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Identification and Characterization of an Endo/exonuclease in Pneumocystis carinii that is Inhibited by Dicationic Diarylfurans with Efficacy Against Pneumocystis Pneumonia
Author(s) -
Hildebrandt Ellen,
Boykin David W.,
Kumar Arvind,
Tidwell Richard R.,
Dykstra Christine C.
Publication year - 1998
Publication title -
journal of eukaryotic microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.067
H-Index - 77
eISSN - 1550-7408
pISSN - 1066-5234
DOI - 10.1111/j.1550-7408.1998.tb05078.x
Subject(s) - pneumocystis carinii , biology , cryptococcus neoformans , in vivo , nuclease , dna , exonuclease , microbiology and biotechnology , candida albicans , biochemistry , virology , pneumocystis jirovecii , dna polymerase , genetics , human immunodeficiency virus (hiv)
ABSTRACT Dicationic diarylfurans and dicationic carbazoles are under development as therapeutic agents against opportunistic infections. While their ability to bind to the minor groove of DNA has been established, the complete mechanism of action has not. We demonstrate here that an effective diarylfuran, 2,5‐bis[4‐(N‐isopropylguanyl)phenyl]furan. inhibits an endo/exonuclease activity present in Pneumocystis carinii, Cryptococcus neoformans, Candida albicans , and Saccharomyces cerevisiae. This activity was purified from the particulate fraction of P. carinii. The enzyme requires Mg ++ or Mn ++ , and shows preferences for single‐ over double stranded DNA and for AT‐rich over GC‐rich domains. A panel of 12 dicationic diarylfurans and eight dicationic carbazoles, previously synthesized, were evaluated for inhibition of the purified nuclease and for efficacy against Pneumocystis pneumonia in rats. Among the diarylfurans, potency of nuclease inhibition, in vivo antimicrobial activity, and DNA binding strength were all strongly correlated (p < 0.001). These findings suggest that one target for antimicrobial action of the diarylfurans may be a nucleolytic or other event requiring unpairing of DNA strands. Dicationic carbazoles which were strong nuclease inhibitors all displayed anti‐ Pneumocystis activity in vivo, but there were also noninhibitory carbazoles with in vivo efficacy.