Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]

Background: Growing insecticide resistance and changes in biting and resting behavior of malaria vectors threaten efficacy of insecticide treated nets and indoor residual spraying. Larval source management (LSM) is a promising approach that can target mosquitoes irrespective of their behavior as adu...

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Main Authors: Joel Odero, Bruno Gomes, Ulrike Fillinger, David Weetman
Format: Article
Language:English
Published: Wellcome 2018-03-01
Series:Wellcome Open Research
Online Access:https://wellcomeopenresearch.org/articles/3-26/v1
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spelling doaj-bb4f1dbd85d14f189edc3cb26f3e21562020-11-24T20:48:11ZengWellcomeWellcome Open Research2398-502X2018-03-01310.12688/wellcomeopenres.14193.115439Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]Joel Odero0Bruno Gomes1Ulrike Fillinger2David Weetman3Malaria Programme, International Centre of Insect Physiology and Ecology, Thomas Odhiambo Campus, P.O. Box 30, Mbita, 40305, KenyaDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, L3 5QA, UKMalaria Programme, International Centre of Insect Physiology and Ecology, Thomas Odhiambo Campus, P.O. Box 30, Mbita, 40305, KenyaDepartment of Vector Biology, Liverpool School of Tropical Medicine, Liverpool, L3 5QA, UKBackground: Growing insecticide resistance and changes in biting and resting behavior of malaria vectors threaten efficacy of insecticide treated nets and indoor residual spraying. Larval source management (LSM) is a promising approach that can target mosquitoes irrespective of their behavior as adults. However, the use of traditional monitoring methods for immature stages of Anopheles mosquitoes is a major challenge to LSM due to the variability in their breeding habitats.  We evaluate the use of an environmental DNA (eDNA) analysis technique in monitoring Anopheles gambiae sensu lato larvae in experimental aquatic habitats. Methods: eDNA was simultaneously sampled and extracted from different volumes of water, number of larvae, and occupation time. Larval presence was detected using PCR and eDNA concentration in samples from 1 L habitats quantified using an IGS and cyt b TaqMan assays. The limit of detection of the two assays was tested and larval density correlated with eDNA positivity. Results: 74% of replicates in the 50 mL habitats were PCR positive with at least 6h required to get a signal from a single larva (0.02 larvae/mL). All 12 replicates where 1 L of water was used were positive with stronger PCR bands than replicates with the same larval density in 50 mL for 24 h. There was a correlation between larval densities and eDNA detection in both assays: IGS, r = 0.503, p = 0.047; and cyt b, r = 0.558, p = 0.025. There was stochasticity in eDNA detection rates, using both PCR and qPCR across all the dilutions. Conclusion: This study has demonstrated the potential use of eDNA analysis for detection and quantification of An. gambiae s.s. mosquito larvae in aquatic habitats. The stochasticity observed in eDNA detection suggest that this technique is best for monitoring aquatic habitats with many larvae at low densities.https://wellcomeopenresearch.org/articles/3-26/v1
collection DOAJ
language English
format Article
sources DOAJ
author Joel Odero
Bruno Gomes
Ulrike Fillinger
David Weetman
spellingShingle Joel Odero
Bruno Gomes
Ulrike Fillinger
David Weetman
Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]
Wellcome Open Research
author_facet Joel Odero
Bruno Gomes
Ulrike Fillinger
David Weetman
author_sort Joel Odero
title Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]
title_short Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]
title_full Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]
title_fullStr Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]
title_full_unstemmed Detection and quantification of Anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental DNA (eDNA). [version 1; referees: 1 approved, 2 approved with reservations]
title_sort detection and quantification of anopheles gambiae sensu lato mosquito larvae in experimental aquatic habitats using environmental dna (edna). [version 1; referees: 1 approved, 2 approved with reservations]
publisher Wellcome
series Wellcome Open Research
issn 2398-502X
publishDate 2018-03-01
description Background: Growing insecticide resistance and changes in biting and resting behavior of malaria vectors threaten efficacy of insecticide treated nets and indoor residual spraying. Larval source management (LSM) is a promising approach that can target mosquitoes irrespective of their behavior as adults. However, the use of traditional monitoring methods for immature stages of Anopheles mosquitoes is a major challenge to LSM due to the variability in their breeding habitats.  We evaluate the use of an environmental DNA (eDNA) analysis technique in monitoring Anopheles gambiae sensu lato larvae in experimental aquatic habitats. Methods: eDNA was simultaneously sampled and extracted from different volumes of water, number of larvae, and occupation time. Larval presence was detected using PCR and eDNA concentration in samples from 1 L habitats quantified using an IGS and cyt b TaqMan assays. The limit of detection of the two assays was tested and larval density correlated with eDNA positivity. Results: 74% of replicates in the 50 mL habitats were PCR positive with at least 6h required to get a signal from a single larva (0.02 larvae/mL). All 12 replicates where 1 L of water was used were positive with stronger PCR bands than replicates with the same larval density in 50 mL for 24 h. There was a correlation between larval densities and eDNA detection in both assays: IGS, r = 0.503, p = 0.047; and cyt b, r = 0.558, p = 0.025. There was stochasticity in eDNA detection rates, using both PCR and qPCR across all the dilutions. Conclusion: This study has demonstrated the potential use of eDNA analysis for detection and quantification of An. gambiae s.s. mosquito larvae in aquatic habitats. The stochasticity observed in eDNA detection suggest that this technique is best for monitoring aquatic habitats with many larvae at low densities.
url https://wellcomeopenresearch.org/articles/3-26/v1
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