Last Updated: 01/09/2025

Drug resistance in malaria infection

Objectives

To address antimalarial drug resistance by identifying the factors and variation in the parasite that affect its susceptibility to antimalarial drugs. 

Specific objectives:

  1. Interrogation of the unique metabolic pathways (eg. Purine transport system) of the parasite in order to identify novel antimalarial drug targets.
  2. Using CRISPR Cas 9 gene editing techniques to identify molecular markers of antimalarial drug resistance and drug target discovery.
  3. Monitoring resistance to antimalarial drugs using WHO recommended standardized methods.
Principal Investigators / Focal Persons

Neils Quarshie

Rationale and Abstract

The malaria parasite, Plasmodium falciparum, has developed resistance to most of the available antimalarial drugs currently in use. Recent report indicates that, elsewhere, the parasites have developed resistance even to the newly introduced artemisinin-based combination therapy (ACT). Going forward, it is important to attempt to understand the mechanisms of resistance to the antimalarial drugs and then identify new drug targets as well as discover novel anti-plasmodia compounds. Concurrently, there is the need to monitor the efficacy of the ACT which are currently in use in most disease endemic areas.

The research has led to the discovery of novel purine transport pathways in Plasmodium falciparum. Data also have been generated from field activities on the efficacy of antimalarial drugs in Ghana. Previously, the use of SYBR Green method was introduced in Ghana which offered a cheap and reliable means of evaluating the outcome of in vitro drug test. Together with external collaborators, the team developed the ‘In Vitro Analysis and Reporting Tool (IVART)’ which removes the subjectivity from in vitro malaria drug sensitivity assay analysis among others.

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