Revue des principales méthodes d’identification des sources de pollutions fécales des eaux et coquillages

Les contaminations fécales des eaux et des coquillages induisent des risques pour la santé humaine et des pertes économiques liées, entre autres, aux interdictions de baignade et à la fermeture des zones de conchyliculture. La réduction des apports à l’origine de cette contamination est facilitée par une identification précise des sources (humaines ou animales) qui peut aussi servir à hié rarchiser les mesures à adopter en cas de besoin. De nombreux marqueurs ont été proposés à ce titre durant les deux dernières décennies. Ils correspondent :-à des micro-organismes (bactéries, virus ou bactériophages) mis en évidence par des approaches culturales, biochimiques ou moléculaires; -à des molécules chimiques présentes naturellement dans les fèces ou associées à l’une des sources de pollution; -et à la mise en évidence de cellules spécifiques de l’hôte dissimulées dans les matières fécales. Cet article présente ces différentes methods d’identification des sources de contaminations fécales en décrivant leur utilisation et la nature des résultats qu’elles permettent d’obtenir. Le principal corollaire de cette revue bibliographique est qu’il semble nécessaire de coupler différents marqueurs pour pouvoir identifier les sources

The host model Galleria mellonella is resistant to taylorellae infection

The genusTaylorellais composed of two species: (i)Taylorella equigenitalis,the causative agent of CEM, a venereally transmitted infection of Equidaeand (ii)Taylorella asinigenitalis, a closely related species considered to benonpathogenic, although experimental infection of mares with this bacteriumresulted in clinical signs of vaginitis, cervicitis or endometritis. Currently, thereis a need for an alternative host model to further study the taylorellae species.In this context, we exploredGalleria mellonellalarvae as potential alternativemodel hosts for taylorellae. Our results showed that infection ofG. mellonellalarvae with a high concentration of taylorellae did not induce overtG. mellonellamortality and that taylorellae were not able to proliferate withinG. mellonella. In conclusion,G. mellonellalarvae are resistant to taylorellaeinfection and therefore do not constitute a relevant alternative system forstudying the virulence of taylorellae species

Identification of general stress genes in Enterococcus faecalis

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Identification of general stress genes for Enterococcus faecalis

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Genetic modifications and introduction of heterologous pdc genes in Enterococcus faecalis for its use in production of bioethanol

Genetically-modified Enterococcus faecalis has a potential of survival and can be used in ethanolic fermentations. Fermentation profiles of E. faecalis JH2-2 were assessed using glucose and lactose as carbon sources. Deletion of lactate dehydrogenase (ldh) genes increased the ethanol production from 0.25 to 0.82 g/l, which was further increased to 0.96 g/l by the insertion of a pyruvate decarboxylase (pdc) gene (from Sarcina ventriculi or Clostridium acetobutylicum) in place ldh1. When grown on lactose, the pdcSv and pdcCa showed 13.6 and 17.6 U mg−1 of pdc specific activity, respectively. Highest activity (47 U mg−1) and ethanol concentration (2.3 g/l) were obtained with pdcCa using an expression plasmid. Formate and acetate were also produced in high quantities. Transcriptional analysis showed that aldehyde alcohol dehydrogenase gene was upregulated up to 16-fold. Further optimizations are required for higher ethanol production

Analyse de l'osmoadaptation chez Enterococcus faecalis

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Characterization of the lacticin 481 operon: the Lactococcus lactis genes lctF, lctE, and lctG encode a putative ABC transporter involved in bacteriocin immunity.

The lantibiotic lacticin 481 is a bacteriocin produced by Lactococcus lactis strains. The genetic determinants of lacticin 481 production are organized as an operon encoded by a 70-kb plasmid. We previously reported the first three genes of this operon, lctA, lctM, and lctT, which are involved in the bacteriocin biosynthesis and export (A. Rincé, A. Dufour, S. Le Pogam, D. Thuault, C. M. Bourgeois, and J.-P. Le Pennec, Appl. Environ. Microbiol. 60:1652-1657, 1994). The operon contains three additional open reading frames: lctF, lctE, and lctG. The hydrophobicity profiles and sequence similarities strongly suggest that the three gene products associate to form an ABC transporter. When the three genes were coexpressed into a lacticin 481-sensitive L. lactis strain, the strain became resistant to the bacteriocin. This protection could not be obtained when any of the three genes was deleted, confirming that lctF, lctE, and lctG are all necessary to provide immunity to lacticin 481. The quantification of the levels of immunity showed that lctF, lctE, and lctG could account for at least 6% and up to 100% of the immunity of the wild-type lacticin 481 producer strain, depending on the gene expression regulation. The lacticin 481 biosynthesis and immunity systems are discussed and compared to other lantibiotic systems

Identification of new genes related to osmotic adaptation in Enterococcus faecalis

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Physiological and molecular aspects of the bile salts response of Enterococcus faecalis

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