Open AccessIn Vitro Efficacies of Nitazoxanide and Other Thiazolides againstNeospora caninumTachyzoites Reveal Antiparasitic Activity Independent of the Nitro Group
Author(s) -
Marco Esposito,
Rebecca Stettler,
Shelley L. Moores,
Chandrakala Pidathala,
Norbert Müller,
Andrew V. Stachulski,
Neil G. Berry,
Jean–François Rossignol,
Andrew Hemphill
Publication year - 2005
Publication title -
antimicrobial agents and chemotherapy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.07
H-Index - 259
eISSN - 1070-6283
pISSN - 0066-4804
DOI - 10.1128/aac.49.9.3715-3723.2005
Subject(s) - nitazoxanide , neospora caninum , biology , oxidoreductase , antiparasitic , antiparasitic agent , nitrofuran , thiazole , nitro , microbiology and biotechnology , stereochemistry , toxoplasma gondii , chemistry , biochemistry , pharmacology , enzyme , immunology , medicine , genetics , alkyl , organic chemistry , pathology , antibody
The thiazolide nitazoxanide [2-acetolyloxy-N-(5-nitro-2-thiazolyl)benzamide] (NTZ) exhibits a broad spectrum of activities against a wide variety of intestinal and tissue-dwelling helminths, protozoa, and enteric bacteria infecting animals and humans. The drug has been postulated to act via reduction of its nitro group by nitroreductases, including pyruvate ferredoxin oxidoreductase. In this study, we investigated the efficacies of nitazoxanide and a number of other thiazolides against Neospora caninum tachyzoites in vitro. We employed real-time-PCR-based monitoring of tachyzoite adhesion, invasion, and intracellular proliferation, as well as electron microscopic visualization of the effects imposed by nitazoxanide. In addition, we investigated several modified versions of this drug. These modifications included on one hand the replacement of the nitro group on the thiazole ring with a bromide, thus removing the most reactive group, and on the other hand the differential positioning of methyl groups on the salicylate ring. We show that the thiazole-associated nitro group is not necessarily required for the action of the drug and that methylation of the salicylate ring can result in complete abrogation of the antiparasitic activity, depending on the positioning of the methyl group. These findings indicate that other mechanisms besides the proposed mode of action involving the pyruvate ferredoxin oxidoreductase enzyme could be responsible for the wide spectrum of antiparasitic activity of NTZ and that modifications in the benzene ring could be important in these alternative mechanisms.