| Literature DB >> 26055366 |
Vito Valiante1, Maria Cândida Monteiro2, Jesús Martín2, Robert Altwasser3, Noureddine El Aouad2, Ignacio González2, Olaf Kniemeyer4, Emilia Mellado5, Sara Palomo2, Nuria de Pedro2, Ignacio Pérez-Victoria2, José R Tormo2, Francisca Vicente2, Fernando Reyes6, Olga Genilloud6, Axel A Brakhage7.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2015 PMID: 26055366 PMCID: PMC4538548 DOI: 10.1128/AAC.00683-15
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191