Diverse evolutionary pathways challenge the use of collateral sensitivity as a strategy to suppress resistance
Year: 2023
Type: article
Abstract: Drug resistance remains a major obstacle to malaria control and eradication efforts, necessitating the development of novel therapeutic strategies to treat this disease. Drug combinations based on collateral sensitivity, wherein resistance to one drug causes increased sensitivity to the partner drug, have been proposed as an evolutionary strategy to suppress the emergence of resistance in pathogen populations. In this study, we explore collateral sensitivity between compounds targeting the Plasmodium dihydroorotate dehydrogenase (DHODH). We profiled the cross-resistance and collateral sensitivity phenotypes of several DHODH mutant lines to a diverse panel of DHODH inhibitors. We focus on one compound, TCMDC-125334, which was active against all mutant lines tested, including the DHODH C276Y line, which arose in selections with the clinical candidate DSM265. We found that selection of the DHODH C276Y mutant with TCMDC-125334 yielded additional genetic changes in the dhodh locus. These double mutant parasites exhibited decreased sensitivity to TCMDC-125334 and were highly resistant to DSM265. Finally, we tested whether collateral sensitivity could be exploited to suppress the emergence of resistance in the context of combination treatment by exposing wildtype parasites to both DSM265 and TCMDC-125334 simultaneously. This selected for parasites with a DHODH V532A mutation which were cross-resistant to both compounds and were as fit as the wildtype parent in vitro . The emergence of these cross-resistant, evolutionarily fit parasites highlights the mutational flexibility of the DHODH enzyme.
Source: eLife
DOI: 10.7554/elife.85023
Language: English
Topic: Malaria Research and Control
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $3,051
Funders: Bill and Melinda Gates Foundation, University of Texas Southwestern Medical Center, Harvard T.H. Chan School of Public Health, Medicines for Malaria Venture, ExxonMobil Foundation, National Institutes of Health, University of California, San Diego, National Institute of General Medical Sciences, National Institute of Allergy and Infectious Diseases
Awards: G1275747955, G1384877631, G1476237564, G1547284777, Targeting the Mitochondrion of P. falciparum, G2387613229, Illumina NovaSeq 6000 Sequencing System, G3549828030, G4523881014, G5918143493, G6154561313, Training Program in Basic and Clinical Genetics, Defining the resistome in P. falciparum: evolution and mechanism
OpenAlex ID: W4386945231
