Michel Treilhou

Neurotoxic effect and metabolic responses induced by a mixture of six pesticides on the earthworm Aporrectodea caliginosa nocturna.

The effects of a mixture of insecticides and/or fungicides at different environmental concentrations were investigated on a Aporrectodea caliginosa nocturna population. This laboratory experiment was carried out in order to reproduce Gaillac (France) vineyard conditions. Neurotoxicity (cholinesterase), metabolisation (glutathione-S-transferase) and oxidative stress (catalase) enzymes were studied as biomarkers in earthworms after short-term exposure in terraria. The aim was to observe the global effects of pesticide exposure, as in a vineyard, rather than focus on each isolated biomarker variation, or on each compounds impact. ChE activity was inhibited after a few days of insecticide and/or fungicide exposure, indicative of a neurotoxic effect in earthworms. The significant increase in GST and CAT activities revealed the metabolisation of these products resulting in the production of reactive oxygen species. After a long period of exposure or high concentrations, earthworms were physiologically damaged: they could not cope with the high toxicity (cellular dysfunction, protein catabolism...). Chemical analysis showed that pesticide bioaccumulation in earthworm tissues, even in those exposed to the highest concentrations and for the longest periods, was very low (under LOD) or absent. However, the study of pesticide residues in terraria after 34 days in a climate chamber suggested that earthworms participate in soil pesticide breakdown.

Development and validation of a rapid multiresidue method for pesticide determination using gas chromatography–mass spectrometry: A realistic case in vineyard soils

A rapid and simultaneous method for residue identification and quantification for seven pesticides in agricultural soils has been developed to study a realistic situation in vineyard. The target compounds are two insecticides, two herbicides and three fungicides, from different chemical families. The procedure is based on a pressurized liquid extraction (PLE) with acetone, before a multiresidue GC-MS analysis. The recovery of PLE is between 53.8+/-2.4 and 99.9+/-4.4% according to pesticide. A limit of detection (LOD) between 1.4 and 4.6 microg kg(-1) of dry soil was obtained for five analytes. This procedure for testing soil contamination is sensitive and easy to perform.

Identification and characterization of a novel antimicrobial peptide from the venom of the ant Tetramorium bicarinatum.

A novel antimicrobial peptide, named Bicarinalin, has been isolated from the venom of the ant Tetramorium bicarinatum. Its amino acid sequence has been determined by de novo sequencing using mass spectrometry and by Edman degradation. Bicarinalin contained 20 amino acid residues and was C-terminally amidated as the majority of antimicrobial peptides isolated to date from insect venoms. Interestingly, this peptide had a linear structure and exhibited no meaningful similarity with any known peptides. Antibacterial activities against Staphylococcus aureus and S. xylosus strains were evaluated using a synthetic replicate. Bicarinalin had a potent and broad antibacterial activity of the same magnitude as Melittin and other hymenopteran antimicrobial peptides such as Pilosulin or Defensin. Moreover, this antimicrobial peptide has a weak hemolytic activity compared to Melittin on erythrocytes, suggesting potential for development into an anti-infective agent for use against emerging antibiotic-resistant pathogens.

Unusual Methyl-Branched α,β-Unsaturated Acyl Chain Substitutions in the Nod Factors of an Arctic Rhizobium,Mesorhizobium sp. Strain N33 (Oxytropis arctobia)

Rhizobia are soil bacteria, now classified in several genera (e.g., Rhizobium, Sinorhizobium, Mesorhizobium, Bradyrhizobium, Azorhizobium), which form a symbiotic association with legume plants. The interaction between bacteria and plants results in the formation of nodules on the host plant roots, in which rhizobia fix atmospheric nitrogen. The association between rhizobia and legumes is specific: each rhizobial strain has a defined host range. For example, Mesorhizobium sp. strain N33, isolated from Oxytropis arctobia, also nodulates Astragalus alpinus and Onobrychis viciifolia (19, 26). In contrast, Sinorhizobium meliloti efficiently nodulates alfalfa (Medicago sativa) as well as Melilotus and Trigonella species. Mesorhizobium sp. strain N33 was isolated in the Canadian high arctic and is able to grow and fix nitrogen at temperatures as low as 5°C. In addition, it was shown that arctic rhizobia promoted better growth of O. viciifolia at low temperatures than did temperate strains (27). Thus, it might be valuable to extend the host range of arctic rhizobia to agronomically important legumes, in order to improve nitrogen fixation by these plants at low temperatures. It is therefore important to understand the molecular mechanisms controlling the nodulation specificity of arctic rhizobia. Earlier work has shown that nodulation and host specificity in rhizobium-legume symbiosis are determined by signal exchanges between the bacteria and the host plant (21). Flavonoids excreted by the plant roots induce the expression of rhizobial nodulation (nod) genes. Most of these genes are involved in the biosynthesis and secretion of bacterial signals, the Nod factors, that can specifically induce symbiotic responses of the host plants. These responses include root hair deformation, division of root cortical cells and, in some instances, nodule formation (8, 32). The structures of Nod factors produced by several rhizobial species have been characterized. They are all lipochito-oligosaccharides (LCOs) consisting of β-1,4-linked oligomers of three to five N-acetylglucosamine residues with an amide-linked acyl chain on the nonreducing terminal residue (8, 10, 25). In addition, the glucosamine residues can carry various substitutions. Nod factor specificity is determined by the nature of these substitutions and of the N-acyl chain. A number of nodulation genes have been identified in Mesorhizobium sp. strain N33 (2, 3, 4). The nodABC genes, which are found in all rhizobial species, are responsible for the synthesis of the lipo-oligosaccharide core common to all Nod factors. In contrast to most rhizobial species, where nodABC belong to one operon, in Mesorhizobium sp. strain N33 nodA and nodBC belong to two different operons (2, 4). In addition to nodABC, several nod genes likely to be involved in Nod factor substitutions have been characterized (3, 4). The nodHPQ genes, which are also found in S. meliloti and Rhizobium tropici, have been shown to specify O sulfation of the Nod factor reducing end in these two species (11, 18, 29). The nodFE genes, which are also present in S. meliloti and R. leguminosarum, determine in these two species the synthesis of various polyunsaturated fatty acids with one or several double bounds conjugated to the carbonyl group (7, 34, 39). Therefore, one might expect the Mesorhizobium sp. strain N33 Nod factors to be sulfated and substituted by a fatty acid with conjugated double bonds. However, given the peculiar host range of this species, the Mesorhizobium sp. strain N33 Nod factors are likely to carry novel substitutions. In this paper, we describe the structure of the Mesorhizobium sp. strain N33 Nod factors. We show that they have original structures with substitutions never described before, and we study several features of their biosynthesis.

Trace determination of linear alkylbenzene sulfonates: application in artificially polluted soil-carrots system.

Surfactants are widely used in household and industrial products. The risk of incorporation of linear alkylbenzene sulfonates (LAS) from biosolids, wastewater, and fertilizers land application to the food chain is being assessed at present by the European Union. In the present work, a complete analytical method for LAS trace determination has been developed and successfully applied to LAS (C10–C13) uptake in carrot plants used as model. These carrots were grown in soil with the trace organics compounds added directly into the plant containers in pure substances form. LAS trace determination (μg kg−1 dry matter) in carrots samples was achieved by Soxtec apparatus and high-performance liquid chromatography-fluorescence detection. The methodology developed provides LAS determination at low detection limits (5 μg kg−1 dry matter) for carrot sample (2 g dry matter) with good recoveries rate (>90%). Transfer of LAS has been followed into the various parts of the carrot plant. LAS are generally found in the carrot leaves and percentage transfer remains very low (0.02%).

Differentiation of O-Acetyl and O-Carbamoyl esters of N-Acetyl-Glucosamine by decomposition of their oxonium ions. application to the structure of the nonreducing terminal residue of Nod factors

Nod factors are substituted N-acyl chito-oligomers secreted by plant symbiotic bacteria of the Rhizobium family. Substitutions on the oligosaccharide core specify their recognition by host plants. A method using tandem mass spectrometry is proposed to locate the O-acetyl and O-carbamoyl substituents on the nonreducing terminal residue of the chito-oligomers. As model compounds, all the positional isomers of monoacetyl and monocarbamoyl esters of 1-O-methyl-N-acetyl-α-D-glucosamine were synthesized. Oxonium ions (MH − CH3OH)+ were generated by liquid secondary ion mass spectrometry (LSIMS) and their decomposition was recorded on a tandem magnetic instrument. Large differences were observed in the relative abundances of ions resulting from elimination of water and of the O-ester substituent from metastable oxonium ions. Deuterium exchange reactions indicated parallel elimination pathways involving either exchangeable or carbon-linked hydrogens. The intensity ratios of some of the ions generated by collisions with helium atoms allowed the isomers to be distinguished. The main dissociation routes were identified. Metastable and collision-induced decomposition of the B1 ions from Nod factors of Sinorhizobium meliloti and Azorhizobium caulinodans resembled that of the 6-O-substituted N-acetylglucosamine models. Decomposition of the B1 ion from Mesorhizobium loti and Rhizobium etli Nod factors, was similar to that of 3-O-carbamoyl N-acetyl-glucosamine and different to that of the 4-O isomer. 6-O- and 3-O-carbamoylation specified by the nodU and nolO genes, respectively, of Rhizobium. sp. NGR234 were confirmed.

Capillary electrophoresis:: theory, teaching approach and separation of oligosaccharides using indirect UV detection

Capillary electrophoresis, a recent analytical method (the first commercial instrument was sold just 10 years ago), offers an efficient alternative means compared to other current separation techniques. Due to a wide application range, this method is becoming more and more important among analytical laboratories. Thus, introductory lectures on this analytical technique are of particular interest. Moreover, the use of capillary electrophoresis aids in the understanding of the numerous parameters which influence electrophoretic migrations, such as ion mobilities, electrical field, pH, pKa, joule heating and buffering capacity. This article presents the theory of capillary electrophoresis and various steps of an analysis of four carbohydrates using this technique. This presentation of the data is similar to the way the students, to whom this analysis was asked, presented theirs. Representative results obtained by four students out of 100 are shown.

ChE, GST and CAT: Evaluation of the efficiency of a combined buffer for protein extraction

Toxicity and biotransformation of several earthworm contaminants are widely evaluated nowadays using biochemical biomarkers. Many investigations track enzyme activities as biomarkers of neurotoxicity (cholinesterase (ChE)), metabolisation (glutathione-S-transferase (GST)) and oxidative stress (catalase (CAT)). This study proposes an evaluation of the use of a combined buffer, to extract proteins from earthworms and then analyse the 3 biomarkers. The method provides good results and allows protein extraction and quantitative determination of biomarkers with the same efficiency as the enzyme-specific buffers. It decreases preparation time and permits a study of the biomarkers on the same individual with only one homogenisation.

Biochemical and biophysical combined study of bicarinalin, an ant venom antimicrobial peptide.

We have recently characterized bicarinalin as the most abundant peptide from the venom of the ant Tetramorium bicarinatum. This antimicrobial peptide is active against Staphylococcus and Enterobacteriaceae. To further investigate the antimicrobial properties of this cationic and cysteine-free peptide, we have studied its antibacterial, antifungal and antiparasitic activities on a large array of microorganisms. Bicarinalin was active against fifteen microorganisms with minimal inhibitory concentrations ranging from 2 and 25μmolL(-1). Cronobacter sakazakii, Salmonella enterica, Candida albicans, Aspergilus niger and Saccharomyces cerevisiae were particularly susceptible to this novel antimicrobial peptide. Resistant strains of Staphylococcus aureus, Pseudomonas aeruginosa and C. albicans were as susceptible as the canonical strains. Interestingly, bicarinalin was also active against the parasite Leishmania infantum with a minimal inhibitory concentrations of 2μmolL(-1). The bicarinalin pre-propeptide cDNA sequence has been determined using a combination of degenerated primers with RACE PCR strategy. Interestingly, the N-terminal domain of bicarinalin pre-propeptide exhibited sequence similarity with the pilosulin antimicrobial peptide family previously described in the Myrmecia venoms. Moreover, using SYTOX green uptake assay, we showed that, for all the tested microorganisms, bicarinalin acted through a membrane permeabilization mechanism. Two dimensional-NMR experiments showed that bicarinalin displayed a 10 residue-long α-helical structure flanked by two N- and C-terminal disordered regions. This partially amphipathic helix may explain the membrane permeabilization mechanism of bicarinalin observed in this study. Finally, therapeutic value of bicarinalin was highlighted by its low cytotoxicity against human lymphocytes at bactericidal concentrations and its long half-life in human serum which was around 15h.

Synthesis and biological evaluation of new bis-indolone-N-oxides

A series of bis-indolone-N-oxides, 1a-f, was prepared from bis(ethynyl)benzenes and o-halonitroaryls and studied for their in vitro antiplasmodial activities against Plasmodium falciparum and representative strains of bacteria and candida as well as for their cytotoxicity against a human tumor cell line (MCF7). They did not cause any haemolysis (300 μgmL(-1)). Of the synthesized bis-indolones, compound 1a had the most potent antiplasmodial activity (IC50=0.763 μmolL(-1) on the FcB1 strain) with a selectivity index (CC50 MCF7/IC50 FcB1) of 35.6. No potency against the tested microbial strains was observed.