Abstract

Plasmodium falciparum infection of human erythrocytes is known to result in the modification of the host cell cytoskeleton by parasite-coded proteins. However, such modifications and corresponding implications in malaria pathogenesis have not been fully explored. Here, we probed the gradual modification of infected erythrocyte cytoskeleton with advancing stages of infection using atomic force microscopy (AFM). We reported a novel strategy to derive accurate and quantitative information on the knob structures and their connections with the spectrin network by performing AFM–based imaging analysis of the cytoplasmic surface of infected erythrocytes. Significant changes on the red cell cytoskeleton were observed from the expansion of spectrin network mesh size, extension of spectrin tetramers and the decrease of spectrin abundance with advancing stages of infection. The spectrin network appeared to aggregate around knobs but also appeared sparser at non-knob areas as the parasite matured. This dramatic modification of the erythrocyte skeleton during the advancing stage of malaria infection could contribute to the loss of deformability of the infected erythrocyte.

Highlights

  • Plasmodium (P.) falciparum causes the most virulent form of human malaria, which attributes to repeated life cycles of growth of the parasite in the erythrocyte

  • We provided the first quantitative study of the gradual changes of the spectrin network of erythrocytes in terms of the mesh size, spectrin protein length and spectrin abundance during P. falciparum infection

  • These findings provide direct evidences of the gradual modification of the cytoskeleton of erythrocytes during malaria infection, and yield insightful clues into the roles the parasiteexported proteins play in modifying the host cell cytoskeleton

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Summary

Introduction

Plasmodium (P.) falciparum causes the most virulent form of human malaria, which attributes to repeated life cycles of growth of the parasite in the erythrocyte. One of the most striking structural alterations on the membrane of the host cell is the formation of knobs, which are composed of parasite-expressed proteins, such as P. falciparum erythrocyte membrane protein 1 (PfEMP1) and knobassociated histidine-rich protein (KAHRP) among others [2]. These knobs interact with the spectrin network via the attachment of KAHRP to the spectrin-actin-protein 4.1 junction [4] or direct binding of KAHRP to spectrin tetramers [5]. The changes in host cell cytoskeleton caused by P. falciparum infection and development have not been well quantitatively elucidated

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