Evidence map›Paper›PMID 35687594›Full record

ArticlePLoS pathogens2022

Using an antimalarial in mosquitoes overcomes Anopheles and Plasmodium resistance to malaria control strategies.

Douglas G Paton, Alexandra S Probst, Erica Ma, Kelsey L Adams, W Robert Shaw, Naresh Singh, Selina Bopp, Sarah K Volkman, Domombele F S Hien, Prislaure S L Paré and 6 more

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.0field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 34 citations in OpenAlex.

  1. Review
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  6. MappingbioRxiv : the preprint server for biology · 2025
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  12. Review
  13. International journal of molecular sciences · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Antimalarial drug discovery: progress and approaches.Nature reviews. Drug discovery · 2023
    Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 3 countries.

Douglas G PatonDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Alexandra S ProbstDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Erica MaDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Kelsey L AdamsDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
W Robert ShawDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Naresh SinghDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Selina BoppDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Sarah K VolkmanDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Domombele F S HienInstitut de Recherche en Sciences de la Santé/Centre Muraz, Bobo-Dioulasso, Burkina Faso.
Prislaure S L ParéInstitut de Recherche en Sciences de la Santé/Centre Muraz, Bobo-Dioulasso, Burkina Faso.
Rakiswendé S YerbangaInstitut de Recherche en Sciences de la Santé/Centre Muraz, Bobo-Dioulasso, Burkina Faso.
Abdoullaye DiabatéInstitut de Recherche en Sciences de la Santé/Centre Muraz, Bobo-Dioulasso, Burkina Faso.
Roch K DabiréInstitut de Recherche en Sciences de la Santé/Centre Muraz, Bobo-Dioulasso, Burkina Faso.
Thierry LefèvreMIVEGEC, IRD, CNRS, University of Montpellier, Montpellier, France.
Dyann F WirthDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Flaminia CatterucciaDepartment of Immunology and Infectious Diseases, Harvard TH Chan School of Public Health, Boston, United States of America.
Boston University · USHarvard University · USInstitut de Recherche en Sciences de la Santé · BFCentre Muraz · BFCentre international de recherche-développement sur l'elevage en zone subhumide · BF

Funding

Novel Genetic Mechanism of Artemisinin Resistance for MalariaR01AI099105 · NIAID · HARVARD SCHOOL OF PUBLIC HEALTH · PI HARTL, DANIEL L, WIRTH, DYANN F · 2013 to 2021
$5.4M
Malaria transmission blocking through mosquito contact with treated surfacesR01AI148646 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI CATTERUCCIA, FLAMINIA · 2020 to 2024
$3.6M
NIAID NIH HHS R01 AI099105NIAID NIH HHS R01 AI148646
6 · The paper itself

Abstract

The spread of insecticide resistance in Anopheles mosquitoes and drug resistance in Plasmodium parasites is contributing to a global resurgence of malaria, making the generation of control tools that can overcome these roadblocks an urgent public health priority. We recently showed that the transmission of Plasmodium falciparum parasites can be efficiently blocked when exposing Anopheles gambiae females to antimalarials deposited on a treated surface, with no negative consequences on major components of mosquito fitness. Here, we demonstrate this approach can overcome the hurdles of insecticide resistance in mosquitoes and drug resistant in parasites. We show that the transmission-blocking efficacy of mosquito-targeted antimalarials is maintained when field-derived, insecticide resistant Anopheles are exposed to the potent cytochrome b inhibitor atovaquone, demonstrating that this drug escapes insecticide resistance mechanisms that could potentially interfere with its function. Moreover, this approach prevents transmission of field-derived, artemisinin resistant P. falciparum parasites (Kelch13 C580Y mutant), proving that this strategy could be used to prevent the spread of parasite mutations that induce resistance to front-line antimalarials. Atovaquone is also highly effective at limiting parasite development when ingested by mosquitoes in sugar solutions, including in ongoing infections. These data support the use of mosquito-targeted antimalarials as a promising tool to complement and extend the efficacy of current malaria control interventions.

Indexed as

AnophelesAntimalarialsMalariaMalaria, FalciparumPlasmodiumAnimalsAtovaquoneFemalePlasmodium falciparumAntimalarialsAtovaquone

Identifiers

PMID35687594
PMCPMC9223321
OpenAlexW4282005103

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.