Veterinary trypanocidal benzoxaboroles are peptidase-activated prodrugs

• Published in: PLoS pathogens Vol. 16; no. 11; p. e1008932
• Main Authors: Giordani, Federica, Paape, Daniel, Vincent, Isabel M., Pountain, Andrew W., Fernández-Cortés, Fernando, Rico, Eva, Zhang, Ning, Morrison, Liam J., Freund, Yvonne, Witty, Michael J., Peter, Rosemary, Edwards, Darren Y., Wilkes, Jonathan M., van der Hooft, Justin J. J., Regnault, Clément, Read, Kevin D., Horn, David, Field, Mark C., Barrett, Michael P.
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 03.11.2020; Public Library of Science (PLoS)
• Subjects: Aldehyde dehydrogenase; Aldehydes; Analysis; Animals; Biology and Life Sciences; Boron Compounds - metabolism; Carboxylic Acids - metabolism; Carboxypeptidase; Carboxypeptidases - metabolism; Chemical compounds; Chemical properties; Chromosome 10; Chromosomes; Cloning; Dosage and administration; Drug dosages; Drug Resistance; Drug therapy; Drugs; Enzyme activation; Female; Forecasts and trends; Gene sequencing; Genes; Genomes; Identification and classification; Infectious diseases; Influence; Livestock; Metabolism; Metabolomics; Methionine; Methylation; Mice; Nucleotide sequence; Parasitemia - veterinary; Parasites; Peptidase; Peptidases; Peptides; Physical Sciences; Prodrugs; Prodrugs - metabolism; Proteases; Protozoan Proteins - metabolism; Research and Analysis Methods; RNA processing; Serine; Serine carboxypeptidase; Splicing; Synteny; Trypanocidal Agents - metabolism; Trypanosoma; Trypanosoma brucei brucei - drug effects; Trypanosoma brucei brucei - enzymology; Trypanosoma congolense - drug effects; Trypanosoma congolense - enzymology; Trypanosoma vivax - drug effects; Trypanosoma vivax - enzymology; Trypanosomiasis, African - drug therapy; Trypanosomiasis, African - parasitology; Trypanosomiasis, African - veterinary; Valine - analogs & derivatives; Valine - metabolism; Veterinary research; Whole genome sequencing; United Kingdom
• ISSN: 1553-7374; 1553-7366; 1553-7374
• DOI: 10.1371/journal.ppat.1008932

Livestock diseases caused by Trypanosoma congolense , T . vivax and T . brucei , collectively known as nagana, are responsible for billions of dollars in lost food production annually. There is an urgent need for novel therapeutics. Encouragingly, promising antitrypanosomal benzoxaboroles are under veterinary development. Here, we show that the most efficacious subclass of these compounds are prodrugs activated by trypanosome serine carboxypeptidases (CBPs). Drug-resistance to a development candidate, AN11736, emerged readily in T . brucei , due to partial deletion within the locus containing three tandem copies of the CBP genes. T . congolense parasites, which possess a larger array of related CBPs , also developed resistance to AN11736 through deletion within the locus. A genome-scale screen in T . brucei confirmed CBP loss-of-function as the primary mechanism of resistance and CRISPR-Cas9 editing proved that partial deletion within the locus was sufficient to confer resistance. CBP re-expression in either T . brucei or T . congolense AN11736-resistant lines restored drug-susceptibility. CBPs act by cleaving the benzoxaborole AN11736 to a carboxylic acid derivative, revealing a prodrug activation mechanism. Loss of CBP activity results in massive reduction in net uptake of AN11736, indicating that entry is facilitated by the concentration gradient created by prodrug metabolism.