Inducible Cell Fusion Permits Use of Competitive Fitness Profiling in the Human Pathogenic Fungus Aspergillus fumigatus
Author(s) -
Darel Macdonald,
Darren D. Thomson,
Anna Johns,
Adriana Contreras Valenzuela,
Jane Mabey Gilsenan,
Kathryn M. Lord,
Paul Bowyer,
David W. Denning,
Nick D. Read,
Michael J. Bromley
Publication year - 2018
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.01615-18
Subject(s) - aspergillus fumigatus , biology , druggability , profiling (computer programming) , microbiology and biotechnology , fungus , aspergillus , fungal pathogen , yeast , filamentous fungus , computational biology , pathogen , genetics , botany , gene , computer science , operating system
Antifungal agents directed against novel therapeutic targets are required for treating invasive, chronic, and allergic Aspergillus infections. Competitive fitness profiling technologies have been used in a number of bacterial and yeast systems to identify druggable targets; however, the development of similar systems in filamentous fungi is complicated by the fact that they undergo cell fusion and heterokaryosis. Here, we demonstrate that cell fusion in Aspergillus fumigatus under standard culture conditions is not predominately constitutive, as with most ascomycetes, but can be induced by a range of extracellular stressors. Using this knowledge, we have developed a barcode-free genetic profiling system that permits high-throughput parallel determination of strain fitness in a collection of diploid A. fumigatus mutants. We show that heterozygous cyp51A and arf2 null mutants have reduced fitness in the presence of itraconazole and brefeldin A, respectively, and a heterozygous atp17 null mutant is resistant to brefeldin A.
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