<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang B</submitter><funding>Guangxi University of Chinese Medicine-Shenzhen Kangtai Biological Products Co.Ltd. Guangxi Hepatitis B Prevention and Control Project</funding><funding>Guangxi University of Chinese Medicine Guipai Xinglin Outstanding Talent Project</funding><funding>| Natural Science Foundation of Guangxi Zhuang Autonomous Region (Guangxi Natural Science Foundation)</funding><funding>广西壮族自治区科学技术厅 | Natural Science Foundation of Guangxi Zhuang Autonomous Region</funding><funding>High Level Talent Cultivation and Innovation Project of Guangxi University of Chinese Medicine</funding><pagination>e0081224</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11575419</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(11)</volume><pubmed_abstract>Individuals with latent tuberculosis infection (LTBI) account for almost 30% of the population worldwide and have the potential to develop active tuberculosis (ATB). Despite this, the current understanding of the pathogenesis of LTBI is limited. The gut microbiome can be altered in tuberculosis patients, and an understanding of the changes associated with the progression from good health to LTBI to ATB can provide novel perspectives for understanding the pathogenesis of LTBI by identifying microbial and molecular biomarkers associated therewith. In this study, fecal samples from healthy controls (HC), individuals with LTBI and ATB patients were collected for gut microbiome and metabolomics analyses. Compared to HC and LTBI subjects, participants with ATB showed a significant decrease in gu</pubmed_abstract><journal>mSystems</journal><pubmed_title>Alterations in purine and pyrimidine metabolism associated with latent tuberculosis infection: insights from gut microbiome and metabolomics analyses.</pubmed_title><pmcid>PMC11575419</pmcid><funding_grant_id>QT022019</funding_grant_id><funding_grant_id>2022A009</funding_grant_id><funding_grant_id>2017GXNSFAA0198330</funding_grant_id><funding_grant_id>2022C010</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Guo X</pubmed_authors><pubmed_authors>Xu R</pubmed_authors><pubmed_authors>Shao K</pubmed_authors><pubmed_authors>Qin X</pubmed_authors><pubmed_authors>Yang B</pubmed_authors><pubmed_authors>Luo D</pubmed_authors><pubmed_authors>Liang D</pubmed_authors><pubmed_authors>Shi C</pubmed_authors><pubmed_authors>Gan L</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Zhong J</pubmed_authors><pubmed_authors>Liu G</pubmed_authors><pubmed_authors>Mo Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Alterations in purine and pyrimidine metabolism associated with latent tuberculosis infection: insights from gut microbiome and metabolomics analyses.</name><description>Individuals with latent tuberculosis infection (LTBI) account for almost 30% of the population worldwide and have the potential to develop active tuberculosis (ATB). Despite this, the current understanding of the pathogenesis of LTBI is limited. The gut microbiome can be altered in tuberculosis patients, and an understanding of the changes associated with the progression from good health to LTBI to ATB can provide novel perspectives for understanding the pathogenesis of LTBI by identifying microbial and molecular biomarkers associated therewith. In this study, fecal samples from healthy controls (HC), individuals with LTBI and ATB patients were collected for gut microbiome and metabolomics analyses. Compared to HC and LTBI subjects, participants with ATB showed a significant decrease in gu</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Nov</publication><modification>2025-04-04T20:38:41.408Z</modification><creation>2025-04-04T20:38:41.408Z</creation></dates><accession>S-EPMC11575419</accession><cross_references><pubmed>39436103</pubmed><doi>10.1128/msystems.00812-24</doi></cross_references></HashMap>