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Understanding the Development of Compensatory Pathways in a Mutant Malaria Parasite Harbouring Hypomorphic Allele of Plant-Like Kinases
Published on: November 22, 2024
Gene encoding a deubiquitinating enzyme is mutated in artesunate- and chloroquine-resistant rodent malaria parasites
Paul Hunt1, Ana Afonso, Alison Creasey
1Institute for Immunology and Infection Research, School of Biological Sciences, University of Edinburgh, Ashworth Laboratory, Kings Buildings, Edinburgh EH9 3JT, UK. Paul.Hunt@ed.ac.uk
Abstract:
Artemisinin- and artesunate-resistant Plasmodium chabaudi mutants, AS-ART and AS-ATN, were previously selected from chloroquine-resistant clones AS-30CQ and AS-15CQ respectively. Now, a genetic cross between AS-ART and the artemisinin-sensitive clone AJ has been analysed by Linkage Group Selection. A genetic linkage group on chromosome 2 was selected under artemisinin treatment. Within this locus, we identified two different mutations in a gene encoding a deubiquitinating enzyme. A distinct mutation occurred in each of the clones AS-30CQ and AS-ATN, relative to their respective progenitors in the AS lineage. The mutations occurred independently in different clones under drug selection with chloroquine (high concentration) or artesunate. Each mutation maps to a critical residue in a homologous human deubiquitinating protein structure. Although one mutation could theoretically account for the resistance of AS-ATN to artemisinin derivates, the other cannot account solely for the resistance of AS-ART, relative to the responses of its sensitive progenitor AS-30CQ. Two lines of Plasmodium falciparum with decreased susceptibility to artemisinin were also selected. Their drug-response phenotype was not genetically stable. No mutations in the UBP-1 gene encoding the P. falciparum orthologue of the deubiquitinating enzyme were observed. The possible significance of these mutations in parasite responses to chloroquine or artemisinin is discussed.
Insights
New mutations in a deubiquitinating enzyme gene on chromosome 2 were identified in Plasmodium chabaudi resistant to artemisinin and artesunate. These independent mutations may contribute to drug resistance, though further study is needed.
Area of Science:
- Malariology
- Parasitic Diseases
- Molecular Biology
Background:
- Plasmodium chabaudi clones resistant to artemisinin and artesunate (AS-ART, AS-ATN) were previously developed.
- These resistant clones originated from chloroquine-resistant progenitors (AS-30CQ, AS-15CQ).
Purpose of the Study:
- To investigate the genetic basis of artemisinin and artesunate resistance in Plasmodium chabaudi.
- To identify specific mutations conferring drug resistance.
Main Methods:
- Genetic crossing between artemisinin-resistant AS-ART and sensitive AJ clones.
- Linkage Group Selection under artemisinin treatment.
- Mutation analysis in a deubiquitinating enzyme gene.
Main Results:
- A genetic linkage group on chromosome 2 was selected under artemisinin pressure.
- Two distinct mutations were identified in a deubiquitinating enzyme gene within this locus.
- Each mutation occurred independently in different resistant clones (AS-30CQ, AS-ATN).
- One mutation partially explains AS-ATN resistance, but not solely AS-ART resistance.
Conclusions:
- Independent mutations in a deubiquitinating enzyme gene are associated with artemisinin and artesunate resistance in Plasmodium chabaudi.
- These mutations map to critical residues in homologous human proteins.
- Further research is needed to fully elucidate the role of these mutations in drug resistance mechanisms.
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