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Whole genome sequencing analysis of Plasmodium vivax using whole genome capture
BACKGROUND: Malaria caused by Plasmodium vivax is an experimentally neglected severe disease with a substantial burden on human health. Because of technical limitations, little is known about the biology of this important human pathogen. Whole genome analysis methods on patient-derived material are...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410760/ https://www.ncbi.nlm.nih.gov/pubmed/22721170 http://dx.doi.org/10.1186/1471-2164-13-262 |
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author | Bright, A Taylor Tewhey, Ryan Abeles, Shira Chuquiyauri, Raul Llanos-Cuentas, Alejandro Ferreira, Marcelo U Schork, Nicholas J Vinetz, Joseph M Winzeler, Elizabeth A |
author_facet | Bright, A Taylor Tewhey, Ryan Abeles, Shira Chuquiyauri, Raul Llanos-Cuentas, Alejandro Ferreira, Marcelo U Schork, Nicholas J Vinetz, Joseph M Winzeler, Elizabeth A |
author_sort | Bright, A Taylor |
collection | PubMed |
description | BACKGROUND: Malaria caused by Plasmodium vivax is an experimentally neglected severe disease with a substantial burden on human health. Because of technical limitations, little is known about the biology of this important human pathogen. Whole genome analysis methods on patient-derived material are thus likely to have a substantial impact on our understanding of P. vivax pathogenesis and epidemiology. For example, it will allow study of the evolution and population biology of the parasite, allow parasite transmission patterns to be characterized, and may facilitate the identification of new drug resistance genes. Because parasitemias are typically low and the parasite cannot be readily cultured, on-site leukocyte depletion of blood samples is typically needed to remove human DNA that may be 1000X more abundant than parasite DNA. These features have precluded the analysis of archived blood samples and require the presence of laboratories in close proximity to the collection of field samples for optimal pre-cryopreservation sample preparation. RESULTS: Here we show that in-solution hybridization capture can be used to extract P. vivax DNA from human contaminating DNA in the laboratory without the need for on-site leukocyte filtration. Using a whole genome capture method, we were able to enrich P. vivax DNA from bulk genomic DNA from less than 0.5% to a median of 55% (range 20%-80%). This level of enrichment allows for efficient analysis of the samples by whole genome sequencing and does not introduce any gross biases into the data. With this method, we obtained greater than 5X coverage across 93% of the P. vivax genome for four P. vivax strains from Iquitos, Peru, which is similar to our results using leukocyte filtration (greater than 5X coverage across 96% ). CONCLUSION: The whole genome capture technique will enable more efficient whole genome analysis of P. vivax from a larger geographic region and from valuable archived sample collections. |
format | Online Article Text |
id | pubmed-3410760 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34107602012-08-03 Whole genome sequencing analysis of Plasmodium vivax using whole genome capture Bright, A Taylor Tewhey, Ryan Abeles, Shira Chuquiyauri, Raul Llanos-Cuentas, Alejandro Ferreira, Marcelo U Schork, Nicholas J Vinetz, Joseph M Winzeler, Elizabeth A BMC Genomics Methodology Article BACKGROUND: Malaria caused by Plasmodium vivax is an experimentally neglected severe disease with a substantial burden on human health. Because of technical limitations, little is known about the biology of this important human pathogen. Whole genome analysis methods on patient-derived material are thus likely to have a substantial impact on our understanding of P. vivax pathogenesis and epidemiology. For example, it will allow study of the evolution and population biology of the parasite, allow parasite transmission patterns to be characterized, and may facilitate the identification of new drug resistance genes. Because parasitemias are typically low and the parasite cannot be readily cultured, on-site leukocyte depletion of blood samples is typically needed to remove human DNA that may be 1000X more abundant than parasite DNA. These features have precluded the analysis of archived blood samples and require the presence of laboratories in close proximity to the collection of field samples for optimal pre-cryopreservation sample preparation. RESULTS: Here we show that in-solution hybridization capture can be used to extract P. vivax DNA from human contaminating DNA in the laboratory without the need for on-site leukocyte filtration. Using a whole genome capture method, we were able to enrich P. vivax DNA from bulk genomic DNA from less than 0.5% to a median of 55% (range 20%-80%). This level of enrichment allows for efficient analysis of the samples by whole genome sequencing and does not introduce any gross biases into the data. With this method, we obtained greater than 5X coverage across 93% of the P. vivax genome for four P. vivax strains from Iquitos, Peru, which is similar to our results using leukocyte filtration (greater than 5X coverage across 96% ). CONCLUSION: The whole genome capture technique will enable more efficient whole genome analysis of P. vivax from a larger geographic region and from valuable archived sample collections. BioMed Central 2012-06-21 /pmc/articles/PMC3410760/ /pubmed/22721170 http://dx.doi.org/10.1186/1471-2164-13-262 Text en Copyright ©2012 Bright et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Article Bright, A Taylor Tewhey, Ryan Abeles, Shira Chuquiyauri, Raul Llanos-Cuentas, Alejandro Ferreira, Marcelo U Schork, Nicholas J Vinetz, Joseph M Winzeler, Elizabeth A Whole genome sequencing analysis of Plasmodium vivax using whole genome capture |
title | Whole genome sequencing analysis of Plasmodium vivax using whole genome capture |
title_full | Whole genome sequencing analysis of Plasmodium vivax using whole genome capture |
title_fullStr | Whole genome sequencing analysis of Plasmodium vivax using whole genome capture |
title_full_unstemmed | Whole genome sequencing analysis of Plasmodium vivax using whole genome capture |
title_short | Whole genome sequencing analysis of Plasmodium vivax using whole genome capture |
title_sort | whole genome sequencing analysis of plasmodium vivax using whole genome capture |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3410760/ https://www.ncbi.nlm.nih.gov/pubmed/22721170 http://dx.doi.org/10.1186/1471-2164-13-262 |
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