Cloning and differential expression of a novel toll-like receptor gene in noble scallop Chlamys nobilis with different total carotenoid content

Fish and Shellfish Immunology

Volumn 56, Issue , 2016, Pages 229-238

  Lu, Yeqing ^a   Zheng, Huaiping ^a   Zhang, Hongkuan ^a   Yang, Jianqin ^a   Wang, Qiang ^a  

^a SHANTOU UNIVERSITY   (China)

Author keywords

Carotenoids; Chlamys nobilis; Lipopolysaccharide (LPS); Noble scallop; Polyinosinic polycytidylic acid (Poly I:C); Toll like receptor; Vibrio parahaemolyticus

Indexed keywords

CAROTENOID; COMPLEMENTARY DNA; LIPOPOLYSACCHARIDE; MESSENGER RNA; POLYINOSINIC POLYCYTIDYLIC ACID; TOLL LIKE RECEPTOR;

AMINO ACID SEQUENCE; ANIMAL; CHEMISTRY; GENETICS; IMMUNOLOGY; INNATE IMMUNITY; METABOLISM; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; PHYLOGENY; PHYSIOLOGY; SCALLOP; SEQUENCE ALIGNMENT; VIBRIO PARAHAEMOLYTICUS;

AMINO ACID SEQUENCE; ANIMALS; BASE SEQUENCE; CAROTENOIDS; CLONING, MOLECULAR; DNA, COMPLEMENTARY; IMMUNITY, INNATE; LIPOPOLYSACCHARIDES; PECTINIDAE; PHYLOGENY; POLY I-C; RNA, MESSENGER; SEQUENCE ALIGNMENT; TOLL-LIKE RECEPTORS; VIBRIO PARAHAEMOLYTICUS;

EID: 84978743997     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2016.07.007     Document Type: Article

References (60)

1. [1] Medzhitov, R., Janeway, C.A. Jr., Innate immunity. New Engl. J. Med. 343 (2000), 338–344.
2. [2] Medzhitov, R., Janeway, C.A. Jr., Decoding the patterns of self and non-self by the innate immune system. Science 296 (2002), 298–300.
3. [3] Janeway, C.A. Jr., Medzhitov, R., Innate immune recognition. Annu. Rev. Immunol. 20 (2002), 197–216.
4. [4] Beutler, B., Jiang, Z., Georgel, P., Crozat, K., Croker, B., Rutschmann, S., Du, X., Hoebe, K., Genetic analysis of host resistance: toll-like receptor signaling and immunity at large. Annu. Rev. Immunol. 24 (2006), 353–389.
5. [5] Hoshino, K., Takeuchi, O., Kawai, T., Sanjo, H., Ogawa, T., Takeda, Y., Taleda, K., Akira, S., Cutting edge: toll-like receptor 4 (TLR4)-deficient mice are hypo-responsive to lipopolysaccharide: evidence for TLR4 as the Lps gene product. J. Immunol. 162 (1999), 3749–3752.
6. [6] Bell, J.K., Mullen, G.E., Leifer, C.A., Mazzoni, A., Davies, D.R., Segal, D.M., Leucine-rich repeats and pathogen recognition in Toll-like receptors. Trends Immunol. 24 (2003), 528–533.
7. [7] Yamamoto, M., Akirz, S., TIR domain-containing adaptors regulate TLR signaling pathways. Adv. Exp. Med. Biol. 560 (2005), 1–9.
8. [8] Lemaitre, B., Nicolas, E., Michaut, L., Reichhart, J.M., Hoffmann, J.A., The dorsoventral regulatory gene cassette spätzle/Toll/cactus controls the potent antifungal response in Drosophila adults. Cell 86:6 (1996), 973–983.
9. [9] Valanne, S., Wang, J.H., Rämet, M., The Drosophila toll signaling pathway. J. Immunol. 186 (2011), 649–656.
10. [10] Zhang, D., Zhang, G., Hayden, M.S., Greenblatt, M.B., Bussey, C., Flavell, R.A., Ghosh, S., A toll-like receptor that prevents infection by uropathogenic bacteria. Science 303:5336 (2004), 1522–1526.
11. [11] Coscia, M.R., Giacomelli, S., Oreste, U., Toll-like receptors: an overview from invertebrates to vertebrates. ISJ-Invertebr. Surviv. J. 8 (2011), 210–226.
12. [12] Qiu, L.M., Song, L.S., Xu, W., Ni, D.J., Yu, Y.D., Molecular cloning and expression of a toll receptor gene homologue from Zhikong Scallop, Chlamys farreri. Fish Shellfish Immunol. 22:5 (2015), 451–466.
13. [13] Zhang, L.L., Li, L., Zhang, G.F., A Crassostrea gigas toll-like receptor and comparative analysis of TLR pathway in invertebrates. Fish Shellfish Immunol. 30:2 (2011), 653–660.
14. [14] Toubiana, M., Gerdol, M., Rosani, U., Pallavicini, A., Venier, P., Roch, P., Toll-like receptors and MyD88 adaptors in Mytilus: complete cds and gene expression levels. Dev. Comp. Immunol. 40:2 (2013), 158–166.
15. [15] Mateo, D.R., Greenwood, S.J., Araya, M.T., Berthe, F.C., Johnson, G.R., Siah, A., Differential gene expression of gamma-actin, Toll-like receptor 2 (TLR-2) and interleukin-1 receptor-associated kinase 4 (IRAK-4) in Mya arenaria haemocytes induced by in vivo infections with two Vibrio splendidus strains. Dev. Comp. Immunol. 34:7 (2010), 710–714.
16. [16] Goodson, M.S., Kojadinovic, M., Troll, J.V., Scheetz, T.E., Casavant, T.L., Soares, M.B., McFall-Ngai, M.J., Identifying components of the NF-kappa B pathway in the beneficial Euprymna scolopes-Vibrio fischeri light organ symbiosis. Appl. Environ. Microbiol. 71 (2005), 6934–6946.
17. [17] Cornet, V., Henry, J., Corre, E., Le Corguillé, G., Zatylny-Gaudin, C., The Toll/NF-kappa B pathway in cuttlefish symbiotic accessory nidamental gland. Dev. Comp. Immunol. 53:1 (2015), 42–46.
18. [18] Wang, M., Yanga, J., Zhoua, Z., Qiu, L., Wang, L., Zhang, H., A primitive Toll-like receptor signaling pathway in mollusk Zhikong scallop Chlamys farreri. Dev. Comp. Immunol. 35 (2011), 511–520.
19. [19] Montagnani, C., Kappler, C., Reichhart, J.M., Escoubas, J.M., Cg-Rel, the first Rel/NF kappa B homolog characterized in a mollusk, the Pacific oyster Crassostrea gigas. FEBS Lett. 561 (2004), 75–82.
20. [20] Montagnani, C., Labreuche, Y., Escoubas, J.M., CgIkappaB. A new member of the I kappa B protein family characterized in the pacific oyster Crassostrea gigas. Dev. Comp. Immunol. 32 (2008), 182–190.
21. [21] Gueguen, Y., Cadoret, J.P., Flament, D., Barreau-Roumiguière, C., Giradot, A.L., Garnier, J., Hoareau, A., Bachère, E., Escpibas, J.M., Immune gene discovery by expressed sequence tags generated from haemocytes of the bacteria-challenged oyster, Crassostrea gigas. Gene 303 (2003), 139–145.
22. [22] Du, Y.S., Zhang, L.L., Huang, B.Y., Guan, X.D., Li, L., Zhang, G.F., Molecular cloning, characterization, and expression of two Myeloid Differentiation Factor 88 (Myd88) in pacific oyster, Crassostrea gigas. J. World Aquac. Soc. 44:6 (2013), 759–774.
23. [23] Roberts, S., Goetz, G., White, S., Goetz, F., Analysis of genes isolated from plated haemocytes of the Pacific oyster, Crassostrea gigas. Mar. Biotech. 11 (2009), 24–44.
24. [24] Salazar, K.A., Joffe, N.R., Dinguirard, N., Houde, P., Castillo, M.G., Transcriptome analysis of the white body of the squid Euprymna tasmanica with emphasis on immune and hematopoietic gene discovery. Plos One, 10(3), 2015 1932–6203.
25. [25] Jiao, Y., Tian, Q.L., Du, X.D., Wang, Q.H., Huang, R.L., Deng, Y.W., Shi, S.L., Molecular characterization of tumor necrosis factor receptor-associated factor 6 (TRAF6) in pearl oyster Pinctada martensii. Genet. Mole Res. 13:4 (2014), 10545–10555.
26. [26] He, C.B., Wang, Y., Liu, W.D., Gao, X.G., Chen, P.H., Li, Y.F., Bao, X.B., Cloning, promoter analysis and expression of the tumor necrosis factor receptor-associated factor 6 (TRAF6) in Japanese scallop (Mizuhopecten yessoensis). Mol. Biol. Rep. 40:8 (2013), 4769–4779.
27. [27] Lee, Y., Whang, I., Umasuthan, N., Zoysa De, M., Oh, C., Choi, C.Y., Park, C.J., Lee, J., Characterization of a novel molluscan MyD88 family protein from manila clam, Ruditapes philippinarum. Fish Shellfish Immunol. 31:6 (2011), 887–893.
28. [28] Maoka, T., Recent progress in structural studies of carotenoids in animals and plants. Arch. Biochem. Biophys. 483:2 (2009), 191–195.
29. [29] Stahl, W., Sies, H., Antioxidant activity of carotenoids. Mole Asp. Medic 24 (2003), 345–351.
30. [30] Stahl, W., Sies, H., Bioactivity and protective effects of natural carotenoids. Biochem. Biophys. Acta-Mole Basis Dis. 1740:2 (2005), 101–107.
31. [31] Rao, A.V., Rao, L.G., Carotenoids and human health. Pharmacol. Res. 55 (2007), 207–216.
32. [32] Kuhnen, S., Lemos, P.M.M., Campestrini, L.H., Ogliari, B.J., Dias, P.F., Maraschin, M., Antiangiogenic properties of carotenoids: a potential role of maize as functional food. J. Funct. Foods 3:1 (2009), 284–290.
33. [33] Maiani, G., Periago Castón, M.J., Catasta, G., Toti1, E., Cambrodón, I.G., Bysted, A., Granado-Lorencio, F., Olmedilla-Alonso, B., Knuthsen, P., Valoti, M., Böhm, V., Mayer-Miebach, E., Behsnilian, D., Schlemmer, U., Carotenoids: actual knowledge on food sources, intakes, stability and bioavailability and their protective role in humans. Mol. Nutr. Food Res. 53:S2 (2009), S194–S218.
34. [34] Bertram, J., Carotenoids and gene regulation. Nutr. Rev. 57 (1999), 182–191.
35. [35] Zhang, Q., Lu, Q.Y., Zheng, H.P., Liu, H.L., Li, S.K., Differential immune response of vitellogenin gene to Vibrio anguillarum in noble scallop Chlamys nobilis and its correlation with total carotenoid content. Fish Shellfish Immunol. 50 (2016), 11–15.
36. [36] Zheng, H.P., Sun, Z.W., Zhang, T., Liu, W.H., Liu, H.L., Inheritance of shell colors in the noble scallop Chlamys nobilis (Bivalve: Pectinidae). Aquac. Res. 44 (2013), 1229–1235.
37. [37] Guo, X.M., Ford, S.E., Zhang, F.S., Molluscan aquaculture in China. J. Shellfish Res. 18 (1999), 19–31.
38. [38] Zheng, H.P., Liu, H.L., Zhang, T., Wang, S.Q., Sun, Z.W., Liu, W.H., Li, Y.Y., Total carotenoid differences in scallop tissues of Chlamys nobilis (Bivalve: Pectinidae) with regard to gender and shell color. Food Chem. 122 (2010), 1164–1167.
39. [39] Huang, Q.F., Primary discussion on suddenly mass death and its control counter measures of Chlamys nobilis. J. Fujian Fish 22:3 (2000), 75–77 (in Chinese).
40. [40] Zhou, R.L., Lv, J.Y., Wu, J.F., Investigation about the cause of suddenly mass death of scallop Chlamys nobilis in Leizhou Peninsula North Bay. Fish. Sci. Technol. 18:2 (2006), 22–23 (in Chinese).
41. [41] Ryan, K.J., Ray, C.G., Sherris Medical Microbiology. fourth ed., 2004, McGraw Hill ISBN 0-8385-8529-9.
42. [42] Brown, C., Losee, E., Observations on natural and induced epizootics of Vibriosis in Crassostrea lirginia larvae. J. Invertebr. Pathol. 31 (1978), 41–47.
43. [43] Elston, R.A., Ellio, E.L., Colwel, R.R., Conchiolin infection and surface coating vibrio: shell fragility, growth depression and mortalities in cultured oyster and clams, Crassostrea virginica, Ostrea edulis and Mercenaria mercenaia. J. Fish. Dis. 5 (1982), 265–284.
44. [44] Li, S., Sun, L., Wu, H., Hu, Z., Liu, W., Li, Y., Wen, X., The intestinal microbial diversity in mud crab (Scylla paramamosain) as determined by PCR-DGGE and clone library analysis. J. Appl. Microbiol. 113 (2012), 1341–1351.
45. [45] Roch, P., Defense mechanisms and disease prevention in farmed marine invertebrates. Aquaculture 172 (1999), 125–145.
46. [46] Lackie, A.M., Invertebrate immunity. Parasitology 80 (1980), 393–412.
47. [47] Liu, H.L., Zheng, H.P., Zhang, H.K., Deng, L.H., Liu, W.H., Wang, S.Q., Meng, F., Wang, Y.J., Guo, Z.C., Li, S.K., Zhang, G.F., A de novo transcriptome of the noble scallop, Chlamys nobilis, focusing on mining transcripts for carotenoid-based coloration. BMC Genom. 16:44 (2015), 1–13.
48. −△△Ct method. Methods 25 (2001), 402–408.
49. [49] Bustin, S.A., Benes, V., Garson, J.A., Hellemans, J., Huggett, J., Kubista, M., Mueller, R., Nolan, T., Pfaffl, M.W., Shipley, G.L., Vandesompele, J., Wittwer, C., The MIQE guidelines-Minimum information for publication of quantitative real-time PCR experiments. Clin. Chem. 55 (2009), 611–622.
50. [50] Bustin, S.A., Beaulieu, J.F., Huggett, J., Kibenge, F.S., Olsvik, P., Penning, L.C., Toegel, S., MIQE précis: practical implementation of minimum standard guidelines for fluorescence based quantitative real-time PCR experiments. BMC Mol. Biol. 11 (2010), 74–79.
51. [51] Yanar, Y., Celik, M., Yanar, M., Seasonal changes in total carotenoid contents of wild marine shrimps (Penaeus semisulcatus and Metapenaeus monoceros) inhabiting the eastern Mediterranean. Food Chem. 88 (2004), 267–269.
52. [52] Yu, A.Q., Jin, X.K., Guo, X.N., Li, S., Wu, M.H., Li, W.W., Wang, Q., Two novel Toll genes (EsToll1 and EsToll2) from Eriocheir sinensis are differentially induced by lipopolysaccharide, peptidoglycan and zymosan. Fish Shellfish Immunol. 35 (2013), 1282–1292.
53. [53] Sun, H.J., Zhou, Z.C., Dong, Y., Yang AF.Jiang, B., Gao, S., Chen, Z., Guan, X.Y., Wang, B., Wang, X.L., Identification and expression analysis of two Toll-like receptor genes from sea cucumber (Apostichopus japonicus). Fish Shellfish Immunol. 34:1 (2013), 147–158.
54. [54] Su, Y.C., Liu, C., Vibro parahaemolyticus: a concern of seafood safety. Food Microbiol. 24:6 (2007), 549–558.
55. [55] Rietschel, E.T., Kirikae, T., Schade, F.U., Mamat, U., Schmidt, G., Loppnow, H., Ulmer, A.J., Zähringer, U., Seydel, U., Di Padova, F., Bacterial endotoxin: molecular relationships of structure to activity and function. FASEB J. 8:2 (1994), 217–225.
56. [56] Fortier, M.E., Kent, S., Ashdown, H., Poole, S., Boksa, P., Luheshi, G.N., The viral mimic, polyinosinic:polycytidylic acid, induces fever in rats via an interleukin-1-dependent mechanism. Am. J. Physiol. Regul. Integr. Comp. Physiol. 287:4 (2004), R759–R766.
57. [57] Sommer, A., Vyas, K.S., A global clinical view on vitamin A and carotenoids. Am. J. Clini Nutri 96:5 (2012), 1204S–1206S.
58. [58] Yagi, A., Fujimoto, K., Michihiro, K., Goh, B., Tsi, D., Nagai, H., The effect of lutein supplementation on visual fatigue: a psychophysiological analysis. Appl. Ergon. 40:6 (2009), 1047–1054.
59. [59] Murakoshi, M., Takayasu, J., Kimura, O., Kohmura, E., Nishino, H., Iwashima, A., Okuzumi, J., Sakai, T., Sugimoto, T., Imanishi, J., Iwasaki, R., Inhibitory effects of α-carotene on proliferation of the human neuroblastoma cell line GOTO. J. Natl. Cancer Inst. 81 (1989), 1649–1652.
60. [60] Obermüller-Jevic, U.C., Francz, P.I., Frank, J., Flaccus, A., Biesalski, H.K., Enhancement of the UVA induction of haem oxygenase-1 expression by β-carotene in human skin fibroblasts. FEBS Lett. 46 (1999), 212–216.