The Kelch13 compartment contains highly divergent vesicle trafficking proteins in malaria parasites

PLoS Pathog. 2023 Dec 1;19(12):e1011814. doi: 10.1371/journal.ppat.1011814. eCollection 2023 Dec.

Abstract

Single amino acid changes in the parasite protein Kelch13 (K13) result in reduced susceptibility of P. falciparum parasites to artemisinin and its derivatives (ART). Recent work indicated that K13 and other proteins co-localising with K13 (K13 compartment proteins) are involved in the endocytic uptake of host cell cytosol (HCCU) and that a reduction in HCCU results in reduced susceptibility to ART. HCCU is critical for parasite survival but is poorly understood, with the K13 compartment proteins among the few proteins so far functionally linked to this process. Here we further defined the composition of the K13 compartment by analysing more hits from a previous BioID, showing that MyoF and MCA2 as well as Kelch13 interaction candidate (KIC) 11 and 12 are found at this site. Functional analyses, tests for ART susceptibility as well as comparisons of structural similarities using AlphaFold2 predictions of these and previously identified proteins showed that vesicle trafficking and endocytosis domains were frequent in proteins involved in resistance or endocytosis (or both), comprising one group of K13 compartment proteins. While this strengthened the link of the K13 compartment to endocytosis, many proteins of this group showed unusual domain combinations and large parasite-specific regions, indicating a high level of taxon-specific adaptation of this process. Another group of K13 compartment proteins did not influence endocytosis or ART susceptibility and lacked detectable vesicle trafficking domains. We here identified the first protein of this group that is important for asexual blood stage development and showed that it likely is involved in invasion. Overall, this work identified novel proteins functioning in endocytosis and at the K13 compartment. Together with comparisons of structural predictions it provides a repertoire of functional domains at the K13 compartment that indicate a high level of adaption of endocytosis in malaria parasites.

MeSH terms

  • Animals
  • Antimalarials* / pharmacology
  • Drug Resistance
  • Malaria, Falciparum* / parasitology
  • Mutation
  • Parasites* / metabolism
  • Plasmodium falciparum / metabolism
  • Protozoan Proteins / genetics
  • Protozoan Proteins / metabolism

Substances

  • Antimalarials
  • Protozoan Proteins

Grants and funding

This project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement No. 101021493). This grant was awarded to TS. HMB acknowledges funding by the Ortrud Mührer Fellowship of the Vereinigung der Freunde des Tropeninstituts Hamburg e.V, https://www.bnitm.de/alumni-und_freunde/vdf. CCP thanks the DAAD (https://www.daad.de/de/) for funding (Personenkennziffer 91726017). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.