Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei

Autores:: Álvarez-Sánchez, Ana R
Nolasco-Soria, Héctor
Mejía-Ruíz, Humberto

Tipo de recurso:: Article of journal

Fecha de publicación:: 2017

Institución:: Universidad de Córdoba

Repositorio:: Repositorio Institucional Unicórdoba

Idioma:: spa

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dc.title.spa.fl_str_mv	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
dc.title.translated.eng.fl_str_mv	In vitro digestibility of specific dsRNA by enzymes of digestive tract of shrimp Litopenaeus vannamei
title	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
spellingShingle	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei Aquaculture balanced feed digestive gland nucleic acids WSSV Ácidos nucleicos acuacultura alimento balanceado glándula digestiva WSSV
title_short	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
title_full	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
title_fullStr	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
title_full_unstemmed	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
title_sort	Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei
dc.creator.fl_str_mv	Álvarez-Sánchez, Ana R Nolasco-Soria, Héctor Mejía-Ruíz, Humberto
dc.contributor.author.spa.fl_str_mv	Álvarez-Sánchez, Ana R Nolasco-Soria, Héctor Mejía-Ruíz, Humberto
dc.subject.eng.fl_str_mv	Aquaculture balanced feed digestive gland nucleic acids WSSV
topic	Aquaculture balanced feed digestive gland nucleic acids WSSV Ácidos nucleicos acuacultura alimento balanceado glándula digestiva WSSV
dc.subject.spa.fl_str_mv	Ácidos nucleicos acuacultura alimento balanceado glándula digestiva WSSV
publishDate	2017
dc.date.accessioned.none.fl_str_mv	2017-05-02 00:00:00 2022-07-01T21:00:23Z
dc.date.available.none.fl_str_mv	2017-05-02 00:00:00 2022-07-01T21:00:23Z
dc.date.issued.none.fl_str_mv	2017-05-02
dc.type.spa.fl_str_mv	Artículo de revista
dc.type.eng.fl_str_mv	Journal article
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dc.identifier.doi.none.fl_str_mv	10.21897/rmvz.1024
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dc.identifier.eissn.none.fl_str_mv	1909-0544
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url	https://repositorio.unicordoba.edu.co/handle/ucordoba/5839 https://doi.org/10.21897/rmvz.1024
dc.language.iso.spa.fl_str_mv	spa
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dc.relation.references.spa.fl_str_mv	Taju G, Madan N, Abdul-Majeed S, Raj-Kumar T, Thamizhvanan S, Otta S, Sahul-Hameed AS. Immune responses of whiteleg shrimp, Litopenaeus vannamei (Boone, 1931), to bacterially expressed dsRNA specific to VP28 gene of white spot syndrome virus. J Fish Dis 2015; 38(5):451-465. https://doi.org/10.1111/jfd.12256 Sudhakaran RT, Mekata T, Kono M, Inada S, Okugawa M, Yoshimine T et al. Double-stranded RNA-mediated silencing of the White Spot Syndrome Virus VP28 gene in Kuruma shrimp, Marsupenaeus japonicus. Aquac Res 2011; 42(8):1153–1162. https://doi.org/10.1111/j.1365-2109.2010.02703.x Robalino J, Bartlett T, Shepard EF, Prior S, Jaramillo G, Scura E, et al. Double-stranded RNA induces sequence-specific antiviral silencing in addition to non-specific immunity in marine shrimp: convergence of RNA interference and innate immunity in the invertebrate antiviral response? J Virology 2005; 79(21):13561–13571. https://doi.org/10.1128/JVI.79.21.13561-13571.2005 Kim CS, Kosuke Z, Nam YK, Kim SK, Kim KH. Protection of shrimp (Penaeus chinensis) against white spot syndrome virus (WSSV) challenge by double-stranded RNA. Fish Shellfish Immunol 2007; 23(1):242–246. https://doi.org/10.1016/j.fsi.2006.10.012 Xu J, Han F, Zhang X. Silencing shrimp white spot syndrome virus (WSSV) genes by siRNA. Antiviral Res 2007; 73(2):126–131. https://doi.org/10.1016/j.antiviral.2006.08.007 Escobedo-Bonilla CM, Vega S, Mejia H. Efficacy of double-stranded RNA against whites pot syndrome virus (WSSV) non-structural (orf89, wsv191) and structural (vp28, vp26) genes in the Pacific white shrimp. J ksus 2015; 27(2):182–188. Sarathi M, Simon MC, Venkatesan C, Thomas J, Ravi M, Madan N, et al. Efficacy of bacterially expressed dsRNA specific to different structural genes of White Spot Syndrome Virus (WSSV) in protection of shrimp from WSSV infection. J Fish Dis 2010; 33(7):603–607. https://doi.org/10.1111/j.1365-2761.2010.01157.x LaFauce K, Owens L. RNA interference with special reference to combating viruses of crustacean. Indian J Virol 2012; 23(2):226-243. https://doi.org/10.1007/s13337-012-0084-1 Papić L, García K, Romero J. Avances y limitaciones en el uso de los dsRNA como estrategias de control y prevención de enfermedades virales en sistemas acuícolas. Lat Am J Aquat Res2015; 43(3):388-401. Agrawal N, Dasaradhi PV, Mohmmed A, Malhotra P, Bhatnagar RK, Mukherjee SK. RNA interference: biology, mechanism, and applications. Microbiol. Mol Biol Rev 2003; 67(4):657–685. https://doi.org/10.1128/MMBR.67.4.657-685.2003 Posiri P, Ongvarrasopone C, Panyim S. A simple one-step method for producing dsRNA from E. coli to inhibit shrimp virus replication. J Virol Meth 2013; 188(2):64-69. https://doi.org/10.1016/j.jviromet.2012.11.033 Plant KP, LaPatra SE. Advances in fish vaccine delivery. Dev Comp Immunol 2011; 35(12):1256-1262. https://doi.org/10.1016/j.dci.2011.03.007 Linggatong GR, Hernandez EP, Talactac MR, Maeda H, Kusakisako K, Umemiya R, Fujisaki K, Tanaka T. Induction of gene silencing in Haemaphysalis longicornis ticks through immersion in double-stranded RNA. Ticks Tick Borne Dis 2016; 7(5):813–816. https://doi.org/10.1016/j.ttbdis.2016.03.018 Sarathi M, Simon MC, Ahmed I, Kumar SR, Sahul-Hameed AS. Silencing vp28 gene of white spot syndrome virus of shrimp by bacterially expressed dsRNA. Mar Biotechnol 2008a; 10(2):198–206. https://doi.org/10.1007/s10126-007-9052-y Sarathi M, Simon MC, Venkatesan C, Sahul-Hameed AS. Oral administration of bacterially expressed vp28 dsRNA to protect Penaeus monodon from white spot syndrome virus. Mar Biotechnol 2008b; 10(3):242–249. https://doi.org/10.1007/s10126-007-9057-6 Somchai P, Jitrakorn S, Thitamadee S, Meetam M, Saksmerprome V. Use of microalgae Chlamydomonas reinhardtii for production of double-stranded RNA against shrimp virus. Aquacult Rep 2016; 3(3):178-183. https://doi.org/10.1016/j.aqrep.2016.03.003 Alexandre D, Ozório R, Derner R, Fracalossi D, Oliveira G, Richard I, Walter R, Silva CP. Spatial distribution of digestive proteinases in the midgut of the Pacific white shrimp (Litopenaeus vannamei) indicates the existence of endo-ectoperitrophic circulation in Crustacea. Comp Biochem Physiol B 2014; 173(10):90–95. https://doi.org/10.1016/j.cbpb.2014.04.010 Magalhães T, Mossolin CE, Mantelatto FL. Gonadosomatic and Hepatosomatic indexes of the freshwater shrimp Macrobrachium olfersii (Decapoda, Palaemonidae) from São Sebastião Island, Southeastern Brazil. Pan-Am J Aquat Sci 2012; 7(1):1-9. Vega-Villasante F, Nolasco H, Civera R. The digestive enzymes of the Pacific brown shrimp Penaeus californiensis. I- Properties of amylase activity in the digestive tract. Comp Biochem Physiol B 1993; 106(6):547-550. https://doi.org/10.1016/0305-0491(93)90130-W Versaw WK, Cuppert SL, Winter DD, Williams LE. An improved colorimetric assay for bacterial lipase in non-fat dry milk. J Food Sci 1989; 54(6):1557-1558. https://doi.org/10.1111/j.1365-2621.1989.tb05159.x Michal G, Schomburg D, editores. Biochemical pathways: an atlas of biochemistry and molecular biology. 2nd ed. New Jersey: John Wiley & Sons; 2012. Hoffman CS, Winston F. A ten- minute DNA preparation from yeast efficiently releases autonomous plasmids for transformation of Escherichia coli. Gene 1987; 57(3):267-272. https://doi.org/10.1016/0378-1119(87)90131-4 Rodríguez-Jaramillo C, Hurtado MA, Romero-Vivas E, Ramírez JL, Manzano M, Palacios E. Gonadal development and histochemistry of the tropical oyster, Crassostrea corteziensis (Hertlein, 1951) during an annual reproductive cycle. J Shellfish Res 2008; 27(5):1129–1141. https://doi.org/10.2983/0730-8000-27.5.1129 Castex M, Chim L, Pham D, Lemaire P, Wabete N, Nicolas JL, Schmidely P, Mariojouls C. Probiotic P. acidilactici application in shrimp Litopenaeus stylirostris culture subject to vibriosis in New Caledonia. Aquaculture 2008; 275(4):182–193. https://doi.org/10.1016/j.aquaculture.2008.01.011 Hernández JC, Murueta JH. Activity of trypsin from Litopenaeus vannamei. Aquaculture 2009; 290(4):190–195. https://doi.org/10.1016/j.aquaculture.2009.02.034 Becerra MJ, Martínez PM, Martínez LR, Rivas ME, López JA, Porchas MA. Production response and digestive enzymatic activity of the Pacific white shrimp Litopenaeus vannamei (Boone 1931) intensively pregrown in microbial heterotrophic and autotrophic-based systems. ScientificWorldJournal 2012; 2012(3):1-6. https://doi.org/10.1100/2012/723654 Cruz–Suárez LE, Ricque-Marie D, Tapia-Salazar M, Olvera-Novoa MA, Civera-Cerecedo R. (Eds.). Avances en Nutrición Acuícola V. Mérida, Yucatán, México; 2000. Sheng LC, We IZ, De SL, Cong HY. Profile of progesterone and estradiol in hepatopancreas, ovary, and hemolymph of shrimp Penaeus chinensis during reproduction cycle. J Fish China 2012; 25(4):304-310. Molthathong S, Senapin S, Klinbunga S, Puanglarp N, Rojtinnakorn J, Flegel TW. Down-regulation of defender against apoptotic death (DAD1) after yellow head virus (YHV) challenge in black tiger shrimp Penaeus monodon. Fish Shellfish Immunol 2008; 24(2):173-179. https://doi.org/10.1016/j.fsi.2007.10.013 Shim MS, Kwon YJ. Efficient and targeted delivery of siRNA in vivo. FEBS J 2010; 277(23):48144827. https://doi.org/10.1111/j.1742-4658.2010.07904.x Lamontagne B, Larose S, Boulanger J, Elela S. The RNase III family: A conserved structure and expanding functions in eukaryotic dsRNA metabolism. Curr Issues Mol Biol 2001; 3(4):71-78. Lemos D, Ezquerra JM, Garcia FL. Protein digestion in penaeid shrimp: digestive proteinases, proteinase inhibitors and feed digestibility. Aquaculture 2000; 186(2):89-105. https://doi.org/10.1016/S0044-8486(99)00371-3 Ongvarrasopone C,Chomchai E, Panyim S. Antiviral effect of PmRab7 knock-down on inhibition of Laem-Singh virus replication in black tiger shrimp. Antiviral Res 2010; 88(1):116-8. https://doi.org/10.1016/j.antiviral.2010.06.013 Varela A, Pe-a N. El Virus del Síndrome de las Manchas Blancas (WSSV): una revisión y su impacto en la camaronicultura costarricense. Rev Costa Rica Cienc Vet 2010; 28(2):51-69. Sellars MJ, Rao M, Arnold SJ, Wade N, Cowley J. Penaeus monodon is protected against gill-associated virus by muscle injection but not oral delivery of bacterially expressed dsRNAs. Dis. Aquat 2011; 95(1):19-30. https://doi.org/10.3354/dao02343 Treerattrakool S, Chartthai C, Phromma-in N, Panyim S, Udomkit A. Silencing of gonad-inhibiting hormone gene expression in Penaeus monodon by feeding with GIH dsRNA enriched Artemia. Aquaculture 2013; 404(1):116–121. https://doi.org/10.1016/j.aquaculture.2013.04.024
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dc.relation.citationedition.spa.fl_str_mv	Núm. 2 , Año 2017 : Revista MVZ Córdoba Volumen 22(2) Mayo-Agosto 2017
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spelling	Álvarez-Sánchez, Ana Redd6959f-6b38-4149-8b4c-939ac355aa9e-1Nolasco-Soria, Héctorfc9ab529-6593-4a76-b5ad-a6f92b51fbc3-1Mejía-Ruíz, Humberto3147bd97-d70f-42b1-979e-59d2fa3e752c-12017-05-02 00:00:002022-07-01T21:00:23Z2017-05-02 00:00:002022-07-01T21:00:23Z2017-05-020122-0268https://repositorio.unicordoba.edu.co/handle/ucordoba/583910.21897/rmvz.1024https://doi.org/10.21897/rmvz.10241909-0544application/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/1024Aquaculturebalanced feeddigestive glandnucleic acidsWSSVÁcidos nucleicosacuaculturaalimento balanceadoglándula digestivaWSSVDigestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannameiIn vitro digestibility of specific dsRNA by enzymes of digestive tract of shrimp 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_970fb48d4fbd8a85Taju G, Madan N, Abdul-Majeed S, Raj-Kumar T, Thamizhvanan S, Otta S, Sahul-Hameed AS. Immune responses of whiteleg shrimp, Litopenaeus vannamei (Boone, 1931), to bacterially expressed dsRNA specific to VP28 gene of white spot syndrome virus. J Fish Dis 2015; 38(5):451-465. https://doi.org/10.1111/jfd.12256Sudhakaran RT, Mekata T, Kono M, Inada S, Okugawa M, Yoshimine T et al. Double-stranded RNA-mediated silencing of the White Spot Syndrome Virus VP28 gene in Kuruma shrimp, Marsupenaeus japonicus. Aquac Res 2011; 42(8):1153–1162. https://doi.org/10.1111/j.1365-2109.2010.02703.xRobalino J, Bartlett T, Shepard EF, Prior S, Jaramillo G, Scura E, et al. Double-stranded RNA induces sequence-specific antiviral silencing in addition to non-specific immunity in marine shrimp: convergence of RNA interference and innate immunity in the invertebrate antiviral response? J Virology 2005; 79(21):13561–13571. https://doi.org/10.1128/JVI.79.21.13561-13571.2005Kim CS, Kosuke Z, Nam YK, Kim SK, Kim KH. Protection of shrimp (Penaeus chinensis) against white spot syndrome virus (WSSV) challenge by double-stranded RNA. Fish Shellfish Immunol 2007; 23(1):242–246. https://doi.org/10.1016/j.fsi.2006.10.012Xu J, Han F, Zhang X. Silencing shrimp white spot syndrome virus (WSSV) genes by siRNA. Antiviral Res 2007; 73(2):126–131. https://doi.org/10.1016/j.antiviral.2006.08.007Escobedo-Bonilla CM, Vega S, Mejia H. Efficacy of double-stranded RNA against whites pot syndrome virus (WSSV) non-structural (orf89, wsv191) and structural (vp28, vp26) genes in the Pacific white shrimp. J ksus 2015; 27(2):182–188.Sarathi M, Simon MC, Venkatesan C, Thomas J, Ravi M, Madan N, et al. Efficacy of bacterially expressed dsRNA specific to different structural genes of White Spot Syndrome Virus (WSSV) in protection of shrimp from WSSV infection. J Fish Dis 2010; 33(7):603–607. https://doi.org/10.1111/j.1365-2761.2010.01157.xLaFauce K, Owens L. RNA interference with special reference to combating viruses of crustacean. Indian J Virol 2012; 23(2):226-243. https://doi.org/10.1007/s13337-012-0084-1Papić L, García K, Romero J. Avances y limitaciones en el uso de los dsRNA como estrategias de control y prevención de enfermedades virales en sistemas acuícolas. Lat Am J Aquat Res2015; 43(3):388-401.Agrawal N, Dasaradhi PV, Mohmmed A, Malhotra P, Bhatnagar RK, Mukherjee SK. RNA interference: biology, mechanism, and applications. Microbiol. Mol Biol Rev 2003; 67(4):657–685. https://doi.org/10.1128/MMBR.67.4.657-685.2003Posiri P, Ongvarrasopone C, Panyim S. A simple one-step method for producing dsRNA from E. coli to inhibit shrimp virus replication. J Virol Meth 2013; 188(2):64-69. https://doi.org/10.1016/j.jviromet.2012.11.033Plant KP, LaPatra SE. Advances in fish vaccine delivery. Dev Comp Immunol 2011; 35(12):1256-1262. https://doi.org/10.1016/j.dci.2011.03.007Linggatong GR, Hernandez EP, Talactac MR, Maeda H, Kusakisako K, Umemiya R, Fujisaki K, Tanaka T. Induction of gene silencing in Haemaphysalis longicornis ticks through immersion in double-stranded RNA. Ticks Tick Borne Dis 2016; 7(5):813–816. https://doi.org/10.1016/j.ttbdis.2016.03.018Sarathi M, Simon MC, Ahmed I, Kumar SR, Sahul-Hameed AS. Silencing vp28 gene of white spot syndrome virus of shrimp by bacterially expressed dsRNA. Mar Biotechnol 2008a; 10(2):198–206. https://doi.org/10.1007/s10126-007-9052-ySarathi M, Simon MC, Venkatesan C, Sahul-Hameed AS. Oral administration of bacterially expressed vp28 dsRNA to protect Penaeus monodon from white spot syndrome virus. Mar Biotechnol 2008b; 10(3):242–249. https://doi.org/10.1007/s10126-007-9057-6Somchai P, Jitrakorn S, Thitamadee S, Meetam M, Saksmerprome V. Use of microalgae Chlamydomonas reinhardtii for production of double-stranded RNA against shrimp virus. Aquacult Rep 2016; 3(3):178-183. https://doi.org/10.1016/j.aqrep.2016.03.003Alexandre D, Ozório R, Derner R, Fracalossi D, Oliveira G, Richard I, Walter R, Silva CP. Spatial distribution of digestive proteinases in the midgut of the Pacific white shrimp (Litopenaeus vannamei) indicates the existence of endo-ectoperitrophic circulation in Crustacea. Comp Biochem Physiol B 2014; 173(10):90–95. https://doi.org/10.1016/j.cbpb.2014.04.010Magalhães T, Mossolin CE, Mantelatto FL. Gonadosomatic and Hepatosomatic indexes of the freshwater shrimp Macrobrachium olfersii (Decapoda, Palaemonidae) from São Sebastião Island, Southeastern Brazil. Pan-Am J Aquat Sci 2012; 7(1):1-9.Vega-Villasante F, Nolasco H, Civera R. The digestive enzymes of the Pacific brown shrimp Penaeus californiensis. I- Properties of amylase activity in the digestive tract. Comp Biochem Physiol B 1993; 106(6):547-550. https://doi.org/10.1016/0305-0491(93)90130-WVersaw WK, Cuppert SL, Winter DD, Williams LE. An improved colorimetric assay for bacterial lipase in non-fat dry milk. J Food Sci 1989; 54(6):1557-1558. https://doi.org/10.1111/j.1365-2621.1989.tb05159.xMichal G, Schomburg D, editores. Biochemical pathways: an atlas of biochemistry and molecular biology. 2nd ed. New Jersey: John Wiley & Sons; 2012.Hoffman CS, Winston F. A ten- minute DNA preparation from yeast efficiently releases autonomous plasmids for transformation of Escherichia coli. Gene 1987; 57(3):267-272. https://doi.org/10.1016/0378-1119(87)90131-4Rodríguez-Jaramillo C, Hurtado MA, Romero-Vivas E, Ramírez JL, Manzano M, Palacios E. Gonadal development and histochemistry of the tropical oyster, Crassostrea corteziensis (Hertlein, 1951) during an annual reproductive cycle. J Shellfish Res 2008; 27(5):1129–1141. https://doi.org/10.2983/0730-8000-27.5.1129Castex M, Chim L, Pham D, Lemaire P, Wabete N, Nicolas JL, Schmidely P, Mariojouls C. Probiotic P. acidilactici application in shrimp Litopenaeus stylirostris culture subject to vibriosis in New Caledonia. Aquaculture 2008; 275(4):182–193. https://doi.org/10.1016/j.aquaculture.2008.01.011Hernández JC, Murueta JH. Activity of trypsin from Litopenaeus vannamei. Aquaculture 2009; 290(4):190–195. https://doi.org/10.1016/j.aquaculture.2009.02.034Becerra MJ, Martínez PM, Martínez LR, Rivas ME, López JA, Porchas MA. Production response and digestive enzymatic activity of the Pacific white shrimp Litopenaeus vannamei (Boone 1931) intensively pregrown in microbial heterotrophic and autotrophic-based systems. ScientificWorldJournal 2012; 2012(3):1-6. https://doi.org/10.1100/2012/723654Cruz–Suárez LE, Ricque-Marie D, Tapia-Salazar M, Olvera-Novoa MA, Civera-Cerecedo R. (Eds.). Avances en Nutrición Acuícola V. Mérida, Yucatán, México; 2000.Sheng LC, We IZ, De SL, Cong HY. Profile of progesterone and estradiol in hepatopancreas, ovary, and hemolymph of shrimp Penaeus chinensis during reproduction cycle. J Fish China 2012; 25(4):304-310.Molthathong S, Senapin S, Klinbunga S, Puanglarp N, Rojtinnakorn J, Flegel TW. Down-regulation of defender against apoptotic death (DAD1) after yellow head virus (YHV) challenge in black tiger shrimp Penaeus monodon. Fish Shellfish Immunol 2008; 24(2):173-179. https://doi.org/10.1016/j.fsi.2007.10.013Shim MS, Kwon YJ. Efficient and targeted delivery of siRNA in vivo. FEBS J 2010; 277(23):48144827. https://doi.org/10.1111/j.1742-4658.2010.07904.xLamontagne B, Larose S, Boulanger J, Elela S. The RNase III family: A conserved structure and expanding functions in eukaryotic dsRNA metabolism. Curr Issues Mol Biol 2001; 3(4):71-78.Lemos D, Ezquerra JM, Garcia FL. 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Silencing of gonad-inhibiting hormone gene expression in Penaeus monodon by feeding with GIH dsRNA enriched Artemia. Aquaculture 2013; 404(1):116–121. https://doi.org/10.1016/j.aquaculture.2013.04.024https://revistamvz.unicordoba.edu.co/article/download/1024/pdfNúm. 2 , Año 2017 : Revista MVZ Córdoba Volumen 22(2) Mayo-Agosto 201758802586722Revista MVZ CórdobaPublicationOREORE.xmltext/xml2665https://repositorio.unicordoba.edu.co/bitstreams/29e5babb-146a-4b4e-a94f-25cf7ffcdfc6/download1f40fe8678804f5267c3a0cbe510c2a5MD51ucordoba/5839oai:repositorio.unicordoba.edu.co:ucordoba/58392023-10-06 00:46:50.092https://creativecommons.org/licenses/by-nc-sa/4.0/metadata.onlyhttps://repositorio.unicordoba.edu.coRepositorio Universidad de Córdobabdigital@metabiblioteca.com

Digestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannamei

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