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Topoisomerase I Is Essential in Cryptococcus neoformans: Role in Pathobiology and as an Antifungal Target
Maurizio Del Poetaa,e, Dena L. Toffalettia, Thomas H. Rudea, Christine C. Dykstraf, Joseph Heitmana,b,c,d, and John R. Perfectaa Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710,
b Department of Genetics, Duke University Medical Center, Durham, North Carolina 27710,
c Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, North Carolina 27710,
d Howard Hughes Medical Institute, Duke University Medical Center, Durham, North Carolina 27710,
e Institute of Infectious Diseases and Public Health, University of Ancona, 60121 Ancona, Italy
f Department of Pathobiology, Auburn University, Auburn, Alabama 36849
Corresponding author: John R. Perfect, Department of Medicine, Division of Infectious Diseases and International Health, Duke University Medical Center, P.O. Box 3353, Durham, NC 27710., perfe001{at}mc.duke.edu (E-mail)
Communicating editor: A. P. MITCHELL
-rays, and camptothecin. In contrast, alterations in topoisomerase I levels had no effect on the toxicity of a novel class of antifungal agents, the dicationic aromatic compounds (DACs), indicating that topoisomerase I is not the target of DACs. In an animal model of cryptococcal meningitis, topoisomerase I regulation was not critically important to established infection, but may impact on the initial stress response to infection. In summary, our studies reveal that topoisomerase I is essential in the human pathogen C. neoformans and represents a novel target for antifungal agents.
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