ABSTRACT
Two snapshot surveys to establish the diversity and ecological preferences of mosquitoes (Diptera: Culicidae) in the terra firme primary rain forest surrounding the Tiputini Biodiversity Station in the UNESCO Yasuní Biosphere Reserve of eastern Amazonian Ecuador were carried out in November 1998 and May 1999. The mosquito fauna of this region is poorly known; the focus of this study was to obtain high quality link-reared specimens that could be used to unequivocally confirm species level diversity through integrated systematic study of all life stages and DNA sequences. A total of 2,284 specimens were preserved; 1,671 specimens were link-reared with associated immature exuviae, all but 108 of which are slide mounted. This study identified 68 unique taxa belonging to 17 genera and 27 subgenera. Of these, 12 are new to science and 37 comprise new country records. DNA barcodes [658-bp of the mtDNA cytochrome c oxidase ( COI ) I gene] are presented for 58 individuals representing 20 species and nine genera. DNA barcoding proved useful in uncovering and confirming new species and we advocate an integrated systematics approach to biodiversity studies in future. Associated bionomics of all species collected are discussed. An updated systematic checklist of the mosquitoes of Ecuador (n = 179) is presented for the first time in 60 years.
Subject(s)
Animals , Biodiversity , Culicidae/classification , Culicidae/genetics , DNA Barcoding, Taxonomic/methods , Ecology/classification , Electron Transport Complex IV/genetics , Ecuador , Oviposition , Polymerase Chain Reaction , RainforestABSTRACT
The morphologically similar taxa Anopheles calderoni, Anopheles punctimacula, Anopheles malefactor and Anopheles guarao are commonly misidentified. Isofamilies collected in Valle de Cauca, Colombia, showed morphological characters most similar to An. calderoni, a species which has never previously been reported in Colombia. Although discontinuity of the postsubcostal pale spots on the costa (C) and first radial (R1) wing veins is purportedly diagnostic for An. calderoni, the degree of overlap of the distal postsubcostal spot on C and R1 were variable in Colombian specimens (0.003-0.024). In addition, in 98.2 percent of larvae, seta 1-X was located off the saddle and seta 3-C had 4-7 branches in 86.7 percent of specimens examined. Correlation of DNA sequences of the second internal transcribed spacer and mtDNA cytochrome c oxidase subunit I gene (COI) barcodes (658 bp of the COI gene) generated from Colombian progeny material and wild-caught mosquitoes from Ecuador with those from the Peruvian type series of An. calderoni confirmed new country records. DNA barcodes generated for the closely related taxa, An. malefactor and An. punctimacula are also presented for the first time. Examination of museum specimens at the University of the Valle, Colombia, revealed the presence of An. calderoni in inland localities across Colombia and at elevations up to 1113 m.
Subject(s)
Animals , Female , Anopheles , Insect Vectors , Wings, Animal , Anopheles , Anopheles , Anopheles , Colombia , DNA, Mitochondrial , Ecuador , Electron Transport Complex IV , Insect Vectors , Insect Vectors , Insect VectorsABSTRACT
The presence of Anopheles (Nyssorhynchus) dunhami Causey in Colombia (Department of Amazonas) is confirmed for the first time through direct comparison of mtDNA cytochrome c oxidase I (COI) barcodes and nuclear rDNA second internal transcribed spacer (ITS2) sequences with topotypic specimens of An. dunhami from Tefé, Brazil. An. dunhami was identified through retrospective correlation of DNA sequences following misidentification as Anopheles nuneztovari s.l. using available morphological keys for Colombian mosquitoes. That An. dunhami occurs in Colombia and also possibly throughout the Amazon Basin, is of importance to vector control programs, as this non-vector species is morphologically similar to known malaria vectors including An. nuneztovari, Anopheles oswaldoi and Anopheles trinkae. Species identification of An. dunhami and differentiation from these closely related species are highly robust using either DNA ITS2 sequences or COI DNA barcode. DNA methods are advocated for future differentiation of these often sympatric taxa in South America.
Subject(s)
Animals , Anopheles , DNA, Ribosomal Spacer , Electron Transport Complex IV , Anopheles , Anopheles/enzymology , Colombia , DNA, Intergenic , DNA, Mitochondrial , DNA, Ribosomal , Sequence Analysis, DNA , Species SpecificityABSTRACT
Malaria transmission in the Southern Colombian state of Putumayo continues despite the absence of traditional vector species, except for the presence of Anopheles darlingi near the southeastern border with the state of Amazonas. In order to facilitate malaria vector incrimination in Putumayo, 2445 morphologically identified Anopheles females were tested for natural infection of Plasmodium vivax by ELISA. Specimens tested included An. apicimacula (n = 2), An. benarrochi B (n = 1617), An. darlingi (n = 29), An. mattogrossensis (n = 7), An. neomaculipalpus (n = 7), An. oswaldoi (n = 362), An. peryassui (n = 1), An. punctimacula (n = 1), An. rangeli (n = 413), and An. triannulatus (n = 6). Despite being overwhelmingly the most anthropophilic species in the region and comprising 66.1 percent of the mosquitoes tested, An. benarrochi B was not shown to be a vector. Thirty-five An. rangeli and one An. oswaldoi were naturally infected with P. vivax VK210. Sequence data were generated for the nuclear second internal transcriber space region of 31 of these 36 vivax positive mosquitoes (86.1 percent) to confirm their morphological identification. An. oswaldoi is known to be a species complex in Latin America, but its internal taxonomy remains unresolved. Herein we show that the An. oswaldoi found in the state of Putumayo is genetically similar to specimens from the state of Amapá in Brazil and from the Ocama region in the state of Amazonas in Venezuela, and that this form harbors natural infections of P. vivax. That An. rangeli and this member of the An. oswaldoi complex are incriminated as malaria vectors in Putumayo, is a novel finding of significance for malaria control in Southern Colombia, and possibly in other areas of Latin America.
Subject(s)
Animals , Female , Anopheles/parasitology , Insect Vectors/parasitology , Plasmodium vivax/physiology , Anopheles/classification , Anopheles/genetics , Colombia , Enzyme-Linked Immunosorbent Assay , Insect Vectors/classification , Insect Vectors/genetics , Molecular Sequence Data , Malaria, Vivax/transmission , Sequence AlignmentABSTRACT
Anopheles (Nyssorhynchus) benarrochi, An. (N.) oswaldoi, and An. (N.) rangeli are the most common anthropophilic mosquitoes in the southern Colombian state of Putumayo. Adult females are most commonly collected in epidemiological studies, and this stage poses significant problems for correct identification, due to overlapping inter-specific morphological characters. Although An. rangeli is easy to identify, the morphological variant of An. benarrochi found in the region and An. oswaldoi are not always easy to separate. Herein we provide a rapid molecular method to distinguish these two species in Southern Colombia. Sequence data for the second internal transcribed spacer (ITS2) region of rDNA was generated for link-reared progeny of An. benarrochi and An. oswaldoi, that had been identified using all life stages. ITS2 sequences were 540 bp in length in An. benarrochi (n = 9) and 531 bp in An. oswaldoi (n = 7). Sequences showed no intra-specific variation and ungapped inter-specific sequence divergence was 6.4 percent. Species diagnostic banding patterns were recovered following digestion of the ITS2 amplicons with the enzyme Hae III as follows: An. benarrochi (365, 137, and 38 bp) and An. oswaldoi (493 and 38 bp). This polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay provides rapid, accurate, and inexpensive species diagnosis of adult females. This will benefit future epidemiological studies and, as PCR amplification can be achieved using a single mosquito leg, the remaining specimen can be either retained as a morphological voucher or further used in vector incrimination studies. That An. benarrochi comprises a complex of at least two species across Latin America is discussed.
Subject(s)
Animals , Female , Anopheles/genetics , DNA, Ribosomal Spacer/genetics , Genes, Insect/genetics , Anopheles/classification , Base Sequence , Colombia , Molecular Sequence Data , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Sequence Analysis, DNAABSTRACT
La identificación correcta de las hembras es esencial para el éxito de cualquier estudio de epidemiología, resistencia a insecticidas o de control de vectores. En el departamento del Putumayo, en el sur de Colombia, la transmisión de malaria continúa siendo un problema, a pesar de la ausencia de los vectores principales de Latinoamérica (Anopheles darlingi Root, Anopheles nuneztovari Gabaldón, Anopheles albimanus Wideman, Anopheles trinkae Faran) en esta región. Se recolectaron. con cebo humano, hembras de Anopheles y se encontró una variante morfológica de Anopheles benarrochi, que en su estadio adulto fácilmente se confunde con Anopheles oswaldoi. La identificación de hembras de Anopheles, particularmente del subgénero Nyssorhynchus, es en general notoriamente difícil debido a la superposición de caracteres morfológicos en el estadio adulto; por tanto, las colecciones deben estar ligadas a la cría de material asociado para identificar correctamente las especies. Esto requiere tiempo y es difícil de obtener en muchas ocasiones. Se presenta un método indirecto de identificación de las especies A. benarrochi, A. oswaldoi y Anopheles rangeli del sur de Colombia usando la morfología de los huevos de hembras silvestres. Los huevos de A. rangeli y A. benarrochi se diferencian por la corona anterior, la cual es apical en A. rangeli y con paredes altas, mientras que en A. benarrochi es ventral y con paredes más cortas. Esta corona está ausente en A. oswaldoi. Estas diferencias fueron obvias incluso bajo un microscopio de luz, lo que hace posible una identificación correcta de estas especies en condiciones de campo. Se muestra cómo la observación de la morfología de los huevos puede permitir la determinación taxonómica correcta, aunque indirecta, de estas tres especies de Nyssorhynchus encontradas en el sur de Colombia, el cual puede ser útil también en otras regiones de Latinoamérica, en donde se encuentre la variante morfológica de A. benarrochi en simpatría con A. oswaldoi.Palabras clave: Nyssorhynchus, huevos, Anopheles, Colombia, microscopia electrónica.Egg morphology as an indirect method to identify Anopheles benarrochi, Anopheles oswaldoi and Anopheles rangeli (Diptera: Culicidae).
Subject(s)
Anopheles , Microscopy, Electron , EggsABSTRACT
Con el propósito de ampliar el conocimiento sobre las especies de Anopheles presentes en el Putumayo, sur de Colombia, y para esclarecer la identidad de los ejemplares clasificados como Anopheles (Nyssorhynchus) evansae en esta región, se recolectaron mosquitos hembra en cebo humano, se alimentaron en pequeños mamíferos y se mantuvieron vivos para la cría de isofamilias. Se realizaron observaciones de las características morfológicas de los huevos, larvas, pupas y adultos de ambos sexos, incluidas las genitalias masculinas. Se obtuvieron 247 posturas de madres identificadas preliminarmente como A. (N) evansee. A 27 de estas familias se le estudió la morfología de los estadios asociados. Todos los especímenes fueron subsecuentemente identificados como Anopheles (N:) benarrochi por la morfología de los huevos, larvas, pupas y genitalias masculinas, lo cual coincidió con las descripciones publicadas para esta especie. Sin embargo, los adultos hembra de Putumayo presentaron la proporción oscura en el tarsómero posterior 2, entre 0.17 y 0,33 de su longitud, inferior a lo informado para esta especie, lo cual se superpone con los rangos de Anopheles (N.) oswaldoi y A. (N.) evansae. Como resultado de la superposición en este carácter, es probable que hembras adultas de A. (N.) benarrochi hayan sido incorrectamente identificadas como A. (N.) evansae y A. (N.) oswaldoi en el sur de Colombia. La presencia de esta variante morfológica ha dificultado la identificación de A. (N.) benarrochi en Putumayo y, probablemente, en otras regiones de Colombia y países vecinos