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BMC Genomics

, 16:458

First Online: 16 June 2015Received: 02 December 2014Accepted: 29 May 2015DOI: 10.1186-s12864-015-1667-1

Cite this article as: Verbruggen, B., Bickley, L.K., Santos, E.M. et al. BMC Genomics 2015 16: 458. doi:10.1186-s12864-015-1667-1

Abstract

BackgroundThe European shore crab, Carcinus maenas, is used widely in biomonitoring, ecotoxicology and for studies into host-pathogen interactions. It is also an important invasive species in numerous global locations. However, the genomic resources for this organism are still sparse, limiting research progress in these fields. To address this resource shortfall we produced a C. maenas transcriptome, enabled by the progress in next-generation sequencing technologies, and applied this to assemble information on the innate immune system in this species.

ResultsWe isolated and pooled RNA for twelve different tissues and organs from C. maenas individuals and sequenced the RNA using next generation sequencing on an Illumina HiSeq 2500 platform. After de novo assembly a transcriptome was generated encompassing 212,427 transcripts 153,699 loci. The transcripts were filtered, annotated and characterised using a variety of tools including BLAST, MEGAN and RSEM and databases including NCBI, Gene Ontology and KEGG. There were differential patterns of expression for between 1,223 and 2,741 transcripts across tissues and organs with over-represented Gene Ontology terms relating to their specific function. Based on sequence homology to immune system components in other organisms, we show both the presence of transcripts for a series of known pathogen recognition receptors and response proteins that form part of the innate immune system, and transcripts representing the RNAi, Toll-like receptor signalling, IMD and JAK-STAT pathways.

ConclusionsWe have produced an assembled transcriptome for C. maenas that provides a significant molecular resource for wide ranging studies in this species. Analysis of the transcriptome has revealed the presence of a series of known targets and functional pathways that form part of their innate immune system and illustrate tissue specific differences in their expression patterns.

AbbreviationsWSSVWhite spot syndrome virus

GOGene ontology

FDRFalse discovery rate

IMDImmune deficiency

MAPKMitogen activated protein kinase

PRRPattern recognition receptors

PAMPPathogen associated molecular patterns

GNBPGram-negative binding proteins

PGRPPeptidoglycan recognition proteins

TLRToll like receptor

FPKMFragments per kilo bases of exons per million mapped reads

ALFAnti-lipopolysaccharide factor

POPhenol oxidase

RNAiRNA interference

Bas Verbruggen and Lisa K. Bickley contributed equally to this work.

Electronic supplementary materialThe online version of this article doi:10.1186-s12864-015-1667-1 contains supplementary material, which is available to authorized users.

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Autor: Bas Verbruggen - Lisa K. Bickley - Eduarda M. Santos - Charles R. Tyler - Grant D. Stentiford - Kelly S. Bateman - Ronn

Fuente: https://link.springer.com/







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