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dc.rights.licenseAtribución-NoComercial 4.0 Internacional
dc.contributor.advisorAriza Botero, Manuel Fernando
dc.contributor.advisorTibatá Rodríguez, Víctor Manuel
dc.contributor.authorPeña Osorio, Leidy Johana
dc.date.accessioned2024-06-27T14:35:33Z
dc.date.available2024-06-27T14:35:33Z
dc.date.issued2024-01-29
dc.identifier.urihttps://repositorio.unal.edu.co/handle/unal/86311
dc.descriptionilustraciones, graficas, fotografías
dc.description.abstractLa estreptococosis en tilapia (Oreochromis sp.) es una enfermedad causada por Streptococcus agalactiae y se caracteriza por tener un gran impacto económico. Como medidas preventivas se ha descrito la vacunación como la mejor opción, sin embargo, esta patología sigue afectando la piscicultura. Por tal razón, es importante entender los diferentes mecanismos de inmunidad humoral frente a este patógeno; tales como la IgM e IgT. A la fecha no hay reporte de expresión de la recientemente descubierta inmunoglobulina T en caso de estreptococosis, por lo tanto, esta investigación tuvo como objetivo determinar los niveles de expresión de las inmunoglobulinas T y M en diferentes tejidos de tilapia roja frente a infección por Streptococcus agalactiae serotipo Ib. Para el estudio se emplearon un total de 48 juveniles de tilapia, con un peso medio inicial de 90g, los cuales se mantuvieron en la sede del remanso de la UDCA, y se inocularon vía intragástrica, intraperitoneal e inmersión con una cepa obtenida de un brote natural, se tomaron muestras de bazo, branquias, hígado, intestino, piel y riñón craneal a las 24h, 3 y 10 días para hallar los niveles de expresión de las inmunoglobulinas por RT-qPCR y para verificar el desarrollo de la enfermedad se tomaron muestras para histopatología y se confirmaron por qPCR. Los niveles de expresión fueron calculados mediante el método 2−ΔΔCt, a partir de los resultados se concluyó que los niveles globales de IgM e IgT, al infectar a los peces con Streptococcus agalactiae serotipo Ib, ocurrieron principalmente, cuando los peces fueron inoculados por inmersión y por vía intraperitoneal y casi sin respuesta por la vía intragástrica. adicionalmente a nivel de órganos, la expresión de IgM e IgT, se dio principalmente en bazo y branquias, mientras que en los demás órganos evaluados hubo una menor expresión de las dos inmunoglobulinas, especialmente de IgM en los tres primeros días. (Texto tomado de la fuente)
dc.description.abstractStreptococcosis in tilapia (Oreochromis sp.) is a disease caused by Streptococcus agalactiae and is characterized by a great economic impact. As preventive measures, vaccination has been described as the best option, however, this pathology continues to affect the fish farming. For this reason, it is important to understand the different mechanisms of humoral immunity against this pathogen, such as IgM and IgT. To date, there is no report of expression of the recently discovered immunoglobulin T in case of streptococcosis, therefore, this research aimed to determine the expression levels of immunoglobulin T and M in different tissues of red tilapia against infection by Streptococcus agalactiae serotype Ib. For the study, a total of 48 juvenile tilapia, with an average initial weight of 90g, were kept at the el remanso headquarters of the UDCA, and were inoculated via intragastric, intraperitoneal and immersion routes with a strain obtained from a natural outbreak. Samples of spleen, gills, liver, instestine, skin and cephalic kidney were taken at 24h, 3 and 10 days to find the levels of expression of immunoglobulins by RT-qPCR and to verify the development of the disease, samples were taken for histopathology and confirmed by qPCR. The expression levels were calculated by the 2 -ΔΔCT method. From the results it was concluded that global levels of IgM and IgT, when infecting fish with Streptococcus agalactiae serotype Ib, occurred mainly when the fish were inoculated by immersion and intraperitoneally and with almost no response by the intragastric route. Additionally, at the organ level, the expression of IgM and IgT occurred mainly in the spleen and gills, while in the other organs evaluated there was a lower expression of the two immunoglobulins, especially IgM in the first three days.
dc.description.sponsorshipVeterinary Molecular Diagnostics and Research . Laboratorio de diagnóstico molecular
dc.format.extent90 páginas
dc.format.mimetypeapplication/pdf
dc.language.isospa
dc.publisherUniversidad Nacional De Colombia
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/
dc.subject.ddc630 - Agricultura y tecnologías relacionadas::636 - Producción animal
dc.titleDeterminación de los niveles de expresión de los genes de IgT E IgM en diferentes tejidos de tilapia roja (Oreochromis sp) frente a infección por Streptococcus agalactiae serotipo Ib
dc.typeTrabajo de grado - Maestría
dc.type.driverinfo:eu-repo/semantics/masterThesis
dc.type.versioninfo:eu-repo/semantics/acceptedVersion
dc.publisher.programBogotá - Medicina Veterinaria y de Zootecnia - Maestría en Salud y Producción Animal
dc.description.degreelevelMaestría
dc.description.degreenameMagíster en Salud Animal o Magíster en Producción Animal
dc.description.researchareaGenética y mejoramiento animal
dc.identifier.instnameUniversidad Nacional de Colombia
dc.identifier.reponameRepositorio Institucional Universidad Nacional de Colombia
dc.identifier.repourlhttps://repositorio.unal.edu.co/
dc.publisher.facultyFacultad de Medicina Veterinaria y de Zootecnia
dc.publisher.placeBogotá, Colombia
dc.publisher.branchUniversidad Nacional de Colombia - Sede Bogotá
dc.relation.referencesAgnew, W.; Barnes, A.C. (2007). Streptococcus iniae: An aquatic pathogen of global veterinary significance and a challenging candidate for reliable vaccination. Vet. Microbiol 122, 1–15
dc.relation.referencesAkhlaghi, M., Munday, B. L., & Whittington, R. J. (1996). Comparison of passive and active immunization of fish against streptococcosis (enterococcosis). Journal of Fish Diseases, 19(3), 251-258.
dc.relation.referencesAmal MN, Zamri-Saad M, Siti-Zahrah A, Zulkafli AR. (2013) Transmission of Streptococcus agalactiae from a hatchery into a newly established red hybrid tilapia, Oreochromis niloticus (L.) × Oreochromis mossambicus (Peters), farm. J Fish Dis. Aug;36(8):735-9. doi: 10.1111/jfd.12056. Epub 2013 Jan 24. PMID: 23347250.
dc.relation.referencesAustin, B., & Austin, D. (1985). Bacterial pathogens of fish. A review. J. Appl. Bacteriol., 58: 483- 506.
dc.relation.referencesBaya, A.M., Navarro, R.B., and Kotopoulis, E. (1996). Streptococcal infections of hybrid striped bass and tilapia. AES Technical Session 1: Open Papers.
dc.relation.referencesBell, J., (2002). Cellular cytotoxicity: complex killing. Nat. Rev. Immunol. 2 (5), 301
dc.relation.referencesBercovier H, Ghittino C and Eldar A. (1997). Immunization with bacterial antigens: infections with Streptococcus and related organisms. Fish Vaccinology. 90:153-160
dc.relation.referencesBerridge, B. R., Bercovier, H., & Frelier, P. F. (2001). Streptococcus agalactiae and Streptococcus difficile 16S–23S intergenic rDNA: genetic homogeneity and species- specific PCR. Veterinary Microbiology, 78(2), 165-173
dc.relation.referencesBland, F., McIntosh, R., Bain, N., Snow, M., (2012). Development and validation of a range of endogenous controls to support the implementation of practical Taqman realtime PCR- based surveillance for fish diseases within aquaculture. J. Fish Dis. 35, 447–454
dc.relation.referencesBondad-Reantaso M.G., Subasinghe R.P., Arthur J.R., Ogawa K., Chinabut S., Adlard R., Tan Z., Shariff M. (2005).Disease and health management in Asian aquaculture. Vet Parasitol.132:249–272
dc.relation.referencesBoomker, J.; Imes, G.D.Jr.; Cameron, C. M.; Naude, T.W., and Schoonbee, H.J. (1979). Trout mortalities as a result of Streptococcus infection. Onderstepoort J. Vet. Res, 46: 71-77.
dc.relation.referencesBowater, R., Forbes‐ Faulkner, J., Anderson, I., Condon, K., Robinson, B., Kong, F., McPherson, G. (2012). Natural outbreak of Streptococcus agalactiae (GBS) infection in wild giant Queensland grouper, Epinephelus lanceolatus (Bloch), and other wild fish in northern Queensland, Australia. Journal of fish diseases, 35(3), 173-186.
dc.relation.referencesBowden, T., Bricknell,I., Ellis, A.E.(2003) Fish Vaccination, an overview. Industry report IntraFish.5-20
dc.relation.referencesBowser, P., Wooster, G., Getchell, R., & Timmons, M. (1998). Streptococcus iniae infection of tilapia Oreochromis niloticus in a recirculation production facility. Journal of the World Aquaculture Society, 29(3), 335-339.
dc.relation.referencesBragg, R., and Broere, J. (1986). Streptococcosis in rainbow trout in South Africa. Bulletin of the European Association of Fish Pathologists (Denmark).
dc.relation.referencesBraunstein H, Tucker EB, Gibson BC. (1969). Identification and significance of Streptococcus agalactiae (Lancefield group B). Am J Clin Pathol 51:207–213 10.1093/ajcp/51.2.207
dc.relation.referencesBromage, E., Thomas, A., & Owens, L. (1999). Streptococcus iniae, a bacterial infection in barramundi Lates calcarifer. Diseases of Aquatic Organisms, 36(3), 177-181
dc.relation.referencesBullock, G. L. (1981). Streptococcal infections of fishes. United States Department of the Interior, Fish and Wildlife Service, Fish Disease Leaflet 63:1-7.
dc.relation.referencesBustin, S.A. (2002). Quantification of mRNA using real-time reverse transcription PCR (RT- PCR): trends and problems. J. Mol. Endocrinol. 29.
dc.relation.referencesBustin, S.A., Benes, V., Nolan, T., Pfaffl, M.W., 2005. Quantitative real-time RT-PCR—a perspective. J. Mol. Endocrinol. 34, 597–601.
dc.relation.referencesBustin, S. A., Benes, V., Garson, J. A., Hellemans, J., Huggett, J., Kubista, M., & Wittwer, C. T. (2009). The MIQE Guidelines: Minimum Information for Publication of Quantitative Real- Time PCR Experiments.
dc.relation.referencesCaipang CMA, Lucanas JB, Lay-yag CM (2014) Updates on the vaccination against bacterial diseases in tilapia, Oreochromis spp. and Asian seabass, Lates calcarifer. AACL Bioflux 7: 184−193
dc.relation.referencesCastillo, A., C. Sánchez, J. Domínguez, S.L. Kaatari & A.J. Villena. (1993). Ontogeny of IgM and IgM-bearing cells in rainbow trout. Dev. Comp. Immunol. 17: 419-424.
dc.relation.referencesCastro, C.D., & Flajnik, M.F. (2014). Putting J Chain Back on the Map: How Might Its Expression Define Plasma Cell Development?. The Journal of Immunology, 193, 3248 - 3255.
dc.relation.referencesCeschia, G.; Giorgetti, G.; Giavenni, R., & Sarti, M. (1992). A new problem for italian trout farms: Streptococcosis in rainbow trout (Oncorhynchus mykiis). Bull. Eur. Assoc. Fish Pathol., 2: 71-72.
dc.relation.referencesChang, P., & Plumb, J. (1996). Histopathology of experimental Streptococcus sp. infection in tilapia, Oreochromis niloticus (L.), and channel catfish, Ictalurus punctatus (Ratinesque). Journal of fish diseases, 19(3), 235-241.
dc.relation.referencesChen, S.L., Li, W., Meng, L., Sha, Z.X., Wang, Z.J., Ren, G.C.(2007). Molecular cloning and expression analysis of a hepcidin antimicrobial peptide gene from turbot (Scophthalmus maximus). Fish Shellfish Immunol. 22, 172–181
dc.relation.referencesChen, M., Li, L. P., Wang, R., Liang, W. W., Huang, Y., Li, J. & Gan, X. (2012). PCR detection and PFGE genotype analyses of streptococcal clinical isolates from tilapia in China. Veterinary microbiology, 159(3-4), 526-530.
dc.relation.referencesChistiakov, D. A., Bobryshev, Y. V., Kozarov, E., Sobenin, I. A., & Orekhov, A. N. (2015). Intestinal mucosal tolerance and impact of gut microbiota to mucosal tolerance. Frontiers in microbiology, 5, 781.
dc.relation.referencesDe Alba Aguayo, David R., & Rueda, Angelica. (2013). Problema bioquímico: Determinación del ciclo umbral y la eficiencia para la PCR cuantitativa en tiempo real. REB. Revista de educación bioquímica, 32(1), 36-39.
dc.relation.referencesDe La Rosa M, D. C. M. (2004). Streptococcus agalactiae. Control Calidad SEIMC.
dc.relation.referencesDelannoy, C.M., Crumlish, M., Fontaine., M.C., Pollock, J., Foster, G., Dagleish, M. P., Zadoks, R.N. (2013). Human Streptococcus agalactiae strains in aquatic mammals and fish. BMC microbiology 13(1), 1
dc.relation.referencesDeloffre, L. A., Andrade, A., Filipe, A. I., & Canario, A. V. (2012). Reference genes to quantify gene expression during oogenesis in a teleost fish. Gene, 506(1), 69-75.
dc.relation.referencesDomeénech, A., Derenaáandez‐ Garayzábal, J., Pascual, C., Garcia, J., Cutuli, M., Moreno, M., Dominguez, L. (1996). Streptococcosis in cultured turbot, Scopthalmus maximus (L.), associated with Streptococcus parauberis. Journal of fish diseases, 19(1), 33-38
dc.relation.referencesDu, Y., Tang, X., Zhan, W., Xing, J., & Sheng, X. (2016). Immunoglobulin tau heavy chain (IgT) in flounder, Paralichthys olivaceus: Molecular cloning, characterization, and expression analyses. International journal of molecular sciences, 17(9), 1571.
dc.relation.referencesDuarte R.S., Miranda O., Bellei B.c., Brito V. And Teixeira L.M. (2004). Phenotypic and molecular characteristics of Streptococcus agalactiae isolates recovered from milk of dairy cows in Brazil. J. Clin. Microbiol. 42: 4214-4222.
dc.relation.referencesDuremdez, R., Al‐ Marzouk, A., Qasem, J., Al‐ Harbi, A., & Gharabally, H. (2004). Isolation of Streptococcus agalactiae from cultured silver pomfret, Pampus argenteus (Euphrasen), in Kuwait. Journal of fish diseases, 27(5), 307-310
dc.relation.referencesEldar, A., Bejerano, Y. and Bercovier, H. (1994). Streptococcus shiloi and Streptococcus difficile: two new streptococcal species causing a meningoencephalitis in fish. Current Microbiology 28:139-143.
dc.relation.referencesEldar, A., Bejerano, Y., Livoff, A., Horovitcz, A., & Bercovier, H. (1995). Experimental streptococcal meningo-encephalitis in cultured fish. Veterinary Microbiology, 43(1), 33-40.
dc.relation.referencesEldar, A., and Guittino, C. (1999).Lactococcus garviae and Streptococcus iniae infections in rainbow trout Oncorhychus mykiis: similar, but different diseases. Dis. Aquat. Org., 36: 227-231.
dc.relation.referencesEvans, J.J., Shoemaker, C.A., & Klesius, P.H. (2000), Experimental Streptococcus iniae infection of hybrid striped bass (Morone chrysops x Morone saxatilis) and tilapia (Oreochromis niloticus) by nares inoculation. Aquaculture,189, 197-210.
dc.relation.referencesEvans, J.J., Klesius, P.H., Gilbert, P.M., Shoemaker, C.A., Sarawi, M.A., Landsberg, J., Duremdez, R., Marzouk, A. Al. and Zenki, S. Al. (2002). Characterization of β-haemolytic group B Streptococcus agalactiae in cultured seabream, Sparus auratus L., and wild mullet, Liza klunzingeri (Day), in Kuwait. Journal fish diseases 25:505-513
dc.relation.referencesFerguson, H. W. (1989). Systemic Pathology of Fish. En A text and atlas of comparative tissue responses in diseases of Teleosts. Iowa State University Press. Pags.: 64- 103
dc.relation.referencesFilby, A. L., & Tyler, C. R. (2007). Appropriate'housekeeping'genes for use in expression profiling the effects of environmental estrogens in fish. BMC molecular biology, 8(1), 1-13.
dc.relation.referencesFry, R.M. (1938). Fatal Infections by Haemolytic Streptococcus Group B. Lancet 1:199–201 10.1016/S0140-6736(00)93202-1
dc.relation.referencesFu, Y., Li, S., Wu, Y. y Chang, Y. (2007). Identification and expression analysis of hepcidinlike cDNAs from pigeon (Columba livia). Mol Cell Biochem. 305: 191–197
dc.relation.referencesFurfaro, L. L., Chang, B. J., & Payne, M. S. (2017). A novel one-step real-time multiplex PCR assay to detect Streptococcus agalactiae presence and serotypes Ia, Ib, and III. Diagnostic Microbiology and Infectious Disease, 89(1), 7-12.
dc.relation.referencesGambón, F.; Sánchez, C.; Magadan, S. (2010). Presence of an unique IgT on the IGH locus in three-spined stickleback fish (Gasterosteus aculeatus) and the very recent generation of a repertoire of VH genes. Dev. Comp. Immunol. 34, 114–122.
dc.relation.referencesGao, Y., Yi, Y., Wu, H., Wang, Q., Qu, J., Zhang, Y. (2014). Molecular cloning and characterization of secretory and membrane-bound IgM of turbot. Fish Shellfish Immunol. 40, 354–361.
dc.relation.referencesGeven, E., Klaren, P. (2017). The teleost head kidney: Integrating thyroid and immune signalling,Developmental & Comparative Immunology, Volume 66, Pages 73-83,ISSN 0145-305X .https://doi.org/10.1016/j.dci.2016.06.025
dc.relation.referencesGibson, R.L., Nizet, V., Rubens, C.E. (1999). Group B streptococcal beta-hemolysin promotes injury of lung microvascular endothelial cells. Pediatric Research 45:626–634
dc.relation.referencesGraves, S.S., D. Evans & D.L. Dawe. (1985). Antiprotozoan activity of nonspecific cytotoxic cells from the channel catfish. J. Immunol. 13:478-85.
dc.relation.referencesGreenlee, A.R., R.A. Brown & S.S. Ristow. 1991. Nonspecific cytotoxic cells of rainbow trout (Oncorhynchus mykiss) kill YAC-1 targets by both necrotic and apoptotic mechanisms. Dev. Comp. Immunol. 15:153-164.
dc.relation.referencesHardie, J. (1986). Genus Streptococcus Rosenbach. In: Sneath, P.; Mair, N.; Sharpe, M., and Holt, J. (eds). Bergey’s manual of systematic bacteriology. Vol. 2. Williams and Wilkins Co., Baltimore, p 1043-1047
dc.relation.referencesHeid, C. A., Stevens, J., Livak, K. J., and Williams, P. M. (1996).Genome Res. 6, 986–994.
dc.relation.referencesHernández EA. 2005. Caracterización epidemiológica, microbiológica e inmunohistoquímica de la Streptococosis en tilapias (Oreochromis sp.) en un brote natural de la enfermedad. Tesis de grado Médico Veterinario. Facultad de Medicina Veterinaria y Zootecnia, Universidad Nacional de Colombia, Bogotá.
dc.relation.referencesHernández, E., Figueroa, J., & Iregui, C. (2009). Streptococcosis on a red tilapia, Oreochromis sp., farm: a case study. Journal of fish diseases, 32(3), 247-252.
dc.relation.referencesHernández, A., Martin Vasallo, P., Torres Ramírez, A., & Salido, E. (1994) RNA analysis: The study of genic expression. NEFROLOGIA 14: 145-162
dc.relation.referencesHoshina T., Sano T. and Morimoto T. 1958. A Streptococcus pathogenic to fish. Journal Tokyo University Fish 44: 57-68
dc.relation.referencesICA. Protección sanitaria de los peces acuícolas. Instituto Colombiano de Agricultura. Recuperado 2 de octubre del 2022 de https://www.ica.gov.co
dc.relation.referencesICA. (2023). Resolución 6535 de 2023. “Por la cual se declara el Estado de Emergencia Sanitaria en el territorio nacional por la presencia de Streptococcus Agalactiae ST7 serotipo Ia”. https://www.ica.gov.co/getattachment/7e70025e-4aac-4a21-8ab0- 2be6dcaa48b6/2023R00006535.aspx
dc.relation.referencesIregui, C., Barato, P., Rey, A., Vasquez, G., and Verjan, N. (2013). Epidemiology of Streptococcus agalactiae and Streptococcosis in Tilapia Fish.
dc.relation.referencesIregui, C., Comas, J., Vásquez, G., & Verján, N. (2016). Experimental early pathogenesis of Streptococcus agalactiae infection in red tilapia Oreochromis spp. Journal of fish diseases, 39(2), 205-215
dc.relation.referencesJiménez, A., Rey, A., Penagos, L., Ariza, M., Figueroa, J., and Iregui, C. (2007). Estado actual de la estreptococosis en tilapias cultivadas en Colombia. Revista Medicina Veterinaria Zootecnia 54, 120-123.
dc.relation.referencesJiménez, A.P. (2010). Detección de Streptococcus agalactiae por PCR en Tejidos de Tilapias rojas (Oreochromis spp.) menores de 20g. Universidad Nacional de Colombia.
dc.relation.referencesJones, H., Everley and Howells, C.H.L. (1968) Neonatal meningitis due to Streptococcus agalactiae. Postgraduate Medical Journal, 44, 549
dc.relation.referencesKillie, J.E., S. Espelid & T. Jorgessen. (1991). The humoral response in atlantic salmon (Salmo salar L.) against the hapten carrier NIP-KLH; the effect of determinant (NIP) density and the isotype profile of anti-NIP antibodies. Fish Shellfish Immunol. 1:33-46.
dc.relation.referencesKim MS, Choi SH, Lee EH, Nam YK, Kim SK, Kim KH. (2007). α-enolase, a plasmin(ogen) binding protein and cell wall associating protein from a fish pathogenic Streptococcus iniae strain. Aquaculture. 265: 55-60.
dc.relation.referencesKitao, T. 1993. Streptococcal infections. In: Inglis, V.; Roberts, R., and Bromage, N. (eds) Bacterial diseases of fish. Blackwell, Oxford, p 196-210.
dc.relation.referencesKlesius, P., Evans, J., Shoemaker, C., Yeh, H., Goodwin, A., Adams, A., & Thompson, K. (2006). Rapid detection and identification of Streptococcus iniae using a monoclonal antibody-based indirect fluorescent antibody technique. Aquaculture 258(1), 180-186.
dc.relation.referencesKnudsen CR, Clark BFC, Degn B, Wiborg O. One-step purification of E. coli elongation factor. Tu Biochem Int. 1992;28:352–362
dc.relation.referencesKoumans-van Diepen, J.C.E., M.H.M. van de Lisdonk, A.J.L. Taverne-Thiele, B.M. Verburg- van Kemenade & J.H.W.M. Rombout. (1994). Characterization of immunoglobulin-binding leucocytes in carp (Cyprinus carpio L.) Dev. Comp. Immunol. 18:45-56.
dc.relation.referencesKvitt, H., and Colorni, A. (2004). Strain variation and geographic endemism in Streptococcus iniae. Diseases of Aquatic Organisms 61:67-73
dc.relation.referencesLancefield,R.C. (1933). A Serological Differentiation of Human and Other Groups of Hemolytic Streptococci. J Exp Med 57:571–595 10.1084/jem.57.4.571.
dc.relation.referencesLancefield RC, Hare R. (1935). The Serological Differentiation of Pathogenic and Non- Pathogenic Strains of Hemolytic Streptococci from Parturient Women. J Exp Med 61:335– 349 10.1084/jem.61.3.335
dc.relation.referencesLee, J., Kim, Y. H., Kim, K., Kim, D., Lee, S. H., & Kim, S. (2022). Selection of stable reference genes for quantitative real‐time PCR in the Varroa mite, Varroa destructor. Archives of Insect Biochemistry and Physiology, 110(3), e21905.
dc.relation.referencesLindahl, G., Stålhammar-Carlemalm, M., & Areschoug, T. (2005). Surface proteins of Streptococcus agalactiae and related proteins in other bacterial pathogens. Clinical microbiology reviews, 18(1), 102-127.
dc.relation.referencesLopardo Horacio A, Predari Silvia C, Vay Carlos. (2018). Manual de Microbiología de la Asociación Argentina de Microbiología. Asociación Argentina de Microbiología. 300pp
dc.relation.referencesMaekawa, S.; Wang, Y.-T.; Yoshida, T.; Wang, P.C.; Chen, S.-C. (2020) Group C Streptococcus dysgalactiae infection in fish. J. Fish Dis. 43, 963–970
dc.relation.referencesMannik M, Baringer JR, Stokes J III. (1962). Infections due to group B beta-hemolytic streptococci. Report of three cases and review of the literature. N Engl J Med 266:910– 913 10.1056/NEJM196205032661803
dc.relation.referencesMarchalonis, J., & Edelman, G. M. (1966). Polypeptide chains of immunoglobulins from the smooth dogfish (Mustelus canis). Science, 154(3756), 1567-1568.
dc.relation.referencesMata A.I., Gibello A., Casamayor A., Blanco M., Domínguez L. and Garayzábal F. (2004). Multiplex PCR assay for detection of bacterial pathogens associated with warm-water streptococcosis in fish. App. Environ. Microbiol. 70: 3183-3187.
dc.relation.referencesMatejusova, I., McKay, P., McBeath, A. J., Collet, B., & Snow, M. (2008). Development of a sensitive and controlled real-time RT-PCR assay for viral haemorrhagic septicaemia virus (VHSV) in marine salmonid aquaculture. Diseases of Aquatic Organisms, 80(2), 137-144.
dc.relation.referencesMcPherson, M. J., Hames, B. D., & Taylor, G. R. (2008). PCR a Practical aproach. First Editon edn. Oxford University Press Oxford. https://www.redalyc.org/pdf/636/63617114013.pdf
dc.relation.referencesMian, G., Godoy, D., Leal, C., Yuhara, T., Costa, G., and Figueiredo, H. (2009). Aspects of the natural history and virulence of S. agalactiae infection in Nile tilapia. Veterinary Microbiology, 136(1), 180-183.
dc.relation.referencesMichel, C.; Nougayrède, P.; Eldar, A.; Sochon, E., and Kinkelin, de P. (1997).Vagococcus salmoninarum, a bacterium of pathological significance in rainbow trout Oncrhynchus mykiss farming. Dis. Aquat. Org., 30: 199-208.
dc.relation.referencesMiller, N.W., R.C. Sizemore & L.W.Clem. (1985). Phylogeny of lymphocyte heterogeneity: the cellular requirements for in vitro antibody responses of channel catfish leukocytes. J. Immunol. 134:2884-2888.
dc.relation.referencesMirete-Bachiller, S., Olivieri, D. N., & Gambón-Deza, F. (2021). Immunoglobulin t genes in actinopterygii. Fish & Shellfish Immunology, 108, 86–93.
dc.relation.referencesMuzquiz, J.L., Royo, F.M., Ortega, C., De Blas, I., Ruiz, I., and Alonso, J.L. (1999). Pathogenicity of streptococcosis in rainbow trout (Oncorhynchus mykiss): dependence on age of diseased fish. Bulletin-European Association Of Fish Pathologists, 19, 114-119.
dc.relation.referencesNakanishi T, Ototake M. (1997). Antigen uptake and immune responses after immersion vaccination. Dev Biol Stand; 90:59–68
dc.relation.referencesNegrutskii BS, El’skaya AV (1998) Eukaryotic translation elongationfactor 1 alpha: structure, expression, functions, and possible role inaminoacyl-tRNA channeling. Prog Nucl Acid Res Mol Biol 60:47–78
dc.relation.referencesNguyen HT, Kanai K y Yoshikoshi K. (2002). Ecological investigation of Streptococcus iniae in cultured Japanese flounder (Paralichthys olivaceus) using selective isolation procedures. Aquaculture. 205: 7-17.
dc.relation.referencesNieto, J., Devesa, S., Quiroga, I., and Toranzo, A. (1995). Pathology of Enterococcus sp. infection in farmed turbot, Scophthalmus maximus L. Journal of fish diseases, 18(1), 21- 30.
dc.relation.referencesNobbs, A.H., Lamont, R.J., and Jenkinson, H.F. (2009). Streptococcus adherence and colonization. Microbiology and Molecular Biology Reviews, 73(3), 407-450
dc.relation.referencesNoga E.J., Silphaduang, U.(2001) Peptide antibiotics in mast cells of fish. Nature; 414:268- 269
dc.relation.referencesNoraini O, Sabri MY, Siti-Zahrah A (2013) Efficacy of spray administration of formalin-killed Streptococcus agalactiae in hybrid red tilapia. J Aquat Anim Health 25: 142−148
dc.relation.referencesNordmo, R., Ramstad, A. (1997). Comparison of different challenge methods to evaluate the efficacy of furunculosis vaccines in Atlantic salmon, Salmo salar L. J. Fish Dis.; 20: 119– 126.
dc.relation.referencesOhlander, C., Perlmann, H., Perlmann, P., (2010). Regulation of IgG-IgM interplay by antibody specificity in human K-cell-mediated cytotoxicity. Scand. J. Immunol. 15 (4), 409–417
dc.relation.referencesOhnishi, K & Jo, Y. (1981). Studies on streptococcal infection in pond-cultured fishes-I. Characteristics of a beta-hemolytic streptococcus isolated from cultured ayu and amago in 1977-1978. Fish Pathology. 16: 63-67.
dc.relation.referencesOlabuenaga, S.E. (2000). Sistema inmune en peces. Gayana (Concepción), 64(2), 205-215. https://dx.doi.org/10.4067/S0717-65382000000200010
dc.relation.referencesParedes, A., Wong, P., and Yow, M.D. (1976). Failure of penicillin to eradicate the carrier state of group B streptococcus in infants. Journal of Pediatrics 89, 191.
dc.relation.referencesParra, D., Takizawa, F., Sunyer, J.O., 2013. Evolution of B cell immunity. Annu. Rev. Anim.Biosci. 1 (1), 65–97
dc.relation.referencesPenagos, G., Barato, P., & Iregui, C. (2009). Sistema inmune y vacunación de peces. Acta Biológica Colombiana, 14(1), 3-24.
dc.relation.referencesPerera, R.P., Johnson, S.K., Collins, M.D., and Lewis, D.H. (1994). Streptococcus iniae associated with mortality of Tilapia nilotica x T. aurea hybrids. Journal of Aquatic Animal Health, 6(4), 335-340
dc.relation.referencesPerera, R.P., Johnson, S.K., and Lewis, D.H. (1997). Epizootiological aspects of Streptococcus iniae affecting tilapia in Texas. Aquaculture, 152 (1), 25-33.
dc.relation.referencesPlumb, J., Schachte, J., Gaines, J., Peltier, W., & Carroll, B. (1974). Streptococcus sp. from marine fishes along the Alabama and northwest Florida coast of the Gulf of Mexico. Transactions of the American Fisheries Society, 103(2), 358-361
dc.relation.referencesPoppert S., Nickel D., Berger A., Yildiz T., Kaestner N.,Mauerer S. and Spellerberg B. (2009). Rapid identification of beta-hemolytic streptococci by fluorescence in situ hybridization (FISH). Internat. J. of Medical Micro. 299: 421–426.
dc.relation.referencesPradeep, P. J., Suebsing, R., Sirthammajak, S., Kampeera, J., Jitrakorn, S., Saksmerprome, V., ... & Withyachumanarnkul, B. (2016). Evidence of vertical transmission and tissue tropism of Streptococcosis from naturally infected red tilapia (Oreochromis spp.). Aquaculture Reports, 3, 58-66.
dc.relation.referencesPreado J., Valeria. (2001). Conceptos microbiológicos de Streptococcus pneumoniae: Basic microbiological aspects. Revista chilena de infectología, 18(Supl. 1), 6-9. https://dx.doi.org/10.4067/S0716-10182001000000002
dc.relation.referencesPretto-Giordano LG, Muller EE, Klesius P, da Silva VG (2010) Efficacy of an experimentally inactivated Streptococcus agalactiae vaccine in Nile tilapia (Oreochromis niloticus) reared in Brazil. Aquacult Res 41: 1539−1544
dc.relation.referencesPridgeon, J. W., & Zhang, D. (2014). Complete genome sequence of a virulent Streptococcus agalactiae strain, 138P, isolated from diseased Nile Tilapia. Genome announcements, 2(2), e00295-00214.
dc.relation.referencesPrieta, J., Doménech, A., Fernández-Garayzábal, J., Collins, M., Rodrıguez, U., Jones, D., Domınguez, L. (1993). Lactococcosis de la trucha arco iris. Medicina Veterinaria 10, 367- 373.
dc.relation.referencesPulido, A., Figueroa, J., and Castro, C.A. (1999). Reporte de streptococcosis en tilapias cultivadas en Colombia.
dc.relation.referencesPulido, A., Figueroa, J., and Castro, C.A. (1999). Reporte de streptococcosis en tilapias cultivadas en Colombia.
dc.relation.referencesPulido, A. (2000). Evaluación clínica y fisiopatológica de un caso de streptoccocosis en la explotación de tilapia roja en la Represa de Hidroprado, Tolima. Tesis, Universidad Nacional de Colombia, Facultad. Medicina Veterinaria Zootecnia, Ibague.
dc.relation.referencesPulido, E., Iregui, C., Figueroa, J., and Klesius, P. (2004). Estreptococosis en tilapias (Oreochromis spp.) cultivadas en Colombia. Revista AquaTIC, 20, 97-106
dc.relation.referencesQuinn, P.J.,Markey,B.K.,Leonard, F.C.,Fitzpatrick,E.S.,Fanning,S.(2016).Elementos de microbiología veterinaria. 2da edición. Ed. Willey- Blackwell. ISBN:9788420011868
dc.relation.referencesR Core Team. (2021). R: A language and environment for statistical computing. R Foundation for Statistical Computing, Vienna, Austria.URL https://www.R-project.org/.
dc.relation.referencesRahl, P. B., & Young, R. A. (2014). MYC and transcription elongation. Cold Spring Harbor perspectives in medicine, 4(1), a020990.
dc.relation.referencesRasheed, V. M. 1983 Streptococcus sp. infection in bullminnows (Fundulus grandis). PhD. dissertation. Department of Fisheries and Allied Aquacultures, Auburn University, Auburn, Alabama. 71 pp
dc.relation.referencesRobinson, J.A. & Meyer, F.P. (1966). Streptococcal fish pathogen. Journal of bacteriology. 92: 512
dc.relation.referencesRomalde J, Malgariños B, Nuñez S, Barja J and Toranzo A. (1996). Host range susceptibility of Enterococcus sp. strains isolated from diseased turbot: possible routes of infection. Appl. Environ. Microbiol., 62: 607-611.
dc.relation.referencesRubio-Godoy, M., 2010. Teleost fish immunology. Review. Revista Mexicana de Ciencias Pecuarias 1, 47-57
dc.relation.referencesRuiz,I., Fernández, A.B., De Blas, I (2003). El sistema inmune de los teleósteos (III): Respuesta inmune específica. Revista AquaTIC. 18:33-38.
dc.relation.referencesRusso, R., Mitchell, H., & Yanong, R. P. E. (2006). Characterization of Streptococcus iniae isolated from ornamental cyprinid fishes. Aquaculture 256, 105-10.
dc.relation.referencesSalinas, I.; Zhang, Y.A.; Sunyer, J.O. (2011). Mucosal immunoglobulins and B cells of teleost fish. Dev. Comp. Immunol. 35, 1346–1365.
dc.relation.referencesSalvador R, Muller EE, Freitas JC, Leonhadt JH, Pretto-Giordano LG, Dias JA. (2005). Isolation and characterization of Streptoccocus spp. group B in Nile tilapias (Oreochromis niloticus) reared in hapas nets and earth nurseries in the northern region of Parana State, Brazil. Ciencia Rural 35(6):1374–1378.
dc.relation.referencesSavan, R.; Aman, A.; Sato, K.; Yamaguchi, R.; Sakai, M. (2005). Discovery of a new class of immunoglobulin heavy chain from fugu. Eur. J. Immunol. 35, 3320–3331
dc.relation.referencesSchauf, V., Deveikis, A., Riff, L., Serota, A. (1976). Antibiotic-killing kinetics of group B streptococci. Journal of Pediatrics 89(2):194–198.
dc.relation.referencesShi, J. y Camus, A. C. (2006). Hepcidins in amphibians and fishes: Antimicrobial peptides or iron-regulatory hormones?. Developmental and Comparative Immunology. 30: 746-755.
dc.relation.referencesShoemaker, C., and Klesius, P. (1997). Streptococcal disease problems and control a review. Fitzsimmons, K.
dc.relation.referencesShoemaker, C.A., Evans, J.J., Klesius, P.H., 2000. Density and dose: factors affecting mortality of Streptococcus iniae infected tilapia (Oreochromis niloticus). Aquaculture 188: 229–235.
dc.relation.referencesSpellerberg, B., Rozdzinski, E., Martin, S., Weber-Heynemann, J., Schnitzler, N., Lütticken, R., and Podbielski, A. (1999). Lmb, a protein with similarities to the LraI adhesin family, mediates attachment of Streptococcus agalactiae to human laminin. Infection and immunity, 67(2), 871-878.
dc.relation.referencesStoffregen, D.A.; Backman, S.C.; Perham, R.E.; Bowser, P.R., and Babish, J.G. (1996). Initial disease report of Streptococcus iniae infection in hybrid striped (sunshine) bass and successful therapeutic intervention with the fluoroquinolone antibacterial enrofloxacin. J. World Aqua. Soc., 4: 420-434.
dc.relation.referencesSu, Y., Wang, B., Zhang, Y., Ruan, Z., Bai, H., Wan, J.& Geng, H. (2019). Mass spectrometric determination of disulfide bonds and free cysteine in grass carp IgM isoforms. Fish & shellfish immunology, 95, 287-296.
dc.relation.referencesSwain P, Dash S, Bal J, Routray P, Sahoo PK, Sahoo SK, et al. (2006). Passive transfer of maternal antibodies and their existence in eggs, larvae and fry of Indian major carp, Labeo rohita (Ham.). Fish Shellfish Immunol; 20:519–527
dc.relation.referencesTamay de Dios, L., Ibarra, C., & Velasquillo, C. (2013). Fundamentos de la reacción en cadena de la polimerasa (PCR) y de la PCR en tiempo real. Investigación en discapacidad, 2(2), 70-78.
dc.relation.referencesTeruo Miyazaki, Saburoh S. Kubota, Noboru Kaige & Toshio Miyashita. Histopathological Study of Streptococcal Disease in Tilapia. Fish Pathology 19(3), 167-172,1984.12
dc.relation.referencesTizard, I. 2001. The phylogeny of the immune system. In:Veterinary Immunology an introduction. W.B. Saunders Company (Ed.). Harcourt Brace Jovanovich, Inc. USA
dc.relation.referencesToranzo, A., Devesa, S., Heinen, P., Riaza, A., Nunez, S., & Barja, J. (1994). Streptococcosis in cultured turbot caused by an Enterococcus-like bacterium. Bulletin of the European Association of Fish Pathologists, 14(1), 19-23
dc.relation.referencesToso, P. W., Diestro, A. D., de la Guarda, R. G., Vallejos, E. C., Herrera, A. M., de Amat Herbozo, C., Álvarez, J. M. (2013). Actividad del Complemento y de la Lisozima Sérica en juveniles de Oncorhynchus mykiss inmunizados con fracciones de membrana externa de una cepa nativa de Flavobacterium psychrophilum. REDVET. Revista Electrónica de Veterinaria, 14(1), 1-10
dc.relation.referencesUtke, K., Bergmann, S., Lorenzen, N., Kollner, B., Ototake, M., y Fischer, U. (2007). Cell- mediated cytotoxicity in rainbow trout, Oncorhynchus mykiss, infected with viral haemorrhagic septicaemia virus. Fish and Shellfish Immunology. 22: 182-196
dc.relation.referencesValasek, M. A., & Repa, J. J. (2005). The power of real-time PCR. Advances in physiology education, 29(3), 151-159.
dc.relation.referencesVásquez, G. M. (2019). Caracterización morfológica de la adherencia e invasión de Streptococcus agalactiae a la mucosa intestinal de la tilapia Oreochromis sp., modelo in vitro. Universidad Nacional de Colombia.
dc.relation.referencesVelázquez, J., Acosta, J., Lugo, J. M., Reyes, E., Herrera, F., González, O., Estrada, M. P. (2018). Discovery of immunoglobulin T in Nile tilapia (Oreochromis niloticus): A potential molecular marker to understand mucosal immunity in this species.Developmental and Comparative Immunology, 88(March), 124–136.https://doi.org/10.1016/j.dci.2018.07.013
dc.relation.referencesVendrell, D., Balcázar, J. L., Ruiz-Zarzuela, I., De Blas, I., Gironés, O., & Múzquiz, J. L. (2006). Lactococcus garvieae in fish: a review. Comparative immunology, microbiology and infectious diseases, 29(4), 177-198
dc.relation.referencesWang, E., Wang, K., Chen, D., Wang, J., He, Y., Long, B., ... & Lai, W. (2015). Evaluation and selection of appropriate reference genes for real-time quantitative PCR analysis of gene expression in Nile tilapia (Oreochromis niloticus) during vaccination and infection. International journal of molecular sciences, 16(5), 9998-10015.
dc.relation.referencesWeijland, A., Harmark, K., Cool, R. H., Anborgh, P. H. & Parmeggiani, A. (1992). Elongation factor Tu: a molecular switch in protein biosynthesis. Mol Microbiol 6, 683–688
dc.relation.referencesWilkinson, H.W. (1978). Group B streptococcal infection in humans. Annual Review of Microbiology.1978;32:41–57
dc.relation.referencesXu, Z.; Parra, D.; Gomez, D.; Salinas, I.; Zhang, Y.A.; Von Gersdorff Jorgensen, L.; Heinecke, R.D.; Buchmann, K.; LaPatra, S.; Sunyer, J.O. (2013).Teleost skin, an ancient mucosal surface that elicits gut-like immune responses. Proc. Natl. Acad. Sci. USA, 110, 13097– 13102
dc.relation.referencesYang W. & Li A. (2009). Isolation and characterization of Streptococcus dysgalactiae from diseased Acipenser schrenckii. Aquaculture 294: 14–17.
dc.relation.referencesYang, C. G., Wang, X. L., Tian, J., Liu, W., Wu, F., Jiang, M., & Wen, H. (2013). Evaluation of reference genes for quantitative real-time RT-PCR analysis of gene expression in Nile tilapia (Oreochromis niloticus). Gene, 527(1), 183-192.
dc.relation.referencesYanong RP, Francis-Floyd R. (2002). Gainesville, FL: IFAS, University of Florida Streptococcal infections of fish. Florida Cooperative Extension Service; pp. 1–5.
dc.relation.referencesYe, JM; Bromage, ES; and Kaattari, SL, The Strength of B Cell Interaction with Antigen Determines the Degree of IgM Polymerization (2010). Journal Of Immunology, 184(2), 844-850.
dc.relation.referencesYin, X., Mu, L., Fu, S., Wu, L., Han, K., Wu, H., ... & Ye, J. (2019). Expression and characterization of Nile tilapia (Oreochromis niloticus) secretory and membrane-bound IgM in response to bacterial infection. Aquaculture, 508, 214-222.
dc.relation.referencesYoshida, T.; Yamada, Y.; Sakai, M.; Inglis, V.; Xie, X.J.; Chen, S.-C., and Kruger, R. (1996). Association of the cell capsule with anti-opsonophagocytosis in β-hemolytic Streptococcus spp. isolated from rainbow trout. J. Aquat. Anim. Health, 8: 223-228.
dc.relation.referencesYuasa, K.; Kitancharoen, N.; Kataoka, Y., and Al-Murbaty, F. (1999). Streptococcus iniae, the causative agent of mass mortality in rabbitfish Siganus canaliculatus in Bahrain. J. Aquat. Anim. Health, 87-93
dc.relation.referencesZamri-Saad M, Amal MNA, Siti-Zahrah A. (2022) Pathological changes in red tilapias (Oreochromis spp.) naturally infected by Streptococcus agalactiae. J Comp Pathol 2010; 143:227–229. Available at: https://pubmed.ncbi.nlm.nih.gov/20334871/.
dc.relation.referencesZhang, Y.-A., Salinas, I., Li, J., Parra, D., Bjork, S., Xu, Z., LaPatra, S. E., Bartholomew, J., & Sunyer, J. O. (2010). Igt, a primitive immunoglobulin class specialized in mucosal immunity. Nature immunology, 11, 827–835.
dc.relation.referencesZheng, W. J., & Sun, L. (2011). Evaluation of housekeeping genes as references for quantitative real time RT-PCR analysis of gene expression in Japanese flounder (Paralichthys olivaceus). Fish & shellfish immunology, 30(2), 638-645.
dc.relation.referencesZhang, R., Zhang, L. L., Ye, X., Tian, Y. Y., Sun, C. F., Lu, M. X., & Bai, J. J. (2013). Transcriptome profiling and digital gene expression analysis of Nile tilapia (Oreochromis niloticus) infected by Streptococcus agalactiae. Molecular biology reports, 40, 5657-56
dc.rights.accessrightsinfo:eu-repo/semantics/openAccess
dc.subject.agrovocStreptococcus agalactiae
dc.subject.agrovocInmunidad humoral
dc.subject.agrovochumoral immunity
dc.subject.agrovocOreochromis
dc.subject.proposalStreptococcus agalactiae
dc.subject.proposalTilapia
dc.subject.proposalInmunoglobulinas
dc.subject.proposalImmunoglobulins
dc.title.translatedDetermination of the levels of expression of IgT and IgM genes in different tissues of red tilapia (Oreochromis sp) in the view of infection by Streptococcus agalactiae serotype Ib
dc.type.coarhttp://purl.org/coar/resource_type/c_bdcc
dc.type.coarversionhttp://purl.org/coar/version/c_ab4af688f83e57aa
dc.type.contentText
dc.type.redcolhttp://purl.org/redcol/resource_type/TM
oaire.accessrightshttp://purl.org/coar/access_right/c_abf2
oaire.fundernameVM Laboratories
dcterms.audience.professionaldevelopmentEstudiantes
dcterms.audience.professionaldevelopmentInvestigadores
dcterms.audience.professionaldevelopmentMaestros
dcterms.audience.professionaldevelopmentPúblico general
dc.contributor.orcidPeña Osorio, Leidy Johana [0000000305882818]


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