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Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica

BACKGROUND: The common liver fluke Fasciola hepatica is the agent of a zoonosis with significant economic consequences in livestock production worldwide, and increasing relevance to human health in developing countries. Although flukicidal drugs are available, re-infection and emerging resistance ar...

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Autores principales: Cancela, Martín, Ruétalo, Natalia, Dell'Oca, Nicolás, da Silva, Edileuza, Smircich, Pablo, Rinaldi, Gabriel, Roche, Leda, Carmona, Carlos, Alvarez-Valín, Fernando, Zaha, Arnaldo, Tort, José F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867827/
https://www.ncbi.nlm.nih.gov/pubmed/20374642
http://dx.doi.org/10.1186/1471-2164-11-227
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author Cancela, Martín
Ruétalo, Natalia
Dell'Oca, Nicolás
da Silva, Edileuza
Smircich, Pablo
Rinaldi, Gabriel
Roche, Leda
Carmona, Carlos
Alvarez-Valín, Fernando
Zaha, Arnaldo
Tort, José F
author_facet Cancela, Martín
Ruétalo, Natalia
Dell'Oca, Nicolás
da Silva, Edileuza
Smircich, Pablo
Rinaldi, Gabriel
Roche, Leda
Carmona, Carlos
Alvarez-Valín, Fernando
Zaha, Arnaldo
Tort, José F
author_sort Cancela, Martín
collection PubMed
description BACKGROUND: The common liver fluke Fasciola hepatica is the agent of a zoonosis with significant economic consequences in livestock production worldwide, and increasing relevance to human health in developing countries. Although flukicidal drugs are available, re-infection and emerging resistance are demanding new efficient and inexpensive control strategies. Understanding the molecular mechanisms underlying the host-parasite interaction provide relevant clues in this search, while enlightening the physiological adaptations to parasitism. Genomics and transcriptomics are still in their infancy in F. hepatica, with very scarce information available from the invasive newly excysted juveniles (NEJ). Here we provide an initial glimpse to the transcriptomics of the NEJ, the first stage to interact with the mammalian host. RESULTS: We catalogued more than 500 clusters generated from the analysis of F. hepatica juvenile expressed sequence tags (EST), several of them not detected in the adult stage. A set of putative F. hepatica specific transcripts, and a group of sequences conserved exclusively in flatworms were identified. These novel sequences along with a set of parasite transcripts absent in the host genomes are putative new targets for future anti-parasitic drugs or vaccine development. Comparisons of the F. hepatica sequences with other metazoans genomes or EST databases were consistent with the basal positioning of flatworms in the bilaterian phylogeny. Notably, GC content, codon usage and amino acid frequencies are remarkably different in Schistosomes to F. hepatica and other trematodes. Functional annotation of predicted proteins showed a general representation of diverse biological functions. Besides proteases and antioxidant enzymes expected to participate in the early interaction with the host, various proteins involved in gene expression, protein synthesis, cell signaling and mitochondrial enzymes were identified. Differential expression of secreted protease gene family members between juvenile and adult stages may respond to different needs during host colonization. CONCLUSION: The knowledge of the genes expressed by the invasive stage of Fasciola hepatica is a starting point to unravel key aspects of this parasite's biology. The integration of the emerging transcriptomics, and proteomics data and the advent of functional genomics tools in this organism are positioning F. hepatica as an interesting model for trematode biology.
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spelling pubmed-28678272010-05-12 Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica Cancela, Martín Ruétalo, Natalia Dell'Oca, Nicolás da Silva, Edileuza Smircich, Pablo Rinaldi, Gabriel Roche, Leda Carmona, Carlos Alvarez-Valín, Fernando Zaha, Arnaldo Tort, José F BMC Genomics Research Article BACKGROUND: The common liver fluke Fasciola hepatica is the agent of a zoonosis with significant economic consequences in livestock production worldwide, and increasing relevance to human health in developing countries. Although flukicidal drugs are available, re-infection and emerging resistance are demanding new efficient and inexpensive control strategies. Understanding the molecular mechanisms underlying the host-parasite interaction provide relevant clues in this search, while enlightening the physiological adaptations to parasitism. Genomics and transcriptomics are still in their infancy in F. hepatica, with very scarce information available from the invasive newly excysted juveniles (NEJ). Here we provide an initial glimpse to the transcriptomics of the NEJ, the first stage to interact with the mammalian host. RESULTS: We catalogued more than 500 clusters generated from the analysis of F. hepatica juvenile expressed sequence tags (EST), several of them not detected in the adult stage. A set of putative F. hepatica specific transcripts, and a group of sequences conserved exclusively in flatworms were identified. These novel sequences along with a set of parasite transcripts absent in the host genomes are putative new targets for future anti-parasitic drugs or vaccine development. Comparisons of the F. hepatica sequences with other metazoans genomes or EST databases were consistent with the basal positioning of flatworms in the bilaterian phylogeny. Notably, GC content, codon usage and amino acid frequencies are remarkably different in Schistosomes to F. hepatica and other trematodes. Functional annotation of predicted proteins showed a general representation of diverse biological functions. Besides proteases and antioxidant enzymes expected to participate in the early interaction with the host, various proteins involved in gene expression, protein synthesis, cell signaling and mitochondrial enzymes were identified. Differential expression of secreted protease gene family members between juvenile and adult stages may respond to different needs during host colonization. CONCLUSION: The knowledge of the genes expressed by the invasive stage of Fasciola hepatica is a starting point to unravel key aspects of this parasite's biology. The integration of the emerging transcriptomics, and proteomics data and the advent of functional genomics tools in this organism are positioning F. hepatica as an interesting model for trematode biology. BioMed Central 2010-04-07 /pmc/articles/PMC2867827/ /pubmed/20374642 http://dx.doi.org/10.1186/1471-2164-11-227 Text en Copyright ©2010 Cancela 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
Cancela, Martín
Ruétalo, Natalia
Dell'Oca, Nicolás
da Silva, Edileuza
Smircich, Pablo
Rinaldi, Gabriel
Roche, Leda
Carmona, Carlos
Alvarez-Valín, Fernando
Zaha, Arnaldo
Tort, José F
Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica
title Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica
title_full Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica
title_fullStr Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica
title_full_unstemmed Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica
title_short Survey of transcripts expressed by the invasive juvenile stage of the liver fluke Fasciola hepatica
title_sort survey of transcripts expressed by the invasive juvenile stage of the liver fluke fasciola hepatica
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2867827/
https://www.ncbi.nlm.nih.gov/pubmed/20374642
http://dx.doi.org/10.1186/1471-2164-11-227
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