Evidence map›Paper›PMID 27460671›Full record

ArticleParasites & vectors2016

Additive effect of knockdown resistance mutations, S989P, V1016G and F1534C, in a heterozygous genotype conferring pyrethroid resistance in Aedes aegypti in Thailand.

Suriya Plernsub, Jassada Saingamsook, Jintana Yanola, Nongkran Lumjuan, Pongsri Tippawangkosol, Kom Sukontason, Catherine Walton, Pradya Somboon

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
10.9field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors at 2 institutions in 2 countries.

Suriya PlernsubDepartment of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Jassada SaingamsookDepartment of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Jintana YanolaDepartment of Medical Technology, Faculty of Associated Medical Sciences, Chiang Mai University, Chiang Mai, Thailand.
Nongkran LumjuanResearch Institute for Health Sciences, Chiang Mai University, Chiang Mai, Thailand.
Pongsri TippawangkosolDepartment of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Kom SukontasonDepartment of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand.
Catherine WaltonFaculty of Life Sciences, University of Manchester, Manchester, UK.
Pradya SomboonDepartment of Parasitology, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand. pradya.somboon@cmu.ac.th.
Chiang Mai University · THUniversity of Manchester · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMutation in the voltage-gated sodium channel gene that results in knockdown resistance (kdr), is a major mechanism of pyrethroid resistance in several mosquito species. In Aedes aegypti, V1016G (occurring with and without S989P) and F1534C mutations are common and widely distributed throughout Asia. The G1016 allele is known to be associated with resistance to type I and II pyrethroids. The C1534 allele is primarily associated with resistance to type I pyrethroids and is known to be a recessive allele in conferring kdr.

methodsWe performed crossing experiments using a P989 + G1016 homozygous mutant strain (UPK-R), a C1534 homozygous mutant strain (PMD-R) and a pyrethroid susceptible strain (PMD) to determine the insecticide susceptibility of different genotypic hybrids. Allele-specific PCR methods were used to confirm the genotypes. Metabolic resistance caused by oxidative enzymes and esterase enzymes was ruled out by the addition of piperonyl butoxide (PBO) and bis(4-nitrophenyl)-phosphate, BNPP), respectively.

resultsThe median lethal concentration (LC50) of deltamethrin susceptibility of a S/P989 + V/G1016 + F/F1534 double heterozygous hybrid from the UPK-R × PMD cross was 0.57 (95 % CI: 0.51-0.63) μgl(-1), which was about 12-fold lower than for UPK-R, 6.98 (6.10-8.04) μgl(-1), and only about 4-fold greater than the susceptible PMD, 0.13 (0.12-0.15) μgl(-1). This resistance returned to 0.08 (0.07-0.09) μgl(-1) on the addition of PBO suggesting that the P989 + G1016 kdr alleles are recessive. The LC50 of the S/P989 + V/G1016 + F/C1534 triple heterozygous hybrid was 3.58 (3.21-3.95) μgl(-1), which was intermediate between that of the homozygous mutant genotypes, being 2-fold higher than the C1534 homozygote and 2-fold lower than the P989 + G1016 homozygote. These minor differences and the high LC50 values of the triple mutated heterozygote indicate there is some degree of functional equivalence of the P989 + G1016 and C1534 alleles in the heterozygote. Addition of PBO decreased the LC50 values by 2-fold, from 3.58 (3.21-3.95) to 1.52 (1.35-1.73) μgl(-1), suggesting that oxidase enzymes play a partial role in resistance. The results are consistent with the median lethal time (LT50) of the triple mutated heterozygote against 0.05 % deltamethrin paper. An adult susceptibility test also revealed that the triple mutated heterozygote was resistant to deltamethrin and permethrin.

conclusionsThe combination of the three kdr alleles in the triple mutated heterozygote, S/P989 + V/G1016 + F/C1534, confers high resistance to pyrethroids. This heterozygous form is common in Ae. aegypti populations throughout Thailand and may have an adverse effect on the efficacy of a mosquito control program using insecticide-based approaches.

Indexed as

Gene Knockdown TechniquesGenotypeInsecticide ResistanceAedesAnimalsCrosses, GeneticInsecticidesPyrethrinsSodium ChannelsThailandInsecticidesPyrethrinsSodium ChannelsAedes aegyptiGeneticsInsecticidekdr

Identifiers

PMID27460671
PMCPMC4962480
OpenAlexW2475543551

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LicenceCC BY
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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.