<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(4)</volume><submitter>Yousuf B</submitter><funding>Canadian Blood Services</funding><funding>Health Canada</funding><pubmed_abstract>&lt;i>Staphylococcus epidermidis&lt;/i> is one of the predominant bacterial contaminants in platelet concentrates (PCs), a blood component used to treat bleeding disorders. PCs are a unique niche that triggers biofilm formation, the main pathomechanism of &lt;i>S. epidermidis&lt;/i> infections. We performed whole genome sequencing of four &lt;i>S. epidermidis&lt;/i> strains isolated from skin of healthy human volunteers (AZ22 and AZ39) and contaminated PCs (ST10002 and ST11003) to unravel phylogenetic relationships and decipher virulence mechanisms compared to 24 complete &lt;i>S. epidermidis&lt;/i> genomes in GenBank. AZ39 and ST11003 formed a separate unique lineage with strains 14.1 .R1 and SE95, while AZ22 formed a cluster with 1457 and ST10002 closely grouped with FDAAGOS_161. The four isolates were assigned</pubmed_abstract><journal>Access microbiology</journal><pagination>000780.v3</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11083402</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparative virulome analysis of four Staphylococcus epidermidis strains from human skin and platelet concentrates using whole genome sequencing.</pubmed_title><pmcid>PMC11083402</pmcid><pubmed_authors>Flint A</pubmed_authors><pubmed_authors>Weedmark K</pubmed_authors><pubmed_authors>Pagotto F</pubmed_authors><pubmed_authors>Ramirez-Arcos S</pubmed_authors><pubmed_authors>Yousuf B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative virulome analysis of four Staphylococcus epidermidis strains from human skin and platelet concentrates using whole genome sequencing.</name><description>&lt;i>Staphylococcus epidermidis&lt;/i> is one of the predominant bacterial contaminants in platelet concentrates (PCs), a blood component used to treat bleeding disorders. PCs are a unique niche that triggers biofilm formation, the main pathomechanism of &lt;i>S. epidermidis&lt;/i> infections. We performed whole genome sequencing of four &lt;i>S. epidermidis&lt;/i> strains isolated from skin of healthy human volunteers (AZ22 and AZ39) and contaminated PCs (ST10002 and ST11003) to unravel phylogenetic relationships and decipher virulence mechanisms compared to 24 complete &lt;i>S. epidermidis&lt;/i> genomes in GenBank. AZ39 and ST11003 formed a separate unique lineage with strains 14.1 .R1 and SE95, while AZ22 formed a cluster with 1457 and ST10002 closely grouped with FDAAGOS_161. The four isolates were assigned</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024</publication><modification>2026-06-01T17:16:18.671Z</modification><creation>2025-07-25T03:08:07.539Z</creation></dates><accession>S-EPMC11083402</accession><cross_references><pubmed>38737800</pubmed><doi>10.1099/acmi.0.000780.v3</doi></cross_references></HashMap>