Enhanced fungal specificity and in vivo therapeutic efficacy of a C-22-modified FK520 analog against C. neoformans

Fungal infections cause significant morbidity and mortality globally. The therapeutic armamentarium against these infections is limited, and the development of antifungal drugs has been hindered by the evolutionary conservation between fungi and the human host. With rising resistance to the current...

Full description

Saved in:
Bibliographic Details
Published in:mBio Vol. 14; no. 5; p. e0181023
Main Authors: Rivera, Angela, Young Lim, Won, Park, Eunchong, Dome, Patrick A, Hoy, Michael J, Spasojevic, Ivan, Sun, Sheng, Averette, Anna Floyd, Pina-Oviedo, Sergio, Juvvadi, Praveen R, Steinbach, William J, Ciofani, Maria, Hong, Jiyong, Heitman, Joseph
Format: Journal Article
Language:English
Published: United States American Society for Microbiology 31-10-2023
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Fungal infections cause significant morbidity and mortality globally. The therapeutic armamentarium against these infections is limited, and the development of antifungal drugs has been hindered by the evolutionary conservation between fungi and the human host. With rising resistance to the current antifungal arsenal and an increasing at-risk population, there is an urgent need for the development of new antifungal compounds. The FK520 analogs described in this study display potent antifungal activity as a novel class of antifungals centered on modifying an existing orally active FDA-approved therapy. This research advances the development of much-needed newer antifungal treatment options with novel mechanisms of action.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:2150-7511
2150-7511
DOI:10.1128/mbio.01810-23