Cargando…
Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery
BACKGROUND: Neglected diseases caused by helminth infections impose a massive hindrance to progress in the developing world. While basic research on parasitic flatworms (platyhelminths) continues to expand, researchers have yet to broadly adopt a free-living model to complement the study of these im...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304616/ https://www.ncbi.nlm.nih.gov/pubmed/25600302 http://dx.doi.org/10.1186/s13071-014-0622-3 |
_version_ | 1782354137109757952 |
---|---|
author | Wheeler, Nicolas J Agbedanu, Prince N Kimber, Michael J Ribeiro, Paula Day, Tim A Zamanian, Mostafa |
author_facet | Wheeler, Nicolas J Agbedanu, Prince N Kimber, Michael J Ribeiro, Paula Day, Tim A Zamanian, Mostafa |
author_sort | Wheeler, Nicolas J |
collection | PubMed |
description | BACKGROUND: Neglected diseases caused by helminth infections impose a massive hindrance to progress in the developing world. While basic research on parasitic flatworms (platyhelminths) continues to expand, researchers have yet to broadly adopt a free-living model to complement the study of these important parasites. METHODS: We report the high-coverage sequencing (RNA-Seq) and assembly of the transcriptome of the planarian Girardia tigrina across a set of dynamic conditions. The assembly was annotated and extensive orthology analysis was used to seed a pipeline for the rational prioritization and validation of putative anthelmintic targets. A small number of targets conserved between parasitic and free-living flatworms were comparatively interrogated. RESULTS: 240 million paired-end reads were assembled de novo to produce a strictly filtered predicted proteome consisting of over 22,000 proteins. Gene Ontology annotations were extended to 16,467 proteins. 2,693 sequences were identified in orthology groups spanning flukes, tapeworms and planaria, with 441 highlighted as belonging to druggable protein families. Chemical inhibitors were used on three targets in pharmacological screens using both planaria and schistosomula, revealing distinct motility phenotypes that were shown to correlate with planarian RNAi phenotypes. CONCLUSIONS: This work provides the first comprehensive and annotated sequence resource for the model planarian G. tigrina, alongside a prioritized list of candidate drug targets conserved among parasitic and free-living flatworms. As proof of principle, we show that a simple RNAi and pharmacology pipeline in the more convenient planarian model system can inform parasite biology and serve as an efficient screening tool for the identification of lucrative anthelmintic targets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-014-0622-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4304616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-43046162015-01-24 Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery Wheeler, Nicolas J Agbedanu, Prince N Kimber, Michael J Ribeiro, Paula Day, Tim A Zamanian, Mostafa Parasit Vectors Research BACKGROUND: Neglected diseases caused by helminth infections impose a massive hindrance to progress in the developing world. While basic research on parasitic flatworms (platyhelminths) continues to expand, researchers have yet to broadly adopt a free-living model to complement the study of these important parasites. METHODS: We report the high-coverage sequencing (RNA-Seq) and assembly of the transcriptome of the planarian Girardia tigrina across a set of dynamic conditions. The assembly was annotated and extensive orthology analysis was used to seed a pipeline for the rational prioritization and validation of putative anthelmintic targets. A small number of targets conserved between parasitic and free-living flatworms were comparatively interrogated. RESULTS: 240 million paired-end reads were assembled de novo to produce a strictly filtered predicted proteome consisting of over 22,000 proteins. Gene Ontology annotations were extended to 16,467 proteins. 2,693 sequences were identified in orthology groups spanning flukes, tapeworms and planaria, with 441 highlighted as belonging to druggable protein families. Chemical inhibitors were used on three targets in pharmacological screens using both planaria and schistosomula, revealing distinct motility phenotypes that were shown to correlate with planarian RNAi phenotypes. CONCLUSIONS: This work provides the first comprehensive and annotated sequence resource for the model planarian G. tigrina, alongside a prioritized list of candidate drug targets conserved among parasitic and free-living flatworms. As proof of principle, we show that a simple RNAi and pharmacology pipeline in the more convenient planarian model system can inform parasite biology and serve as an efficient screening tool for the identification of lucrative anthelmintic targets. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-014-0622-3) contains supplementary material, which is available to authorized users. BioMed Central 2015-01-20 /pmc/articles/PMC4304616/ /pubmed/25600302 http://dx.doi.org/10.1186/s13071-014-0622-3 Text en © Wheeler et al.; licensee BioMed Central. 2015 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 Wheeler, Nicolas J Agbedanu, Prince N Kimber, Michael J Ribeiro, Paula Day, Tim A Zamanian, Mostafa Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
title | Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
title_full | Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
title_fullStr | Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
title_full_unstemmed | Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
title_short | Functional analysis of Girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
title_sort | functional analysis of girardia tigrina transcriptome seeds pipeline for anthelmintic target discovery |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4304616/ https://www.ncbi.nlm.nih.gov/pubmed/25600302 http://dx.doi.org/10.1186/s13071-014-0622-3 |
work_keys_str_mv | AT wheelernicolasj functionalanalysisofgirardiatigrinatranscriptomeseedspipelineforanthelmintictargetdiscovery AT agbedanuprincen functionalanalysisofgirardiatigrinatranscriptomeseedspipelineforanthelmintictargetdiscovery AT kimbermichaelj functionalanalysisofgirardiatigrinatranscriptomeseedspipelineforanthelmintictargetdiscovery AT ribeiropaula functionalanalysisofgirardiatigrinatranscriptomeseedspipelineforanthelmintictargetdiscovery AT daytima functionalanalysisofgirardiatigrinatranscriptomeseedspipelineforanthelmintictargetdiscovery AT zamanianmostafa functionalanalysisofgirardiatigrinatranscriptomeseedspipelineforanthelmintictargetdiscovery |