Contribution à l’étude des sillons subverticaux intéressant des facettes interproximales

Des restes dentaires néandertaliens ont été mis au jour dans la grotte de Rochelot (Charente, France) reconnue comme un repaire d’hyènes. Deux dents, PM1 et PM2 gauches, présentent des sillons subverticaux sur leurs facettes d’attrition interproximales et antagonistes. L’étude macroscopique et microscopique (MEB) révèle que chaque sillon d’une facette interproximale présente une concordance d’orientation et de dimensions avec son antagoniste. L’analyse bibliographique et notre expérimentation sur des dents actuelles nous conduisent à l’élaboration d’une classification chronologique des phénomènes aboutissant à la formation ante mortem de ces sillons subverticaux.Neanderthal dental remains were discovered in the cave at Rochelot (Charente, France) which is known to have been inhabited by hyenas. Two left teeth, PM1 and PM2, presented subvertical grooves located on their antagonist interproximal facets. Macroscopic and microscopic examination revealed that each vertical groove of an interproximal facet resembled its antagonist groove. Bibliographical research and our experiments on modern teeth have led us to develop a chonological classification of the elements leading to the ante mortem formation of these subvertical grooves

Species indicators of ecosystem recovery after reducing large herbivore density: Comparing taxa and testing species combinations

Indicator species have been used successfully for estimating ecosystem integrity, but comparative studies for defining optimal taxonomic group remain scarce. Furthermore, species combinations may constitute more integrative tools than single species indicators, but case studies are needed to test their efficiency. We used Indicator Species Analysis, which statistically determines the association of species to one or several groups of sites, to obtain indicators of ecosystem recovery after various deer density reductions. We used five taxonomic groups: plants, carabid beetles, bees, moths and songbirds. To test whether species combinations could complement single indicator species, we used plants as a model taxon and examined the indicator value of joint occurrence of two or three plant species. Our study relies on experimental controlled browsing enclosures established for six years on Anticosti Island (Quebec). Four levels of deer density (0, 7.5 and 15 deer km−2 and natural densities between 27 and 56 deer km−2) were studied in two vegetation cover types (uncut forests and cut-over areas), in a full factorial design for a total of eight experimental treatments. For all taxa but bees, we tested 54 treatment groups consisting in one specific density or in a sequence of two or more consecutive deer densities in one or both cover types (ten groups for bees, sampled only in cut-over areas). We found 12 plants, 11 moths and one songbird to be single species indicators of ecosystem conditions obtained under 12 different treatment groups. Six treatment groups were indicated by plants and six different ones by moths, of which one group was also identified by a songbird species. Moths were thus worth the extra sampling effort, especially since the groups they indicated were more treatment-specific (mainly one or two deer density treatments). We tested the same 54 treatment groups for plant species combinations represented by two or three co-occurring species. Plant combinations efficiently complemented plant singletons for detecting ecosystem conditions obtained under various deer densities. In fact, although singletons were highly predictive, 17 additional treatment groups were identified exclusively with two- and three-species combinations, some being more treatment-specific. Our findings show that plants and moths provide complementary indicators of ecosystem conditions under various deer densities, and that computing species combinations increases our capacity to monitor ecosystem recovery after reducing herbivore densities.Funding was provided by the Natural Sciences and Engineering Research Council of Canada (NSERC)-Produits forestiers Anticosti Industrial Chair to SDC, the Ministère des Ressources Naturelles et de la Faune du Québec, the Canadian Forest Service of Natural Resources Canada and an NSERC scholarship to MB and NSERC DG to MP and SP. We are grateful to the Centre de la Science de la Biodiversité du Québec and Centre d’études nordiques for scholarships

Impact of enological tannins on laccase activity

Aims: The aim of this research was to determine and quantify the ability of enological tannins to reduce laccase activity and, consequently, to protect wine color against enzymatic browning and/or oxidasic haze. Methods and results: Botrytized grape juice with laccase activity was obtained by inoculating Botrytis cinerea in healthy mature grapes. Laccase activity was determined in grape juice before and after supplementation with enological tannins using the syringaldazine method. White micro-fermentations were performed in the presence or not of laccase activity and supplemented or not with enological tannins in order to determine how the color was affected. Similarly, red micro-fermentations were performed using white grape juice supplemented with malvidin-3-O-glucoside. All enological tannins inhibited laccase activity and protected the wine color. Conclusion: Supplementation with enological tannins is an interesting tool to inhibit laccase activity and protect the color of white wines from browning and the color of red wines from oxidasic haze. Significance and impact of the study: This is the first scientific study evidencing the inhibitory effect of enological tannins on laccase activity in winemaking conditions. Keywords: enological tannins, Botrytis cinerea, grey mould, laccase activity, contact time, dose effec

Low Penetrance, Broad Resistance, and Favorable Outcome of Interleukin 12 Receptor β1 Deficiency: Medical and Immunological Implications

The clinical phenotype of interleukin 12 receptor β1 chain (IL-12Rβ1) deficiency and the function of human IL-12 in host defense remain largely unknown, due to the small number of patients reported. We now report 41 patients with complete IL-12Rβ1 deficiency from 17 countries. The only opportunistic infections observed, in 34 patients, were of childhood onset and caused by weakly virulent Salmonella or Mycobacteria (Bacille Calmette-Guérin -BCG- and environmental Mycobacteria). Three patients had clinical tuberculosis, one of whom also had salmonellosis. Unlike salmonellosis, mycobacterial infections did not recur. BCG inoculation and BCG disease were both effective against subsequent environmental mycobacteriosis, but not against salmonellosis. Excluding the probands, seven of the 12 affected siblings have remained free of case-definition opportunistic infection. Finally, only five deaths occurred in childhood, and the remaining 36 patients are alive and well. Thus, a diagnosis of IL-12Rβ1 deficiency should be considered in children with opportunistic mycobacteriosis or salmonellosis; healthy siblings of probands and selected cases of tuberculosis should also be investigated. The overall prognosis is good due to broad resistance to infection and the low penetrance and favorable outcome of infections. Unexpectedly, human IL-12 is redundant in protective immunity against most microorganisms other than Mycobacteria and Salmonella. Moreover, IL-12 is redundant for primary immunity to Mycobacteria and Salmonella in many individuals and for secondary immunity to Mycobacteria but not to Salmonella in most

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Background Suicide is a leading cause of death worldwide, and nonfatal suicide attempts, which occur far more frequently, are a major source of disability and social and economic burden. Both have substantial genetic etiology, which is partially shared and partially distinct from that of related psychiatric disorders. Methods We conducted a genome-wide association study (GWAS) of 29,782 suicide attempt (SA) cases and 519,961 controls in the International Suicide Genetics Consortium (ISGC). The GWAS of SA was conditioned on psychiatric disorders using GWAS summary statistics via multitrait-based conditional and joint analysis, to remove genetic effects on SA mediated by psychiatric disorders. We investigated the shared and divergent genetic architectures of SA, psychiatric disorders, and other known risk factors. Results Two loci reached genome-wide significance for SA: the major histocompatibility complex and an intergenic locus on chromosome 7, the latter of which remained associated with SA after conditioning on psychiatric disorders and replicated in an independent cohort from the Million Veteran Program. This locus has been implicated in risk-taking behavior, smoking, and insomnia. SA showed strong genetic correlation with psychiatric disorders, particularly major depression, and also with smoking, pain, risk-taking behavior, sleep disturbances, lower educational attainment, reproductive traits, lower socioeconomic status, and poorer general health. After conditioning on psychiatric disorders, the genetic correlations between SA and psychiatric disorders decreased, whereas those with nonpsychiatric traits remained largely unchanged. Conclusions Our results identify a risk locus that contributes more strongly to SA than other phenotypes and suggest a shared underlying biology between SA and known risk factors that is not mediated by psychiatric disorders.Peer reviewe

Endogenous (In)Formal Institutions.

Despite the huge evidence documenting the relevance of inclusive political institutions and a culture of cooperation, we still lack a framework that identifies their origins and interaction. In a model in which an elite and a citizenry try to cooperate in consumption risk-sharing and investment, we show that a rise in the investment value encourages the elite to introduce more inclusive political institutions to convince the citizenry that a sufficient part of the returns on joint investments will be shared. In addition, accumulation of culture rises with the severity of consumption risk if this is not too large and thus cheating is not too appealing. Finally, the citizenry may over-accumulate culture to credibly commit to cooperate in investment when its value falls and so inclusive political institutions are at risk. These predictions are consistent with the evolution of activity-specific geographic factors, monasticism, and political institutions in a panel of 90 European regions spanning the 1000-1600 period. Evidence from several identification strategies suggests that the relationships we uncover are causal

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study

Background Huntington's disease is caused by a CAG repeat expansion in the huntingtin gene, HTT. Age at onset has been used as a quantitative phenotype in genetic analysis looking for Huntington's disease modifiers, but is hard to define and not always available. Therefore, we aimed to generate a novel measure of disease progression and to identify genetic markers associated with this progression measure. Methods We generated a progression score on the basis of principal component analysis of prospectively acquired longitudinal changes in motor, cognitive, and imaging measures in the 218 indivduals in the TRACK-HD cohort of Huntington's disease gene mutation carriers (data collected 2008–11). We generated a parallel progression score using data from 1773 previously genotyped participants from the European Huntington's Disease Network REGISTRY study of Huntington's disease mutation carriers (data collected 2003–13). We did a genome-wide association analyses in terms of progression for 216 TRACK-HD participants and 1773 REGISTRY participants, then a meta-analysis of these results was undertaken. Findings Longitudinal motor, cognitive, and imaging scores were correlated with each other in TRACK-HD participants, justifying use of a single, cross-domain measure of disease progression in both studies. The TRACK-HD and REGISTRY progression measures were correlated with each other (r=0·674), and with age at onset (TRACK-HD, r=0·315; REGISTRY, r=0·234). The meta-analysis of progression in TRACK-HD and REGISTRY gave a genome-wide significant signal (p=1·12 × 10−10) on chromosome 5 spanning three genes: MSH3, DHFR, and MTRNR2L2. The genes in this locus were associated with progression in TRACK-HD (MSH3 p=2·94 × 10−8 DHFR p=8·37 × 10−7 MTRNR2L2 p=2·15 × 10−9) and to a lesser extent in REGISTRY (MSH3 p=9·36 × 10−4 DHFR p=8·45 × 10−4 MTRNR2L2 p=1·20 × 10−3). The lead single nucleotide polymorphism (SNP) in TRACK-HD (rs557874766) was genome-wide significant in the meta-analysis (p=1·58 × 10−8), and encodes an aminoacid change (Pro67Ala) in MSH3. In TRACK-HD, each copy of the minor allele at this SNP was associated with a 0·4 units per year (95% CI 0·16–0·66) reduction in the rate of change of the Unified Huntington's Disease Rating Scale (UHDRS) Total Motor Score, and a reduction of 0·12 units per year (95% CI 0·06–0·18) in the rate of change of UHDRS Total Functional Capacity score. These associations remained significant after adjusting for age of onset. Interpretation The multidomain progression measure in TRACK-HD was associated with a functional variant that was genome-wide significant in our meta-analysis. The association in only 216 participants implies that the progression measure is a sensitive reflection of disease burden, that the effect size at this locus is large, or both. Knockout of Msh3 reduces somatic expansion in Huntington's disease mouse models, suggesting this mechanism as an area for future therapeutic investigation