Evidence map›Paper›PMID 26047119›Full record

ArticlePesticide biochemistry and physiology2015

Carbamate and pyrethroid resistance in the akron strain of Anopheles gambiae.

James M Mutunga, Troy D Anderson, Derek T Craft, Aaron D Gross, Daniel R Swale, Fan Tong, Dawn M Wong, Paul R Carlier, Jeffrey R Bloomquist

Open access · greenAbstract read
In one paragraph

Article in Pesticide biochemistry and physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

20 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
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  3. Mechanisms of carbamate resistance in the malaria vector:Parasite epidemiology and control · 2026
    Review
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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

9 authors at 2 institutions in 1 country.

James M MutungaDepartment of Entomology, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Troy D AndersonDepartment of Entomology, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Derek T CraftDepartment of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Aaron D GrossEmerging Pathogens Institute, Department of Entomology and Nematology, University of Florida, Gainesville, FL 32610, USA.
Daniel R SwaleEmerging Pathogens Institute, Department of Entomology and Nematology, University of Florida, Gainesville, FL 32610, USA.
Fan TongEmerging Pathogens Institute, Department of Entomology and Nematology, University of Florida, Gainesville, FL 32610, USA.
Dawn M WongDepartment of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Paul R CarlierDepartment of Chemistry, Virginia Polytechnic Institute and State University, Blacksburg, VA 24061, USA.
Jeffrey R BloomquistEmerging Pathogens Institute, Department of Entomology and Nematology, University of Florida, Gainesville, FL 32610, USA. Electronic address: jbquist@epi.ufl.edu.
Virginia Tech · USUniversity of Florida · US

Funding

Development of vector-specific, resistance-breaking insecticides to reduce malariR01AI082581 · NIAID · VIRGINIA POLYTECHNIC INST AND ST UNIV · PI CARLIER, PAUL R · 2009 to 2013
$3.4M
NIAID NIH HHS R01 AI082581NIAID NIH HHS R01AI082581
6 · The paper itself

Abstract

Insecticide resistance in the malaria vector, Anopheles gambiae, is a serious problem, epitomized by the multi-resistant Akron strain, originally isolated in the country of Benin. Here we report resistance in this strain to pyrethroids and DDT (13-fold to 35-fold compared to the susceptible G3 strain), but surprisingly little resistance to etofenprox, a compound sometimes described as a "pseudo-pyrethroid." There was also strong resistance to topically-applied commercial carbamates (45-fold to 81-fold), except for the oximes aldicarb and methomyl. Biochemical assays showed enhanced cytochrome P450 monooxygenase and carboxylesterase activity, but not that of glutathione-S-transferase. A series of substituted α,α,α,-trifluoroacetophenone oxime methylcarbamates were evaluated for enzyme inhibition potency and toxicity against G3 and Akron mosquitoes. The compound bearing an unsubstituted phenyl ring showed the greatest toxicity to mosquitoes of both strains. Low cross resistance in Akron was retained by all analogs in the series. Kinetic analysis of acetylcholinesterase activity and its inhibition by insecticides in the G3 strain showed inactivation rate constants greater than that of propoxur, and against Akron enzyme inactivation rate constants similar to that of aldicarb. However, inactivation rate constants against recombinant human AChE were essentially identical to that of the G3 strain. Thus, the acetophenone oxime carbamates described here, though potent insecticides that control resistant Akron mosquitoes, require further structural modification to attain acceptable selectivity and human safety.

Indexed as

Insecticide ResistanceAcetylcholinesteraseAnimalsAnophelesCarbamatesDDTEsterasesGlutathione TransferaseInsecticidesPyrethrinsAcetylcholinesteraseCarbamatesDDTEsterasesGlutathione TransferaseInsecticidesPyrethrinsAcetylcholinesteraseAnticholinesteraseKnockdown resistanceMetabolic resistanceMosquito

Identifiers

PMID26047119
PMCPMC4457939
OpenAlexW2019649325

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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 OpenQuestion graph.