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dc.contributorAUDREY LENHART
dc.contributorMIKE DUNBAR
dc.contributorPABLO MANRIQUE SAIDE
dc.coverage.spatialGeneración de conocimiento
dc.creatorANUAR MEDINA BARREIRO
dc.creatorEDGAR ULISES KOYOC CARDEÑA
dc.creatorAZAEL COHUO RODRIGUEZ
dc.creatorNORMA DEL ROSARIO PAVIA RUZ
dc.creatorGUADALUPE AYORA TALAVERA
dc.creatorGONZALO VAZQUEZ PROKOPEC
dc.date2019-03-21
dc.date.accessioned2021-06-22T17:38:14Z
dc.date.available2021-06-22T17:38:14Z
dc.identifierhttps://parasitesandvectors.biomedcentral.com/articles/10.1186/s13071-019-3503-y
dc.identifier.urihttp://redi.uady.mx:8080/handle/123456789/4982
dc.description.abstractQuantifcation of adult Aedes aegypti abundance indoors has relied on estimates of relative density (e.g. number of adults per unit of sampling or time), most commonly using traps or timed collections using aspirators. The lack of estimates of the sensitivity of collections and lack of a numerical association between relative and the absolute density of adult Ae. aegypti represent a significant gap in vector surveillance. Here, we describe the use of sequential removal sampling to estimate absolute numbers of indoor resting Ae. aegypti and to calculate calibration coeficients for timed Prokopack aspirator collections in the city of Merida, Yucatan State, Mexico. The study was performed in 200 houses that were selected based on recent occurrence of Aedes-borne viral illness in residents. Removal sampling occurred in 10-minute sampling rounds performed sequentially until no Ae. aegypti adult was collected for 3 hours or over 2 consecutive 10-minute periods. Results: A total of 3439 Ae. aegypti were collected. The sensitivity of detection of positive houses in the first sampling round was 82.5% for any adult Ae. aegypti, 78.5% for females, 75.5% for males and 73.3% for blood-fed females. The total number of Ae. aegypti per house was on average ~5 times higher than numbers collected for the first sampling round. There was a positive linear relationship between the relative density of Ae. aegypti collected during the first 10-min round and the absolute density for all adult metrics. Coefcients from the linear regression were used to calibrate numbers from 10-min collections into estimates of absolute indoor Ae. aegypti density for all adults, females and males. Conclusions: Exhaustive removal sampling represents a promising method for quantifcation of absolute indoor Ae. aegypti density, leading to improved entomological estimates of mosquito distribution, a key measure in the assess ments of the risk pathogen transmission, disease modeling and the evaluation of vector control interventions.
dc.languageeng
dc.publisherParasites and Vectors
dc.relationcitation:0
dc.rightsinfo:eu-repo/semantics/openAccess
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/4.0
dc.sourceurn:issn:1756-3305
dc.subjectinfo:eu-repo/classification/cti/2
dc.subjectBIOLOGÍA Y QUÍMICA
dc.subjectinfo:eu-repo/classification/cti/3
dc.subjectMEDICINA Y CIENCIAS DE LA SALUD
dc.subjectSampling
dc.subjectEntomology
dc.subjectPopulation abundance
dc.titleEstimating absolute indoor density of Aedes aegypti (Stegomyia) using removal sampling
dc.typeinfo:eu-repo/semantics/article


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