Cognitive decline, obesity and gut dysfunction or microbial dysbiosis occur in association. Our aim was to identify gut microbiota-metabolomics signatures preceding dementia in genetically prone (3xtg) mice, with and without superimposed high-fat diet. We examined the composition and diversity of their gut microbiota, and serum and faecal metabolites. 3xtg mice showed brain hypometabolism typical of pre-demented stage, and lacked the physiological bacterial diversity between caecum and colon seen in controls. Cluster analyses revealed distinct profiles of microbiota, and serum and fecal metabolome across groups. Elevation in Firmicutes-to-Bacteroidetes abundance, and exclusive presence of Turicibacteraceae, Christensenellaceae, Anaeroplasmataceae and Ruminococcaceae, and lack of Bifidobacteriaceae, were also observed. Metabolome analysis revealed a deficiency in unsaturated fatty acids and choline, and an overabundance in ketone bodies, lactate, amino acids, TMA and TMAO in 3xtg mice, with additive effects of high-fat diet. These metabolic alterations were correlated with high prevalence of Enterococcaceae, Staphylococcus, Roseburia, Coprobacillus and Dorea, and low prevalence of S24.7, rc4.4 and Bifidobacterium, which in turn related to cognitive impairment and cerebral hypometabolism. Our results indicate an effect of transgenic background on gut microbiome-metabolome, enhanced by high-fat diet. The resulting profiles may precede overt cognitive impairment, suggesting their predictive or risk-stratifying potential.
Abnormalities in the intestinal microbiota have been described in association with numerous diseases, most frequently obesity and bowel inflammation1,2. Recent evidence suggests that the microbiota may be strongly involved in the pathogenesis of neuropathologies3. Among them, psychiatric conditions, autism and Parkinson’s disease have received most attention, whereas there seem to be no studies addressing Alzheimer’s disease (AD) and dementia. These epidemic diseases are growing in prevalence at an alarming rate, fostered by population aging, and by an increasing frequency and severity of predisposing conditions4. Recent findings document that in mice and humans with AD, neurodegenerative changes occur in the gut, similar to the brain5,6. Obesity is among commonest risk factors for cognitive decline and AD, and high-fat diet has been shown to accelerate cognitive deterioration, especially in genetically predisposed models7,8. High-fat diets are known to modify gut function and bacteria composition9.
Microbiota-mediated signals can reach the brain via neural and circulating routes10. The microbiota regulates the transport of nutrients across the gut barrier, and produces absorbable or non-absorbable metabolites, affecting circulating and faecal metabolic profiles11,12. These can modulate systemic inflammation, i.e. a hallmark of obesity and neurodegenerative diseases, or cross the blood-brain barrier to act directly on the brain12,13,14. Metabolites, whose synthesis, modification or absorption have been ascribed to the microbiota include lipids and lipoproteins, amino acids, glutamate, choline, acetate, butyrate, glycerol and modulators of inflammation and oxidative stress, which are considered crucial in regulating neurological development and preservation15,16,17,18,19,20,21,22,23.
In spite of the notion that the gastrointestinal environment varies profoundly from the proximal to the distal end of the intestine, affecting bacteria composition, most of the available knowledge is based on faecal bacteria obtained from the very end of the intestine24.
Here, we postulated that the combined characterization of microbiome, and circulating and faecal metabolome might reveal signatures and provide mechanistic insight related to neurodegenerative disease, and its accentuation by high-fat feeding. We studied 3xtg transgenic mice at an early cerebral disease stage and control mice, both undergoing normal or high-fat feeding. We examined their caecum and colon microbiota composition and diversity (within and between intestinal segments), and also metabolites in faeces (caecum and colon) and serum. In vivo cerebral metabolism and cognitive function were assessed to confirm the subclinical disease stage.
We characterized n = 45 mice, grouped in normal diet-fed (ND, n = 9), high-fat diet-fed (HFD, n = 9), ND-fed triple transgenic (3xtg, n = 8) and HFD-fed 3xtg mice (3xtg-HFD, n = 7). Diet was administered up to 8 months of age, when body weight, cognitive performance by Y-maze test, and brain glucose metabolism by 18F-2-fluoro-2-deoxyglucose positron emission tomography/computed tomography ([18F]FDG PET/CT) were assessed. At the end of the dieting period, 8-month-old HFD mice were heavier than ND mice (51.8 ± 2.6 vs 41.7 ± 1.5, p < 0.01; growth curves, Fig. S1), whereas a tendency was shown in 3xtg-HFD vs 3xtg mice (39.7 ± 1.8 vs 35.5 ± 1.0, p = 0.1). As per design, we aimed to target the pre-demented stage, thus the Y-maze test showed a non-significant ∼20–40% cognitive decline in 3xtg models. Two [18F]FDG PET/CT images of control ND mice were excluded due to persistent hyperglycaemia on the imaging day. A marked (∼30–40%) reduction in cerebral [18F]FDG extraction was observed in 3xtg and 3xtg-HFD mice compared to controls, especially in the hippocampus and temporal cortex, consistent with a pre-demented state (Table 1).
Impact on the metabolome
We quantified 77 and 99 metabolites in all serum and faecal (caecum and colon) samples, respectively (Tables S1-2), and built chemometric models for detecting global and individual metabolic trends (Fig. 1, Figs S2–5). Serum analysis by Principal Component Analysis (PCA) showed distinct clusters in 3xtg compared to control mice, indicating genotype-induced changes in metabolome (Fig. 1a). More specifically, we observed a clear separation along the first Principal Component (PC1, 46.54% of variance) between 3xtg and control mice, regardless of diet, suggesting a stronger metabolic impact of 3xtg genotype than HFD. Serum metabolites explaining this separation pattern are given in the PCA loading plot (Fig. S2). Metabolites and samples segregation in response to diet and disease were attenuated at faecal level, where a greater effect of HFD compared to 3xtg genotype was observed in the determination of samples segregation (Fig. 1b,c). To further explore the metabolomic relationships between 3xtg genotype and diet, we built separated partial least-squares discriminant analysis (PLS-DA) models discriminating 3xtg and control mice, under ND or HFD (Figs S3–5). These plots highlighted a strong separation between 3xtg and controls in both serum and fecal extracts, regardless of diet, and revealed greater HFD-mediated separation in 3xtg compared to control mice. For serum and faecal metabolites, we quantified relative fold-changes in all possible binary comparisons to evaluate the extent of metabolomic variations in the different groups (Figs 2–3), thus observing that both 3xtg genotype and HFD affect some metabolites in the same direction, but to a different extent, prevailing for the 3xtg background.
Impact of diet
A significant increase in inflammatory marker (glycoprotein acetylation biomarker, GlycA), lactate and albumin lysil serum levels was observed in HFD compared to ND mice (Fig. 2). At faecal level, group comparisons did not show regional differences between colon and caecum tracts (Fig. 3) and a large interindividual variation in metabolic profiles seemed to attenuate group effects. A tendency towards higher ribose, threonine, threonine-ornithyne, glycerol and fatty acid levels, and lower proline, acetate and ethanol amounts was observed in HFD compared to control mice (especially in colon), but only colon ribose levels achieved statistical significance.
Impact of disease
The 3xtg genotype induced strong metabolic changes in host (serum) metabolome, but minor changes in host-microbial co-metabolome (faeces) (Figs 2–3). Differences in serum metabolome of 3xtg compared to control mice, regardless of diet, included elevation in inflammatory markers (GlycA), lactate, albumin lysil, leucine and isoleucine, and deficient levels of unsaturated fatty acids, very low density lipoprotein (VLDL), and choline. In addition, higher levels of trimethylamine (TMA) and a tendency to trimethylamine N-oxide (TMAO) elevation occurred in 3xtg mice compared to controls. At faecal level, 3xtg mice were characterized by a pronounced increase in ornithine-tyrosine levels compared to controls, in both colon and caecum.
Combined impact of diet and disease
The combined effect of HFD and 3xtg genotype amplified the changes observed in each component alone. As expected, the comparison of 3xtg genotype under HFD vs control animals under ND showed the largest number of statically significant differences and fold changes (Fig. 2). Similar to 3xtg mice, high aminoacids (leucine, isoleucine, glycine) and albumin lysil serum levels were detected compared to controls. The amount of systemic inflammatory markers (GlycA) was elevated, but not higher than in 3xtg under ND, due to already high inflammatory levels in this group. Instead, a further elevation in glucose, lactate, glycerol and glutamate levels was observed compared to controls and to 3xtg under ND. Likewise, fatty acid (but not VLDL) deficiencies were also amplified in 3xtg-HFD, compared to each condition (3xtg or HFD) alone. Finally, TMA and TMAO levels were progressively greater from ND to 3xtg and to 3xtg-HFD. Important, the combination of HFD and 3xtg genotype affected ketone bodies pathways in an alternative way compared to the above listed metabolites, due to the opposing effects of HFD, lowering and 3xtg, elevating acetoacetate and 3-hydroxibutyrate. The net effect resulted in a significant reduction of ketone bodies in 3xtg-HFD mice compared to controls. In faeces, ornithine-threonine and acetoin levels were significantly higher in the colon of 3xtg-HFD compared to ND mice (Fig. 3).
Impact on the microbiome
A total of 2,895,848 quality-filtered 16 S rDNA sequences were obtained from caecum and colon faecal extracts (52,651.8 ± 34,735.2 seq/sample) and clustered into 23,874 Operational Taxonomic Units (OTUs).
Impact of location
Analysis of Similarity (ANOSIM) test showed significant differences at OTU level between colon and caecum microbiome (R = 0.184, p = 0.039). In group analysis, they were significant in ND (R = 0.184, p = 0.043) but not in 3xtg mice (R = 0.007, p = 0.412).
Higher Bacteroidetes (27.57% vs 13.0%, p = 0.0016, p Bonferroni correction = 0.0096, false discovery rate, FDR = 0.0075) and lower Firmicutes (64.41% vs 81.97%, p = 0.0025, p Bonferroni correction = 0.015, FDR = 0.0075) were present in colon compared to caecum samples in ND mice. However, no differences at phylum level were observed between colon and caecum samples in the 3xtg group.
At family level, caecum samples showed higher levels of Lachnospiraceae (18.02% vs 10.28%, p = 0.036) and lower levels of S24.7 (13% vs 27.56%, p = 0.0016) than colon samples in ND. Conversely, only Enterococcaceae family was significantly different between colon and caecum samples in 3xtg mice (2.31% vs 0.09%, respectively, p = 0.012). In linear discriminant analysis effect size (LEfSe) tests, S24.7 family was significantly enriched in ND colon compared to caecum samples (linear discriminant analysis, LDA, score > 5, p < 0.05), while Enterococcaceae family was enriched in 3xtg colon compared to caecum samples (LDA score = 4.5, p < 0.05). At OTU level, we found significant differences in 30 OTU belonging mostly to Firmicutes and Bacteroidetes phyla when ND colon and caecum samples were compared, while only 8 OTU significantly differed in 3xtg. Higher abundance of Oscillospira (p = 0.035) and lower abundance of Enterococcus spp. (p = 0.05) genera was detected in caecum compared to colon samples in 3xtg (data not shown).
Higher Shannon diversity index (p = 0.022), but no differences in microbial richness measured by Chao1 index (p = 0.512), was observed in caecum compared to colon samples in ND. Conversely, no alpha diversity (Shannon and Chao1 indexes), was reported between colon and caecum samples in 3xtg mice (Fig. S6).
Impact of diet
Redundancy Analysis (RDA) showed significant differences in microbial composition between HFD and ND mice, in colon (p = 0.006) and caecum samples (p = 0.001) (Fig. 4b), as confirmed by ANOSIM tests (colon: R = 0.209, p = 0.023; caecum: R = 0.213, p = 0.032).
At family level, lower abundance of Bifidobacteriaceae (p = 0.029), Lactobacillaceae (p = 0.071) and S24.7 (p = 0.055) and higher abundance of Rikenellaceae (p = 0.0013, FDR = 0.023), Mogibacteriaceae. (p = 0.0074, FDR = 0.074), Lachnospiraceae (p = 0.012, FDR = 0.072) Enterococcaceae (p = 0.022, FDR = 0.09), were detected in HFD compared to ND colon samples. Similar results were found in caecum samples, where lower levels of Bifidobacteriaceae (p = 0.063) and S24.7 (p = 0.029), and higher abundance of Rikenellaceae (p = 0.00077, FDR = 0.013), Enterococcaceae (p = 0.0088, FDR = 0.052) and Staphylococcaceae (p = 0.0092, FDR = 0.052) were observed in the HFD compared to ND group.
At genus level, lower abundance of Unclassified Peptococcaceae (p = 0.013), Bifidobacterium and Lactobacillus spp (p = 0.029 and 0.072, respectively) and higher abundance of Unclassified Rikenellaceae (p = 0.0013, FDR = 0.042), Unclassified Mogibacteriaceae (p = 0.007), and Unclassified Enterococcaceae (p = 0.022) were observed in HFD compared to ND colon samples.
DESeq 2 test confirmed diet-based differences between groups, specifically lower abundance of Bifidobacterium and Lactobacillus were found in HFD than ND mice (p < 0.0001, FDR < 0.0001 for both). In caecum samples, we also observed lower abundance of Bifidobacterium spp (p = 0.036) and Ruminococcus (p = 0.043), and higher abundance of Staphylococcus (p = 0.009) and Clostridium spp (p = 0.07) genera in HFD compared to ND mice. Most significant findings in pooled samples (caecum and colon) are shown in Supplementary Figure 7.
At OTU level, we found significant differences in 37 OTU belonging mostly to Firmicutes, Bacteroidetes and Actinobacteria phyla (Table S3) in colon, and also 37 OTU in caecum when ND and HFD groups were compared (Table S4). No differences in Shannon diversity index and lower Chao1 richness index (p = 0.086, colon; p = 0.0223, caecum) were observed in HFD compared to ND groups (Fig. S6). LEfSe tests revealed that at family level in ND mice, S24.7 was significantly enriched in colon, while Bifidobacteriaceae were highly abundant in caecum (Fig. 5a). In HFD mice, Enterococcaceae and Rikenellaceae were representative of colon, whereas Lachnospiraceae and Staphylococcaecae were abundant in caecum samples. Venn diagram showed a core of 13 families shared between diet groups and locations (Fig. 5c). Bifidobacteriaceae family was exclusively present in ND colon and caecum. Christensenellaceae, Mogibacteriaceae and Rikenellaceae were present in HFD colon and caecum. Staphylococcaceae and Enterococcaceae, were shared between ND colon and HFD colon and caecum.
Impact of disease
RDA showed differences in the microbial composition of colon (p = 0.001) and caecum samples (p = 0.001), between ND and 3xtg (Fig. 4c,d), as confirmed by ANOSIM tests (colon: R = 0.696, p = 0.001; caecum: R = 0.326, p = 0.001).
At family level, lower abundance of S24.7 (p = 0.018) and higher abundance of Enterococcaceae (p = 0.0077, FDR = 0.081) and Turicibacteraceae (p = 0.0081, FDR = 0.081) were detected in 3xtg compared to ND colon samples. Similar results were found in caecum samples, in which lower levels of S24.7 (p = 0.029) and Bifidobacteriaceae (p = 0.045) were detected in 3xtg compared to ND mice. At genus level, lower abundance of Bifidobacterium spp (p = 0.045) and rc4.4 (p = 0.042), and higher abundance of Roseburia (p = 0.049) were detected in 3xtg compared to ND caecum. LEfSe analyses confirmed that, at family level S24.7 and Lachnospiraceae was significantly enriched in ND colon and caecum, respectively, while Enterococcaceae and Turicibacteriaceae were associated to 3xtg colon samples (Fig. 5b). Families belonging to Ruminococcaceae and Anaeroplasmataceae were representative of 3xtg caecum samples. At genus level, Turicibacter and Staphylococcus were significantly enriched in 3xtg colon samples, whereas Anaeroplasma was associated to 3xtg caecum samples. Most significant findings in pooled samples (caecum and colon) are shown in Supplementary Figure 7.
Venn diagram showed a core of 13 families shared between 3xtg and control mice in both locations (Fig. 5d). Turicibacteraceae family was associated to 3xtg colon, while Christensenellaceae to 3xtg caecum. Bifidobacteriaceae was related to ND colon and caecum, whereas Anaeroplasmataceae was linked to 3xtg colon and caecum. Finally, Staphylococcaceae and Enterococcaceae families were shared between ND colon and 3xtg colon and caecum.
At OTU level, we found significant differences in 48 OTU (Table S5) in colon and 62 OTU in caecum (Table S6) when ND and 3xtg groups were compared. Alpha diversity analysis showed no group differences in Shannon diversity index, but lower Chao1 richness index (p = 0.0195) in 3xtg than ND colon samples (Fig. S6). No significant difference was found in caecum, though the tendency was the same.
Impact of combined location, diet and disease
Principal Coordinates Analysis (PCoA) of the samples clearly separated 3xtg from control animals, in both weighted (Fig. 6a) and unweighed (Fig. 6b) plots (PC1 accounting for 8.7% and 30.94% of the variance in unweighted and weighted UniFrac analysis, respectively), indicating that the microbiota between groups is compositionally distinct. In addition, the different diet groups are well defined and clustered. ANOSIM tests confirmed the overall significant difference between groups and intestinal locations (R = 0.477, p = 0.001). Similar results were found when microbiome of ND, HDF, 3xtg and 3xtg-HFD groups in each intestinal location (colon: R = 0.53, p = 0.001; caecum: R = 0.589, p = 0.001) were compared.
Together with UniFrac data, ADONIS (permutational manova, PERMANOVA) showed significant differences at OTU level between diet groups and sample location (p = 0.0006). In addition, RDA highlighted significant differences in the microbial composition between the diets and disease status in colon (p = 0.001) and caecum (p = 0.001) (Fig. 6c,d).
Alpha diversity analysis showed no differences in Shannon diversity index, but higher Chao1 richness index (p < 0.0001 in colon and p = 0.0256 in caecum) between groups and locations, as higher richness was found in ND followed by HFD group (Fig. S6).
Microbiome and metabolome associations
Heatmap generated to examine correlations between colon microbiota and serum metabolome in ND and 3xtg mice (Fig. 7) showed three main clusters: I) lactate, malate, acetylcarnitine, glutamate, succinylacetone, glycerol, citrate, etc; II) proline, methylalanine, methionine, creatine phosphate, leucine, isoleucine, glutamine, alanine, methylsuccinate, etc; III) cholesterol, lipoproteins and fatty acids. Bifidobacterium and Unclassified s24.7 levels, which were shown to be defective 3xtg mice, were related to high lactate, malate and aminoacid levels, and to low cholesterol, low density lipoprotein (LDL) and fatty acid amounts. Coprobacillus, Dorea and other bacterial strains were also negatively related to cholesterol and fatty acid levels. Abundance of rc4.4, which was shown to be deficient in 3xtg mice, was associated negatively with circulating aminoacids and positively with cholesterol and fatty acids levels. Both Unclassified s24.7 and rc4.4 were negatively correlated with the amount of circulating choline compounds and inflammatory marker GlycA. Conversely, Staphylococcus and Unclassified Enterococcus (shown to be overabundant in 3xtg) were positively associated with lactate, malate, acetylcarnitine, succinylacetone, pyruvate and aminoacid levels. Overall, bacteria correlating with an adverse metabolic profile, as defined by 3xtg characteristics, were primarily Enterococcaceae, Staphylococcus, followed by Roseburia, Coprobacillus, Dorea, Enterococcus, Christenellaceae. The ones relating to the reverse healthier profile were s24.7, rc4.4, Bifidobacterium, Dehalobacterium, Peptococcaceae, Acinetobacter.
Microbiome and brain associations
Heatmap generated to examine correlations between caecum-colon microbiota and cerebral parameters (Alternation triplets, n and %, and glucose metabolism) across groups (Fig. 8) showed that cerebral hypometabolism was associated with higher abundance of Firmicutes phylum, Anaeroplasmataceae and Erysipelotrichaceae families, and Coprobacillus, Clostridium, Anaeroplasma and Roseburia genera, and lower abundance of Bacteroidetes phylum, Peptococcaceae, Rikenellaceae, Dehalobacteriaceae and s24.7 families, and rc4.4, Dehalobacterium, Unclassified Coriobacteriacea, Unclassified Rikenellaceae, Unclassified s24.7.
Furthermore, we observed that higher abundance of Bifidobacteriaceae and Erysipelotrichaceae families, and Bifidobacterium and rc4.4 genera were positively correlated with cognitive function, whereas negative associations occurred with Coprobacillus, Dorea, Roseburia, and Unclassified Peptococcaceae.
The emerging biology of gut-brain crosstalk has revealed the existence of a complex bidirectional system25, in which neurodegenerative processes affecting the brain also occur in the gut5,6, and vice versa, factors primarily influencing the gut microbiota, e.g. high-fat diets, increase the risk of neurodegeneration. We addressed these interrelations by comparing normal and high-fat feeding in control mice and in a transgenic mouse model of neurodegenerative disease. This model was studied prior to the development of full-blown cognitive deficits, which we have shown to occur later in life26. In the current disease stage, our 3xtg mice showed the typical cerebral hypometabolism that precedes dementia in humans27. Several novel results emerged from our study.
The most salient finding was the dramatic rightward and clear-cut shift occurring in the overall composition of the microbiota in 3xtg compared to ND mice, and defining a global microbiota pattern which enabled to clearly identify subjects that are going to be demented. Another specific trait of 3xtg mice was the loss of differences in microbial diversity between caecum and colon, as opposed to control mice, in which the caecum showed superior diversity than the colon, due to higher amounts of Firmicutes and lower Bacteroidetes at phylum level, and higher Lachnospiraceae and lower S24.7 at family level. Bacterial richness was also defective in 3xtg mice, as documented by Chao1 indices. In normal gut physiology, the caecum and colon reflect very different functions, and a greater diversity in their microbial composition - as observed in our healthy mice - is therefore expected. The lack of this trait in our 3xtg mice may indicate that these intestinal segments have lost their distinctive milieu. In fact, recent reports document that neurodegeneration involves intestinal walls (beyond brain), leading to functional abnormalities in 3xtg mice5,6. This may affect microbial composition and function. Notably, 3xtg mice were characterized by an elevation in Firmicutes compared to Bacteroidetes abundance in both gut tract, and these traits were associated with cerebral hypometabolism. Most important, specific families were exclusively represented in the 3xtg model, and absent in ND mice. These were Turicibacteraceae (colon), Christensenellaceae (caecum) and Anaeroplasmataceae (both colon and caecum). Conversely, Bifidobacteriaceae were absent in 3xtg mice, while being well represented in the control ND model (colon and caecum), in agreement with their positive association with cognitive function. In the colon, 3xtg mice also showed higher amounts of Enterococcaceae. In the caecum, lower abundance of S24.7 and rc4.4, and higher amounts of Ruminoccaceae and Roseburia occurred. Some, but not all of these bacterial alterations, along with the reduction in bacterial diversity and richness have been described in dysmetabolic, low-grade inflammatory and inflammatory bowel states28,29,30,31, in agreement the high serum levels of GlycA (marker of inflammation) observed in our 3xtg mice. Our data lend support to the concept that abundance differences in very selected bacterial families are specifically related to a high-risk to develop dementia in our mouse model, and warrant studies to examine direct cause-effect relationships.
We explored serum and faecal metabolomes, and their correlations with bacteria. Notably, our PCA analysis explained 46% of changes in serum metabolites occurring in 3xtg compared to ND mice, indicating a strong and selective relationship between disease and metabolome. In fact, subgroup analyses showed well-defined serum and faecal metabolite clusters in 3xtg versus control mice. Also important was that these metabolomics alterations were significantly correlated with the prevalence of Enterococcaceae, Coprobacillus, Staphylococcus, Roseburia and Dorea, belonging to the Firmicutes phylum, mostly in the Clostridia and Lachnospiraceae class and families, and with deficiencies in S24.7, rc4.4, Bifidobacterium, Dehalobacterium. Coherently, associations between most of these taxa and cerebral metabolism and/or cognitive function were also detected. One striking finding in faecal metabolites was the elevated presence of amino acids ornithine and thyrosine. Ornithine provides cerebral protection against ammonia, whereas thyrosine has neuroexcitatory properties, and Clostridia modulate amino acid metabolism. The pathophysiological significance of this finding in the context of neurodegeneration deserves further investigation. Serum metabolomics patterns seen in 3xtg mice were typical of neurodegenerative diseases. First, reductions in unsaturated fatty acids, LDL and VLDL, as seen in 3xtg mice, compromise the important contribution of lipids to neuronal cell structure (50% of neuronal membranes), energy storage and signal transduction, and relate to the development of AD16,17,18. Second, the brain is an avid consumer of glucose, and our 3xtg mice showed a gross impairment in brain glucose uptake. The accompanying increase in ketone bodies, i.e. β-hydroxybutyrate, acetoacetate, and acetone may serve as protective alternative fuel during brain glucose starvation, as suggested in humans with mild-cognitive impairment (MCI)32. The impairment in brain glucose metabolism has been implicated in the pathogenesis of hyperglycemia and hyperlactatemia in patients with MCI and AD32,33, and these substrate excesses were found in our 3xtg mice. Lactate is a modulator of cerebral Aβ production, and its levels are abnormal in brain and cerebrospinal fluid (CSF) of AD subjects34,35. Third, remarkable alterations were found in amino acid metabolism in 3xtg mice, consisting in high levels of methionine (precursor of homocysteine), leucine (activator of the mammalian target of rapamycin, mTOR, signalling36) and isoleucine (relating to insulin resistance with other branched-chain amino acids37), alanine and glutamate (important in neurotransmission). These pathways have been implicated in the pathogenesis of cerebrovascular disease and dementia38, β-amyloid brain accumulation39, enhanced neurofibrillar tangle formation40, and glutamatergic dysregulation21. We also report elevated TMA, TMAO levels (regulating tau aggregation41), and choline deficiency (precursor of acetylcholine, a cholinergic neurotransmitter implicated in memory and AD42), in 3xtg mice. Altogether, these results suggest that metabolite changes known to compromise brain structure and function occur in 3xtg mice, prior to the development of overt dementia, and correlate with the abundance of selected gut bacteria, revealing potential mechanisms underlying the complex interaction linking gut and neurodegenerative disease.
High-fat diets have a profound impact on gut microbiota9. Extending previous observations, we found that a HFD modifies bacterial composition in both colon and caecum, also leading to lower richness compared to ND. In both caecum and colon, HFD mice showed high relative abundances of Firmicutes than Bacteroidetes at phylum levels, Rikenellaceae, Lachnospiraceae, Enterococcaceae and S24.7 at family level, as well as increased amount of faecal ribose. Higher post-prandial colonic motility has been described in response to HFD consumption, and ribose affects gut activity43,44. Elevations in Clostridium and Staphylococcus were also observed in the caecum. HFD mice were depleted in protective Bifidobacteriaceae and Lactobacillaceae (Bifidobacterium and Lactobacillus at genus level), which maintain mucosal barrier integrity and constrain endotoxin formation, preventing inflammation and metabolic complications45,46. Coherently with this, GlycA levels were high in our HFD mice.
We and others have shown that a HFD promotes cognitive impairment in both humans and mice, and that the acceleration of cognitive decline is particularly evident in older 3xtg-HFD mice26. In this study, compared to HFD or 3xtg alone, summative outcomes were seen in selected microbial families and genera in 3xtg-HFD mice, resulting in severe depletion of S24.7, Peptococcaceae, Dehalobacteriaceae families, and rc4.4 genus, and excess of Clostridium genus abundance. In the metabolome of HFD and 3xtg mice, most changes occurred in a similar direction, leading to strong additive effects in 3xtg-HFD mice, compared to HFD and 3xtg alone. One important distinctive feature was also noted, as 3-hydroxybutyrate and acetoacetate were high in 3xtg and low in HFD, compared to ND mice. Ketones are considered protective in Alzheimer’s brains, as they may compensate for cerebral glucose hypometabolism47,48. Therefore, the ketone deficiency caused by HFD in our 3xtg-HFD mice can be an important mechanism whereby HFD accelerates progression of cognitive impairment in 3xtg mice26.
The study has some limitations. It involved male mice to limit data variability, considering that males seem more vulnerable than females to the impact of HFD-induced obesity (i.e. a target risk factor for dementia), on weight gain, metabolic alterations, deficits of learning, and hippocampal synaptic plasticity49. However, it would be relevant to extend findings to females, since the number of women with obesity and/or dementia is also high. Furthermore, the study was conducted in mice, and therefore its translational significance remains to be examined.
In conclusion, our study shows that high-fat feeding and genetic predisposition to neurodegenerative disease share abnormalities in the resulting microbiome and metabolome, which are additive and seem unfavourable to brain health. Most important, distinctive signatures, including selected microbial families and metabolic changes, and the lack of bacterial diversity between colon and caecum were exclusively found in association with 3xtg mice, and coherent associations were identified between microbiota changes and cognitive reductions or cerebral hypometabolism. Our findings have important implications, as an excellent discrimination was shown in microbial-metabolome profiles between groups, and 3xtg mice were pre-demented, suggesting that the above clear-cut microbiome-metabolome deviations occur early in the course of neurodegenerative disease.
Animal model and study design
The study involved n = 18 B6129SF2/J (stock no:101045, The Jackson Laboratory, Bar Harbor, Maine) and n = 15 triple transgenic (3xtg) male mice (B6;129-Psen1tm1MpmTg[APPSwe, tauP301L]1Lfa/Mmjax stock no:004807, MMRRC034830, The Jackson Laboratory), randomly stratified as follow: I) normal diet-fed mice (ND, B6129SF2J, n = 9, 11% kcals from fat, Mucedola, Italy); II) high-fat diet-fed mice (HFD, B6129SF2J, n = 9, 58% kcals from fat, Mucedola); III) ND-fed 3xtg mice (3xtg, n = 8) and IV) HFD-fed 3xtg mice (3xtg-HFD, n = 7). The slight discrepancy in group sizes was due to higher 3xtg mortality. Animals were housed in standard cages (n = 4–5 mice/cage) under controlled conditions (12-hour light/12-hour dark cycles, 22 °C), with ad libitum access to food and water. Veterinary and animal care staffs were responsible for the monitoring of animal welfare and health for all the duration of the study. Diet was administered from 2 to 8 months of age, when body weight, cognitive performance and brain glucose metabolism were assessed. Then, animals were euthanized by an anaesthetic overdose, and blood and faecal samples (caecum and colon) collected for analyses of serum and faecal metabolome, and gut microbiota. The experimental protocol was notified to the Ministry of Health (Dept. of Public Veterinary Health) in accordance with the D.L.116/92 implementation of directive EEC 609/86 regarding the protection of animals used for experimental and other scientific purposes, and adheres to standards articulated in Reporting of In Vivo Experiments (ARRIVE) guidelines.
Cognitive analysis by Y-maze test
Cognitive performance was measured by a spontaneous alternation test (Y-maze, Panlab, Harvard Apparatus, Spain). Each subjects was allowed to freely move through the maze for 8 minutes, whereas a visual automatic tracking system (Panlab) recorded the number of alternation triplets explored.
Brain glucose metabolism by [18F]FDG PET/CT
On the experimental day, each animal was transferred to the imaging facility. Anaesthesia was induced and maintained in overnight-fasted mice by ∼2% (v/v) isofluorane inhalation (IsoFlo®, Abbott Laboratories, IL, USA), a standard method for rodent based on minimal handling and safety, and breath frequency and body temperature were monitored. Then, a 60-minute dynamic PET scan was acquired after i.p. 18F]FDG injection, by an IRIS PET/CT small-animal tomograph (Inviscan SAS, France). Volumes of interest were manually drawn on PET/CT images by AMIDE software (AMIDE-bin 1.0.5) in the hippocampus, frontal and temporal cortex. Regional [18F]FDG uptake was expressed as standardized uptake value (SUV), i.e. the ratio between tissue activity (kBq/ml) at 60 min post-injection, and weight-normalized injected dose (kBq/g).
Serum and faecal metabolites by 1H-NMR Spectroscopy
Blood samples (n = 33) were centrifuged (2200 RCF, 10 min) to obtain serum. Faecal samples (n = 27, caecum; n = 28, colon) were suspended in Milliq water (100 µL) and centrifuged (14800 rpm, 5 minutes) for 3 consecutive times to obtain the extract. Extracts (20 μl) supplemented with D2O (2 μl) were transferred into 1-mm NMR tubes. 1H-NMR spectra (8000 Hz width) were recorded in a Bruker Avance DRX 600 spectrometer (Valencia, Spain), equipped with a triple resonance 1 H/13 C/31 P probe. Samples were measured at 310 K and a single-pulse presaturation experiment was acquired in all samples. The water signal was saturated with weak irradiation during the recycle delay. Data were Fourier transformed after the free induction decay was multiplied by a 0.3 Hz exponential line-broadening function. Spectra were processed using MestReNova 8.1 (Mestrelab Research S.L., Spain) and transferred to MATLAB (MathWorks, 2012) using in-house scripts for data analysis. The chemical shift region including resonances 0.50–4.70 ppm (the aliphatic region) and 5.20–10.00 ppm (the aromatic region) was investigated. Metabolite spin systems and resonances were identified by literature data and Chenomx resonances database (Chenomx NMR 7.6). Spectra were normalized to total aliphatic spectral area to eliminate differences in metabolite total concentration, binned into 0.01 ppm buckets and then subjected to mean-centering before multivariate analysis. Signals belonging to selected metabolites were integrated and quantified using semi-automated in-house MATLAB peak-fitting routines. Final metabolite levels were calculated in arbitrary units as peak area normalized to total spectral area.
NMR profile and statistical analyses
Metabolomics data analysis was performed using in-house MATLAB scripts and PLS_Toolbox (Eigenvector Research). PCA was applied to NMR spectra data sets, to find low-dimensional embeddings of multivariate data. PCs were chosen to explain at least 70% of the variance. The loading plots of the corresponding PC were used to detect the position of most discriminative variables in the NMR spectra. To maximize the separation between samples, PLS-DA was applied. Permutation test was performed to check overfitting of the PLS-DA models. The multivariate chemometric models were cross-validated with 10-fold Venetian blind cross-validation. In each run, 10% of data were left out of the training and used to test the model. Spectral regions with high variable importance in projections (VIP) coefficients obtained during PLS-DA are more important in providing class separation during analysis, while those with small VIP coefficients provide little contribution to classification. P-values ≤ 0.05 were regarded as statistically significant.
Faecal microbiome by 16S rDNA gene sequencing
Total DNA was isolated from faecal samples (n = 27, caecum; n = 28, colon) by MasterPure Complete DNA&RNA Purification Kit (Epicentre, Illumina, WI, USA), with some modifications, as previously described50. Isolated DNA concentrations were measured using a Qubit® 2.0 Fluorometer (Life Technology, CA, USA) and normalized to 10 ng/μL. The V3-V4 region of 16 S rDNA gene was amplified by PCR using Illumina adapter overhang nucleotide sequences following Illumina protocols. The multiplexing step was performed using Nextera XT Index Kit (Illumina, CA, USA). PCR product was checked with a Bioanalyzer DNA 1000 chip (Agilent Technologies, CA, USA) and libraries were sequenced using a 2 × 300 pb paired-end run (MiSeq Reagent kit v3) on a MiSeq-Illumina platform (FISABIO sequencing service, Valencia, Spain) according to manufacturer’s instructions (Illumina). Reagents employed for DNA extraction and PCR amplification were also sequenced as controls.
Bioinformatics and statistical analysis
Quality assessment was performed by prinseq-lite program (min_length:50; trim_qual_right:20; trim_qual_type:mean; trim_qual_window:2051). R1 and R2 from sequencing where joined using fastq-join from ea-tools suite52. Data were obtained using an ad-hoc pipeline written in RStatistics environment53 and data processing was performed by QIIME pipeline (version 1.9.0)54. Chimeric sequences and sequences that could not be aligned were removed. The clustered sequences were utilized to construct OTUs tables (97% identity), then classified into phylum, family, genus taxonomic levels based on the Greengenes database. Sequences, that could not be classified, or classified as Cyanobacteria and Chloroplasts (representing ingested plant material), were removed. Alpha diversity indices (Chao1 and Shannon), UniFrac beta diversity, and PERMANOVA were used to test significance. ANOSIM test was employed for group-comparison in microbiota communities. Calypso software version 7.36 (http://cgenome.net/calypso/) was used with total sum normalization (TSS) for the statistical analysis, and also Cumulative Sum Scaling normalisation (CSS) for multivariate tests (RDA). Venn diagram for shared phylotypes was generated with the same software. LEfSe was used to detect unique biomarkers (LDA score >3.0) in relative abundance of bacterial taxonomy55. P-values ≤ 0.05 were regarded as statistically significant.
The datasets generated and analysed during the current study are not publicly available, but will be available from the corresponding author on reasonable request.
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The study was conducted at the Institute of Clinical Physiology of the National Research Council (CNR) in Pisa, Italy. Metabolomic and microbiome analyses were carried out at the Health Research Institute of the Clinical Hospital INCLIVA and the Institute of Agrochemistry and Food Technologies of the Spanish Council for Scientific Research, Valencia, Spain. Bacterial 16 S rDNA gene sequencing by Illumina Technology was conducted at FISABIO (Sequencing and Bioinformatics Service), Valencia, Spain. We acknowledge the Animal Care Unit staff at CNR, Pisa, Italy, for their support in chronic mice studies. Data on cerebral hypometabolism and cognitive decline were presented at the European Congress on Obesity 2015 (ECO, Prague, Czech Republic May 2015). This work was supported by the Ministry of Economy, Industry and Competitiveness of Spain (MINECO-Spanish Government, grant numbers SAF2014–52875R to DM, and AGL2015–707487-P to MCC), Instituto de Salud Carlos III and co-funded by ‘FEDER’ (grant number PIE15/00013 to DM), and the European DORIAN-Health-FP7 project (GA 278603 to PI).