<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>15(1)</volume><submitter>Huang M</submitter><pubmed_abstract>The purpose of this research is to examine the impact of key type VI secretion system (T6SS) proteins hemolysin coregulated protein (Hcp) and valine-glycine repeat protein G (VgrG) on the metabolism of Acinetobacter baumannii (A. baumannii). Homologous recombination technology was used to construct hcp knockout strain (ATCC17978Δhcp), vgrG knockout strain (ATCC17978ΔvgrG), and a combined hcp and vgrG knockout strain (ATCC17978ΔhcpΔvgrG), with the wild-type A. baumannii strain (ATCC17978) used as a control. These strains were co-cultured with human pulmonary alveolar epithelial cells (HPAEpiC), respectively. Subsequently, a non-targeted metabolomic analysis of the co-culture supernatant, bacteria, and cells was conducted using liquid chromatography-tandem mass spectrometry (LC-MS/MS). In th</pubmed_abstract><journal>Scientific reports</journal><pagination>34632</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12494896</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Impact of hcp and vgrG on Acinetobacter baumannii biofilm formation during infection of human pulmonary alveolar epithelial cells.</pubmed_title><pmcid>PMC12494896</pmcid><pubmed_authors>Qin P</pubmed_authors><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Liu M</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Huang M</pubmed_authors><pubmed_authors>Yu D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Impact of hcp and vgrG on Acinetobacter baumannii biofilm formation during infection of human pulmonary alveolar epithelial cells.</name><description>The purpose of this research is to examine the impact of key type VI secretion system (T6SS) proteins hemolysin coregulated protein (Hcp) and valine-glycine repeat protein G (VgrG) on the metabolism of Acinetobacter baumannii (A. baumannii). Homologous recombination technology was used to construct hcp knockout strain (ATCC17978Δhcp), vgrG knockout strain (ATCC17978ΔvgrG), and a combined hcp and vgrG knockout strain (ATCC17978ΔhcpΔvgrG), with the wild-type A. baumannii strain (ATCC17978) used as a control. These strains were co-cultured with human pulmonary alveolar epithelial cells (HPAEpiC), respectively. Subsequently, a non-targeted metabolomic analysis of the co-culture supernatant, bacteria, and cells was conducted using liquid chromatography-tandem mass spectrometry (LC-MS/MS). In th</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Oct</publication><modification>2026-06-04T02:04:26.008Z</modification><creation>2026-05-04T03:13:44.437Z</creation></dates><accession>S-EPMC12494896</accession><cross_references><pubmed>41044369</pubmed><doi>10.1038/s41598-025-18287-1</doi></cross_references></HashMap>