<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(1)</volume><submitter>Kong C</submitter><pubmed_abstract>Staphylococcus aureus is a major cause of nosocomial infections and secretes a diverse spectrum of virulence determinants as well as forms biofilm. The emergence of antibiotic-resistant S. aureus highlights the need for alternative forms of therapeutics other than conventional antibiotics. One route to meet this need is screening small molecule derivatives for potential anti-infective activity. Using a previously optimized C. elegans - S. aureus small molecule screen, we identified a benzimidazole derivative, UM-C162, which rescued nematodes from a S. aureus infection. UM-C162 prevented the formation of biofilm in a dose-dependent manner without interfering with bacterial viability. To examine the effect of UM-C162 on the expression of S. aureus virulence genes, a genome-wide transcriptome</pubmed_abstract><journal>Scientific reports</journal><pagination>2758</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5807447</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Suppression of Staphylococcus aureus biofilm formation and virulence by a benzimidazole derivative, UM-C162.</pubmed_title><pmcid>PMC5807447</pmcid><pubmed_authors>Thomas N</pubmed_authors><pubmed_authors>Abd Rahman N</pubmed_authors><pubmed_authors>Nathan S</pubmed_authors><pubmed_authors>Chee CF</pubmed_authors><pubmed_authors>Richter K</pubmed_authors><pubmed_authors>Kong C</pubmed_authors></additional><is_claimable>false</is_claimable><name>Suppression of Staphylococcus aureus biofilm formation and virulence by a benzimidazole derivative, UM-C162.</name><description>Staphylococcus aureus is a major cause of nosocomial infections and secretes a diverse spectrum of virulence determinants as well as forms biofilm. The emergence of antibiotic-resistant S. aureus highlights the need for alternative forms of therapeutics other than conventional antibiotics. One route to meet this need is screening small molecule derivatives for potential anti-infective activity. Using a previously optimized C. elegans - S. aureus small molecule screen, we identified a benzimidazole derivative, UM-C162, which rescued nematodes from a S. aureus infection. UM-C162 prevented the formation of biofilm in a dose-dependent manner without interfering with bacterial viability. To examine the effect of UM-C162 on the expression of S. aureus virulence genes, a genome-wide transcriptome</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Feb</publication><modification>2026-05-04T09:33:47.834Z</modification><creation>2019-03-26T23:02:12Z</creation></dates><accession>S-EPMC5807447</accession><cross_references><pubmed>29426873</pubmed><doi>10.1038/s41598-018-21141-2</doi></cross_references></HashMap>