induced in vitro cytokine production were assessed at admission and at regular intervals during ICU stay. TNF alpha and IL-6 were the most frequently detected circulating cytokines. Despite the fact that IL-1 alpha is the main cytokine found within monocytes upon in vitro activation of cells from healthy individuals, it was very rarely detected within freshly isolated monocytes from septic patients, and levels of cell-associated IL-1 beta were lower than those of TNF alpha. Cell-associated IL-1 beta and TNF alpha were not correlated with corresponding levels in plasma. Upon LPS stimulation, we observed a profound decrease of in vitro IL-1 alpha production by monocytes in all patients, and of IL-1 beta, IL-6, and TNF alpha in septic patients. This reduced LPS-induced production of cytokines was most pronounced in patients with gram-negative infections. Finally, monocytes from survival patients, but not from nonsurvival ones recovered their capacity to produce normal amounts of cytokines upon LPS stimulation. In conclusion, our data indicate an in vivo activation of circulating monocytes during sepsis as well as in noninfectious shock and suggest that complex regulatory mechanisms can downregulate the production of cytokines by monocytes during severe infections

Evaluation of nonnatural L-iminosugar C,C-glycosides, a new class of C-branched iminosugars, as glycosidase inhibitors

International audienceCapitalizing on a previously developed Staudinger/azaWittig/Grignard (SAWG)-ring contraction sequence that furnished protected six-membered L-iminosugar C,C-glycosides bearing an allyl group and various substituents at the pseudoanomeric position, the synthesis and glycosidase inhibition of a small library of six- and seven-membered L-iminosugar C,C-glycosides is reported. Their hydrogenolysis or cyclization by RCM followed by deprotection afforded eleven L-iminosugars including spirocyclic derivatives. All compounds adopt a 1C4 conformation in solution according to NMR data. Compared to previously reported branched L-iminosugars, the L-iminosugar C,C-glycosides reported herein were less potent glycosidase inhibitors. However, some of these compounds showed micromolar inhibition of human lysosome β-glucocerebrosidase suggesting that such iminosugars could be useful to access potent CGase inhibitors by adjusting the structure/length of the pseudoanomeric substituents