Indoles from commensal bacteria extend healthspan
Open accessAbstract
Significance: Increases in human life expectancy over the next century will be accompanied by increased frailty and massive and unsustainable health care costs. Developing means to extend the time that individuals remain healthy and free of age-related infirmities, called healthspan, has therefore become a critical goal of aging research. We show that small molecules produced by the microbiota and related to indole extend healthspan in geriatric worms, flies, and mice, without attendant effects on lifespan. Indoles act via the aryl hydrocarbon receptor and cause animals to retain a youthful gene expression profile. Indoles may represent a new class of therapeutics that improve the way we age as opposed to simply extending how long we live.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Healthy ageing correlates with increased indoles, gut bacterial tryptophan degradation products that mediate immune homeostasis via aryl hydrocarbon and IL-10 receptors.
“healthy ageing correlates with an increased presence of certain indoles, which are gut bacterial degradation products of tryptophan that mediate immune homeostasis upon binding to aryl hydrocarbon receptors and IL-10 receptors15–17”
From Gut OncoMicrobiome Signatures (GOMS) as next-generation biomarkers for cancer immunotherapy (2023) · cites this paper as [16]
Recent animal studies have shown that metabolic byproducts of intestinal bacteria have great relevance in prolonging healthspan.
“and that the metabolic byproducts of intestinal bacteria have a great relevance in prolonging healthspan [140].”
From Gut Microbiota, Muscle Mass and Function in Aging: A Focus on Physical Frailty and Sarcopenia (2019) · cites this paper as [140]
Cites
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106 · see citing works
The Sequence Alignment/Map format and SAMtools
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G., Durbin, R., & 1000 Genome Project Data Processing Subgroup (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp352 · Cited by 62,041 · see citing works
STAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709 · see citing works
Cutadapt removes adapter sequences from high-throughput sequencing reads
Martin, M. (2011) · EMBnet.journal · doi:10.14806/ej.17.1.200 · Cited by 33,889 · see citing works
HTSeq—a Python framework to work with high-throughput sequencing data
Anders, S., Pyl, P. T., & Huber, W. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btu638 · Cited by 21,464 · see citing works
Guide for the Care and Use of Laboratory Animals: Eighth Edition
(2011) · doi:10.17226/12910 · Cited by 16,199 · see citing works
One-step inactivation of chromosomal genes in Escherichia coli K-12 using PCR products.
Datsenko, K., & Wanner, B. (2000) · Proceedings of the National Academy of Sciences of the United States of America · doi:10.1073/pnas.120163297 · Cited by 15,902 · see citing works
THE GENETICS OF CAENORHABDITIS ELEGANS
Brenner, S. (1974) · Genetics · doi:10.1093/genetics/77.1.71 · Cited by 14,984 · see citing works
Inflamm‐aging: An Evolutionary Perspective on Immunosenescence
FRANCESCHI, C., BONAFÈ, M., VALENSIN, S., OLIVIERI, F., DE LUCA, M., OTTAVIANI, E., & DE BENEDICTIS, G. (2000) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2000.tb06651.x · Cited by 5,358 · see citing works
Chronic Inflammation (Inflammaging) and Its Potential Contribution to Age-Associated Diseases
Franceschi, C., & Campisi, J. (2014) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glu057 · Cited by 3,891 · see citing works
A C. elegans mutant that lives twice as long as wild type
Kenyon, C., Chang, J., Gensch, E., Rudner, A., & Tabtiang, R. (1993) · Nature · doi:10.1038/366461a0 · Cited by 3,387 · see citing works
An Immunomodulatory Molecule of Symbiotic Bacteria Directs Maturation of the Host Immune System
Mazmanian, S. K., Liu, C. H., Tzianabos, A. O., & Kasper, D. L. (2005) · Cell · doi:10.1016/j.cell.2005.05.007 · Cited by 2,910 · see citing works
The Nematode Caenorhabditis elegans
Wood, W. B. (1988) · Cold Spring Harbor Laboratory eBooks · Cited by 2,821 · see citing works
Zelante, T., Iannitti, R. G., Cunha, C., De Luca, A., Giovannini, G., Pieraccini, G., Zecchi, R., D’Angelo, C., Massi-Benedetti, C., Fallarino, F., et al. (2013) · Immunity · doi:10.1016/j.immuni.2013.08.003 · Cited by 2,614 · see citing works
Bifidobacteria can protect from enteropathogenic infection through production of acetate
Fukuda, S., Toh, H., Hase, K., Oshima, K., Nakanishi, Y., Yoshimura, K., Tobe, T., Clarke, J. M., Topping, D. L., Suzuki, T., et al. (2011) · Nature · doi:10.1038/nature09646 · Cited by 2,387 · see citing works
[C. elegans: of neurons and genes].
Gally, C., & Bessereau, J. (2003) · Medecine sciences : M/S · doi:10.1051/medsci/20031967725 · Cited by 2,194 · see citing works
AmiGO: online access to ontology and annotation data
Carbon, S., Ireland, A., Mungall, C., Shu, S., Marshall, B., Lewis, S., Hub, T. A., & the Web Presence Working Group (2008) · Bioinformatics · doi:10.1093/bioinformatics/btn615 · Cited by 1,918 · see citing works
Methods for cell and particle tracking.
Meijering, E., Dzyubachyk, O., & Smal, I. (2012) · Methods in Enzymology · doi:10.1016/b978-0-12-391857-4.00009-4 · Cited by 1,471 · see citing works
Stochastic and genetic factors influence tissue-specific decline in ageing C. elegans
Herndon, L. A., Schmeissner, P. J., Dudaronek, J. M., Brown, P. A., Listner, K. M., Sakano, Y., Paupard, M. C., Hall, D. H., & Driscoll, M. (2002) · Nature · doi:10.1038/nature01135 · Cited by 1,214 · see citing works
Guide for the Care and Use of Laboratory Animals
Studies, D. O. E. A. L. (2011) · National Academies Press eBooks · doi:10.17226/25801 · Cited by 1,134 · see citing works
Interleukin-22 promotes intestinal-stem-cell-mediated epithelial regeneration
Lindemans, C. A., Calafiore, M., Mertelsmann, A. M., O'Connor, M. H., Dudakov, J. A., Jenq, R. R., Velardi, E., Young, L. F., Smith, O. M., Lawrence, G., et al. (2015) · Nature · doi:10.1038/nature16460 · Cited by 1,112 · see citing works
Lee, J. S., Cella, M., McDonald, K. G., Garlanda, C., Kennedy, G. D., Nukaya, M., Mantovani, A., Kopan, R., Bradfield, C. A., Newberry, R. D., et al. (2012) · Nature Immunology · doi:10.1038/ni.2187 · Cited by 777 · see citing works
Gut microbiota–generated metabolites in animal health and disease
Lee, W.-J., & Hase, K. (2014) · Nature Chemical Biology · doi:10.1038/nchembio.1535 · Cited by 756 · see citing works
The gut microbiota, obesity and insulin resistance
Shen, J., Obin, M. S., & Zhao, L. (2013) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2012.11.001 · Cited by 599 · see citing works
Transcriptional Responses to the Auxin Hormone
Weijers, D., & Wagner, D. (2016) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-043015-112122 · Cited by 547 · see citing works
Roles of indole as an interspecies and interkingdom signaling molecule
Lee, J.-H., Wood, T. K., & Lee, J. (2015) · Trends in Microbiology · doi:10.1016/j.tim.2015.08.001 · Cited by 516 · see citing works
On the Control of Oocyte Meiotic Maturation and Ovulation inCaenorhabditis elegans
McCarter, J. P., Bartlett, B. M., Dang, T., et al. (1999) · Developmental Biology · doi:10.1006/dbio.1998.9109 · Cited by 501 · see citing works
Microbial shifts in the aging mouse gut
Langille, M. G., Meehan, C. J., Koenig, J. E., Dhanani, A. S., Rose, R. A., Howlett, S. E., & Beiko, R. G. (2014) · Microbiome · doi:10.1186/s40168-014-0050-9 · Cited by 437 · see citing works
Commensal bacteria-dependent indole production enhances epithelial barrier function in the colon
Shimada, Y., Kinoshita, M., Harada, K., Mizutani, M., Masahata, K., Kayama, H., & Takeda, K. (2013) · PLoS ONE · doi:10.1371/journal.pone.0080604 · Cited by 404 · see citing works
Adaptation of the human aryl hydrocarbon receptor to sense microbiota-derived indoles
Hubbard, T. D., Murray, I. A., Bisson, W. H., Lahoti, T. S., Gowda, K., Amin, S. G., Patterson, A. D., & Perdew, G. H. (2015) · Scientific Reports · doi:10.1038/srep12689 · Cited by 377 · see citing works
Uncoupling lifespan and healthspan in <i>Caenorhabditis elegans</i> longevity mutants
Bansal, A., Zhu, L. J., Yen, K., & Tissenbaum, H. A. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1412192112 · Cited by 367 · see citing works
Kunde, S., Pham, A., Bonczyk, S., Crumb, T., Duba, M., Conrad, H., Cloney, D., & Kugathasan, S. (2013) · Journal of Pediatric Gastroenterology and Nutrition · doi:10.1097/mpg.0b013e318292fa0d · Cited by 314 · see citing works
Modulation of a Circulating Uremic Solute via Rational Genetic Manipulation of the Gut Microbiota
Devlin, A. S., Marcobal, A. M., Dodd, D., Nayfach, S., Plummer, N. S., Meyer, T., Pollard, K. S., Sonnenburg, J. L., & Fischbach, M. A. (2016) · Cell Host & Microbe · doi:10.1016/j.chom.2016.10.021 · Cited by 300 · see citing works
TGF-β and Insulin Signaling Regulate Reproductive Aging via Oocyte and Germline Quality Maintenance
Luo, S., Kleemann, G. A., Ashraf, J. M., Shaw, W. M., & Murphy, C. T. (2010) · Cell · doi:10.1016/j.cell.2010.09.013 · Cited by 286 · see citing works
Li, G., & Young, K. D. (2013) · Microbiology · doi:10.1099/mic.0.064139-0 · Cited by 266 · see citing works
An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans
Budovskaya, Y. V., Wu, K., Southworth, L. K., Jiang, M., Tedesco, P., Johnson, T. E., & Kim, S. K. (2008) · Cell · doi:10.1016/j.cell.2008.05.044 · Cited by 253 · see citing works
Richards, J. L., Yap, Y. A., McLeod, K. H., Mackay, C. R., & Mariño, E. (2016) · Clinical & Translational Immunology · doi:10.1038/cti.2016.29 · Cited by 250 · see citing works
The microbiota in inflammatory bowel disease
Sheehan, D., Moran, C. P., & Shanahan, F. (2015) · Journal of Gastroenterology · doi:10.1007/s00535-015-1064-1 · Cited by 249 · see citing works
Lactobacilli Modulate Epithelial Cytoprotection through the Nrf2 Pathway
Jones, R. M., Desai, C., Darby, T. M., Luo, L., Wolfarth, A. A., Scharer, C. D., Ardita, C., Reedy, A. R., Keebaugh, E. S., & Neish, A. S. (2015) · Cell Reports · doi:10.1016/j.celrep.2015.07.042 · Cited by 231 · see citing works
Self-citationDiet and Inflammatory Bowel Disease: Review of Patient-Targeted Recommendations
Hou, J. K., Lee, D. Y., & Lewis, J. D. (2013) · Clinical Gastroenterology and Hepatology · doi:10.1016/j.cgh.2013.09.063 · Cited by 204 · see citing works
Acute Gastrointestinal Syndrome in High-Dose Irradiated Mice
Booth, C. E., Tudor, G. L., Tudor, J., Katz, B. P., & MacVittie, T. J. (2012) · Health Physics · doi:10.1097/hp.0b013e318266ee13 · Cited by 200 · see citing works
Weber, D., Oefner, P. J., Hiergeist, A., Koestler, J., Gessner, A., Weber, M., Hahn, J., Wolff, D., Stämmler, F., Spang, R., et al. (2015) · Blood · doi:10.1182/blood-2015-04-638858 · Cited by 195 · cited 1× · see citing works
“The indole metabolite 3-indoxyl sulfate, an indirect measure of indole production by intestinal microbes (29, 30), was readily detected in urine from animals colonized with K12, but appeared at significantly lower levels in animals colonized with K12ΔtnaA (Fig.”
BackgroundXenobiotic detoxification in the nematode Caenorhabditis elegans
Lindblom, T. H., & Dodd, A. K. (2006) · Journal of Experimental Zoology Part A Comparative Experimental Biology · doi:10.1002/jez.a.324 · Cited by 188 · see citing works
Trends In Medical Spending By Age, 1963–2000
Meara, E. R., White, C., & Cutler, D. (2004) · Health Affairs · doi:10.1377/hlthaff.23.4.176 · Cited by 171 · see citing works
Role of the microbiome, probiotics, and ‘dysbiosis therapy’ in critical illness
Wischmeyer, P. E., McDonald, D. T., & Knight, R. D. (2016) · Current Opinion in Critical Care · doi:10.1097/mcc.0000000000000321 · Cited by 161 · see citing works
Anyanful, A., Dolan‐Livengood, J. M., Lewis, T., Sheth, S., DeZalia, M. N., Sherman, M. A., Kalman, L. V., Benian, G. M., & Kalman, D. (2005) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.04739.x · Cited by 154 · see citing works
Self-citationCho, H., Seon, M. R., Lee, Y. M., Kim, J., Kim, J.-K., Kim, S. G., & Park, J. H. Y. (2008) · Journal of Nutrition · doi:10.1093/jn/138.1.17 · Cited by 130 · see citing works
Genetics, Life Span, Health Span, and the Aging Process in Caenorhabditis elegans
Tissenbaum, H. A. (2012) · The Journals of Gerontology Series A · doi:10.1093/gerona/gls088 · Cited by 118 · see citing works
Fecal Microbiota Transplantation for Ulcerative Colitis: A Systematic Review and Meta-Analysis
Shi, Y., Dong, Y., Huang, W., Zhu, D., Mao, H., & Su, P. (2016) · PLoS ONE · doi:10.1371/journal.pone.0157259 · Cited by 117 · see citing works
Saltzman, J. R., & Russell, R. M. (1998) · Gastroenterology Clinics of North America · doi:10.1016/s0889-8553(05)70005-4 · Cited by 115 · see citing works
Rouse, M. D., Singh, N. P., Nagarkatti, P. S., & Nagarkatti, M. (2013) · British Journal of Pharmacology · doi:10.1111/bph.12205 · Cited by 111 · see citing works
How a Mutation that Slows Aging Can Also Disproportionately Extend End-of-Life Decrepitude
Podshivalova, K., Kerr, R. A., & Kenyon, C. J. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.03.062 · Cited by 109 · see citing works
The C. elegans healthspan and stress-resistance assay toolkit
Keith, S. A., Amrit, F. R. G., Ratnappan, R., & Ghazi, A. (2014) · Methods · doi:10.1016/j.ymeth.2014.04.003 · Cited by 105 · see citing works
A Family of Indoles Regulate Virulence and Shiga Toxin Production in Pathogenic E. coli
Bommarius, B., Anyanful, A., Izrayelit, Y., Bhatt, S., Cartwright, E. J., Wang, W., Swimm, A. I., Benian, G. M., Schroeder, F. C., & Kalman, D. (2013) · PLoS ONE · doi:10.1371/journal.pone.0054456 · Cited by 99 · see citing works
Self-citationZhang, W. B., Sinha, D. B., Pittman, W. E., Hvatum, E., Stroustrup, N., & Pincus, Z. (2016) · Cell Systems · doi:10.1016/j.cels.2016.09.003 · Cited by 98 · see citing works
Changes in Small‐Intestine Permeability with Aging
Saltzman, J. R., Kowdley, K. V., Perrone, G., & Russell, R. M. (1995) · Journal of the American Geriatrics Society · doi:10.1111/j.1532-5415.1995.tb06382.x · Cited by 94 · see citing works
Anyanful, A., Easley, K. A., Benian, G. M., & Kalman, D. (2009) · Cell Host & Microbe · doi:10.1016/j.chom.2009.04.012 · Cited by 94 · see citing works
Self-citationLeatham, M. P., Stevenson, S. J., Gauger, E. J., Krogfelt, K. A., Lins, J. J., Haddock, T. L., Autieri, S. M., Conway, T., & Cohen, P. S. (2005) · Infection and Immunity · doi:10.1128/iai.73.12.8039-8049.2005 · Cited by 93 · see citing works
The aryl hydrocarbon receptor promotes aging phenotypes across species
Eckers, A., Jakob, S., Heiß, C., Haarmann‐Stemmann, T., Goy, C., Brinkmann, V., Cortese-Krott, M. M., Sansone, R., Esser, C., Ale‐Agha, N., et al. (2016) · Scientific Reports · doi:10.1038/srep19618 · Cited by 86 · see citing works
Measures of Healthspan as Indices of Aging in Mice—A Recommendation
Richardson, A., Fischer, K. E., Speakman, J. R., de Cabo, R., Mitchell, S. J., Peterson, C. A., Rabinovitch, P., Chiao, Y. A., Taffet, G., Miller, R. A., et al. (2016) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glv080 · Cited by 81 · see citing works
Hill, K. L., & L’Hernault, S. W. (2001) · Developmental Biology · doi:10.1006/dbio.2000.0136 · Cited by 71 · see citing works
Hansen, D. A., Esakky, P., Drury, A. M., Lamb, L. E., & Moley, K. H. (2013) · Biology of Reproduction · doi:10.1095/biolreprod.113.108845 · Cited by 62 · see citing works
Probiotic Therapy in Radiation‐Induced Intestinal Injury and Repair
Ciorba, M. A., & Stenson, W. F. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04029.x · Cited by 52 · see citing works
Huffman, D. M., Justice, J. N., Stout, M. B., Kirkland, J. L., Barzilai, N., & Austad, S. N. (2016) · The Journals of Gerontology Series A: Biological Sciences and Medical Sciences · doi:10.1093/gerona/glw106 · Cited by 52 · see citing works
Tatar, M. (2009) · The Journals of Gerontology Series A · doi:10.1093/gerona/gln067 · Cited by 49 · see citing works
Melnick, M. B., Noll, E., & Perrimon, N. (1993) · Genetics · doi:10.1093/genetics/135.2.553 · Cited by 41 · see citing works
Stress Response and Aging in Caenorhabditis elegans
Lithgow, G. J. (2000) · Results and problems in cell differentiation · doi:10.1007/978-3-540-48003-7_7 · Cited by 29 · see citing works
How’s your microbiota? Let’s check your urine.
Jenq, R. R. (2015) · Blood · doi:10.1182/blood-2015-08-661504 · Cited by 11 · see citing works
Detecting Reactive Oxygen Species Generation and Stem Cell Proliferation in the Drosophila Intestine
Luo, L., Reedy, A. R., & Jones, R. M. (2016) · Methods in molecular biology · doi:10.1007/978-1-4939-3603-8_10 · Cited by 9 · see citing works
Self-citationHuang, H., Arocho, G. M. R., Davis, C. D., et al. (2016) · The FASEB Journal · doi:10.1096/fasebj.30.1_supplement.1176.26 · Cited by 3 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Cryan, J. F., O'Riordan, K. J., Cowan, C. S. M., Sandhu, K. V., Bastiaanssen, T. F. S., Boehme, M., Codagnone, M. G., Cussotto, S., Fulling, C., Golubeva, A. V., et al. (2019) · Physiological Reviews · doi:10.1152/physrev.00018.2018 · Cited by 5,286 · see citing works
Microbial tryptophan catabolites in health and disease
Roager, H. M., & Licht, T. R. (2018) · Nature Communications · doi:10.1038/s41467-018-05470-4 · Cited by 2,236 · see citing works
Gut Microbiota, Muscle Mass and Function in Aging: A Focus on Physical Frailty and Sarcopenia
Ticinesi, A., Nouvenne, A., Cerundolo, N., Catania, P., Prati, B., Tana, C., & Meschi, T. (2019) · Nutrients · doi:10.3390/nu11071633 · Cited by 418 · see citing works
Ticinesi, A., Lauretani, F., Milani, C., Nouvenne, A., Tana, C., Del Rio, D., Maggio, M., Ventura, M., & Meschi, T. (2017) · Nutrients · doi:10.3390/nu9121303 · Cited by 401 · see citing works
The Gut Microbiota and Unhealthy Aging: Disentangling Cause from Consequence
DeJong, E. N., Surette, M. G., & Bowdish, D. M. E. (2020) · Cell Host & Microbe · doi:10.1016/j.chom.2020.07.013 · Cited by 370 · see citing works
BiT age: A transcriptome‐based aging clock near the theoretical limit of accuracy
Meyer, D. H., & Schumacher, B. (2021) · Aging Cell · doi:10.1111/acel.13320 · Cited by 165 · see citing works
Gut OncoMicrobiome Signatures (GOMS) as next-generation biomarkers for cancer immunotherapy
Thomas, A. M., Fidelle, M., Routy, B., Kroemer, G., Wargo, J. A., Segata, N., & Zitvogel, L. (2023) · Nature Reviews Clinical Oncology · doi:10.1038/s41571-023-00785-8 · Cited by 141 · see citing works
Christian, C. J., & Benian, G. M. (2020) · Aging Cell · doi:10.1111/acel.13223 · Cited by 113 · see citing works
Self-citationHeterochronic faecal transplantation boosts gut germinal centres in aged mice
Stebegg, M., Silva-Cayetano, A., Innocentin, S., Jenkins, T. P., Cantacessi, C., Gilbert, C., & Linterman, M. A. (2019) · Nature Communications · doi:10.1038/s41467-019-10430-7 · Cited by 107 · see citing works
The intestinal microbiome and its relevance for functionality in older persons
Ticinesi, A., Tana, C., & Nouvenne, A. (2019) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000521 · Cited by 80 · see citing works
Brinkmann, V., Ale-Agha, N., Haendeler, J., & Ventura, N. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2019.01561 · Cited by 71 · see citing works
- Authors
- Sonowal, R., Swimm, A., Sahoo, A., Luo, L., Matsunaga, Y., Wu, Z., Bhingarde, J. A., Ejzak, E. A., Ranawade, A., Qadota, H., Powell, D. N., Capaldo, C. T., Flacker, J. M., Jones, R. M., Benian, G. M., & Kalman, D.
- Affiliations
- Emory University (US)
- McMaster University (CA)
- Department of Pediatrics, Emory University School of Medicine, Atlanta, GA 30322;
- ORCID
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2017-08-21
- Volume
- 114
- Issue
- 36
- Pages
- E7506-E7515
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC5594673
- OpenAlex
- W2747253994
- Cited by
- 197
- References
- 70
- Citations by year
- 2026: 20 · 2025: 19 · 2024: 28 · 2023: 15 · 2022: 30 · 2021: 23 · 2020: 30 · 2019: 12 · 2018: 18 · 2017: 2
- FWCI
- 7.22
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (2R01DK074731)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- indole, commensal bacteria, gut microbiota, healthspan, healthy aging, aging, fecundity, oogenesis, reproductive period, frailty, gene expression
- MeSH terms
- Aging, Animals, Bacteria, Drosophila melanogaster, Indoles, Longevity, Mice, Inbred BALB C, Mice, Inbred C57BL, Mutation, Reproduction, Caenorhabditis elegans, Receptors, Aryl Hydrocarbon, Caenorhabditis elegans Proteins, Mice, Transcriptome
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review