| Literature DB >> 33431834 |
Janette Reader1, Mariëtte E van der Watt1, Dale Taylor2, Claire Le Manach2, Nimisha Mittal3, Sabine Ottilie3, Anjo Theron4, Phanankosi Moyo1, Erica Erlank5, Luisa Nardini5, Nelius Venter5, Sonja Lauterbach6, Belinda Bezuidenhout6, Andre Horatscheck2, Ashleigh van Heerden1, Natalie J Spillman7, Anne N Cowell3, Jessica Connacher1, Daniel Opperman1, Lindsey M Orchard8, Manuel Llinás8,9, Eva S Istvan7, Daniel E Goldberg7, Grant A Boyle2, David Calvo10, Dalu Mancama4, Theresa L Coetzer6, Elizabeth A Winzeler3, James Duffy11, Lizette L Koekemoer5, Gregory Basarab2, Kelly Chibale2,12, Lyn-Marié Birkholtz13.
Abstract
Chemical matter is needed to target the divergent biology associated with the different life cycle stages of Plasmodium. Here, we report the parallel de novo screening of the Medicines for Malaria Venture (MMV) Pandemic Response Box against Plasmodium asexual and liver stage parasites, stage IV/V gametocytes, gametes, oocysts and as endectocides. Unique chemotypes were identified with both multistage activity or stage-specific activity, including structurally diverse gametocyte-targeted compounds with potent transmission-blocking activity, such as the JmjC inhibitor ML324 and the antitubercular clinical candidate SQ109. Mechanistic investigations prove that ML324 prevents histone demethylation, resulting in aberrant gene expression and death in gametocytes. Moreover, the selection of parasites resistant to SQ109 implicates the druggable V-type H+-ATPase for the reduced sensitivity. Our data therefore provides an expansive dataset of compounds that could be redirected for antimalarial development and also point towards proteins that can be targeted in multiple parasite life cycle stages.Entities:
Year: 2021 PMID: 33431834 DOI: 10.1038/s41467-020-20629-8
Source DB: PubMed Journal: Nat Commun ISSN: 2041-1723 Impact factor: 14.919