<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>18(1)</volume><submitter>Tigabu A</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The gut microbiota (GM) harbors diverse antibiotic resistance genes (ARGs), which are primarily disseminated through horizontal gene transfer (HGT), contributing to the emergence and spread of multidrug-resistant (MDR) pathogens. Broad-spectrum antibiotics are commonly used to treat a wide range of bacterial infections; however, they also exert collateral effects on non-target microbes. A comprehensive understanding of the impact of broad-spectrum antibiotic treatment on GM composition and the resistome is essential for the effective management of dysbiosis-related complications.&lt;h4>Methods&lt;/h4>Twenty-one fecal samples were collected from randomly selected study participants. Metagenomic sequencing was performed using the Illumina NovaSeq 6000 platform. FastQC v0.12.1, T</pubmed_abstract><journal>Gut pathogens</journal><pagination>18</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12950245</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Broad-spectrum antibiotic treatment reshapes the gut microbiome, resistome, and colonization potential of opportunistic pathogens: a metagenomics study.</pubmed_title><pmcid>PMC12950245</pmcid><pubmed_authors>Tigabu A</pubmed_authors><pubmed_authors>Leung PHM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Broad-spectrum antibiotic treatment reshapes the gut microbiome, resistome, and colonization potential of opportunistic pathogens: a metagenomics study.</name><description>&lt;h4>Background&lt;/h4>The gut microbiota (GM) harbors diverse antibiotic resistance genes (ARGs), which are primarily disseminated through horizontal gene transfer (HGT), contributing to the emergence and spread of multidrug-resistant (MDR) pathogens. Broad-spectrum antibiotics are commonly used to treat a wide range of bacterial infections; however, they also exert collateral effects on non-target microbes. A comprehensive understanding of the impact of broad-spectrum antibiotic treatment on GM composition and the resistome is essential for the effective management of dysbiosis-related complications.&lt;h4>Methods&lt;/h4>Twenty-one fecal samples were collected from randomly selected study participants. Metagenomic sequencing was performed using the Illumina NovaSeq 6000 platform. FastQC v0.12.1, T</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-17T01:10:34.252Z</modification><creation>2026-07-12T03:13:02.836Z</creation></dates><accession>S-EPMC12950245</accession><cross_references><pubmed>41593761</pubmed><doi>10.1186/s13099-026-00795-8</doi></cross_references></HashMap>