{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T21:47:28Z","timestamp":1791323248271,"version":"4.3.1"},"reference-count":55,"publisher":"Portland Press Ltd.","issue":"1","content-domain":{"domain":["portlandpress.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2014,2,1]]},"abstract":"<jats:p>Mycolactone is a polyketide macrolide lipid-like secondary metabolite synthesized by Mycobacterium ulcerans, the causative agent of BU (Buruli ulcer), and is the only virulence factor for this pathogen identified to date. Prolonged exposure to high concentrations of mycolactone is cytotoxic to diverse mammalian cells (albeit with varying efficiency), whereas at lower doses it has a spectrum of immunosuppressive activities. Combined, these pleiotropic properties have a powerful influence on local and systemic cellular function that should explain the pathophysiology of BU disease. The last decade has seen significant advances in our understanding of the molecular mechanisms underlying these effects in a range of different cell types. The present review focuses on the current state of our knowledge of mycolactone function, and its molecular and cellular targets, and seeks to identify commonalities between the different functional and cellular systems. Since mycolactone influences fundamental cellular processes (cell division, cell death and inflammation), getting to the root of how mycolactone achieves this could have a profound impact on our understanding of eukaryotic cell biology.<\/jats:p>","DOI":"10.1042\/bst20130133","type":"journal-article","created":{"date-parts":[[2014,1,23]],"date-time":"2014-01-23T12:09:46Z","timestamp":1390478986000},"page":"177-183","update-policy":"https:\/\/doi.org\/10.1042\/crossmark_policy","source":"Crossref","is-referenced-by-count":51,"title":["Pleiotropic molecular effects of the<i>Mycobacterium ulcerans<\/i>virulence factor mycolactone underlying the cell death and immunosuppression seen in Buruli ulcer"],"prefix":"10.1042","volume":"42","author":[{"given":"Belinda","family":"Hall","sequence":"first","affiliation":[{"name":"Department of Microbial and Cellular Sciences, Institute of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey GU2 7XH, U.K."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rachel","family":"Simmonds","sequence":"additional","affiliation":[{"name":"Department of Microbial and Cellular Sciences, Institute of Biosciences and Medicine, Faculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey GU2 7XH, U.K."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"288","published-online":{"date-parts":[[2014,1,23]]},"reference":[{"key":"2021111720033495000_B1","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.det.2010.09.006","article-title":"Buruli ulcer: advances in understanding Mycobacterium ulcerans infection","volume":"29","author":"Walsh","year":"2011","journal-title":"Dermatol. 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