The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Gut Microbiomes of Malawian Twin Pairs Discordant for Kwashiorkor
Open accessAbstract
Not Just Wasting: Malnutrition is well known in Malawi, including a severe form—kwashiorkor—in which children do not simply waste away, they also suffer edema, liver damage, skin ulceration, and anorexia. Smith et al. (p. 548 ; see the Perspective by Relman ) investigated the microbiota of pairs of twins in Malawian villages and found notable differences in the composition of the gut microbiota in children with kwashiorkor. In these children, a bacterial species related to Desulfovibrio , which has been associated with bowel disease and inflammation, was noticeable. When the fecal flora from either the healthy or the sick twin was transplanted into groups of germ-free mice, the mice that received the kwashiorkor sample started to lose weight, like their human counterpart.
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In the citing paper
“when the mice are fed a peanut-based, ‘ready-to-use’ therapeutic food, their weight transiently increases and their microbiota normalize115.”
From Diet–microbiota interactions as moderators of human metabolism (2016) · cites this paper as [115]
In the citing paper
“germ-free mice that have been colonized with a ‘kwashiorkor’ microbiota experience weight loss when they are fed a typical Malawian diet, which is based on tomatoes and corn.”
From Diet–microbiota interactions as moderators of human metabolism (2016) · cites this paper as [115]
In the citing paper
“Twins that are discordant for kwashiorkor have distinct microbiotas”
From Diet–microbiota interactions as moderators of human metabolism (2016) · cites this paper as [115]
In the citing paper
“For example, several diet-induced host phenotypes are sufficiently mediated by changes in the gut microbiota (85–88).”
From Emerging Roles for the Gut Microbiome in Autism Spectrum Disorder (2017) · cites this paper as [86]
In the citing paper
“The microbiota/microbiome in turn plays an important role in extracting and metabolizing dietary ingredients9-14.”
From Persistent gut microbiota immaturity in malnourished Bangladeshi children (2014) · cites this paper as [12]
In the citing paper
“Food is a major factor that shapes the proportional representation of organisms present in the gut microbial community (microbiota), and its gene content (microbiome).”
From Persistent gut microbiota immaturity in malnourished Bangladeshi children (2014) · cites this paper as [12]
In the citing paper
“Seminal studies using germ‐free mice confirmed the role of the gut microbiome in a number of diseases, including obesity,47 Kwashiorkor,48 and autism‐spectrum disorder,49 by inducing disease features in recipient animals following transfer of a patient‐associated microbiome.”
From The oral microbiome: Role of key organisms and complex networks in oral health and disease (2021) · cites this paper as [48]
In the citing paper
“Importantly, animal data further suggest that this “fasting” microbiome also contributes to malnourishment in the host, as a microbial transplant from individuals with Kwashiorkor (a form of severe protein-energy malnutrition) induced weight loss and altered protein and carbohydrate metabolism in the recipient mice [77].”
In the citing paper
“Transfer of fecal samples from undernourished children to GF mice elicited metabolic and immune dysregulations in the mouse model similar to those observed in the human host, suggesting that the manifestations of malnutrition could in part be attributed to the absence of certain beneficial microbes (280).”
From Diet and the Microbiota–Gut–Brain Axis: Sowing the Seeds of Good Mental Health (2021) · cites this paper as [280]
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Cites
Breiman, L. (2001) · Machine Learning · doi:10.1023/a:1010933404324 · Cited by 133,538
QIIME allows analysis of high-throughput community sequencing data
Caporaso, J. G., Kuczynski, J., Stombaugh, J., Bittinger, K., Bushman, F. D., Costello, E. K., Fierer, N., Peña, A. G., Goodrich, J. K., Gordon, J. I., et al. (2010) · Nature Methods · doi:10.1038/nmeth.f.303 · Cited by 34,887
Self-citationUltra-high-throughput microbial community analysis on the Illumina HiSeq and MiSeq platforms
Caporaso, J. G., Lauber, C. L., Walters, W. A., Berg-Lyons, D., Huntley, J., Fierer, N., Owens, S. M., Betley, J., Fraser, L., Bauer, M., et al. (2012) · The ISME Journal · doi:10.1038/ismej.2012.8 · Cited by 8,839
Self-citationA core gut microbiome in obese and lean twins
Turnbaugh, P. J., Hamady, M., Yatsunenko, T., Cantarel, B. L., Duncan, A., Ley, R. E., Sogin, M. L., Jones, W. J., Roe, B. A., Affourtit, J. P., et al. (2009) · Nature · doi:10.1038/nature07540 · Cited by 7,823
Self-citationHuman gut microbiome viewed across age and geography
Yatsunenko, T., Rey, F. E., Manary, M. J., Trehan, I., Dominguez-Bello, M. G., Contreras, M., Magris, M., Hidalgo, G., Baldassano, R. N., Anokhin, A. P., et al. (2012) · Nature · doi:10.1038/nature11053 · Cited by 7,815
Self-citationMaternal and child undernutrition: global and regional exposures and health consequences
Black, R. E., Allen, L. H., Bhutta, Z. A., Caulfield, L. E., de Onis, M., Ezzati, M., Mathers, C., & Rivera, J. (2008) · The Lancet · doi:10.1016/s0140-6736(07)61690-0 · Cited by 6,443
Sokol, H., Pigneur, B., Watterlot, L., Lakhdari, O., Bermúdez-Humarán, L. G., Gratadoux, J.-J., Blugeon, S., Bridonneau, C., Furet, J.-P., Corthier, G., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804812105 · Cited by 4,413
WHO Child Growth Standards based on length/height, weight and age
de Onís, M. (2006) · Acta Paediatrica · doi:10.1111/j.1651-2227.2006.tb02378.x · Cited by 3,991
Beckonert, O. P., Keun, H. C., Ebbels, T. M. D., Bundy, J. G., Holmes, E. C., Lindon, J. C., & Nicholson, J. K. (2007) · Nature Protocols · doi:10.1038/nprot.2007.376 · Cited by 2,181
Self-citationDietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice
Devkota, S., Wang, Y., Musch, M. W., Leone, V., Fehlner-Peach, H., Nadimpalli, A., Antonopoulos, D. A., Jabri, B., & Chang, E. B. (2012) · Nature · doi:10.1038/nature11225 · Cited by 1,904
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Research works printed but not linked: 2
- C. Gopalan in Calorie Deficiencies and Protein Deficiencies: Kwashiorkor and Marasmus: Evolution and Distinguishing Features R. A. McCance E. M. Widdowson Eds. (Churchill London 1968) pp. 48–58.
- Subcommittee on Laboratory Animal Nutrition Committee on Animal Nutrition Board on Agriculture National Research Council Nutrient Requirements of Laboratory Animals (The National Academies Press Washington DC ed. 4 1995).
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Fan, Y., & Pedersen, O. (2021) · Nature Reviews Microbiology · doi:10.1038/s41579-020-0433-9 · Cited by 4,724
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Shin, N.-R., Whon, T. W., & Bae, J.-W. (2015) · Trends in Biotechnology · doi:10.1016/j.tibtech.2015.06.011 · Cited by 3,954
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Sonnenburg, J. L., & Bäckhed, F. (2016) · Nature · doi:10.1038/nature18846 · Cited by 2,257
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Suez, J., Korem, T., Zeevi, D., Zilberman-Schapira, G., Thaiss, C. A., Maza, O., Israeli, D., Zmora, N., Gilad, S., Weinberger, A., et al. (2014) · Nature · doi:10.1038/nature13793 · Cited by 2,067
Metadata
- Authors
- Smith, M. I., Yatsunenko, T., Manary, M. J., Trehan, I., Mkakosya, R., Cheng, J., Kau, A. L., Rich, S. S., Concannon, P., Mychaleckyj, J. C., Liu, J., Houpt, E., Li, J. V., Holmes, E., Nicholson, J., Knights, D., Ursell, L. K., Knight, R., & Gordon, J. I.
- Affiliations
- Washington University in St. Louis (US)
- University of Malawi (MW)
- University of Virginia (US)
- Imperial College London (GB)
- University of Colorado Boulder (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Smith, Michelle I.
- Yatsunenko, Tanya
- Gordon, Jeffrey I.
- ORCID
- Venue
- Science
- Published
- 2013-02
- Volume
- 339
- Issue
- 6119
- Pages
- 548-554
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3667500
- OpenAlex
- W2097478615
- Cited by
- 1,173
- References
- 48
- Citations by year
- 2026: 40 · 2025: 49 · 2024: 67 · 2023: 73 · 2022: 66 · 2021: 71 · 2020: 101 · 2019: 82 · 2018: 101 · 2017: 92 · 2016: 126 · 2015: 105 · 2014: 119 · 2013: 77
- FWCI
- 63.95
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Spiral (Imperial College London) (submittedVersion)
- Funders
- National Institute of General Medical Sciences (T32GM008759, T32GM142607)
- National Institute of Diabetes and Digestive and Kidney Diseases (R37DK030292, DK-30292, DK078669, P01DK078669, T35DK074375, R01DK030292)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD049338)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gut microbiota and health
- Health Sciences › Nursing › Nutrition and Dietetics › Child Nutrition and Water Access
- Health Sciences › Nursing › Nutrition and Dietetics › Infant Nutrition and Health
- Keywords
- kwashiorkor, gut microbiota, acute malnutrition, discordant twins, ready-to-use therapeutic food, microbial transplantation, gnotobiotic mice, infant nutrition, Malawi, microbial metabolic functions, weight loss
- MeSH terms
- Amino Acids, Animals, Child, Preschool, Diseases in Twins, Feces, Female, Germ-Free Life, Humans, Infant, Kwashiorkor, Longitudinal Studies, Malawi, Male, Mice, Inbred C57BL, Arachis, Gastrointestinal Tract, Carbohydrate Metabolism, Mice, Metagenome
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