| Literature DB >> 34643906 |
Katharina Röltgen1, Gerd Pluschke2,3.
Abstract
The acquisition by a Mycobacterium marinum-like progenitor of a plasmid encoding enzymes for the biosynthesis of the highly potent macrolide toxin mycolactone has set off the evolution of M. ulcerans toward a new mycobacterial species. While the selective advantage of producing mycolactone for survival in environmental niche(s) of the pathogen is unclear, there is no doubt that the cytotoxic, immunomodulatory, and analgesic properties of mycolactone are key for the establishment and progression of M. ulcerans infections in the host. Improved procedures for the isolation, handling, and detection of the amphiphilic and light-sensitive toxin have facilitated studies to unravel molecular mechanisms of mycolactone action on host cells in vitro and on cellular and immune responses in animal models. The pivotal role of mycolactone in the pathology of Buruli ulcer and the fact that the toxin has not been associated with other pathogens make it an ideal target for therapeutics/vaccines aiming at mycolactone neutralization and for the development of assays for the diagnosis of the disease.Entities:
Keywords: Apoptosis; Buruli ulcer; Mycobacterium ulcerans disease; Mycolactone
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Year: 2022 PMID: 34643906 DOI: 10.1007/978-1-0716-1779-3_11
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745