The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.

Invasion of host cells by apicomplexan parasites such as Toxoplasma and Plasmodium spp requires the sequential secretion of the parasite apical organelles, the micronemes and the rhoptries. The claudin-like apicomplexan microneme protein (CLAMP) is a conserved protein that plays an essential role du...

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Main Authors: Manon Loubens, Carine Marinach, Clara-Eva Paquereau, Soumia Hamada, Bénédicte Hoareau-Coudert, David Akbar, Jean-François Franetich, Olivier Silvie
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-03-01
Series:PLoS Pathogens
Online Access:https://doi.org/10.1371/journal.ppat.1011261
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author Manon Loubens
Carine Marinach
Clara-Eva Paquereau
Soumia Hamada
Bénédicte Hoareau-Coudert
David Akbar
Jean-François Franetich
Olivier Silvie
author_facet Manon Loubens
Carine Marinach
Clara-Eva Paquereau
Soumia Hamada
Bénédicte Hoareau-Coudert
David Akbar
Jean-François Franetich
Olivier Silvie
author_sort Manon Loubens
collection DOAJ
description Invasion of host cells by apicomplexan parasites such as Toxoplasma and Plasmodium spp requires the sequential secretion of the parasite apical organelles, the micronemes and the rhoptries. The claudin-like apicomplexan microneme protein (CLAMP) is a conserved protein that plays an essential role during invasion by Toxoplasma gondii tachyzoites and in Plasmodium falciparum asexual blood stages. CLAMP is also expressed in Plasmodium sporozoites, the mosquito-transmitted forms of the malaria parasite, but its role in this stage is still unknown. CLAMP is essential for Plasmodium blood stage growth and is refractory to conventional gene deletion. To circumvent this obstacle and study the function of CLAMP in sporozoites, we used a conditional genome editing strategy based on the dimerisable Cre recombinase in the rodent malaria model parasite P. berghei. We successfully deleted clamp gene in P. berghei transmission stages and analyzed the functional consequences on sporozoite infectivity. In mosquitoes, sporozoite development and egress from oocysts was not affected in conditional mutants. However, invasion of the mosquito salivary glands was dramatically reduced upon deletion of clamp gene. In addition, CLAMP-deficient sporozoites were impaired in cell traversal and productive invasion of mammalian hepatocytes. This severe phenotype was associated with major defects in gliding motility and with reduced shedding of the sporozoite adhesin TRAP. Expansion microscopy revealed partial colocalization of CLAMP and TRAP in a subset of micronemes, and a distinct accumulation of CLAMP at the apical tip of sporozoites. Collectively, these results demonstrate that CLAMP is essential across invasive stages of the malaria parasite, and support a role of the protein upstream of host cell invasion, possibly by regulating the secretion or function of adhesins in Plasmodium sporozoites.
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spelling doaj.art-1926ed2b342e4f58a1d86fc22a73057f2023-04-12T05:31:26ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742023-03-01193e101126110.1371/journal.ppat.1011261The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.Manon LoubensCarine MarinachClara-Eva PaquereauSoumia HamadaBénédicte Hoareau-CoudertDavid AkbarJean-François FranetichOlivier SilvieInvasion of host cells by apicomplexan parasites such as Toxoplasma and Plasmodium spp requires the sequential secretion of the parasite apical organelles, the micronemes and the rhoptries. The claudin-like apicomplexan microneme protein (CLAMP) is a conserved protein that plays an essential role during invasion by Toxoplasma gondii tachyzoites and in Plasmodium falciparum asexual blood stages. CLAMP is also expressed in Plasmodium sporozoites, the mosquito-transmitted forms of the malaria parasite, but its role in this stage is still unknown. CLAMP is essential for Plasmodium blood stage growth and is refractory to conventional gene deletion. To circumvent this obstacle and study the function of CLAMP in sporozoites, we used a conditional genome editing strategy based on the dimerisable Cre recombinase in the rodent malaria model parasite P. berghei. We successfully deleted clamp gene in P. berghei transmission stages and analyzed the functional consequences on sporozoite infectivity. In mosquitoes, sporozoite development and egress from oocysts was not affected in conditional mutants. However, invasion of the mosquito salivary glands was dramatically reduced upon deletion of clamp gene. In addition, CLAMP-deficient sporozoites were impaired in cell traversal and productive invasion of mammalian hepatocytes. This severe phenotype was associated with major defects in gliding motility and with reduced shedding of the sporozoite adhesin TRAP. Expansion microscopy revealed partial colocalization of CLAMP and TRAP in a subset of micronemes, and a distinct accumulation of CLAMP at the apical tip of sporozoites. Collectively, these results demonstrate that CLAMP is essential across invasive stages of the malaria parasite, and support a role of the protein upstream of host cell invasion, possibly by regulating the secretion or function of adhesins in Plasmodium sporozoites.https://doi.org/10.1371/journal.ppat.1011261
spellingShingle Manon Loubens
Carine Marinach
Clara-Eva Paquereau
Soumia Hamada
Bénédicte Hoareau-Coudert
David Akbar
Jean-François Franetich
Olivier Silvie
The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.
PLoS Pathogens
title The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.
title_full The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.
title_fullStr The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.
title_full_unstemmed The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.
title_short The claudin-like apicomplexan microneme protein is required for gliding motility and infectivity of Plasmodium sporozoites.
title_sort claudin like apicomplexan microneme protein is required for gliding motility and infectivity of plasmodium sporozoites
url https://doi.org/10.1371/journal.ppat.1011261
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