Whole genome sequencing analysis of Plasmodium vivax using whole genome capture

被引:45
作者
Bright, A. Taylor [1 ,2 ]
Tewhey, Ryan [3 ,4 ]
Abeles, Shira [5 ]
Chuquiyauri, Raul [5 ,6 ]
Llanos-Cuentas, Alejandro [6 ]
Ferreira, Marcelo U. [7 ]
Schork, Nicholas J. [3 ,8 ]
Vinetz, Joseph M. [5 ]
Winzeler, Elizabeth A. [2 ,9 ]
机构
[1] Univ Calif San Diego, Biomed Sci Program, La Jolla, CA 92093 USA
[2] Scripps Res Inst, Dept Genet, La Jolla, CA 92037 USA
[3] Scripps Res Inst, Scripps Translat Sci Inst, La Jolla, CA 92037 USA
[4] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Dept Med, Div Infect Dis, La Jolla, CA 92093 USA
[6] Univ Peruana Cayetano Heredia, Alexander von Humboldt Inst Trop Med, Lima, Peru
[7] Univ Sao Paulo, Inst Biomed Sci, Dept Parasitol, Sao Paulo, Brazil
[8] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA 92037 USA
[9] Novartis Res Fdn, Genom Inst, San Diego, CA USA
来源
BMC GENOMICS | 2012年 / 13卷
基金
美国国家卫生研究院;
关键词
Malaria; HYBRID SELECTION; RESISTANCE;
D O I
10.1186/1471-2164-13-262
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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% of the genome). 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.
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页数:9
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