Bacterial Taxa Associated with High Adherence to Mediterranean Diet in a Spanish Population †
Abstract
:1. Introduction
2. Material and Methods
2.1. Subjects
2.2. Anthropometric and Biochemical Measurements
2.3. Dietary Estimation
2.4. Faecal Sample Collection and DNA Extraction
2.4.1. Metagenomic Data: Library Preparation
2.4.2. Metagenomics Data: Analysis and Processing
2.5. Statistical Analysis
3. Results
4. Discussion
5. Conclusions
Author Contributions
Funding
Conflicts of Interest
References
- Maslowski, K.M.; Mackay, C.R. Diet, gut microbiota and immune responses. Nat. Immunol. 2011, 12, 5–9. [Google Scholar] [CrossRef] [PubMed]
- Rook, G.A.W. 99th Dahlem Conference on Infection, Inflammation and Chronic Inflammatory Disorders: Darwinian medicine and the ‘hygiene’ or ‘old friends’ hypothesis. Clin. Exp. Immunol. 2010, 160, 70–79. [Google Scholar] [CrossRef] [PubMed]
- Sofi, F.; Macchi, C.; Abbate, R.; Gensini, G.F.; Casini, A. Mediterranean diet and health status: An updated meta-analysis and a proposal for a literature-based adherence score. Public Health Nutr. 2014, 17, 2769–2782. [Google Scholar] [CrossRef] [PubMed]
- Le Chatelier, E.; Nielsen, T.; Qin, J.; Prifti, E.; Hildebrand, F.; Falony, G.; Almeida, M.; Arumugam, M.; Batto, J.-M.; Kennedy, S.; et al. Richness of human gut microbiome correlates with metabolic markers. Nature 2013, 500, 541–546. [Google Scholar] [CrossRef] [PubMed]
- Rivière, A.; Selak, M.; Lantin, D.; Leroy, F.; De Vuyst, L. Bifidobacteria and Butyrate-Producing Colon Bacteria: Importance and Strategies for Their Stimulation in the Human Gut. Front. Microbiol. 2016, 7, 979. [Google Scholar] [CrossRef]
- Shatenstein, B.; Nadon, S.; Godin, C.; Ferland, G. Development and Validation of a Food Frequency Questionnaire. Can. J. Diet. Pract. Res. 2005, 66, 67–75. [Google Scholar] [CrossRef]
- Martínez-González, M.A.; García-Arellano, A.; Toledo, E.; Salas-Salvadó, J.; Buil-Cosiales, P.; Corella, D.; Covas, M.I.; Schröder, H.; Arós, F.; Gómez-Gracia, E.; et al. A 14-Item Mediterranean Diet Assessment Tool and Obesity Indexes among High-Risk Subjects: The PREDIMED Trial. PLoS ONE 2012, 7, e43134. [Google Scholar] [CrossRef]
- Hildebrand, F.; Tito, R.Y.; Voigt, A.; Bork, P.; Raes, J. Correction: LotuS: An efficient and user-friendly OTU processing pipeline. Microbiome 2014, 2, 37. [Google Scholar] [CrossRef]
- Altschul, S.F.; Gish, W.; Miller, W.; Myers, E.W.; Lipman, D.J. Basic local alignment search tool. J. Mol. Biol. 1990, 215, 403–410. [Google Scholar] [CrossRef]
- Ritari, J.; Salojärvi, J.; Lahti, L.; de Vos, W.M. Improved taxonomic assignment of human intestinal 16S rRNA sequences by a dedicated reference database. BMC Genom. 2015, 16, 1056. [Google Scholar] [CrossRef]
- Gentleman, R.C.; Carey, V.J.; Bates, D.M.; Bolstad, B.; Dettling, M.; Dudoit, S.; Ellis, B.; Gautier, L.; Ge, Y.; Gentry, J.; et al. Bioconductor: Open software development for computational biology and bioinformatics. Genome Biol. 2004, 5, R80. [Google Scholar] [CrossRef] [PubMed]
- Dhariwal, A.; Chong, J.; Habib, S.; King, I.L.; Agellon, L.B.; Xia, J. MicrobiomeAnalyst: A Web-Based Tool for Comprehensive Statistical, Visual and Meta-Analysis of Microbiome Data. Available online: https://academic.oup.com/nar/article-abstract/45/W1/W180/3760191 (accessed on 21 April 2020).
- Lobionda, S.; Sittipo, P.; Kwon, H.Y.; Lee, Y.K. The role of gut microbiota in intestinal inflammation with respect to diet and extrinsic stressors. Microorganisms 2019, 7, 271. [Google Scholar] [CrossRef] [PubMed]
- Mendez, M.A.; Popkin, B.M.; Jakszyn, P.; Berenguer, A.; Tormo, M.J.; Sanchéz, M.J.; Quirós, J.R.; Pera, G.; Navarro, C.; Martinez, C.; et al. Adherence to a Mediterranean Diet Is Associated with Reduced 3-Year Incidence of Obesity. J. Nutr. 2006, 136, 2934–2938. [Google Scholar] [CrossRef] [PubMed]
- Lopez-Legarrea, P.; Fuller, N.R.; Zulet, M.A.; Martinez, J.A.; Caterson, I.D. The influence of Mediterranean, carbohydrate and high protein diets on gut microbiota composition in the treatment of obesity and associated inflammatory state. Asia Pac. J. Clin. Nutr. 2014, 23, 360–368. [Google Scholar]
- AlEssa, H.B.; Malik, V.S.; Yuan, C.; Willett, W.C.; Huang, T.; Hu, F.B.; Tobias, D.K. Dietary patterns and cardiometabolic and endocrine plasma biomarkers in US women. Am. J. Clin. Nutr. 2017, 105, 432–441. [Google Scholar] [CrossRef]
- Million, M.; Maraninchi, M.; Henry, M.; Armougom, F.; Richet, H.; Carrieri, P.; Valero, R.; Raccah, D.; Vialettes, B.; Raoult, D. Obesity-associated gut microbiota is enriched in Lactobacillus reuteri and depleted in Bifidobacterium animalis and Methanobrevibacter smithii. Int. J. Obes. 2012, 36, 817–825. [Google Scholar] [CrossRef]
- Horiuchi, H.; Kamikado, K.; Aoki, R.; Suganuma, N.; Nishijima, T.; Nakatani, A.; Kimura, I. Bifidobacterium animalis subsp. lactis GCL2505 modulates host energy metabolism via the short-chain fatty acid receptor GPR43. Sci. Rep. 2020, 10, 1–8. [Google Scholar] [CrossRef]
- Den Besten, G.; Van Eunen, K.; Groen, A.K.; Venema, K.; Reijngoud, D.J.; Bakker, B.M. The role of short-chain fatty acids in the interplay between diet, gut microbiota, and host energy metabolism. J. Lipid Res. 2013, 54, 2325–2340. [Google Scholar] [CrossRef]
- Robert, C.; Chassard, C.; Lawson, P.A.; Bernalier-Donadille, A. Bacteroides cellulosilyticus sp. nov., a cellulolytic bacterium from the human gut microbial community. Int. J. Syst. Evol. Microbiol. 2007, 57, 1516–1520. [Google Scholar] [CrossRef]
- McNulty, N.P.; Wu, M.; Erickson, A.R.; Pan, C.; Erickson, B.K.; Martens, E.C.; Pudlo, N.A.; Muegge, B.D.; Henrissat, B.; Hettich, R.L.; et al. Effects of Diet on Resource Utilization by a Model Human Gut Microbiota Containing Bacteroides cellulosilyticus WH2, a Symbiont with an Extensive Glycobiome. PLoS Biol. 2013, 11, e1001637. [Google Scholar] [CrossRef]
- Morotomi, M.; Nagai, F.; Sakon, H.; Tanaka, R. Paraprevotella clara gen. nov., sp. nov. and Paraprevotella xylaniphila sp. nov., members of the family “Prevotellaceae” isolated from human faeces. Int. J. Syst. Evol. Microbiol. 2009, 59, 1895–1900. [Google Scholar] [CrossRef] [PubMed]
- Flint, H.J.; Bayer, E.A.; Rincon, M.T.; Lamed, R.; White, B.A. Polysaccharide utilization by gut bacteria: Potential for new insights from genomic analysis. Nat. Rev. Microbiol. 2008, 6, 121–131. [Google Scholar] [CrossRef] [PubMed]
- Iino, T.; Mori, K.; Tanaka, K.; Suzuki, K.I.; Harayama, S. Oscillibacter valericigenes gen. nov., sp. nov., a valerate-producing anaerobic bacterium isolated from the alimentary canal of a Japanese corbicula clam. Int. J. Syst. Evol. Microbiol. 2007, 57, 1840–1845. [Google Scholar] [CrossRef] [PubMed]
- Yuille, S.; Reichardt, N.; Panda, S.; Dunbar, H.; Mulder, I.E. Human gut bacteria as potent class I histone deacetylase inhibitors in vitro through production of butyric acid and valeric acid. PLoS ONE 2018, 13, e0201073. [Google Scholar] [CrossRef]
- Borrelli, L.; Coretti, L.; Dipineto, L.; Bovera, F.; Menna, F.; Chiariotti, L.; Nizza, A.; Lembo, F.; Fioretti, A. Insect-based diet, a promising nutritional source, modulates gut microbiota composition and SCFAs production in laying hens. Sci. Rep. 2017, 7. [Google Scholar] [CrossRef]
- Kasai, C.; Sugimoto, K.; Moritani, I.; Tanaka, J.; Oya, Y.; Inoue, H.; Tameda, M.; Shiraki, K.; Ito, M.; Takei, Y.; et al. Comparison of the gut microbiota composition between obese and non-obese individuals in a Japanese population, as analyzed by terminal restriction fragment length polymorphism and next-generation sequencing. BMC Gastroenterol. 2015, 15, 100. [Google Scholar] [CrossRef]
- Konikoff, T.; Gophna, U. Oscillospira: A Central, Enigmatic Component of the Human Gut Microbiota. Trends Microbiol. 2016, 24, 523–524. [Google Scholar] [CrossRef]
- Ryan, K.K.; Tremaroli, V.; Clemmensen, C.; Kovatcheva-Datchary, P.; Myronovych, A.; Karns, R.; Wilson-Pérez, H.E.; Sandoval, D.A.; Kohli, R.; Bäckhed, F.; et al. FXR is a molecular target for the effects of vertical sleeve gastrectomy. Nature 2014, 509, 183–188. [Google Scholar] [CrossRef]
- Lau, S.K.P.; Mcnabb, A.; Woo, G.K.S.; Hoang, L.; Fung, A.M.Y.; Chung, L.M.W.; Woo, P.C.Y.; Yuen, K.-Y.; Hospital, M.; Kong, H. Catabacter hongkongensis gen. nov., sp. nov., Isolated from Blood Cultures of Patients from Hong Kong and Canada. J. Clin. Microbiol. 2007, 45, 395–401. [Google Scholar] [CrossRef]
- Venkataraman, A.; Sieber, J.R.; Schmidt, A.W.; Waldron, C.; Theis, K.R.; Schmidt, T.M. Variable responses of human microbiomes to dietary supplementation with resistant starch. Microbiome 2016, 4, 33. [Google Scholar] [CrossRef]
- Peng, L.; Li, Z.-R.; Green, R.S.; Holzman, I.R.; Lin, J. Butyrate Enhances the Intestinal Barrier by Facilitating Tight Junction Assembly via Activation of AMP-Activated Protein Kinase in Caco-2 Cell Monolayers. J. Nutr. 2009, 139, 1619–1625. [Google Scholar] [CrossRef] [PubMed]
- Ruemmele, F.M.; Schwartz, S.; Seidman, E.G.; Dionne, S.; Levy, E.; Lentze, M.J. Butyrate induced Caco-2 cell apoptosis is mediated via the mitochondrial pathway. Gut 2003, 52, 94–100. [Google Scholar] [CrossRef] [PubMed]
- Mikkelsen, K.H.; Allin, K.H.; Knop, F.K. Effect of antibiotics on gut microbiota, glucose metabolism and body weight regulation: A review of the literature. Diabetes Obes. Metab. 2016, 18, 444–453. [Google Scholar] [CrossRef] [PubMed]
- Furusawa, Y.; Obata, Y.; Fukuda, S.; Endo, T.A.; Nakato, G.; Takahashi, D.; Nakanishi, Y.; Uetake, C.; Kato, K.; Kato, T.; et al. Commensal microbe-derived butyrate induces the differentiation of colonic regulatory T cells. Nature 2013, 504, 446–450. [Google Scholar] [CrossRef]
- Midtvedt, T.; Gustafsson, B.E. Microbial conversation of bilirubin to urobilins in vitro and in vivo. Acta Pathol. Microbiol. Scand. Sect. B Microbiol. 2009, 89B, 57–60. [Google Scholar] [CrossRef]
- Biagi, E.; Nylund, L.; Candela, M.; Ostan, R.; Bucci, L.; Pini, E.; Nikkïla, J.; Monti, D.; Satokari, R.; Franceschi, C.; et al. Through ageing, and beyond: Gut microbiota and inflammatory status in seniors and centenarians. PLoS ONE 2010, 5, e10667. [Google Scholar] [CrossRef]
High Adherence (3rd tertile) | Low Adherence (1st tertile) | ||
---|---|---|---|
Species | FDR | Species | FDR |
Bifidobacterium animalis | 1.21 × 10−7 | OTU100|NN=Eubacterium saphenum GU427005|D=91 | 4.44 × 10−5 |
Bacteroides cellulosilyticus | 4.47 × 10−7 | OTU375|NN=Succinivibrio dextrinosolvens Y17600|D=97 | 0.0001 |
OTU946|NN=Paraprevotella clara AB331896|D=86.8 | 1.72 × 10−5 | OTU759|NN=Gordonibacter pamelaeae AB566419|D=87.6 | 0.0005 |
OTU1682|NN=Oscillibacter valericigenes AB238598|D=91.1 | 3.42 × 10−5 | OTU11|NN=Butyricicoccus pullicaecorum EU410376|D=89.5 | 0.0002 |
OTU1065|NN=Oscillospira (Flavonifractor) plautii Y18187|D=86.6 | 3.42 × 10−5 | Christensenella minuta | 0.0020 |
OTU1173|NN=Roseburia faecis AY804149|D=94.9 | 0.0008 | Parabacteroides goldsteinii | 0.0073 |
OTU1517|NN=Catabacter hongkongensis AB671763|D=87 | 0.0008 | OTU1625|NN=Anaerotruncus colihominis DQ002932|D=89.9 | 0.0120 |
OTU1296|NN=Ruminococcus bromii DQ882649|D=92.3 | 0.0120 | Alistipes timonensis | 0.0155 |
Erysipelatoclostridium ramosum | 0.0176 | Prevotella corporis | 0.0192 |
OTU521|NN=Papillibacter cinnamivorans AF167711|D=89 | 0.0463 |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Rosés, C.; Cuevas-Sierra, A.; Quintana, S.; Riezu-Boj, J.I.; Martínez, J.A.; Milagro, F.I.; Barceló, A. Bacterial Taxa Associated with High Adherence to Mediterranean Diet in a Spanish Population. Proceedings 2020, 61, 10. https://doi.org/10.3390/IECN2020-07001
Rosés C, Cuevas-Sierra A, Quintana S, Riezu-Boj JI, Martínez JA, Milagro FI, Barceló A. Bacterial Taxa Associated with High Adherence to Mediterranean Diet in a Spanish Population. Proceedings. 2020; 61(1):10. https://doi.org/10.3390/IECN2020-07001
Chicago/Turabian StyleRosés, Carles, Amanda Cuevas-Sierra, Salvador Quintana, José I. Riezu-Boj, J. Alfredo Martínez, Fermín I. Milagro, and Anna Barceló. 2020. "Bacterial Taxa Associated with High Adherence to Mediterranean Diet in a Spanish Population" Proceedings 61, no. 1: 10. https://doi.org/10.3390/IECN2020-07001
APA StyleRosés, C., Cuevas-Sierra, A., Quintana, S., Riezu-Boj, J. I., Martínez, J. A., Milagro, F. I., & Barceló, A. (2020). Bacterial Taxa Associated with High Adherence to Mediterranean Diet in a Spanish Population. Proceedings, 61(1), 10. https://doi.org/10.3390/IECN2020-07001