Contamination du lait caillé et de l’oeuf consommé en Côte d’Ivoire par des pesticides organochlorés

La présente étude vise à évaluer l’aspect sanitaire de l’alimentation humaine à travers deux produits à forte consommation en Côte d’Ivoire : le lait caillé et l’oeuf. Ainsi, 30 échantillons de lait caillé ont été achetés et 30 échantillons d’oeufs de poulet ont été collectés dans trois fermes dans la ville d’Abidjan. Ces échantillons ont été traités dans le but de déterminer les résidus de 12 POC (Pesticides OrganoChlorés). Les analyses ont été réalisées au CG sur colonne capillaire avec un détecteur à capture d'électrons. Les résultats observés révèlent une contamination du lait caillé et de l’oeuf par 5 POC. Ainsi, des charges moyennes en μg/kg des isomères hexachlorocyclohexane (HCH) allant de 0,125 à 0,997 et de 1,870 à 35,907, de l’endosulfan allant de 0,045 à 0,563 et non détecté, de la dieldrine allant de 0,025 à 0,263 et de 5,727 à 69,710 et du Dichlorodiphenyltrichloroethane (DDT) et métabolites allant de 0,133 à 0,813 et de 21,105 à 75,22, ont été respectivement déterminées dans le lait caillé et dans l’oeuf. La teneur résiduelle moyenne des isomères HCH, des cyclodiènes (dieldrine, et endosulfane) et du DDT et ses métabolites constituent respectivement 40%, 40% et 20% de la moyenne du total des POC mesurés dans le lait caillé et respectivement 20%, 20% et 60% de celle mesurée dans l’oeuf.Mots-clés: pesticides organochlorés, lait caillé, oeuf, Côte d’Ivoire. Contamination of the curdled milk and the egg consumed in Ivory Coast by organochlorinated pesticides This study aims to determine the levels of organochlorinated pesticides (OCPs) in the curdled milk and egg. Thus, 30 samples of curdled milk were purchased and 30 egg samples were collected from three farms in the area of the lagoons. These samples were processed in order to determine the residues 12 OCPs. Analyses were performed by GC capillary column with electron capture detector. The observed results indicate contamination of curdled milk and egg by 5 OCPs. Thus, average loads in μg/kg of hexachlorocyclohexane (HCH) isomers ranging from 0.125 to 0.997 and 1.870 to 35.907, endosulfan ranging from 0.045 to 0.563 and undetected, dieldrin ranging from 0.025 to 0.263 and 5.727 to 69.710 and dichlorodiphenyltrichloroethane (DDT) and metabolites ranging from 0.133 to 0.813 and 21, 105 to 75.22, respectively, were determined in the curdled milk and egg. The average residual HCH isomers, cyclodiene (dieldrin and endosulfan) and DDT and its metabolites is respectively 40%, 40% and 20% of the average total OCPs measured in curdled milk and respectively 20%, 20 % and 60% of that measured in the bud.Keywords: organochlorinated pesticides, curdled milk, egg, Ivory Coast

Vulnerability of Polarised Intestinal Porcine Epithelial Cells to Mycotoxin Deoxynivalenol Depends on the Route of Application

BACKGROUND AND AIMS: Deoxynivalenol (DON) is a Fusarium derived mycotoxin, often occurring on cereals used for human and animal nutrition. The intestine, as prominent barrier for nutritional toxins, has to handle the mycotoxin from the mucosa protected luminal side (apical exposure), as well as already absorbed toxin, reaching the cells from basolateral side via the blood stream. In the present study, the impact of the direction of DON exposure on epithelial cell behaviour and intestinal barrier integrity was elucidated. METHODS: A non-transformed intestinal porcine epithelial cell line (IPEC-J2), cultured in membrane inserts, serving as a polarised in vitro model to determine the effects of deoxynivalenol (DON) on cellular viability and tight junction integrity. RESULTS: Application of DON in concentrations up to 4000 ng/mL for 24, 48 and 72 hours on the basolateral side of membrane cultured polarised IPEC-J2 cells resulted in a breakdown of the integrity of cell connections measured by transepithelial electrical resistance (TEER), as well as a reduced expression of the tight junction proteins ZO-1 and claudin 3. Epithelial cell number decreased and nuclei size was enlarged after 72 h incubation of 4000 ng/mL DON from basolateral. Although necrosis or caspase 3 mediated apoptosis was not detectable after basolateral DON application, cell cycle analysis revealed a significant increase in DNA fragmentation, decrease in G0/G1 phase and slight increase in G2/M phase after 72 hours incubation with DON 2000 ng/mL. CONCLUSIONS: Severity of impact of the mycotoxin deoxynivalenol on the intestinal epithelial barrier is dependent on route of application. The epithelium appears to be rather resistant towards apical (luminal) DON application whereas the same toxin dose from basolateral severely undermines barrier integrity

Circulating microRNAs in sera correlate with soluble biomarkers of immune activation but do not predict mortality in ART treated individuals with HIV-1 infection: A case control study

Introduction: The use of anti-retroviral therapy (ART) has dramatically reduced HIV-1 associated morbidity and mortality. However, HIV-1 infected individuals have increased rates of morbidity and mortality compared to the non-HIV-1 infected population and this appears to be related to end-organ diseases collectively referred to as Serious Non-AIDS Events (SNAEs). Circulating miRNAs are reported as promising biomarkers for a number of human disease conditions including those that constitute SNAEs. Our study sought to investigate the potential of selected miRNAs in predicting mortality in HIV-1 infected ART treated individuals. Materials and Methods: A set of miRNAs was chosen based on published associations with human disease conditions that constitute SNAEs. This case: control study compared 126 cases (individuals who died whilst on therapy), and 247 matched controls (individuals who remained alive). Cases and controls were ART treated participants of two pivotal HIV-1 trials. The relative abundance of each miRNA in serum was measured, by RTqPCR. Associations with mortality (all-cause, cardiovascular and malignancy) were assessed by logistic regression analysis. Correlations between miRNAs and CD4+ T cell count, hs-CRP, IL-6 and D-dimer were also assessed. Results: None of the selected miRNAs was associated with all-cause, cardiovascular or malignancy mortality. The levels of three miRNAs (miRs -21, -122 and -200a) correlated with IL-6 while miR-21 also correlated with D-dimer. Additionally, the abundance of miRs -31, -150 and -223, correlated with baseline CD4+ T cell count while the same three miRNAs plus miR- 145 correlated with nadir CD4+ T cell count. Discussion: No associations with mortality were found with any circulating miRNA studied. These results cast doubt onto the effectiveness of circulating miRNA as early predictors of mortality or the major underlying diseases that contribute to mortality in participants treated for HIV-1 infection