Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.

Plasmodium falciparum is the main cause of disease and death from malaria. P. falciparum virulence resides in the ability of infected erythrocytes (IEs) to sequester in various tissues through the interaction between members of the polymorphic P. falciparum erythrocyte membrane protein 1 (PfEMP1) ad...

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Main Authors: Dominique Dorin-Semblat, Marilou Tétard, Aurélie Claës, Jean-Philippe Semblat, Sébastien Dechavanne, Zaineb Fourati, Romain Hamelin, Florence Armand, Graziella Matesic, Sofia Nunes-Silva, Anand Srivastava, Stéphane Gangnard, Jose-Juan Lopez-Rubio, Marc Moniatte, Christian Doerig, Artur Scherf, Benoît Gamain
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-06-01
Series:PLoS Biology
Online Access:https://doi.org/10.1371/journal.pbio.3000308
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spelling doaj-99d6e1fa67c54645ad056545942995652021-07-02T16:29:11ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852019-06-01176e300030810.1371/journal.pbio.3000308Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.Dominique Dorin-SemblatMarilou TétardAurélie ClaësJean-Philippe SemblatSébastien DechavanneZaineb FouratiRomain HamelinFlorence ArmandGraziella MatesicSofia Nunes-SilvaAnand SrivastavaStéphane GangnardJose-Juan Lopez-RubioMarc MoniatteChristian DoerigArtur ScherfBenoît GamainPlasmodium falciparum is the main cause of disease and death from malaria. P. falciparum virulence resides in the ability of infected erythrocytes (IEs) to sequester in various tissues through the interaction between members of the polymorphic P. falciparum erythrocyte membrane protein 1 (PfEMP1) adhesin family to various host receptors. Here, we investigated the effect of phosphorylation of variant surface antigen 2-CSA (VAR2CSA), a member of the PfEMP1 family associated to placental sequestration, on its capacity to adhere to chondroitin sulfate A (CSA) present on the placental syncytium. We showed that phosphatase treatment of IEs impairs cytoadhesion to CSA. MS analysis of recombinant VAR2CSA phosphosites prior to and after phosphatase treatment, as well as of native VAR2CSA expressed on IEs, identified critical phosphoresidues associated with CSA binding. Site-directed mutagenesis on recombinant VAR2CSA of 3 phosphoresidues localised within the CSA-binding region confirmed in vitro their functional importance. Furthermore, using clustered regularly interspaced short palindromic repeats/CRISPR-associated protein-9 nuclease (CRISPR/Cas9), we generated a parasite line in which the phosphoresidue T934 is changed to alanine and showed that this mutation strongly impairs IEs cytoadhesion to CSA. Taken together, these results demonstrate that phosphorylation of the extracellular region of VAR2CSA plays a major role in IEs cytoadhesion to CSA and provide new molecular insights for strategies aiming to reduce the morbidity and mortality of PM.https://doi.org/10.1371/journal.pbio.3000308
collection DOAJ
language English
format Article
sources DOAJ
author Dominique Dorin-Semblat
Marilou Tétard
Aurélie Claës
Jean-Philippe Semblat
Sébastien Dechavanne
Zaineb Fourati
Romain Hamelin
Florence Armand
Graziella Matesic
Sofia Nunes-Silva
Anand Srivastava
Stéphane Gangnard
Jose-Juan Lopez-Rubio
Marc Moniatte
Christian Doerig
Artur Scherf
Benoît Gamain
spellingShingle Dominique Dorin-Semblat
Marilou Tétard
Aurélie Claës
Jean-Philippe Semblat
Sébastien Dechavanne
Zaineb Fourati
Romain Hamelin
Florence Armand
Graziella Matesic
Sofia Nunes-Silva
Anand Srivastava
Stéphane Gangnard
Jose-Juan Lopez-Rubio
Marc Moniatte
Christian Doerig
Artur Scherf
Benoît Gamain
Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.
PLoS Biology
author_facet Dominique Dorin-Semblat
Marilou Tétard
Aurélie Claës
Jean-Philippe Semblat
Sébastien Dechavanne
Zaineb Fourati
Romain Hamelin
Florence Armand
Graziella Matesic
Sofia Nunes-Silva
Anand Srivastava
Stéphane Gangnard
Jose-Juan Lopez-Rubio
Marc Moniatte
Christian Doerig
Artur Scherf
Benoît Gamain
author_sort Dominique Dorin-Semblat
title Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.
title_short Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.
title_full Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.
title_fullStr Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.
title_full_unstemmed Phosphorylation of the VAR2CSA extracellular region is associated with enhanced adhesive properties to the placental receptor CSA.
title_sort phosphorylation of the var2csa extracellular region is associated with enhanced adhesive properties to the placental receptor csa.
publisher Public Library of Science (PLoS)
series PLoS Biology
issn 1544-9173
1545-7885
publishDate 2019-06-01
description Plasmodium falciparum is the main cause of disease and death from malaria. P. falciparum virulence resides in the ability of infected erythrocytes (IEs) to sequester in various tissues through the interaction between members of the polymorphic P. falciparum erythrocyte membrane protein 1 (PfEMP1) adhesin family to various host receptors. Here, we investigated the effect of phosphorylation of variant surface antigen 2-CSA (VAR2CSA), a member of the PfEMP1 family associated to placental sequestration, on its capacity to adhere to chondroitin sulfate A (CSA) present on the placental syncytium. We showed that phosphatase treatment of IEs impairs cytoadhesion to CSA. MS analysis of recombinant VAR2CSA phosphosites prior to and after phosphatase treatment, as well as of native VAR2CSA expressed on IEs, identified critical phosphoresidues associated with CSA binding. Site-directed mutagenesis on recombinant VAR2CSA of 3 phosphoresidues localised within the CSA-binding region confirmed in vitro their functional importance. Furthermore, using clustered regularly interspaced short palindromic repeats/CRISPR-associated protein-9 nuclease (CRISPR/Cas9), we generated a parasite line in which the phosphoresidue T934 is changed to alanine and showed that this mutation strongly impairs IEs cytoadhesion to CSA. Taken together, these results demonstrate that phosphorylation of the extracellular region of VAR2CSA plays a major role in IEs cytoadhesion to CSA and provide new molecular insights for strategies aiming to reduce the morbidity and mortality of PM.
url https://doi.org/10.1371/journal.pbio.3000308
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