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Antimicrobial Agents and Chemotherapy, January 2006, p. 162-170, Vol. 50, No. 1
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.1.162-170.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.

In Vitro Effects of Thiazolides on Giardia lamblia WB Clone C6 Cultured Axenically and in Coculture with Caco2 Cells

Joachim Müller,1* Géraldine Rühle,1 Norbert Müller,1 Jean-François Rossignol,2 and Andrew Hemphill1,2*

Institute of Parasitology, University of Bern, Länggass-Strasse 122, CH-3012 Bern, Switzerland,1 The Romark Institute for Medical Research, Tampa, Florida 336072

Received 21 September 2005/ Returned for modification 12 October 2005/ Accepted 18 October 2005

The thiazolides represent a novel class of anti-infective drugs, with the nitrothiazole nitazoxanide [2-acetolyloxy-N-(5-nitro 2-thiazolyl) benzamide] (NTZ) as the parent compound. NTZ exhibits a broad spectrum of activities against a wide variety of helminths, protozoa, and enteric bacteria infecting animals and humans. In vivo, NTZ is rapidly deacetylated to tizoxanide (TIZ), which exhibits similar activities. We have here comparatively investigated the in vitro effects of NTZ, TIZ, a number of other modified thiazolides, and metronidazole (MTZ) on Giardia lamblia trophozoites grown under axenic culture conditions and in coculture with the human cancer colon cell line Caco2. The modifications of the thiazolides included, on one hand, the replacement of the nitro group on the thiazole ring with a bromide, and, on the other hand, the differential positioning of methyl groups on the benzene ring. Of seven compounds with a bromo instead of a nitro group, only one, RM4820, showed moderate inhibition of Giardia proliferation in axenic culture, but not in coculture with Caco2 cells, with a 50% inhibitory concentration (IC50) of 18.8 µM; in comparison, NTZ and tizoxanide had IC50s of 2.4 µM, and MTZ had an IC50 of 7.8 µM. Moreover, the methylation or carboxylation of the benzene ring at position 3 resulted in a significant decrease of activity, and methylation at position 5 completely abrogated the antiparasitic effect of the nitrothiazole compound. Trophozoites treated with NTZ showed distinct lesions on the ventral disk as soon as 2 to 3 h after treatment, whereas treatment with metronidazole resulted in severe damage to the dorsal surface membrane at later time points.


* Corresponding author. Mailing address: Institute of Parasitology, University of Bern, Länggass-Strasse 122, CH-3012 Bern, Switzerland. Phone: 41 31 6312384. Fax: 41 31 6312477. E-mail for Andrew Hemphill: hemphill{at}ipa.unibe.ch. E-mail for Joachim Müller: joachim.mueller{at}ipa.unibe.ch.


Antimicrobial Agents and Chemotherapy, January 2006, p. 162-170, Vol. 50, No. 1
0066-4804/06/$08.00+0     doi:10.1128/AAC.50.1.162-170.2006
Copyright © 2006, American Society for Microbiology. All Rights Reserved.




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