{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,27]],"date-time":"2026-05-27T18:54:05Z","timestamp":1779908045138,"version":"3.53.1"},"reference-count":52,"publisher":"Oxford University Press (OUP)","issue":"10","license":[{"start":{"date-parts":[[2023,10,1]],"date-time":"2023-10-01T00:00:00Z","timestamp":1696118400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/journals\/pages\/open_access\/funder_policies\/chorus\/standard_publication_model"}],"funder":[{"name":"Science and Technology Development Plan Project","award":["20190103080JH"],"award-info":[{"award-number":["20190103080JH"]}]},{"name":"Science and Technology Project","award":["JJKH20230985KJ"],"award-info":[{"award-number":["JJKH20230985KJ"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2023,10,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n               <jats:sec>\n                  <jats:title>Aims<\/jats:title>\n                  <jats:p>Disabling bacterial virulence with small molecules has been proposed as a potential strategy to prevent bacterial pathogenicity. The von Willebrand factor-binding protein of Staphylococcus aureus was identified previously as a key virulence determinant. Our objective was to discover a von Willebrand-factor binding protein (vWbp) inhibitor distinct from the antibiotics used to prevent infections resulting from S. aureus.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Methods and results<\/jats:title>\n                  <jats:p>Using coagulation assays, we found that the sesquiterpene trilactone bilobalide blocks coagulation mediated by vWbp, but has no impact on the growth of S. aureus at a concentration of 128\u00a0\u03bcg ml\u22121. Moreover, a mouse model of pneumonia caused by S. aureus indicated that bilobalide could attenuate S. aureus virulence in vivo. This effect is achieved not by interfering with the expression of vWbp but by binding to vWbp, as demonstrated by western blotting, thermal shift assays, and fluorescence quenching assays. Using molecular dynamic simulations and point mutagenesis analysis, we identified that the Q17A and R453A residues are key residues for the binding of bilobalide to vWbp.<\/jats:p>\n               <\/jats:sec>\n               <jats:sec>\n                  <jats:title>Conclusions<\/jats:title>\n                  <jats:p>Overall, we tested the ability of bilobalide to inhibit S. aureus infections by targeting vWbp and explored the potential mechanism of this activity.<\/jats:p>\n               <\/jats:sec>","DOI":"10.1093\/jambio\/lxad233","type":"journal-article","created":{"date-parts":[[2023,10,14]],"date-time":"2023-10-14T01:55:48Z","timestamp":1697248548000},"source":"Crossref","is-referenced-by-count":1,"title":["Inhibitory effect of bilobalide on <i>Staphylococcus aureus<\/i> von Willebrand factor-binding protein and its therapeutic effect in mice with pneumonia"],"prefix":"10.1093","volume":"134","author":[{"given":"Juan","family":"Hou","sequence":"first","affiliation":[{"name":"College of Integrated Traditional Chinese and Western Medicine, Changchun University of Chinese Medicine , Changchun 130017 , China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yijing","family":"Jiang","sequence":"additional","affiliation":[{"name":"College of Integrated Traditional Chinese and Western Medicine, Changchun University of Chinese Medicine , Changchun 130017 , China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yangming","family":"Xu","sequence":"additional","affiliation":[{"name":"College of Integrated Traditional Chinese and Western Medicine, Changchun University of Chinese Medicine , Changchun 130017 , China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chunhui","family":"Zhao","sequence":"additional","affiliation":[{"name":"College of Integrated Traditional Chinese and Western 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