Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease

Se realizó una primera caracterización del bacterioma intestinal de triatominos capturados en condiciones naturales en Colombia dada la falta de información sobre este bacterioma y los cambios que puede tener cuando Trypanosoma cruzi está presente o la fuente alimenticia del insecto cambia

Autores:

Tipo de recurso:

Fecha de publicación:: 2019

Institución:: Universidad del Rosario

Repositorio:: Repositorio EdocUR - U. Rosario

Idioma:: spa

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network_acronym_str	EDOCUR2
network_name_str	Repositorio EdocUR - U. Rosario
repository_id_str
dc.title.spa.fl_str_mv	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
title	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
spellingShingle	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease Secuenciación de última generación Bacterioma Triatominae Trypanosoma cruzi Fuente alimenticia Enfermedades Next-generation sequencing Bacteriome Triatominae Trypanosoma cruzi Feeding source Enfermedad de chagas Hemipteros
title_short	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
title_full	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
title_fullStr	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
title_full_unstemmed	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
title_sort	Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease
dc.contributor.advisor.none.fl_str_mv	Ramírez, Juan David
dc.subject.spa.fl_str_mv	Secuenciación de última generación Bacterioma Triatominae Trypanosoma cruzi Fuente alimenticia
topic	Secuenciación de última generación Bacterioma Triatominae Trypanosoma cruzi Fuente alimenticia Enfermedades Next-generation sequencing Bacteriome Triatominae Trypanosoma cruzi Feeding source Enfermedad de chagas Hemipteros
dc.subject.ddc.spa.fl_str_mv	Enfermedades
dc.subject.keyword.spa.fl_str_mv	Next-generation sequencing Bacteriome Triatominae Trypanosoma cruzi Feeding source
dc.subject.lemb.spa.fl_str_mv	Enfermedad de chagas Hemipteros
description	Se realizó una primera caracterización del bacterioma intestinal de triatominos capturados en condiciones naturales en Colombia dada la falta de información sobre este bacterioma y los cambios que puede tener cuando Trypanosoma cruzi está presente o la fuente alimenticia del insecto cambia
publishDate	2019
dc.date.accessioned.none.fl_str_mv	2019-02-11T19:12:51Z
dc.date.available.none.fl_str_mv	2019-02-11T19:12:51Z
dc.date.created.none.fl_str_mv	2019-02-05
dc.date.issued.none.fl_str_mv	2019
dc.type.eng.fl_str_mv	bachelorThesis
dc.type.coar.fl_str_mv	http://purl.org/coar/resource_type/c_7a1f
dc.type.document.spa.fl_str_mv	Artículo
dc.type.spa.spa.fl_str_mv	Trabajo de grado
dc.identifier.doi.none.fl_str_mv	https://doi.org/10.48713/10336_19038
dc.identifier.uri.none.fl_str_mv	http://repository.urosario.edu.co/handle/10336/19038
url	https://doi.org/10.48713/10336_19038 http://repository.urosario.edu.co/handle/10336/19038
dc.language.iso.none.fl_str_mv	spa
language	spa
dc.rights.spa.fl_str_mv	Atribución-NoComercial-SinDerivadas 2.5 Colombia Atribución-NoComercial-SinDerivadas 2.5 Colombia
dc.rights.coar.fl_str_mv	http://purl.org/coar/access_right/c_abf2
dc.rights.acceso.spa.fl_str_mv	Abierto (Texto Completo)
dc.rights.uri.none.fl_str_mv	http://creativecommons.org/licenses/by-nc-nd/2.5/co/
rights_invalid_str_mv	Atribución-NoComercial-SinDerivadas 2.5 Colombia Abierto (Texto Completo) http://creativecommons.org/licenses/by-nc-nd/2.5/co/ http://purl.org/coar/access_right/c_abf2
dc.format.mimetype.none.fl_str_mv	application/pdf
dc.publisher.spa.fl_str_mv	Universidad del Rosario
dc.publisher.department.spa.fl_str_mv	Facultad de Ciencias Naturales y Matemáticas
dc.publisher.program.spa.fl_str_mv	Biología
institution	Universidad del Rosario
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Montoya-Porras LM, Omar T-C, Alzate JF, Moreno-Herrera CX, Cadavid-Restrepo GE. 16S rRNA gene amplicon sequencing reveals dominance of Actinobacteria in Rhodnius pallescens compared with Triatoma maculata midgut microbiota in natural populations of vector insects from Colombia. Acta Trop. 2018;178:327–32. Pompanon F, Deagle BE, Symondson WO, Brown DS, Jarman SN, Taberlet P. Who is eating what: diet assessment using next generation sequencing. Mol Ecol. 2012;21:1931–50. Noireau F, Abad-Franch F, Valente SA, Dias-Lima A, Lopes CM, Cunha V, et al. Trapping Triatominae in silvatic habitats. Mem Inst Oswaldo Cruz. 2002;97:61–3. Duffy T, Cura CI, Ramirez JC, Abate T, Cayo NM, Parrado R, et al. Analytical performance of a multiplex real-time PCR assay using TaqMan probes for quantification of Trypanosoma cruzi satellite DNA in blood samples. PLoS Negl Trop Dis. 2013;7:e2000. Ramirez JD, Guhl F, Umezawa ES, Morillo CA, Rosas F, Marin-Neto JA, et al. Evaluation of adult chronic Chagas’ heart disease diagnosis by molecular and serological methods. J Clin Microbiol. 2009;47:3945–51. Sadowsky MJ, Staley C, Heiner C, Hall R, Kelly CR, Brandt L, et al. Analysis of gut microbiota – An ever changing landscape. Gut Microbes 2017;8:268–75. Caporaso JG, Kuczynski J, Stombaugh J, Bittinger K, Bushman FD, Costello EK, et al. QIIME allows analysis of high-throughput community sequencing data. Nat Methods 2010;7:335–6. Pellecer MJ, Dorn PL, Bustamante DM, Rodas A, Monroy MC. Vector blood meals are an early indicator of the effectiveness of the Ecohealth approach in halting Chagas transmission in Guatemala. Am J Trop Med Hyg. 2013;88:638–44. Waleckx E, Suarez J, Richards B, Dorn PL. Triatoma sanguisuga blood meals and potential for Chagas disease, Louisiana, USA. Emerg Infect Dis. 2014;20:2141–3. Wang Q, Garrity GM, Tiedje JM, Cole JR. Naive Bayesian classifier for rapid assignment of rRNA sequences into the new bacterial taxonomy. Appl Environ Microbiol. 2007;73:5261–7. Caporaso JG, Bittinger K, Bushman FD, DeSantis TZ, Andersen GL, Knight R. PyNAST: a flexible tool for aligning sequences to a template alignment. Bioinformatics 2010;26:266–7. Edgar RC. Search and clustering orders of magnitude faster than BLAST. Bioinformatics 2010;26:2460–1. Krzywinski M, Schein J, Birol I, Connors J, Gascoyne R, Horsman D, et al. Circos: An information aesthetic for comparative genomics. Genome Res. 2009;19:1639–45. Silva MBA, Menezes KR, Farias MCG, Andrade MS, Victor CCA, Lorosa ES, et al. Description of the feeding preferences of triatominae in the Chagas disease surveillance study for the State of Pernambuco, Brazil (Hemiptera: Reduviidae). Rev Soc Bras Med Trop. 2017;50:543–546. Oliveira JL, Cury JC, Gurgel-Gonçalves R, Bahia AC, Monteiro FA. Field-collected Triatoma sordida from central Brazil display high microbiota diversity that varies with regard to developmental stage and intestinal segmentation. PLoS Negl Trop Dis. 2018;12:e0006709. Engel P, Moran NA. The gut microbiota of insects – diversity in structure and function. FEMS Microbiol Rev. 2013;37:699–735. Vieira CS, Waniek PJ, Castro DP, Mattos DP, Moreira OC, Azambuja P. Impact of Trypanosoma cruzi on antimicrobial peptide gene expression and activity in the fat body and midgut of Rhodnius prolixus. Parasit Vectors 2016;9:119. Yun J-H, Roh SW, Whon TW, Jung MJ, Kim MS, Park DS, et al. Insect gut bacterial diversity determined by environmental habitat, diet, developmental stage, and phylogeny of host. Appl Environ Microbiol. 2014;80:5254–64. Garcia ES, Castro DP, Figueiredo MB, Azambuja P. Immune homeostasis to microorganisms in the guts of triatomines (Reduviidae)--a review. Mem Inst Oswaldo Cruz. 2010;105:605–10. Ventura M, Canchaya C, Tauch A, Chandra G, Fitzgerald GF, Chater KF, et al. Genomics of Actinobacteria: Tracing the evolutionary history of an ancient phylum. Microbiol Mol Biol Rev. 2007;71:495–548. Shin N-R, Whon TW, Bae J-W. Proteobacteria: microbial signature of dysbiosis in gut microbiota. Trends Biotechnol. 2015;33:496–503. Bradley PH, Pollard KS. Proteobacteria explain significant functional variability in the human gut microbiome. Microbiome 2017;5:36. Wexler HM. Bacteroides: the Good, the Bad, and the Nitty-Gritty. Clin Microbiol Rev. 2007;20:593–621. Thomas F, Hehemann J-H, Rebuffet E, Czjzek M, Michel G. Environmental and gut bacteroidetes: the food connection. Front Microbiol. 2011;2:93. Ramakrishna BS. Role of the gut microbiota in human nutrition and metabolism. J Gastroenterol Hepatol. 2013;28:9–17. Salem H, Kreutzer E, Sudakaran S, Kaltenpoth M. Actinobacteria as essential symbionts in firebugs and cotton stainers (Hemiptera, Pyrrhocoridae). Environ Microbiol. 2013;15:1956–68. Wang X, Liu T, Wu Y, Zhong D, Zhou G, Su X, et al. Bacterial microbiota assemblage in Aedes albopictus mosquitoes and its impacts on larval development. Mol Ecol. 2018;27:2972–85. Hehemann J-H, Correc G, Barbeyron T, Helbert W, Czjzek M, Michel G. Transfer of carbohydrate-active enzymes from marine bacteria to Japanese gut microbiota. Nature 2010;464:908–12. Pais R, Lohs C, Wu Y, Wang J, Aksoy S. The obligate mutualist Wigglesworthia glossinidia influences reproduction, digestion, and immunity processes of its host, the Tsetse fly. Appl Environ Microbiol. 2008;74:5965–74. Weiss BL, Maltz M, Aksoy S. Obligate symbionts activate immune system evelopment in the Tsetse fly. J Immunol. 2012;188:3395–403. Engel P, Martinson VG, Moran NA. Functional diversity within the simple gut microbiota of the honey bee. Proc Natl Acad Sci U S A. 2012;109:11002–7. Villegas LM, Pimenta PFP. Metagenomics, paratransgenesis and the Anopheles microbiome: a portrait of the geographical distribution of the anopheline microbiota based on a meta-analysis of reported taxa. Mem Inst Oswaldo Cruz. 2014;109:672–84. Espino CI, Gómez T, González G, Brazil do Santos MF, Solano J, Sousa O, et al. 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Malacrinò A, Schena L, Campolo O, Laudani F, Mosca S, Giunti G. A metabarcoding survey on the fungal microbiota associated to the olive fruit fly. Microb Ecol. 2017;73:677–84. Duarte APM, Ferro M, Rodrigues A, Bacci M Jr, Nagamoto NS, Forti LC, et al. Prevalence of the genus Cladosporium on the integument of leaf-cutting ants characterized by 454 pyrosequencing. Antonie Van Leeuwenhoek 2016;109:1235–43. Lage-Moraes AM, Reis-de-Figueiredo A, Vieira-Junqueira AC, Lara-da-Costa G, Aguiar RK, Cunha-de-Oliveira P. Fungal flora of the digestive tract of Panstrongylus megistus (Reduviidae) used for experimental xenodiagnosis of Trypanosoma (Schizotripanum) cruzi Chagas, 1909. Rev Iberoam Micol. 2001;18:79–82. Moraes AML de, Junqueira ACV, Celano V, Lara da Costa G, Rodrigues Coura J. Fungal flora of the digestive tract of Rhodnius prolixus, Rhodnius neglectus, Diptelanogaster maximus and Panstrongylus megistus, vectors of Trypanosoma cruzi, Chagas, 1909. 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spelling	Ramírez, Juan David1011716118600Arias-Giraldo, Luisa M.Muñoz, Claudia MarinaHernández Castro, Diana CarolinaHerrera Ossa, Giovanny AndrésCaicedo Garzón, ValentinaVelásquez-Ortiz, NataliaCantillo, OmarUrbano, PlutarcoBiólogoFull time9325ec59-afd4-44a7-8f36-99f36e34797a600966e0593-a04b-498b-81d7-a39434da9caf600f401d21c-a327-4fc5-9043-0963b38c932e600db65c9d8-a7e8-4f0e-84e7-d5b2655cc062600578e3d3c-f2f9-46c9-b26d-a86520d4698360030f14eb2-f36a-4a70-bc45-ab294c25876660080f15593-2cd2-4c43-b949-8694a201fb2e6007a058964-b13e-4d0d-9ed5-d4f0668ba0146002019-02-11T19:12:51Z2019-02-11T19:12:51Z2019-02-052019Se realizó una primera caracterización del bacterioma intestinal de triatominos capturados en condiciones naturales en Colombia dada la falta de información sobre este bacterioma y los cambios que puede tener cuando Trypanosoma cruzi está presente o la fuente alimenticia del insecto cambiaWe provide a first characterization of the gut bacteriome of triatomines captured in natural conditions in Colombia given the lack of information about this bacteriome and the possible changes it can undergo when Trypanosoma cruzi is present or the feeding source of the triatomine varies2021-02-12 01:01:01: Script de automatizacion de embargos. info:eu-repo/date/embargoEnd/2021-02-11application/pdfhttps://doi.org/10.48713/10336_19038 http://repository.urosario.edu.co/handle/10336/19038spaUniversidad del RosarioFacultad de Ciencias Naturales y MatemáticasBiologíaAtribución-NoComercial-SinDerivadas 2.5 ColombiaAtribución-NoComercial-SinDerivadas 2.5 ColombiaAbierto (Texto Completo)EL AUTOR, manifiesta que la obra objeto de la presente autorización es original y la realizó sin violar o usurpar derechos de autor de terceros, por lo tanto la obra es de exclusiva autoría y tiene la titularidad sobre la misma.http://creativecommons.org/licenses/by-nc-nd/2.5/co/http://purl.org/coar/access_right/c_abf2Rassi A, Rassi A, Marin-Neto JA. 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Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera : Reduviidae), vectors of Chagas disease

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