| Literature DB >> 27895021 |
Sergio H Szajnman1, Tamila Galaka1, Zhu-Hong Li2, Catherine Li2, Nathan M Howell2, María N Chao1, Boris Striepen2, Vasant Muralidharan2, Silvia N J Moreno3, Juan B Rodriguez4.
Abstract
We tested a series of sulfur-containing linear bisphosphonates against Toxoplasma gondii, the etiologic agent of toxoplasmosis. The most potent compound (compound 22; 1-[(n-decylsulfonyl)ethyl]-1,1-bisphosphonic acid) is a sulfone-containing compound, which had a 50% effective concentration (EC50) of 0.11 ± 0.02 μM against intracellular tachyzoites. The compound showed low toxicity when tested in tissue culture with a selectivity index of >2,000. Compound 22 also showed high activity in vivo in a toxoplasmosis mouse model. The compound inhibited the Toxoplasma farnesyl diphosphate synthase (TgFPPS), but the concentration needed to inhibit 50% of the enzymatic activity (IC50) was higher than the concentration that inhibited 50% of growth. We tested compound 22 against two other apicomplexan parasites, Plasmodium falciparum (EC50 of 0.6 ± 0.01 μM), the agent of malaria, and Cryptosporidium parvum (EC50 of ∼65 μM), the agent of cryptosporidiosis. Our results suggest that compound 22 is an excellent novel compound that could lead to the development of potent agents against apicomplexan parasites.Entities:
Keywords: Cryptosporidium parvum; Plasmodium falciparum; Toxoplasma gondii; bisphosphonates; farnesyl diphosphate synthase; isoprenoids
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Year: 2017 PMID: 27895021 PMCID: PMC5278718 DOI: 10.1128/AAC.01590-16
Source DB: PubMed Journal: Antimicrob Agents Chemother ISSN: 0066-4804 Impact factor: 5.191