{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T05:49:23Z","timestamp":1788846563312,"version":"build-2803163510"},"reference-count":55,"publisher":"Oxford University Press (OUP)","issue":"9","license":[{"start":{"date-parts":[[2024,9,1]],"date-time":"2024-09-01T00:00:00Z","timestamp":1725148800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"funder":[{"name":"Fifth Batch of National Traditional Chinese Medicine Excellent Clinical Talents Training Project"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,9,2]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Aims<\/jats:title>\n                  <jats:p>Coagulase (Coa), a crucial virulence factor of Staphylococcus aureus (S. aureus), is considered a vital target for anti-virulence strategies. The research aimed to discover a natural compound capable of inhibiting S. aureus infection by targeting the virulence factor Coa.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods and results<\/jats:title>\n                  <jats:p>The study showed that sinensetin at a concentration of 128\u2009\u03bcg mL\u22121 effectively inhibited both Coa-induced coagulation and biofilm formation in S. aureus. However, western blot results indicated that sinensetin did not impact the expression of Coa protein, suggesting that sinensetin may directly target Coa to counteract the virulence of S. aureus. Thermal shift assay results demonstrated that sinensetin enhanced the thermal stability of Coa, supporting the theory of direct binding. Molecular docking and point mutation experiments identified two key binding sites for sinensetin to Coa as R73A-Coa and R204A-Coa. In vivo studies on mice revealed that sinensetin not only reduced lung tissue damage caused by S. aureus infection, but also decreased inflammatory factors in the lung lavage fluid. Furthermore, combining sinensetin with oxacillin improved the survival rates of the Galleria mellonella and mice.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>Sinensetin is a promising natural compound that acts as a direct inhibitor of Coa against S. aureus infections.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/jambio\/lxae235","type":"journal-article","created":{"date-parts":[[2024,9,17]],"date-time":"2024-09-17T17:09:51Z","timestamp":1726592991000},"source":"Crossref","is-referenced-by-count":4,"title":["Sinensetin interferes with <i>Staphylococcus aureus<\/i> infections by targeting <i>staphylocoagulase<\/i> and improves infection survival rates in mouse model of pneumonia"],"prefix":"10.1093","volume":"135","author":[{"given":"Bin","family":"Ge","sequence":"first","affiliation":[{"name":"Changchun University of Chinese Medicine , Changchun 130117 , 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