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Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis

BACKGROUND: More than 20% of the world’s population is at risk for infection by filarial nematodes and >180 million people worldwide are already infected. Along with infection comes significant morbidity that has a socioeconomic impact. The eight filarial nematodes that infect humans are Wucherer...

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Autores principales: Tallon, Luke J, Liu, Xinyue, Bennuru, Sasisekhar, Chibucos, Marcus C, Godinez, Alvaro, Ott, Sandra, Zhao, Xuechu, Sadzewicz, Lisa, Fraser, Claire M, Nutman, Thomas B, Dunning Hotopp, Julie C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175631/
https://www.ncbi.nlm.nih.gov/pubmed/25217238
http://dx.doi.org/10.1186/1471-2164-15-788
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author Tallon, Luke J
Liu, Xinyue
Bennuru, Sasisekhar
Chibucos, Marcus C
Godinez, Alvaro
Ott, Sandra
Zhao, Xuechu
Sadzewicz, Lisa
Fraser, Claire M
Nutman, Thomas B
Dunning Hotopp, Julie C
author_facet Tallon, Luke J
Liu, Xinyue
Bennuru, Sasisekhar
Chibucos, Marcus C
Godinez, Alvaro
Ott, Sandra
Zhao, Xuechu
Sadzewicz, Lisa
Fraser, Claire M
Nutman, Thomas B
Dunning Hotopp, Julie C
author_sort Tallon, Luke J
collection PubMed
description BACKGROUND: More than 20% of the world’s population is at risk for infection by filarial nematodes and >180 million people worldwide are already infected. Along with infection comes significant morbidity that has a socioeconomic impact. The eight filarial nematodes that infect humans are Wuchereria bancrofti, Brugia malayi, Brugia timori, Onchocerca volvulus, Loa loa, Mansonella perstans, Mansonella streptocerca, and Mansonella ozzardi, of which three have published draft genome sequences. Since all have humans as the definitive host, standard avenues of research that rely on culturing and genetics have often not been possible. Therefore, genome sequencing provides an important window into understanding the biology of these parasites. The need for large amounts of high quality genomic DNA from homozygous, inbred lines; the availability of only short sequence reads from next-generation sequencing platforms at a reasonable expense; and the lack of random large insert libraries has limited our ability to generate high quality genome sequences for these parasites. However, the Pacific Biosciences single molecule, real-time sequencing platform holds great promise in reducing input amounts and generating sufficiently long sequences that bypass the need for large insert paired libraries. RESULTS: Here, we report on efforts to generate a more complete genome assembly for L. loa using genetically heterogeneous DNA isolated from a single clinical sample and sequenced on the Pacific Biosciences platform. To obtain the best assembly, numerous assemblers and sequencing datasets were analyzed, combined, and compared. Quiver-informed trimming of an assembly of only Pacific Biosciences reads by HGAP2 was selected as the final assembly of 96.4 Mbp in 2,250 contigs. This results in ~9% more of the genome in ~85% fewer contigs from ~80% less starting material at a fraction of the cost of previous Roche 454-based sequencing efforts. CONCLUSIONS: The result is the most complete filarial nematode assembly produced thus far and demonstrates the utility of single molecule sequencing on the Pacific Biosciences platform for genetically heterogeneous metazoan genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-788) contains supplementary material, which is available to authorized users.
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spelling pubmed-41756312014-09-27 Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis Tallon, Luke J Liu, Xinyue Bennuru, Sasisekhar Chibucos, Marcus C Godinez, Alvaro Ott, Sandra Zhao, Xuechu Sadzewicz, Lisa Fraser, Claire M Nutman, Thomas B Dunning Hotopp, Julie C BMC Genomics Research Article BACKGROUND: More than 20% of the world’s population is at risk for infection by filarial nematodes and >180 million people worldwide are already infected. Along with infection comes significant morbidity that has a socioeconomic impact. The eight filarial nematodes that infect humans are Wuchereria bancrofti, Brugia malayi, Brugia timori, Onchocerca volvulus, Loa loa, Mansonella perstans, Mansonella streptocerca, and Mansonella ozzardi, of which three have published draft genome sequences. Since all have humans as the definitive host, standard avenues of research that rely on culturing and genetics have often not been possible. Therefore, genome sequencing provides an important window into understanding the biology of these parasites. The need for large amounts of high quality genomic DNA from homozygous, inbred lines; the availability of only short sequence reads from next-generation sequencing platforms at a reasonable expense; and the lack of random large insert libraries has limited our ability to generate high quality genome sequences for these parasites. However, the Pacific Biosciences single molecule, real-time sequencing platform holds great promise in reducing input amounts and generating sufficiently long sequences that bypass the need for large insert paired libraries. RESULTS: Here, we report on efforts to generate a more complete genome assembly for L. loa using genetically heterogeneous DNA isolated from a single clinical sample and sequenced on the Pacific Biosciences platform. To obtain the best assembly, numerous assemblers and sequencing datasets were analyzed, combined, and compared. Quiver-informed trimming of an assembly of only Pacific Biosciences reads by HGAP2 was selected as the final assembly of 96.4 Mbp in 2,250 contigs. This results in ~9% more of the genome in ~85% fewer contigs from ~80% less starting material at a fraction of the cost of previous Roche 454-based sequencing efforts. CONCLUSIONS: The result is the most complete filarial nematode assembly produced thus far and demonstrates the utility of single molecule sequencing on the Pacific Biosciences platform for genetically heterogeneous metazoan genomes. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1471-2164-15-788) contains supplementary material, which is available to authorized users. BioMed Central 2014-09-12 /pmc/articles/PMC4175631/ /pubmed/25217238 http://dx.doi.org/10.1186/1471-2164-15-788 Text en © Tallon et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Article
Tallon, Luke J
Liu, Xinyue
Bennuru, Sasisekhar
Chibucos, Marcus C
Godinez, Alvaro
Ott, Sandra
Zhao, Xuechu
Sadzewicz, Lisa
Fraser, Claire M
Nutman, Thomas B
Dunning Hotopp, Julie C
Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis
title Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis
title_full Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis
title_fullStr Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis
title_full_unstemmed Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis
title_short Single molecule sequencing and genome assembly of a clinical specimen of Loa loa, the causative agent of loiasis
title_sort single molecule sequencing and genome assembly of a clinical specimen of loa loa, the causative agent of loiasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4175631/
https://www.ncbi.nlm.nih.gov/pubmed/25217238
http://dx.doi.org/10.1186/1471-2164-15-788
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