The LDRs were carried

out in a final volume of 20 μl with 50 fmol of PCR product. Two hundred and fifty fmol of synthetic template (5’-AGCCGCGAACACCACGATCGACCGGCGCGCGCAGCTGCAGCTTGCTCATG-3) were used for normalization purposes. All HTF-Microbi.Array experiments were performed in independent duplicates. Data analysis All arrays were scanned and processed according to the protocol and parameters already described by Candela et al.[24]. Fluorescence intensities (IF) were normalized on the basis of the synthetic ligation control signal: (a) outlier values (2.5-fold above or below the average) were discarded; (b) a correction factor was calculated in order to set the average IF of the ligation control to 50000 (n = 6); (c) the correction factor https://www.selleckchem.com/products/AG-014699.html was applied to both the probes and background IF values. Reproducibility of the experiments was assessed by calculating Pearson’s correlation

of the fluorescence signals between the two replicates. LDR experiments showing a Pearson’s correlation coefficient <0.95 were repeated. Mean data from two replicated experiments were obtained and utilized for principal component analysis (PCA), box plot analysis and calculation of the probe relative IF contribution. Non-parametric Kruskal-Wallis test was used to determine whether the contribution of each bacterial group was significantly different between atopics and controls. Two-sided t-test was applied to evaluate whether the relative percentage contribution Selleck MK-1775 of each bacterial group was significantly different between the two groups. Correlation between variables was N-acetylglucosamine-1-phosphate transferase computed by Spearman rank correlation coefficient. Statistical analyses were performed by using Canoco package for Windows [30] and the

R statistical software (http://​www.​r-project.​org). Quantitative PCR qPCR was Compound C carried out in a LightCycler instrument (Roche). Quantification of the 16 S rRNA gene of A. muciniphila, Faecalibacterium prausnitzii, Enterobacteriaceae, Clostridium cluster IV, Bifidobacterium and Lactobacillus group was performed with the genus-, group- or species-specific primers reported in Table 2. SYBR Green I fluorophore was used to correlate the amount of PCR product with the fluorescent signal. For quantification, standard curves were generated with known amounts of pCR2.1 (Invitrogen)-cloned 16 S rRNA gene from A. muciniphila (DSM22959), F. prausnitzii (DSM17677), E. coli (ATCC11105), Clostridium leptum (DSM753), Bifidobacterium animalis subsp. lactis (BI-07) and Lactobacillus acidophilus (LA-14). Amplification was carried out in a 20 μl final volume containing 100 ng of faecal DNA, 0.5 μM of each primer and 4 μl of LightCycler-FastStart DNA Master SYBR Green I (Roche).