<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(2)</volume><submitter>Jimi S</submitter><pubmed_abstract>We investigated the drug-resistant mechanisms of intracellular survival of methicillin-resistant S. aureus (MRSA). Our established MRSA clinical strain, OJ-1, with high biofilm-forming ability, and a macrophage cell line, J774A, were used. After ingestion of OJ-1 by J774A, the cells were incubated for ten days with vancomycin at doses 30 times higher than the minimum inhibitory concentration. The number of phagocytosed intracellular OJ-1 gradually decreased during the study but plateaued after day 7. In J774A cells with intracellular OJ-1, the expression of LysoTracker-positive lysosomes increased until day 5 and then declined from day 7. In contrast, LysoTracker-negative and OJ-1-retaining J774A cells became prominent from day 7, and intracellular OJ-1 also escaped from the autophagosome.</pubmed_abstract><journal>Microorganisms</journal><pagination>348</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8874447</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Intracellular Survival of Biofilm-Forming MRSA OJ-1 by Escaping from the Lysosome and Autophagosome in J774A Cells Cultured in Overdosed Vancomycin.</pubmed_title><pmcid>PMC8874447</pmcid><pubmed_authors>Yoshimura M</pubmed_authors><pubmed_authors>Saparov A</pubmed_authors><pubmed_authors>Mashima K</pubmed_authors><pubmed_authors>Ueda Y</pubmed_authors><pubmed_authors>Miyazaki M</pubmed_authors><pubmed_authors>Jimi S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Intracellular Survival of Biofilm-Forming MRSA OJ-1 by Escaping from the Lysosome and Autophagosome in J774A Cells Cultured in Overdosed Vancomycin.</name><description>We investigated the drug-resistant mechanisms of intracellular survival of methicillin-resistant S. aureus (MRSA). Our established MRSA clinical strain, OJ-1, with high biofilm-forming ability, and a macrophage cell line, J774A, were used. After ingestion of OJ-1 by J774A, the cells were incubated for ten days with vancomycin at doses 30 times higher than the minimum inhibitory concentration. The number of phagocytosed intracellular OJ-1 gradually decreased during the study but plateaued after day 7. In J774A cells with intracellular OJ-1, the expression of LysoTracker-positive lysosomes increased until day 5 and then declined from day 7. In contrast, LysoTracker-negative and OJ-1-retaining J774A cells became prominent from day 7, and intracellular OJ-1 also escaped from the autophagosome.</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Feb</publication><modification>2025-04-04T08:24:17.517Z</modification><creation>2025-04-04T08:24:17.517Z</creation></dates><accession>S-EPMC8874447</accession><cross_references><pubmed>35208802</pubmed><doi>10.3390/microorganisms10020348</doi></cross_references></HashMap>