User menu

Accès à distance ? S'identifier sur le proxy UCLouvain

De novo adult transcriptomes of two European brittle stars: spotlight on opsin-based photoreception

  • Open access
  • PDF
  • 3.18 M
  1. , Sodergren E., Weinstock G. M., Davidson E. H, Cameron R. A., Gibbs R. A., Angerer R. C., Angerer L. M., Arnone M. I., Burgess D. R., Burke R. D., Coffman J. A., Dean M., Elphick M. R., Ettensohn C. A., Foltz K. R., Hamdoun A., Hynes R. O., Klein W. H., Marzluff W., McClay D. R., Morris R. L., Mushegian A., Rast J. P., Smith L. C., Thorndyke M. C., Vacquier V. D., Wessel G. M., Wray G., Zhang L., Elsik C. G., Ermolaeva O., Hlavina W., Hofmann G., Kitts P., Landrum M. J., Mackey A. J., Maglott D., Panopoulou G., Poustka A. J., Pruitt K., Sapojnikov V., Song X., Souvorov A., Solovyev V., Wei Z., Whittaker C. A., Worley K., Durbin K. J., Shen Y., Fedrigo O., Garfield D., Haygood R., Primus A., Satija R., Severson T., Gonzalez-Garay M. L., Jackson A. R., Milosavljevic A., Tong M., Killian C. E., Livingston B. T., Wilt F. H., Adams N., Belle R., Carbonneau S., Cheung R., Cormier P., Cosson B., Croce J., Fernandez-Guerra A., Geneviere A.-M., Goel M., Kelkar H., Morales J., Mulner-Lorillon O., Robertson A. J., Goldstone J. V., Cole B., Epel D., Gold B., Hahn M. E., Howard-Ashby M., Scally M., Stegeman J. J., Allgood E. L., Cool J., Judkins K. M., McCafferty S. S., Musante A. M., Obar R. A., Rawson A. P., Rossetti B. J., Gibbons I. R., Hoffman M. P., Leone A., Istrail S., Materna S. C., Samanta M. P., Stolc V., Tongprasit W., Tu Q., Bergeron K.-F., Brandhorst B. P., Whittle J., Berney K., Bottjer D. J., Calestani C., Peterson K., Chow E., Yuan Q. A., Elhaik E., Graur D., Reese J. T., Bosdet I., Heesun S., Marra M. A., Schein J., Anderson M. K., Brockton V., Buckley K. M., Cohen A. H., Fugmann S. D., Hibino T., Loza-Coll M., Majeske A. J., Messier C., Nair S. V., Pancer Z., Terwilliger D. P., Agca C., Arboleda E., Chen N., Churcher A. M., Hallbook F., Humphrey G. W., Idris M. M., Kiyama T., Liang S., Mellott D., Mu X., Murray G., Olinski R. P., Raible F., Rowe M., Taylor J. S., Tessmar-Raible K., Wang D., Wilson K. H., Yaguchi S., Gaasterland T., Galindo B. E., Gunaratne H. J., Juliano C., Kinukawa M., Moy G. W., Neill A. T., Nomura M., Raisch M., Reade A., Roux M. M., Song J. L., Su Y.-H., Townley I. K., Voronina E., Wong J. L., Amore G., Branno M., Brown E. R., Cavalieri V., Duboc V., Duloquin L., Flytzanis C., Gache C., Lapraz F., Lepage T., Locascio A., Martinez P., Matassi G., Matranga V., Range R., Rizzo F., Rottinger E., Beane W., Bradham C., Byrum C., Glenn T., Hussain S., Manning F. G., Miranda E., Thomason R., Walton K., Wikramanayke A., Wu S.-Y., Xu R., Brown C. T., Chen L., Gray R. F., Lee P. Y., Nam J., Oliveri P., Smith J., Muzny D., Bell S., Chacko J., Cree A., Curry S., Davis C., Dinh H., Dugan-Rocha S., Fowler J., Gill R., Hamilton C., Hernandez J., Hines S., Hume J., Jackson L., Jolivet A., Kovar C., Lee S., Lewis L., Miner G., Morgan M., Nazareth L. V., Okwuonu G., Parker D., Pu L.-L., Thorn R., Wright R., The Genome of the Sea Urchin Strongylocentrotus purpuratus, 10.1126/science.1133609
  2. Cameron R. A., Samanta M., Yuan A., He D., Davidson E., SpBase: the sea urchin genome database and web site, 10.1093/nar/gkn887
  3. Du Huixia, Bao Zhenmin, Hou Rui, Wang Shan, Su Hailin, Yan Jingjing, Tian Meilin, Li Yan, Wei Wen, Lu Wei, Hu Xiaoli, Wang Shi, Hu Jingjie, Transcriptome Sequencing and Characterization for the Sea Cucumber Apostichopus japonicus (Selenka, 1867), 10.1371/journal.pone.0033311
  4. Zhou Z. C., Dong Y., Sun H. J., Yang A. F., Chen Z., Gao S., Jiang J. W., Guan X. Y., Jiang B., Wang B., Transcriptome sequencing of sea cucumber (Apostichopus japonicus) and the identification of gene-associated markers, 10.1111/1755-0998.12147
  5. Vaughn Roy, Garnhart Nancy, Garey James R, Thomas W, Livingston Brian T, Sequencing and analysis of the gastrula transcriptome of the brittle star Ophiocoma wendtii, 10.1186/2041-9139-3-19
  6. Burns Gavin, Thorndyke Michael C., Peck Lloyd S., Clark Melody S., Transcriptome pyrosequencing of the Antarctic brittle star Ophionotus victoriae, 10.1016/j.margen.2012.05.003
  7. Gillard Gareth B, Garama Daniel J, Brown Chris M, The transcriptome of the NZ endemic sea urchin Kina (Evechinus chloroticus), 10.1186/1471-2164-15-45
  8. Mashanov Vladimir S, Zueva Olga R, García-Arrarás José E, Transcriptomic changes during regeneration of the central nervous system in an echinoderm, 10.1186/1471-2164-15-357
  9. Wygoda Jennifer A., Yang Yee, Byrne Maria, Wray Gregory A., Transcriptomic Analysis of the Highly Derived Radial Body Plan of a Sea Urchin, 10.1093/gbe/evu070
  10. Dilly G. F., Gaitán-Espitia J. D., Hofmann G. E., Characterization of the Antarctic sea urchin (Sterechinus neumayeri) transcriptome and mitogenome: a molecular resource for phylogenetics, ecophysiology and global change biology, 10.1111/1755-0998.12316
  11. Tu Qiang, Cameron R. Andrew, Davidson Eric H., Quantitative developmental transcriptomes of the sea urchin Strongylocentrotus purpuratus, 10.1016/j.ydbio.2013.11.019
  12. Ma Deyou, Yang Hongsheng, Sun Lina, Profiling and comparison of color body wall transcriptome of normal juvenile sea cucumber (Apostichopus japonicus) and those produced by crossing albino, 10.1007/s11802-014-2297-y
  13. Ma Deyou, Yang Hongsheng, Sun Lina, Chen Muyan, Transcription profiling using RNA-Seq demonstrates expression differences in the body walls of juvenile albino and normal sea cucumbers Apostichopus japonicus, 10.1007/s00343-014-3041-6
  14. Ma Deyou, Yang Hongsheng, Sun Lina, Xu Dongxue, Comparative analysis of transcriptomes from albino and control sea cucumbers, Apostichopus japonicus, 10.1007/s13131-014-0464-z
  15. Hennebert E., Wattiez R., Demeuldre M., Ladurner P., Hwang D. S., Waite J. H., Flammang P., Sea star tenacity mediated by a protein that fragments, then aggregates, 10.1073/pnas.1400089111
  16. Purushothaman Sruthi, Saxena Sandeep, Meghah Vuppalapaty, Swamy Cherukuvada V. Brahmendra, Ortega-Martinez Olga, Dupont Sam, Idris Mohammed, Transcriptomic and proteomic analyses of Amphiura filiformis arm tissue-undergoing regeneration, 10.1016/j.jprot.2014.08.011
  17. Telford M. J., Lowe C. J., Cameron C. B., Ortega-Martinez O., Aronowicz J., Oliveri P., Copley R. R., Phylogenomic analysis of echinoderm class relationships supports Asterozoa, 10.1098/rspb.2014.0479
  18. Reich Adrian, Dunn Casey, Akasaka Koji, Wessel Gary, Phylogenomic Analyses of Echinodermata Support the Sister Groups of Asterozoa and Echinozoa, 10.1371/journal.pone.0119627
  19. Delroisse Jérôme, Ortega-Martinez Olga, Dupont Sam, Mallefet Jérôme, Flammang Patrick, De novo transcriptome of the European brittle star Amphiura filiformis pluteus larvae, 10.1016/j.margen.2015.05.014
  20. Elphick Maurice R., Semmens Dean C., Blowes Liisa M., Levine Judith, Lowe Christopher J., Arnone Maria I., Clark Melody S., Reconstructing SALMFamide Neuropeptide Precursor Evolution in the Phylum Echinodermata: Ophiuroid and Crinoid Sequence Data Provide New Insights, 10.3389/fendo.2015.00002
  21. Wang Zhong, Gerstein Mark, Snyder Michael, RNA-Seq: a revolutionary tool for transcriptomics, 10.1038/nrg2484
  22. Hodkinson Brendan P., Grice Elizabeth A., Next-Generation Sequencing: A Review of Technologies and Tools for Wound Microbiome Research, 10.1089/wound.2014.0542
  23. Morozova Olena, Hirst Martin, Marra Marco A., Applications of New Sequencing Technologies for Transcriptome Analysis, 10.1146/annurev-genom-082908-145957
  24. TW Cronin, 105 (2014)
  25. Raible Florian, Tessmar-Raible Kristin, Arboleda Enrique, Kaller Tobias, Bork Peer, Arendt Detlev, Arnone Maria I., Opsins and clusters of sensory G-protein-coupled receptors in the sea urchin genome, 10.1016/j.ydbio.2006.08.070
  26. Ullrich-Luter E. M., Dupont S., Arboleda E., Hausen H., Arnone M. I., Unique system of photoreceptors in sea urchin tube feet, 10.1073/pnas.1018495108
  27. J Delroisse, Cah Biol, 54, 721 (2013)
  28. Ullrich-Lüter Esther M., D’Aniello Salvatore, Arnone Maria I., C-opsin Expressing Photoreceptors in Echinoderms, 10.1093/icb/ict050
  29. Delroisse Jérôme, Ullrich-Lüter Esther, Ortega-Martinez Olga, Dupont Sam, Arnone Maria-Ina, Mallefet Jérôme, Flammang Patrick, High opsin diversity in a non-visual infaunal brittle star, 10.1186/1471-2164-15-1035
  30. D'Aniello S., Delroisse J., Valero-Gracia A., Lowe E.K., Byrne M., Cannon J.T., Halanych K.M., Elphick M.R., Mallefet J., Kaul-Strehlow S., Lowe C.J., Flammang P., Ullrich-Lüter E., Wanninger A., Arnone M.I., Opsin evolution in the Ambulacraria, 10.1016/j.margen.2015.10.001
  31. Hendler Gordon, Brittlestar Color-Change and Phototaxis (Echinodermata: Ophiuroidea: Ophiocomidae)., 10.1111/j.1439-0485.1984.tb00131.x
  32. Hendler Gordon, Byrne Maria, Fine structure of the dorsal arm plate of Ophiocoma wendti: Evidence for a photoreceptor system (Echinodermata, Ophiuroidea), 10.1007/bf00312172
  33. T Heinzeller (2005)
  34. Aizenberg Joanna, Tkachenko Alexei, Weiner Steve, Addadi Lia, Hendler Gordon, Calcitic microlenses as part of the photoreceptor system in brittlestars, 10.1038/35090573
  35. WJ Gehring, Developmental Biology, 3, 1 (2014)
  36. Johnsen S., Identification and Localization of a Possible Rhodopsin in the Echinoderms Asterias forbesi (Asteroidea) and Ophioderma brevispinum (Ophiuroidea), 10.2307/1542739
  37. D Arendt, International Journal of Developmental Biology, 47, 563 (2003)
  38. Andrews S. FastQC: A quality control application for high throughput sequence data. Babraham Institute Project page: http://www.bioinformatics.bbsrc.ac.uk/projects/fastqc. 2012.
  39. Grabherr Manfred G, Haas Brian J, Yassour Moran, Levin Joshua Z, Thompson Dawn A, Amit Ido, Adiconis Xian, Fan Lin, Raychowdhury Raktima, Zeng Qiandong, Chen Zehua, Mauceli Evan, Hacohen Nir, Gnirke Andreas, Rhind Nicholas, di Palma Federica, Birren Bruce W, Nusbaum Chad, Lindblad-Toh Kerstin, Friedman Nir, Regev Aviv, Full-length transcriptome assembly from RNA-Seq data without a reference genome, 10.1038/nbt.1883
  40. Pertea G., Huang X., Liang F., Antonescu V., Sultana R., Karamycheva S., Lee Y., White J., Cheung F., Parvizi B., Tsai J., Quackenbush J., TIGR Gene Indices clustering tools (TGICL): a software system for fast clustering of large EST datasets, 10.1093/bioinformatics/btg034
  41. Li R., Li Y., Kristiansen K., Wang J., SOAP: short oligonucleotide alignment program, 10.1093/bioinformatics/btn025
  42. Parra G., Bradnam K., Korf I., CEGMA: a pipeline to accurately annotate core genes in eukaryotic genomes, 10.1093/bioinformatics/btm071
  43. C Iseli (1999)
  44. Conesa A., Gotz S., Garcia-Gomez J. M., Terol J., Talon M., Robles M., Blast2GO: a universal tool for annotation, visualization and analysis in functional genomics research, 10.1093/bioinformatics/bti610
  45. V Hemandezl, 2006 (2006)
  46. Ye J., Fang L., Zheng H., Zhang Y., Chen J., Zhang Z., Wang J., Li S., Li R., Bolund L., Wang J., WEGO: a web tool for plotting GO annotations, 10.1093/nar/gkl031
  47. Ogata H., Goto S., Sato K., Fujibuchi W., Bono H., Kanehisa M., KEGG: Kyoto Encyclopedia of Genes and Genomes, 10.1093/nar/27.1.29
  48. M Kanehisa, Nucleic acids research, 36, D480 (2008)
  49. Altschul Stephen F., Gish Warren, Miller Webb, Myers Eugene W., Lipman David J., Basic local alignment search tool, 10.1016/s0022-2836(05)80360-2
  50. E Gasteiger (2005)
  51. Jones D. T., Taylor W. R., Thornton J. M., A Model Recognition Approach to the Prediction of All-Helical Membrane Protein Structure and Topology, 10.1021/bi00176a037
  52. Gouy M., Guindon S., Gascuel O., SeaView Version 4: A Multiplatform Graphical User Interface for Sequence Alignment and Phylogenetic Tree Building, 10.1093/molbev/msp259
  53. Edgar R. C., MUSCLE: multiple sequence alignment with high accuracy and high throughput, 10.1093/nar/gkh340
  54. Tamura K., Dudley J., Nei M., Kumar S., MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0, 10.1093/molbev/msm092
  55. Kumar S., Nei M., Dudley J., Tamura K., MEGA: A biologist-centric software for evolutionary analysis of DNA and protein sequences, 10.1093/bib/bbn017
  56. Plachetzki D. C., Fong C. R., Oakley T. H., The evolution of phototransduction from an ancestral cyclic nucleotide gated pathway, 10.1098/rspb.2009.1797
  57. Feuda R., Hamilton S. C., McInerney J. O., Pisani D., Metazoan opsin evolution reveals a simple route to animal vision, 10.1073/pnas.1204609109
  58. Feuda Roberto, Rota-Stabelli Omar, Oakley Todd H., Pisani Davide, The Comb Jelly Opsins and the Origins of Animal Phototransduction, 10.1093/gbe/evu154
  59. Guindon Stéphane, Gascuel Olivier, Rannala Bruce, A Simple, Fast, and Accurate Algorithm to Estimate Large Phylogenies by Maximum Likelihood, 10.1080/10635150390235520
  60. Guindon Stéphane, Delsuc Frédéric, Dufayard Jean-François, Gascuel Olivier, Estimating Maximum Likelihood Phylogenies with PhyML, Methods in Molecular Biology (2009) ISBN:9781588299109 p.113-137, 10.1007/978-1-59745-251-9_6
  61. K Tamura, Molecular biology and evolution, mst197 (2013)
  62. Ronquist Fredrik, Teslenko Maxim, van der Mark Paul, Ayres Daniel L., Darling Aaron, Höhna Sebastian, Larget Bret, Liu Liang, Suchard Marc A., Huelsenbeck John P., MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space, 10.1093/sysbio/sys029
  63. K-W Yau, Cell, 139, 246 (2009)
  64. Tong D., Rozas N. S., Oakley T. H., Mitchell J., Colley N. J., McFall-Ngai M. J., Evidence for light perception in a bioluminescent organ, 10.1073/pnas.0904571106
  65. Fain Gordon L., Hardie Roger, Laughlin Simon B., Phototransduction and the Evolution of Photoreceptors, 10.1016/j.cub.2009.12.006
  66. Schnitzler Christine E, Pang Kevin, Powers Meghan L, Reitzel Adam M, Ryan Joseph F, Simmons David, Tada Takashi, Park Morgan, Gupta Jyoti, Brooks Shelise Y, Blakesley Robert W, Yokoyama Shozo, Haddock Steven HD, Martindale Mark Q, Baxevanis Andreas D, Genomic organization, evolution, and expression of photoprotein and opsin genes in Mnemiopsis leidyi: a new view of ctenophore photocytes, 10.1186/1741-7007-10-107
  67. Pairett Autum N., Serb Jeanne M., De Novo Assembly and Characterization of Two Transcriptomes Reveal Multiple Light-Mediated Functions in the Scallop Eye (Bivalvia: Pectinidae), 10.1371/journal.pone.0069852
  68. M�rkel Konrad, R�ser Ursula, Comparative morphology of echinoderm calcified tissues: Histology and ultrastructure of ophiuroid scales (Echinodermata, Ophiuroida), 10.1007/bf00312157
  69. HENDLER GORDON, Ophiuroid Skeleton Ontogeny Reveals Homologies Among Skeletal Plates of Adults: A Study ofAmphiura filiformis, Amphiura stimpsoniiandOphiophragmus filograneus(Echinodermata), 10.2307/1541755
  70. M Byrne, Microscopic anatomy of invertebrates, 14, 247 (1994)
  71. Falkner I., Byrne M., Skeletal characters for identification of juvenile Ophiactis resiliens and Amphiura constricta (Echinodermata): cryptic ophiuroids in coralline turf habitat, 10.1017/s0025315406014196
  72. Stöhr Sabine, O'Hara Timothy D., Thuy Ben, Global Diversity of Brittle Stars (Echinodermata: Ophiuroidea), 10.1371/journal.pone.0031940
  73. R Rosenberg, Marine Biology, 145, 651 (2004)
  74. JM Lawrence (1987)
  75. Astley H. C., Getting around when you're round: quantitative analysis of the locomotion of the blunt-spined brittle star, Ophiocoma echinata, 10.1242/jeb.068460
  76. Oppenheim Sara J., Baker Richard H., Simon Sabrina, DeSalle Rob, We can't all be supermodels: the value of comparative transcriptomics to the study of non-model insects : Comparative transcriptomics of non-model insects, 10.1111/imb.12154
  77. Tao Xiang, Gu Ying-Hong, Wang Hai-Yan, Zheng Wen, Li Xiao, Zhao Chuan-Wu, Zhang Yi-Zheng, Digital Gene Expression Analysis Based on Integrated De Novo Transcriptome Assembly of Sweet Potato [Ipomoea batatas (L.) Lam.], 10.1371/journal.pone.0036234
  78. Hahn Daniel A, Ragland Gregory J, Shoemaker D. DeWayne, Denlinger David L, Gene discovery using massively parallel pyrosequencing to develop ESTs for the flesh fly Sarcophaga crassipalpis, 10.1186/1471-2164-10-234
  79. Clark Melody S., Thorne Michael A. S., Toullec Jean-Yves, Meng Yan, Guan Le Luo, Peck Lloyd S., Moore Stephen, Antarctic Krill 454 Pyrosequencing Reveals Chaperone and Stress Transcriptome, 10.1371/journal.pone.0015919
  80. Franchini Paolo, van der Merwe Mathilde, Roodt-Wilding Rouvay, Transcriptome characterization of the South African abalone Haliotis midae using sequencing-by-synthesis, 10.1186/1756-0500-4-59
  81. Zhao Ye, Yang Hongsheng, Storey Kenneth B., Chen Muyan, Differential gene expression in the respiratory tree of the sea cucumber Apostichopus japonicus during aestivation, 10.1016/j.margen.2014.07.001
  82. Y Zhao, Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, 10, 30 (2014)
  83. Tatusov Roman L, Fedorova Natalie D, Jackson John D, Jacobs Aviva R, Kiryutin Boris, Koonin Eugene V, Krylov Dmitri M, Mazumder Raja, Mekhedov Sergei L, Nikolskaya Anastasia N, Rao B Sridhar, Smirnov Sergei, Sverdlov Alexander V, Vasudevan Sona, Wolf Yuri I, Yin Jodie J, Natale Darren A, 10.1186/1471-2105-4-41
  84. Tatusov R. L., The COG database: new developments in phylogenetic classification of proteins from complete genomes, 10.1093/nar/29.1.22
  85. Terakita Akihisa, Koyanagi Mitsumasa, Tsukamoto Hisao, Yamashita Takahiro, Miyata Takashi, Shichida Yoshinori, Counterion displacement in the molecular evolution of the rhodopsin family, 10.1038/nsmb731
  86. Bellingham James, Chaurasia Shyam S, Melyan Zara, Liu Cuimei, Cameron Morven A, Tarttelin Emma E, Iuvone P. Michael, Hankins Mark W, Tosini Gianluca, Lucas Robert J, Evolution of Melanopsin Photoreceptors: Discovery and Characterization of a New Melanopsin in Nonmammalian Vertebrates, 10.1371/journal.pbio.0040254
  87. Shichida Y., Matsuyama T., Evolution of opsins and phototransduction, 10.1098/rstb.2009.0051
  88. Kozmik Zbynek, Ruzickova Jana, Jonasova Kristyna, Matsumoto Yoshifumi, Vopalensky Pavel, Kozmikova Iryna, Strnad Hynek, Kawamura Shoji, Piatigorsky Joram, Paces Vaclav, Vlcek Cestmir, Assembly of the cnidarian camera-type eye from vertebrate-like components, 10.1073/pnas.0800388105
  89. A Terakita, Wiley Interdisciplinary Reviews: Membrane Transport and Signaling, 1, 104 (2012)
  90. Yau King-Wai, Hardie Roger C., Phototransduction Motifs and Variations, 10.1016/j.cell.2009.09.029
  91. Zuker Charles S., Scott Kristin, 10.1038/27448
  92. Cao P., Sun W., Kramp K., Zheng M., Salom D., Jastrzebska B., Jin H., Palczewski K., Feng Z., Light-sensitive coupling of rhodopsin and melanopsin to Gi/o and Gq signal transduction in Caenorhabditis elegans, 10.1096/fj.11-197798
  93. Bailes H. J., Lucas R. J., Human melanopsin forms a pigment maximally sensitive to blue light ( max   479 nm) supporting activation of Gq/11 and Gi/o signalling cascades, 10.1098/rspb.2012.2987
  94. Hao Wenshan, Fong Henry K. W., The Endogenous Chromophore of Retinal G Protein-coupled Receptor Opsin from the Pigment Epithelium, 10.1074/jbc.274.10.6085
  95. Chen Pu, Hao Wenshan, Rife Lawrence, Wang Xiao Peng, Shen Daiwei, Chen Jeannie, Ogden Thomas, Van Boemel Gretchen B., Wu Lanyin, Yang Mao, Fong Henry K.W., 10.1038/90089
  96. Matsumoto Yoshifumi, Fukamachi Shoji, Mitani Hiroshi, Kawamura Shoji, Functional characterization of visual opsin repertoire in Medaka (Oryzias latipes), 10.1016/j.gene.2005.12.005
  97. Yewers M. S., McLean C. A., Moussalli A., Stuart-Fox D., Bennett A. T. D., Knott B., Spectral sensitivity of cone photoreceptors and opsin expression in two colour-divergent lineages of the lizard Ctenophorus decresii, 10.1242/jeb.119404
Bibliographic reference Delroisse, Jérôme ; Mallefet, Jérôme ; Flammang, Patrick . De novo adult transcriptomes of two European brittle stars: spotlight on opsin-based photoreception. In: PLoS One, Vol. 11, no.4, p. e0152988 (2016)
Permanent URL http://hdl.handle.net/2078.1/175178