Colección de Microorganismos con Interés en Salud Animal (CMISA) (bacterias y virus - ectoparásitos y hemoparásitos)

dc.creatorTorres Higuera, Ligia Denise
dc.creatorJiménez Velásquez, Sabrina del Carmen
dc.creatorLópez Ardila, David Emigdio
dc.creatorBeltrán, Óscar Gabriel
dc.creatorRengifo Ibáñez, María Camila
dc.date.accessioned2022-04-08T16:46:59Z
dc.date.available2022-04-08T16:46:59Z
dc.date.created2022-04-08T16:46:59Z
dc.date.issued2021
dc.identifierhttp://hdl.handle.net/20.500.12324/37079
dc.identifierreponame:Biblioteca Digital Agropecuaria de Colombia
dc.identifierrepourl:https://repository.agrosavia.co
dc.identifierinstname:Corporación colombiana de investigación agropecuaria AGROSAVIA
dc.description.abstractEn nuestro país, los sistemas de producción animal están amenazados por la presencia de microorganismos patógenos causantes de enfermedades bacterianas como leptospirosis, mastitis, brucelosis, salmonelosis, enfermedad de Newcastle y enfermedades producidas por hemoparásitos, como anaplasmosis, babesiosis y tripanosomiasis. Estas patologías ocasionan pérdidas económicas importantes asociadas con la incidencia de casos de abortos, infertilidad, anemia, emaciación y cuadros febriles, entre otros signos clínicos que provocan disminución en la calidad de la leche, la carne y demás subproductos, así como también la presencia de animales persistentemente infectados, la aparición de residuos antimicrobianos en alimentos, la generación de resistencia antimicrobiana y la muerte de grupos de animales (Adler & De la Peña Moctezuma, 2010; Balamurugan et al., 2013) . La CMISA ha sido conformada con cepas de referencia y aislamientos, por medio de colectas realizadas en diferentes departamentos del territorio colombiano, con el objetivo de contar con material biológico que pueda ser utilizado en diversos trabajos de investigación y para el desarrollo de productos biotecnológicos como inmunógenos experimentales o comerciales, pruebas de diagnóstico y estudios epidemiológicos. Dentro de las colecciones de microorganismos encontramos la colección de bacterias-virus y de ectoparásitos-hemoparásitos, cuya viabilidad, pureza y actividad biológica son año tras año objeto de activida-des de monitoreo.
dc.languagespa
dc.publisherCorporación colombiana de investigación agropecuaria - AGROSAVIA
dc.publisherMosquera (Colombia)
dc.relation165
dc.relation213
dc.relationdamu, L., Turaki, U. A., Bukar-Kolo, Y. M., Husainy, A. Y., Dauda, I., Wakil, Y., Gulani, I. A., Abadam, F. A., & Mani, A. U. (2016). Current updates on diagnostic methodologies for tick-borne hemoparasitic diseases in equids: A review. Journal of Advanced Veterinary and Animal Research, 3(2), 84-91. https://doi.org/10.5455/javar.2016.c148
dc.relationAdler, B., & De la Peña Moctezuma, A. (2010). Leptospira and leptospirosis. Veterinary Microbiology, 140(3-4), 287-296. https://doi.org/10.1016/j.vetmic.2009.03.012
dc.relationAsfour, H., & Darwish, S. (2011). Phenotypic and genotypic detection of both mecA- and blaZ-genes mediated ß-lactam resistance in staphylococcus strains isolated from bovine mastitis. Global Veterinaria, 6(1), 39-50. https://www.researchgate.net/publication/283157921_Phenotypic_and_genotypic_detection_of_both_mecA-_and_blaZ-genes_mediated_b-lactam_resistance_in_sta-phylococcus_strains_isolated_from_bovine_mastitis
dc.relationBezerra da Silva, J., Carvalho, E., Hartskeerl, R. A., & Ho, P. L. (2011). Evaluation of the use of selective pcr amplification of lps biosynthesis genes for molecular typing of Leptospira at the serovar level. Current Microbiology, 62, 518-524. https://doi.org/10.1007/s00284-010-9738-7
dc.relationBonar, E., Wójcik, I., & Wladyka, B. (2015). Proteomics in studies of Staphylococcus aureus virulence. Acta Biochimica Polonica, 62(3), 367-381. https://doi.org/10.18388/abp.2015_1083
dc.relationBoonsilp, S., Thaipadungpanit, J., Amornchai, P., Wuthiekanun, V., Chierakul, W., Limmathurotsakul, D., Day, N. P., & Peacock, S. J. (2011). Molecular detection and speciation of pathogenic Leptospira spp. in blood from patients with culture-negative leptospirosis. bmc Infectious Diseases, 11, artículo 338. https://doi.org/10.1186/1471-2334-11-338
dc.relationBricker, B. J., & Halling, S. M. (1994). Differentiation of Brucella abortus bv. 1, 2, and 4, Brucella meliten-sis, Brucella ovis, and Brucella suis bv. 1 by pcr. Journal of Clinical Microbiology, 32(11), 2.660-2.666. https://doi.org/10.1128/JCM.32.11.2660-2666.1994
dc.relationBustos, F. (1999). Caracterización biológica y molecular de cepas del virus de Newcastle en Colombia. Avicultores, 53, 38-43.
dc.relationBustos, F., & Marín, C. (1995). La enfermedad de Newcastle: generalidades y situación en Colombia. Revista del Ceisa, 2(2), 31-35.
dc.relationCortez, A. P., Rodrigues, A. C., Garcia, H. A., Neves, L., Batista, J. S., Bengaly, Z., Paiva, F., & Teixeira, M. M. G. (2009). Cathepsin L-like genes of Trypanosoma vivax from Africa and South America − Characterization, relationships and diagnostic implications. Molecular and Cellular Probes, 23(1), 44-51. https://doi.org/10.1016/j.mcp.2008.11.003
dc.relationDastmalchi Saei, H., Ahmadi, M., Mardani, K., & Batavani, R. A. (2009). Molecular typing of Staphylo-coccus aureus isolated from bovine mastitis based on polymorphism of the coagulase gene in the north west of Iran. Veterinary Microbiology, 137(1-2), 202-206. https://doi.org/10.1016/j.vetmic.2009.01.001
dc.relationDíaz-Sánchez, S., Sánchez, S., Sánchez, M., Herrera-León, S., Hanning, I., & Vidal, D. (2012). Detec-tion and characterization of Shiga toxin-producing Escherichia coli in game meat and ready-to-eat meat products. International Journal of Food Microbiology, 160(2), 179-182. https://doi.org/10.1016/j.ijfoodmicro.2012.09.016
dc.relationDieser, S. A., Fessia, A. S., Ferrari, M. P., Raspanti, C. G., & Odierno, L. M. (2017). Streptococcus uberis: In vitro biofilm production in response to carbohydrates and skim milk. Revista Argentina de Microbiología, 49(4), 305-310. https://doi.org/10.1016/j.ram.2017.04.007
dc.relationDrummond, R. O., & Whetstone, T. M. (1970). Oviposition of the Gulf Coast tick. Journal of Economic Entomology, 63(5), 1.547-1.551. https://doi.org/10.1093/jee/63.5.1547
dc.relationDubernet, S., Desmasures, N., & Guéguen, M. (2002). A PCR-based method for identification of lac-tobacilli at the genus level. fems Microbiology Letters, 214(2), 271-275. https://doi.org/10.1016/S0378-1097(02)00895-9
dc.relationGonzález, A., Borrero, R., Ruiz, J., Batista, N., Fernández, Y., Valdés, Y., & González, M. (2006). Medio emjh modificado para el cultivo de Leptospira interrogans serogrupo Ballum. Revista Argentina de Microbiología, 38(2), 61-68. https://www.redalyc.org/articulo.oa?id=213016795003
dc.relationGonzález Rodríguez, A., Rodríguez Jiménez, Y., Batista Santiesteban, N., Valdés Abreu, Y., & González González, M. (2003). Caracterización microbiológica de cepas candidatas vacunales de Leptos-pira interrogans serogrupo Ballum. Revista Cubana de Medicina Tropical, 55(3), 146-152. http://scielo.sld.cu/scielo.php?script=sci_arttext&pid=S0375-07602003000300003
dc.relationGuglielmini, J., Bourhy, P., Schiettekatte, O., Zinini, F., Brisse, S., & Picardeau, M. (2019). Genus-wide Leptospira core genome multilocus sequence typing for strain taxonomy and global surveillance. PLoS Neglected Tropical Diseases, 13(4), artículo e0007374. https://doi.org/10.1371/journal.pntd.0007374
dc.relationGuillemi, E., Ruybal, P., Lia, V., González, S., Farber, M., & Wilkowsky, S. E. (2013). Multi-locus typing scheme for Babesia bovis and Babesia bigemina reveals high levels of genetic variability in strains from Northern Argentina. Infection, Genetics and Evolution, 14, 214-222. https://doi.or-g/10.1016/j.meegid.2012.12.005
dc.relationHan, L., Pu, T., Wang, X., Liu, B., Wang, Y., Feng, J., & Zhang, X. (2018). Optimization of a protective medium for enhancing the viability of freeze-dried Bacillus amyloliquefaciens B1408 based on response surface methodology. Cryobiology, 81, 101-106. https://doi.org/10.1016/j.cryobiol.2018.02.003
dc.relationIbrahim, G. M., & Morin, P. M. (2018). Salmonella serotyping using whole genome sequencing. Fron-tiers in Microbiology, 9. https://doi.org/10.3389/fmicb.2018.02993
dc.relationKoval, A. A., Brihuega, B. F., Grune Loffler, S., López, S., Saint Martin, M., Lagioia, G. G., & Insaugarat, J. R. (2020). Primer aislamiento de Leptospira borgpetersenii serovar Hardjo tipo Hardjo Bovis a partir de un caso clínico en Argentina. Revista Argentina de Microbiología, 52(3), 198-201. https://doi.org/10.1016/j.ram.2019.10.002
dc.relationKrishnamoorthy, P., Satyanarayana, M. L., & Shome, B. R. (2016). Coagulase negative staphylococcal species mastitis: An overview. Research Journal of Veterinary Sciences, 9(1), 1-10. https://doi.org/10.3923/rjvs.2016.1.10
dc.relationKumar, A., Grover, S., & Kumar Batish, V. (2013). Application of multiplex pcr assay based on uidR and fliCH7 genes for detection of Escherichia coli O157:H7 in milk. TheJournal of General and Applied Microbiology, 59(1), 11-19. https://doi.org/10.2323/jgam.59.011
dc.relationKupletskaya, M. B., & Netrusov, A. I. (2011). Viability of lyophilized microorganisms after 50-year stor-age. Microbiology, 80(6), 850-853. https://doi.org/10.1134/S0026261711060129
dc.relationLakew, B. T., Fayera, T., & Ali, Y. M. (2019). Risk factors for bovine mastitis with the isolation and identification of Streptococcus agalactiae from farms in and around Haramaya district, eastern Ethiopia. Tropical Animal Health and Production, 51(6), 1.507-1.513. https://doi.org/10.1007/s11250-019-01838-w
dc.relationLedwaba, M. B., Gomo, C., Lekota, K. E., Le Flèche, P., Hassim, A., Vergnaud, G., & Van Heerden, H. (2019). Molecular characterization of Brucella species from Zimbabwe. PLoS Neglected Tropical Diseases, 13(5), 1-16. https://doi.org/10.1371/journal.pntd.0007311
dc.relationMérien, F., Amouriaux, P., Perolat, P., Baranton, G., & Saint Girons, I. (1992). Polymerase chain reaction for detection of Leptospira spp. in clinical samples. Journal of Clinical Microbiology, 30(9), 2.219-2.224. https://doi.org/10.1128/JCM.30.9.2219-2224.1992
dc.relationMinst, K., Märtlbauer, E., Miller, T., & Meyer, C. (2012). Short communication: Streptococcus species iso-lated from mastitis milk samples in Germany and their resistance to antimicrobial agents. Journal of Dairy Science, 95(12), 6.957-6.962. https://doi.org/10.3168/jds.2012-5852
dc.relationMiyamoto-Shinohara, Y., Sukenobe, J., Imaizumi, T., & Nakahara, T. (2006). Survival curves for mi-crobial species stored by freeze-drying. Cryobiology, 52(1), 27-32. https://doi.org/10.1016/j.cryobiol.2005.09.002
dc.relationMorey, R. E., Galloway, R. L., Bragg, S. L., Steigerwalt, A. G., Mayer, L. W., & Levett, P. N. (2006). Spe-cies-specific identification of Leptospiraceae by 16S rRNA gene sequencing. Journal of Clinical Microbiology, 44(10), 3.510-3.516. https://doi.org/10.1128/JCM.00670-06
dc.relationMunderloh, U. G., & Kurtti, T. J. (1989). Formulation of medium for tick cell culture. Experimental & Applied Acarology, 7(3), 219-229. https://doi.org/10.1007/BF01194061
dc.relationNagano, H., Hirochi, T., Fujita, K., Wakamori, Y., Takeshi, K., & Yano, S. (2004). Phenotypic and genotypic characterization of ß-D-glucuronidase- positive Shiga toxin-producing Escherichia coli O157:H7 isolates from deer. Journal of Medical Microbiology, 53(10), 1.037-1.043. https://doi.org/10.1099/jmm.0.05381-0
dc.relationPalomares Velosa, J. E., & Rodríguez Bautista, J. L. (2011). Fluctuación en el comportamiento del perfil de resistencia a acaricidas piretroides sintéticos (ps) y organofosforados (op) de la cepa Palma de Vino de Rhipicephalus (Boophilus) microplus. En Parasitología. Abstracts, Revista Colombiana de Cien-cias Pecuarias, 24(3), 500-510. https://revistas.udea.edu.co/index.php/rccp/article/view/32470
dc.relationPavan, M. E., Brihuega, B., Pettinari, M. J., & Cairó, F. (2011). Multiple-locus variable-number tandem repeat analysis of reference strains used for the diagnosis of leptospirosis in Argentina. Revista Ar-gentina de Microbiología, 43(4), 251-255. https://doi.org/10.1590/S0325-75412011000400003
dc.relationPavan, M. E., Cairó, F., Brihuega, B., & Samartino, L. (2008). Multiple-locus variable-number tandem repeat analysis (mlva) of Leptospira interrogans serovar Pomona from Argentina reveals four new genotypes. Comparative Immunology, Microbiology and Infectious Diseases, 31(1), 37-45. https://doi.org/10.1016/j.cimid.2007.03.004
dc.relationPhilip, N., Garba, B., & Neela, V. K. (2018). Long-term preservation of Leptospira spp.: Challenges and prospects. Applied Microbiology and Biotechnology, 102(13), 5.427-5.435. https://doi.org/10.1007/s00253-018-9047-9
dc.relationPolo, L., Mañes-Lázaro, R., Olmeda, I., Cruz-Pio, L. E., Medina, A., Ferrer, S., & Pardo, I. (2017). Influ-ence of freezing temperatures prior to freeze-drying on viability of yeasts and lactic acid bacteria isolated from wine. Journal of Applied Microbiology, 122(6), 1.603-1.614. https://doi.org/10.1111/jam.13465
dc.relationPortner, D. C., Leuschner, R. G. K., & Murray, B. S. (2007). Optimising the viability during storage of freeze-dried cell preparations of Campylobacter jejuni. Cryobiology, 54(3), 265-270. https://doi.org/10.1016/j.cryobiol.2007.03.002
dc.relationRato, M. G., Bexiga, R., Florindo, C., Cavaco, L. M., Vilela, C. L., & Santos-Sanches, I. (2013). Antimicrobial resistance and molecular epidemiology of streptococci from bovine mastitis. Veterinary Microbi-ology, 161(3-4), 286-294. https://doi.org/10.1016/j.vetmic.2012.07.043
dc.relationRavindra, P. V., Tiwari, A. K., Ratta, B., Chaturvedi, U., Palia, S. K., & Chauhan, R. S. (2009). Newcastle disease virus-induced cytopathic effect in infected cells is caused by apoptosis. Virus Research, 141(1), 13-20. https://doi.org/10.1016/j.virusres.2008.12.008
dc.relationReinoso, E. B., Lasagno, M. C., & Odierno, L. M. (2015). Genetic patterns of Streptococcus uberisisolated from bovine mastitis. Revista Argentina de Microbiología, 47(2), 108-111. https://doi.org/10.1016/j.ram.2015.02.001
dc.relationRen, D., Zhu, J., Gong, S., Liu, H., & Yu, H. (2018). Antimicrobial characteristics of lactic acid bacteria iso-lated from homemade fermented foods. BioMed Research International, 2018, artículo 5416725. https://doi.org/10.1155/2018/5416725
dc.relationRezasoltani, S., Dabiri, H., Khaki, P., Nejad, M. R., Karimnasab, N., & Modirrousta, S. (2015). Charac-terization of Leptospira interrogans serovars by polymorphism variable number tandem repeat analysis. Jundishapur Journal of Microbiology, 8(10), artículo e22819. https://doi.org/10.5812/jjm.22819
dc.relationRomaniuk, J. A. H., & Cegelski, L. (2015). Bacterial cell wall composition and the influence of antibiotics by cell-wall and whole-cell nmr. Philosophical Transactions of the Royal Society B: Biological Sciences, 370(1.679). https://doi.org/10.1098/rstb.2015.0024
dc.relationThibeaux, R., Girault, D., Bierque, E., Soupé-Gilbert, M.-E., Rettinger, A., Douyère, A., Meyer, M., Irao-la, G., Picardeau, M., & Goarant, C. (2018). Biodiversity of environmental Leptospira: Improving identification and revisiting the diagnosis. Frontiers in Microbiology, 9. https://doi.org/10.3389/fmicb.2018.00816
dc.relationThibeaux, R., Iraola, G., Ferrés, I., Bierque, E., Girault, D., Soupé-Gilbert, M.-E., Picardeau, M., & Goarant, C. (2018). Deciphering the unexplored Leptospira diversity from soils uncovers genomic evolution to virulence. Microbial Genomics, 4(1). https://doi.org/10.1099/mgen.0.000144
dc.relationTitze, I., & Krömker, V. (2020). Antimicrobial activity of a phage mixture and a lactic acid bacterium against Staphylococcusaureus from bovine mastitis. Veterinary Sciences, 7(1). https://doi.org/10.3390/vetsci7010031
dc.relationTomazi, T., Freu, G., Gomes Alves, B., De Souza Filho, A. F., Heinemann, M. B., & Dos Santos, M. V. (2019). Genotyping and antimicrobial resistance of Streptococcus uberis isolated from bovine cli-nical mastitis. PLoS ONE, 14(10), artículo e0223719. https://doi.org/10.1371/journal.pone.0223719
dc.relationTorres Higuera, L. D., Jiménez Velásquez, S. del C., Rodríguez Bautista, J. L., & Patiño Burbano, R. E. (2019). Identification of Brucella abortus biovar 4 of bovine origin in Colombia. Revista Argentina de Microbiología, 51(3), 221-228. https://doi.org/10.1016/j.ram.2018.08.002
dc.relationTorres Higuera, L. D., Ortiz Ortega, D., Rodríguez Bautista, J. L., & Patiño Burbano, R. E. (2008). Com-paración de tres tratamientos para la crioconservación de serovares de Leptospira en nitró-geno líquido. Revista Corpoica − Ciencia y Tecnología Agropecuaria, 9(2), 72-76. https://doi.org/10.21930/rcta.vol9_num2_art:120
dc.relationWhatmore, A. M., Davison, N., Cloeckaert, A., Al Dahouk, S., Zygmunt, M. S., Brew, S. D., Perrett, L. L., Koylass, M. S., Vergnaud, G., Quance, C., Scholz, H. C., Dick Jr., E. J., Hubbard, G., & Schlabritz-Lout-sevitch, N. E. (2014). Brucella papionis sp. nov., isolated from baboons (Papio spp.). International Journal of Systematic and Evolutionary Microbiology, 64, 4.120-4.128. https://doi.org/10.1099/ijs.0.065482-0
dc.relationWoo, P. T. K. (1969). The haematocrit centrifuge for the detection of trypanosomes in blood. Canadian Journal of Zoology, 47(5), 921-923. https://doi.org/10.1139/z69-150
dc.relationZarantonelli, L., Suanes, A., Meny, P., Buroni, F., Nieves, C., Salaberry, X., Briano, C., Ashfield, N., Da Silva Silveira, C., Dutra, F., Easton, C., Fraga, M., Giannitti, F., Hamond, C., Macías-Rioseco, M., Menén-dez, C., Mortola, A., Picardeau, M., Quintero, J., ... Buschiazzo, A. (2018). Isolation of pathogenicLeptospira strains from naturally infected cattle in Uruguay reveals high serovar diversity, and uncovers a relevant risk for human leptospirosis. PLoS Neglected Tropical Diseases, 12(9), artículo e0006694. https://doi.org/10.1371/journal.pntd.0006694
dc.relationZhang, J., Liu, Q., Chen, W., Du, G., & Chen, J. (2016). Short communication: Protection of lyophilized milk starter Lactobacillus casei Zhang by glutathione. Journal of Dairy Science, 99(3). https://doi.org/10.3168/jds.2015-9540
dc.relationZhao, G., & Zhang, G. (2005). Effect of protective agents, freezing temperature, rehydration media on viability of malolactic bacteria subjected to freeze-drying. Journal of Applied Microbiology, 99(2), 333-338. https://doi.org/10.1111/j.1365-2672.2005.02587.x
dc.relationZuerner, R. L. (2005). Laboratory maintenance of pathogenic Leptospira. Current Protocols in Micro-biology, 00(1). https://doi.org/10.1002/9780471729259.mc12e01s00
dc.relation36935 ; Conservación y manejo de la diversidad microbiana en los bancos de germoplasma para la alimentación y la agricultura en Colombia
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.titleColección de Microorganismos con Interés en Salud Animal (CMISA) (bacterias y virus - ectoparásitos y hemoparásitos)


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