122 research outputs found

    Molecular diversity of antimicrobial effectors in the oyster Crassostrea gigas

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    Background: To gain insight into the molecular diversity of antimicrobial peptides and proteins in the oyster Crassostrea gigas, we characterized and compared the sequence polymorphism of the antimicrobial peptides (AMPs), Cg-Defensins (Cg-Defs) and Cg-Proline Rich peptide (Cg-Prp), and of the bactericidal permeability increasing protein, Cg-BPI. For that, we analyzed genomic and transcript sequences obtained by specific PCR amplification and in silico searches. Results: High diversification among the three antimicrobial effectors was evidenced by this polymorphism survey. On the basis of sequence phylogenies, each AMP aggregates into clearly defined groups of variants and is the product of a multigenic family displaying a variety of gene structures. In contrast, Cg-bpi forms a single group and is encoded by a single gene copy. Moreover, we identified for both AMPs several genetic mechanisms of diversification such as recombination, parallel mutations leading to phylogenetic homoplasy and indel events. In addition, the non synonymous to synonymous substitutions ratio by codon (dN/dS) revealed several negatively and positively selected sites for both AMPs, suggesting that directional selection pressures have shaped their sequence variations. Conclusions: This study shows for the first time in a mollusc that antimicrobial peptides and proteins have been subject to distinct patterns of diversification and we evidence the existence of different evolutionary routes leading to such sequence variability

    Acute and late-onset optic atrophy due to a novel OPA1 mutation leading to a mitochondrial coupling defect

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    PurposeAutosomal dominant optic atrophy (ADOA, OMIM 165500), an inherited optic neuropathy that leads to retinal ganglion cell degeneration and reduced visual acuity during the early decades of life, is mainly associated with mutations in the OPA1 gene. Here we report a novel ADOA phenotype associated with a new pathogenic OPA1 gene mutation. Methods The patient, a 62-year-old woman, was referred for acute, painless, and severe visual loss in her right eye. Acute visual loss in her left eye occurred a year after initial presentation. MRI confirmed the diagnosis of isolated atrophic bilateral optic neuropathy. We performed DNA sequencing of the entire coding sequence and the exon/intron junctions of the OPA1 gene, and we searched for the mitochondrial DNA mutations responsible for Leber hereditary optic atrophy by sequencing entirely mitochondrial DNA. Mitochondrial respiratory chain complex activity and mitochondrial morphology were investigated in skin fibroblasts from the patient and controls. Results We identified a novel heterozygous missense mutation (c.2794C>T) in exon 27 of the OPA1 gene, resulting in an amino acid change (p.R932C) in the protein. This mutation, which affects a highly conserved amino acids, has not been previously reported, and was absent in 400 control chromosomes. Mitochondrial DNA sequence analysis did not reveal any mutation associated with Leber hereditary optic neuropathy or any pathogenic mutations. The investigation of skin fibroblasts from the patient revealed a coupling defect of oxidative phosphorylation and a larger proportion of short mitochondria than in controls. Conclusions The presence of an OPA1 mutation indicates that this sporadic, late-onset acute case of optic neuropathy is related to ADOA and to a mitochondrial energetic defect. This suggests that the mutational screening of the OPA1 gene would be justified in atypical cases of optic nerve atrophy with no evident cause

    Generation and analysis of a 29,745 unique Expressed Sequence Tags from the Pacific oyster (Crassostrea gigas) assembled into a publicly accessible database: the GigasDatabase

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    Background: Although bivalves are among the most-studied marine organisms because of their ecological role and economic importance, very little information is available on the genome sequences of oyster species. This report documents three large-scale cDNA sequencing projects for the Pacific oyster Crassostrea gigas initiated to provide a large number of expressed sequence tags that were subsequently compiled in a publicly accessible database. This resource allowed for the identification of a large number of transcripts and provides valuable information for ongoing investigations of tissue-specific and stimulus-dependant gene expression patterns. These data are crucial for constructing comprehensive DNA microarrays, identifying single nucleotide polymorphisms and microsatellites in coding regions, and for identifying genes when the entire genome sequence of C. gigas becomes available. Description: In the present paper, we report the production of 40,845 high-quality ESTs that identify 29,745 unique transcribed sequences consisting of 7,940 contigs and 21,805 singletons. All of these new sequences, together with existing public sequence data, have been compiled into a publicly-available Website http://public-contigbrowser.sigenae.org:9090/Crassostrea_gigas/index.htm l. Approximately 43% of the unique ESTs had significant matches against the SwissProt database and 27% were annotated using Gene Ontology terms. In addition, we identified a total of 208 in silico microsatellites from the ESTs, with 173 having sufficient flanking sequence for primer design. We also identified a total of 7,530 putative in silico, single-nucleotide polymorphisms using existing and newly-generated EST resources for the Pacific oyster. Conclusion: A publicly-available database has been populated with 29,745 unique sequences for the Pacific oyster Crassostrea gigas. The database provides many tools to search cleaned and assembled ESTs. The user may input and submit several filters, such as protein or nucleotide hits, to select and download relevant elements. This database constitutes one of the most developed genomic resources accessible among Lophotrochozoans, an orphan clade of bilateral animals. These data will accelerate the development of both genomics and genetics in a commercially-important species with the highest annual, commercial production of any aquatic organism

    A pearl of a partnership

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    Pearl farming is essential to the economy of French Polynesia, generating thousands of jobs for the islands. What are the main concerns for the current state of pearl farming in the region

    Molecular diversity of antimicrobial effectors in the oyster Crassostrea gigas and role in the antimicrobial response

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    Ce travail a contribuĂ© Ă  la comprĂ©hension des bases molĂ©culaires de l'immunitĂ© de l'huĂźtre creuse par la caractĂ©risation la diversitĂ© de trois effecteurs antimicrobiens de C. gigas et par l'apprĂ©hension du rĂŽle de cette diversitĂ© dans les mĂ©canismes de dĂ©fense. Des analyses phylogĂ©nĂ©tiques de deux peptides antimicrobiens (AMPs), Cg-DĂ©fensines (Cg-Defs) et Cg-Proline rich peptide (Cg-Prp), et d'une protĂ©ine de type Bactericidal Permeability Increasing protein, Cg-BPI, nous a permis montrer la grande diversitĂ© pour les 2 AMPs, qui est gĂ©nĂ©rĂ©e par plusieurs mĂ©canismes gĂ©nĂ©tiques et par des pressions de sĂ©lection directionnelles, suggĂšrant une diversitĂ© fonctionnelle des variants. L'importance biologique de cette diversitĂ© a Ă©tĂ© Ă©tudiĂ©e pour trois variants de Cg-Defs. Une forte activitĂ© antimicrobienne a Ă©tĂ© mise en Ă©vidence contre les bactĂ©ries Ă  Gram positive, mais celle-ci diffĂšre selon les variants. De plus, nous avons dĂ©montrĂ© que le mĂ©canisme d'action des Cg-Defs contre S. aureus repose sur l'inhibition de la biosynthĂšse du peptidoglycane par le piegeage de son prĂ©curseur, le lipide II. Finalement, l'expression des transcrits et la localisation de ces effecteurs en rĂ©ponse Ă  une infection par un Vibrio pathogĂšne ont montrĂ© un rĂ©seau complexe des profils d'expression des diffĂ©rents antimicrobiens, au niveau des populations hĂ©mocytaires et des tissus d'huĂźtre, suggĂ©rant une interaction entre les antimicrobiens du fait de leur colocalization. La combinaison entre les familles ou entre les variants d'une mĂȘme famille produit de fortes activitĂ©s synergiques qui Ă©largissent les spectres d'activitĂ©. Ainsi, la diversitĂ© produit par la coĂ©volution entre hĂŽte et pathogĂšnes pourrait amĂ©liorer l'activitĂ© des AMPs d'huĂźtre, lui confĂ©rant une plus grande protection contre les pathogĂšnes de son environnement.This work contributed to the knowledge of the molecular bases of oyster immunity by the characterization of the diversity of three antimicrobials of C. gigas and the understanding of the role played by their diversity in the oyster antimicrobial response. Phylogenetic analyses of two antimicrobial peptides (AMPs), Cg-Defensins (Cg-Defs) and Cg-Proline rich peptide (Cg-Prp), and one Bactericidal Permeability Increasing protein, Cg-BPI, led us to the identification of a high diversity for both AMPs. Further analyses showed that this diversity is generated by gene duplication, allelic recombination and directional selection pressures, suggesting their functional diversification. The biological meaning of AMP diversity was investigated for the three major variants of Cg-Defs, which revealed a strong but variable potency against Gram-positive bacteria. We evidenced that oyster defensins kill S. aureus through binding to the cell wall precursor lipid II, resulting in the inhibition of peptidoglycan biosynthesis. Finally, transcript expression and localization of oyster antimicrobials after a pathogenic infection evidenced a complex network in their expression profiles in hemocyte populations and oyster tissues, suggesting a potential interplay between antimicrobials as a result of their colocalization. Indeed, the combination of oyster antimicrobials produced strong synergistic activities that enlarged their antimicrobial spectra. Thus, the diversity of oyster antimicrobials may provide significant means in acquiring functional divergence, probably concerned in the evolutionary arms race between hosts and their pathogens.From our data, it would provide oysters with a higher protection against the potential pathogens from their environment.MONTPELLIER-BU Sciences (341722106) / SudocSudocFranceF

    Strategie d'echantillonnage des lieux du REPHY Sanitaire et REPHYTOX en Occitanie - Année 2023

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    Cette spĂ©cification technique a pour objet de dĂ©crire la stratĂ©gie d’échantillonnage des lieux de surveillance du REPHY Sanitaire et REPHYTOX en Occitanie. Les logigrammes, prĂ©sentĂ©s par secteur gĂ©ographique, indiquent la logique opĂ©rationnelle Ă  suivre entre les lieux de surveillance du REPHY et du REPHYTOX dans le cadre de la mise en oeuvre des stratĂ©gies de ces rĂ©seaux. Ces stratĂ©gies sont dĂ©taillĂ©es dans le document de procĂ©dure nationale REPHYTOX (version en vigueur) et plus particuliĂšrement dans le paragraphe « STRATEGIE D'ECHANTILLONNAGE »

    Evaluation de la qualitĂ© des zones de production conchylicole d’Occitanie. PĂ©riode 2020-2022

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    AprĂšs un rappel des objectifs, du fonctionnement et de la mĂ©thode d’interprĂ©tation des rĂ©sultats du rĂ©seau de surveillance microbiologique (REMI) et du rĂ©seau de surveillance chimique (ROCCH), ce rapport comprend un bilan national et dĂ©crit le programme annuel 2022 de la rĂ©gion Occitanie. Il prĂ©sente l’ensemble des rĂ©sultats obtenus, en particulier l’estimation de la qualitĂ© microbiologique et chimique des zones classĂ©es de production de coquillages. En 2022, 23 zones de production ont Ă©tĂ© suivies par le REMI en Occitanie dont 10 dans l’Aude, 12 dans l’HĂ©rault et 1 dans le Gard au travers de 29 points de suivi. Le taux de rĂ©alisation de la surveillance rĂ©guliĂšre microbiologique en 2022 est de 95.7%, et 40 alertes ont Ă©tĂ© dĂ©clenchĂ©es au cours de l’annĂ©e. La qualitĂ© microbiologique estimĂ©e en 2023 Ă  partir des rĂ©sultats de la pĂ©riode 2020-2022 est : « A » pour 2 zones (8,7%), « B » pour 12 zones (52,2%), « C » pour 6 zones (26.1%) et « trĂšs mauvaise » pour 3 zones (13%). Parmi ces zones, 16 ont un classement sanitaire concordant avec l’estimation de leur qualitĂ©, 7 ont un classement sanitaire plus favorable que l’estimation de leur qualitĂ©. La qualitĂ© chimique est satisfaisante pour l’ensemble des points suivis
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