Ontology highlight
ABSTRACT: Background
Antimalarial resistance, especially artemisinin resistance, in Plasmodium falciparum threatens global malaria control. Molecular surveillance of Plasmodium falciparum drug resistance is critical for monitoring the efficacy of artemisinin-based combination therapies (ACTs). Current molecular surveillance tools for Plasmodium falciparum artemisinin resistance are restricted to predefined polymorphism hotspots in limited loci (Pfk13 domain), failing to capture novel mutations in emerging resistance genes (Pfcoronin, Pfubp1, Pfap2μ) or cover complete coding regions. This study addresses this gap by developing an optimized long-amplicon panel for comprehensive, full-gene resistance surveillance.Methods
Six genes were selected for the multiplex PCR amplification, inclu
SUBMITTER: Li F
PROVIDER: S-EPMC12539163 | biostudies-literature | 2025 Oct
REPOSITORIES: biostudies-literature