Diet Drives Convergence in Gut Microbiome Functions Across Mammalian Phylogeny and Within Humans

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Science  20 May 2011:
Vol. 332, Issue 6032, pp. 970-974
DOI: 10.1126/science.1198719


Coevolution of mammals and their gut microbiota has profoundly affected their radiation into myriad habitats. We used shotgun sequencing of microbial community DNA and targeted sequencing of bacterial 16S ribosomal RNA genes to gain an understanding of how microbial communities adapt to extremes of diet. We sampled fecal DNA from 33 mammalian species and 18 humans who kept detailed diet records, and we found that the adaptation of the microbiota to diet is similar across different mammalian lineages. Functional repertoires of microbiome genes, such as those encoding carbohydrate-active enzymes and proteases, can be predicted from bacterial species assemblages. These results illustrate the value of characterizing vertebrate gut microbiomes to understand host evolutionary histories at a supraorganismal level.

Comparative culture-independent metagenomic studies of the microbial species assemblages that compose mammalian gut microbiota, and the functions that these communities encode in their aggregate genomes (microbiomes), can provide a complementary perspective to comparative studies of host genomes. A previous bacterial 16S ribosomal RNA (rRNA)–based study of 59 mammalian species revealed that their fecal microbiota clustered according to diet rather than host phylogeny (1). This finding raises several questions: What is the functional evolution of the gut microbiome in relation to diet? Is the process unique to each mammalian lineage? To what extent does microbial phylogeny predict function within microbial communities? Could analysis of interspecific differences among mammals create a pipeline for deciphering intraspecific differences among humans in response to varied diets or other factors? Therefore, we have extended our 16S rRNA studies to a broader sampling of microbial genes in total fecal community DNA prepared from herbivores, omnivores, and carnivores.

We generated shotgun pyrosequencing data sets from 33 mammalian species, along with newly collected bacterial 16S rRNA data. These adult animals represent 10 Orders and varied digestive physiologies (hindgut-fermenters, foregut-fermenters, and simple-gut). In some cases, free-living and captive representatives of a given species were sampled (Table 1 and table S1). Methods for classifying diets and for collecting and processing fecal samples for metagenomic analyses have been described (1). Multiplex pyrosequencing of amplicons generated from the V2 region of bacterial 16S rRNA genes yielded 149,675 high-quality de-noised reads (average = 3838 ± 1080 per sample) (table S2) (2). After chimera removal, 8541 operational taxonomic units (OTUs) were identified in the combined data set (an OTU was defined as reads sharing ≥97% nucleotide sequence identity). Shotgun sequencing of the same fecal DNA preparations produced 2,163,286 reads [mean = 55,469 ± 28,724 (SD) per sample; 261 ± 83 nt per read] (table S3) (2). Shotgun reads were functionally annotated using three databases: KEGG [for KEGG Orthology (KO) groups and Enzyme Commission (E.C.) numbers], CAZy (for carbohydrate-active enzymes), and MEROPS (for peptidases) (35). When shotgun reads were assigned to phylogenetic bins using the program MEGAN (6), the results revealed that fecal microbiomes were dominated by members of Bacteria, had low levels of Eukarya (0.15 to 5.35% of identifiable reads), and archaeons were variably represented (0 to 1.77% of assignable reads, with none detected in any carnivore microbiome). Seventeen samples had reads assigned to known viruses (table S4) (2).

Table 1

Overview of mammals in this study. Sample abbreviations used in figures and tables are noted in parentheses. See table S1 for additional details.

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Procrustes analysis (least-squares orthogonal mapping) was used to test whether the functional properties of a microbiome can be predicted from the bacterial species that compose it (2). Procrustes analysis attempts to stretch and rotate the points in one matrix, such as points obtained by principal coordinates analysis (PCoA), to be as close as possible to points in the other matrix, thus preserving the relative distances between points within each matrix (7, 8) (Fig. 1A). We first took the 16S rRNA data set and used the UniFrac metric to compare the overlap between each pair of communities in terms of their evolutionary distance (9). The similarity in functional profiles was then determined using the Bray-Curtis distance metric applied to KO groups, E.C.s, CAZYmes, or peptidases. Principal-coordinates reduction was performed separately on the 16S rRNA and annotated shotgun (microbiome) data sets, and the point clouds were aligned using Procrustes. For each comparison, the goodness of fit, or M2 value, of the transformed data sets was measured over the first three dimensions. The statistical significance of the goodness of the fit was measured by a Monte Carlo label permutation approach (2).

Fig. 1

Procrustes analysis shows that mammalian gut bacterial lineages and microbiome gene content give similar clustering patterns. (A) Cartoon illustrating Procrustes analysis. The Procrustes transformation of the blue and red data types (i) results in a good fit, whereas the transformation of the green and red data (ii) yields a worse fit, with large distances separating data from samples B and C. (B to E) Procrustes analysis of 16S rRNA sequences (weighted UniFrac) against KO groups, CAZymes (glycoside hydrolases), MEROPS peptidases, and E.C.s. Every sphere represents a single mammalian fecal community and is colored by host diet. The black end of each line connects to the 16S rRNA data for the sample, whereas the orange end is connected to the functional annotation data. The fit of each Procrustes transformation over the first three dimensions is reported as the M2 value.

The agreement between phylogenetic and functional measurements was remarkable for all mammals, regardless of their diet, host lineage, or gut physiology. Figure 1, B to E, shows how the goodness of fit was robust to different functional databases. The analysis was also robust to taxon- or phylogenetic-based species classification, weighted or unweighted metrics, and whether one or more member of each mammalian species was considered (fig. S1). For both bacterial 16S rRNA and whole community gene data sets, the PCoA plots separated carnivores and omnivores from herbivores, emphasizing the importance of diet in differentiating gut microbial communities (P < 0.05) (2). Our previous study using full-length 16S rRNA sequences revealed that the fecal microbiota of conspecifics were significantly more similar than the communities of different host species (1). The V2 16S rRNA data generated in this study confirmed this result, using both weighted and unweighted UniFrac distances (P < 0.05 by 1000 Monte Carlo permutations) (2).

The Procrustes results prompted us to use a nearest-neighbor model to test whether the functional configuration of a microbiome could be predicted from its 16S rRNA sequences. Using a fecal sample’s nearest neighbor, as defined by unweighted or weighted UniFrac, to predict the sample’s functional profile generated a significantly better prediction than a random neighbor; this was true for KOs, E.C.s, CAZymes, and peptidases (P < 0.0001, 106 Monte Carlo permutations) (2).

The concordance of diet and microbiome structure and function raises the question of whether it is caused primarily by coevolution between mammals and their gut microbiota and microbiome, or by the many parallel dietary shifts that have occurred over the course of mammalian evolution (10). We tested which of these hypotheses, which have traditionally been viewed as competing but need not be mutually exclusive, were supported by looking for congruence between mammalian phylogeny and subsets of bacterial species, KOs, CAZymes, peptidases, or other enzymatic activities. Briefly, the mammalian phylogenetic tree defines sets of organisms that are monophyletic; that is, groups containing all and only the descendants of a common ancestor. We reasoned that if bacterial taxa or functions originated rarely, then these taxa or functions should be vertically transmitted during mammalian speciation. Therefore, there should be more cases in which a given taxon or function occurred in all members of a monophyletic mammalian group than chance would predict. Using this analytic approach (2), we found that the overall distribution of microbial species and microbiome functions in the gut does not mirror mammalian phylogeny. 198 different named bacterial genera were detected in our data set; of these, only 3 were significantly associated with the mammalian phylogenetic tree more than would be expected by chance (Prevotella, Barnesiella, and Bacteroides). No CAZymes or peptidases and only 18 of the 3866 KOs tested were associated with host phylogeny. We repeated the analysis using a more relaxed constraint that a taxon or function occurs in a given monophyletic group more frequently than expected by chance rather than requiring strict presence or absence agreement (2). The relaxed definition gave similar results; only three additional genera and a total of 90 KOs were detected as having a significant association with the mammalian tree. We concluded that bacterial taxa and functions are evolutionarily labile and do not explain the concordance between bacterial communities and microbiome functions.

Bipartite network analysis provided an additional tool for exploring the interrelationship between host diet, host lineage, gut physiology, and shared and unique bacteria taxa (1). Mammalian hosts and bacterial OTUs were used as nodes in a bipartite graph, with edges connecting OTU nodes to the hosts in which they are found (2). Using 1900 V2 16S rRNA sequences from each mammalian host, the network shows clear separation of fecal communities by host diet (Fig. 2A), mirroring our earlier results based on smaller numbers of full-length 16S rRNA sequences (1).

Fig. 2

Mammalian gut bacterial communities share a functional core. (A and B) Bipartite network diagrams of evenly sampled bacterial 16S rRNA–derived OTUs (A) or KOs (B). Edges connecting mammalian nodes (circles) to species-level OTUs or KOs found in that sample are colored by host diet. Sample labels are removed from the KO diagram for legibility (a high-resolution image of removed labels is presented in fig. S2). (C) Mammalian gut communities share a core suite of KOs. Using evenly subsampled OTU or KO data sets, the distribution of counts is plotted as a function of the number of mammalian host microbiomes where the KO or phylotype was detected. The results demonstrate exponential decay for the 16S rRNA data (OTU, species, and genus), with no OTU or bacterial species found in all samples, although a core set of KOs is detectable in all fecal communities sampled.

We reasoned that the bipartite graph approach could also be used to connect mammalian samples to individual microbial gene functions from shotgun reads. The power of the bipartite graph approach is to represent both genes and mammalian species explicitly as nodes, thus visualizing which genes connect with which species. The clear separation by diet disappears when we consider gene functions (Fig. 2B and fig. S2), suggesting that rather than a diet- or physiology-specific set of genes, the relationship among mammalian gut microbiomes is that they share a large core repertoire of functions. We confirmed this result by plotting the frequency of shared taxa in the 39 mammalian fecal samples, and also species- and genus-level OTU bins (2). All of the curves demonstrate an essentially exponential decay as successive samples are added, with no OTUs found in more than 30 samples (Fig. 2C). However, the plot of KO frequency flattens out, with 35 KOs found in all samples. This effect cannot be due to differences in the number of OTUs relative to KOs: There are more OTUs than KOs, and fewer assigned species or assigned genera, yet all the taxonomic curves show the same rapid decay, unlike the KOs.

This result does not imply that there are no differences among the functional configurations of microbiomes of host species having different diets. Rather, it suggests that the differences between microbiomes probably stem from differing abundances of shared functions, such as enzymes that break down chemical substrates in the host diet. We identified 495 E.C.s with significantly different proportional abundance in the 7 carnivorous and 21 herbivorous mammalian microbiomes, using the program Shotgun FunctionalizeR (adjusted P < 0.001 after multiple hypothesis correction) (table S5) (11). Many of the enzymes distinguishing carnivorous and herbivorous fecal microbiomes are involved in amino acid metabolism. Microbiomes from herbivores were enriched in enzymes that map to biosynthetic reactions for 12 amino acids, whereas no carnivore samples were enriched in amino acid biosynthetic enzymes (table S6). In contrast, nine amino acid degradation pathways contained enzymes that were significantly increased in carnivores, whereas the only degradative enzymes whose representation was significantly greater in herbivores were those involved in the breakdown of branched-chain amino acids (Val, Leu, and Ile). Glutamate metabolism is particularly illustrative of these trends. Both the adenosine triphosphate (ATP)–dependent and ATP-independent pathways for glutamate biosynthesis are significantly increased in herbivore microbiomes, whereas the catabolic reactions to break down glutamate and glutamine are increased in carnivores (Fig. 3A). These results suggest that carnivorous microbiomes have specialized to degrade proteins as an energy source, whereas herbivorous communities have specialized to synthesize amino acid building blocks.

Fig. 3

Differences in metabolic features encoded in fecal microbiomes among herbivores versus carnivores. (A) Carnivorous and herbivorous microbiomes indicate opposing directionality for amino acid metabolism. Colored arrows denote enzyme functions whose representation is significantly (P < 0.001) greater in the fecal microbiomes of herbivores (green) or carnivores (red). (B) Carnivorous and herbivorous microbiomes suggest opposing directionality at the central PEP-pyruvate-OAA node. The coloring scheme is as in (A). Abbreviations: 2-OG, alpha-ketoglutarate; Ck, carboxykinase; Cx, carboxylase; DH, dehydrogenase; Dx, decarboxylase; GABA, γ-aminobutyrate; GDH, Glu DH; ODx, OAA Dx; PPDk, Pyr-phosphate dikinase; Pyr, pyruvate; SSA, succinate-semialdehyde.

The distinctiveness of carnivorous and herbivorous microbiomes was also revealed at a central anaplerotic node (Fig. 3B). When gluconeogenesis is required, oxaloacetate (OAA) can be converted to phosphoenolpyruvate (PEP) and pyruvate. When tricarboxylic acid cycle intermediates are withdrawn for biosynthesis, they are replenished by converting PEP and pyruvate directly to OAA (12). All of the genes encoding enzymes catalyzing OAA production from pyruvate or PEP are significantly increased in the carnivore microbiomes, whereas the reverse reactions are catalyzed by enzymes whose representation is increased in herbivore microbiomes.

Our studies comparing mammalian species revealed a relationship between host diet and gut microbial community structure and function. We next asked whether similar trends could be detected using diet variation within a single free-living host species, namely humans. Quantitative studies of diet in most human populations are complicated by the known inaccuracy of self-reported data (13), so we turned to a group of adults known to keep meticulous records about their daily food composition and consumption. The selected cohort consisted of 18 lean members of the Calorie Restriction Society who typically measure and record all components of their diets on a daily basis with computer software to insure optimal nutrition despite reduced energy intake (14, 15). We collected their dietary records for a 4-day period (conservatively encompassing at least one complete intestinal transit time) before obtaining a single fecal sample, and analyzed macro- and micronutrient consumption using a validated protocol (2, 16). An average of 3642 ± 3826 bacterial V2 16S rRNA reads and 54,295 ± 28,086 shotgun reads were obtained per sample (tables S7 to S10).

Procrustes analysis revealed a significant association between the bacterial phylogenetic structure of their fecal communities (16S rRNA) and the functions encoded in their microbiomes [P < 0.05 for KOs, E.C.s, and CAZymes (glycoside hydrolases)]; not significant for peptidases (P = 0.061) (fig. S3). These results suggest that the processes that drive the functional differentiation of microbiomes within an individual host species may be fundamentally similar to those that drive their differentiation across mammalian evolution.

Documentation of the weight of each ingredient in each meal consumed by these individuals (table S7) allowed us to perform a follow-up analysis examining the impact on fecal bacterial community configuration of three dietary components (total protein, carbohydrate, and insoluble fiber intake). We chose these diet categories because protein intake is markedly different between carnivores and herbivores, and because an extensive literature exists about the impact of ingested polysaccharides and fiber on the gut microbiota (17). Linear regression of the three dietary categories against the position of each individual’s microbiome along principal coordinate 1 of the PCoA plots revealed that total protein intake was significantly associated with KO data [adjusted linear regression coefficient of determination (R2) value = 0.307, adjusted P value = 0.030] (2). In contrast, insoluble dietary fiber was significantly associated with bacterial OTU content (Bray-Curtis metric; adjusted R2 value = 0.371; adjusted P value = 0.013) (table S11). These results confirm that within a single free-living species, both the structure and function of the gut microbiome are significantly associated with dietary intake.

Taken together with our prior work (1), these results teach us that even fecal samples from mammals living in zoos and human samples from a single self-selected population can provide insights into the factors driving the evolution of the gut microbiome. They also compel us, at a time when complete genomes are to be sequenced for 10,000 vertebrates (18), to take the next step and perform systematic studies that rigorously test specific mechanisms that drive the evolution of hosts and their (gut) microbial symbionts. These studies should be guided by experts who can choose taxa that radiated at different points in their evolutionary history, with parallel shifts in their diet, morphology, biogeography, or other key factors known or hypothesized to influence evolution. The results should help address questions such as what functional features in host intestinal environments (including the biochemical characteristics of mucosal surfaces) are related to the representation of specific bacterial taxa and microbiome functions, and how readily microbial populations have been acquired and reacquired during the course of vertebrate evolution. Additionally, our findings emphasize the need to sample humans across the globe with a variety of extreme diets and life-styles, including relatively ancestral hunter-gatherer lifestyles, in order to provide new insights into the limits of variation within a host species and the possibility that our microbes, in coevolving with our bodies and our cultures, have helped shaped our physiological differences and environmental adaptations.

Supporting Online Material

Materials and Methods

Figs. S1 to S3

Tables S1 to S11

References (1934)

References and Notes

  1. See supporting material on Science Online.
  2. Acknowledgments: We thank J. Manchester and S. Wagoner for technical assistance; B. Cantarel, V. Lombard, C. Rancurel, and P. Coutinho for CAZyme annotation; R. Ley and members of the Gordon lab for their suggestions; and S. Bircher, R. Ramey, M. Schlegel, M. Schrenzel, T. Tucker, and P. Turnbaugh for past help in procuring mammalian fecal samples. This work was supported by grants from NIH (DK30292, DK70977, DK078669, and UL1 RR024992), the Crohn’s and Colitis Foundation of America, and NIH Institutional Training Grant T32-A1007172 (to B.D.M.). The National Center for Biotechnology Information Sequence Read Archive accession number for the bacterial 16S rRNA and shotgun data sets related to our studies of mammalian and Calorie Restriction Society member human fecal microbiomes is SRA030940. Sequence data have also been deposited in MG-Rast with project accession numbers qiime:625, qiime:626, qiime:627, and qiime:628.
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