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

dc.contributor.authorÁlvarez-Sánchez, Ana Rspa
dc.contributor.authorNolasco-Soria, Héctorspa
dc.contributor.authorMejía-Ruíz, Humbertospa
dc.date.accessioned2017-05-02 00:00:00
dc.date.accessioned2022-07-01T21:00:23Z
dc.date.available2017-05-02 00:00:00
dc.date.available2022-07-01T21:00:23Z
dc.date.issued2017-05-02
dc.format.mimetypeapplication/pdfspa
dc.identifier.doi10.21897/rmvz.1024
dc.identifier.eissn1909-0544
dc.identifier.issn0122-0268
dc.identifier.urihttps://repositorio.unicordoba.edu.co/handle/ucordoba/5839
dc.identifier.urlhttps://doi.org/10.21897/rmvz.1024
dc.language.isospaspa
dc.publisherUniversidad de Córdobaspa
dc.relation.bitstreamhttps://revistamvz.unicordoba.edu.co/article/download/1024/pdf
dc.relation.citationeditionNúm. 2 , Año 2017 : Revista MVZ Córdoba Volumen 22(2) Mayo-Agosto 2017spa
dc.relation.citationendpage5880
dc.relation.citationissue2spa
dc.relation.citationstartpage5867
dc.relation.citationvolume22spa
dc.relation.ispartofjournalRevista MVZ Córdobaspa
dc.relation.referencesTaju 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.12256spa
dc.relation.referencesSudhakaran 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.xspa
dc.relation.referencesRobalino 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.79.21.13561-13571.2005spa
dc.relation.referencesKim 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.2006.10.012spa
dc.relation.referencesXu 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.2006.08.007spa
dc.relation.referencesEscobedo-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.spa
dc.relation.referencesSarathi 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.xspa
dc.relation.referencesLaFauce 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/s13337-012-0084-1spa
dc.relation.referencesPapić 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.spa
dc.relation.referencesAgrawal 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.67.4.657-685.2003spa
dc.relation.referencesPosiri 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.2012.11.033spa
dc.relation.referencesPlant KP, LaPatra SE. Advances in fish vaccine delivery. Dev Comp Immunol 2011; 35(12):1256-1262. https://doi.org/10.1016/j.dci.2011.03.007spa
dc.relation.referencesLinggatong 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.2016.03.018spa
dc.relation.referencesSarathi 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-yspa
dc.relation.referencesSarathi 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/s10126-007-9057-6spa
dc.relation.referencesSomchai 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.2016.03.003spa
dc.relation.referencesAlexandre 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.2014.04.010spa
dc.relation.referencesMagalhães 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.spa
dc.relation.referencesVega-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-Wspa
dc.relation.referencesVersaw 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.xspa
dc.relation.referencesMichal G, Schomburg D, editores. Biochemical pathways: an atlas of biochemistry and molecular biology. 2nd ed. New Jersey: John Wiley & Sons; 2012.spa
dc.relation.referencesHoffman 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)90131-4spa
dc.relation.referencesRodríguez-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/10.2983/0730-8000-27.5.1129spa
dc.relation.referencesCastex 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.2008.01.011spa
dc.relation.referencesHernández JC, Murueta JH. Activity of trypsin from Litopenaeus vannamei. Aquaculture 2009; 290(4):190–195. https://doi.org/10.1016/j.aquaculture.2009.02.034spa
dc.relation.referencesBecerra 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/10.1100/2012/723654spa
dc.relation.referencesCruz–Suárez LE, Ricque-Marie D, Tapia-Salazar M, Olvera-Novoa MA, Civera-Cerecedo R. (Eds.). Avances en Nutrición Acuícola V. Mérida, Yucatán, México; 2000.spa
dc.relation.referencesSheng 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.spa
dc.relation.referencesMolthathong 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.2007.10.013spa
dc.relation.referencesShim 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.xspa
dc.relation.referencesLamontagne 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.spa
dc.relation.referencesLemos 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)00371-3spa
dc.relation.referencesOngvarrasopone 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.2010.06.013spa
dc.relation.referencesVarela 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.spa
dc.relation.referencesSellars 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/dao02343spa
dc.relation.referencesTreerattrakool 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.2013.04.024spa
dc.rights.accessrightsinfo:eu-repo/semantics/openAccessspa
dc.rights.coarhttp://purl.org/coar/access_right/c_abf2spa
dc.rights.urihttps://creativecommons.org/licenses/by-nc-sa/4.0/spa
dc.sourcehttps://revistamvz.unicordoba.edu.co/article/view/1024spa
dc.subjectAquacultureeng
dc.subjectbalanced feedeng
dc.subjectdigestive glandeng
dc.subjectnucleic acidseng
dc.subjectWSSVeng
dc.subjectÁcidos nucleicosspa
dc.subjectacuaculturaspa
dc.subjectalimento balanceadospa
dc.subjectglándula digestivaspa
dc.subjectWSSVspa
dc.titleDigestibilidad in vitro del dsRNA específico por enzimas del tracto digestivo del camarón Litopenaeus vannameispa
dc.title.translatedIn vitro digestibility of specific dsRNA by enzymes of digestive tract of shrimp Litopenaeus vannameieng
dc.typeArtículo de revistaspa
dc.typeJournal articleeng
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dspace.entity.typePublication
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