1. Academic Validation
  2. Novel Minor Groove Binders Cure Animal African Trypanosomiasis in an in Vivo Mouse Model

Novel Minor Groove Binders Cure Animal African Trypanosomiasis in an in Vivo Mouse Model

  • J Med Chem. 2019 Mar 28;62(6):3021-3035. doi: 10.1021/acs.jmedchem.8b01847.
Federica Giordani Abedawn I Khalaf 1 Kirsten Gillingwater 2 3 Jane C Munday Harry P de Koning Colin J Suckling 1 Michael P Barrett 4 Fraser J Scott 5
Affiliations

Affiliations

  • 1 Department of Pure and Applied Chemistry, WestCHEM , University of Strathclyde , Glasgow G1 1XL , U.K.
  • 2 Parasite Chemotherapy, Department of Medical Parasitology and Infection Biology , Swiss Tropical and Public Health Institute , Basel 4051 , Switzerland.
  • 3 University of Basel , Basel 4001 , Switzerland.
  • 4 Glasgow Polyomics , University of Glasgow , Glasgow G61 1QH , U.K.
  • 5 Department of Biological and Geographical Sciences, School of Applied Sciences , University of Huddersfield , Huddersfield HD1 3DH , U.K.
Abstract

Animal African trypanosomiasis (AAT) is a significant socioeconomic burden for sub-Saharan Africa because of its huge impact on livestock health. Existing therapies including those based on minor groove binders (MGBs), such as the diamidines, which have been used for decades, have now lost efficacy in some places because of the emergence of resistant parasites. Consequently, the need for new chemotherapies is urgent. Here, we describe a structurally distinct class of MGBs, Strathclyde MGBs (S-MGBs), which display excellent in vitro activities against the principal causative organisms of AAT: Trypanosoma congolense, and Trypanosoma vivax. We also show the cure of T. congolense-infected mice by a number of these compounds. In particular, we identify S-MGB-234, compound 7, as curative by using two applications of 50 mg/kg intraperitoneally. Crucially, we demonstrate that S-MGBs do not show cross-resistance with the current diamidine drugs and are not internalized via the transporters used by diamidines. This study demonstrates that S-MGBs have significant potential as novel therapeutic agents for AAT.

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