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Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation

BACKGROUND: Hookworm infection is one of the most important neglected diseases in developing countries, with approximately 1 billion people infected worldwide. To better understand hookworm biology and nematode parasitism, the present study generated a near complete transcriptome of the canine hookw...

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Autores principales: Wang, Zhengyuan, Abubucker, Sahar, Martin, John, Wilson, Richard K, Hawdon, John, Mitreva, Makedonka
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882930/
https://www.ncbi.nlm.nih.gov/pubmed/20470405
http://dx.doi.org/10.1186/1471-2164-11-307
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author Wang, Zhengyuan
Abubucker, Sahar
Martin, John
Wilson, Richard K
Hawdon, John
Mitreva, Makedonka
author_facet Wang, Zhengyuan
Abubucker, Sahar
Martin, John
Wilson, Richard K
Hawdon, John
Mitreva, Makedonka
author_sort Wang, Zhengyuan
collection PubMed
description BACKGROUND: Hookworm infection is one of the most important neglected diseases in developing countries, with approximately 1 billion people infected worldwide. To better understand hookworm biology and nematode parasitism, the present study generated a near complete transcriptome of the canine hookworm Ancylostoma caninum to a very high coverage using high throughput technology, and compared it to those of the free-living nematode Caenorhabditis elegans and the parasite Brugia malayi. RESULTS: The generated transcripts from four developmental stages, infective L3, serum stimulated L3, adult male and adult female, covered 93% of the A. caninum transcriptome. The broad diversity among nematode transcriptomes was confirmed, and an impact of parasitic adaptation on transcriptome diversity was inferred. Intra-population analysis showed that A. caninum has higher coding sequence diversity than humans. Examining the developmental expression profiles of A. caninum revealed major transitions in gene expression from larval stages to adult. Adult males expressed the highest number of selectively expressed genes, but adult female expressed the highest number of selective parasitism-related genes. Genes related to parasitism adaptation and A. caninum specific genes exhibited more expression selectivity while those conserved in nematodes tend to be consistently expressed. Parasitism related genes were expressed more selectively in adult male and female worms. The comprehensive analysis of digital expression profiles along with transcriptome comparisons enabled identification of a set of parasitism genes encoding secretory proteins in animal parasitic nematode. CONCLUSIONS: This study validated the usage of deep sequencing for gene expression profiling. Parasitic adaptation of the canine hookworm is related to its diversity and developmental dynamics. This comprehensive comparative genomic and expression study substantially improves our understanding of the basic biology and parasitism of hookworms and, is expected, in the long run, to accelerate research toward development of vaccines and novel anthelmintics.
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spelling pubmed-28829302010-06-10 Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation Wang, Zhengyuan Abubucker, Sahar Martin, John Wilson, Richard K Hawdon, John Mitreva, Makedonka BMC Genomics Research Article BACKGROUND: Hookworm infection is one of the most important neglected diseases in developing countries, with approximately 1 billion people infected worldwide. To better understand hookworm biology and nematode parasitism, the present study generated a near complete transcriptome of the canine hookworm Ancylostoma caninum to a very high coverage using high throughput technology, and compared it to those of the free-living nematode Caenorhabditis elegans and the parasite Brugia malayi. RESULTS: The generated transcripts from four developmental stages, infective L3, serum stimulated L3, adult male and adult female, covered 93% of the A. caninum transcriptome. The broad diversity among nematode transcriptomes was confirmed, and an impact of parasitic adaptation on transcriptome diversity was inferred. Intra-population analysis showed that A. caninum has higher coding sequence diversity than humans. Examining the developmental expression profiles of A. caninum revealed major transitions in gene expression from larval stages to adult. Adult males expressed the highest number of selectively expressed genes, but adult female expressed the highest number of selective parasitism-related genes. Genes related to parasitism adaptation and A. caninum specific genes exhibited more expression selectivity while those conserved in nematodes tend to be consistently expressed. Parasitism related genes were expressed more selectively in adult male and female worms. The comprehensive analysis of digital expression profiles along with transcriptome comparisons enabled identification of a set of parasitism genes encoding secretory proteins in animal parasitic nematode. CONCLUSIONS: This study validated the usage of deep sequencing for gene expression profiling. Parasitic adaptation of the canine hookworm is related to its diversity and developmental dynamics. This comprehensive comparative genomic and expression study substantially improves our understanding of the basic biology and parasitism of hookworms and, is expected, in the long run, to accelerate research toward development of vaccines and novel anthelmintics. BioMed Central 2010-05-14 /pmc/articles/PMC2882930/ /pubmed/20470405 http://dx.doi.org/10.1186/1471-2164-11-307 Text en Copyright ©2010 Wang 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 Research Article
Wang, Zhengyuan
Abubucker, Sahar
Martin, John
Wilson, Richard K
Hawdon, John
Mitreva, Makedonka
Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
title Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
title_full Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
title_fullStr Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
title_full_unstemmed Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
title_short Characterizing Ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
title_sort characterizing ancylostoma caninum transcriptome and exploring nematode parasitic adaptation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2882930/
https://www.ncbi.nlm.nih.gov/pubmed/20470405
http://dx.doi.org/10.1186/1471-2164-11-307
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