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Growth of Plasmodium falciparum in response to a rotating magnetic field

BACKGROUND: Plasmodium falciparum is the deadliest strain of malaria and the mortality rate is increasing because of pathogen drug resistance. Increasing knowledge of the parasite life cycle and mechanism of infection may provide new models for improved treatment paradigms. This study sought to inve...

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Autores principales: Gilson, Rebecca C., Deissler, Robert J., Bihary, Richard F., Condit, William C., Thompson, Mary E., Blankenship, D’Arbra, Grimberg, Kerry O., Brown, Robert W., Grimberg, Brian T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934852/
https://www.ncbi.nlm.nih.gov/pubmed/29724219
http://dx.doi.org/10.1186/s12936-018-2333-2
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author Gilson, Rebecca C.
Deissler, Robert J.
Bihary, Richard F.
Condit, William C.
Thompson, Mary E.
Blankenship, D’Arbra
Grimberg, Kerry O.
Brown, Robert W.
Grimberg, Brian T.
author_facet Gilson, Rebecca C.
Deissler, Robert J.
Bihary, Richard F.
Condit, William C.
Thompson, Mary E.
Blankenship, D’Arbra
Grimberg, Kerry O.
Brown, Robert W.
Grimberg, Brian T.
author_sort Gilson, Rebecca C.
collection PubMed
description BACKGROUND: Plasmodium falciparum is the deadliest strain of malaria and the mortality rate is increasing because of pathogen drug resistance. Increasing knowledge of the parasite life cycle and mechanism of infection may provide new models for improved treatment paradigms. This study sought to investigate the paramagnetic nature of the parasite’s haemozoin to inhibit parasite viability. RESULTS: Paramagnetic haemozoin crystals, a byproduct of the parasite’s haemoglobin digestion, interact with a rotating magnetic field, which prevents their complete formation, causing the accumulation of free haem, which is lethal to the parasites. Plasmodium falciparum cultures of different stages of intraerythrocytic growth (rings, trophozoites, and schizonts) were exposed to a magnetic field of 0.46 T at frequencies of 0 Hz (static), 1, 5, and 10 Hz for 48 h. The numbers of parasites were counted over the course of one intraerythrocytic life cycle via flow cytometry. At 10 Hz the schizont life stage was most affected by the rotating magnetic fields (p = 0.0075) as compared to a static magnetic field of the same strength. Parasite growth in the presence of a static magnetic field appears to aid parasite growth. CONCLUSIONS: Sequestration of the toxic haem resulting from haemoglobin digestion is key for the parasites’ survival and the focus of almost all existing anti-malarial drugs. Understanding how the parasites create the haemozoin molecule and the disruption of its creation aids in the development of drugs to combat this disease.
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spelling pubmed-59348522018-05-11 Growth of Plasmodium falciparum in response to a rotating magnetic field Gilson, Rebecca C. Deissler, Robert J. Bihary, Richard F. Condit, William C. Thompson, Mary E. Blankenship, D’Arbra Grimberg, Kerry O. Brown, Robert W. Grimberg, Brian T. Malar J Research BACKGROUND: Plasmodium falciparum is the deadliest strain of malaria and the mortality rate is increasing because of pathogen drug resistance. Increasing knowledge of the parasite life cycle and mechanism of infection may provide new models for improved treatment paradigms. This study sought to investigate the paramagnetic nature of the parasite’s haemozoin to inhibit parasite viability. RESULTS: Paramagnetic haemozoin crystals, a byproduct of the parasite’s haemoglobin digestion, interact with a rotating magnetic field, which prevents their complete formation, causing the accumulation of free haem, which is lethal to the parasites. Plasmodium falciparum cultures of different stages of intraerythrocytic growth (rings, trophozoites, and schizonts) were exposed to a magnetic field of 0.46 T at frequencies of 0 Hz (static), 1, 5, and 10 Hz for 48 h. The numbers of parasites were counted over the course of one intraerythrocytic life cycle via flow cytometry. At 10 Hz the schizont life stage was most affected by the rotating magnetic fields (p = 0.0075) as compared to a static magnetic field of the same strength. Parasite growth in the presence of a static magnetic field appears to aid parasite growth. CONCLUSIONS: Sequestration of the toxic haem resulting from haemoglobin digestion is key for the parasites’ survival and the focus of almost all existing anti-malarial drugs. Understanding how the parasites create the haemozoin molecule and the disruption of its creation aids in the development of drugs to combat this disease. BioMed Central 2018-05-03 /pmc/articles/PMC5934852/ /pubmed/29724219 http://dx.doi.org/10.1186/s12936-018-2333-2 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Gilson, Rebecca C.
Deissler, Robert J.
Bihary, Richard F.
Condit, William C.
Thompson, Mary E.
Blankenship, D’Arbra
Grimberg, Kerry O.
Brown, Robert W.
Grimberg, Brian T.
Growth of Plasmodium falciparum in response to a rotating magnetic field
title Growth of Plasmodium falciparum in response to a rotating magnetic field
title_full Growth of Plasmodium falciparum in response to a rotating magnetic field
title_fullStr Growth of Plasmodium falciparum in response to a rotating magnetic field
title_full_unstemmed Growth of Plasmodium falciparum in response to a rotating magnetic field
title_short Growth of Plasmodium falciparum in response to a rotating magnetic field
title_sort growth of plasmodium falciparum in response to a rotating magnetic field
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5934852/
https://www.ncbi.nlm.nih.gov/pubmed/29724219
http://dx.doi.org/10.1186/s12936-018-2333-2
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