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Comparative genomics of clinical and environmental isolates of Vibrio spp.: implications of traits associated with virulence and resistance
dc.contributor.advisor | Arboleda Valencia, Jorge | |
dc.contributor.advisor | Rodriguez-Rey, Ghennie T | |
dc.contributor.author | Pérez Duque, Alejandra María | |
dc.date.accessioned | 2021-12-09T15:14:44Z | |
dc.date.available | 2022-04-11 | |
dc.date.available | 2021-12-09T15:14:44Z | |
dc.date.issued | 2021-12-02 | |
dc.identifier.uri | https://repositorio.ucaldas.edu.co/handle/ucaldas/17239 | |
dc.description | Ilustraciones | spa |
dc.description.abstract | spa:El género Vibrio comprende más de 100 especies bacterianas presentes en hábitats acuáticos y marinos como organismos de vida libre o asociados a organismos acuáticos, pese a que la mayoría de estas especies son consideradas no patógenas, existe una preocupación generalizada por el aumento en los casos de infecciones humanas y enfermedades en organismos acuáticos causadas por especies patógenas de Vibrio en el mundo, la emergencia de linajes epidémicos y la gran diversidad del género. Colombia no está exento de posibles brotes de cólera o vibriosis dada su ubicación geográfica y la presencia de las costas Pacífico y Atlántico. Por lo tanto, se ha establecido una vigilancia activa por parte del Instituto Nacional de Salud. En muestreos realizados durante 2010 y 2013, encontraron aislamientos de Vibrio circulando en el país, estos aislamientos no han sido caracterizados a nivel de genoma. Este estudio se enfoca en la diversidad genómica de aislamientos de Vibrio spp. para determinar sus relaciones genéticas e identificar potenciales rasgos de virulencia y resistencia. Sesenta aislamientos de Vibrio spp provenientes de muestras clínicas y ambientales de las costas Pacífico y Atlántico de Colombia fueron secuenciados, ensamblados y anotados. Se llevaron a cabo análisis de pangenoma y filogenómica para cada especie. Se caracterizaron las especies más importantes en salud pública de acuerdo con el esquema de tipificación multilocus y filogenómica. Se encontraron seis especies de Vibrio (V. parahaemolyticus (17), V. vulnificus (9), V. fluvialis (16), V. furnissii (6), V. alginolyticus (10) y V. diabolicus (4). En V. parahaemolyticus encontramos aislamientos pertenecientes al clon pandémico ST3 y ST120 y en V. vulnificus encontramos aislamientos pertenecientes al Linaje 1 y 2. El pangenoma de cada especie mostró que todos los aislamientos compartían importantes categorías relacionadas con virulencia. Se encontraron genes de virulencia homólogos entre las especies incluso en especies clasificadas como no patógenas como V. diabolicus. Se encontraron categorías relacionadas con mobiloma, elementos móviles y genes de resistencia asociados a plásmidos tanto en aislamientos ambientales como en clínicos. Este estudio permitió identificar posibles focos de vibriosis contribuyendo al fortalecimiento del sistema de vigilancia intensificada implementado por el Instituto Nacional de Salud de Colombia para predecir futuros brotes de vibriosis en el país. | spa |
dc.description.abstract | eng:There is widespread concern about the increase in cases of human and animal infections caused by pathogenic Vibrio species due to the emergence of epidemic lineages. In Colombia, active sur-veillance by the National Institute of Health (INS) has confirmed the presence of Vibrio; however, in routine surveillance, these isolates are not genomically characterized. This study focused on the pangenome analysis of six Vibrio species: V. parahaemolyticus, V. vulnificus, V. alginolyticus, V. fluvialis, V. diabolicus and V. furnissii to determine the genetic architectures of potentially virulent and an-timicrobial resistance traits. Isolates from environmental and clinical samples were genome se-quenced, assembled and annotated. The most important species in public health were further characterized by multilocus sequence typing and phylogenomics. For V. parahaemolyticus, we found the virulent ST3 and ST120 genotypes. For V. vulnificus, we identified isolates belonging to lineages 1 and 2. Virulence gene homologues between species were found even in non-pathogenic species such as V. diabolicus. Annotations related to the mobilome, integrative mobile and conjugative elements and resistance genes were obtained from environmental and clinical isolates. This study contributes genomic information to the intensified surveillance program implemented by the INS to establish potential sources of vibriosis in Colombia. | eng |
dc.description.tableofcontents | Agradecimientos / Resumen Y Abstract / Lista de tablas / Lista de anexos / 1. Introducción / 1.1. Campo temático / 1.2. Planteamiento del problema / 1.3. Justificación / 1.4. Objetivos / 1.4.1. Objetivo general / 1.4.2. Objetivos específicos / 2. Referente teórico y antecedentes / 2.1. Género Vibrio / 2.1.1. Generalidades y hábitat / 2.1.2. Especies patógenas / 2.1.3. Principales especies patógenas de Vibrio / 2.1.3 Genoma de Vibrio / 2.1.4 Patógenos emergentes / 2.1.5 Resistencia a antibióticos / 2.1.6 Herramientas moleculares para el estudio de Vibrio / 2.1.7 Sistemas de vigilancia a nivel mundial / 3 Primer artículo / 4 Conclusiones generales / 4.1 Contribuciones del trabajo de grado / 4.2 Impactos potenciales del trabajo de grado / 4.3 Recomendaciones y trabajos futuros / ANEXOS | spa |
dc.format.mimetype | application/pdf | spa |
dc.language.iso | eng | spa |
dc.language.iso | spa | spa |
dc.title | Comparative genomics of clinical and environmental isolates of Vibrio spp.: implications of traits associated with virulence and resistance | eng |
dc.type | Artículo de revista | spa |
dc.type | Trabajo de grado - Maestría | spa |
dc.contributor.educationalvalidator | González Muñoz, Andrea | |
dc.contributor.researcher | Arboleda Valencia, Jorge | |
dc.contributor.researcher | Vivas Aguas, Lizbeth Janet | |
dc.contributor.researcher | Córdoba Meza, Tania | |
dc.contributor.researcher | Rodríguez Rey, Ghennie Tatiana | |
dc.contributor.researcher | Díaz Guevara, Paula | |
dc.contributor.researcher | Martinez Urtaza, Jaime | |
dc.contributor.researcher | Wiesner Reyes, Magdalena | |
dc.description.degreelevel | Maestría | spa |
dc.identifier.instname | Universidad de Caldas | spa |
dc.identifier.reponame | Repositorio Institucional Universidad de Caldas | spa |
dc.identifier.repourl | https://repositorio.ucaldas.edu.co | spa |
dc.publisher.faculty | Facultad de Ingeniería | spa |
dc.publisher.place | Manizales, Caldas | spa |
dc.relation.references | Arias, T., Alexander, J., Higuita, J. C., López, M., & Ospina Martínez, V. (2013). Plan Estratégico de Ciencia, Tecnología e Innovación para el departamento de Caldas. | spa |
dc.relation.references | Baker-Austin, C., Oliver, J. D., Alam, M., Ali, A., Waldor, M. K., Qadri, F., & Martinez-Urtaza, J. (2018). Vibrio spp. infections. Nature Reviews Disease Primers, 4(1). https://doi.org/10.1038/s41572- 018-0005-8 | spa |
dc.relation.references | Baker-Austin, C., Stockley, L., Rangdale, R., & Martinez-Urtaza, J. (2010). Environmental occurrence and clinical impact of Vibrio vulnificus and Vibrio parahaemolyticus: A European perspective. Environmental Microbiology Reports, 2(1), 7–18. https://doi.org/10.1111/j.1758- 2229.2009.00096.x | spa |
dc.relation.references | Bruto, M., Labreuche, Y., James, A., Piel, D., Chenivesse, S., Petton, B., Polz, M. F., & Le Roux, F. (2018). Ancestral gene acquisition as the key to virulence potential in environmental Vibrio populations. ISME Journal, 12(12), 2954–2966. https://doi.org/10.1038/s41396-018-0245-3 | spa |
dc.relation.references | CDC. (n.d.). Vibrio Species Causing Vibriosis. 2020. Retrieved February 2, 2021, from https://www.cdc.gov/vibrio/index.html | spa |
dc.relation.references | Escobar, L. E., Ryan, S. J., Stewart-Ibarra, A. M., Finkelstein, J. L., King, C. A., Qiao, H., & Polhemus, M. E. (2015). A global map of suitability for coastal Vibrio cholerae under current and future climate conditions. Acta Tropica, 149, 202–211. https://doi.org/10.1016/j.actatropica.2015.05.028 | spa |
dc.relation.references | Gobierno de Caldas, G. (2017). Plan Departamental de Desarrollo 2016-2019. Caldas Territorio de Oportunidades. | spa |
dc.relation.references | Hernández-Flórez, C. E., & Cáceres-Manrique, F. de M. (2014). Cólera, ¿se aproxima una nueva pandemia? Medicas UIS, 27(2), 67–83. | spa |
dc.relation.references | Khouadja, S., Suffredini, E., Baccouche, B., Croci, L., & Bakhrouf, A. (2014). Occurrence of virulence genes among Vibrio cholerae and Vibrio parahaemolyticus strains from treated wastewaters. Environmental Monitoring and Assessment, 186(10), 6935–6945. https://doi.org/10.1007/s10661-014-3900-9 | spa |
dc.relation.references | Klein, S., Pipes, S., & Lovell, C. R. (2018). Occurrence and significance of pathogenicity and fitness islands in environmental vibrios. AMB Express, 8(1). https://doi.org/10.1186/s13568-018-0704- 2 | spa |
dc.relation.references | López, M. (2012). Acciones de vigilancia intensificada de cólera ante posible reintroducción en los componentes de vigilancia epidemiológica y laboratorio, Colombia, 2011-2012. 2011–2012. | spa |
dc.relation.references | Mohamad, N., Amal, M. N. A., Saad, M. Z., Yasin, I. S. M., Zulkiply, N. A., Mustafa, M., & Nasruddin, N. S. (2019). Virulence-associated genes and antibiotic resistance patterns of Vibrio spp. isolated from cultured marine fishes in Malaysia. BMC Veterinary Research, 15(1), 1–13. https://doi.org/10.1186/s12917-019-1907-8 | spa |
dc.relation.references | Mok, J. S., Ryu, A., Kwon, J. Y., Kim, B., & Park, K. (2019). Distribution of Vibrio species isolated from bivalves and bivalve culture environments along the Gyeongnam coast in Korea: Virulence and antimicrobial resistance of Vibrio parahaemolyticus isolates. Food Control, 106(June), 106697. https://doi.org/10.1016/j.foodcont.2019.06.023 | spa |
dc.relation.references | Mok, J. S., Ryu, A., Kwon, J. Y., Park, K., & Shim, K. B. (2019). Abundance, antimicrobial resistance, and virulence of pathogenic Vibrio strains from molluscan shellfish farms along the Korean coast. Marine Pollution Bulletin, 149(April), 110559. https://doi.org/10.1016/j.marpolbul.2019.110559 | spa |
dc.relation.references | Nathamuni, S., Jangam, A. K., Katneni, V. K., Selvaraj, A., Krishnan, K., Kumar, S., Avunje, S., Balasubramaniam, S., Grover, M., Alavandi, S. V., & Koyadan, V. K. (2019). Insights on genomic diversity of Vibrio spp. through Pan-genome analysis. Annals of Microbiology, 69(13), 1547– 1555. https://doi.org/10.1007/s13213-019-01539-7 | spa |
dc.relation.references | OMS. (2019). Cólera. https://www.who.int/es/news-room/fact-sheets/detail/cholera | spa |
dc.relation.references | Raszl, S. M., Froelich, B. A., Vieira, C. R. W., Blackwood, A. D., & Noble, R. T. (2016). Vibrio parahaemolyticus and Vibrio vulnificus in South America: water, seafood and human infections. Journal of Applied Microbiology, 121(5), 1201–1222. https://doi.org/10.1111/jam.13246 | spa |
dc.relation.references | Soto, Z., Pérez, L., & Estrada, D. (2016). Bacterias causantes de enfermedades transmitidas por alimentos: Una mirada en Colombia. Salud Uninorte, 32(1), 105–122. http://www.scielo.org.co/pdf/sun/v32n1/v32n1a10.pdf | spa |
dc.relation.references | Vezzulli, L., Pezzati, E., Brettar, I., Höfle, M., & Pruzzo, C. (2015). Effects of Global Warming on Vibrio Ecology . Microbiology Spectrum, 3(3). https://doi.org/10.1128/microbiolspec.ve-0004-2014 | spa |
dc.relation.references | Baker-Austin, C., Oliver, J. D., Alam, M., Ali, A., Waldor, M. K., Qadri, F., & Martinez-Urtaza, J. (2018). Vibrio spp. infections. Nature Reviews Disease Primers, 4(1). https://doi.org/10.1038/s41572- 018-0005-8 | spa |
dc.relation.references | Baker-Austin, C., Stockley, L., Rangdale, R., & Martinez-Urtaza, J. (2010). Environmental occurrence and clinical impact of Vibrio vulnificus and Vibrio parahaemolyticus: A European perspective. Environmental Microbiology Reports, 2(1), 7–18. https://doi.org/10.1111/j.1758- 2229.2009.00096.x | spa |
dc.relation.references | Balloux, F., Brønstad Brynildsrud, O., van Dorp, L., Shaw, L. P., Chen, H., Harris, K. A., Wang, H., & Eldholm, V. (2018). From Theory to Practice: Translating Whole-Genome Sequencing (WGS) into the Clinic. Trends in Microbiology, 26(12), 1035–1048. https://doi.org/10.1016/j.tim.2018.08.004 | spa |
dc.relation.references | Bhunia, A. K. (2018). Vibrio vulnificus, Vibrio parahaemolyticus, and Vibrio cholerae. 2013, 315–329. https://doi.org/10.1007/978-1-4939-7349-1_18 | spa |
dc.relation.references | Bisharat, N., Koton, Y., & Oliver, J. D. (2020). Phylogeography of the marine pathogen, Vibrio vulnificus, revealed the ancestral scenarios of its evolution. MicrobiologyOpen, 9(9), 1–8. https://doi.org/10.1002/mbo3.1103 | spa |
dc.relation.references | Bruto, M., James, A., Petton, B., Labreuche, Y., Chenivesse, S., Alunno-Bruscia, M., Polz, M. F., & Le Roux, F. (2017). Vibrio crassostreae, a benign oyster colonizer turned into a pathogen after plasmid acquisition. ISME Journal, 11(4), 1043–1052. https://doi.org/10.1038/ismej.2016.162 | spa |
dc.relation.references | Castillo, D., Kauffman, K., Hussain, F., Kalatzis, P., Rørbo, N., Polz, M. F., & Middelboe, M. (2018). Widespread distribution of prophage-encoded virulence factors in marine Vibrio communities. Scientific Reports, 8(1), 2–10. https://doi.org/10.1038/s41598-018-28326-9 | spa |
dc.relation.references | Dobrindt, U., Hochhut, B., Hentschel, U., & Hacker, J. (2004). Genomic islands in pathogenic and environmental microorganisms. Nature Reviews Microbiology, 2(5), 414–424. https://doi.org/10.1038/nrmicro884 | spa |
dc.relation.references | Elmahdi, S., DaSilva, L. V., & Parveen, S. (2016). Antibiotic resistance of Vibrio parahaemolyticus and Vibrio vulnificus in various countries: A review. Food Microbiology, 57, 128–134. https://doi.org/10.1016/j.fm.2016.02.008 | spa |
dc.relation.references | Gavilan, R. G., Zamudio, M. L., & Martinez-Urtaza, J. (2013). Molecular Epidemiology and Genetic Variation of Pathogenic Vibrio parahaemolyticus in Peru. PLoS Neglected Tropical Diseases, 7(5). https://doi.org/10.1371/journal.pntd.0002210 | spa |
dc.relation.references | Gennari, M., Ghidini, V., Caburlotto, G., & Lleo, M. M. (2012). Virulence genes and pathogenicity islands in environmental Vibrio strains nonpathogenic to humans. FEMS Microbiology Ecology, 82(3), 563–573. https://doi.org/10.1111/j.1574-6941.2012.01427.x | spa |
dc.relation.references | González-Escalona, N., Martinez-Urtaza, J., Romero, J., Espejo, R. T., Jaykus, L. A., & DePaola, A. (2008). Determination of molecular phylogenetics of Vibrio parahaemolyticus strains by multilocus sequence typing. Journal of Bacteriology, 190(8), 2831–2840. https://doi.org/10.1128/JB.01808-07 | spa |
dc.relation.references | Hazen, T. H., Pan, L., Gu, J. D., & Sobecky, P. A. (2010). The contribution of mobile genetic elements to the evolution and ecology of Vibrios. FEMS Microbiology Ecology, 74(3), 485–499. https://doi.org/10.1111/j.1574-6941.2010.00937.x | spa |
dc.relation.references | Heidelberg, J. F., Elsen, J. A., Nelson, W. C., Clayton, R. A., Gwinn, M. L., Dodson, R. J., Haft, D. H., Hickey, E. K., Peterson, J. D., Umayam, L., Gill, S. R., Nelson, K. E., Read, T. D., Tettelin, H., Richardson, D., Ermolaeva, M. D., Vamathevan, J., Bass, S., Halving, Q., … Fraser, C. M. (2000). DNA sequence of both chromosomes of the cholera pathogen Vibrio cholerae. Nature, 406(6795), 477–483. https://doi.org/10.1038/35020000 | spa |
dc.relation.references | Hernández-Cabanyero, C., & Amaro, C. (2020). Phylogeny and life cycle of the zoonotic pathogen Vibrio vulnificus. Environmental Microbiology, 22(10), 4133–4148. https://doi.org/10.1111/1462- 2920.15137 | spa |
dc.relation.references | Hernández, M., Quijada, N. M., Rodríguez-Lázaro, D., & Eiros, J. M. (2020). Bioinformatics of next generation sequencing in clinical microbiology diagnosis. Revista Argentina de Microbiologia, 52(2), 150–161. https://doi.org/10.1016/j.ram.2019.06.003 | spa |
dc.relation.references | Horseman, M. A., & Surani, S. (2011). A comprehensive review of Vibrio vulnificus: An important cause of severe sepsis and skin and soft-tissue infection. International Journal of Infectious Diseases, 15(3), e157–e166. https://doi.org/10.1016/j.ijid.2010.11.003 | spa |
dc.relation.references | Ina-Salwany, M. Y., Al-saari, N., Mohamad, A., Mursidi, F. A., Mohd-Aris, A., Amal, M. N. A., Kasai, H., Mino, S., Sawabe, T., & Zamri-Saad, M. (2019). Vibriosis in Fish: A Review on Disease Development and Prevention. Journal of Aquatic Animal Health, 31(1), 3–22. https://doi.org/10.1002/aah.10045 | spa |
dc.relation.references | Janda, J. M., Newton, A. E., & Bopp, C. A. (2015). Vibriosis. Clinics in Laboratory Medicine, 35(2), 273–288. https://doi.org/10.1016/j.cll.2015.02.007 | spa |
dc.relation.references | Julie, D., Solen, L., Antoine, V., Jaufrey, C., Annick, D., & Dominique, H. H. (2010). Ecology of pathogenic and non-pathogenic Vibrio parahaemolyticus on the French Atlantic coast. Effects of temperature, salinity, turbidity and chlorophyll a. Environmental Microbiology, 12(4), 929– 937. https://doi.org/10.1111/j.1462-2920.2009.02136.x | spa |
dc.relation.references | Klemm, E., & Dougan, G. (2016). Advances in understanding bacterial pathogenesis gained from whole-genome sequencing and phylogenetics. Cell Host and Microbe, 19(5), 599–610. https://doi.org/10.1016/j.chom.2016.04.015 | spa |
dc.relation.references | Kwong, J. C., Mccallum, N., Sintchenko, V., & Howden, B. P. (2015). Whole genome sequencing in clinical and public health microbiology. Pathology, 47(3), 199–210. https://doi.org/10.1097/PAT.0000000000000235 | spa |
dc.relation.references | Le Roux, F., Wegner, K. M., Baker-Austin, C., Vezzulli, L., Osorio, C. R., Amaro, C., Ritchie, J. M., Defoirdt, T., Destoumieux-Garzón, D., Blokesch, M., Mazel, D., Jacq, A., Cava, F., Gram, L., Wendling, C. C., Strauch, E., Kirschner, A., & Huehn, S. (2015). The emergence of Vibrio pathogens in Europe: Ecology, evolution and pathogenesis (Paris, 11-12 March 2015). Frontiers in Microbiology, 6(JUL), 1–8. https://doi.org/10.3389/fmicb.2015.00830 | spa |
dc.relation.references | Letchumanan, V., Chan, K. G., & Lee, L. H. (2014). Vibrio parahaemolyticus: A review on the pathogenesis, prevalence, and advance molecular identification techniques. Frontiers in Microbiology, 5(DEC), 1–13. https://doi.org/10.3389/fmicb.2014.00705 | spa |
dc.relation.references | Leyton, Y., & Riquelme, C. (2008). Vibrios en los sistemas marinos costeros. Revista de Biologia Marina y Oceanografia, 43(3), 441–456. https://doi.org/10.4067/s0718-19572008000300004 | spa |
dc.relation.references | Logar-Henderson, C., Ling, R., Tuite, A. R., & Fisman, D. N. (2019). Effects of large-scale oceanic phenomena on mon-cholera vibriosis Incidence in the United States: Implications for climate change. BioRxiv. https://doi.org/10.1101/528893 | spa |
dc.relation.references | López, L., Ganiveth, M., Herrera, L., Montes, A., Olascuaga, Y., & Ortega, R. (2010). Estudio piloto para el aislamiento de Vibrio spp. en ostras (Crassostrea rhizophorae) capturadas en la ciénada de la Vírgen, Cartagena, Colombia. 1 | spa |
dc.relation.references | López, M. (2012). Acciones de vigilancia intensificada de cólera ante posible reintroducción en los componentes de vigilancia epidemiológica y laboratorio, Colombia, 2011-2012. 2011–2012. | spa |
dc.relation.references | Martinez-Urtaza, J., Bowers, J. C., Trinanes, J., & DePaola, A. (2010). Climate anomalies and the increasing risk of Vibrio parahaemolyticus and Vibrio vulnificus illnesses. Food Research International, 43(7), 1780–1790. https://doi.org/10.1016/j.foodres.2010.04.001 | spa |
dc.relation.references | Mohamad, N., Amal, M. N. A., Saad, M. Z., Yasin, I. S. M., Zulkiply, N. A., Mustafa, M., & Nasruddin, N. S. (2019). Virulence-associated genes and antibiotic resistance patterns of Vibrio spp. isolated from cultured marine fishes in Malaysia. BMC Veterinary Research, 15(1), 1–13. https://doi.org/10.1186/s12917-019-1907-8 | spa |
dc.relation.references | Mok, J. S., Ryu, A., Kwon, J. Y., Kim, B., & Park, K. (2019). Distribution of Vibrio species isolated from bivalves and bivalve culture environments along the Gyeongnam coast in Korea: Virulence and antimicrobial resistance of Vibrio parahaemolyticus isolates. Food Control, 106(June), 106697. https://doi.org/10.1016/j.foodcont.2019.06.023 | spa |
dc.relation.references | Muhling, B. A., Jacobs, J., Stock, C. A., Gaitan, C. F., & Saba, V. S. (2017). Projections of the future occurrence, distribution, and seasonality of three Vibrio species in the Chesapeake Bay under a high-emission climate change scenario. GeoHealth, 1(7), 278–296. https://doi.org/10.1002/2017GH000089 | spa |
dc.relation.references | Newton, A., Kendall, M., Vugia, D. J., Henao, O. L., & Mahon, B. E. (2012). Increasing rates of vibriosis in the United States, 1996-2010: Review of surveillance data from 2 systems. Clinical Infectious Diseases, 54(SUPPL.5), 391–395. https://doi.org/10.1093/cid/cis243OMS. (2019). Cólera. https://www.who.int/es/news-room/fact-sheets/detail/cholera | spa |
dc.relation.references | Raszl, S. M., Froelich, B. A., Vieira, C. R. W., Blackwood, A. D., & Noble, R. T. (2016). Vibrio parahaemolyticus and Vibrio vulnificus in South America: water, seafood and human infections. Journal of Applied Microbiology, 121(5), 1201–1222. https://doi.org/10.1111/jam.13246 | spa |
dc.relation.references | Rivera, I. N. G., Souza, K. M. C., Souza, C. P., & Lopes, R. M. (2012). Free-living and planktonassociated vibrios: Assessment in ballast water, Harbor areas, and coastal ecosystems in Brazil. Frontiers in Microbiology, 3(JAN), 1–8. https://doi.org/10.3389/fmicb.2012.00443 | spa |
dc.relation.references | Rodríguez-Castro, A. M. (2012). Origen, distribución y caracterización de Vibrios patógenos humanos en el medio ambiente marino de Galicia. Santiago de Compostela. | spa |
dc.relation.references | Rouli, L., Merhej, V., Fournier, P. E., & Raoult, D. (2015). The bacterial pangenome as a new tool for analysing pathogenic bacteria. New Microbes and New Infections, 7, 72–85. https://doi.org/10.1016/j.nmni.2015.06.005 | spa |
dc.relation.references | Sawabe, T., Ogura, Y., Matsumura, Y., Feng, G., Rohul Amin, A. K. M., Mino, S., Nakagawa, S., Sawabe, T., Kumar, R., Fukui, Y., Satomi, M., Matsushima, R., Thompson, F. L., Gomez-Gil, B., Christen, R., Maruyama, F., Kurokawa, K., & Hayashi, T. (2013). Updating the Vibrio clades defined by multilocus sequence phylogeny: Proposal of eight new clades, and the description of Vibrio tritonius sp. nov. Frontiers in Microbiology, 4(DEC), 1–14. https://doi.org/10.3389/fmicb.2013.00414 | spa |
dc.relation.references | Song, X., Zang, J., Yu, W., Shi, X., & Wu, Y. (2020). Occurrence and identification of pathogenic Vibrio contaminants in common seafood available in a chinese traditional market in Qingdao, Shandong Province. Frontiers in Microbiology, 11(June), 1–6. https://doi.org/10.3389/fmicb.2020.01488 | spa |
dc.relation.references | Soto, Z., Pérez, L., & Estrada, D. (2016). Bacterias causantes de enfermedades transmitidas por alimentos: Una mirada en Colombia. Salud Uninorte, 32(1), 105–122. http://www.scielo.org.co/pdf/sun/v32n1/v32n1a10.pdf | spa |
dc.relation.references | Sun, Y., Bernard, E., Hammer, B., & Miyashiro, T. (2013). Competence and Natural Transformation in Vibrios. 23(1), 1–7. https://doi.org/10.1111/mmi.12307.Competence | spa |
dc.relation.references | Thompson, F. L., Iida, T., & Swings, J. (2004). Biodiversity of Vibrios. Journal of Clinical Microbiology. https://doi.org/10.1128/MMBR.68.3.403 | spa |
dc.relation.references | Velazquez-Roman, J., León-Sicairos, N., Hernández-Díaz, L. de J., & Canizalez-Roman, A. (2014). Pandemic Vibrio parahaemolyticus O3: K6 on the American continent. Frontiers in Cellular and Infection Microbiology, 3(JAN), 1–14. https://doi.org/10.3389/fcimb.2013.00110 | spa |
dc.relation.references | Vezzulli, L., Pezzati, E., Brettar, I., Höfle, M., & Pruzzo, C. (2015). Effects of Global Warming on Vibrio Ecology . Microbiology Spectrum, 3(3). https://doi.org/10.1128/microbiolspec.ve-0004- 2014 | spa |
dc.relation.references | Xu, M., Xu, M., & Tu, Q. (2021). Comparative evaluation of Vibrio delineation methodologies in postgenomic era. Environmental Microbiology Reports, 13, 209–217. https://doi.org/10.1111/1758- 2229.12928 | spa |
dc.relation.references | Zago, V., Veschetti, L., Patuzzo, C., Malerba, G., & Lleo, M. M. (2020). Resistome, mobilome and virulome analysis of shewanella algae and vibrio spp. Strains isolated in italian aquaculture centers. Microorganisms, 8(4). https://doi.org/10.3390/microorganisms8040572 | spa |
dc.relation.references | Zheng, L. L., Li, Y. X., Ding, J., Guo, X. K., Feng, K. Y., Wang, Y. J., Hu, L. Le, Cai, Y. D., Hao, P., & Chou, K. C. (2012). A comparison of computational methods for identifying virulence factors. PLoS ONE, 7(8). https://doi.org/10.1371/journal.pone.0042517 | spa |
dc.relation.references | Baker-Austin, C.; Oliver, J.D.; Alam, M.; Ali, A.; Waldor, M.K.; Qadri, F.; Martinez-Urtaza, J. Vibrio spp. infections. Nat. Rev. Dis. Primers 2018, 4, 1–19. https://doi.org/10.1038/s41572-018-0005-8. | spa |
dc.relation.references | OMS. Cólera. 2019. Available online: https://www.who.int/es/news-room/fact-sheets/detail/cholera (accessed on 25 January 2021). | spa |
dc.relation.references | CDC. Vibrio Species Causing Vibriosis. 2020. Available online: https://www.cdc.gov/vibrio/index.html (accessed on 2 February 2021). | spa |
dc.relation.references | CDC. Vibrio Species Causing Vibriosis. 2020. Available online: https://www.cdc.gov/vibrio/index.html (accessed on 2 February 2021). | spa |
dc.relation.references | Mok, J.S.; Ryu, A.; Kwon, J.Y.; Kim, B.; Park, K. Distribution of Vibrio species isolated from bivalves and bivalve culture environments along the Gyeongnam coast in Korea: Virulence and antimicrobial resistance of Vibrio parahaemolyticus isolates. Food Control 2019, 106, 106697. https://doi.org/10.1016/j.foodcont.2019.06.023. | spa |
dc.relation.references | Baker-Austin, C.; Trinanes, J.; Gonzalez-Escalona, N.; Martinez-Urtaza, J. Non-Cholera Vibrios: The Microbial Barometer of Climate Change. Trends Microbiol. 2017, 25, 76–84. https://doi.org/10.1016/j.tim.2016.09.008. | spa |
dc.relation.references | Hernández-Flórez, C.E.; Cáceres-Manrique, F.D.M. Cólera, ¿se aproxima una nueva pandemia? Med. UIS 2014, 27, 67–83. Available online: http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0121- 03192014000200008 (accessed on 12 January 2021). | spa |
dc.relation.references | Escobar, L.E.; Ryan, S.J.; Stewart-Ibarra, A.M.; Finkelstein, J.L.; King, C.A.; Qiao, H.; Polhemus, M.E. A global map of suitability for coastal Vibrio cholerae under current and future climate conditions. Acta Trop. 2015, 149, 202–211. https://doi.org/10.1016/j.actatropica.2015.05.028. | spa |
dc.relation.references | Raszl, S.M.; Froelich, B.A.; Vieira, C.R.W.; Blackwood, A.D.; Noble, R.T. Vibrio parahaemolyticus and Vibrio vulnificus in South America: Water, seafood and human infections. J. Appl. Microbiol. 2016, 121, 1201–1222. https://doi.org/10.1111/jam.13246. | spa |
dc.relation.references | López, M. Acciones de Vigilancia Intensificada de Cólera Ante Posible Reintroducción en Los Componentes de Vigilancia Epidemiológica y Laboratorio, Colombia, 2011–2012. 2012. Available online: https://www.ins.gov.co/buscadoreventos/IQEN/IQEN%20vol%2018%202013%20num%2024.pdf(accessed on 11 November 2021). | spa |
dc.relation.references | Instituto Nacional de Salud. Vigilancia Fenotípica y Genotípica de Vibrio Cholerae 2010–2013. 1–11. 2013. Available online: https://www.ins.gov.co/buscador/Informacin%20de%20laboratorio/Vigilancia%20C%C3%B3lera%20Colo mbia%202013.pdf (accessed on 10 October 2021). | spa |
dc.relation.references | Mohamad, N.; Amal MN, A.; Saad, M.Z.; Yasin, I.S.M.; Zulkiply, N.A.; Mustafa, M.; Nasruddin, N.S. Virulence-associated genes and antibiotic resistance patterns of Vibrio spp. isolated from cultured marine fishes in Malaysia. BMC Vet. Res. 2019, 15, 1–13. https://doi.org/10.1186/s12917-019-1907-8 | spa |
dc.relation.references | Bruto, M.; Labreuche, Y.; James, A.; Piel, D.; Chenivesse, S.; Petton, B.; Polz, M.F.; Le Roux, F. Ancestral gene acquisition as the key to virulence potential in environmental Vibrio populations. ISME J. 2018, 12, 2954–2966. https://doi.org/10.1038/s41396-018-0245-3. | spa |
dc.relation.references | Klein, S.; Pipes, S.; Lovell, C.R. Occurrence and significance of pathogenicity and fitness islands in environmental vibrios. AMB Express 2018, 8, 177. https://doi.org/10.1186/s13568-018-0704-2. | spa |
dc.relation.references | Nathamuni, S.; Jangam, A.K.; Katneni, V.K.; Selvaraj, A.; Krishnan, K.; Kumar, S.; Avunje, S.; Balasubramaniam, S.; Grover, M.; Alavandi, S.V.; et al. Insights on genomic diversity of Vibrio spp. through Pan-genome analysis. Ann. Microbiol. 2019, 69, 1547–1555. https://doi.org/10.1007/s13213-019-01539-7. | spa |
dc.relation.references | Mok, J.S.; Ryu, A.; Kwon, J.Y.; Park, K.; Shim, K.B. Abundance, antimicrobial resistance, and virulence of pathogenic Vibrio strains from molluscan shellfish farms along the Korean coast. Mar. Pollut. Bull. 2019, 149, 110559. https://doi.org/10.1016/j.marpolbul.2019.110559 | spa |
dc.relation.references | Thompson, F.L.; Iida, T.; Swings, J. Biodiversity of Vibrios. J. Clin. Microbiol. 2004, 68, 403–431. https://doi.org/10.1128/MMBR.68.3.403-431.2004. | spa |
dc.relation.references | Castillo, D.; Kauffman, K.; Hussain, F.; Kalatzis, P.; Rørbo, N.; Polz, M.F.; Middelboe, M. Widespread distribution of prophage-encoded virulence factors in marine Vibrio communities. Sci. Rep. 2018, 8, 2–10. https://doi.org/10.1038/s41598-018-28326-9. | spa |
dc.relation.references | Dobrindt, U.; Hochhut, B.; Hentschel, U.; Hacker, J. Genomic islands in pathogenic and environmental microorganisms. Nat. Rev. Microbiol. 2004, 2, 414–424. https://doi.org/10.1038/nrmicro884. | spa |
dc.relation.references | Nishino, K.; Senda, Y.; Yamaguchi, A. CRP regulator modulates multidrug resistance of Escherichia coli by repressing the mdtEF multidrug efflux genes. J. Antibiot. 2008, 61, 120–127. https://doi.org/10.1038/ja.2008.120. | spa |
dc.relation.references | Roig, F.J.; González-Candelas, F.; Sanjuán, E.; Fouz, B.; Feil, E.J.; Llorens, C.; Baker-Austin, C.; Oliver, J.D.; Danin-Poleg, Y.; Gibas, C.J.; et al. Phylogeny of Vibrio vulnificus from the analysis of the core-genome: Implications for intra-species taxonomy. Front. Microbiol. 2018, 8, 1–13. https://doi.org/10.3389/fmicb.2017.02613 | spa |
dc.relation.references | Thompson, C.C.; Vicente, A.C.P.; Souza, R.C.; Vasconcelos, A.T.R.; Vesth, T.; Alves, N.; Ussery, D.W.; Iida, T.; Thompson, F.L. Genomic taxonomy of vibrios. BMC Evol. Biol. 2009, 9, 1–16. https://doi.org/10.1186/1471-2148-9-258. | spa |
dc.relation.references | Gavilan, R.G.; Zamudio, M.L.; Martinez-Urtaza, J. Molecular Epidemiology and Genetic Variation of Pathogenic Vibrio parahaemolyticus in Peru. PLoS Negl. Trop. Dis. 2013, 7, e2210. https://doi.org/10.1371/journal.pntd.0002210 | spa |
dc.relation.references | Baker-Austin, C.; Jenkins, C.; Dadzie, J.; Mestanza, O.; Delgado, E.; Powell, A.; Bean, T.; Martinez-Urtaza, J. Genomic epidemiology of domestic and travel-associated Vibrio parahaemolyticus infections in the UK, 2008–2018. Food Control 2020, 115, 107244. https://doi.org/10.1016/j.foodcont.2020.107244. | spa |
dc.relation.references | Gonzalez-Escalona, N.; Gavilan, R.G.; Toro, M.; Zamudio, M.L.; Martinez-Urtaza, J. Outbreak of Vibrio parahaemolyticus sequence type 120, Peru, 2009. Emerg. Infect. Dis. 2016, 22, 1235–1237. https://doi.org/10.3201/eid2207.151896. | spa |
dc.relation.references | Velazquez-Roman, J.; León-Sicairos, N.; Hernández-Díaz, L.D.J.; Canizalez-Roman, A. Pandemic Vibrio parahaemolyticus O3: K6 on the American continent. Front. Cell. Infect. Microbiol. 2014, 3, 1–14. https://doi.org/10.3389/fcimb.2013.00110. | spa |
dc.relation.references | Boyd, E.F.; Cohen, A.L.V.; Naughton, L.M.; Ussery, D.W.; Binnewies, T.T.; Stine, O.C.; Parent, M.A. Molecular analysis of the emergence of pandemic Vibrio parahaemolyticus. BMC Microbiol. 2008, 8, 1–14. https://doi.org/10.1186/1471-2180-8-110. | spa |
dc.relation.references | Kim, Y.R.; Lee, S.E.; Kook, H.; Yeom, J.A.; Na, H.S.; Kim, S.Y.; Chung, S.S.; Choy, H.E.; Rhee, J.H. Vibrio vulnificus RTX toxin kills host cells only after contact of the bacteria with host cells. Cell. Microbiol. 2008, 10, 848–862. https://doi.org/10.1111/j.1462-5822.2007.01088.x. | spa |
dc.relation.references | Jones, M.K.; Oliver, J.D. Vibrio vulnificus: Disease and pathogenesis. Infect. Immun. 2009, 77, 1723–1733. https://doi.org/10.1128/IAI.01046-08. | spa |
dc.relation.references | Xie, Z.Y.; Hu, C.Q.; Chen, C.; Zhang, L.P.; Ren, C.H. Investigation of seven Vibrio virulence genes among Vibrio alginolyticus and Vibrio parahaemolyticus strains from the coastal mariculture systems in Guangdong, China. Lett. Appl. Microbiol. 2005, 41, 202–207. https://doi.org/10.1111/j.1472-765X.2005.01688.x. | spa |
dc.relation.references | Hernández-Robles, M.F.; Álvarez-Contreras, A.K.; Juárez-García, P.; Natividad-Bonifacio, I.; CurielQuesada, E.; Vázquez-Salinas, C.; Quiñones-Ramírez, E.I. Virulence factors and antimicrobial resistance in environmental strains of Vibrio alginolyticus. Int. Microbiol. 2016, 19, 191–198. https://doi.org/10.2436/20.1501.01.277 | spa |
dc.relation.references | Osorio, C.R. T3SS effectors in Vibrios: Homology in sequence, diversity in biological functions? Virulence 2018, 9, 721–723. https://doi.org/10.1080/21505594.2018.1435965. | spa |
dc.relation.references | Song, J.; Liu, X.; Wu, C.; Zhang, Y.; Fan, K.; Zhang, X.; Wei, Y. Isolation, identification and pathogenesis study of Vibrio diabolicus. Aquaculture 2021, 533, 736043. https://doi.org/10.1016/j.aquaculture.2020.736043 | spa |
dc.relation.references | Chibani, C.M.; Roth, O.; Liesegang, H.; Wendling, C.C. Genomic variation among closely related Vibrio alginolyticus strains is located on mobile genetic elements. BMC Genom. 2020, 21, 1–14. https://doi.org/10.1186/s12864-020-6735-5 | spa |
dc.relation.references | Ramamurthy, T.; Chowdhury, G.; Pazhani, G.P.; Shinoda, S. Vibrio fluvialis: An emerging human pathogen. Front. Microbiol. 2014, 5, 1–8. https://doi.org/10.3389/fmicb.2014.00091. | spa |
dc.relation.references | Liu, X.; Pan, J.; Gao, H.; Han, Y.; Zhang, A.; Huang, Y.; Liu, P.; Kan, B.; Liang, W. CqsA/LuxS-HapR Quorum sensing circuit modulates type VI secretion system VflT6SS2 in Vibrio fluvialis. Emerg. Microbes Infect. 2021, 10, 589–601. https://doi.org/10.1080/22221751.2021.1902244. | spa |
dc.relation.references | Liu, M.; Li, X.; Xie, Y.; Bi, D.; Sun, J.; Li, J.; Tai, C.; Deng, Z.; Ou, H.Y. ICEberg 2.0: An updated database of bacterial integrative and conjugative elements. Nucleic Acids Res. 2019, 47, D660–D665. https://doi.org/10.1093/nar/gky1123. | spa |
dc.relation.references | Cattoir, V.; Poirel, L.; Mazel, D.; Soussy, C.J.; Nordmann, P. Vibrio splendidus as the source of plasmidmediated QnrS-like quinolone resistance determinants. Antimicrob. Agents Chemother. 2007, 51, 2650–2651. https://doi.org/10.1128/AAC.00070-07. | spa |
dc.relation.references | Sarkar, A.; Morita, D.; Ghosh, A.; Chowdhury, G.; Mukhopadhyay, A.K.; Okamoto, K.; Ramamurthy, T. Altered Integrative and Conjugative Elements (ICEs) in Recent Vibrio cholerae O1 Isolated From Cholera Cases, Kolkata, India. Front. Microbiol. 2019, 10, 1–13. https://doi.org/10.3389/fmicb.2019.02072 | spa |
dc.relation.references | Loo, K.Y.; Letchumanan, V.; Law, J.W.F.; Pusparajah, P.; Goh, B.H.; Ab Mutalib, N.S.; He, Y.W.; Lee, L.H. Incidence of antibiotic resistance in Vibrio spp. Rev. Aquac. 2020, 12, 2590–2608. https://doi.org/10.1111/raq.12460. | spa |
dc.relation.references | Paul, B.; Dixit, G.; Murali, T.S.; Satyamoorthy, K. Genome Based Taxonomic Classification. Genome 2019, 62, 1–17. https://doi.org/https://doi.org/10.1139/gen-2018-0072. | spa |
dc.relation.references | Lepuschitz, S.; Baron, S.; Larvor, E.; Granier, S.A.; Pretzer, C.; Mach, R.L.; Farnleitner, A.H.; Ruppitsch, W.; Pleininger, S.; Indra, A.; et al. Phenotypic and Genotypic Antimicrobial Resistance Traits of Vibrio cholerae Non-O1/Non-O139 Isolated From a Large Austrian Lake Frequently Associated With Cases of Human Infection. Front. Microbiol. 2019, 10, 1–9. https://doi.org/10.3389/fmicb.2019.02600 | spa |
dc.relation.references | Gennari, M.; Ghidini, V.; Caburlotto, G.; Lleo, M.M. Virulence genes and pathogenicity islands in environmental Vibrio strains nonpathogenic to humans. FEMS Microbiol. Ecol. 2012, 82, 563–573. https://doi.org/10.1111/j.1574-6941.2012.01427.x | spa |
dc.relation.references | Sánchez, L.P.; Martínez, M.; León, T.; Córdoba, T.; Díaz, P.; Calvo, M.; Montaño, A.; Escandón, P.; Narváez, S.; Vivas, J.; et al. Desarrollo e Implementación de una PCR Multiplex Para la Detección de Cuatro Especies de Vibrio spp. Biomédica, Volume 39. 2019. Available online: https://revistabiomedica.org/index.php/biomedica/issue/download/171/58 (accessed on 8 September 2021). | spa |
dc.relation.references | Instituto Nacional de Salud. Manual de Procedimientos Para la Toma, Conservación y Envío de Muestras al Laboratorio Nacional de Referencia. Dirección Redes en Salud Pública. Available online: https://www.ins.gov.co/Direcciones/RedesSaludPublica/DocumentosdeInteresSRNL/Manual_toma_envi o_muestras_INS-2019.pdf (accessed on 20 September 2021) | spa |
dc.relation.references | Williams; Wilkins. Bergey’s Manual of Systematic Bacteriology. In The Proteobacteria, 2nd ed.; Garrity, G., Ed.; Springer-Verlag US, 1984; Volume 2. | spa |
dc.relation.references | Instituto Nacional de Salud Dirección Redes en Salud Pública. Guía Para la Vigilancia por Laboratorio de Vibrio Cholerae (p. 17). Dirección Redes en Salud Pública. 2017. Available online: https://www.ins.gov.co/buscadoreventos/Informacin%20de%20laboratorio/Gu%C3%ADa%20para%20la%20vigilancia%20por%20laborato rio%20de%20Vibrio%20cholerae.pdf (accessed on 11 November 2021). | spa |
dc.relation.references | Menzel, P.; Ng, K.L.; Krogh, A. Fast and sensitive taxonomic classification for metagenomics with Kaiju. Nat. Commun. 2016, 7, 11257. https://doi.org/10.1038/ncomms11257. | spa |
dc.relation.references | Ondov, B.D.; Bergman, N.H.; Phillippy, A.M. Interactive metagenomic visualization in a Web browser. BMC Bioinform. 2011, 12, 385. https://doi.org/10.1186/1471-2105-12-385. | spa |
dc.relation.references | Li, H. Seqtk. 2013. Available online: https://github.com/lh3/seqtk (accessed on 17 August 2021). | spa |
dc.relation.references | Lischer, H.E.L.; Shimizu, K.K. Reference-guided de novo assembly approach improves genome reconstruction for related species. BMC Bioinform. 2017, 18, 1–12. https://doi.org/10.1186/s12859-017-1911- 6 | spa |
dc.relation.references | Bankevich, A.; Nurk, S.; Antipov, D.; Gurevich, A.A.; Dvorkin, M.; Kulikov, A.S.; Lesin, V.M.; Nikolenko, S.I.; Pham, S.; Prjibelski, A.D.; et al. SPAdes: A new genome assembly algorithm and its applications to single-cell sequencing. J. Comput. Biol. A J. Comput. Mol. Cell Biol. 2012, 19, 455–477. https://doi.org/10.1089/cmb.2012.0021. | spa |
dc.relation.references | Andrews; Simon. FastQC: A Quality Control Tool for High Throughput Sequence Data. 2017. Available online: http://www.bioinformatics.babraham.ac.uk/projects/fastqc (accessed on 10 January 2021). | spa |
dc.relation.references | Ewels, P.; Magnusson, M.; Lundin, S.; Käller, M. MultiQC: Summarize analysis results for multiple tools and samples in a single report. Bioinformatics 2016, 32, 3047–3048. https://doi.org/10.1093/bioinformatics/btw354. | spa |
dc.relation.references | Bolger, A.M.; Lohse, M.; Usadel, B. Trimmomatic: A flexible trimmer for Illumina sequence data. Bioinformatics 2014, 30, 2114–2120. https://doi.org/10.1093/bioinformatics/btu170. | spa |
dc.relation.references | Langmead, B.; Salzberg, S.L. Fast gapped-read alignment with Bowtie 2. Nat. Methods 2012, 9, 357–359. https://doi.org/10.1038/nmeth.1923. | spa |
dc.relation.references | Li, H.; Handsaker, B.; Wysoker, A.; Fennell, T.; Ruan, J.; Homer, N.; Marth, G.; Abecasis, G.; Durbin, R. The Sequence Alignment/Map format and SAMtools. Bioinformatics 2009, 25, 2078–2079. https://doi.org/10.1093/bioinformatics/btp352 | spa |
dc.relation.references | Quinlan, A.R.; Hall, I.M. BEDTools: A flexible suite of utilities for comparing genomic features. Bioinformatics 2010, 26, 841–842. https://doi.org/10.1093/bioinformatics/btq033. | spa |
dc.relation.references | Li, H. A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data. Bioinformatics 2011, 27, 2987–2993. https://doi.org/10.1093/bioinformatics/btr509. | spa |
dc.relation.references | Pop, M.; Phillippy, A.; Delcher, A.L.; Salzberg, S.L. Comparative genome assembly. Brief. Bioinform. 2004, 5, 237–248. https://doi.org/10.1093/bib/5.3.237 | spa |
dc.relation.references | Van der Auwera, G.A.; Carneiro, M.O.; Hartl, C.; Poplin, R.; Del Angel, G.; Levy-Moonshine, A.; Jordan, T.; Shakir, K.; Roazen, D.; Thibault, J.; et al. From FastQ data to high confidence variant calls: The Genome Analysis Toolkit best practices pipeline. Curr. Protoc. Bioinform. 2013, 43, 11.10.1–11.10.33. https://doi.org/10.1002/0471250953.bi1110s43 | spa |
dc.relation.references | McKenna, A.; Hanna, M.; Banks, E.; Sivachenko, A.; Cibulskis, K.; Kernytsky, A.; Garimella, K.; Altshuler, D.; Gabriel, S.; Daly, M.; et al. The Genome Analysis Toolkit: A MapReduce framework for analyzing nextgeneration DNA sequencing data. Genome Res. 2010, 20, 1297–1303. https://doi.org/10.1101/gr.107524.110. | spa |
dc.relation.references | Delcher, A.L.; Salzberg, S.L.; Phillippy, A.M. Using MUMmer to identify similar regions in large sequence sets. Curr. Protoc. Bioinform. 2003, 10.3.1–10.3.18. https://doi.org/10.1002/0471250953.bi1003s00. | spa |
dc.relation.references | Luo, R.; Liu, B.; Xie, Y.; Li, Z.; Huang, W.; Yuan, J.; He, G.; Chen, Y.; Pan, Q.; Liu, Y.; et al. SOAPdenovo2: An empirically improved memory-efficient short-read de novo assembler. GigaScience 2012, 1, 18. https://doi.org/10.1186/2047-217X-1-18. | spa |
dc.relation.references | Gurevich, A.; Saveliev, V.; Vyahhi, N.; Tesler, G. QUAST: Quality assessment tool for genome assemblies. Bioinformatics 2013, 29, 1072–1075. https://doi.org/10.1093/bioinformatics/btt086. | spa |
dc.relation.references | Simão, F.A.; Waterhouse, R.M.; Ioannidis, P.; Kriventseva, E.V.; Zdobnov, E.M. BUSCO: Assessing genome assembly and annotation completeness with single-copy orthologs. Bioinformatics 2015, 31, 3210–3212. https://doi.org/10.1093/bioinformatics/btv351. | spa |
dc.relation.references | Jain, C.; Rodriguez-R, L.M.; Phillippy, A.M.; Konstantinidis, K.T.; Aluru, S. High throughput ANI analysis of 90K prokaryotic genomes reveals clear species boundaries. Nat. Commun. 2018, 9, 1–8. https://doi.org/10.1038/s41467-018-07641-9. | spa |
dc.relation.references | Wickham, H. Ggplot2. Wiley Interdiscip. Rev. Comput. Stat. 2011, 3, 180–185. https://doi.org/10.1002/wics.147. | spa |
dc.relation.references | GitHub—Tseemann/Mlst: Scan Contig Files against PubMLST Typing Schemes. Available online: https://github.com/tseemann/mlst (accessed on 18 August 2021). | spa |
dc.relation.references | Jolley, K.A.; Bray, J.E.; Maiden, M.C.J. Open-access bacterial population genomics: BIGSdb software, the PubMLST.org website and their applications. Wellcome Open Res. 2018, 3, 1–20. https://doi.org/10.12688/wellcomeopenres.14826.1 | spa |
dc.relation.references | Treangen, T.J.; Ondov, B.D.; Koren, S.; Phillippy, A.M. The harvest suite for rapid core-genome alignment and visualization of thousands of intraspecific microbial genomes. Genome Biol. 2014, 15, 1–15. https://doi.org/10.1186/s13059-014-0524-x | spa |
dc.relation.references | Nguyen, L.T.; Schmidt, H.A.; Von Haeseler, A.; Minh, B.Q. IQ-TREE: A fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 2015, 32, 268–274. https://doi.org/10.1093/molbev/msu300. | spa |
dc.relation.references | Release FigTree v1.4.4 · Rambaut/Figtree · GitHub. Available online: https://github.com/rambaut/figtree/releases/tag/v1.4.4 (accessed on 20 August 2021). | spa |
dc.relation.references | Eren, A.M.; Esen, O.C.; Quince, C.; Vineis, J.H.; Morrison, H.G.; Sogin, M.L.; Delmont, T.O. Anvi’o: An advanced analysis and visualization platformfor’omics data. PeerJ 2015, 2015, 1–29. https://doi.org/10.7717/peerj.1319. | spa |
dc.relation.references | Tatusov, R.L.; Galperin, M.Y.; Natale, D.A.; Koonin, E.V. The COG database: A tool for genome-scale analysis of protein functions and evolution. Nucleic Acids Res. 2000, 28, 33–36. https://doi.org/10.1093/nar/28.1.33. | spa |
dc.relation.references | Shaiber, A.; Willis, A.D.; Delmont, T.O.; Roux, S.; Chen, L.X.; Schmid, A.C.; Yousef, M.; Watson, A.R.; Lolans, K.; Esen, Ö.C.; et al. Functional and genetic markers of niche partitioning among enigmatic members of the human oral microbiome. BioRxiv 2020, 1–35. https://doi.org/10.1101/2020.04.29.069278. | spa |
dc.relation.references | GitHub—Tseemann/Abricate: Mass Screening of Contigs for Antimicrobial and Virulence Genes. Available online: https://github.com/tseemann/abricate (accessed on 18 August 2021). | spa |
dc.relation.references | Feldgarden, M.; Brover, V.; Haft, D.H.; Prasad, A.B.; Slotta, D.J.; Tolstoy, I.; Tyson, G.H.; Zhao, S.; Hsu, C.H.; McDermott, P.F.; et al. Validating the AMRFINder tool and resistance gene database by using antimicrobial resistance genotype-phenotype correlations in a collection of isolates. Antimicrob. Agents Chemother. 2019, 63. https://doi.org/10.1128/AAC.00483-19. | spa |
dc.relation.references | Jia, B.; Raphenya, A.R.; Alcock, B.; Waglechner, N.; Guo, P.; Tsang, K.K.; Lago, B.A.; Dave, B.M.; Pereira, S.; Sharma, A.N.; et al. CARD 2017: Expansion and model-centric curation of the comprehensive antibiotic resistance database. Nucleic Acids Res. 2017, 45, D566–D573. https://doi.org/10.1093/NAR/GKW1004. | spa |
dc.relation.references | Liu, B.; Zheng, D.; Jin, Q.; Chen, L.; Yang, J. VFDB 2019: A comparative pathogenomic platform with an interactive web interface. Nucleic Acids Res. 2019, 47, D687–D692. https://doi.org/10.1093/nar/gky1080. | spa |
dc.relation.references | Hernández, M., Quijada, N. M., Rodríguez-Lázaro, D., & Eiros, J. M. (2020). Bioinformatics of next generation sequencing in clinical microbiology diagnosis. Revista Argentina de Microbiologia, 52(2), 150–161. https://doi.org/10.1016/j.ram.2019.06.003 | spa |
dc.rights.accessrights | info:eu-repo/semantics/closedAccess | spa |
dc.rights.accessrights | info:eu-repo/semantics/closedAccess | spa |
dc.rights.accessrights | info:eu-repo/semantics/closedAccess | spa |
dc.rights.accessrights | info:eu-repo/semantics/closedAccess | spa |
dc.subject.proposal | Vibriosis | spa |
dc.subject.proposal | Virulencia | spa |
dc.subject.proposal | Resistencia | spa |
dc.subject.proposal | Genómica comparativa | spa |
dc.subject.proposal | Salud pública | spa |
dc.subject.proposal | Vibriosis | eng |
dc.subject.proposal | Virulence | eng |
dc.subject.proposal | Antibiotic resistance | eng |
dc.subject.proposal | Antibiotic resistance | eng |
dc.subject.proposal | Pangenome | eng |
dc.subject.proposal | Whole genome sequencing | eng |
dc.subject.unesco | Microorganismo | |
dc.subject.unesco | Microbiología | |
dc.type.coar | http://purl.org/coar/resource_type/c_bdcc | spa |
dc.type.content | Text | spa |
dc.type.driver | info:eu-repo/semantics/masterThesis | spa |
dc.type.version | info:eu-repo/semantics/publishedVersion | spa |
oaire.version | http://purl.org/coar/version/c_ab4af688f83e57aa | spa |
oaire.accessrights | http://purl.org/coar/access_right/c_f1cf | spa |
dc.description.degreename | Magister en Bioinformática y Biología Computacional (EN CONVENIO) | spa |
dc.publisher.program | Maestría en Bioinformática y Biología Computacional (En convenio) | spa |
dc.rights.coar | http://purl.org/coar/access_right/c_14cb | spa |