Eficiencia de lectinas como inmunoindicadores en juveniles de camarón blanco, Litopenaeus vannamei (Malacostraca: Penaeidae)

Autores/as

  • Angel Isidro Campa Cordova Centro de Investigaciones Biológicas del Noroeste, S.C.

DOI:

https://doi.org/10.24275/uam/izt/dcbs/hidro/2018v28n3/Martin

Palabras clave:

anticuerpos monoclonales, inmunoestimulantes, lectinas, Litopenaeus vannamei

Resumen

 Antecedentes: Las lectinas actúan como unidades de reconocimiento para facilitar la eliminación de pató­genos invasivos en plantas y animales, participan en mecanismos de defensa y actúan como mediadores de reconocimiento en la respuesta inmune de invertebrados. Existen pocos estudios dirigidos a evaluar el efecto de inmunoestimulantes sobre la activación de lectinas en crustáceos. Objetivos: Evaluar la concentración de lectina en juveniles de camarón blanco tratados con inmunoestimulantes de origen microbiano y comer­cial. Métodos: Se utilizaron cinco tratamientos agregados directamente al agua de cultivo cada tercer día durante 12 días: 1) laminarina (0.5 mg ml-1); 2) mezcla 1 (Bacillus tequilensis y B. licheniformis; 2 x 106 UFC ml-1, proporción 1:1); 3) mezcla 2 (B. endophyticus, cepa YC3-B y cepa C2-2; 2 x 106 UFC ml-1, proporción 1:1); 4) Debaryomyces hansenii (1 x 106 UFC ml-1); 5) control (sin inmunoestimulantes). Después de los 12 días de tratamiento se tomaron muestras de hemolinfa a las 24, 48 y 72 h para la cuantificación de lectina en plasma, para ello se utilizaron anticuerpos monoclonales contra la lectina de Macrobrachium rosenbergii (MrL). Resultados: A las 24 h posteriores a la última aplicación del tratamiento, se registraron diferencias significativas (p < 0.05) en la concentración de lectina en el plasma de L. vannamei de los camarones ex­puestos al inmunoestimulante comercial laminarina respecto al grupo control, seguida por la mezcla 1 y la mezcla 2 a las 72 horas después de la aplicación de los tratamientos. A las 48 h no hubo diferencias signi­ficativas (p > 0.05) entre los tratamientos y el grupo control. No se encontraron diferencias significativas en los camarones expuestos a la cepa de D. hansenii respecto al grupo control. Conclusiones: Se observó que la concentración de lectina en el plasma de camarón blanco puede incrementarse por el uso de inmunoesti­mulantes y utilizarse como herramienta bioindicadora de inmunoestimulación.

Descargas

Los datos de descargas todavía no están disponibles.

Biografía del autor/a

Angel Isidro Campa Cordova, Centro de Investigaciones Biológicas del Noroeste, S.C.

Departamento de Acuicultura. Investigador Titular

Citas

Agundis, C., A. Pereyra, R. Zenteno, C. Brassart, C. Sierra, L. Vazquez& E. Zenteno. 2000. Cuantification of lectin in freshwater prawn (Macro¬brachium rosembergii) hemolymph by ELISA. 2000. Comparative Biochemistry and Physiology Part B 127: 165-172. DOI:10.1016/ S0305-0491(00)00248-0

Alpuche, J., C. Agundis, C. Solórzano & A. PereyraA. 2005. Lectina en L. Se¬tiferus: una alternativa en cultivo ante enfermedades que afectan al cultivo de camarones. REDVET 12: 1-12.

Alpuche, J., A. Pereyra, C. Agundis, C. Rosas, C. Pascual, M. C. Slomianny, L. Vázquez& E. Zenteno. 2005. Purification and characterization of a lectin from the White shrimp Litopenaeus setiferus (Crustacea de¬capoda) hemolymph. Biochimica et Biophysica Acta 1724: 86-93. DOI:10.1016/j.bbagen.2005.04.014

Amparyup, P., J. Sutthangkul, W. Charoensapsri & A. Tassanakajon. 2016. Pattern recognition protein binds to lipopolysaccharide and β-1,3-glucan and activates shrimp prophenoloxidase system. The Journal of Biological Chemistry 291 (20): 10949. DOI:10.1074/jbc. M111.294744

Bae, S. H., B. R. Kim, B. J. Kang, N. Tsutsui, T. Okutsu, J. Shinji, I. K. Jang, C. H. Han & M. N. Wilder. 2012. Molecular cloning of prophenoloxidase and the effects of dietary β-glucan and rutin on immune response in hemocytes of the fleshy shrimp, Fenneropenaeus chinensis. Fish & Shellfish Immunology 33: 597-604. DOI:10.1016/j.fsi.2012.06.034

Bollag, D. M., M. D. Rozycki & S. J. Edelsteein. 1996. Protein methods. Wiley-Liss. 432 p.

Bradford, M. 1976. A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Pro¬tein-Dye Binding. Analytical Biochemistry 72:248-254.

Campa-Córdova, A. I., N. Y. Hernández-Saavedra, R. De Philippis & F. Ascencio. 2002. Generation of superoxide anion and SOD activity in haemo¬cytes and muscle of American white shrimp (Litopenaeus vanna¬mei) as a response to β-glucan and sulphated polysaccharide. Fish & Shellfish Immunology 12: 353-366. DOI:10.1006/fsim.2001.0377

Campa-Córdova, A. I., N. Y. Hernández-Saavedra, G. Aguirre-Guzmán & F. As¬cencio. 2005. Respuesta inmunomoduladora de la superóxido dis¬mutasa en juveniles de camarón blanco (Litopenaeus vannamei) expuestos a inmunoestimulantes. Ciencias Marinas 31: 661-669.

Chai, P. C., X. L. Song, G. F. Chen, H. Xu & J. Huang. 2016. Dietary supple¬mentation of probiotic Bacillus PC465 isolated from the gut of Fen¬neropenaeus chinensis improves the health status and resistance of Litopenaeus vannamei against white spot syndrome virus. Fish & Shellfish Immunology 54: 602-611. DOI: 10.1016/j.fsi.2016.05.011

Chen, Y. Y., J. C. Chen, Y. H. Kuo, Y. C. Lin, Y. H. Chang, H. Y. Gong & C. L. Huang. 2016. Lipopolysaccharide and β-1,3-glucan-binding protein (LGBP) bind to seaweed polysaccharides and activate the prophe¬noloxidase system in white shrimp Litopenaeus vannamei. Develo¬pmental & Comparative Immunology 55: 144-151. DOI:10.1016/j. dci.2015.10.023

Denis, M., K. Thayappan, S. M. Ramasamy & A. Munusamy. 2016. Lectin in innate immunity of crustacea. Austin Biology 1 (1): 1-7.

Itami, T. 2002. Promising strategies against WSSV for kuruma shrimp in Japan. Asian Aquaculture 24: 9-10.

Laemmli, U. K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-685.

Li, H., Y. Chen, M. Li, S. Wang, H. Zuo, X. Xu, S. Weng, J. He & C. Li. 2015. A C-type lectin (LvCTL4) from Litopenaeus vannamei is a downs¬tream molecule of the NF-κB signaling pathway and participates in antibacterial immune response. Fish & Shellfish Immunology 43: 257-263. DOI:10.1016/fsi.2014.12.024

Li, F. & J. Xiang. 2013. Signaling pathways regulating innate immune responses in shrimp. Fish & Shellfish Immunology 34: 973-980. DOI:10.1026/fsi.2012.08.023

Li, J., B. Tan, K. Mai. 2009. Dietary probiotic Bacillus OJ and isomal¬tooligosaccharides influence the intestine microbial populations, immune responses and resistance to white spot syndrome virus in shrimp (Litopenaeus vannamei). Aquaculture 291: 35-40.

Li, M., C. Li, C. Ma, H. Li, H. Zuo, S. Weng, X. Chen, D. Zeng, J. He & X. Xu. 2014. Identification of a C-type lectin with antiviral and antibacte¬rial activity from pacific white shrimp Litopenaeus vannamei. Deve¬lopmental & Comparative Immunology 46: 231-240. DOI:10.1016/j. dci.2014.04.014

Lu, J., Z. Yu, C. Mu, R. Li, W. Song & C. Wang. 2017. Characterization and functional analysis of a novel C-type lectin from the swimming crab Portunus trituberculatus. Fish & Shellfish Immunology 64: 185-192. DOI:10.1016/j.fsi.2017.03.013

Luis-Villaseñor, I., M. E. Macías-Rodríguez, B. Gómez-Gil, F. Ascencio-Valle & A. I. Campa-Córdova. 2011. Beneficial effects of four Bacillus strains on the larval cultivation of Litopenaeus vannamei. Aquaculture 321: 136-144. DOI:10.1016/j.aquaculture.2011.08.036

Luis-Villaseñor, I., T. Castellanos-Cervantes, B. Gómez-Gil, A. E. Carrillo-Gar¬cía, A. I. Campa-Córdova& F. Ascencio. 2013. Probiotics in the intestinal tract of juvenile whiteleg shrimp Litopenaeus vannamei: modula¬tion of the bacterial community. World Journal of Microbiology and Biotechnology 29: 257-265. DOI:10.1007/s11274-012-1177-0

Luo, Z., J. Zhang, F. Li, X. Zhang, C. Liu & J. Xiang. 2011. Identification of a novel C-type lectin from the shrimp Litopenaeus vannamei and its role in defense against pathogens infection. Chinese Journal of Oceanography and Limnology 29 (5): 942-951. DOI: 10.1007/ s00343-011-0249-6

Pacheco-Marges, M. R., A. I. Campa-Córdova, G. Aguirre-Guzmán, A. Luna-Gon¬zález, M. A. Guzmán-Murillo & F. Ascencio. 2012. Efecto de Debar¬yomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei. Revista MVZ Córdoba 17 (1): 2820-2826.

Pan, M. V., R. F. M. Traifalgar, A. E. Jr. Serrano & V. L. Jr. Corre. 2015. Immunomodulatory and growth promoting effects of peptidoglycan supplementation in Black tiger shrimp Penaeus monodon Fabricius 1798. Asian Fisheries Science 28: 60-71.

Pais, R., R. Khushiramani, I. Karunasagar & I. Karunasagar. 2008. Effect of immunostimulants on the haemolymph haemagglutinins of tiger shrimp Penaeus monodon. Aquaculture Research 39: 1339-1345. DOI:10.1111/j.1365-2109.2008.02004.x

Pereyra, A., C. Agundis, B. Barrera, J. Alpuche, C. Sierra, R. Zenteno, E. Zente¬no & L. Vazquez. 2009. The use of monoclonal antibodies anti-lectin form freshwater prawn Macrobrachium rosenbergii (DeMan, 1879) in the recognition of protein with lectin activity in decapod´s he¬molymph. Preparative Biochemistry and Biotechnology 39: 308- 322. DOI: 10.1080/10826060902953384

Pereyra, A., J. Alpuche, J. C. Sainz, E. Zenteno & C. Agundis. 2012. Purifi¬cation and partial characterization of a lectin from the prawn Ma¬crobrachium americanum (Decapoda, Palaemonidae). Crustaceana 85: 1253-1267.

Purivirojkul, W., N. Areechon & P. Srisapoome. 2006. The effect of peptido¬glycan on immune response in Black Tiger Shrimp (Penaeus mo¬nodon Fabricius). Kasetsart Journal: Natural Sciencie 40: 11-187.

Sarlin, P. J. & R. Philip. 2011. Efficacy of marine yeasts and baker´s yeast as immunostimulants in Fenneropenaeus indicus: A compa¬rative study. Aquaculture 321: 173-178. DOI: 10.1016/j.aquacultu-re.2011.08.039

Sivakamavalli, J. & B. Vaseeharan. 2014. Purification, characterization and functional role of lectin from green tiger shrimp Penaeus semisul¬catus. International Journal of Biological Macromolecules 67: 64- 70. DOI:10.1016/j.ijbiomac.2014.03.008

Sivakamavalli, J., S. K. Tripathi, S. K. Singh & B. Vaseeharan. 2015. Homology modeling, molecular dynamics, and docking studies of pattern-re¬cognition transmembrane protein-lipopolysaccharide and β-1,3 glucan-binding protein from Fenneropenaeus indicus. Journal of Biomolecular Structure and Dynamics 33: 1269-1280. DOI:10.10 80/07391102.2014.943807

Smith, V. J. & K. Söderhäll. 1983. β-1,3 glucan activation of crustacean hemocytes in vitro and in vivo. Biological Bulletin 164: 299-314. DOI:10.2307/1541146

Sritunyalucksana, K., P. Sithisarn, B. Withayachumnarnkul& T. W. Flegel. 1999. Activation of prophenoloxidase, agglutinin and antibacterial acti¬vity in haemolymph of the black tiger prawn, Penaeus monodon, by immunoestimulants. Fish & Shellfish Immunology 9: 21-30. DOI:10.1006/fsim.1998.0161

Sukumaran, V., D. W. Lowman, T. P. Sajeevan & R. Philip. 2010. Marine yeast glucans confer better protection than that of baker’s yeast in Penaeus monodon against white spot syndrome virus infec¬tion. Aquaculture Research 41: 1799-1805. DOI:10.1111/j.1365- 2109.2010.02520.x

Sung, H. H., G. H. Kou & L. Song. 1994. Vibriosis resistance induced by glucan treatment in tiger shrimp (Penaeus monodon). Fish Patholo¬gy 29: 11-17. DOI:10.3147/jsfp.29.11

Tassanakajon, A., Somboonwiwat, K., Supungul, P. & S. Tang. 2013. Discovery of immune molecules and their crucial functions in shrimp im¬munity. Fish & Shellfish Immunology 34: 954-967. DOI:10.1016/j. fsi.2012.09.021

Towbin, H., T. Staehelin & J. Gordon. 1979. Electrophoretic transfer of pro¬teins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proceedings of the National Academy of Sciences 76: 4350-4354.

Vargas-Albores, F., M. A. Guzman, J. L. Ochoa. 1993. An anticoagulant so¬lution for haemolymph collection and prophenoloxidase studies of penaeid shrimp (Penaeus californiensis). 1993. Comparative Bio¬chemistry and Physiology 106A: 299-303.

Wang, X. W. & J. X. Wang. 2013. Diversity and multiple functions of lectins in shrimp immunity. Developmental & Comparative Immunology 39: 27-38. DOI:10.1016/j.dci.2012.04.009

Wang, X. W., J. D. Xu, X. F. Zhao, G. R. Vasta& J. X. Wang. 2014. A shrimp C-type lectin inhibits proliferation of the hemolymph microbiota by maintaining the expression of antimicrobial peptides. Jour¬nal of Biological Chemistry 289: 11779-11790. DOI:10.1074/jbc. M114.552307

Wei, X., X. Liu, J. Yang, J. Fang, H. Qiao, Y. Zhang & J. Yang. 2012. Two C-type lectins from shrimp Litopenaeus vannamei that might be involved in immune response against bacteria and virus. Fish & Shellfish Immunology 32: 132-140. DOI:10.1016/j.fsi.2011.11.001

Wilson, W., D. Lowman, S. P. Antony, J. Puthumana, I. S. Bright Singh & R. Philip. 2015. Immune gene expression profile of Penaeus monodon in response to marine yeast glucan application and white spot sy¬ndrome virus challenge. Fish & Shellfish Immunology 43: 346-56. DOI:10.1016/j.fsi.2014.12.032

Xu, Y. H., W.J. Bi, X. W. Wang, Y. R. Zhao, X. F. Zhao & J. X. Wang. 2014a. Two novel C-type lectins with a low-density lipoprotein receptor class A domain have antiviral function in the shrimp Marsupenaeus ja-ponicus. Developmental & Comparative Immunology 42: 323-332.

Xu, S., L. Wang, X. W. Wang, Y. R. Zhao, W. J. Bi, X. F. Zhao & J. X. Wang. 2014b. L-Type lectin from the kuruma shrimp Marsupenaeus ja¬ponicus promotes hemocyte phagocytosis. Developmental & Com¬parative Immunology 44: 397-405. DOI:10.1016/j.dci.2014.01.016

Zhang, Q., B. Tan, K. Mai, W. Zhang, H. Ma, Q. Ai, X. Wang & Z. Liufu. 2011. Die¬tary administration of Bacillus (B. licheniformis and B. subtilis) and isomaltooligosaccharide influences the intestinal microflora, im-munological parameters and resistance against Vibrio alginolyticus in shrimp, Penaeus japonicus (Decapoda: Penaeidae). Aquaculture Research 42: 943-952. DOI:10.1111/j.1365-2109.2010.02677.x

Zhao, H. X., J. M. Cao, A. L. Wang, Z. Y. Du, C. X. Ye, Y. H. Huang, H. B. Lan, T. T. Zhou & L. G. L. Li. 2012. Effect of long-term administration of dietary B 1,3 glucan on growth, physiological, and immune responses in Litopenaeus vannamei (Boone, 1931). Aquaculture International 20: 145-158. DOI:10.1007/s10499-011-9448-6

Descargas

Publicado

2018-12-11

Cómo citar

Campa Cordova, A. I. (2018). Eficiencia de lectinas como inmunoindicadores en juveniles de camarón blanco, Litopenaeus vannamei (Malacostraca: Penaeidae). HIDROBIOLÓGICA, 28(3). https://doi.org/10.24275/uam/izt/dcbs/hidro/2018v28n3/Martin

Número

Sección

Artículos