Web of Science: 2 citations, Scopus: 3 citations, Google Scholar: citations,
Extending Immunological Profiling in the Gilthead Sea Bream, Sparus aurata, by Enriched cDNA Library Analysis, Microarray Design and Initial Studies upon the Inflammatory Response to PAMPs
Boltaña Harms, Sebastian (Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí")
Castellana, Barbara (The Child & Family Research Institute (Vancouver, Canadà))
Goetz, Giles (Northwest Fisheries Science Centre (Seattle, Estats Units d'Amèrica))
Tort Bardolet, Lluís (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia)
Teles, Mariana (Universitat Autònoma de Barcelona. Departament de Biologia Cel·lular, de Fisiologia i d'Immunologia)
Mulero, Víctor (Universidad de Murcia. Department de Biología Celular e Histología)
Novoa, Beatriz (Instituto de Investigaciones Marinas (Vigo, Espanya))
Figueras, Antonio (Instituto de Investigaciones Marinas (Vigo, Espanya))
Goetz, Frederick W. (Northwest Fisheries Science Centre (Seattle, Estats Units d'Amèrica))
Gallardo-Escarate, Cristian (Universidad de Concepción (Concepción, Xile))
Planas, Josep V. (Universitat de Barcelona. Departament de Fisiologia i Immunologia)
Mackenzie, Simon A. (Institut de Biotecnologia i de Biomedicina "Vicent Villar Palasí")

Date: 2017
Abstract: This study describes the development and validation of an enriched oligonucleotide-microarray platform for Sparus aurata (SAQ) to provide a platform for transcriptomic studies in this species. A transcriptome database was constructed by assembly of gilthead sea bream sequences derived from public repositories of mRNA together with reads from a large collection of expressed sequence tags (EST) from two extensive targeted cDNA libraries characterizing mRNA transcripts regulated by both bacterial and viral challenge. The developed microarray was further validated by analysing monocyte/macrophage activation profiles after challenge with two Gram-negative bacterial pathogen-associated molecular patterns (PAMPs; lipopolysaccharide (LPS) and peptidoglycan (PGN)). Of the approximately 10,000 EST sequenced, we obtained a total of 6837 EST longer than 100 nt, with 3778 and 3059 EST obtained from the bacterial-primed and from the viral-primed cDNA libraries, respectively. Functional classification of contigs from the bacterial- and viral-primed cDNA libraries by Gene Ontology (GO) showed that the top five represented categories were equally represented in the two libraries: metabolism (approximately 24% of the total number of contigs), carrier proteins/membrane transport (approximately 15%), effectors/modulators and cell communication (approximately 11%), nucleoside, nucleotide and nucleic acid metabolism (approximately 7. 5%) and intracellular transducers/signal transduction (approximately 5%). Transcriptome analyses using this enriched oligonucleotide platform identified differential shifts in the response to PGN and LPS in macrophage-like cells, highlighting responsive gene-cassettes tightly related to PAMP host recognition. As observed in other fish species, PGN is a powerful activator of the inflammatory response in S. aurata macrophage-like cells. We have developed and validated an oligonucleotide microarray (SAQ) that provides a platform enriched for the study of gene expression in S. aurata with an emphasis upon immunity and the immune response.
Rights: Aquest document està subjecte a una llicència d'ús Creative Commons. Es permet la reproducció total o parcial, la distribució, la comunicació pública de l'obra i la creació d'obres derivades, fins i tot amb finalitats comercials, sempre i quan es reconegui l'autoria de l'obra original. Creative Commons
Language: Anglès.
Document: article ; recerca ; publishedVersion
Subject: Expressed sequence tags (EST) ; Oligo-nucleotide microarray ; Pathogen-associated molecular patterns (PAMPs) ; Lipopolysaccharide (LPS) ; Peptidoglycan (PGN) ; Macrophages
Published in: International Journal of Molecular Sciences, Vol. 18 Núm. 2 (2017) , p. 1-21, ISSN 1422-0067

DOI: 10.3390/ijms18020317
PMID: 28165358


21 p, 4.7 MB

The record appears in these collections:
Articles > Research articles
Articles > Published articles

 Record created 2017-02-14, last modified 2019-02-04



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