Journal
JOURNAL OF INFECTIOUS DISEASES
Volume 183, Issue 7, Pages 1093-1099Publisher
UNIV CHICAGO PRESS
DOI: 10.1086/319272
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Funding
- NHLBI NIH HHS [HL-59842] Funding Source: Medline
- NIAID NIH HHS [AI-01489, AI-13342, AI-22774] Funding Source: Medline
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Cryptococcus neoformans is a major fungal pathogen and is a relatively common cause of life-threatening meningoencephalitis. Glyphosate is a widely used herbicide that inhibits the synthesis of aromatic amino acids via the shikimate acid pathway. This study investigated the effects of glyphosate on C. neoformans growth, melanization, and murine infection. C. neoformans was relatively resistant to glyphosate, requiring concentrations >250 mg/mL for inhibition. Melanization of C. neoformans in the presence of L-dopa was inhibited by subinhibitory concentrations of glyphosate. Glyphosate inhibited autopolymerization of L-dopa and oxidation of L-epinephrine by cryptococcal cells, which is mediated by a laccase. Administration of glyphosate to mice infected with C. neoformans delayed melanization of yeast cells in vivo and prolonged average mouse survival. The results suggest that inhibition of melanization in vivo may facilitate control of C. neoformans infection.
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