Abstract
ABSTRACTHeme-biosynthetic pathway of malaria parasite is dispensable for asexual stages, but essential for sexual and liver stages. Despite having backup mechanisms to acquire hemoglobin-heme, pathway intermediates and/or enzymes from the host, asexual parasites express heme pathway enzymes and synthesize heme. Here we show heme synthesized in asexual stages promotes cerebral pathogenesis by enhancing hemozoin formation. Hemozoin is a parasite molecule associated with inflammation, aberrant host-immune responses, disease severity and cerebral pathogenesis. The heme pathway knockout parasites synthesize less hemozoin, and mice infected with knockout parasites are completely protected from cerebral malaria and death due to anaemia is delayed. Biosynthetic heme regulates food vacuole integrity and the food vacuoles from knockout parasites are compromised in pH, lipid unsaturation and proteins, essential for hemozoin formation. Targeting parasite heme synthesis by griseofulvin - a FDA-approved drug, prevents cerebral malaria in mice and provides a new adjunct therapeutic option for cerebral and severe malaria.
Publisher
Cold Spring Harbor Laboratory
Reference88 articles.
1. World Health Organization. World Malaria Report (2020). https://www.mmv.org/sites/default/files/uploads/docs/publications/World_Malaria_Report_2020.pdf
2. Severe Malaria
3. Persistent cognitive impairment after cerebral malaria: models, mechanisms and adjunctive therapies;Expert Rev. Anti. Infect. Ther,2014
4. Adjunctive therapy for severe malaria: a review and critical appraisal;Malar. J,2018
5. Cerebral malaria: why experimental murine models are required to understand the pathogenesis of disease