Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei
- Autores:
-
Pacheco M, María
Campa C, Ángel
Aguirre G, Gabriel
Luna G, Antonio
Guzmán M, María
Ascencio, Felipe
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2012
- Institución:
- Universidad de Córdoba
- Repositorio:
- Repositorio Institucional Unicórdoba
- Idioma:
- spa
- OAI Identifier:
- oai:repositorio.unicordoba.edu.co:ucordoba/5470
- Acceso en línea:
- https://repositorio.unicordoba.edu.co/handle/ucordoba/5470
https://doi.org/10.21897/rmvz.249
- Palabra clave:
- Debaryomyces hansenii
immunostimulation
Litopenaeus vannamei
- Rights
- openAccess
- License
- https://creativecommons.org/licenses/by-nc-sa/4.0/
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Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| dc.title.translated.eng.fl_str_mv |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| title |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| spellingShingle |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei Debaryomyces hansenii immunostimulation Litopenaeus vannamei |
| title_short |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| title_full |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| title_fullStr |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| title_full_unstemmed |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| title_sort |
Efecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannamei |
| dc.creator.fl_str_mv |
Pacheco M, María Campa C, Ángel Aguirre G, Gabriel Luna G, Antonio Guzmán M, María Ascencio, Felipe |
| dc.contributor.author.spa.fl_str_mv |
Pacheco M, María Campa C, Ángel Aguirre G, Gabriel Luna G, Antonio Guzmán M, María Ascencio, Felipe |
| dc.subject.spa.fl_str_mv |
Debaryomyces hansenii immunostimulation Litopenaeus vannamei |
| topic |
Debaryomyces hansenii immunostimulation Litopenaeus vannamei |
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2012 |
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2012-01-04 00:00:00 2022-07-01T20:58:41Z |
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2012-01-04 00:00:00 2022-07-01T20:58:41Z |
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2012-01-04 |
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Aguirre-Guzmán G, Sánchez-Martínez JG, Campa-Córdova AI, Luna-González A, Ascencio F. Penaeid shrimp immune system: A Minireview. Thai J Vet Med 2009; 39: 205-215. Zhen-Ming C, Liu G, Zhao S, Li J, Peng Y. Marine yeasts as biocontrol agents and producers of bio-products. Appl Microbiol Biotechnol 2010; 86:1227-1241. http://dx.doi.org/10.1007/s00253-010-2483-9 Vici V, Bright Sing IS, Bhat SG. Application of bacterins and yeast Acremonium dyosporii to protect the larvae of Macrobrachium rosenbergii from vibriosis. Fish Shellfish Immunol 2000; 10:559-563. http://dx.doi.org/10.1006/fsim.2000.0278 Robles R, Sorgeloos P, Van Duffel H, Nelis H. Progress in biomedication using live foods. J Appl Ichthyol 1998; 14:207-212. http://dx.doi.org/10.1111/j.1439-0426.1998.tb00643.x Miles DJC, Polchana J, Lilley JH, Kanchanakhan S, Thompson KD, Adams A. Immunostimulation of striped snakehead Channa striata against epizootic ulcerative syndrome. Aquaculture 2001; 195:1-15. http://dx.doi.org/10.1016/S0044-8486(00)00529-9 Gatesoupe FJ. Live yeasts in the gut: natural occurrence, dietary introduction, and their effects on fish health and development. Aquaculture 2007; 267:20-30. http://dx.doi.org/10.1016/j.aquaculture.2007.01.005 Reyes-Becerril M, Salinas I, Cuesta A, Meseguer J, Tovar-Ramirez D, AscencioValle F, Esteban MA. Oral delivery of live yeast Debaryomyces hansenii modulates the main innate immune parameters and the expression of immune-relevant genes in the gilthead seabream (Sparus aurata L.). Fish Shellfish Immunol 2008a; 25:731-739. Reyes-Becerril M, Tovar-Ramirez D, AscencioValle F, Civera-Cerecedo R, Gracia-López V, Barbosa-Solomieu V. Effects of dietary live yeast Debaryomyces hansenii on the immune and antioxidant system in juvenile leopard grouper Mycteroperca rosacea exposed to stress. Aquaculture 2008b; 280: 39–44. Sukumaran V, Williams DL, Sajeevan TP, Rosamma P. Marine yeast glucans confer better protection than that of baker's yeast in Penaeus monodon against white spot syndrome virus infection. Aquac Res 2010; 41: 1799-1805. http://dx.doi.org/10.1111/j.1365-2109.2010.02520.x Mu-oz M, Cedeno R, Rodriguez J, Knaap WPW, Mialhe E, Bachere E. Measurement of reactive oxygen intermediate production in haemocytes of penaeid shrimp, Penaeus vannamei. Aquaculture 2000; 191: 89-107. http://dx.doi.org/10.1016/S0044-8486(00)00420-8 Campa-Córdova AI, Hernández-Saavedra NY, Philippis R De, Ascencio F. Generation of superoxide anion and SOD activity in haemocytes and muscle of American white shrimp (Litopenaeus vannamei) as a response to β-glucan and sulphated polysaccharide. Fish Shellfish Immunol 2002; 12: 353-366. http://dx.doi.org/10.1006/fsim.2001.0377 Silakes S, Supamattaya K. Immunostimulant and vaccination in Black Tiger shrimp, Penaeus monodon Fabricius: II Production of vaccine from Vibrio harveyi and its application in Black Tiger shrimp, Penaeus monodon Fabricius. Songklanakarin J Sci Technol 2000; 22(Suppl.): 663-676. Sajeevan TP, Lowman DW, Williams DL, Selven S, Anas A, Rosamma P. Marine yeast diet confers better protection than its cell wall component (1-3)-b-D-glucan as an immunostimulant in Fenneropenaeus indicus. Aquac Res 2009; 40: 1723-1730. http://dx.doi.org/10.1111/j.1365-2109.2009.02275.x Yang SP, Wu ZH, Jian JC, Zhang XZ. Effect of marine red yeast Rhodosporium paludigenum on growth and antioxidant competence of Litopenaeus vannamei. Aquaculture 2010; 309: 62-65. http://dx.doi.org/10.1016/j.aquaculture.2010.09.032 Tovar D, Zambonino-Infante J, Cahu C, Gatesoupe FJ, Vázquez-Juárez R. Influence of dietary live yeast on European sea bass (Dicentrarchus labrax) larval development. Aquaculture 2004; 234: 415–427. 16. Shupantharika M, Khunrae P, Thanardkit P, Verduyn C. Preparation of spent brewer's yeast β-glucans with potential application as an immunostimulant for black tiger shrimp, Penaeus monodon. Bioresource Technol 2003; 88: 55-60. 17. Macey BM, Coyne VE. Improved growth rate and disease resistance in farmed Haliotis midae through probiotic treatment. Aquaculture 2005; 245: 249-261. http://dx.doi.org/10.1016/j.aquaculture.2004.11.031 Vine NG, Leukes WD, Horst K. Probiotics in marine larviculture. FEMS Microbiol Rev 2006; 30: 404-427. http://dx.doi.org/10.1111/j.1574-6976.2006.00017.x Boonyaratpalin M, Supamattaya K, Verakunpiriya V, Suprasert D. Effects of aflatoxin B1 on growth performance, blood components, immune function and histopathological changes in black tiger shrimp (Penaeus monodon Fabricius). Aquac Res 2001; 32: 388-398. http://dx.doi.org/10.1046/j.1355-557x.2001.00046.x Sritunyalucksana K, Gangnonngiw W, Archakunakorn S, Fegan D, Flegel TW. Bacterial clearance rate and a new differential hemocyte staining method to assess immunostimulant activity in shrimp. Dis Aquat Org 2005; 63: 89–94. http://dx.doi.org/10.3354/dao063089 Laria RE, Cruz Y, Silveira R, Martínez M, González N. Effects of formalin on total haemocytes count and histopathological changes in the shrimp Litopenaeus schmitti (Pérez-Farfante & Kensley 1997). Aquac Res 2008; 39: 1316-1321. http://dx.doi.org/10.1111/j.1365-2109.2008.01997.x Sajeevan TP, Selven S, Rosamma P. b-Mercapto-ethanol-treated yeast showed better protection against white spot syndrome virus infection in Indian white shrimp Fenneropenaeus indicus. 2010. Aquac Res 2010; 41: e715-e718. Downs C, Fauth JE, Woodley CM. Assessing the health of grass shrimp (Palaemonetes pugio) exposed to natural and anthropogenic stressors: A molecular biomarker system. Mar Biotechnol 2001; 3: 380-397. http://dx.doi.org/10.1007/s10126-001-0008-3 Moreno I, Pichardo S, Jose A, GómezAmores L, Mate A, Vázquez CM, Camean AM. Antioxidant enzyme activity and lipid peroxidation in liver and kidney of rats exposed to microcystin-LR administered intraperitoneally. Toxicon 2005; 45:395-402. http://dx.doi.org/10.1016/j.toxicon.2004.11.001 Van de Braak K. Hemocytic defense in black tiger shrimp (Penaeus monodon). [Doctor degree thesis]. The Netherlands: Wageningen University. Wageningen Institute of Animal Science; 2002. Liu CH, Yeh SP, Kuo CH, Cheng W, Chou CH. The effect of sodium alginate on the immune response of tiger shrimp via dietary administration: Activity and gene transcription. Fish Shellfish Immunol 2006; 21:442-452. http://dx.doi.org/10.1016/j.fsi.2006.02.003 Guertler C, Schleder DD, Barracco MA, Perazzolo LM. Comparative study of the intracellular superoxide anion production in different penaeid species through the NBT-reduction assay. Aquac Res 2010; 41: 1082-1088. |
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Pacheco M, Maríaed2133c6-e765-425b-a3d4-6c52e695579a-1Campa C, Ángelf1e905b4-819e-4c7c-9002-0235a81a5160-1Aguirre G, Gabriel6eea3447-5e2f-40a2-9326-ad0ff9aa0295-1Luna G, Antonio6b9742c1-5991-4bd4-878c-c90d7759c1fb-1Guzmán M, Maríaab5507b4-baba-416e-bb7c-6f87276cd6b4-1Ascencio, Felipe58d6f905-43be-490e-8609-f4f0888828ee-12012-01-04 00:00:002022-07-01T20:58:41Z2012-01-04 00:00:002022-07-01T20:58:41Z2012-01-040122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/547010.21897/rmvz.249https://doi.org/10.21897/rmvz.2491909-0544application/pdfspaUniversidad de Córdobahttps://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2https://revistamvz.unicordoba.edu.co/article/view/249Debaryomyces hanseniiimmunostimulationLitopenaeus vannameiEfecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannameiEfecto de Debaryomyces hansenii en la respuesta antioxidante de juveniles de camarón blanco Litopenaeus vannameiArtículo de revistaJournal articleinfo:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/publishedVersionTexthttp://purl.org/redcol/resource_type/ARTREFhttp://purl.org/coar/version/c_970fb48d4fbd8a85Aguirre-Guzmán G, Sánchez-Martínez JG, Campa-Córdova AI, Luna-González A, Ascencio F. Penaeid shrimp immune system: A Minireview. Thai J Vet Med 2009; 39: 205-215.Zhen-Ming C, Liu G, Zhao S, Li J, Peng Y. Marine yeasts as biocontrol agents and producers of bio-products. Appl Microbiol Biotechnol 2010; 86:1227-1241. http://dx.doi.org/10.1007/s00253-010-2483-9Vici V, Bright Sing IS, Bhat SG. Application of bacterins and yeast Acremonium dyosporii to protect the larvae of Macrobrachium rosenbergii from vibriosis. Fish Shellfish Immunol 2000; 10:559-563. http://dx.doi.org/10.1006/fsim.2000.0278Robles R, Sorgeloos P, Van Duffel H, Nelis H. Progress in biomedication using live foods. J Appl Ichthyol 1998; 14:207-212. http://dx.doi.org/10.1111/j.1439-0426.1998.tb00643.xMiles DJC, Polchana J, Lilley JH, Kanchanakhan S, Thompson KD, Adams A. Immunostimulation of striped snakehead Channa striata against epizootic ulcerative syndrome. Aquaculture 2001; 195:1-15. http://dx.doi.org/10.1016/S0044-8486(00)00529-9Gatesoupe FJ. Live yeasts in the gut: natural occurrence, dietary introduction, and their effects on fish health and development. Aquaculture 2007; 267:20-30. http://dx.doi.org/10.1016/j.aquaculture.2007.01.005Reyes-Becerril M, Salinas I, Cuesta A, Meseguer J, Tovar-Ramirez D, AscencioValle F, Esteban MA. Oral delivery of live yeast Debaryomyces hansenii modulates the main innate immune parameters and the expression of immune-relevant genes in the gilthead seabream (Sparus aurata L.). Fish Shellfish Immunol 2008a; 25:731-739.Reyes-Becerril M, Tovar-Ramirez D, AscencioValle F, Civera-Cerecedo R, Gracia-López V, Barbosa-Solomieu V. Effects of dietary live yeast Debaryomyces hansenii on the immune and antioxidant system in juvenile leopard grouper Mycteroperca rosacea exposed to stress. Aquaculture 2008b; 280: 39–44.Sukumaran V, Williams DL, Sajeevan TP, Rosamma P. Marine yeast glucans confer better protection than that of baker's yeast in Penaeus monodon against white spot syndrome virus infection. Aquac Res 2010; 41: 1799-1805. http://dx.doi.org/10.1111/j.1365-2109.2010.02520.xMu-oz M, Cedeno R, Rodriguez J, Knaap WPW, Mialhe E, Bachere E. Measurement of reactive oxygen intermediate production in haemocytes of penaeid shrimp, Penaeus vannamei. Aquaculture 2000; 191: 89-107. http://dx.doi.org/10.1016/S0044-8486(00)00420-8Campa-Córdova AI, Hernández-Saavedra NY, Philippis R De, Ascencio F. Generation of superoxide anion and SOD activity in haemocytes and muscle of American white shrimp (Litopenaeus vannamei) as a response to β-glucan and sulphated polysaccharide. Fish Shellfish Immunol 2002; 12: 353-366. http://dx.doi.org/10.1006/fsim.2001.0377Silakes S, Supamattaya K. Immunostimulant and vaccination in Black Tiger shrimp, Penaeus monodon Fabricius: II Production of vaccine from Vibrio harveyi and its application in Black Tiger shrimp, Penaeus monodon Fabricius. Songklanakarin J Sci Technol 2000; 22(Suppl.): 663-676.Sajeevan TP, Lowman DW, Williams DL, Selven S, Anas A, Rosamma P. Marine yeast diet confers better protection than its cell wall component (1-3)-b-D-glucan as an immunostimulant in Fenneropenaeus indicus. Aquac Res 2009; 40: 1723-1730. http://dx.doi.org/10.1111/j.1365-2109.2009.02275.xYang SP, Wu ZH, Jian JC, Zhang XZ. Effect of marine red yeast Rhodosporium paludigenum on growth and antioxidant competence of Litopenaeus vannamei. Aquaculture 2010; 309: 62-65. http://dx.doi.org/10.1016/j.aquaculture.2010.09.032Tovar D, Zambonino-Infante J, Cahu C, Gatesoupe FJ, Vázquez-Juárez R. Influence of dietary live yeast on European sea bass (Dicentrarchus labrax) larval development. Aquaculture 2004; 234: 415–427. 16. Shupantharika M, Khunrae P, Thanardkit P, Verduyn C. Preparation of spent brewer's yeast β-glucans with potential application as an immunostimulant for black tiger shrimp, Penaeus monodon. Bioresource Technol 2003; 88: 55-60. 17. Macey BM, Coyne VE. Improved growth rate and disease resistance in farmed Haliotis midae through probiotic treatment. Aquaculture 2005; 245: 249-261. http://dx.doi.org/10.1016/j.aquaculture.2004.11.031Vine NG, Leukes WD, Horst K. Probiotics in marine larviculture. FEMS Microbiol Rev 2006; 30: 404-427. http://dx.doi.org/10.1111/j.1574-6976.2006.00017.xBoonyaratpalin M, Supamattaya K, Verakunpiriya V, Suprasert D. Effects of aflatoxin B1 on growth performance, blood components, immune function and histopathological changes in black tiger shrimp (Penaeus monodon Fabricius). Aquac Res 2001; 32: 388-398. http://dx.doi.org/10.1046/j.1355-557x.2001.00046.xSritunyalucksana K, Gangnonngiw W, Archakunakorn S, Fegan D, Flegel TW. Bacterial clearance rate and a new differential hemocyte staining method to assess immunostimulant activity in shrimp. Dis Aquat Org 2005; 63: 89–94. http://dx.doi.org/10.3354/dao063089Laria RE, Cruz Y, Silveira R, Martínez M, González N. Effects of formalin on total haemocytes count and histopathological changes in the shrimp Litopenaeus schmitti (Pérez-Farfante & Kensley 1997). Aquac Res 2008; 39: 1316-1321. http://dx.doi.org/10.1111/j.1365-2109.2008.01997.xSajeevan TP, Selven S, Rosamma P. b-Mercapto-ethanol-treated yeast showed better protection against white spot syndrome virus infection in Indian white shrimp Fenneropenaeus indicus. 2010. Aquac Res 2010; 41: e715-e718.Downs C, Fauth JE, Woodley CM. Assessing the health of grass shrimp (Palaemonetes pugio) exposed to natural and anthropogenic stressors: A molecular biomarker system. Mar Biotechnol 2001; 3: 380-397. http://dx.doi.org/10.1007/s10126-001-0008-3Moreno I, Pichardo S, Jose A, GómezAmores L, Mate A, Vázquez CM, Camean AM. Antioxidant enzyme activity and lipid peroxidation in liver and kidney of rats exposed to microcystin-LR administered intraperitoneally. Toxicon 2005; 45:395-402. http://dx.doi.org/10.1016/j.toxicon.2004.11.001Van de Braak K. Hemocytic defense in black tiger shrimp (Penaeus monodon). [Doctor degree thesis]. The Netherlands: Wageningen University. Wageningen Institute of Animal Science; 2002.Liu CH, Yeh SP, Kuo CH, Cheng W, Chou CH. The effect of sodium alginate on the immune response of tiger shrimp via dietary administration: Activity and gene transcription. Fish Shellfish Immunol 2006; 21:442-452. http://dx.doi.org/10.1016/j.fsi.2006.02.003Guertler C, Schleder DD, Barracco MA, Perazzolo LM. Comparative study of the intracellular superoxide anion production in different penaeid species through the NBT-reduction assay. Aquac Res 2010; 41: 1082-1088.https://revistamvz.unicordoba.edu.co/article/download/249/318Núm. 1 , Año 2012 : Revista MVZ Córdoba Volumen 17(1) Enero-Abril 201228261282017Revista MVZ CórdobaPublicationOREORE.xmltext/xml2789http://172.16.14.198/bitstreams/852fed5d-c61e-4ccc-bb1e-de8eb2a13338/download344f9cac539f3d254dc3d0b4ee2d6341MD51ucordoba/5470oai:172.16.14.198:ucordoba/54702023-10-06 00:45:19.723https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttp://172.16.14.198Repositorio Universidad de Córdobabdigital@metabiblioteca.com |