The lipid sensor oleoylethanolamide (OEA), an endogenous high-affinity agonist of peroxisome proliferator-activated receptor-α (PPAR-α) secreted in the proximal intestine, is endowed with several distinctive homeostatic properties, such as control of appetite, anti-inflammatory activity, stimulation of lipolysis and fatty acid oxidation. When administered exogenously, OEA has beneficial effects in several cognitive paradigms; therefore, in all respects, OEA can be considered a hormone of the gut-brain axis. Here we report an unexplored modulatory effect of OEA on the intestinal microbiota and on immune response. Our study shows for the first time that sub-chronic OEA administration to mice fed a normal chow pellet diet, changes the faecal microbiota profile, shifting the Firmicutes:Bacteroidetes ratio in favour of Bacteroidetes (in particular Bacteroides genus) and decreasing Firmicutes (Lactobacillus), and reduces intestinal cytokines expression by immune cells isolated from Peyer’s patches. Our results suggest that sub-chronic OEA treatment modulates gut microbiota composition towards a “lean-like phenotype”, and polarises gut-specific immune responses mimicking the effect of a diet low in fat and high in polysaccharides content.
Gut microorganisms are indispensable for the regulation of the host metabolism by protecting the intestine against exogenous pathogens and potentially harmful resident microorganisms. Several mechanisms converge to establish a healthy status of the host, which include a constant dialogue between microbiota and intestinal immune system. The intestinal microbial community plays a pivotal role in the development of the innate immune system and is essential in shaping adaptive immunity1. In turn, intestinal immune responses regulate the composition of the microbiota2,3. The intestinal immune system has particular features to control the proliferation and composition of intestinal microbes. Peyer’s patches are gut-associated lymphoid follicles that, by their ability to transport luminal antigens and bacteria, can be considered as the immune sensors of the intestine. Peyer’s patches functions, such as induction of immune tolerance or defence against pathogens, result from the complex interplay between immune cells located in the lymphoid follicles and the follicle-associated epithelium. Hence, Peyer’s patches sampling of the lumen is crucial for protective mucosal immune responses4. Dysbiosis disrupts gut homeostasis and increases the risk of inflammatory responses and it is now broadly accepted that changes in the microbiota are associated with not only intestinal5, but also immunological and metabolic diseases6. In addition, changes in the microbiota may affect the central nervous system through the gut-brain axis and may contribute to signs and symptoms of neurological diseases7,8,9,10. Diet has a fundamental role in shaping the gut microbiota profile; for instance, an animal-fat based diet leads to fall in bacterial diversity and shifts the proportions of the two most abundant phyla of gut microbiota, Firmicutes and Bacteroidetes11. On the contrary, a fiber-rich diet promotes bacterial diversity that affords an anti-inflammatory outcome, as it ameliorates pathological profiles as for instance in type-2 diabetes12. It has been proposed that diet-induced obesity is associated with dysbiosis that creates a permissive gut inflammatory environment13. Although the literature reports some discrepancies regarding how the inflammatory state in the intestine relates to obesity and metabolic diseases, some studies have shown that obesity is associated with an increased intestinal inflammation and elevated levels of intestinal TH1 and TH17 lymphocytes at the relative expense of TH2 and anti-inflammatory T regulatory (Treg) lymphocytes. For instance, Treg levels decrease following prolonged high fat diet in mice14,15.
A newly discovered player in the homeostasis of intestinal functions is the endocannabinoid system16. In this regard, oleoylethanolamide (OEA) a potent agonist of PPAR-α, has a prominent role in gut physiology17. OEA is synthesized in the gastro-intestinal tract and was first described as a fat sensor that mediates satiety18,19. In addition, the levels of OEA activation may change in response to inflammation20, diet21,22 or food intake18,23,24. A vast literature suggests that endogenous acylethanolamides, signalling through PPAR-α exert a tonic inhibitory control on the induction of nociception and inflammation therefore helping to maintain host-defence homeostasis by preventing inappropriate reactions25,26. OEA is mobilized in the proximal intestine after a meal27, but it is currently unclear whether it also affects intestinal homeostasis by changing the profile of the microbiota and intestinal lymphocytes activity. To answer these questions, we examined the consequences of sub-chronic OEA administration on the faecal microbiota profile and intestinal cytokines expression by immune cells of the mouse Peyer’s Patches.
OEA treatment decreases body weight and food consumption
As shown in Fig. 1A mice treated with OEA (10 mg/kg i.p.) gained significantly less weight than control mice treated with vehicle (2 way Anova repeated measures and Bonferroni post hoc test; Fdays×treatment 11,220 = 2.217, P < 0.05 Fdays 11,220 = 6.126, P < 0.001; Ftreatment 1,220 = 11.59, P < 0.01; n = 9–13), although this difference was lost on the last day of treatment. The modest weight loss was associated with a moderate but significant reduction of food intake (Fig. 1B,C. Unpaired Student’s t test; *P < 0.05; **P < 0.01). Hence, mice did not develop tolerance to the anorexic effect of OEA, as previously reported in rats19.
Effect of OEA sub-chronic treatment on gut microbiota profiles in mice
In order to evaluate the effect of OEA sub-chronic treatment on gut microbiota, we analysed faecal microbial profiles in a subgroup of mice before treatment at steady state (T0; n = 14) and after treatment with OEA 10 mg/kg, i.p. for 11 days (OEA_T11; n = 7). We then compared the microbiota composition of OEA-treated mice with that of vehicle-treated mice (VEH_T11 group; n = 7), used as controls.
Alpha diversity was estimated by observed OTUs (a measure of microbial richness), Shannon entropy, a measure of entropy accounting for both abundance and evenness of bacterial species, Dominance, an index indicating whether one taxon dominates the community completely, and Equitability, a measure of the evenness with which bacterial species are divided among the taxa (see Methods). Although the differences were not statistical significant, the observed OTUs showed a trend of increased species richness in OEA-treated mice (T11) compared to T0, and a trend of higher microbial diversity (as indicated by Shannon index) after OEA treatment (T11) compared to T0 and vehicle-treated mice (Fig. 2A,B). We also observed that no taxon dominates bacterial community after OEA treatment, as observed by Dominance index, and that no differences in evenness of bacterial communities were found among T0, OEA treatment and controls, as observed by Equitability index (Fig. 2C,D).
To evaluate differences in faecal microbiota communities between groups, we analysed beta diversity by using Non-metric Multi-Dimensional Scaling (NMDS) and Principal Coordinates Analysis (PCoA) on Bray-Curtis distances. Both ordinations showed a clear separation of OEA-treated mice samples with respect to samples at T0 and that of vehicle-treated mice (Fig. 2E,F; P = 0.035 PERMANOVA), suggesting an effect of OEA on gut microbiota profiles.
We then performed a meta-taxonomic analysis at different taxonomic levels. In Fig. 3, the most abundant bacterial phyla and genera (>1%) in mice at T0 and after OEA treatment and in controls at T11 are shown.
Linear discriminant analysis Effect Size analysis (LEfSe) showed differentially enriched phyla at T0 and after OEA treatment (OEA_T11; Fig. 4A). Firmicutes were enriched at T0 and in vehicle-treated mice at T11 (relative abundance on average, 52% at T0 and 41% for vehicle treated mice vs 35% after OEA treatment; Fig. 4B). Bacteroidetes on the other hand, were enriched at T11 after OEA treatment when compared with both T0 (on average, 39% after OEA treatment vs 28% at T0) and with vehicle treated mice at T11 (34%).
At the genus level, we observed that, when compared to T0, OEA treatment enriched the microbiota of Bacteroides (on average 16% at T0 vs 34% at T11 of OEA-treated mice), Prevotella (on average 2% at T0 vs 5% at T11 of OEA-treated mice), and Parabacteroides (on average 2% at T0 vs 5% at T11 OEA-treated mice; Fig. 4C). When compared to vehicle-treated mice, Bacteroides were enriched in OEA-treated mice (34% OEA treated-mice vs 15% control mice; Fig. 4D), whereas the observed different abundances of Prevotella and Parabacteroides between vehicle- and OEA-treated mice at T11 were not significant (Fig. 4D). Sequence alignments by BLASTn indicated that the majority of Bacteroides sequences in microbiota of OEA-treated mice were attributable with 97–98% of identity (see section “Methods”) to B. acidifaciens and to a lesser extent to B. sartorii.
Furthermore, LEfSe analysis showed that Lactobacillus was significantly reduced after OEA treatment, in comparison with either T0 or vehicle-treated mice at T11 (22% vs 49% vs 42%, respectively; Fig. 4C,D). Sequence alignments by BLASTn indicated that Lactobacillus sequences were attributable from 97% to 99% of identity to different species, especially L. reuteri and L. gasseri, and to a lesser extent to L. murinus and L. johnsonii.
Prediction of functional metabolic profiles of gut microbiota in OEA-treated mice
In order to predict how the observed differences in microbial profiles affected by OEA treatment, reflect differentially enriched functional pathways in mice, we applied PICRUSt (Phylogenetic Investigation of Communities by Reconstruction of Unobserved States). We observed functional classes (KEGG categories) differentially enriched in mice at T0 and after OEA treatment at T11 (Fig. 5A). In particular, among the metabolic functions significantly enriched in the microbiome of OEA-treated mice compared to T0, we found KEGG categories related to amino acids metabolism, (such as arginine and proline metabolism, glycine, serine and threonine metabolism, phenylalanine metabolism and tryptophan metabolism), together with functions related to glycan biosynthesis and metabolism (including functions related to other glycan degradation and glycosaminoglycan degradation). Other significant enriched functions were sphingolipid metabolism, glycosphingolipid metabolism and lipoic acid metabolism. Functions related to carbohydrate metabolism (such as butanoate metabolism and propanoate metabolism), and lipid metabolism (such as biosynthesis of unsaturated fatty acids), were reduced in OEA-treated mice compared to T0.
When vehicle and OEA treatment were compared at T11 (Fig. 5B), the metabolic functions enriched in the microbiome of OEA-treated mice regarded the metabolism of simple sugars and polysaccharides (such as pentose and glucoronate interconversions and other glycan degradation), and sphingolipid metabolism, whereas propanoate metabolism was reduced.
OEA sub-chronic treatment modulates cytokines expression in intestinal Peyer’s patches
Peyer’s patches, together with small intestine epithelial cells, are thought to be the first station for the discrimination between pathogens and commensal bacteria. As OEA modified the microbiota profile, we also investigated Peyer’s patches response to the sub-chronic administration of OEA. In order to study cytokine production of Peyer’s patches isolated cells, we tested two mitogens that activate different immune cell populations. Isolated Peyer’s patches cells were incubated in either the lymphocyte mitogen phytohaemmagglutin (PHA), that mainly induces IL2, IFNγ and TNFα production by indirect T cell receptor cross linking; the other mitogen tested was lipopolysaccharide (LPS) that induces the production of critical proinflammatory cytokines necessary to activate immune responses by binding to TLR4 and triggers the NFkB pathway in innate immune cells (e.g. dendritic cells, macrophages), lymphocytes and intestinal epithelial cells (IECs, reviewed in28).
As shown in Fig. 6A, a variety of cytokines and chemokines released by lymphocytes were differentially affected by OEA treatment. Cytokine regulation in response to OEA included a significant decrease of pro-inflammatory IFNγ, IL6, IL17, IL4, TNFα compared to vehicle treated mice (Unpaired Student’s t test, *p < 0.01, **p < 0.001, ***p < 0.0001; n = 5 animals X group). We observed a trend of IL10 increase that did not reach statistical significance. Furthermore, OEA decreased the release of the chemokines CXCL1 and CXCL2 that are required for recruitment of neutrophils during inflammatory responses following bacterial infections and injury29. In the presence of LPS, immune cells from Peyer’s patches of OEA-treated mice produced significantly less IFNγ, IL6, IL17, whereas no significant differences were observed for the other cytokines and for chemokines (Fig. 6B; unpaired Student’s T test, *P < 0.05, **P < 0.01, ***P < 0.001).
Treatment with OEA modifies lymphocytes transcription factor expression
We also evaluated if the modulation of lymphocytic cytokines production was due to the activation of different subsets of T lymphocytes by analysing the relative expression of cMaf, Tbet, RORc GATA3 and FOXP3, transcription factors that affect the functional capabilities
and flexibility of CD4+ T cell subsets30. We found that OEA treatment significantly increased cMaf associated with TH2 (IL10 producing lymphocytes) and macrophages6,31,32 and decreased RORc (associated with TH17 lymphocytes) expression (Fig. 7; Unpaired Student’s t test, ***P < 0.001 and **P = 0.03), whereas the observed decrease of TH1 associated Tbet, GATA3 (TH2 lineage-specifying factor) and Foxp3 (Treg lineage-specifying factor) did not reach statistical significance. These results strongly suggest a trend towards TH2 polarization at the expenses of TH17, an observation also corroborated by the significant decrease of IL17, IL6 expression in the Peyer’s patches of OEA-treated mice.
This study shows for the first time that OEA treatment changes the microbiota composition of mice in a way that mimics the effect of a diet low in fat and high in polysaccharides content, and is also able to polarise gut-specific immune responses. We also confirmed that OEA treatment is associated with the reduction of body weight and, in agreement with previously reported results19,23, we observed that the change in body weight was associated with a small reduction of food consumption. In our hands, the overall effects of OEA are in line with those reported by other authors in rats and mice19,33,34. When comparing our results to those of other authors though, OEA treatment did not have the same effect on body weight change at all time points. Different experimental settings such as difference in the day time at which OEA was administered, animal strains, single-caging may be responsible of the discrepancies.
Compared with steady state (T0) and control treatment (vehicle at T11), sub-chronic OEA treatment modified microbial profiles in faeces of mice, as observed by analysis of biodiversity. This diversity is reflected in the populations of the gut microbiota, as OEA shifted the Firmicutes:Bacteroidetes ratio in favour of Bacteroidetes, in particular the genus Bacteroides, and reduced Firmicutes, in particular the genus Lactobacillus. This Firmicutes:Bacteroidetes trend was observed for the first time in ob/ob versus lean mice by Ley and co-workers35 and subsequently in human obese subjects36. These effects of OEA on the microbiota profile are very much like those afforded by a fiber-rich diet that promotes the survival of saccharolytic bacteria, such as Bacteroides, able to use dietary-derived glycans as energy sources, thanks to the high number of glycoside hydrolases and polysaccharide lyases (reviewed in11,37).
In agreement with the body weight reduction induced by OEA, a previous study demonstrated that Bacteroides and Prevotella are negatively correlated with fat mass development in diet-induced obese mice38. Relevant to our study, within Bacteroides genus, the observed enrichment of B. acidifaciens is associated with lower body weight, fat mass and improvement of insulin resistance in hepatic autophagy-related gene 7 (Atg7)-deficient mice39. Of note, B. acidifaciens promoted the expression of PPAR-α in epididymal adipose tissue39.
On the other hand, a high fat/high refined carbohydrates diet leads to a prevalence of Firmicutes40. In our study, the reduction of Lactobacillus genus following OEA treatment involved L. murinus, L. johnsonii, and in particular L. gasseri and L. reuteri. In humans and animals, weight modifications, either weight loss or gain, were significantly associated with different Lactobacillus species and strains, and these modifications are believed to be host-specific as reported by two meta-analyses41,42. Some studies have shown that in pigs, turkeys and rats, L. reuteri induced a significant weight gain41,43,44, and in some cases, even if there is no clear evidence, an association with obesity45,46,47. Thus, our findings suggest, in the opposite direction, an association between OEA-induced diminished weight gain and reduced abundance of some commensal bacteria, such as Lactobacillus, but not of Bacteroides, in particular B. acidifaciens. Overall, our results suggest that OEA sub-chronic treatment shifts gut microbiota towards a “lean-like phenotype”. Prediction analysis (PICRUSt) of the metabolic pathways by metagenomic data as well suggests that OEA-induced shift of microbial profiles produces significant modifications of microbiome functions, suggesting relevant consequences on host metabolism and intestinal immune homeostasis.
OEA treatment, by activating PPAR-α, not only induces food-satiety and a modest weight loss19,34, as confirmed by our results, but it also enhances lipid utilization by stimulating fatty acid uptake, intracellular transport and lipolysis, fat oxidation, and can also modulate lipid levels in tissues and circulation17,34. In addition, OEA participates in the physiologic inhibition of intestinal motility48 presumably in a PPAR-α independent manner49, enhances long-chain fatty acid uptake in enterocytes39, and increases intestinal epithelial cells resistance50. These metabolic and homeostatic effects of OEA may change the intestinal environment and the ecological fitness of bacterial community, favouring the enrichment of Bacteroides at the expenses of other genera, such as Lactobacillus. We cannot exclude though, that the rapid effect on body weight induced by OEA contributes to the microbiota modification. Further studies should be performed to understand the role of direct and/or indirect mechanisms on the intestinal microbiota.
Several lines of evidence suggest that endogenous ligands of PPAR-α exert a tonic inhibitory control over the induction of inflammatory responses25. Whereas the anti-inflammatory effects of the PPAR-α agonist palmitoylethanolamide (PEA) are well documented20, less studied is the direct contribution of OEA to the production of inflammatory or regulatory cytokines, even more so in the gut-associated lymphoid tissues.
We found that OEA profoundly affects the polarization of TH lymphocytes in the Peyer’s patches towards an anti-inflammatory profile, in agreement with previous reports that indicated how stimulation of PPAR-α competes with other transcription factors that are major mediators of inflammatory response in lymphocytes, monocyte and macrophages51,52. Furthermore, it is well established that PPAR-α genetic deletion results in increased TH1/TH17 response of cells isolated from the intestine lamina propria at steady state conditions and the condition is exacerbated in colitis53. Our observation of the concomitant change in microbiota and Peyer’s patches environment in vivo suggests a double, if not related, effect of OEA in the intestine, that may be exploited to counteract obesity induced regional and systemic inflammation54, balancing the reduction of a tolerant milieu associated with skewing toward TH1/TH17 immune profile in the liver, adipose and muscle tissue13. Immune responses are orchestrated by the production of pro- and anti-inflammatory cytokines, as the lymphonodes in the Peyer’s patches must continuously distinguish between commensal bacteria and pathogens, with consequences on systemic immunity. Therefore, the fact that OEA is acting on Peyer’s patches immune cells decreasing pro-inflammatory cytokines production and, at the molecular level, transcription factors responsible for TH1 and TH17 differentiation may be exploited in order to modulate gut inflammation. OEA and PEA in vivo decrease plasma and cortical TNFα mRNA levels55 and our experiments add further knowledge to this observation: in our hands TNFα, that in turn induces CXCL1 and CXCL2 production, is down modulated when Peyer’s patches derived cells are stimulated with PHA, but not with LPS, suggesting that OEA is promoting a less inflammatory mileu, without significantly affecting innate immune response and the ability of neutrophils recall, when necessary. In the future, it would be of interest to check if OEA anti-inflammatory effect is present in all intestinal regions and associated to immune cells, as in fact these may not behave in the same way as cells isolated from Peyer’s patches56.
Several intriguing questions remain unanswered as for instance whether the homeostatic effects of OEA on Peyer’s patches immune cells responses and microbiota are independent phenomena or whether they influence each other. Our results can be explained by two equally valid hypotheses: (i) the induction of a tolerogenic milieu in itself determines differences in the microbiome, or (ii) OEA-induced changes in the microbiome primes anti-inflammatory responses. There is evidence that bioactive lipids (e.g. palmytoylethanolamide, anandamide, short chain fatty acids) participate in physiological processes correlated with the maintenance of gut-barrier function, inflammation and energy metabolism20,57,58. Dysregulation of the endocannabinoid system might play a crucial role in the etiopathogenesis of intestinal disorders59. Enhancing endogenous OEA synthesis could represent a new therapeutic strategy to treat such diseases.
Overall, the present study stimulates future investigation addressed at solving the causal effects, also measuring the microbial metabolites produced by OEA treatment, to provide further useful insights on role of OEA in the gut-brain axis.
SV129 male mice aged 8–12 weeks were bred in our colony in the animal facility where they were single-housed in macrolon cages at 20–24 °C. Mice were allowed free access to chow pellets (Mucedola, Milano Italy) and water, and kept on a 12-h-light/-dark cycle (light started at 7:00 am). All experimental manipulations were performed in strict compliance with the EEC recommendations for the care and use of laboratory animals (2010/63/EU) approved by the Animal Care Committee of the Dipartimento di Scienze della Salute, Universitá di Firenze (I). Ethical policy of the Universitá di Firenze complies with the Guide for the Care and Use of Laboratory Animals of the Council Directive of the European Community (2010/63/EU) and the Italian Decreto Legislativo 26 (13/03/2014). Every effort was made to minimize animal suffering and to reduce the number of animals used. Mice were handled for at least 4 days before experiments begun, to let them acclimatise to human contact. Body weight and food consumption were measured daily, starting the day before administration of OEA or vehicle. OEA (Tocris Bioscience, UK) was dissolved in saline/polyethylene glycol/Tween80 (90/5/5, v/v) and administered at a dose of 10 mg/kg i.p. 30 min before lights off, once daily for 11 days. The dose of OEA was within the range of i.p. doses that have been reported in the literature and that do not cause harmful or unwanted side effects19,60,61,62. Mice were weighted and food consumption measured in the morning, and faecal pellets collected right after.
Faecal samples collection and bacterial genomic DNA extraction
Faeces was collected (i) at steady state (T0) from each mice group, (ii) after 11 days of OEA treatment (OEA_T11), and (iii) after 11 days of vehicle-treatment (Vehicle_T11). For each group of mice, the pellets were collected in sterile conditions and stored at −80 °C until extraction of nucleic acids. The bacterial genomic DNA extraction was carried out with DNeasy PowerLyzer PowerSoil Kit (Qiagen, Hilden, Germania) following the manufacturer’s instructions. DNA quality was assessed by gel electrophoresis and spectrophotometry, measuring OD 260/280.
16S Ribosomal RNA Gene Amplicons preparation and Illumina MiSeq sequencing
Library of 16S rRNA gene amplicons was prepared by IGA Technology Services (Udine, Italy) through amplification of the V3-V4 hypervariable region by using specific-barcoded primers with overhang adapters. The standard protocol was followed according to the 16S metagenomic sequencing library preparation guide from Illumina (Part #15044223 Rev. B; https://support.illumina.com/). Pooled V3-V4 amplicon libraries were sequenced using the Illumina MiSeq platform.
Sequence data are available at http://www.ebi.ac.uk/ena/data/view/ PRJEB26276, under the accession number PRJEB26276. The 300-bp paired-end reads obtained from Illumina MiSeq platform for each sample were demultiplexed and quality checked using FastQC 0.11.5. Reads were further processed using the MICCA pipeline (version 1.6, ttp://compmetagen.github.io/micca/)63. Briefly, Illumina paired-end reads was merged by using the mergepairs function. Forward and reverse primers was trimmed, and reads did not contain the forward or the reverse primer was discarded, as well as both sequences preceding the forward or succeeding the reverse primers was removed. Quality filtering were performed by using mica-filter (according to the maximum allowed expected error rate % reported in filterstats), truncating reads shorter than 300 nt (quality threshold = 18), in order to produce high-quality reads. Denovo sequence clustering, chimera filtering and taxonomy assignment were performed by micca-otu-denovo. Operational Taxonomic Units (OTUs) were assigned by clustering the sequences with a threshold of 97% pair-wise identity. The representative sequences were classified using the RDP classifier version 2.7 against RDP 11 database (update 5) of 16S rRNA. Template-guided multiple sequence alignment was performed using PyNAST (version 0.1) against the multiple alignment of the Greengenes 16S rRNA gene database (release 13_05) and filtering at 97% similarity. A total of 3570 Operational Taxonomic Units (OTUs) were assigned by clustering the sequences with a threshold of 97% pair-wise identity. OUT tables for each taxonomic level were created by mica-tabletotax and used for further statistical analysis.
For Bacteroides and Lactobacillus genera, depth at species level was obtained by sequence alignment using Basic Local Alignment Search Tool nucleotide (BLASTn) software in the National Center for Biotechnology Information (NCBI) database. The highest percentage of identity (Query cover 100–99% and Identity 99 or 95%). Expectation value (E-value) was used to select significant BLAST hits, keeping only outcomes with the lowest E-value (minimal E-value of 10−3).
Alpha diversity was estimated by observed OTUs (a measure of microbial richness), Shannon entropy (a measure of entropy accounting for both abundance and evenness of bacterial species), Dominance (1-Simpson index), and Equitability (Shannon diversity divided by the logarithm of number of taxa), by using Paleontological Statistics Software Package (PAST3 v.3.12). Beta diversity was performed to evaluate differences in overall bacterial communities by Principal Coordinates Analysis (PCoA) and Non-metric Multidimensional Scaling (NMDS), based on Bray-Curtis dissimilarities, using the phyloseq package of the R software suite. The significance of between-groups differentiation on Bray-Curtis dissimilarity was assessed by PERMANOVA using the adonis() function of the R package vegan with 999 permutations.
To infer the functional pathways (KEGG categories) that differ between mice groups (treated with OEA vs control mice), we applied Phylogenetic Investigation of Communities by Reconstruction of Unobserved States- PICRUSt64 on 16S rDNA sequencing data set. We obtained the final output from metagenome prediction as an annotated table of predicted gene family counts for each sample, where the encoded function of each gene family be orthologous groups or other identifiers such as KEGG orthologs (KOs).
Metagenomic biomarker discovery and related statistical significance were assessed by using the linear discriminant analysis (LDA) effect size (LEfSe) method, based on the bacterial relative abundances. In LEfSe, Kruskal–Wallis rank-sum test is used to identify significantly different taxa abundances among groups of mice, and LDA to estimate the size effect of each feature. An alpha significance level of 0.05, either for the factorial Kruskal-Wallis test among classes or for the pairwise Wilcoxon test between subclasses, was used. A size-effect threshold of 2.0 on the logarithmic LDA score was applied for discriminative microbial biomarkers. LEfSe was also performed on PICRUSt data to discover bacterial functional biomarkers among groups of mice based on different treatments.
For PICRUSt analysis, statistical analysis and visualization of results were performed by using STAMP package (Statistical Analysis of Metagenomic and other Profiles; version Profiles65; version 2.1.3). Multiple comparison testing was performed using non-parametric Kruskal Wallis test. Two-group comparison was performed by White’s non-parametric t-test, using an alpha of 0.05, with Storey false discovery rate correction.
Peyer’s patches isolation and cytokines determination
Mice were sacrificed by cerebral dislocation without anaesthesia. Peyer’s Patches were freshly isolated from the intestine and transferred in a 15 ml tube with PBS + 1% Pen/Strep (Lonza, Germany) to prevent drying. Peyer’s patches were digested with collagenase D (1 mg/ml) (Sigma-Aldrich, USA) in a 37 °C and 5% CO2 incubator for 5 minutes. All Peyer’s patches were transferred in a 70 µm cell strainer (Falcon, USA) placed over 50 ml tube and mechanically dissociated. During dissociation filters were washed with RPMI + 1% PEN/Strep. Peyer’s patches-single cells flowed through the filter and were suspended in 15 ml of RPMI, 10% FBS, 1%Pen/Strep, 0,01% beta-mercaptoethanol, 1% L-glutammin, 1% Na-Pir and 1% Hepes (complete medium). Cells were centrifuged at 1300 rpm at room temperature for 10 minutes, then the supernatant was discarded and pellets were suspended in complete medium. Peyer’s patches cells were counted with Thomas chamber using trypan blue dye exclusion. Cells were plated at the concentration of 1 × 105 cells/100 \(\mu \)l (1 × 106 cells/ml) in 96-well plate in the presence of PHA (5 ug/ml), LPS (1 ug/ml) (Sigma-Aldrich, USA) or vehicle for 48 h, in a 37 °C and 5% CO2 incubator. After incubation cell supernatants were collected for the determination of the following soluble factors: IFNγ, IL4, IL6, IL10, IL17, TNFα, CXCL1, CXCL2, by Luminex Technologies (Procartaplex, Life Technologies, USA).
Peyer’s patches cells were transferred in QIAzol (QIAGEN, Germany) lysis buffer, for RNA extraction. RT-PCR was carried out on 0.5–1 ng total RNA using Quantitec Reversion Transcription kit (QIAGEN, Germany) as first-strand primer. Real-time quantitative PCR was performed using TaqMan Universal PCR Master Mix, according to the manufacturer’s instructions (ThermoFisher Scientific, USA). The cDNA fragments corresponding to mouse Tbet, Rorc, GATA3, cMaf and Foxp3 were amplified using specific pairs of primers (Life Technologies, USA). All samples were run in triplicate on 96-well using optical PCR plates (Life Technologies, USA). Data were expressed as arbitrary units relative to expression of the gene encoding ubiquitin. The reference gene for RT-PCR, ubiquitin, was selected among others normally in use that are not involved in the process under examination, e.g. GADPH-R, 16S rRNA. To date no published indications are available for PP. Differences were revealed by unpaired Student’s t test, and significance was set at P < 0.05.
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The authors would like to thank C. Manuelli for Technical assistance in the real time PCR experiments, E. Conti and L. Pavarini for performing the preliminary experiments and data analysis. This work was supported by a grant from JPI-HDHL” “Nutrition and cognitive function”, Ambrosiac to M.B.P. G.P. was supported by Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq Brazil, process 201511/2014-2), and Fondazione Umberto Veronesi grants; A.C. was supported by Ministero della Salute, Bando Ricerca Finalizzata e Giovani Ricercatori 2011e2012 (GR-201102346829).
The authors declare no competing interests.
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Di Paola, M., Bonechi, E., Provensi, G. et al. Oleoylethanolamide treatment affects gut microbiota composition and the expression of intestinal cytokines in Peyer’s patches of mice. Sci Rep 8, 14881 (2018). https://doi.org/10.1038/s41598-018-32925-x
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