Effects of dietary oxidized konjac glucomannan sulfates (OKGMS) and acidolysis-oxidized konjac glucomannan (A-OKGM) on the immunity and expression of immune-related genes of Schizothorax prenanti

Fish and Shellfish Immunology

Volumn 56, Issue , 2016, Pages 96-105

  Chen, Mingrui ^a   Wang, Hongjie ^a   Yan, Qiuping ^a   Zheng, Qiaoran ^a   Yang, Min ^a   Lv, Zhenzhen ^a   He, Mei ^a   Feng, Limei ^a   Zhao, Jiaqi ^a   Tang, Tingting ^a   Wu, Yinglong ^a  

^a SICHUAN AGRICULTURAL UNIVERSITY   (China)

Author keywords

Acidolysis oxidized konjac glucomannan; Immunity; Interferon regulatory factors7; Myeloid differentiation factor 88; Oxidized konjac glucomannan sulfates; Toll like receptor 22

Indexed keywords

(1-6)-ALPHA-GLUCOMANNAN; FISH PROTEIN; INTERFERON REGULATORY FACTOR 7; MANNAN; MYELOID DIFFERENTIATION FACTOR 88; SULFATE; TOLL LIKE RECEPTOR;

ANALYSIS; ANIMAL; ANIMAL FOOD; CYPRINIDAE; DIET; DIETARY SUPPLEMENT; DOSE RESPONSE; GENE EXPRESSION REGULATION; GENETICS; IMMUNOLOGY; INNATE IMMUNITY; METABOLISM; OXIDATION REDUCTION REACTION; RANDOMIZATION; VETERINARY;

ANIMAL FEED; ANIMALS; CYPRINIDAE; DIET; DIETARY SUPPLEMENTS; DOSE-RESPONSE RELATIONSHIP, DRUG; FISH PROTEINS; GENE EXPRESSION REGULATION; IMMUNITY, INNATE; INTERFERON REGULATORY FACTOR-7; MANNANS; MYELOID DIFFERENTIATION FACTOR 88; OXIDATION-REDUCTION; RANDOM ALLOCATION; SULFATES; TOLL-LIKE RECEPTORS;

EID: 84978792823     PISSN: 10504648     EISSN: 10959947     Source Type: Journal    
DOI: 10.1016/j.fsi.2016.07.003     Document Type: Article

References (54)

1. [1] Mu, X.J., Pridgeon, J.W., Klesius, P.H., Comparative transcriptional analysis reveals distinct expression patterns of channel catfish genes after the first infection and re-infection with Aeromonas hydrophila. Fish Shellfish Immunol. 35 (2013), 1566–1576.
2. [2] Yeh, S.P., Chang, C.A., Chang, C.Y., Liu, C.H., Cheng, W.T., Dietary sodium alginate administration affects fingerling growth and resistance to Streptococcus sp. and iridovirus, and juvenile non-specific immune responses of the orangespotted grouper, Epinephelus coioides. Fish Shellfish Immunol. 25 (2008), 19–27.
3. [3] Yin, G.J., Ardo´, L., Thompson, K.D., Adams, A., Jeney, Z., Jeney, G., Chinese herbs(Astragalus radix and Ganoderma lucidum) enhance immune response of carp, Cyprinus carpio, and protection against Aeromonas hydrophila. Fish Shellfish Immunol. 26 (2009), 140–145.
4. [4] Falco, A., Frost, P., Miest, J., Pionnier, N., et al. Reduced inflammatory response to Aeromonas salmonicida infection in common carp (Cyprinus carpio L.) fed with β-glucan supplements. Fish Shellfish Immunol. 32 (2012), 1051–1057.
5. [5] Tester, R.F., Al-Ghazzewi, F.H., Mannans and health, with a special focus on glucomannans. Food Res. Int. 50 (2013), 384–391.
6. [6] Zhang, Y.Q., Xie, B.J., Gan, X., Advance in the applications of konjac glucomannan and its derivatives. Carbohydr. Polym. 60 (2005), 27–31.
7. [7] Xiao, M., Wan, L., Corke, H., Yan, W., Ni, X.W., Fang, Y.P., Jiang, F.T., Characterization of konjac glucomannan-ethyl cellulose filmformation via microscopy. Int. J. Biol. Macromol. 85 (2016), 434–441.
8. [8] Chen, L.G., Liu, Z.L., Zhuo, R.X., Synthesis and properties of degradable hydrogels of konjac glucomannan grafted acrylic acid for colon-specific drug delivery. Polymer 46 (2005), 6274–6281.
9. [9] Zhu, Z.Y., Liu, Y., Si, C.L., Yuan, J., Lv, Q., Li, Y.Y., Dong, G.L., Liu, A.J., Zhang, Y.M., Sulfated modification of the polysaccharide from Cordyceps gunnii mycelia and its biological activities. Carbohydr. Polym. 92 (2013), 872–876.
10. [10] Jiang, J., Meng, F.Y., He, Z., Ning, Y.L., Li, X.H., Song, H., Wang, J., Zhou, R., Sulfated modification of longan polysaccharide and its immunomodulatory and antitumor activity in vitro. Int. J. Biol. Macromol. 67 (2014), 323–329.
11. [11] Kojima, T., Tabata, K., Itoh, W., et al. Molecular weight dependence of the anti-tumor activity of schizophyllan. Agric. Biol. Chem. 50 (1986), 231–232.
12. [12] Li, B., Xie, B.j., Study on molecular chain morphology of Konjac glucoman nan. Sci. Agric. Sin. 37 (2004), 280–284.
13. [13] Liu, W., Wang, H.Y., Yao, W.B., Gao, X.D., (Lucy) Yu, L.L., Effects of sulfation on the physicochemical and functional properties of a water-insoluble polysaccharide preparation from Ganoderma lucidum. J. Agric. Food Chem. 58 (2010), 3336–3341.
14. [14] Lim, D.W., Whang, H.S., Yoon, K.J., Ko, S.W., Synthesis and absorbency of a superabsorbent from sodium starch sulfate-g-polyacrylonitrile. J. Appl. Polym. Sci. 78 (2001), 1423–1430.
15. [15] Nie, H.R., Shen, X.X., Zhou, Z.H., Jiang, Q.S., Chen, Y.W., Xie, A., et al. Electrospinning and characterization of konjac glucomannan/chitosan nanofibrous scaffolds favoring the growth of bone mesenchymal stem cells. Carbohydr. Polym. 85 (2011), 681–686.
16. [16] Krichen, F., Karoud, W., Sila, A., Abdelmalek, B.E., Ghorbel, R., Ellouz-Chaabouni, S., Bougatef, A., Extraction, characterization and antimicrobial activity of sulfated polysaccharides from fish skins. Int. J. Biol. Macromol. 75 (2015), 283–289.
17. [17] Wu, W.T., Yang, L.C., Chen, H.L., Effects of konjac glucomannan, inulin and cellulose on acute colonic responses to genotoxic azoxymethane. Food Chem. 155 (2014), 304–310.
18. [18] Onishi, N., Kawamoto, S., Ueda, K., Yamanaka, Y., Katayama, A., Suzuki, H., et al. Dietary pulverised konjac glucomannan prevents the development of allergic rhinitis-like symptoms and IgE response in mice. Bioscience. Biotechnol. Biochem. 71 (2007), 2551–2556.
19. [19] Chen, H.L., Fan, Y.H., Chen, M.E., Chan, Y., Unhydrolyzed and hydrolyzed konjac glucomannans modulated cecal and fecal microflora in Balb/c mice. Nutrition 21 (2005), 1059–1064.
20. [20] Chen, Y., Zhang, H., Wang, Y.X., Nie, S.P., Li, C., Xie, M.Y., Sulfated modification of the polysaccharides from Ganoderma atrum and their antioxidant and immunomodulating activities. Food Chem. 186 (2015), 231–238.
21. [21] Yuan, Y., Macquarrie, D., Microwave assisted extraction of sulfated polysaccharides (fucoidan) from Ascophyllum nodosum and its antioxidant activity. Carbohydr. Polym. 129 (2015), 101–107.
22. [22] Dawood, M.A.O., Koshio, S., Ishikawa, M., et al. Interaction effects of dietary supplementation of heat-killed Lactobacillus plantarum and β-glucan on growth performance, digestibility and immune response of juvenile red sea bream, Pagrus major. Fish Shellfish Immunol. 45 (2015), 33–42.
23. [23] Torrecillas, S., Makol, A., Benítez-Santana, T., et al. Reduced gut bacterial translocation in European sea bass (Dicentrarchus labrax) fed mannan oligosaccharides (MOS). Fish shellfish Immunol. 30 (2011), 674–681.
24. [24] Grinde, B., Lysozyme from rainbow trout, Salmo gairdneri Richardson, as an antibacterial agent against fish pathogens. J. Fish Dis. 12 (1989), 95–104.
25. [25] Jollès, P., Jollès, J., What's new in lysozyme research?. Mol. Cell. Biochem. 63 (1984), 165–189.
26. [26] Zhu, L.Y., Nie, L., Zhu, G., Xiang, L.X., Shao, J.Z., Advances in research of fish immune-relevant genes: a comparative overview of innate and adaptive immunity in teleosts. Dev. Comp. Immunol. 39 (2013), 39–62.
27. [27] Gonzalez, S.F., Buchmann, K., Nielsen, M.E., Complement expression in common carp (Cyprinus carpio L.) during infection with Ichthyophthirius multifiliis. Dev.Comparative Immunol. 31 (2007), 576–586.
28. [28] Pionnier, N., Falco, A., Miest, J.J., Shrive, A.K., Hoole, D., Feeding common carp Cyprinus carpio with β-glucan supplemented diet stimulates C-reactive protein and complement immune acute phase responses following PAMPs injection. Fish Shellfish Immunol. 39 (2014), 285–295.
29. [29] Aramli, M.S., Kamangar, B., Nazari, R.M., Effects of dietary β-glucan on the growth and innate immune response of juvenile Persian sturgeon, Acipenser persicus. Fish Shellfish Immunol. 47 (2015), 606–610.
30. [30] Ghaedi, G., Keyvanshokooh, S., Azarm, H.M., Akhlaghi, M., Effects of dietary β-glucan on maternal immunity and fry quality of rainbow trout (Oncorhynchus mykiss). Aquaculture 441 (2015), 78–83.
31. [31] Kunihiko, K., Susumu, T., Tadashi, K., A second class of immunoglobulin other than IgM present in the serum of a cartilaginous fish, the skate, Raja kenojei: isolation and characterization. Mol. Immunol. 21 (1984), 397–404.
32. [32] Zhang, L., Wu, Y.L., Wang, L., et al. Effects of Oxidized Konjac glucomannan (OKGM) on growth and immune function of Schizothorax prenanti. Fish Shellfish Immunol. 35 (2013), 1105–1110.
33. [33] Gomez-Anduro, G.A., Barillas-Mury, C.V., Peregrino-Uriarte, A.B., Gupta, L., et al. The cytosolic manganese superoxide dismutase from the shrimp Litopenaeus vannamei: molecular cloning and expression. Dev. Comp. Immunol. 30 (2006), 893–900.
34. [34] Younghun, J., Nowak, T.S., Zhang, S.M., Hertel, L.A., et al. Manganese superoxide dismutase from Biomphalaria glabrata. J. Invertebr. Pathol. 90 (2005), 59–63.
35. [35] Ni, D.J., Song, L.S., Gao, Q., Wu, L.T., et al. The cDNA cloning and mRNA expression of cytoplasmic Cu, Zn superoxide dismutase (SOD) gene in scallop Chlamys farreri. Fish Shellfish Immunol. 23 (2007), 1032–1042.
36. [36] Kutlu, M., Susuz, F., Biochemical properties of glutathione peroxidase in Gammarus pulex. Bull. Environ. Contam. Toxicol. 73 (2004), 432–436.
37. [37] Zhang, J., Liu, Y.J., Tian, L.X., Yang, H.J., Liang, G.Y., Xu, D.H., Effects of dietary mannan oligosaccharide on growth performance, gut morphology and stress tolerance of juvenile Pacific white shrimp, Litopenaeus vannamei. Fish Shellfish Immunol. 33 (2012), 1027–1032.
38. [38] Kim, Y.S., Ke, F., Zhang, Q.Y., Effect of β-glucan on activity of antioxidant enzymes and Mx gene expression in virus infected grass carp. Fish Shellfish Immunol. 27 (2009), 336–340.
39. [39] Gu, M., Ma, H.M., Mai, K.S., Zhang, W.B., et al. Effects of dietary β-glucan, mannan oligosaccharide and their combinations on growth performance, immunity and resistance against Vibrio splendidus of sea cucumber, Apostichopus japonicus. Fish Shellfish Immunol. 31 (2011), 303–309.
40. [40] Bricknell, I., Dalmo, R.A., The use of immunostimulants in fish larval aquaculture. Fish Shellfish Immunol. 19 (2005), 457–472.
41. [41] Roach, J.C., Gustavo, G., Lee, R., Amardeep, K., Purcell, M.K., et al. The evolution of vertebrate Toll-like receptors. Proc. Natl. Acad. Sci. 102 (2005), 9577–9582.
42. [42] Aoki, T., Takano, T., Santos, M.D., Kondo, H., Hirono, I., Molecular innate immunity in teleost fish: review and future perspectives. 5th World Fisheries Congress, 2008, 263–276.
43. [43] Hu, G.B., Zhang, S.F., Yang, X., Liu, D.H., Liu, Q.M., Zhang, S.C., Cloning and expression analysis of a Toll-like receptor 22 (tlr22) gene from turbot, Scophthalmus maximus. Fish Shellfish Immunol. 44 (2015), 399–409.
44. [44] Zheng, Q.R., Wu, Y.L., Xu, H.L., Yao, Y.F., Xia, X.J., et al. The effects of dietary oxidized konjac glucomannan and its acidolysis products on the immune response, expression of immune related genes and disease resistance of Schizothorax prenanti. Fish Shellfish Immunol. 45 (2015), 551–559.
45. [45] Feng, Z.F., Wang, Z.X., Yang, M., Zhou, L.J., Bao, Y.X., Polysaccharopeptide exerts immunoregulatory effects via MyD88-dependent signaling pathway. Int. J. Biol. Macromol. 82 (2016), 201–207.
46. [46] Ning, X.H., Wang, R.J., Li, X., Wang, S.Y., Zhang, M.G., et al. Genome-wide identification and characterization of five MyD88 duplication genes in Yesso scallop (Patinopecten yessoensis) and expression changes in response to bacterial challenge. Fish Shellfish Immunol. 46 (2015), 181–191.
47. [47] Wen, R., Li, F.H., Sun, Z., Li, S.H., Xiang, J.H., Shrimp MyD88 responsive to bacteria and white spot syndrome virus. Fish Shellfish Immunol. 34 (2013), 574–581.
48. [48] Lin, J.Y., Hu, G.B., Yu, C.H., Li, S., Liu, Q.M., Zhang, S.C., Molecular cloning and expression studies of the adapter molecule myeloid differentiation factor 88 (MyD88) in turbot (Scophthalmus maximus). Dev. Comp. Immunol. 52 (2015), 166–171.
49. [49] Betsy, B., Barbora, L., Pitha, P.M., On the role of IRF in host defense. J. Interferon & Cytokine Res. 22 (2002), 59–71.
50. [50] Zhang, J., Kong, X.H., Zhou, C.J., Li, L., Toll-like receptor recognition of bacteria in fish: ligand specificity and signal pathways. Fish Shellfish Immunol. 41 (2014), 380–388.
51. [51] Zhang, Y.B., Gui, J.F., Molecular regulation of interferon antiviral response in fish. Dev. Comp. Immunol. 38 (2012), 193–202.
52. [52] Hu, G.B., Xia, J., Lou, H.M., Liu, Q.M., et al. Cloning and expression analysis of interferon regulatory factor 7 (IRF-7) in turbot, Scophthalmus maximus. Dev. Comp. Immunol. 35 (2011), 416–420.
53. [53] Yu, F.F., Zhang, Y.B., Liu, T.K., Liu, Y., Sun, F., et al. Fish virus-induced interferon exerts antiviral function through Stat1 pathway. Mol. Immunol. 47 (2010), 2330–2341.
54. [54] Kileng, Ø., Bergan, V., Workenhe, S.T., Robertsen, B., Structural and functional studies of an IRF-7-like gene from Atlantic salmon. Dev. Comp. Immunol. 33 (2009), 18–27.