Journalartikel

Amidochelocardin Overcomes Resistance Mechanisms Exerted on Tetracyclines and Natural Chelocardin


AutorenlisteHennessen, Fabienne; Miethke, Marcus; Zaburannyi, Nestor; Loose, Maria; Lukezic, Tadeja; Bernecker, Steffen; Huettel, Stephan; Jansen, Rolf; Schmiedel, Judith; Fritzenwanker, Moritz; Imirzalioglu, Can; Vogel, Joerg; Westermann, Alexander J.; Hesterkamp, Thomas; Stadler, Marc; Wagenlehner, Florian; Petkovic, Hrvoje; Herrmann, Jennifer; Mueller, Rolf

Jahr der Veröffentlichung2020

ZeitschriftAntibiotics

Bandnummer9

Heftnummer9

ISSN2079-6382

Open Access StatusGold

DOI Linkhttps://doi.org/10.3390/antibiotics9090619

VerlagMDPI


Abstract
The reassessment of known but neglected natural compounds is a vital strategy for providing novel lead structures urgently needed to overcome antimicrobial resistance. Scaffolds with resistance-breaking properties represent the most promising candidates for a successful translation into future therapeutics. Our study focuses on chelocardin, a member of the atypical tetracyclines, and its bioengineered derivative amidochelocardin, both showing broad-spectrum antibacterial activity within the ESKAPE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, andEnterobacterspecies) panel. Further lead development of chelocardins requires extensive biological and chemical profiling to achieve favorable pharmaceutical properties and efficacy. This study shows that both molecules possess resistance-breaking properties enabling the escape from most common tetracycline resistance mechanisms. Further, we show that these compounds are potent candidates for treatment of urinary tract infections due to their in vitro activity against a large panel of multidrug-resistant uropathogenic clinical isolates. In addition, the mechanism of resistance to natural chelocardin was identified as relying on efflux processes, both in the chelocardin producerAmycolatopsis sulphureaand in the pathogenKlebsiella pneumoniae.Resistance development in Klebsiellaled primarily to mutations in ram R, causing increased expression of the acrAB-tol Cefflux pump. Most importantly, amidochelocardin overcomes this resistance mechanism, revealing not only the improved activity profile but also superior resistance-breaking properties of this novel antibacterial compound.



Zitierstile

Harvard-ZitierstilHennessen, F., Miethke, M., Zaburannyi, N., Loose, M., Lukezic, T., Bernecker, S., et al. (2020) Amidochelocardin Overcomes Resistance Mechanisms Exerted on Tetracyclines and Natural Chelocardin, Antibiotics, 9(9), Article 619. https://doi.org/10.3390/antibiotics9090619

APA-ZitierstilHennessen, F., Miethke, M., Zaburannyi, N., Loose, M., Lukezic, T., Bernecker, S., Huettel, S., Jansen, R., Schmiedel, J., Fritzenwanker, M., Imirzalioglu, C., Vogel, J., Westermann, A., Hesterkamp, T., Stadler, M., Wagenlehner, F., Petkovic, H., Herrmann, J., & Mueller, R. (2020). Amidochelocardin Overcomes Resistance Mechanisms Exerted on Tetracyclines and Natural Chelocardin. Antibiotics. 9(9), Article 619. https://doi.org/10.3390/antibiotics9090619



Schlagwörter


AcrAB-TolC efflux pumpACTIVATORS SOXSAMYCOLATOPSIS-SULFUREAatypical tetracyclinesbroad-spectrum antibioticschelocardinsclinical isolatesmechanism of resistancePRIMARY TARGETPUMP ACRAB-TOLCresistance-breaking propertiesURINARY-TRACT-INFECTIONSurinary tract infection (UTI)Uropathogens


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Zuletzt aktualisiert 2025-10-06 um 11:17