Genetics, Vol. 152, 167-178, May 1999, Copyright © 1999

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. Perfecta
a 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

Topisomerase I is the target of several toxins and chemotherapy agents, and the enzyme is essential for viability in some organisms, including mice and drosophila. We have cloned the TOP1 gene encoding topoisomerase I from the opportunistic fungal pathogen Cryptococcus neoformans. The C. neoformans topoisomerase I contains a fungal insert also found in topoisomerase I from Candida albicans and Saccharomyces cerevisiae that is not present in the mammalian enzyme. We were unable to disrupt the topoisomerase I gene in this haploid organism by homologous recombination in over 8000 transformants analyzed. When a second functional copy of the TOP1 gene was introduced into the genome, the topoisomerase I gene could be readily disrupted by homologous recombination (at 7% efficiency). Thus, topoisomerase I is essential in C. neoformans. This new molecular strategy with C. neoformans may also be useful in identifying essential genes in other pathogenic fungi. To address the physiological and pathobiological functions of the enzyme, the TOP1 gene was fused to the GAL7 gene promoter. The resulting GAL7::TOP1 fusion gene was modestly regulated by carbon source in a serotype A strain of C. neoformans. Modest overexpression of topoisomerase I conferred sensitivity to heat shock, {gamma}-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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