ABSTRACT
Dengue is known to transmit between humans and A. aegypti mosquitoes living in neighboring houses. Although transmission is thought to be highly heterogeneous in both space and time, little is known about the patterns and drivers of transmission in groups of houses in endemic settings. We carried out surveys of PCR positivity in children residing in 2-block patches of highly endemic cities of Colombia. We found high levels of heterogeneity in PCR positivity, varying from less than 30% in 8 of the 10 patches to 56 and 96%, with the latter patch containing 22 children simultaneously PCR positive (PCR22) for DEN2. We then used an agent-based model to assess the likely eco-epidemiological context of this observation. Our model, simulating daily dengue dynamics over a 20 year period in a single two block patch, suggests that the observed heterogeneity most likely derived from variation in the density of susceptible people. Two aspects of human adaptive behavior were critical to determining this density: external social relationships favoring viral introduction (by susceptible residents or infectious visitors) and immigration of households from non-endemic areas. External social relationships generating frequent viral introduction constituted a particularly strong constraint on susceptible densities, thereby limiting the potential for explosive outbreaks and dampening the impact of heightened vectorial capacity. Dengue transmission can be highly explosive locally, even in neighborhoods with significant immunity in the human population. Variation among neighborhoods in the density of local social networks and rural-to-urban migration is likely to produce significant fine-scale heterogeneity in dengue dynamics, constraining or amplifying the impacts of changes in mosquito populations and cross immunity between serotypes.
Subject(s)
Dengue Virus/pathogenicity , Dengue/transmission , Population Density , Residence Characteristics , Social Behavior , Aedes/virology , Animals , Child , Colombia , Dengue/virology , Disease Outbreaks , Humans , Insect Vectors/virology , Polymerase Chain Reaction , Population Dynamics , RNA, Viral/bloodABSTRACT
Introducción.A pesar del control de los insectos domiciliados, se siguen presentando casos de enfermedad de Chagas con la participación en la transmisión de especies peridomiciliarias y selváticas, una de las cuales es Rhodnius robustus, especie reportada con infecciones naturales de Trypanosoma cruzi y T. rangeli. Objetivo. Describir el comportamiento de R. robustus durante su alimentación en condiciones de laboratorio. Materiales y métodos. En cada estadio de desarrollo de R. robustus se analizó el tiempo promedio para alcanzar la repleción, número promedio de deyecciones, porcentaje de individuos que defecan durante la comida y ganancia de peso después de la alimentación. Resultados. Rhodnius robustus tardó entre 19:26 y 44:55 (minutos:segundos) en alimentarse a repleción; los insectos defecaron en todos sus diferentes estadios durante la alimentación. El porcentaje de individuos que defecan durante la alimentación varía de 13,3 % a 93,3 %. Por otro lado, el consumo promedio de sangre en el quinto estadio, 337,19 mg, duplica la cantidad ingerida por los adultos, 161,25 mg. Conclusiones. En todos los estadios de R. robustus hay defecación durante la alimentación, factor que favorece su competencia vectorial. Sin embargo, el tiempo para la primera deyección, el porcentaje de deyecciones y los individuos que defecan durante la comida, así como la cantidad de sangre ingerida, varían entre los estadios, lo cual indica que el comportamiento alimenticio está mediado por variables dependientes de la edad/estadio.
Introduction: Despite of indoor insect control measures, American trypanosomiasis cases still occur, with the participation of both peridomestic and sylvan species. One of these species is Rhodnius robustus, which has been found naturally infected with Trypanosoma cruzi and Trypanosoma rangeli. Objective: To describe the feeding behavior of R. robustus under laboratory conditions. Materials and methods: We analyzed time spent for repletion, the number of defecations, the percentage and number of times insects defecated during blood intake, and the weight gained after blood feeding in each nymph stage of R. robustus. Results: Repletion for R. robustus took between 19:26 to 44:55 (minutes:seconds) and all nymph stages defecated during blood feeding. The proportion of individuals which defecated during blood feeding varied between 13.3% and 93.3%. On the other hand, the highest average blood intake was observed in the fifth stage (337.19 mg), which is twice the blood intake of adults (161.25 mg). Conclusions: All stages of R. robustus dejected during blood feeding, which is an important factor for its vectorial competence. Nevertheless, the time prior to the first dejection, the percentage of dejections and number of individuals that dejected upon blood feeding, as well as the amount of ingested blood varied among stages, which means that feeding behavior is mediated by variables depending on age/stage.
Subject(s)
Animals , Female , Male , Rhodnius/physiology , Animals, Laboratory , Defecation , Feeding BehaviorABSTRACT
INTRODUCTION: Despite of indoor insect control measures, American trypanosomiasis cases still occur, with the participation of both peridomestic and sylvan species. One of these species is Rhodnius robustus, which has been found naturally infected with Trypanosoma cruzi and Trypanosoma rangeli. OBJECTIVE: To describe the feeding behavior of R. robustus under laboratory conditions. MATERIALS AND METHODS: We analyzed time spent for repletion, the number of defecations, the percentage and number of times insects defecated during blood intake, and the weight gained after blood feeding in each nymph stage of R. robustus. RESULTS: Repletion for R. robustus took between 19:26 to 44:55 (minutes:seconds) and all nymph stages defecated during blood feeding. The proportion of individuals which defecated during blood feeding varied between 13.3% and 93.3%. On the other hand, the highest average blood intake was observed in the fifth stage (337.19 mg), which is twice the blood intake of adults (161.25 mg). CONCLUSIONS: All stages of R. robustus dejected during blood feeding, which is an important factor for its vectorial competence. Nevertheless, the time prior to the first dejection, the percentage of dejections and number of individuals that dejected upon blood feeding, as well as the amount of ingested blood varied among stages, which means that feeding behavior is mediated by variables depending on age/stage.