Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.

Rapidly emerging insecticide resistance is creating an urgent need for new active ingredients to control the adult mosquitoes that vector malaria. Biopesticides based on the spores of entomopathogenic fungi have shown considerable promise by causing very substantial mortality within 7-14 days of exp...

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Main Authors: Simon Blanford, Wangpeng Shi, Riann Christian, James H Marden, Lizette L Koekemoer, Basil D Brooke, Maureen Coetzee, Andrew F Read, Matthew B Thomas
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21897846/?tool=EBI
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author Simon Blanford
Wangpeng Shi
Riann Christian
James H Marden
Lizette L Koekemoer
Basil D Brooke
Maureen Coetzee
Andrew F Read
Matthew B Thomas
author_facet Simon Blanford
Wangpeng Shi
Riann Christian
James H Marden
Lizette L Koekemoer
Basil D Brooke
Maureen Coetzee
Andrew F Read
Matthew B Thomas
author_sort Simon Blanford
collection DOAJ
description Rapidly emerging insecticide resistance is creating an urgent need for new active ingredients to control the adult mosquitoes that vector malaria. Biopesticides based on the spores of entomopathogenic fungi have shown considerable promise by causing very substantial mortality within 7-14 days of exposure. This mortality will generate excellent malaria control if there is a high likelihood that mosquitoes contact fungi early in their adult lives. However, where contact rates are lower, as might result from poor pesticide coverage, some mosquitoes will contact fungi one or more feeding cycles after they acquire malaria, and so risk transmitting malaria before the fungus kills them. Critics have argued that 'slow acting' fungal biopesticides are, therefore, incapable of delivering malaria control in real-world contexts. Here, utilizing standard WHO laboratory protocols, we demonstrate effective action of a biopesticide much faster than previously reported. Specifically, we show that transient exposure to clay tiles sprayed with a candidate biopesticide comprising spores of a natural isolate of Beauveria bassiana, could reduce malaria transmission potential to zero within a feeding cycle. The effect resulted from a combination of high mortality and rapid fungal-induced reduction in feeding and flight capacity. Additionally, multiple insecticide-resistant lines from three key African malaria vector species were completely susceptible to fungus. Thus, fungal biopesticides can block transmission on a par with chemical insecticides, and can achieve this where chemical insecticides have little impact. These results support broadening the current vector control paradigm beyond fast-acting chemical toxins.
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spelling doaj.art-01cd96ec7ab945568b018cfe701abfc72022-12-21T21:34:34ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0168e2359110.1371/journal.pone.0023591Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.Simon BlanfordWangpeng ShiRiann ChristianJames H MardenLizette L KoekemoerBasil D BrookeMaureen CoetzeeAndrew F ReadMatthew B ThomasRapidly emerging insecticide resistance is creating an urgent need for new active ingredients to control the adult mosquitoes that vector malaria. Biopesticides based on the spores of entomopathogenic fungi have shown considerable promise by causing very substantial mortality within 7-14 days of exposure. This mortality will generate excellent malaria control if there is a high likelihood that mosquitoes contact fungi early in their adult lives. However, where contact rates are lower, as might result from poor pesticide coverage, some mosquitoes will contact fungi one or more feeding cycles after they acquire malaria, and so risk transmitting malaria before the fungus kills them. Critics have argued that 'slow acting' fungal biopesticides are, therefore, incapable of delivering malaria control in real-world contexts. Here, utilizing standard WHO laboratory protocols, we demonstrate effective action of a biopesticide much faster than previously reported. Specifically, we show that transient exposure to clay tiles sprayed with a candidate biopesticide comprising spores of a natural isolate of Beauveria bassiana, could reduce malaria transmission potential to zero within a feeding cycle. The effect resulted from a combination of high mortality and rapid fungal-induced reduction in feeding and flight capacity. Additionally, multiple insecticide-resistant lines from three key African malaria vector species were completely susceptible to fungus. Thus, fungal biopesticides can block transmission on a par with chemical insecticides, and can achieve this where chemical insecticides have little impact. These results support broadening the current vector control paradigm beyond fast-acting chemical toxins.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21897846/?tool=EBI
spellingShingle Simon Blanford
Wangpeng Shi
Riann Christian
James H Marden
Lizette L Koekemoer
Basil D Brooke
Maureen Coetzee
Andrew F Read
Matthew B Thomas
Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.
PLoS ONE
title Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.
title_full Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.
title_fullStr Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.
title_full_unstemmed Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.
title_short Lethal and pre-lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors.
title_sort lethal and pre lethal effects of a fungal biopesticide contribute to substantial and rapid control of malaria vectors
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21897846/?tool=EBI
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