Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays
Abstract Background Direct membrane feeding assays (DMFA) are an important tool to study parasite transmission to mosquitoes. Mosquito feeding rates in these artificial systems require optimization, as there are a number of factors that potentially influence the feeding rates and there are no standa...
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doaj-136075e210754d4ca8e10b43ccceaffe2021-07-11T11:31:41ZengBMCParasites & Vectors1756-33052021-07-011411910.1186/s13071-021-04842-yOptimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assaysLincoln Timinao0Rebecca Vinit1Michelle Katusele2Louis Schofield3Thomas R. Burkot4Stephan Karl5Papua New Guinea Institute of Medical ResearchPapua New Guinea Institute of Medical ResearchPapua New Guinea Institute of Medical ResearchAustralian Institute of Tropical Health and Medicine, James Cook UniversityAustralian Institute of Tropical Health and Medicine, James Cook UniversityPapua New Guinea Institute of Medical ResearchAbstract Background Direct membrane feeding assays (DMFA) are an important tool to study parasite transmission to mosquitoes. Mosquito feeding rates in these artificial systems require optimization, as there are a number of factors that potentially influence the feeding rates and there are no standardized methods that apply to all anopheline species. Methods A range of parameters prior to and during direct membrane feeding (DMF) were evaluated for their impact on Anopheles farauti sensu stricto feeding rates, including the starving conditions and duration of starving prior to feeding, membrane type, DMF exposure time, mosquito age, feeding in the light versus the dark, blood volume, mosquito density and temperature of water bath. Results The average successful DMFA feeding rate for An. farauti s.s. colony mosquitoes increased from 50 to 85% when assay parameters were varied. Overnight starvation and Baudruche membrane yielded the highest feeding rates but rates were also affected by blood volume in the feeder and the mosquito density in the feeding cups. Availability of water during the pre-feed starvation period did not significantly impact feeding rates, nor did the exposure duration to blood in membrane feeders, the age of mosquitoes (3, 5 and 7 days post-emergence), feeding in the light versus the dark, or the temperature (34 °C, 38 °C, 42 °C and 46 °C) of the water bath. Conclusion Optimal feeding conditions in An. farauti s.s. DMFA were to offer 50 female mosquitoes in a cup (with a total surface area of ~ 340 cm2 with 1 mosquito/6.8 cm2) that were starved overnight 350–500 µL of blood (collected in heparin-coated Vacutainer tubes) per feeder in feeders with a surface area ~ 5 cm2 (with a maximum capacity of 1.5 mL of blood) via a Baudruche membrane, for at least 10–20 min. Graphical Abstracthttps://doi.org/10.1186/s13071-021-04842-yDirect membrane feeding assayAnopheles farautiPapua New Guinea |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Lincoln Timinao Rebecca Vinit Michelle Katusele Louis Schofield Thomas R. Burkot Stephan Karl |
spellingShingle |
Lincoln Timinao Rebecca Vinit Michelle Katusele Louis Schofield Thomas R. Burkot Stephan Karl Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays Parasites & Vectors Direct membrane feeding assay Anopheles farauti Papua New Guinea |
author_facet |
Lincoln Timinao Rebecca Vinit Michelle Katusele Louis Schofield Thomas R. Burkot Stephan Karl |
author_sort |
Lincoln Timinao |
title |
Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays |
title_short |
Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays |
title_full |
Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays |
title_fullStr |
Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays |
title_full_unstemmed |
Optimization of the feeding rate of Anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays |
title_sort |
optimization of the feeding rate of anopheles farauti s.s. colony mosquitoes in direct membrane feeding assays |
publisher |
BMC |
series |
Parasites & Vectors |
issn |
1756-3305 |
publishDate |
2021-07-01 |
description |
Abstract Background Direct membrane feeding assays (DMFA) are an important tool to study parasite transmission to mosquitoes. Mosquito feeding rates in these artificial systems require optimization, as there are a number of factors that potentially influence the feeding rates and there are no standardized methods that apply to all anopheline species. Methods A range of parameters prior to and during direct membrane feeding (DMF) were evaluated for their impact on Anopheles farauti sensu stricto feeding rates, including the starving conditions and duration of starving prior to feeding, membrane type, DMF exposure time, mosquito age, feeding in the light versus the dark, blood volume, mosquito density and temperature of water bath. Results The average successful DMFA feeding rate for An. farauti s.s. colony mosquitoes increased from 50 to 85% when assay parameters were varied. Overnight starvation and Baudruche membrane yielded the highest feeding rates but rates were also affected by blood volume in the feeder and the mosquito density in the feeding cups. Availability of water during the pre-feed starvation period did not significantly impact feeding rates, nor did the exposure duration to blood in membrane feeders, the age of mosquitoes (3, 5 and 7 days post-emergence), feeding in the light versus the dark, or the temperature (34 °C, 38 °C, 42 °C and 46 °C) of the water bath. Conclusion Optimal feeding conditions in An. farauti s.s. DMFA were to offer 50 female mosquitoes in a cup (with a total surface area of ~ 340 cm2 with 1 mosquito/6.8 cm2) that were starved overnight 350–500 µL of blood (collected in heparin-coated Vacutainer tubes) per feeder in feeders with a surface area ~ 5 cm2 (with a maximum capacity of 1.5 mL of blood) via a Baudruche membrane, for at least 10–20 min. Graphical Abstract |
topic |
Direct membrane feeding assay Anopheles farauti Papua New Guinea |
url |
https://doi.org/10.1186/s13071-021-04842-y |
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