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Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes

Plasmodium falciparum infections can cause severe malaria, but not every infected person develops life-threatening complications. In particular, carriers of the structural haemoglobinopathies S and C and infants are protected from severe disease. Protection is associated with impaired parasite-induc...

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Autores principales: Cyrklaff, Marek, Srismith, Sirikamol, Nyboer, Britta, Burda, Kvetoslava, Hoffmann, Angelika, Lasitschka, Felix, Adjalley, Sophie, Bisseye, Cyrille, Simpore, Jacques, Mueller, Ann-Kristin, Sanchez, Cecilia P., Frischknecht, Friedrich, Lanzer, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105170/
https://www.ncbi.nlm.nih.gov/pubmed/27824335
http://dx.doi.org/10.1038/ncomms13401
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author Cyrklaff, Marek
Srismith, Sirikamol
Nyboer, Britta
Burda, Kvetoslava
Hoffmann, Angelika
Lasitschka, Felix
Adjalley, Sophie
Bisseye, Cyrille
Simpore, Jacques
Mueller, Ann-Kristin
Sanchez, Cecilia P.
Frischknecht, Friedrich
Lanzer, Michael
author_facet Cyrklaff, Marek
Srismith, Sirikamol
Nyboer, Britta
Burda, Kvetoslava
Hoffmann, Angelika
Lasitschka, Felix
Adjalley, Sophie
Bisseye, Cyrille
Simpore, Jacques
Mueller, Ann-Kristin
Sanchez, Cecilia P.
Frischknecht, Friedrich
Lanzer, Michael
author_sort Cyrklaff, Marek
collection PubMed
description Plasmodium falciparum infections can cause severe malaria, but not every infected person develops life-threatening complications. In particular, carriers of the structural haemoglobinopathies S and C and infants are protected from severe disease. Protection is associated with impaired parasite-induced host actin reorganization, required for vesicular trafficking of parasite-encoded adhesins, and reduced cytoadherence of parasitized erythrocytes in the microvasculature. Here we show that aberrant host actin remodelling and the ensuing reduced cytoadherence result from a redox imbalance inherent to haemoglobinopathic and fetal erythrocytes. We further show that a transient oxidative insult to wild-type erythrocytes before infection with P. falciparum induces the phenotypic features associated with the protective trait of haemoglobinopathic and fetal erythrocytes. Moreover, pretreatment of mice with the pro-oxidative nutritional supplement menadione mitigate the development of experimental cerebral malaria. Our results identify redox imbalance as a causative principle of protection from severe malaria, which might inspire host-directed intervention strategies.
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spelling pubmed-51051702016-11-18 Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes Cyrklaff, Marek Srismith, Sirikamol Nyboer, Britta Burda, Kvetoslava Hoffmann, Angelika Lasitschka, Felix Adjalley, Sophie Bisseye, Cyrille Simpore, Jacques Mueller, Ann-Kristin Sanchez, Cecilia P. Frischknecht, Friedrich Lanzer, Michael Nat Commun Article Plasmodium falciparum infections can cause severe malaria, but not every infected person develops life-threatening complications. In particular, carriers of the structural haemoglobinopathies S and C and infants are protected from severe disease. Protection is associated with impaired parasite-induced host actin reorganization, required for vesicular trafficking of parasite-encoded adhesins, and reduced cytoadherence of parasitized erythrocytes in the microvasculature. Here we show that aberrant host actin remodelling and the ensuing reduced cytoadherence result from a redox imbalance inherent to haemoglobinopathic and fetal erythrocytes. We further show that a transient oxidative insult to wild-type erythrocytes before infection with P. falciparum induces the phenotypic features associated with the protective trait of haemoglobinopathic and fetal erythrocytes. Moreover, pretreatment of mice with the pro-oxidative nutritional supplement menadione mitigate the development of experimental cerebral malaria. Our results identify redox imbalance as a causative principle of protection from severe malaria, which might inspire host-directed intervention strategies. Nature Publishing Group 2016-11-08 /pmc/articles/PMC5105170/ /pubmed/27824335 http://dx.doi.org/10.1038/ncomms13401 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Cyrklaff, Marek
Srismith, Sirikamol
Nyboer, Britta
Burda, Kvetoslava
Hoffmann, Angelika
Lasitschka, Felix
Adjalley, Sophie
Bisseye, Cyrille
Simpore, Jacques
Mueller, Ann-Kristin
Sanchez, Cecilia P.
Frischknecht, Friedrich
Lanzer, Michael
Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
title Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
title_full Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
title_fullStr Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
title_full_unstemmed Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
title_short Oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
title_sort oxidative insult can induce malaria-protective trait of sickle and fetal erythrocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5105170/
https://www.ncbi.nlm.nih.gov/pubmed/27824335
http://dx.doi.org/10.1038/ncomms13401
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