New Insight into Amphotericin B Resistance in Aspergillus terreus
Author(s) -
Gerhard Blum,
Caroline Hörtnagl,
Emina Jukic,
Thomas Erbeznik,
Thomas Pümpel,
Hermann Dietrich,
Markus Nagl,
Cornelia Speth,
Günter Rambach,
Cornelia LassFlörl
Publication year - 2013
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.01283-12
Subject(s) - aspergillus terreus , ergosterol , amphotericin b , microbiology and biotechnology , intracellular , biology , in vivo , in vitro , efflux , drug resistance , biochemistry , antifungal
Amphotericin B (AMB) is the predominant antifungal drug, but the mechanism of resistance is not well understood. We compared thein vivo virulence of an AMB-resistantAspergillus terreus (ATR) isolate with that of an AMB-susceptibleA. terreus isolate (ATS) using a murine model for disseminated aspergillosis. Furthermore, we analyzed the molecular basis of intrinsic AMB resistancein vitro by comparing the ergosterol content, cell-associated AMB levels, AMB-induced intracellular efflux, and prooxidant effects between ATR and ATS. Infection of immunosuppressed mice with ATS or ATR showed that the ATS strain was more lethal than the ATR strain. However, AMB treatment improved the outcome in ATS-infected mice while having no positive effect on the animals infected with ATR. Thein vitro data demonstrated that ergosterol content is not the molecular basis for AMB resistance. ATR absorbed less AMB, discharged more intracellular compounds, and had better protection against oxidative damage than the susceptible strain. Our experiments showed that ergosterol content plays a minor role in intrinsic AMB resistance and is not directly associated with intracellular cell-associated AMB content. AMB might exert its antifungal activity by oxidative injury rather than by an increase in membrane permeation.
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