Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia

Presentamos la primera aproximación de diversidad genética, relaciones filogenéticas y estructura poblacional de Panstrongylus geniculatus en Colombia. Compilamos un amplio muestreo para construir una filogenia y estimar la estructura genética de las poblaciones encontradas.

Detalles Bibliográficos
Autor Principal: Caicedo Garzón, Valentina
Otros Autores: Ramírez, Juan David
Formato: Trabajo de grado (Bachelor Thesis)
Lenguaje:Español (Spanish)
Publicado: Universidad del Rosario 2019
Materias:
Acceso en línea:http://repository.urosario.edu.co/handle/10336/19037
id ir-10336-19037
recordtype dspace
institution EdocUR - Universidad del Rosario
collection DSpace
language Español (Spanish)
topic Panstrongylus geniculatus
Triatominae
Dispersión
Diversificación genética
Enfermedad de Chagas
Enfermedades
Enfermedad de chagas
Trypanosoma cruzi
Panstrongylus geniculatus
Dispersal
Triatominae
Chagas disease
Genetic diversification
spellingShingle Panstrongylus geniculatus
Triatominae
Dispersión
Diversificación genética
Enfermedad de Chagas
Enfermedades
Enfermedad de chagas
Trypanosoma cruzi
Panstrongylus geniculatus
Dispersal
Triatominae
Chagas disease
Genetic diversification
Caicedo Garzón, Valentina
Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia
description Presentamos la primera aproximación de diversidad genética, relaciones filogenéticas y estructura poblacional de Panstrongylus geniculatus en Colombia. Compilamos un amplio muestreo para construir una filogenia y estimar la estructura genética de las poblaciones encontradas.
author2 Ramírez, Juan David
author_facet Ramírez, Juan David
Caicedo Garzón, Valentina
format Trabajo de grado (Bachelor Thesis)
author Caicedo Garzón, Valentina
author_sort Caicedo Garzón, Valentina
title Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia
title_short Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia
title_full Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia
title_fullStr Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia
title_full_unstemmed Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia
title_sort spatial diversification of panstrongylus geniculatus (reduviidae : triatominae) in colombia
publisher Universidad del Rosario
publishDate 2019
url http://repository.urosario.edu.co/handle/10336/19037
_version_ 1694382534073253888
spelling ir-10336-190372021-02-11T06:01:01Z Spatial diversification of Panstrongylus geniculatus (Reduviidae : Triatominae) in Colombia Caicedo Garzón, Valentina Ramírez, Juan David Salazar, Camilo Salgado Roa, Fabian Camilo Sanchez-Herrera, Melissa Hernández Castro, Carolina Arias Giraldo, Luisa María Garcia, Lineth Vallejo, Gustavo Cantillo, Omar Tovar, Catalina Aristeu da Rosa, Joao Carrasco, Hernán Panstrongylus geniculatus Triatominae Dispersión Diversificación genética Enfermedad de Chagas Enfermedades Enfermedad de chagas Trypanosoma cruzi Panstrongylus geniculatus Dispersal Triatominae Chagas disease Genetic diversification Presentamos la primera aproximación de diversidad genética, relaciones filogenéticas y estructura poblacional de Panstrongylus geniculatus en Colombia. Compilamos un amplio muestreo para construir una filogenia y estimar la estructura genética de las poblaciones encontradas. We present the first approximation of genetic diversity, phylogenetic relationships and population structure of Panstrongylus geniculatus in Colombia. We compiled an extensive sampling to construct a phylogeny and estimate the genetic structure of the populations found. 2019-10-08 12:50:01: Script de automatizacion de embargos. Correo recibido el jueves 7 feb 2019 El día de ayer subí mi tesis de pregrado al repositorio y solicité el acceso restringido debido a que estamos en proceso de someter el artículo a la revista "Plos Neglected Tropical Diseases". Está revista es de acceso libre, sin embargo, nos gustaría proteger los derechos de autor durante el tiempo de revisión del artículo. De ante mano muchas gracias, Valentina Caicedo Garzón Respuesta correo 7 deb 2019 Hemos recibido su solicitud, al momento de realizar la publicación del documento agregaremos el embargo solicitado. Le recordamos que los embargos se realizan por un periodo de tiempo de dos años, si usted desea al finalizar este tiempo puede volver a solicitar el embargo por otro periodo igual. Tenga en cuenta que los documentos en acceso abierto propician una mejor visibilidad de su producción académica y científica, y la Universidad del Rosario es pionera en la región en políticas de acceso abierto. Se recibió una llamada de Valentina el 8 de octubre de 2019 diciendo que el documento se encuentra completo en Semantic Scholar. Se descarga, se cambia el nombre y se vuelve a embargar 2021-02-11 01:01:01: Script de automatizacion de embargos. info:eu-repo/date/embargoEnd/2021-02-11 2019-02-05 2019-02-11T17:36:47Z info:eu-repo/semantics/bachelorThesis info:eu-repo/semantics/acceptedVersion http://repository.urosario.edu.co/handle/10336/19037 spa Atribución-NoComercial-SinDerivadas 2.5 Colombia Atribución-NoComercial-SinDerivadas 2.5 Colombia http://creativecommons.org/licenses/by-nc-nd/2.5/co/ info:eu-repo/semantics/openAccess application/pdf Universidad del Rosario Biología Facultad de Ciencias Naturales y Matemáticas instname:Universidad del Rosario reponame:Repositorio Institucional EdocUR Hernández C, Salazar C, Brochero H, Teherán A, Buitrago LS, Vera M, et al. Untangling the transmission dynamics of primary and secondary vectors of Trypanosoma cruzi in Colombia: parasite infection, feeding sources and discrete typing units. Parasit Vectors [Internet]. 2016 Dec 1;9:620. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131512/ Coura JR, Borges-Pereira J. Chagas disease: 100 years after its discovery. A systemic review. Acta Trop. 2010;115(1–2):5–13. Galvão C, Carcavallo R, Rocha DDS, Jurberg J. A checklist of the current valid species of the subfamily Triatominae Jeannel, 1919 (Hemiptera, Reduviidae) and their geographical distribution, with nomenclatural and taxonomic notes. Zootaxa [Internet]. 2003 [cited 2018 Feb 26];202(1):1. Available from: https://www.researchgate.net/profile/Cleber_Galvao/publication/237163007_A_checklist_of_the_current_valid_species_of_the_subfamily_Triatominae_Jeannel_1919_Hemiptera_Reduviidae_and_their_geographical_distribution_with_nomenclatural_and_taxonomic_notes_Zoo Patterson JS, Barbosa SE, Feliciangeli MD. On the genus Panstrongylus Berg 1879: Evolution, ecology and epidemiological significance. Acta Trop. 2009;110(2–3):187–99. Molina J a, Gualdrón LE, Brochero HL, Olano V, Barrios D, Guhl F. Distribución actual e importancia epidemiológica de las especies de triatominos ( Reduviidae : Triatominae ) en Colombia. Biomédica. 2000;20:344–60. Jácome-Pinilla D, Hincapie-Peñaloza E, Ortiz MI, Ramírez JD, Guhl F, Molina J. Risks associated with dispersive nocturnal flights of sylvatic Triatominae to artificial lights in a model house in the northeastern plains of Colombia. Parasit Vectors [Internet]. 2015 Nov 19;8:600. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4652337/ Carrasco HJ, Segovia M, Londoño JC, Ortegoza J, Rodríguez M, Martínez CE. Panstrongylus geniculatus and four other species of triatomine bug involved in the Trypanosoma cruzi enzootic cycle: high risk factors for Chagas’ disease transmission in the Metropolitan District of Caracas, Venezuela. Parasit Vectors [Internet]. 2014 Dec 23;7:602. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4307744/ Guhl F, Restrepo M, Angulo VM, Antunes CMF, Campbell-Lendrum D, Davies CR. Lessons from a national survey of Chagas disease transmission risk in Colombia. Trends Parasitol [Internet]. 2005 Jun 1 [cited 2018 Apr 26];21(6):259–62. Available from: https://www.sciencedirect.com/science/article/pii/S1471492205001042?via%3Dihub Carrasco HJ, Torrellas A, García C, Segovia M, Feliciangeli MD. Risk of Trypanosoma cruzi I (Kinetoplastida: Trypanosomatidae) transmission by Panstrongylus geniculatus (Hemiptera: Reduviidae) in Caracas (Metropolitan District) and neighboring States, Venezuela. Int J Parasitol. 2005;35(13):1379–84. Valente VC, Valente SA, Noireau F, Carrasco HJ, Miles MA. Chagas disease in the Amazon Basin: association of Panstrongylus geniculatus (Hemiptera: Reduviidae) with domestic pigs. J Med Entomol [Internet]. 1998;35(2):99–103. Available from: http://www.ncbi.nlm.nih.gov/pubmed/9538568 Wolff M, Castillo D. Evidencias de domesticación y aspectos biológicos de "Panstrongylus Geniculatus (Latreille, 1811) (Hemiptera: Reduviidae). Acta entomológica Chil [Internet]. 2000;(24):77–83. Available from: http://dialnet.unirioja.es/servlet/articulo?codigo=2013609 Urdaneta-morales S. Urban Trypanosoma cruzi : biological characterization of isolates from Panstrongylus geniculatus. 1988;(June). Guhl F, Aguilera G, Pinto NA, Vergara D. Actualización de la distribución geográfica y ecoepidemiología de la fauna de triatominos (Reduviidae: Triatominae) en Colombia. Biomédica [Internet]. 2007 [cited 2018 Dec 29];27. Available from: http://www.scielo.org.co/pdf/bio/v27s1/v27s1a16.pdf Dib J, Barnabe C, Tibayrenc M, Triana O. Incrimination of Eratyrus cuspidatus (Stal) in the transmission of Chagas’ disease by molecular epidemiology analysis of Trypanosoma cruzi isolates from a geographically restricted area in the north of Colombia. Acta Trop. 2009;111(3):237–42. Aldana E, Heredia-Coronado E, Avendaño-Rangel F, Lizano E, Concepcióm JL, Bonfante-Cabarcas R, et al. Análisis morfométrico de Panstrongylus geniculatus de Caracas, Venezuela. Biomédica [Internet]. 2011;31:108–17. Available from: http://www.scielo.org.co/scielo.php?script=sci_arttext&pid=S0120-41572011000100013&nrm=iso Santos C, Jurberg J, Galvão C, Rocha D da S, Fernandez JIR. Morphometric study of the genus Panstrongylus Berg, 1879 (Hemiptera, Reduviidae, Triatominae). Mem Inst Oswaldo Cruz [Internet]. 2003;98:939–44. Available from: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762003000700014&nrm=iso Lorosa ES, Dos Santos CM, Jurberg J. Foco de doença de Chagas em São Fidélis, no Estado do Rio de Janeiro. Rev Soc Bras Med Trop. 2008;41(4):419–20. Marcilla A, Bargues MD, Abad-Franch F, Panzera F, Carcavallo RU, Noireau F, et al. Nuclear rDNA ITS-2 sequences reveal polyphyly of Panstrongylus species (Hemiptera: Reduviidae: Triatominae), vectors of Trypanosoma cruzi. Infect Genet Evol. 2002;1(3):225–35. Justi SA, Russo CAM, Mallet JRDS, Obara MT, Galvão C. Molecular phylogeny of Triatomini (Hemiptera: Reduviidae: Triatominae). Parasites and Vectors [Internet]. 2014 [cited 2018 Apr 26];7(1):1–12. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4021723/pdf/1756-3305-7-149.pdf Lent H, Wygodzinsky PW. Revision of the Triatominae (Hemiptera, Reduviidae), and their significance as vectors of Chagas’ disease. 1979 [cited 2018 Apr 7]; Available from: http://digitallibrary.amnh.org/handle/2246/1282 Qiagen. DNeasy ® Blood & Tissue Handbook For purification of total DNA from animal blood animal tissue. DNeasy ® Blood Tissue Handb Purif Total DNA from Anim blood Anim tissue [Internet]. 2006;(July):1–59. Available from: http://www.qiagen.com/products/genomicdnastabilizationpurification/dneasytissuesystem/dneasybloodtissuekit.aspx#Tabs=t0 Díaz S, Panzera F, Jaramillo-O N, Pérez R, Fernández R, Vallejo G, et al. Genetic, cytogenetic and morphological trends in the evolution of the Rhodnius (Triatominae: Rhodniini) trans-Andean group. PLoS One [Internet]. 2014 [cited 2018 Dec 16];9(2):e87493. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24498330 Gómez-Palacio A, Triana O. Molecular Evidence of Demographic Expansion of the Chagas Disease Vector Triatoma dimidiata (Hemiptera, Reduviidae, Triatominae) in Colombia. Dumonteil E, editor. PLoS Negl Trop Dis [Internet]. 2014 Mar 13 [cited 2018 Dec 16];8(3):e2734. Available from: https://dx.plos.org/10.1371/journal.pntd.0002734 Geneious. Geneious 11.0.5 [Internet]. [cited 2018 Dec 23]. Available from: https://www.geneious.com Larkin MA, Blackshields G, Brown NP, Chenna R, McGettigan PA, McWilliam H, et al. Clustal W and Clustal X version 2.0. Bioinformatics [Internet]. 2007 Nov 1 [cited 2018 Dec 23];23(21):2947–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17846036 Librado P, Rozas J. DnaSP v5: A software for comprehensive analysis of DNA polymorphism data. Bioinformatics. 2009;25(11):1451–2. Berchtold A. Sequence Analysis and Transition Models. Encycl Anim Behav [Internet]. 2010 Jan 1 [cited 2018 Dec 23];139–45. Available from: https://www.sciencedirect.com/science/article/pii/B9780080453378002333 Trifinopoulos J, Nguyen L-T, von Haeseler A, Minh BQ. W-IQ-TREE: a fast online phylogenetic tool for maximum likelihood analysis. Nucleic Acids Res [Internet]. 2016 Jul 8;44(Web Server issue):W232–5. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4987875/ Bouckaert R, Heled J, Kühnert D, Vaughan T, Wu C-H, Xie D, et al. BEAST 2: A Software Platform for Bayesian Evolutionary Analysis. Prlic A, editor. PLoS Comput Biol [Internet]. 2014 Apr 10;10(4):e1003537. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985171/ Poinar G. Panstrongylus hispaniolae sp. n. (Hemiptera: Reduviidae: Triatominae), a new fossil triatomine in Dominican amber, with evidence of gut flagellates. Palaeodiversity [Internet]. 2013 [cited 2018 Dec 23]; Available from: http://www.palaeodiversity.org/pdf/06/S-01_Poinar.pdf Tracer. Tracer v1.7.1 [Internet]. [cited 2018 Dec 23]. Available from: http://tree.bio.ed.ac.uk/software/tracer/ Rambaut A. FigTree v1.4.4 [Internet]. 2012. Available from: http://tree.bio.ed.ac.uk/software/figtree/ Leigh JW, Bryant D. POPART: Full-feature software for haplotype network construction. Methods Ecol Evol. 2015;6(9):1110–6. Wrigh S. The genetical structure of populations. Ann Eugen [Internet]. 1949 Mar [cited 2018 Dec 23];15(1):323–54. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24540312 Nei M, Miller’ JC. A Simple Method for Estimating Average Number of Nucleotide Substitutions Within and Between Populations From Restriction Data MATHEMATICAL FORMULATION [Internet]. 1990 [cited 2018 Dec 23]. Available from: http://www.genetics.org/content/genetics/125/4/873.full.pdf Mantel N. The Detection of Disease Clustering and a Generalized Regression Approach. CANCER Res [Internet]. 1967 [cited 2018 May 14];27(1):209–20. Available from: http://cancerres.aacrjournals.org/content/27/2_Part_1/209.full-text.pdf Oksanen J, Blanchet FG, Friendly M, Kindt R, Legendre P, Mcglinn D, et al. Package “vegan” Title Community Ecology Package. 2018 [cited 2018 May 14]; Available from: https://github.com/vegandevs/vegan/issues Rousset F. GENEPOP’007: A complete re-implementation of the GENEPOP software for Windows and Linux. Mol Ecol Resour. 2008;8(1):103–6. Hijmans RJ. Spherical Trigonometry [R package geosphere version 1.5-7]. 2016 [cited 2018 May 14]; Available from: https://cran.r-project.org/web/packages/geosphere/index.html Legendre P, Fortin MJ. Comparison of the Mantel test and alternative approaches for detecting complex multivariate relationships in the spatial analysis of genetic data. Mol Ecol Resour [Internet]. 2010 Sep [cited 2019 Jan 5];10(5):831–44. Available from: http://doi.wiley.com/10.1111/j.1755-0998.2010.02866.x Justi SA, Galvão C. The Evolutionary Origin of Diversity in Chagas Disease Vectors. Trends Parasitol [Internet]. 2017;33(1):42–52. Available from: http://dx.doi.org/10.1016/j.pt.2016.11.002 Crossa RP, Hernández M, Caraccio MN, Rose V, Valente SAS, Valente V da C, et al. Chromosomal evolution trends of the genus Panstrongylus (Hemiptera, Reduviidae), vectors of Chagas disease. Infect Genet Evol. 2002;2(1):47–56. Kvist L, Martens J, Nazarenko AA, Orell M. Paternal Leakage of Mitochondrial DNA in the Great Tit (Parus major). Mol Biol Evol [Internet]. 2003 Feb 1 [cited 2018 Dec 25];20(2):243–7. Available from: http://www.ncbi.nlm.nih.gov/pubmed/12598691 Messenger LA, Llewellyn MS, Bhattacharyya T, Franzén O, Lewis MD, Ramírez JD, et al. Multiple Mitochondrial Introgression Events and Heteroplasmy in Trypanosoma cruzi Revealed by Maxicircle MLST and Next Generation Sequencing. Traub-Csekö YM, editor. PLoS Negl Trop Dis [Internet]. 2012 Apr 10 [cited 2018 Dec 29];6(4):e1584. Available from: https://dx.plos.org/10.1371/journal.pntd.0001584 Fontaine KM, Cooley JR, Simon C. Evidence for paternal leakage in hybrid periodical cicadas (Hemiptera: Magicicada spp.). Crusio W, editor. PLoS One [Internet]. 2007 Sep 12 [cited 2018 Dec 25];2(9):e892. Available from: http://www.ncbi.nlm.nih.gov/pubmed/17849021 Russell O, Turnbull D. Mitochondrial DNA disease-molecular insights and potential routes to a cure [Internet]. Vol. 325, Experimental Cell Research. Elsevier; 2014 [cited 2018 Dec 25]. p. 38–43. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24675282 Stewart JB, Chinnery PF. The dynamics of mitochondrial DNA heteroplasmy: implications for human health and disease. Nat Rev Genet [Internet]. 2015 Sep 1 [cited 2018 Dec 29];16(9):530–42. Available from: http://www.ncbi.nlm.nih.gov/pubmed/26281784 Campos-Soto R, Torres-Pérez F, Solari A. Phylogenetic incongruence inferred with two mitochondrial genes in Mepraia spp. and Triatoma eratyrusiformis(Hemiptera, Reduviidae). Genet Mol Biol [Internet]. 2015 [cited 2018 Dec 25];38(3):390–5. Available from: http://www.ncbi.nlm.nih.gov/pubmed/26500444 Magnacca KN, Brown MJF. Tissue segregation of mitochondrial haplotypes in heteroplasmic Hawaiian bees: Implications for DNA barcoding. Mol Ecol Resour [Internet]. 2010 Jan [cited 2018 Dec 25];10(1):60–8. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21564991 White DJ, Wolff JN, Pierson M, Gemmell NJ. Revealing the hidden complexities of mtDNA inheritance [Internet]. Vol. 17, Molecular Ecology. 2008 [cited 2018 Dec 25]. p. 4925–42. Available from: http://www.ncbi.nlm.nih.gov/pubmed/19120984 Zhang D-X, Hewitt GM. Nuclear DNA analyses in genetic studies of populations: practice, problems and prospects. Mol Ecol [Internet]. 2003 Mar 1 [cited 2018 Dec 25];12(3):563–84. Available from: http://doi.wiley.com/10.1046/j.1365-294X.2003.01773.x Ballard JWO, Whitlock MC. The incomplete natural history of mitochondria. Mol Ecol [Internet]. 2004 Apr 1 [cited 2018 Dec 25];13(4):729–44. Available from: http://doi.wiley.com/10.1046/j.1365-294X.2003.02063.x Eo SH, DeWoody JA. Evolutionary rates of mitochondrial genomes correspond to diversification rates and to contemporary species richness in birds and reptiles. Proceedings Biol Sci [Internet]. 2010 Dec 7 [cited 2018 Dec 25];277(1700):3587–92. Available from: http://www.ncbi.nlm.nih.gov/pubmed/20610427 Bromham L, Leys R. Sociality and the Rate of Molecular Evolution. Mol Biol Evol [Internet]. 2005 Jun 1 [cited 2018 Dec 25];22(6):1393–402. Available from: http://academic.oup.com/mbe/article/22/6/1393/1111798/Sociality-and-the-Rate-of-Molecular-Evolution Li WH, Gojobori T, Nei M. Pseudogenes as a paradigm of neutral evolution. Nature [Internet]. 1981 Jul 16 [cited 2018 Dec 25];292(5820):237–9. Available from: http://www.ncbi.nlm.nih.gov/pubmed/7254315 Ibarra-Cerdeña CN, Zaldívar-Riverón A, Peterson AT, Sánchez-Cordero V, Ramsey JM. Phylogeny and Niche Conservatism in North and Central American Triatomine Bugs (Hemiptera: Reduviidae: Triatominae), Vectors of Chagas’ Disease. Dumonteil E, editor. PLoS Negl Trop Dis [Internet]. 2014 Oct 30 [cited 2018 Dec 25];8(10):e3266. Available from: https://dx.plos.org/10.1371/journal.pntd.0003266 de la Rúa NM, Bustamante DM, Menes M, Stevens L, Monroy C, Kilpatrick CW, et al. Towards a phylogenetic approach to the composition of species complexes in the North and Central American Triatoma, vectors of Chagas disease. Infect Genet Evol [Internet]. 2014 Jun [cited 2018 Dec 24];24:157–66. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24681261 Hypša V, Tietz DF, Zrzavý J, Rego RO., Galvao C, Jurberg J. Phylogeny and biogeography of Triatominae (Hemiptera: Reduviidae): molecular evidence of a New World origin of the Asiatic clade. Mol Phylogenet Evol [Internet]. 2002 Jun [cited 2018 Dec 24];23(3):447–57. Available from: http://linkinghub.elsevier.com/retrieve/pii/S1055790302000234 Justi SA, Galvão C, Schrago CG. Geological Changes of the Americas and their Influence on the Diversification of the Neotropical Kissing Bugs (Hemiptera: Reduviidae: Triatominae). PLoS Negl Trop Dis [Internet]. 2016 [cited 2018 Apr 26];10(4). Available from: http://journals.plos.org/plosntds/article/file?id=10.1371/journal.pntd.0004527&type=printable Justi SA, Cahan S, Stevens L, Monroy C, Lima R, Dorn L. Vectors of Diversity: Genome wide diversity across the geographic range of the Chagas disease vector Triatoma dimidiata sensu lato (Hemiptera: Reduviidae). 2017; Abad-Franch F, Monteiro FA. Biogeography and evolution of Amazonian triatomines (Heteroptera: Reduviidae): Implications for Chagas disease surveillance in humid forest ecoregions. In: Memorias do Instituto Oswaldo Cruz [Internet]. Fundação Oswaldo Cruz; 2007 [cited 2018 Dec 29]. p. 57–69. Available from: http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0074-02762007000900011&lng=en&tlng=en Cuervo AM. Evolutionary Assembly of the Neotropical Montane Avifauna. 2013; Dorn PL, de la Rúa NM, Axen H, Smith N, Richards BR, Charabati J, et al. Hypothesis testing clarifies the systematics of the main Central American Chagas disease vector, Triatoma dimidiata (Latreille, 1811), across its geographic range. Infect Genet Evol [Internet]. 2016 Oct [cited 2018 Dec 26];44:431–43. Available from: http://www.ncbi.nlm.nih.gov/pubmed/27496718 Ramírez CJ, Jaramillo CA, Delgado M del P, Pinto NA, Aguilera G, Guhl F. Genetic structure of sylvatic, peridomestic and domestic populations of Triatoma dimidiata (Hemiptera: Reduviidae) from an endemic zone of Boyaca, Colombia. Acta Trop [Internet]. 2005 Jan [cited 2018 Dec 26];93(1):23–9. Available from: http://linkinghub.elsevier.com/retrieve/pii/S0001706X04002049 Gómez-Palacio A, Triana O, Jaramillo-O N, Dotson EM, Marcet PL. Eco-geographical differentiation among Colombian populations of the Chagas disease vector Triatoma dimidiata (Hemiptera: Reduviidae). Infect Genet Evol [Internet]. 2013 Dec [cited 2018 Dec 26];20:352–61. Available from: http://www.ncbi.nlm.nih.gov/pubmed/24035810 Monteiro FA, Peretolchina T, Lazoski C, Harris K, Dotson EM, Abad-Franch F, et al. Phylogeographic Pattern and Extensive Mitochondrial DNA Divergence Disclose a Species Complex within the Chagas Disease Vector Triatoma dimidiata. Oliveira PL, editor. PLoS One [Internet]. 2013 Aug 5 [cited 2018 Dec 26];8(8):e70974. Available from: https://dx.plos.org/10.1371/journal.pone.0070974 Bargues MD, Klisiowicz DR, Gonzalez-Candelas F, Ramsey JM, Monroy C, Ponce C, et al. Phylogeography and genetic variation of Triatoma dimidiata, the main Chagas disease vector in Central America, and its position within the genus Triatoma. PLoS Negl Trop Dis [Internet]. 2008 May 7 [cited 2018 Dec 26];2(5):e233. Available from: http://www.ncbi.nlm.nih.gov/pubmed/18461141 Campos R, Torres-Pérez F, Botto-Mahan C, Coronado X, Solari A. High phylogeographic structure in sylvatic vectors of Chagas disease of the genus Mepraia (Hemiptera: Reduviidae). Infect Genet Evol [Internet]. 2013 Oct [cited 2018 Dec 26];19:280–6. Available from: https://linkinghub.elsevier.com/retrieve/pii/S1567134813001858 Gourbière S, Dorn P, Tripet F, Dumonteil E. Genetics and evolution of triatomines: From phylogeny to vector control [Internet]. Vol. 108, Heredity. Nature Publishing Group; 2012 [cited 2018 Dec 30]. p. 190–202. Available from: http://www.ncbi.nlm.nih.gov/pubmed/21897436 WHO. Weekly epidemiological record - Chagas diseases in Latin America: an epidemiological update based on 2010 estimates. 2015 [cited 2018 Feb 26]; Available from: http://www.who.int/wer/2015/wer9006.pdf?ua=1 Neves D, Farias LM, Godoy MF. Epidemiologia da Doença de Chagas na Zona Rural do Município de Teresina-Piauí, Brasil. Rev Soc Bras Med Trop. 1992;25(1):51–8. Omahmaharaj I. Studies on Vectors of Trypanosoma-Cruzi in Trinidad, West-Indies. Med Vet Entomol. 1992;6(2):115–20. Castillo D, Wolff M. Aspectos del comportamiento de los triatominos ( Hemiptera : Reduviidae ), vectores de la enfermedad de Chagas. Biomédica. 2000;20(1):59–64. Arias-Giraldo L, Muñoz M, Hernández C, Herrera G, Caicedo-Garzon V, Velásquez Ortíz N, et al. Portraying the gut bacterial communities and blood feeding sources of triatomine bugs (Hemiptera: Reduviidae), vectors of Chagas disease. submitted. McCoy KD. The population genetic structure of vectors and our understanding of disease epidemiology. Parasite [Internet]. 2008 Sep 15 [cited 2018 Dec 27];15(3):444–8. Available from: http://www.parasite-journal.org/10.1051/parasite/2008153444 Barrett T V, Hoff RH, Mott KE, Miles MA, Godfrey DG, Teixeira R, et al. Epidemiological aspects of three Trypanosoma cruzi zymodemes in Bahia State, Brazil. Trans R Soc Trop Med Hyg [Internet]. 1980 [cited 2018 Dec 27];74(1):84–90. Available from: http://www.ncbi.nlm.nih.gov/pubmed/6776664 de Noya BA, González ON. An ecological overview on the factors that drives to Trypanosoma cruzi oral transmission. Acta Trop [Internet]. 2015;151(1):94–102. Available from: http://dx.doi.org/10.1016/j.actatropica.2015.06.004 Urdaneta-Morales S. Chagas Disease: An Emergent Urban Zoonosis. The Caracas Valley (Venezuela) as an Epidemiological Model. Front Public Heal [Internet]. 2014;2(December):1–13. Available from: http://journal.frontiersin.org/article/10.3389/fpubh.2014.00265/abstract Rabinovich JE, Feliciangeli MD. Vital Statistics of Triatominae (Hemiptera: Reduviidae) under Laboratory Conditions: IV. Panstrongylus geniculatus. J Med Entomol. 2015;52(5):797–805. Monteiro FA, Escalante AA, Beard CB. Molecular tools and triatomine systematics: a public health perspective. Trends Parasitol [Internet]. 2001 Jul [cited 2018 Dec 27];17(7):344–7. Available from: http://linkinghub.elsevier.com/retrieve/pii/S1471492201019213
score 12,131701