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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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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. |
format | Online Article Text |
id | pubmed-5105170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
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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