Many neurological disorders have a distinctive colonic microbiome (CM) signature. Particularly, children with autism spectrum disorders (ASD) exhibit a very dissimilar CM when compared to neurotypical (NT) ones, mostly at the species level. Thus far, knowledge on this matter comes from high-throughput (yet very expensive and time-consuming) analytical platforms, such as massive high-throughput sequencing of bacterial 16S rRNA. Here, pure (260/280 nm, ~1.85) stool DNA samples (200 ng.µL−1) from 48 participants [39 ASD, 9 NT; 3–13 y] were used to amplify four candidate differential CM markers [Bacteroides fragilis (BF), Faecalibacterium prausnitzii (FP), Desulfovibrio vulgaris (DV), Akkermansia muciniphila (AM)], using micro-organism-specific oligonucleotide primers [265 bp (BF), 198 bp (FP), 196 bp (DV), 327 bp (AM)] and a standardized two-step [low (step 1: °Tm—5 °C) to high (stage 2: °Tm—0 °C) astringent annealing] PCR protocol (2S-PCR). The method was sensitive enough to differentiate all CM biomarkers in the studied stool donors [↑ abundance: NT (BF, FP, AM), ASD (DV)], and phylogenetic analysis confirmed the primers’ specificity.
Calcium is the only dietary factor that affects both non‐heme and heme iron absorption in humans. Mechanisms behind this effect are not elucidated. An hypothesis is that calcium may modify gene expression of proteins involved in iron absorption. An interesting experimental model for evaluating this effect is the human cell line Caco‐2, which is easy to use and produces results that strongly correlate with the absorption of iron in humansObjectiveTo evaluate the effect of calcium on expression of proteins involved on both heme, and non‐hemeiron absorption by Caco‐2 cells.MethodologyCaco‐2 cells were seeded by 1h in a 2 μM de iron solution (ferrous sulfate) and calcium (chloride); calcium: iron molar ratios 0:1 to 1000:1. Iron absorption was determined by ferritin method, and gene expression by qRT‐PCR. Changes in ferritin and gene expression were reported as increment respect to a control (calcium: iron molar ratio=0:1). Differences between experimental conditions were evaluated by a one‐way ANOVA test; p<0.05 was considered significant.ResultsCalcium does not affect iron absorption. Calcium increases genes involved in non‐heme iron uptake: DcytB (p=0.003), and DMT1 (p=0.016). Otherwise, calcium decreases genes involved in heme iron uptake: HCP1 (p=0.002), and HMOX‐1 (p=0.012). Expression of FPN gene (efflux protein for both heme, and non‐heme iron) decreased by calcium exposition (p<0.0001).ConclusionThe calcium effect of calcium on expression of gene involved on heme, and non‐heme iron uptake is opposite. Nevertheless, it decreases FPN expression which is the only protein involved on two iron types efflux from the enterocytes. This effect may explained the negative effect of calcium on iron absorption previously described in humans.Support or Funding InformationCODI, Universidad de Antioquia.Corporación Vidarium, Centro de Investigación en Nutrición Salud y Bienestar.
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