DETECCIÓN DE INFECCIÓN NATURAL POR Trypanosoma cruzi (TRYPANOSOMATIDAE) EN TRIATOMINOS DEL MUNICIPIO DE COLOSÓ, COLOMBIA / Detection of Natural Infection with Trypanosoma cruzi (Trypanosomatidae) in Triatomines From the Municipality of Colosó, Colombia

RESUMEN El reporte de triatominos infectados por Trypanosoma cruzi en un área silvestre del municipio de Colosó, hizo necesario determinar las especies de vectores en cercanía a las viviendas de la vereda Jorro, por ser el asentamiento rural próximo al hallazgo. En la presente nota, se informa por primera vez para el municipio la presencia de especies de triatominos de importancia epidemiológica con un alto porcentaje de infección por el parásito, además, de ampliar la distribución de estos vectores en el departamento de Sucre. Para ello, se realizaron capturas de los insectos en 13 viviendas por búsqueda activa, vigilancia comunitaria y trampas de luz. La determinación de la infección natural se llevó a cabo por observación directa al microscopio y amplificación por PCR del ADN de T. cruzi presente en el contenido intestinal de los triatominos. En total se capturaron 40 ejemplares de las especies Panstrongylus geniculatus, Rhodnius pallescens, Eratyrus cuspidatus y Triatoma dimidiata. La mayoría de los individuos fueron recolectados en el extradomicilio, con un menor porcentaje de insectos adultos encontrados en ambientes domésticos y la tasa de infección natural en los insectos fue del 85 %.

ABSTRACT The report of triatomines infected with Trypanosoma cruzi in a wild area of the municipality of Colosó, made it necessary to determine the species of vectors near the houses in the village Jorro, because it is the closest rural settlement to this finding. The presence of triatomine species with epidemiological importance was reported by first time, with a high percentage of infection with the parasite, in addition to expanding the distribution of these vectors in the department of Sucre. The researchers captured insects in 13 dwellings through active search, community surveillance and light traps, and demonstrated the natural infection by direct observation under the microscope and PCR amplification DNA from T. cruzi present in the intestinal content of the triatomines. Were captured 40 specimens belonging to the species Panstrongylus geniculatus, Rhodnius pallescens, Eratyrus cuspidatus and Triatoma dimidiata. The majority of the specimens were collected in the extradomicile, with a lower percentage of adult insects found in domestic environments. The natural infection rate in the insects was 85 %.

DNA barcoding to identify species of phlebotomine sand fly (Diptera: Psychodidae) in the mixed leishmaniasis focus of the Colombian Caribbean.

Identification of the species of phlebotomine sand flies present in each focus of leishmaniasis is necessary to incriminate vectors and implement vector control strategies. Although the cytochrome oxidase I (COI) gene has been proposed as a barcode for the identification of animal species, less than 20% of New World phlebotomines have been characterized to date. In this study DNA barcoding was used to identify phlebotomine species of the mixed leishmaniasis focus in the Colombian Caribbean by means of three evolutionary models: Kimura's two parameter (K2P) nucleotide substitution model, that of (Tamura and Nei, 1993) (TN93) and proportional sequence divergence (p-distances). A 681bp sequence of the COI gene was obtained from 66 individuals belonging to 19 species of the genus Lutzomyia (Lu. abonnenci, Lu. atroclavata, Lu. bicolor, Lu. carpenteri, Lu. cayennensis cayennensis, Lu. dubitans, Lu. evansi, Lu. gomezi, Lu. gorbitzi, Lu. longipalpis, Lu. micropyga, Lu. migonei, Lu. panamensis, Lu. (Psathyromyia) sp., Lu. rangeliana, Lu. serrana, Lu. shannoni, Lu. trinidadensis and Lu. venezuelensis) and one of Brumptomyia (B. mesai). The genetic divergence values for TN93 among individuals of the same species fluctuated up to 3.2% (vs. 2.9% for K2P and 2.8% for p-distances), while the values between species ranged from 8.8-43.7% (vs. 6.8-19.6% for K2P and 6.6-17.4% for p-distances). A dendrogram constructed by means of the Neighbor-Joining method grouped phlebotomines into 20 clusters according to species, with bootstrap values of up to 100% in those with more than one individual. However, loss of the phylogenetic signal of the gene COI was observed at the supraspecific level as a consequence of substitutional saturation. In conclusion, irrespective of the evolutionary model selected, all phlebotomines were correctly assigned to species, showing 100% concordance with morphological identification.

Evidence for anthropophily in five species of phlebotomine sand flies (Diptera: Psychodidae) from northern Colombia, revealed by molecular identification of bloodmeals.

Identification of the bloodmeal sources of phlebotomine sand flies is fundamental to determining which species are anthropophilic and understanding the transmission of Leishmania parasites in natural epidemiological settings. The objective of this study was to identify sand fly bloodmeals in the mixed leishmaniasis focus of the department of Sucre, northern Colombia. In all 141 engorged female sand flies were analyzed, after being captured in intradomiciliary, peridomiciliary and extradomiciliary habitats with Shannon and CDC traps and by active searching in diurnal resting sites. Bloodmeals were identified by sequencing and analysis of a 358bp fragment of the mitochondrial gene Cytochrome b (CYB) and a 330bp fragment of the nuclear gene prepronociceptin (PNOC). Using both genes 105 vertebrate bloodmeals were identified, with an efficiency of 72% for CYB but only 7% for PNOC. Ten species of vertebrates were identified as providing bloodmeal sources for 8 sand fly species: Homo sapiens (Lutzomyia evansi, Lutzomyia panamensis, Lutzomyia micropyga, Lutzomyia shannoni and Lutzomyia atroclavata), Equus caballus (L. evansi, L. panamensis and Lutzomyia cayennensis cayennensis), Equus asinus (L. evansi and L. panamensis), Bos taurus (L. evansi, L. panamensis and L. c. cayennensis), Tamandua mexicana (L. shannoni and Lutzomyia trinidadensis), Proechimys guyanensis (L. evansi, L. panamensis and L. c. cayennensis), Mabuya sp. (Lutzomyia micropyga), Anolissp. (L. micropyga), Sus scrofa (L. evansi and Lutzomyia gomezi) and Gallus gallus (L. evansi). Cattle, donkeys, humans and pigs were significantly more important than other animals (P=0.0001) as hosts of L. evansi, this being the most abundant sand fly species. The five Lutzomyia species in which blood samples of human origin were detected included L. micropyga and L. atroclavata, constituting the first evidence of anthropophily in both species.