Super-resolution dissection of coordinated events during malaria parasite invasion of the human erythrocyte

Date

2011

Authors

Riglar, D.
Richard, D.
Wilson, D.
Boyle, M.
Dekiwadia, C.
Turnbull, L.
Angrisano, F.
Marapana, D.
Rogers, K.
Whitchurch, C.

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Citation

Cell Host and Microbe, 2011; 9(1):9-20

Statement of Responsibility

David T. Riglar, Dave Richard, Danny W. Wilson, Michelle J. Boyle, Chaitali Dekiwadia, Lynne Turnbull, Fiona Angrisano, Danushka S. Marapana, Kelly L. Rogers, Cynthia B. Whitchurch, James G. Beeson, Alan F. Cowman, Stuart A. Ralph, and Jake Baum

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Abstract

Erythrocyte invasion by the merozoite is an obligatory stage in Plasmodium parasite infection and essential to malaria disease progression. Attempts to study this process have been hindered by the poor invasion synchrony of merozoites from the only in vitro culture-adapted human malaria parasite, Plasmodium falciparum. Using fluorescence, three-dimensional structured illumination, and immunoelectron microscopy of filtered merozoites, we analyze cellular and molecular events underlying each discrete step of invasion. Monitoring the dynamics of these events revealed that commitment to the process is mediated through merozoite attachment to the erythrocyte, triggering all subsequent invasion events, which then proceed without obvious checkpoints. Instead, coordination of the invasion process involves formation of the merozoite-erythrocyte tight junction, which acts as a nexus for rhoptry secretion, surface-protein shedding, and actomyosin motor activation. The ability to break down each molecular step allows us to propose a comprehensive model for the molecular basis of parasite invasion.

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© 2011 Elsevier Inc.

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