Fungal infections have increased dramatically in the last 2 decades, and fighting infectious diseases requires innovative approaches such as the combination of two drugs acting on different targets or even targeting a salvage pathway of one of the drugs. The fungal cell wall biosynthesis is inhibited by the clinically used antifungal drug caspofungin. This antifungal activity has been found to be potentiated by humidimycin, a new natural product identified from the screening of a collection of 20,000 microbial extracts, which has no major effect when used alone. An analysis of transcriptomes and selected Aspergillus fumigatus mutants indicated that humidimycin affects the high osmolarity glycerol response pathway. By combining humidimycin and caspofungin, a strong increase in caspofungin efficacy was achieved, demonstrating that targeting different signaling pathways provides an excellent basis to develop novel anti-infective strategies.
Hitting the caspofungin salvage pathway of human-pathogenic fungi with the novel lasso peptide humidimycin (MDN-0010).
利用新型套索肽 humidimycin (MDN-0010) 攻击人类致病真菌的卡泊芬净补救途径
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作者:Valiante Vito, Monteiro Maria Cândida, MartÃn Jesús, Altwasser Robert, El Aouad Noureddine, González Ignacio, Kniemeyer Olaf, Mellado Emilia, Palomo Sara, de Pedro Nuria, Pérez-Victoria Ignacio, Tormo José R, Vicente Francisca, Reyes Fernando, Genilloud Olga, Brakhage Axel A
| 期刊: | Antimicrobial Agents and Chemotherapy | 影响因子: | 4.500 |
| 时间: | 2015 | 起止号: | 2015 Sep;59(9):5145-53 |
| doi: | 10.1128/AAC.00683-15 | 研究方向: | 微生物学 |
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