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A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings

Plasmodium vivax infects a hundred million people annually and endangers 40% of the world's population. Unlike Plasmodium falciparum, P. vivax parasites can persist as a dormant stage in the liver, known as the hypnozoite, and these dormant forms can cause malaria relapses months or years after...

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Autores principales: Bright, Andrew Taylor, Manary, Micah J., Tewhey, Ryan, Arango, Eliana M., Wang, Tina, Schork, Nicholas J., Yanow, Stephanie K., Winzeler, Elizabeth A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046966/
https://www.ncbi.nlm.nih.gov/pubmed/24901334
http://dx.doi.org/10.1371/journal.pntd.0002882
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author Bright, Andrew Taylor
Manary, Micah J.
Tewhey, Ryan
Arango, Eliana M.
Wang, Tina
Schork, Nicholas J.
Yanow, Stephanie K.
Winzeler, Elizabeth A.
author_facet Bright, Andrew Taylor
Manary, Micah J.
Tewhey, Ryan
Arango, Eliana M.
Wang, Tina
Schork, Nicholas J.
Yanow, Stephanie K.
Winzeler, Elizabeth A.
author_sort Bright, Andrew Taylor
collection PubMed
description Plasmodium vivax infects a hundred million people annually and endangers 40% of the world's population. Unlike Plasmodium falciparum, P. vivax parasites can persist as a dormant stage in the liver, known as the hypnozoite, and these dormant forms can cause malaria relapses months or years after the initial mosquito bite. Here we analyze whole genome sequencing data from parasites in the blood of a patient who experienced consecutive P. vivax relapses over 33 months in a non-endemic country. By analyzing patterns of identity, read coverage, and the presence or absence of minor alleles in the initial polyclonal and subsequent monoclonal infections, we show that the parasites in the three infections are likely meiotic siblings. We infer that these siblings are descended from a single tetrad-like form that developed in the infecting mosquito midgut shortly after fertilization. In this natural cross we find the recombination rate for P. vivax to be 10 kb per centimorgan and we further observe areas of disequilibrium surrounding major drug resistance genes. Our data provide new strategies for studying multiclonal infections, which are common in all types of infectious diseases, and for distinguishing P. vivax relapses from reinfections in malaria endemic regions. This work provides a theoretical foundation for studies that aim to determine if new or existing drugs can provide a radical cure of P. vivax malaria.
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spelling pubmed-40469662014-06-09 A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings Bright, Andrew Taylor Manary, Micah J. Tewhey, Ryan Arango, Eliana M. Wang, Tina Schork, Nicholas J. Yanow, Stephanie K. Winzeler, Elizabeth A. PLoS Negl Trop Dis Research Article Plasmodium vivax infects a hundred million people annually and endangers 40% of the world's population. Unlike Plasmodium falciparum, P. vivax parasites can persist as a dormant stage in the liver, known as the hypnozoite, and these dormant forms can cause malaria relapses months or years after the initial mosquito bite. Here we analyze whole genome sequencing data from parasites in the blood of a patient who experienced consecutive P. vivax relapses over 33 months in a non-endemic country. By analyzing patterns of identity, read coverage, and the presence or absence of minor alleles in the initial polyclonal and subsequent monoclonal infections, we show that the parasites in the three infections are likely meiotic siblings. We infer that these siblings are descended from a single tetrad-like form that developed in the infecting mosquito midgut shortly after fertilization. In this natural cross we find the recombination rate for P. vivax to be 10 kb per centimorgan and we further observe areas of disequilibrium surrounding major drug resistance genes. Our data provide new strategies for studying multiclonal infections, which are common in all types of infectious diseases, and for distinguishing P. vivax relapses from reinfections in malaria endemic regions. This work provides a theoretical foundation for studies that aim to determine if new or existing drugs can provide a radical cure of P. vivax malaria. Public Library of Science 2014-06-05 /pmc/articles/PMC4046966/ /pubmed/24901334 http://dx.doi.org/10.1371/journal.pntd.0002882 Text en © 2014 Bright et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Bright, Andrew Taylor
Manary, Micah J.
Tewhey, Ryan
Arango, Eliana M.
Wang, Tina
Schork, Nicholas J.
Yanow, Stephanie K.
Winzeler, Elizabeth A.
A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
title A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
title_full A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
title_fullStr A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
title_full_unstemmed A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
title_short A High Resolution Case Study of a Patient with Recurrent Plasmodium vivax Infections Shows That Relapses Were Caused by Meiotic Siblings
title_sort high resolution case study of a patient with recurrent plasmodium vivax infections shows that relapses were caused by meiotic siblings
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4046966/
https://www.ncbi.nlm.nih.gov/pubmed/24901334
http://dx.doi.org/10.1371/journal.pntd.0002882
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