4.6 Article

A novel fluorescence and DNA combination for versatile, long-term marking of mosquitoes

Journal

METHODS IN ECOLOGY AND EVOLUTION
Volume 12, Issue 6, Pages 1008-1016

Publisher

WILEY
DOI: 10.1111/2041-210X.13592

Keywords

Anopheles gambiae; dispersal; DNA; fluorescent; Mark– release– recapture

Categories

Funding

  1. Division of Intramural Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health

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The study introduced a novel and long-lasting marking method using a combination of fluorescent dye and synthetic DNA tags for efficient marking of adult mosquitoes. The method allows separation of multiple insect subpopulations by utilizing unlimited length and sequence variation in the synthetic DNA tags, making it suitable for field deployment. The marking did not affect survival, oviposition, or Plasmodium competence of the tested mosquitoes, and the retention of DNA and fluorescence was 100% up to 3 weeks.
Current mark-release-recapture methodologies are limited in their ability to address complex problems in vector biology, such as studying multiple groups overlapping in space and time. Additionally, limited mark retention, reduced post-marking survival and the large effort in marking, collection and recapture all complicate effective insect tracking. We have developed and evaluated a marking method using a fluorescent dye (SmartWater(R)) combined with synthetic DNA tags to informatively and efficiently mark adult mosquitoes using an airbrush pump and nebulizer. Using a handheld UV flashlight, the fluorescent marking enabled quick and simple initial detection of recaptures in a field-ready and non-destructive approach that when combined with an extraction-free PCR on individual mosquito legs provides potentially unlimited marking information. This marking, first tested in the laboratory with Anopheles gambiae s.l. mosquitoes, did not affect survival (median ages 24-28 days, p-adj > 0.25), oviposition (median eggs/female of 28.8, 32.5, 33.3 for water, green, red dyes, respectively, p-adj > 0.44) or Plasmodium competence (mean oocysts 5.56-10.6, p-adj > 0.95). DNA and fluorescence had 100% retention up to 3 weeks (longest time point tested) with high intensity, indicating marks would persist longer. We describe a novel, simple, no/low-impact and long-lasting marking method that allows separation of multiple insect subpopulations by combining unlimited length and sequence variation in the synthetic DNA tags. This method can be readily deployed in the field for marking multiple groups of mosquitoes or other insects.

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