<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Bertrand BP</submitter><funding>NIAID NIH HHS</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>e0042822</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9670962</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>90(11)</volume><pubmed_abstract>Biofilms are bacterial communities characterized by antibiotic tolerance. Staphylococcus aureus is a leading cause of biofilm infections on medical devices, including prosthetic joints, which represent a significant health care burden. The major leukocyte infiltrate associated with S. aureus prosthetic joint infection (PJI) is granulocytic myeloid-derived suppressor cells (G-MDSCs), which produce IL-10 to promote biofilm persistence by inhibiting monocyte and macrophage proinflammatory activity. To determine how S. aureus biofilm responds to G-MDSCs and macrophages, biofilms were cocultured with either leukocyte population followed by RNA sequencing. Several genes involved in fermentative pathways were significantly upregulated in S. aureus biofilm following G-MDSC coculture, including for</pubmed_abstract><journal>Infection and immunity</journal><pubmed_title>Role of Staphylococcus aureus Formate Metabolism during Prosthetic Joint Infection.</pubmed_title><pmcid>PMC9670962</pmcid><funding_grant_id>P30 CA036727</funding_grant_id><funding_grant_id>P30 GM110768</funding_grant_id><funding_grant_id>P20 GM103427</funding_grant_id><funding_grant_id>P01 AI083211</funding_grant_id><funding_grant_id>R01 AI125588</funding_grant_id><pubmed_authors>West SC</pubmed_authors><pubmed_authors>Ali H</pubmed_authors><pubmed_authors>Heim CE</pubmed_authors><pubmed_authors>Thomas VC</pubmed_authors><pubmed_authors>Kielian T</pubmed_authors><pubmed_authors>Bertrand BP</pubmed_authors><pubmed_authors>Chaudhari SS</pubmed_authors></additional><is_claimable>false</is_claimable><name>Role of Staphylococcus aureus Formate Metabolism during Prosthetic Joint Infection.</name><description>Biofilms are bacterial communities characterized by antibiotic tolerance. Staphylococcus aureus is a leading cause of biofilm infections on medical devices, including prosthetic joints, which represent a significant health care burden. The major leukocyte infiltrate associated with S. aureus prosthetic joint infection (PJI) is granulocytic myeloid-derived suppressor cells (G-MDSCs), which produce IL-10 to promote biofilm persistence by inhibiting monocyte and macrophage proinflammatory activity. To determine how S. aureus biofilm responds to G-MDSCs and macrophages, biofilms were cocultured with either leukocyte population followed by RNA sequencing. Several genes involved in fermentative pathways were significantly upregulated in S. aureus biofilm following G-MDSC coculture, including for</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Nov</publication><modification>2026-06-13T06:16:14.778Z</modification><creation>2025-04-06T14:10:09.067Z</creation></dates><accession>S-EPMC9670962</accession><cross_references><pubmed>36286525</pubmed><doi>10.1128/iai.00428-22</doi></cross_references></HashMap>