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PLOS ONE  2012 

High-Throughput Sequence Analysis of Turbot (Scophthalmus maximus) Transcriptome Using 454-Pyrosequencing for the Discovery of Antiviral Immune Genes

DOI: 10.1371/journal.pone.0035369

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Abstract:

Background Turbot (Scophthalmus maximus L.) is an important aquacultural resource both in Europe and Asia. However, there is little information on gene sequences available in public databases. Currently, one of the main problems affecting the culture of this flatfish is mortality due to several pathogens, especially viral diseases which are not treatable. In order to identify new genes involved in immune defense, we conducted 454-pyrosequencing of the turbot transcriptome after different immune stimulations. Methodology/Principal Findings Turbot were injected with viral stimuli to increase the expression level of immune-related genes. High-throughput deep sequencing using 454-pyrosequencing technology yielded 915,256 high-quality reads. These sequences were assembled into 55,404 contigs that were subjected to annotation steps. Intriguingly, 55.16% of the deduced protein was not significantly similar to any sequences in the databases used for the annotation and only 0.85% of the BLASTx top-hits matched S. maximus protein sequences. This relatively low level of annotation is possibly due to the limited information for this specie and other flatfish in the database. These results suggest the identification of a large number of new genes in turbot and in fish in general. A more detailed analysis showed the presence of putative members of several innate and specific immune pathways. Conclusions/Significance To our knowledge, this study is the first transcriptome analysis using 454-pyrosequencing for turbot. Previously, there were only 12,471 EST and less of 1,500 nucleotide sequences for S. maximus in NCBI database. Our results provide a rich source of data (55,404 contigs and 181,845 singletons) for discovering and identifying new genes, which will serve as a basis for microarray construction, gene expression characterization and for identification of genetic markers to be used in several applications. Immune stimulation in turbot was very effective, obtaining an enormous variety of sequences belonging to genes involved in the defense mechanisms.

References

[1]  Nielsen JG (1986) Scophtalmidae. In: Whitehead PJP, Bauchot ML, Hureau JC, Nielsen J, Tortonese E., editors. Fishes of the North-eastern Atlantic and the Mediterranean. Paris: Unesco. pp. 1287–1293.
[2]  Federation of European Aquaculture Producers (FEAP) (2008) Production and price reports of member associations of the F.E.A.P. Liège: FEAP.
[3]  Food and Agriculture Organization of the United Nations (FAO) (2010) The state of world fisheries and aquaculture. Rome: FAO.
[4]  Toranzo AE, Magari?os B, Romalde JL (2005) A review of the main bacterial fish diseases in mariculture systems. Aquaculture 246: 37–61.
[5]  Walker PJ, Winton JR (2010) Emerging viral diseases of fish and shrimp. Vet Res 41: 51–75.
[6]  álvarez-Pellitero P (2008) Fish immunity and parasite infections: from innate immunity to immunoprophylactic prospects. Vet Immunol Immunopathol 126: 171–198.
[7]  Sarmasik A (2002) Antimicrobial peptides: a potential therapeutic alternative for the treatment of fish diseases. Turk J Biol 26: 201–207.
[8]  Biragyn A (2005) Defensins – Non-antibiotic use for vaccine development. Curr Protein Pept Sci 6: 53–60.
[9]  Bowdish DME, Davidson DJ, Hancock REW (2006) Immunomodulatory properties of defensins and cathelicidins. CTMI 306: 27–66.
[10]  Jenssen H, Hamill P, Hancock REW (2006) Peptide Antimicrobial Agents. Clin Microbiol Rev 19: 491–511.
[11]  Kornbluth RS, Stone GW (2006) Immunostimulatory combinations: designing the next generation of vaccine adjuvants. J Leuk Biol 80: 1084–1102.
[12]  Mookherjee N, Hancock REW (2007) Cationic host defense peptides: innate immune regulatory peptides as a novel approach for treating infections. Cell Mol Life Sci 64: 922–933.
[13]  Smith VJ, Desbois AP, Dyrynda EA (2010) Conventional and unconventional antimicrobials from fish, marine invertebrates and micro-algae. Mar Drugs 8: 1213–1262.
[14]  Nicholls EF, Madera L, Hancock REW (2010) Immunomodulators as adjuvants for vaccines and antimicrobial therapy. Ann N Y Acad Sci 1213: 46–61.
[15]  Marra MA, Hillier L, Waterston RH (1998) Expressed sequence tags-ESTablishing bridges between genomes. Trends Genet 14: 4–7.
[16]  Nagaraj SH, Gasser RB, Ranganathan S (2007) A hitchhike?s guide to expressed sequence tag (EST) analysis. Brief Bioinform 8: 6–21.
[17]  Wang C, Zhang XH, Jia A, Chen J, Austin B (2008) Identification of immune-related genes from kidney and spleen of turbot, Psetta maxima (L.), by suppression subtractive hybridization following challenge with Vibrio harveyi. J Fish Dis 31: 505–514.
[18]  Pardo BG, Fernández C, Millán A, Bouza C, Vázquez-López A, et al. (2008) Expressed sequence tags (ESTs) from immune tissues of turbot (Scophthalmus maximus) challenged with pathogens. BMC Vet Res 4: 37.
[19]  Park KC, Osborne JA, Montes A, Dios S, Nerland AH, et al. (2009) Immunological responses of turbot (Psetta maxima) to nodavirus infection or polyriboinosinic polyribocytidylic acid (pIC) stimulation, using expressed sequence tags (ESTs) analysis and cDNA microarrays. Fish Shellfish Immunol 26: 91–108.
[20]  Yeh Y, Feeney RE (1996) Antifreeze proteins: structures and mechanisms of function. Chem Rev 96: 601–617.
[21]  Ewart KV, Fletcher GL (1993) Herring antifreeze protein: primary structure and evidence for a C-type lectin evolutionary origin. Mol Mar Biol Biotechnol 2: 20–27.
[22]  Millan A, Gomez-Tato A, Fernandez C, Pardo BG, Alvarez-Dios JA, et al. (2010) Design and performance of a turbot (Scophthalmus maximus) oligo-microarray based on ESTs from immune tissues. Mar Biotechnol 12: 452–465.
[23]  Kilpatrick DC (2002) Animal lectins: a historical introduction and overview. BBA-Gen Subjects 1572: 187–197.
[24]  Choudhury M, Yamada S, Komatsu M, Kishimura H, Ando S (2009) Homologue of mammalian apolipoprotein A-II in non-mammalian vertebrates. Acta Biochim Biophys Sin 41: 370–378.
[25]  Bolanos-García VM, Miguel RN (2003) On the structure and function of apolipoproteins: more than a family of lipid-binding proteins. Prog Biophys Mol Biol 83: 47–68.
[26]  Srinivas RV, Venkatachalapathi YV, Rui Z, Owens RJ, Gupta KB, et al. (1991) Inhibition of virus-induced cell fusion by apolipoprotein A-I and its amphipathic peptide analogs. J Cell Biochem 45: 224–237.
[27]  Tada N, Sakamoto T, Kagami A, Mochizuki K, Kurosaka K (1993) Antimicrobial activity of lipoprotein particles containing apolipoprotein Al. Mol Cell Biochem 119: 171–178.
[28]  Motizuki M, Satoh T, Takey T, Itoh T, Yokota S, et al. (2002) Structure-activity analysis of an antimicrobial peptide derived from bovine apolipoprotein A-II. J Biochem 132: 115–119.
[29]  Concha MI, Molina S, Oyarzún C, Villanueva J, Amthauer R (2003) Local expression of apolipoprotein A-I gene and a possible role for HDL in primary defence in the carp skin. Fish Shellfish Immunol 14: 259–273.
[30]  Concha MI, Smith VJ, Castro K, Bastias A, Romero A, et al. (2004) Apolipoproteins A-I and A-II are potentially important effectors of innate immunity in the teleost fish Cyprinus carpio. Eur J Biochem 271: 2984–2990.
[31]  Chang MX, Nie P, Liu GY, Song Y, Gao Q (2005) Identification of immune genes in grass carp Ctenopharyngodon idella in response to infection of the parasitic copepod Sinergasilus major. Parasitol Res 96: 224–229.
[32]  Villarroel F, Bastias , A , Casado A, Amthauer R, Concha MI (2007) Apolipoprotein A-I, an antimicrobial protein in Oncorhynchus mykiss: evaluation of its expression in primary defence barriers and plasma levels in sick and healthy fish. Fish Shellfish Immunol 23: 197–209.
[33]  Akerstr?m B, L?gdberg L, Berggard T, Osmark P, Lindqvist A (2000) α1-Microglobulin: a yellow-brown lipocalin. Biochim Biophys Acta 1482: 172–184.
[34]  L?gdberg L, Wester L (2000) Immunocalins: a lipocalin subfamily that modulates immune and inflammatory responses. Biochim Biophys Acta 1482: 284–297.
[35]  Pott GB, Chan ED, Dinarello CA, Shapiro L (2009) α1-Antitrypsin is an endogenous inhibitor of proinflammatory cytokine production in whole blood. J Leukoc Biol 85: 886–895.
[36]  Steinhoff M, Buddenkotte J, Shpacovitch V, Rattenholl A, Moormann C, et al. (2005) Proteinase-activated receptors: transducers of proteinase-mediated signaling in inflammation and immune response. Endocr Rev 26: 1–43.
[37]  Maeda K, Hirota M, Kimura Y, Ichihara A, Ohmuraya M, et al. (2005) Proinflammatory role of trypsin and protease-activated receptor-2 in a rat model of acute pancreatitis. Pancreas 31: 54–62.
[38]  Jensen T, Kierulf P, Sandset PM, Klingenberg O, Jo? GB, et al. (2007) Fibrinogen and fibrin induce synthesis of proinflammatory cytokines from isolated peripheral blood mononuclear cells. Thromb Haemost 97: 822–829.
[39]  Lu PP, Liu JT, Liu N, Guo F, Ji YY, et al. (2011) Pro-inflammatory effect of fibrinogen and FDP on vascular smooth muscle cells by IL-6, TNF-α and iNOS. Life Sci 88: 839–845.
[40]  Jiang D, Liang J, Noble PW (2011) Hyaluronan as an immune regulator in human diseases. Physiol Rev 91: 221–264.
[41]  Hallquist NA, Klasing KC (1994) Serotransferrin, ovotransferrin and metallothionein levels during an immune response in chickens. Comp Biochem Physiol Biochem Mol Biol 108: 375–384.
[42]  Quaye IK (2008) Haptoglobin, inflammation and disease. Trans R Soc Trop Med Hyg 102: 735–742.
[43]  Tolosano E, Fagoonee S, Morello N, Vinchi F, Fiorito V (2010) Heme scavenging and the other facets of hemopexin. Antioxid Redox Signal 12: 305–320.
[44]  Office International des Epizooties (OIE) (2009) Manual of Diagnostic test for Aquatic Animals. Paris: OIE.
[45]  Drakesmith H, Prentice A (2008) Viral infection and iron metabolism. Nat Rev Microbiol 6: 541–552.
[46]  Law RHP, Lukoyanova N, Voskoboinik I, Caradoc-Davies TT, Baran K, et al. (2010) The structural basis for membrane binding and pore formation by lymphocyte perforin. Nature 468: 447–453.
[47]  G?tz S, García-Gómez JM, Terol J, Williams TD, Nagaraj SH, et al. (2008) High-throughput functional annotation and data mining with the Blast2GO suite. Nucleic Acids Res 36: 3420–3435.
[48]  Conesa A, G?tz S, García-Gómez JM, Terol J, Talon M, et al. (2005) Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research. Bioinformatics 21: 3674–3676.
[49]  Salem M, Rexroad CE III, Wang J, Thorgaard GH, Yao J (2010) Characterization of the rainbow trout transcriptome using Sanger and 454-pyrosequencing approaches. BMC Genomics 11: 564.
[50]  Zhang Z, Wang Y, Wang S, Liu J, Warren W, et al. (2011) Transcriptome analysis of female and male Xiphophorus maculatus Jp 163 A. PLoS ONE 6: e18379.
[51]  Coppe A, Pujolar JM, Maes GE, Larsen PF, Hansen MM, et al. (2010) Sequencing, de novo annotation and analysis of the first Anguilla anguilla transcriptome: EeellBase opens new perspectives for the study of the critically endangered european eel. BMC Genomics 11: 635.
[52]  Wang JPZ, Lindsay BG, Leebens-Mack J, Cui L, Wall K, et al. (2004) EST clustering error evaluation and correction. Bioinformatics 20: 2973–2984.
[53]  Serazin AC, Dana AN, Hillenmeyer ME, Lobo NF, Coulibaly MB, et al. (2009) Comparative analysis of the global transcriptome of Anopheles funestus from Mali, West Africa. PLoS ONE 4: e7976.
[54]  Carroll MC (2004) The complement system in regulation of adaptive immunity. Nat Immunol 5: 981–986.
[55]  Gasque P (2004) Complement: a unique innate immune sensor for danger signals. Mol Immunol 41: 1089–1098.
[56]  Barton , GM , Medzhitov R (2003) Toll-Like Receptor Signaling Pathways. Science 300: 1524–1525.
[57]  Takeda K, Akira S (2004) TLR signaling pathways. Sem Immunol 16: 3–9.
[58]  Kurosaki T, Shinohara H, Baba Y (2010) B cell signaling and fate decision. Annu Rev Immunol 28: 21–55.
[59]  Batista FD, Neuberger MS (1998) Affinity dependence of the B cell response to antigen: a threshold, a ceiling, and the importance of off-rate. Immunity 8: 751–759.
[60]  Starr TK, Jameson SC, Hogquist KA (2003) Positive and negative selection of T cells. Annu Rev Immunol 21: 139–176.
[61]  Germain RN (1994) MHC-dependent antigen processing and peptide presentation: providing ligands for T lymphocyte activation. Cell 76: 287–299.
[62]  Mosmann TR, Coffman RL (1989) TH1 and TH2 cells: different patterns of lymphokine secretion lead to different functional properties. Annu Rev Immunol 7: 145–173.
[63]  Chaplin DD (2010) Overview of the immune response. J Allergy Clin Immunol 125: S3–S23.
[64]  Elmore S (2007) Apoptosis: a review of programmed cell death. Toxicol Pathol 35: 495–516.
[65]  Crawford ED, Wells JA (2011) Caspase substrates and cellular remodeling. Annu Rev Biochem 80: 1055–1087.
[66]  Townsend MJ, McKenzie AN (2000) Unravelling the net? cytokines and diseases. J Cell Sci 113: 3549–3550.
[67]  Feliciani C, Gupta AK, Saucier DN (1996) Keratinocytes and Cytokine/Growth Factors. CROBM 7: 300–318.
[68]  Miller MD, Krangel MS (1992) Biology and biochemistry of the chemokines: a family of chemotactic and inflammatory cytokines. Crit Rev Immunol 12: 17–46.
[69]  Wang H, Czura CJ, Tracey KJ (2003) Tumor necrosis factor. In: Thomson AW, Lotze MT, editors. The Cytokine Handbook. Amsterdam: Academic Press. pp. 837–860.
[70]  Clark SC, Kamen R (1987) The human hematopoietic colony stimulating factors. Science 236: 1229–1237.
[71]  Grotmol S, Nerland AH, Biering E, Totland GK, Nishizawa T (2000) Characterization of the capsid protein gene from a nodavirus strain affecting the Atlantic halibut Hippoglossus hippoglossus and design of an optimal reverse-transcriptase polymerase chain reaction (RT-PCR) detection assay. Dis Aquat Organ 39: 79–88.
[72]  Ross K, McCarthy U, Huntly PJ, Wood BP, Stuart D, et al. (1994) An outbreak of viral haemorrhagic septicaemia (VHS) in turbot (Scophthalmus maximus) in Scotland. Bull Eur Assoc Fish Pathol 14: 213–214.
[73]  Dios S, Poisa-Beiro L, Figueras A, Novoa B (2007) Suppression subtraction hybridization (SSH) and macroarray techniques reveal differential gene expression profiles in brain of sea bream infected with nodavirus. Mol Immunol 44: 2195–2204.
[74]  Poisa-Beiro L, Dios S, Montes A, Aranguren R, Figueras A, Novoa B (2008) Nodavirus increases the expression of Mx and inflammatory cytokines in fish brain. Mol Immunol 45: 218–225.
[75]  Shagin DA, Rebrikov DV, Kozhemyako VB, Altshuler IM, Shcheglov AS, et al. (2002) A novel method for SNP detection using a new duplex-specific nuclease from crab hepatopancreas. Genome Res 12: 1935–42.
[76]  Zhulidov PA, Bogdanova EA, Shcheglov AS, Vagner LL, Khaspekov GL, et al. (2004) Simple cDNA normalization using kamchatka crab duplex-specific nuclease. Nucleic Acids Res 32: e37.
[77]  Chevreux B, Pfisterer T, Drescher B, Driesel AJ, Müller WE, et al. (2004) Using the miraEST Assembler for Reliable and Automated mRNA Transcript Assembly and SNP Detection in Sequenced ESTs. Genome Res 14: 1147–1159.
[78]  Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215: 403–410.
[79]  Kanehisa M, Goto S (2000) KEGG: Kyoto Encyclopedia of Genes and Genomes. Nucleic Acids Res 28: 27–30.

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