<?xml version="1.0" encoding="UTF-8"?><rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcq="http://purl.org/dc/terms/"><records count="1" morepages="false" start="1" end="1"><record rownumber="1"><dc:product_type>Journal Article</dc:product_type><dc:title>Responses to chemical cross-talk between the Mycobacterium ulcerans toxin, mycolactone, and Staphylococcus aureus</dc:title><dc:creator>Dhungel, Laxmi; Burcham, Lindsey; Park, Joo Youn; Sampathkumar, Harshini Devi; Cudjoe, Albert; Seo, Keun Seok; Jordan, Heather</dc:creator><dc:corporate_author/><dc:editor>null</dc:editor><dc:description>Abstract                          Buruli ulcer is a neglected tropical disease caused by the environmental pathogen,              Mycobacterium ulcerans              whose major virulence factor is mycolactone, a lipid cytotoxic molecule. Buruli ulcer has high morbidity, particularly in rural West Africa where the disease is endemic. Data have shown that infected lesions of Buruli ulcer patients can be colonized by quorum sensing bacteria such as              Staphylococcus aureus, S. epidermidis,              and              Pseudomonas aeruginosa              , but without typical pathology associated with those pathogens’ colonization.              M. ulcerans              pathogenesis may not only be an individual act but may also be dependent on synergistic or antagonistic mechanisms within a polymicrobial network. Furthermore, co-colonization by these pathogens may promote delayed wound healing, especially after the initiation of antibiotic therapy. Hence, it is important to understand the interaction of              M. ulcerans              with other bacteria encountered during skin infection. We added mycolactone to              S. aureus              and incubated for 3, 6 and 24 h. At each timepoint,              S. aureus              growth and hemolytic activity was measured, and RNA was isolated to measure virulence gene expression through qPCR and RNASeq analyses. Results showed that mycolactone reduced              S. aureus              hemolytic activity, suppressed              hla              promoter activity, and attenuated virulence genes, but did not affect              S. aureus              growth              .              RNASeq data showed mycolactone greatly impacted              S. aureus              metabolism. These data are relevant and significant as mycolactone and              S. aureus              sensing and response at the transcriptional, translational and regulation levels will provide insight into biological mechanisms of interspecific interactions that may play a role in regulation of responses such as effects between              M. ulcerans              , mycolactone, and              S. aureus              virulence that will be useful for treatment and prevention.</dc:description><dc:publisher/><dc:date>2021-12-01</dc:date><dc:nsf_par_id>10253911</dc:nsf_par_id><dc:journal_name>Scientific Reports</dc:journal_name><dc:journal_volume>11</dc:journal_volume><dc:journal_issue>1</dc:journal_issue><dc:page_range_or_elocation/><dc:issn>2045-2322</dc:issn><dc:isbn/><dc:doi>https://doi.org/10.1038/s41598-021-89177-5</dc:doi><dcq:identifierAwardId>1911457</dcq:identifierAwardId><dc:subject/><dc:version_number/><dc:location/><dc:rights/><dc:institution/><dc:sponsoring_org>National Science Foundation</dc:sponsoring_org></record></records></rdf:RDF>