Genome-wide functional screening of drug-resistance genes in Plasmodium falciparum.
Shiroh IwanagaRie KubotaTsubasa NishiSumalee KamchonwongpaisanSomdet SrichairatanakoolNaoaki ShinzawaDin SyafruddinMasao YudaChairat UthaipibullPublished in: Nature communications (2022)
The global spread of drug resistance is a major obstacle to the treatment of Plasmodium falciparum malaria. The identification of drug-resistance genes is an essential step toward solving the problem of drug resistance. Here, we report functional screening as a new approach with which to identify drug-resistance genes in P. falciparum. Specifically, a high-coverage genomic library of a drug-resistant strain is directly generated in a drug-sensitive strain, and the resistance gene is then identified from this library using drug screening. In a pilot experiment using the strain Dd2, the known chloroquine-resistant gene pfcrt is identified using the developed approach, which proves our experimental concept. Furthermore, we identify multidrug-resistant transporter 7 (pfmdr7) as a novel candidate for a mefloquine-resistance gene from a field-isolated parasite; we suggest that its upregulation possibly confers the mefloquine resistance. These results show the usefulness of functional screening as means by which to identify drug-resistance genes.
Keyphrases
- plasmodium falciparum
- genome wide
- genome wide identification
- drug resistant
- multidrug resistant
- copy number
- dna methylation
- bioinformatics analysis
- acinetobacter baumannii
- genome wide analysis
- transcription factor
- klebsiella pneumoniae
- emergency department
- adverse drug
- gene expression
- smoking cessation
- study protocol
- health insurance
- drug induced
- life cycle
- affordable care act