Prof. Dr. Tanja Schneider
Institute for Pharmaceutical Microbiology
tschneider@uni-bonn.de View member: Prof. Dr. Tanja Schneider
The ISME journal
Many bacteria produce antimicrobial compounds such as lantibiotics to gain advantage in the competitive natural environments of microbiomes. Epilancins constitute an until now underexplored family of lantibiotics with an unknown ecological role and unresolved mode of action. We discovered production of an epilancin in the nasal isolate Staphylococcus epidermidis A37. Using bioinformatic tools, we found that epilancins are frequently encoded within staphylococcal genomes, highlighting their ecological relevance. We demonstrate that production of epilancin A37 contributes to S. epidermidis competition specifically against natural corynebacterial competitors. Combining microbiological approaches with quantitative in vivo and in vitro fluorescence microscopy and cryo-electron tomography, we show that A37 enters the corynebacterial cytoplasm through a partially transmembrane-potential driven uptake without impairing the cell membrane function. Upon intracellular aggregation, A37 induces the formation of intracellular membrane vesicles, which are heavily loaded with the compound and are essential for the antibacterial activity of the epilancin. Our work sheds light on the ecological role of epilancins for staphylococci mediated by a mode of action previously unknown for lantibiotics.
© The Author(s) [2024]. Published by Oxford University Press on behalf of the International Society for Microbial Ecology.
PMID: 38470311
Institute for Pharmaceutical Microbiology
tschneider@uni-bonn.de View member: Prof. Dr. Tanja SchneiderMedical Microbiology, Immunology and Parasitology
View member: Prof. Hans-Georg Sahl