Leukocyte susceptibility and immune response against Vibrio parahaemolyticus in Totoaba macdonaldi

Developmental and Comparative Immunology

Volumn 65, Issue , 2016, Pages 258-267

  Reyes Becerril, Martha ^a   Alamillo, Erika ^a   Sánchez Torres, Luvia ^a   Ascencio Valle, Felipe ^a   Perez Urbiola, Juan C ^a   Angulo, Carlos ^a  

^a INSTITUTO POLITÉCNICO NACIONAL   (Mexico)

Author keywords

Apoptosis; Cellular immune response; Gene expression; Phagocytic activity; Totoaba; Vibrio parahaemolyticus

Indexed keywords

INTERLEUKIN 1BETA; INTERLEUKIN 8; LIPOCORTIN 5; MESSENGER RNA; PROPIDIUM IODIDE; FISH PROTEIN;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL DEATH; CELL PHAGOCYTOSIS; CELL SURVIVAL; CELL VIABILITY; CELLULAR IMMUNITY; CONTROLLED STUDY; DOWN REGULATION; FISH; HEAD; IN VITRO STUDY; IN VIVO STUDY; INTESTINE; KIDNEY; LEUKOCYTE; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RESPIRATORY BURST; SPLEEN; THYMUS; TOTOABA MACDONALDI; UPREGULATION; VIBRIO PARAHAEMOLYTICUS; ANIMAL; CELL CULTURE; GENETICS; HEAD KIDNEY; IMMUNOLOGY; INNATE IMMUNITY; METABOLISM; PERCIFORMES; PHAGOCYTOSIS; VIBRIOSIS; VIROLOGY;

ANIMALS; APOPTOSIS; CELLS, CULTURED; FISH PROTEINS; HEAD KIDNEY; IMMUNITY, INNATE; INTERLEUKIN-1BETA; INTERLEUKIN-8; LEUKOCYTES; PERCIFORMES; PHAGOCYTOSIS; RESPIRATORY BURST; UP-REGULATION; VIBRIO INFECTIONS; VIBRIO PARAHAEMOLYTICUS;

EID: 84982847358     PISSN: 0145305X     EISSN: 18790089     Source Type: Journal    
DOI: 10.1016/j.dci.2016.07.016     Document Type: Article

References (50)

1. Bachére, E., Mialhe, E., Noël, D., Boulo, V., Morvan, A., Rodriguez, J., Knowledge and research prospects in marine mollusk and crustacean immunology. Aquaculture 132 (1995), 17–32.
2. Baillie, J., Groombridge, B., IUCN Red List of Threatened Animals. 1996, IUCN, Gland, Switzerland, 378.
3. Barrera-Guevara, J.C., The conservation of Totoaba macdonaldi (Gilbert), (Pisces: Sciaenidae), in the Gulf of California, Mexico. J. Fish. Biol. 37 (1990), 201–202.
4. Bobadilla, M., Alvarez-Borrego, S., Avila-Foucat, S., Lara-Valencia, F., Espejel, I., Evolution of environmental policy instruments implemented for the protection of totoaba and the vaquita porpoise in the Upper Gulf of California. Environm. Sci. Policy 14 (2011), 998–1007.
5. Bowden, T.J., Cook, P., Rombout, J.H.W.M., Development and function of the thymus in teleosts. Fish. Shellfish Immunol. 19 (2005), 413–427.
6. Broberg, C.A., Calder, T.J., Orth, K., Vibrio parahaemolyticus cell biology and pathogenicity determinants. Microbes Infect. 13 (2011), 992–1001.
7. Caipang, C.M., Lazado, C.C., Brinchmann, M.F., Kiron, V., Infection-induced changes in expression of antibacterial and cytokine genes in the gill epithelial cells of Atlantic cod, Gadus morhua during incubation with bacterial pathogens. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 156 (2010), 319–325.
8. Cardenas, R.T., Angulo, C., Hori, O.S., Velazquez, L.E., Reyes-Becerril, M., B-cell activating CpG ODN 1668 enhance the immune response of Pacific red snapper (Lutjanus Peru) exposed to Vibrio parahaemolitycus. Dev. Comp. Immunol. 62 (2016), 72–81.
9. Carol, M., Borruel, N., Antolin, M., Llopis, M., Casellas, F., Guarner, F., et al. Modulation of apoptosis in intestinal lymphocytes by a probiotic bacteria in Crohn's disease. J. Leukoc. Biol. 79 (2006), 917–922.
10. Cisneros-Mata, M., Botsford, L.W., Quinn, J.F., Projecting viability of Totoaba macdonaldi, a population with unknown age-dependent variability. Ecol. Applic 7 (1997), 968–980.
11. Elmadfa, I., Klein, P., Meyer, A.L., Immune-stimulating effects of lactic acid bacteria in vivo and in vitro. Proc. Nutr. Soc. 69 (2010), 416–420.
12. Froese, R., Pauly, D., (Eds.), FishBase. World Wide Web Electronic Publication. www.fishbase.org version (10/2004).
13. Gao, Q., Min, M., Zhang, C., Peng, S., Shi, Z., Ability of Lactobacillus plantarum lipoteichoic acid to inhibit Vibrio anguillarum-induced inflammation and apoptosis in silvery pomfret (Pampus argenteus) intestinal epithelial cells. Fish. Shellfish Immunol. 54 (2016), 573–579.
14. Hassanpour, M., Joss, J., Mohammad, M.G., Functional analyses of lymphocytes and granulocytes isolated from the thymus, spiral valve intestine, spleen, and kidney of juvenile Australian lungfish, Neoceratodus forsteri. Fish. Shellfish Immunol. 35 (2013), 107–114.
15. Haugland, G.T., Rønneseth, A., Wergeland, H.I., Flow cytometry analyses of phagocytic and respiratory burst activities and cytochemical characterization of leucocytes isolated from wrasse (Labrus bergylta A.). Fish Shellfish Immunol. 39 (2014), 51–60.
16. Henderson, L.M., Chappell, J.B., Dihydrorhodamine 123: a fluorescent probe for superoxide generation?. Eur. J. Biochem. 217 (1993), 973–980.
17. Herath, H.M.L.P.B., Elvitigala, D.A.S., Godahewa, G.I., Umasuthan, N., Whang, I., Noh, J.K., Lee, J., Molecular characterization and comparative expression analysis of two teleostean pro-inflammatory cytokines, IL-1β and IL-8, from Sebastes schlegeli. Gene 575 (2016), 732–742.
18. Hilbi, H., Zychlinsky, A., Sansonetti, P.J., Macrophage apoptosis in microbial infections. Parasitol 115 (1997), S79–S87.
19. Huang, X.-N., Wang, Z.-Y., Yao, C.-L., Characterization of Toll-like receptor 3 gene in large yellow croaker, Pseudosciaena crocea. Fish. Shellfish Immunol. 3 (2011), 98–106.
20. Kalendar, R., Lee, D., Schulman, A.H., FastPCR software for PCR primer and probe design and repeat search. Genes Genomes Genomics 3 (2009), 1–14.
21. Laing, K.J., Secombes, C.J., Chemokines. Dev. Comp. Immunol. 28 (2004), 443–460.
22. Lee, P.T., Zou, J., Holland, J.W., Martin, S.A.M., Collet, B., Kanellos, T., Secombes, C.J., Identification and characterisation of TLR18-21genes in Atlantic salmon (Salmo salar). Fish. Shellfish Immunol. 41 (2014), 549–559.
23. Lercari, D., Chavez, E.A., Possible causes related to historic stock depletion of the totoaba, Totoaba macdonaldi (Perciformes: Sciaenidae), endemic to the Gulf of California. Fish. Res. 86 (2007), 136–142.
24. Li, C., Yao, C.L., Molecular and expression characterizations of interleukin-8 gene in large yellow croaker (Larimichthys crocea). Fish. Shellfish Immunol. 34 (2013), 799–809.
25. Lin, T., Zhang, D., Liu, X., Xiao, D., Variations of immune parameters in the lined seahorse Hippocampus erectus after infection with enteritis pathogen of Vibrio parahaemolyticus. Fish. Shellfish Immunol. 50 (2016), 247–254.
26. Livak, K.J., Schmittgen, T.D., Analysis of relative gene expression data using real time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 25 (2001), 402–408.
27. López, L.M., Flores-Ibarra, M., Bañuelos-Vargas, I., Galaviz, M.A., True, C.D., Effect of fishmeal replacement by soy protein concentrate with taurine supplementation on growth performance, hematological and biochemical status, and liver histology of totoaba juveniles (Totoaba macdonaldi). Fish. Physiol. Biochem. 41 (2015), 921–936.
28. Márquez-Farías, J.F., Rosales-Juárez, F.J., Intrinsic rebound potential of the endangered (Totoaba macdonaldi) population, endemic to the Gulf of California, México. Fish. Res. 147 (2013), 150–153.
29. Mata-Sotres, J.A., Lazo, J.P., Baron-Sevilla, B., Effect of age on weaning success in totoaba (Totoaba macdonaldi) larval culture. Aquaculture 437 (2015), 292–296.
30. Minjarez-Osorio, C., González-Félix, M.L., Perez-Velazquez, M., Biological performance of Totoaba macdonaldi in response to dietary protein level. Aquaculture 362–363 (2012), 50–54.
31. Muñoz, M., Cedeño, R., Rodríguez, J., Van der Knaap, W.P., Mialhe, E., Bachére, E., Measurement of reactive oxygen intermediate production in haemocytes of the penaeid shrimp, Penaeus vannamei. Aquaculture 191 (2000), 89–107.
32. Muñoz-Atienza, E., Araújo, C., Lluch, N., Hernandez, P.E., Herranz, C., Cintas, L.M., Magadan S. Different impact of heat-inactivated and viable lactic acid bacteria of aquatic origin on turbot (Scophthalmus maximus L.) head-kidney leucocytes. Fish. Shellfish Immunol. 44 (2015), 214–223.
33. Pang, H., Chen, L., Hoare, R., Huang, Y., Wu, Z., Jian, J., Identification of DLD, by immunoproteomic analysis and evaluation as a potential vaccine antigen against three Vibrio species in Epinephelus coioides. Vaccine 34 (2016), 1225–1231.
34. Pfaffl, M.W., A new mathematical model for relative quantification in realtime RT-PCR. Nucleic Acids Res., 2001, 29–45.
35. Press, C.M., Evensen, O., The morphology of the immune system in teleost fishes. Fish. Shellfish Immunol. 9 (1999), 309–318.
36. Raida, M.K., Buchmann, K., Innate immune response in rainbow trout (Oncorhynchus mykiss) against primary and secondary infections with Yersinia ruckeri O1. Dev. Comp. Immunol. 33 (2009), 35–45.
37. Reyes-Becerril, M., López, M.T., Ascencio, F., Esteban, M.A., Immune response of gilthead seabream (Sparus aurata) following experimental infection with Aeromonas hydrophila. Fish. Shellfish Immunol. 31 (2011), 564–570.
38. Reyes-Becerril, M., Ascencio, V.F., Hirono, I., Kondo, H., Jirapongpairoj, W., Esteban, M.A., Alamillo, E., Angulo, C., TLR21's agonists in combination with Aeromonas antigens synergistically up-regulate functional TLR21 and cytokine gene expression in yellowtail leucocytes. Dev. Comp. Immunol. 61 (2016), 107–115.
39. Rodriguez, A., Esteban, M.A., Meseguer, J., Phagocytosis and peroxidase response to yeast cells. Anat. Rec. 272 (2003), 415–423.
40. Sahoo, P.K., Das,Mahapatra, K., Saha, J.N., Barat, A., Sahoo, M., Mohanty, B.R., et al. Family association between immune parameters and resistance to Aeromonas hydrophila infection in the Indian major carp, Labeo rohita. Fish. Shellfish Immunol. 25 (2008), 163–169.
41. Secombes, C.J., Fletcher, T.C., The role of phagocytes in the protective mechanisms of fish. Annu. Rev. Fish Dis. 2 (1992), 53–71.
42. Secombes, C., Hardie, L., Daniels, G., Cytokines in fish: an update. Fish. Shellfish Immunol. 6 (1996), 291–304.
43. Seppola, M., Larsen, A.N., Steiro, K., Robertsen, B., Jensen, I., Characterisation and expression analysis of the interleukin genes, IL-1β, IL-8 and IL-10, in Atlantic cod (Gadus morhua L.). Mol. Immunol. 45 (2008), 887–897.
44. Shimohata, T., Nakano, M., Lian, X., Shigeyama, T., Iba, H., et al. Vibrio parahaemolyticus infection induces modulation of IL-8 secretion through dual pathway via VP1680 in Caco-2 cells. Biochem. Mol. Biol. 156 (2010), 319–325.
45. Trichet, V.V., Nutrition and immunity: an update. Aquac. Res. 41 (2010), 356–372.
46. True, C.D., Castro, N.C., Acquisition of broodstock of Totoaba macdonaldi: field handling, decompression, and prophylaxis of an endangered species. Fish-Culturist 59 (1997), 246–248.
47. Xu, X.J., Sang, B.H., Chen, W.B., Yan, Q.P., Xiong, Z.Y., Su, J.B., Zou, W.Z., Intracellular survival of virulence and low-virulence strains of Vibrio parahaemolyticus in Epinephelus awoara macrophages and peripheral leukocytes. Genet. Mol. Res. 30 (2015), 706–718.
48. Yao, C.L., Kong, P., Wang, Z.Y.J.P.F., Liu, X.D., Cai, M.Y., Han, X.Z., Molecular cloning and expression of MyD88 in large yellow croaker, Pseudosciaena crocea. Fish. Shellfish Immun. 26 (2009), 249–255.
49. Zapata, A., Diez, B., Cejalvo, T., Gutierrez de Frias, C., Cortes, A., Ontogeny of the immune system of fish. Fish. Shellfish Immunol. 20 (2006), 126–136.
50. Zhang, Q., Dong, X., Chen, B., Zhang, Y., Zu, Y., Li, W., Zebrafish as a useful model for zoonotic Vibrio parahaemolyticus pathogenicity in fish and human. Dev. Comp. Immunol. 55 (2016), 159–168.