- Short report
- Open Access
Unusual sub-genus associations of faecal Prevotella and Bacteroides with specific dietary patterns
© The Author(s). 2016
- Received: 30 June 2016
- Accepted: 12 October 2016
- Published: 21 October 2016
Diet has a recognized effect in shaping gut microbiota. Many studies link an increase in Prevotella to high-fibre diet, while Bacteroides abundance is usually associated with the consumption of animal fat and protein-rich diets. Nevertheless, closely related species and strains may harbour different genetic pools; therefore, further studies should aim to understand whether species of the same genus are consistently linked to dietary patterns or equally responsive to diet variations. Here, we used oligotyping of 16S rRNA gene sequencing data to exploit the diversity within Prevotella and Bacteroides genera in faecal samples of omnivore and non-omnivore subjects from a previously studied cohort.
A great heterogeneity was found in oligotype composition. Nevertheless, different oligotypes within the same genus showed distinctive correlation patterns with dietary components and metabolome. We found that some Prevotella oligotypes are significantly associated with the plant-based diet but some are associated with animal-based nutrients, and the same applies to Bacteroides. Therefore, an indiscriminate association of Bacteroidetes genera with specific dietary patterns may lead to an oversimplified vision that does not take into account sub-genus diversity and the different possible responses to dietary components.
We demonstrated that Prevotella and Bacteroides oligotypes show distinctive correlation patterns with dietary components and metabolome. These results substantiate a current oversimplification of diet-dependent microbe-host associations and highlighted that sub-genus differences must be taken into account when planning gut microbiota modulation for health benefits
- Gut microbiota
- Plant-based diet
- Omnivore diet
The important contribution of the gut microbiota to human health and disease is widely recognized . Habitual diet plays a key role in shaping the gut microbial community composition [2–6], and sudden dietary changes are reflected in a prompt response of the gut symbionts . Bacteroidetes are among the most abundant bacterial groups found in the gut, and many genera within this phylum are recognized to be diet-responsive; in particular, high-fibre diet is commonly associated with an increase in Prevotella, while Bacteroides abundance is linked to the consumption of diet rich in animal fat and protein [3–5, 7, 8]. Nevertheless, closely related species and strains may harbour different genetic pools [9–11].
No studies have so far posed the question of whether species of the same genus are consistently linked to dietary patterns or equally responsive to diet variations. The high genetic diversity found between and within Prevotella spp. might explain the highly different behaviour observed when considering the genus-level identification . In fact, only some of the subjects reported an increase of this genus after administration of a fibre-rich diet , while P. copri was supposed to drive chronic inflammation in HIV patients  and to induce insulin resistance . Therefore, species and even strain variability have to be considered in order to understand how to modulate the gut microbiota for therapeutic purposes . The current knowledge is limited by the common use of a de novo clustering approach, relying on the clustering of sequences into operational taxonomic units (OTUs) at 97 % of similarity, often resulting in phylogenetically mixed units  and leading to taxonomic assignment at the genus level . This approach may fail to resolve ecologically important differences between closely related organisms . On the contrary, even small differences in ribosomal RNA (rRNA) sequence can predict substantial genomic and ecological variation [14, 17]. Oligotyping is an alternative approach, which decomposes a given taxon, or 97 % OTU, into high-resolution units (“oligotypes”) by considering the nucleotide positions identified as the most information-rich and allows resolution at the species level and below .
In a recent cohort study, we investigated the associations of microbiota and metabolome with habitual diets, and the OTU-based analyses of the 16S rRNA gene sequences yielded the usual associations of Prevotella with plant-based and Bacteroides with animal-based diets . Gut Prevotella oligotypes were recently supposed to be host-specific and suggested as possible markers useful to track the origin of faecal contamination [18, 19]. Here, we explored the diversity of Bacteroidetes genera in faecal samples of omnivore and non-omnivore subjects of the previously studied cohort  using oligotyping of 16S rRNA gene sequencing data and highlight for the first time that heterogeneity within Prevotella and Bacteroides prevent a comprehensive association of these genera with specific dietary patterns.
We used the oligotyping technique to explore differences within Bacteroides and Prevotella populations in omnivore (n = 44) and non-omnivore (self-declared ovo-lacto vegetarians and vegans, n = 93) subjects of a previously studied cohort . Subject recruitment, DNA extraction, sequencing of the V1–V3 regions of rRNA gene, and metabolomics were carried out as recently described . Raw reads were quality-filtered as follows: reads were trimmed at the first ambiguous base or when the average quality score dropped below 25 within a 50-bp-long window, and reads shorter than 500 bp and with >1 primer mismatch were discarded. High-quality reads were aligned to the Greengenes alignment template by using PyNAST 1.2.1 , and alignment was further trimmed to equal length by using the o-smart-trim script included in the oligotyping package v.1.0 . In order to avoid biases due to different sequencing depths, all samples were rarefied at 4500 reads after raw read quality filtering. Taxonomy assignment of all the reads was carried out by using the RDP classifier . Reads assigned to Prevotella or Bacteroides genera were extracted, and entropy analysis and oligotyping were carried out separately as described by the developers. High-entropy positions were chosen to compute the oligotypes (-C option): 106, 121, 137, 272, 349, 462, 502, 544, 549, 739, 746, 778, 851 and 98 and 251, 319, 432, 440, 462, 463, 471, 477, 502, 526, 528, 549, 578, 746, 778, 847 and 851 for Prevotella and Bacteroides dataset, respectively. To minimize the impact of sequencing errors, we required an oligotype to be represented by at least 100 reads (-M option). Moreover, rare oligotypes present in less than 10 samples were discarded (-s option). These parameters led to 61 (omnivores n = 17; non-omnivores n = 44) and 136 (omnivores n = 44; non-omnivores n = 92) samples left in Prevotella and Bacteroides dataset, respectively. BLASTn (match/mismatch scores: 1, −2; gap cost: linear) was used to query the representative sequences against the NCBI nr database, and the top hit was considered for taxonomic assignment. Statistical analyses and plotting were carried out in R environment (https://www.r-project.org). Pairwise Wilcoxon tests were used in order to determine significant differences in specific oligotype abundance according to diets. Pairwise Spearman’s correlations between oligotype relative abundance and diet or metabolome were computed and plotted by using the psych and made4 packages. A cladogram of representative sequences was generated using MrBayes (http://mrbayes.sourceforge.net) and depicted using the Interactive Tree of Life (http://itol.embl.de).
Gut microbiota is a complex consortium of microbial species and strains . However, analyses based on OTU clustering methodology often result in genus-level classification and may underestimate this diversity . This oversimplified vision does not take into account the possible different responses that species or strains belonging to the same genus may have to dietary components [8, 10]. The oligotyping approach was proposed as a powerful tool allowing resolution at the species level and below. It was successfully used to explain the microbial complexity of the oral microbiota  and to associate diversity within Blautia and Prevotella genera to different animal hosts [13, 18]. Moreover, differentiations in faecal Bacteroides oligotype composition were previously observed in Western and agrarian populations . Here, we oligotyped Bacteroides and Prevotella 16S rRNA gene sequences in human faecal samples and demonstrated that specific oligotypes within these genera may be associated with the habitual diet. Consistently, oligotypes associated with an omnivore diet were positively correlated to TMAO levels, a metabolite derived from carnitine and choline catabolism and related to the development of cardiovascular diseases . On the contrary, those linked to a vegetable-based diet showed positive correlations with SCFA, derived from carbohydrate fermentation and associated with beneficial outcomes for the host, such as anti-inflammatory and anti-carcinogenic effects [23, 24]. Our results highlighted how an indiscriminate association of a whole genus with a specific dietary pattern may lead to an oversimplified vision of the correlations between gut microbiota and diet, which does not take into account the diversity existing within the same genus or even within the same species [9, 11] and the possible different responses of these variants to dietary components [8, 10].
Sub-genus-level diversity can play a key role in establishing the interconnection between gut microbiome, diet, microbial metabolome and host response, and this should be taken into account in diet-based intervention studies aiming at changing gut microbiota structure and functions in order to gather specific health benefits. The consistency of the correlative patterns between oligotypes, diet and metabolome suggests the intriguing presence of a diet-driven adaptive selection, associated with different metabolic and enzymatic profiles. Different Prevotella and Bacteroides oligotypes, although identified as the same species, showed differential relative abundance in omnivores and non-omnivores and a consistent correlation pattern with foodstuffs/nutrients and metabolome, highlighting a possible distinct behaviour below the genus level never demonstrated before and the presence of different putative strains with diverse metabolic potential, possibly selected by the habitual diet.
This study was supported by the Italian Ministry of University and Research (MIUR) programme PRIN 2010–2011 (grant number 2010WZ2NJN). Francesca De Filippis was supported by a grant from Regione Campania within the programme POR Campania FSE 2007/2013–2014/2020.
Availability of data and materials
The 16S rRNA gene sequences are available at the Sequence Read Archive of NCBI (accession number SRP042234).
FDF, MG and DE conceived and designed the experiments. FDF, NP and LL performed the experiments. FDF and DE analysed the data. FDF wrote the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
Consent for publication
Ethics approval and consent to participate
The study was approved by the Ethics Committee of (a) Azienda Sanitaria Locale (Bari) (protocol N.1050), (b) Azienda Ospedaliera Universitaria of Bologna (protocol N.0018396), (c) the Province of Parma (protocol N.22884) and (d) the University of Torino (protocol N.1/2013/C).
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
- Aron-Wisnewsky J, Clément K. The gut microbiome, diet, and links to cardiometabolic and chronic disorders. Nat Rev Nephrol. 2016;12(3):169–81.View ArticlePubMedGoogle Scholar
- De Filippis F, Pellegrini N, Vannini L, Jeffery IB, La Storia A, Laghi L, et al. High-level adherence to a Mediterranean diet beneficially impacts the gut microbiota and associated metabolome. Gut. 2016;65:1812–21.View ArticleGoogle Scholar
- Schnorr SL, Candela M, Rampelli S, Centanni M, Consolandi C, Basaglia G, et al. Gut microbiome of the Hadza hunter-gatherers. Nat Commun. 2014;5:3654.View ArticlePubMedPubMed CentralGoogle Scholar
- De Filippo C, Cavalieri D, Di Paola M, Ramazzotti M, Poullet JB, Massart S, et al. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc Natl Acad Sci U S A. 2010;107(33):14691–6.View ArticlePubMedPubMed CentralGoogle Scholar
- Wu GD, Chen J, Hoffmann C, Bittinger K, Chen YY, Keilbaugh SA, et al. Linking long-term dietary patterns with gut microbial enterotypes. Science. 2011;334(6052):105–8.View ArticlePubMedPubMed CentralGoogle Scholar
- Zhernakova A, Kurilshikov A, Bonder MJ, Tigchelaar EF, Schirmer M, Vatanen T, et al. Population-based metagenomics analysis reveals markers for gut microbiome composition and diversity. Science. 2016;352(6285):565–9.View ArticlePubMedGoogle Scholar
- David LA, Maurice CF, Carmody RN, Gootenberg DB, Button JB, Wolfe BE, et al. Diet rapidly and reproducibly alters the human gut microbiome. Nature. 2014;505(7484):559–63.View ArticlePubMedGoogle Scholar
- Kovatcheva-Datchary P, Nilsson A, Akrami R, Lee YS, De Vadder F, Arora T, et al. Dietary fiber-induced improvement in glucose metabolism is associated with increased abundance of Prevotella. Cell Metab. 2015;22(6):971–82.View ArticlePubMedGoogle Scholar
- Greenblum S, Carr R, Borenstein E. Extensive strain-level copy-number variation across human gut microbiome species. Cell. 2015;160(4):583–94.View ArticlePubMedPubMed CentralGoogle Scholar
- Wu M, McNulty NP, Rodionov DA, Khoroshkin MS, Griffin NW, Cheng J, et al. Genetic determinants of in vivo fitness and diet responsiveness in multiple human gut Bacteroides. Science. 2015;350(6256):aac5992.View ArticlePubMedPubMed CentralGoogle Scholar
- Ley RE. Gut microbiota in 2015: Prevotella in the gut: choose carefully. Nat Rev Gastroenterol Hepatol. 2016;13(2):69–70.View ArticlePubMedGoogle Scholar
- Dillon SM, Lee EJ, Kotter CV, Austin GL, Gianella S, Siewe B, et al. Gut dendritic cell activation links an altered colonic microbiome to mucosal and systemic T-cell activation in untreated HIV-1 infection. Mucosal Immunol. 2015;9:24–37.View ArticlePubMedPubMed CentralGoogle Scholar
- Pedersen HK, Gudmundsdottir V, Nielsen HB, Hyotylainen T, Nielsen T, Jensen BA, et al. Human gut microbes impact host serum metabolome and insulin sensitivity. Nature. 2016;535(7612):376–81.View ArticlePubMedGoogle Scholar
- Eren MA, Sogin ML, Morrison HG, Vineis JH, Fisher JC, Newton RJ, et al. A single genus in the gut microbiome reflects host preference and specificity. ISME J. 2015;9(1):90–100.View ArticlePubMedGoogle Scholar
- Eren MA, Borisy GG, Huse SM, Mark Welch JL. Oligotyping analysis of the human oral microbiome. Proc Natl Acad Sci U S A. 2014;111(28):E2875–84.View ArticlePubMedPubMed CentralGoogle Scholar
- Eren AM, Maignien L, Sul WL, Murphy LG, Grim SL, Morrison HG, et al. Oligotyping: differentiating between closely related microbial taxa using 16S rRNA gene data. Methods Ecol Evol. 2013;4(12):1111–9.View ArticlePubMed CentralGoogle Scholar
- Zaneveld JR, Lozupone C, Gordon JI, Knight R. Ribosomal RNA diversity predicts genome diversity in gut bacteria and their relatives. Nucleic Acids Res. 2010;38(12):3869–79.View ArticlePubMedPubMed CentralGoogle Scholar
- Koskey AM, Fisher JC, Eren AM, Ponce-Terashima R, Reis MG, Blanton RE, et al. Blautia and Prevotella sequences distinguish human and animal fecal pollution in Brazil surface waters. Environ Microbiol Rep. 2014;6(6):696–704.View ArticlePubMedPubMed CentralGoogle Scholar
- Fisher JC, Eren AM, Green HC, Shanks OC, Morrison HG, Vineis JH, et al. Comparison of sewage and animal fecal microbiomes by using oligotyping reveals potential human fecal indicators in multiple taxonomic groups. Appl Environ Microbiol. 2015;81(20):7023–33.View ArticlePubMedPubMed CentralGoogle Scholar
- Caporaso JG, Bittinger K, Bushman FD, De Santis TZ, Andersen GL, Knight R. PyNAST: a flexible tool for aligning sequences to a template alignment. Bioinformatics. 2010;26:266–7.View ArticlePubMedGoogle Scholar
- Wang Q, Garrity GM, Tiedje JM, Cole JR. Naïve Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl Environ Microbiol. 2007;73(16):5261–7.View ArticlePubMedPubMed CentralGoogle Scholar
- Stock J. Gut microbiota: an environmental risk factor for cardiovascular disease. Atherosclerosis. 2013;229(2):440–2.View ArticlePubMedGoogle Scholar
- Louis P, Hold GL, Flint HJ. The gut microbiota, bacterial metabolites and colorectal cancer. Nat Rev Microbiol. 2014;12(10):661–72.View ArticlePubMedGoogle Scholar
- Smith PM, Howitt MR, Panikov N, Michaud M, Gallini CA, Bohlooly-Y M, et al. The microbial metabolites, short-chain fatty acids, regulate the colonic Treg cell homeostasis. Science. 2013;341(6145):569–73.View ArticlePubMedGoogle Scholar