Multiple triclosan targets in Trypanosoma brucei

Kimberly S. Paul, Cyrus J. Bacchi, Paul T. Englund

Research output: Contribution to journalArticle

Abstract

Trypanosoma brucei genes encoding putative fatty acid synthesis enzymes are homologous to those encoding type II enzymes found in bacteria and organelles such as chloroplasts and mitochondria. It was therefore not surprising that triclosan, an inhibitor of type II enoyl-acyl carrier protein (enoyl-ACP) reductase, killed both procyclic forms and bloodstream forms of T. brucei in culture with 50% effective concentrations (EC50S) of 10 and 13 μM, respectively. Triclosan also inhibited cell-free fatty acid synthesis, though much higher concentrations were required (EC50S of 100 to 200 μM). Unexpectedly, 100 μM triclosan did not affect the elongation of [ 3H] laurate (C12:0) to myristate (C14:0) in cultured bloodstream form parasites, suggesting that triclosan killing of trypanosomes may not be through specific inhibition of enoyl-ACP reductase but through some other mechanism. Interestingly, 100 μM triclosan did reduce the level of incorporation of [3H] myristate into glycosyl phosphatidylinositol species (GPIs). Furthermore, we found that triclosan inhibited fatty acid remodeling in a cell-free assay in the same concentration range required for killing T. brucei in culture. In addition, we found that a similar concentration of triclosan also inhibited the myristate exchange pathway, which resides in a distinct subcellular compartment. However, GPI myristoylation and myristate exchange are specific to the bloodstream form parasite, yet triclosan kills both the bloodstream and procyclic forms. Therefore, triclosan killing may be due to a nonspecific perturbation of subcellular membrane structure leading to dysfunction in sensitive membrane-resident biochemical pathways.

Original languageEnglish (US)
Pages (from-to)855-861
Number of pages7
JournalEukaryotic Cell
Volume3
Issue number4
DOIs
StatePublished - Aug 1 2004

ASJC Scopus subject areas

  • Microbiology
  • Molecular Biology

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    Paul, K. S., Bacchi, C. J., & Englund, P. T. (2004). Multiple triclosan targets in Trypanosoma brucei. Eukaryotic Cell, 3(4), 855-861. https://doi.org/10.1128/EC.3.4.855-861.2004