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Artificial sweeteners induce glucose intolerance by altering the gut microbiota


Non-caloric artificial sweeteners (NAS) are among the most widely used food additives worldwide, regularly consumed by lean and obese individuals alike. NAS consumption is considered safe and beneficial owing to their low caloric content, yet supporting scientific data remain sparse and controversial. Here we demonstrate that consumption of commonly used NAS formulations drives the development of glucose intolerance through induction of compositional and functional alterations to the intestinal microbiota. These NAS-mediated deleterious metabolic effects are abrogated by antibiotic treatment, and are fully transferrable to germ-free mice upon faecal transplantation of microbiota configurations from NAS-consuming mice, or of microbiota anaerobically incubated in the presence of NAS. We identify NAS-altered microbial metabolic pathways that are linked to host susceptibility to metabolic disease, and demonstrate similar NAS-induced dysbiosis and glucose intolerance in healthy human subjects. Collectively, our results link NAS consumption, dysbiosis and metabolic abnormalities, thereby calling for a reassessment of massive NAS usage.

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Figure 1: Artificial sweeteners induce glucose intolerance transferable to germ-free mice.
Figure 2: Functional characterization of saccharin-modulated microbiota.
Figure 3: Saccharin directly modulates the microbiota.
Figure 4: Acute saccharin consumption impairs glycaemic control in humans by inducing dysbiosis.

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European Nucleotide Archive

Data deposits

Sequencing data are deposited in the European Nucleotide Archive accession PRJEB6996.


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We thank the members of the Elinav and Segal laboratories for discussions. We acknowledge C. Bar-Nathan for germ-free mouse caretaking. We thank the Weizmann Institute management and the Nancy and Stephen Grand Israel National Center for Personalized Medicine (INCPM) for providing financial and infrastructure support. We thank G. Malka, N. Kosower and R. Bikovsky for coordinating the human clinical trials, and M. Pevsner-Fischer, T. Avnit-Sagi and M. Lotan-Pompan for assistance with microbiome sample processing. C.A.T. is the recipient of a Boehringer Ingelheim Fonds PhD Fellowship. G.Z.-S. is supported by the Morris Kahn Fellowships for Systems Biology. This work was supported by grants from the National Institute of Health (NIH) and the European Research Council (ERC) to E.S., and support and grants to E.E. provided by Y. and R. Ungar, the Abisch Frenkel Foundation for the Promotion of Life Sciences, the Gurwin Family Fund for Scientific Research, Leona M. and Harry B. Helmsley Charitable Trust, Crown Endowment Fund for Immunological Research, estate of J. Gitlitz, estate of L. Hershkovich, Rising Tide foundation, Minerva Stiftung foundation, and the European Research Council. E.E. is the incumbent of the Rina Gudinski Career Development Chair.

Author information

Authors and Affiliations



J.S. conceived the project, designed and performed experiments, interpreted the results, and wrote the manuscript. T.K., D.Z. and G.Z.-S. performed the computational and metagenomic microbiota analysis and the analysis of the retrospective and prospective human study, and are listed alphabetically. C.A.T., O.M., A.W. and H.S. helped with experiments. Y.K. helped with the metabolic cage experiments. S.G. designed the metagenomic library protocols and generated the libraries. I.K.-G. performed the SCFA quantification experiments. D.I., N.Z., and Z.H. performed and supervised human experimentation. A.H. supervised the germ-free mouse experiments. E.S. and E.E. conceived and directed the project, designed experiments, interpreted the results, and wrote the manuscript.

Corresponding authors

Correspondence to Eran Segal or Eran Elinav.

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Competing interests

The authors declare no competing financial interests.

Extended data figures and tables

Extended Data Figure 1 Experimental scheme.

10-week-old C57Bl/6 male mice were treated with the following dietary regimes. a, Drinking commercially available non-caloric artificial sweeteners (NAS; saccharin, sucralose and aspartame) or glucose, sucrose or water as controls and fed a normal-chow (NC) diet. b, Drinking commercially available saccharin or glucose as control and fed a high-fat diet (HFD). c, Drinking pure saccharin or water and fed HFD. d, As in c, but with outbred Swiss-Webster mice. Glucose tolerance tests, microbiome analysis and supplementation of drinking water with antibiotics were performed on the indicated time points. e, Schematic of faecal transplant experiments.

Extended Data Figure 2 Artificial sweeteners induce glucose intolerance.

a, AUC of mice fed HFD and commercial saccharin (N = 10) or glucose (N = 9). b, AUC of HFD-fed mice drinking 0.1 mg ml−1 saccharin or water for 5 weeks (N = 20), followed by ‘antibiotics A’ (N = 10). c, d, OGTT and AUC of HFD-fed outbred Swiss-Webster mice (N = 5) drinking pure saccharin or water. e, f, Faecal samples were transferred from donor mice (N = 10) drinking commercially available, pure saccharin, glucose or water controls into 8-week-old male Swiss-Webster germ-free recipient mice. AUC of germ-free mice 6 days following transplant of microbiota from commercial saccharin- (N = 12) and glucose-fed mice (N = 11) (e); or pure saccharin- (N = 16) and water-fed (N = 16) donors (f). Symbols (GTT) or horizontal lines (AUC), means; error bars, s.e.m. *P < 0.05, **P < 0.01, ***P < 0.001, ANOVA and Tukey post hoc analysis (GTT) or unpaired two-sided Student t-test (AUC). Each experiment was repeated twice.

Extended Data Figure 3 Metabolic characterization of mice consuming commercial NAS formulations.

10-week-old C57Bl/6 mice (N = 4) were given commercially available artificial sweeteners (saccharin, sucralose and aspartame) or controls (water, sucrose or glucose, N = 4 in each group) and fed normal-chow diet. After 11 weeks, metabolic parameters were characterized using the PhenoMaster metabolic cages system for 80 h. Light and dark phases are denoted by white and black rectangles on the x-axis, respectively, and grey bars for the dark phase. a, Liquids intake. b, AUC of a. c, Chow consumption. d, AUC of c. e, Total caloric intake from chow and liquid during 72 h (see methods for calculation). f, Respiratory exchange rate (RER). g, AUC of f. h, Physical activity as distance. i, AUC of h. j, Energy expenditure. k, Mass change compared to original mouse weight during 15 weeks (N = 10). l, AUC of k. The metabolic cages characterization and weight-gain monitoring were repeated twice.

Extended Data Figure 4 Metabolic characterization of mice consuming HFD and pure saccharin or water.

10-week-old C57Bl/6 mice (N = 8) were fed HFD, with or without supplementing drinking water with 0.1 mg ml−1 pure saccharin. After 5 weeks, metabolic parameters were characterized using the PhenoMaster metabolic cages system for 70 h. Light and dark phases are denoted by white and black rectangles on the x-axis, respectively, and grey bars for the dark phase. a, Liquids intake. b, AUC of a. c, Chow consumption. d, AUC of c. e, Respiratory exchange rate (RER). f, AUC of e. g, Physical activity as distance. h, AUC of g. i, Energy expenditure. The metabolic cages characterization was repeated twice.

Extended Data Figure 5 Glucose intolerant NAS-drinking mice display normal insulin levels and tolerance.

a, Fasting plasma insulin measured after 11 weeks of commercial NAS or controls (N = 10). b, Same as a, but measured after 5 weeks of HFD and pure saccharin or water (N = 20). c, Insulin tolerance test performed after 12 weeks of commercial NAS or controls (N = 10). Horizontal lines (a, b) or symbols (c) represent means; error bars, s.e.m. All measurements were performed on two independent cohorts.

Extended Data Figure 6 Dysbiosis in saccharin-consuming mice and germ-free recipients.

Heat map representing W11 logarithmic-scale fold taxonomic differences between commercial saccharin and water or caloric sweetener consumers (N = 5 in each group). Right column, taxonomical differences in germ-free mice following faecal transplantation from commercial saccharin- (recipients N = 15) or glucose-consuming mice (N = 13). OTU number (GreenGenes) and the lowest taxonomic level identified are denoted.

Extended Data Figure 7 Functional analysis of saccharin-modulated microbiota.

a, b, Changes in bacterial relative abundance occur throughout the bacterial genome. Shown are changes in sequencing coverage along 10,000 bp genomic regions of Bacteroides vulgatus (a) and Akkermansia muciniphila (b), with bins ordered by abundance in week 0 of saccharin-treated mice. c, Fold change in relative abundance of modules belonging to phosphotransferase systems (PTS) between week 11 and week 0 in mice drinking commercial saccharin, glucose or water. Module diagram source: KEGG database. d, Enriched KEGG pathways (fold change > 1.38 as cutoff) in mice consuming HFD and pure saccharin versus water compared to the fold change in relative abundance of the same pathways in mice consuming commercial saccharin (week 11/week 0).

Extended Data Figure 8 Saccharin directly modulates the microbiota.

a, Experimental schematic. b, Relative taxonomic abundance of anaerobically cultured microbiota. c, AUC of germ-free mice 6 days following transplantation with saccharin-enriched or control faecal cultures (N = 10 and N = 9, respectively). Horizontal lines, means; error bars, s.e.m. **P < 0.01, unpaired two-sided Student t-test. The experiment was repeated twice.

Extended Data Figure 9 Impaired glycaemic control associated with acute saccharin consumption in humans is transferable to germ-free mice.

a, Experimental schematic (N = 7). b, c, Daily incremental AUC of days 1–4 versus days 5–7 in four responders (b) or three non-responders (c). d, Principal coordinates analysis (PCoA) of weighted UniFrac distances of 16S rRNA sequences demonstrating separation on principal coordinates 2 (PC2), 3 (PC3) and 4 (PC4) of microbiota from responders (N samples = 12) versus non-responders (N = 8) during days 5–7. e, Order-level relative abundance of taxa samples from days 1–7 of responders and non-responders. f, AUC in germ-free mice (N = 6) 6 days following faecal transplantation from samples of responder 1 (R1) collected before and after 7 days of saccharin consumption. g, h, OGTT and AUC in germ-free mice (N = 5) 6 days after receiving faecal samples collected from responder 4 (R4) before and after 7 days of saccharin consumption. i, AUC in germ-free mice (N = 5) 6 days following faecal transplantation from samples of non-responder 3 (NR3) collected before and after 7 days of saccharin consumption. j, k, OGTT and AUC in germ-free mice (N = 5) 6 days after receiving faecal samples collected from non-responder 2 (NR2) before and after 7 days of saccharin consumption. l, Fold taxonomical abundance changes of selected OTUs, altered in germ-free recipients of D7 versus D1 microbiomes from R1. Dot colour same as in e, bacterial orders. Symbols (GTT) or horizontal lines (AUC), means; error bars, s.e.m. *P < 0.05, **P < 0.01, ***P < 0.001, two-way ANOVA and Bonferroni post-hoc analysis (GTT), unpaired two-sided Student t-test (AUC).

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Suez, J., Korem, T., Zeevi, D. et al. Artificial sweeteners induce glucose intolerance by altering the gut microbiota. Nature 514, 181–186 (2014).

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