<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Raman AS</submitter><funding>NIDDK NIH HHS</funding><funding>NIAID NIH HHS</funding><funding>National Institutes of Health</funding><funding>Bill and Melinda Gates Foundation</funding><pagination>eaau4735</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6683326</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>365(6449)</volume><pubmed_abstract>Characterizing the organization of the human gut microbiota is a formidable challenge given the number of possible interactions between its components. Using a statistical approach initially applied to financial markets, we measured temporally conserved covariance among bacterial taxa in the microbiota of healthy members of a Bangladeshi birth cohort sampled from 1 to 60 months of age. The results revealed an "ecogroup" of 15 covarying bacterial taxa that provide a concise description of microbiota development in healthy children from this and other low-income countries, and a means for monitoring community repair in undernourished children treated with therapeutic foods. Features of ecogroup population dynamics were recapitulated in gnotobiotic piglets as they transitioned from exclusive </pubmed_abstract><journal>Science (New York, N.Y.)</journal><pubmed_title>A sparse covarying unit that describes healthy and impaired human gut microbiota development.</pubmed_title><pmcid>PMC6683326</pmcid><funding_grant_id>R01 DK030292</funding_grant_id><funding_grant_id>DK030292</funding_grant_id><funding_grant_id>AI043596</funding_grant_id><funding_grant_id>OPP1134649</funding_grant_id><funding_grant_id>R01 AI043596</funding_grant_id><pubmed_authors>Chang HW</pubmed_authors><pubmed_authors>Raman AS</pubmed_authors><pubmed_authors>Gehrig JL</pubmed_authors><pubmed_authors>Kosek MN</pubmed_authors><pubmed_authors>Ahmed T</pubmed_authors><pubmed_authors>Mahfuz M</pubmed_authors><pubmed_authors>Venkatesh S</pubmed_authors><pubmed_authors>Petri WA</pubmed_authors><pubmed_authors>Leyn SA</pubmed_authors><pubmed_authors>Haque R</pubmed_authors><pubmed_authors>Bessong PO</pubmed_authors><pubmed_authors>Lima AAM</pubmed_authors><pubmed_authors>Gordon JI</pubmed_authors><pubmed_authors>Kang G</pubmed_authors><pubmed_authors>Osterman AL</pubmed_authors><pubmed_authors>Islam M</pubmed_authors><pubmed_authors>Huq S</pubmed_authors><pubmed_authors>Barratt MJ</pubmed_authors><pubmed_authors>Hibberd MC</pubmed_authors><pubmed_authors>Rodionov DA</pubmed_authors><pubmed_authors>Arzamasov AA</pubmed_authors><pubmed_authors>Subramanian S</pubmed_authors><pubmed_authors>Mostafa I</pubmed_authors></additional><is_claimable>false</is_claimable><name>A sparse covarying unit that describes healthy and impaired human gut microbiota development.</name><description>Characterizing the organization of the human gut microbiota is a formidable challenge given the number of possible interactions between its components. Using a statistical approach initially applied to financial markets, we measured temporally conserved covariance among bacterial taxa in the microbiota of healthy members of a Bangladeshi birth cohort sampled from 1 to 60 months of age. The results revealed an "ecogroup" of 15 covarying bacterial taxa that provide a concise description of microbiota development in healthy children from this and other low-income countries, and a means for monitoring community repair in undernourished children treated with therapeutic foods. Features of ecogroup population dynamics were recapitulated in gnotobiotic piglets as they transitioned from exclusive </description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jul</publication><modification>2026-07-14T15:48:10.558Z</modification><creation>2025-05-31T22:25:45.659Z</creation></dates><accession>S-EPMC6683326</accession><cross_references><pubmed>31296739</pubmed><doi>10.1126/science.aau4735</doi></cross_references></HashMap>