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This is a microscopic image of human red blood cells infected with Malaria Parasite Plasmodium falciparum (blue), which kills half a million people in the developing world every year. Courtesy of SUTD
A Singapore-India collaborative research project between the Singapore University of Technology & Design (SUTD) and CSIR-National Chemical Laboratories (NCL) completed phenotypic screening of a large collection of potent chemical inhibitors (known as MMV Malaria Box), against pathogenic parasites Toxoplasma gondii and Plasmodium falciparum, causative agents of human toxoplasmosis and malaria. This knowledge opens up new avenues to study unique stages of infectious cycle that are affected by inhibitor classes towards anti-parasitic drug development.
Plasmodium parasites cause malaria and morbidly impact the economies of the developing world. Although, asymptomatic and not as deadly as malaria, toxoplasmosis can lead to serious health concerns in pregnant women (and in immuno-compromised individuals). Towards reducing the global burden of malaria and other neglected diseases, millions of compounds were screened, prioritized and assembled by the WHO-supported Medicines for Malaria Venture (MMV) as the MMV 'Malaria Box' collection of 400 chemically diverse small molecules. However, how these inhibitors kill the parasites remain largely unknown. Through complementary and comparative screening, the SUTD-NCL team has now discovered and segregated the MMV box library based on the life-stage events affected by individual inhibitors.
The team used complementary phenotypic screens on P. falciparum and T. gondii to identify phenotype-specific hits based on: Inhibition of overall parasite growth, Apicoplast segregation, and egress or host invasion and cross-validated between the two related, yet distinct parasitic forms.
They identified 24 molecules with nanomolar potency against both parasites, 30 molecules causing delayed death (in toxoplasma), out of which three interfere with apicoplast segregation, an essential process for the formation of new daughter cells. They also identified 26 molecules that specifically inhibit parasite release or host cell invasion of P. falciparum. Five of their 'hits' were also active against the release of T. gondii tachyzoites from mammalian cells, highlighting pathways that can be exploited in both parasites using the same class of molecules.
Principal investigator Rajesh Chandramohanadas from SUTD said, "MMV malaria Box represents an excellent starting point for anti-parasitic drug development due to chemical diversity, potency and open access. However, more information is needed on cellular pathways and targets affected by these inhibitors before pharmacological optimizations can be pursued. Having completed the phenotypic characterization and stage-specificity studies, we have now shortlisted a handful of excellent inhibitors for detailed mode-of-action and medicinal chemistry studies towards novel drug development."
"Egress and invasion are significantly similar between malaria and toxoplasma parasites. Therefore, identification of molecules that affect both parasites during their release from infected host cells not only highlights robustness of the complementary screening approach we adopted, but also conserved drug targets for pan anti-parasitic drug development," Dr. Dhanasekaran Shanmugam from NCL added.
This research appeared in mSphere, published by the American Society of Microbiology and its first authors are graduate students Subramanian Gowtham (SUTD) and Meenakshi Belekar (NCL). Other senior investigators in the team include Dr. Srinivasa Reddy (NCL), professor Kevin Tan (National University of Singapore), and professor Peter Preiser (Nanyang Technological University).
This work was jointly funded by the Agency for Science, Technology and Research (A*Star), Singapore- and the Department of Science and Technology (DST), India under the Singapore-India Joint Grant.