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Evidence for gene duplication in the voltage-gated sodium channel gene of Aedes aegypti

https://doi.org/10.1093/emph/eot012
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ps.1574openalex-snapshot
Pyrethroids, knockdown resistance and sodium channels
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Knockdown resistance to DDT and pyrethroids: from target‐site mutations to molecular modelling
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Gene amplification and insecticide resistance
inferredcites →https://doi.org/10.1007/bf00267238openalex-snapshot
Temperature-sensitive mutations in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/0092-8674(89)90512-6openalex-snapshot
Molecular analysis of the para locus, a sodium channel gene in Drosophila
inferredcites →https://doi.org/10.1016/j.actatropica.2008.08.004openalex-snapshot
Development and application of a simple colorimetric assay reveals widespread distribution of sodium channel mutations in Thai populations of Aedes aegypti
inferredcites →https://doi.org/10.1016/j.bbrc.2011.03.060openalex-snapshot
Sodium channel genes and their differential genotypes at the L-to-F kdr locus in the mosquito Culex quinquefasciatus
inferredcites →https://doi.org/10.1016/j.cbpb.2008.03.008openalex-snapshot
Comparison of Anopheles gambiae and Culex pipiens acetycholinesterase 1 biochemical properties
inferredcites →https://doi.org/10.1016/j.ibmb.2007.09.007openalex-snapshot
Genomic analysis of detoxification genes in the mosquito Aedes aegypti
inferredcites →https://doi.org/10.1016/j.ibmb.2009.01.001openalex-snapshot
A novel amino acid substitution in a voltage-gated sodium channel is associated with knockdown resistance to permethrin in Aedes aegypti
inferredcites →https://doi.org/10.1016/j.ibmb.2009.09.006openalex-snapshot
The discovery of a novel sodium channel in the cockroach Periplaneta americana: Evidence for an early duplication of the para-like gene
inferredcites →https://doi.org/10.1016/j.ibmb.2010.06.001openalex-snapshot
Genomic structures of Cyp9m10 in pyrethroid resistant and susceptible strains of Culex quinquefasciatus
inferredcites →https://doi.org/10.1016/j.ibmb.2012.01.005openalex-snapshot
Molecular characterization of DSC1 orthologs in invertebrate species
inferredcites →https://doi.org/10.1016/j.taap.2008.10.006openalex-snapshot
Molecular determinants on the insect sodium channel for the specific action of type II pyrethroid insecticides
inferredcites →https://doi.org/10.1016/s0896-6273(00)81133-2openalex-snapshot
From Ionic Currents to Molecular Mechanisms
inferredcites →https://doi.org/10.1016/s0896-6273(04)00148-5openalex-snapshot
A Voltage-Gated Calcium-Selective Channel Encoded by a Sodium Channel-like Gene
inferredcites →https://doi.org/10.1017/s001667230100547xopenalex-snapshot
Insecticide resistance genes induce a mating competition cost in Culex pipiens mosquitoes
inferredcites →https://doi.org/10.1017/s0016672304006792openalex-snapshot
Insecticide resistance genes confer a predation cost on mosquitoes, Culex pipiens
inferredcites →https://doi.org/10.1038/167855a0openalex-snapshot
Inheritance of Resistance to DDT in the Housefly, Musca domestica L.
inferredcites →https://doi.org/10.1038/168193a0openalex-snapshot
Mechanism of Resistance to Insecticide in Houseflies
inferredcites →https://doi.org/10.1038/hdy.1993.43openalex-snapshot
Stability of insecticide resistance due to amplification of esterase genes in Culex pipiens
inferredcites →https://doi.org/10.1038/nature01771openalex-snapshot
Dosage sensitivity and the evolution of gene families in yeast
inferredcites →https://doi.org/10.1038/nrg2482openalex-snapshot
Turning a hobby into a job: How duplicated genes find new functions
inferredcites →https://doi.org/10.1042/bj20051925openalex-snapshot
Modelling insecticide-binding sites in the voltage-gated sodium channel
inferredcites →https://doi.org/10.1046/j.1365-2915.2003.00412.xopenalex-snapshot
Pyrethroid and DDT cross‐resistance in Aedes aegypti is correlated with novel mutations in the voltage‐gated sodium channel gene
inferredcites →https://doi.org/10.1046/j.1471-4159.1996.67052115.xopenalex-snapshot
Existence of Two Acetylcholinesterases in the Mosquito Culex pipiens (Diptera: Culicidae)
inferredcites →https://doi.org/10.1073/pnas.68.5.890openalex-snapshot
Temperature-Sensitive Mutations in Drosophila melanogaster , VII. A Mutation ( para ts ) Causing Reversible Adult Paralysis
inferredcites →https://doi.org/10.1073/pnas.76.6.2858openalex-snapshot
Fixation of a deleterious allele at one of two "duplicate" loci by mutation pressure and random drift.
inferredcites →https://doi.org/10.1080/15216540701352042openalex-snapshot
DDT, pyrethrins, pyrethroids and insect sodium channels
inferredcites →https://doi.org/10.1093/ilar.52.1.e8openalex-snapshot
The Brazilian Legal Framework on the Scientific Use of Animals
inferredcites →https://doi.org/10.1093/molbev/msm025openalex-snapshot
Independent Duplications of the Acetylcholinesterase Gene Conferring Insecticide Resistance in the Mosquito Culex pipiens
inferredcites →https://doi.org/10.1098/rstb.1998.0322openalex-snapshot
An overview of the evolution of overproduced esterases in the mosquito Culex pipiens
inferredcites →https://doi.org/10.1101/gr.087916.108openalex-snapshot
Two duplicated P450 genes are associated with pyrethroid resistance in Anopheles funestus, a major malaria vector
inferredcites →https://doi.org/10.1111/j.1365-2583.2006.00672.xopenalex-snapshot
A deficit of detoxification enzymes: pesticide sensitivity and environmental response in the honeybee
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00733.xopenalex-snapshot
A comparative study of voltage‐gated sodium channels in the Insecta: implications for pyrethroid resistance in Anopheline and other Neopteran species
inferredcites →https://doi.org/10.1111/j.1365-2583.2007.00774.xopenalex-snapshot
A mutation in the voltage‐gated sodium channel gene associated with pyrethroid resistance in Latin American Aedes aegypti
inferredcites →https://doi.org/10.1111/j.1365-3156.2009.02378.xopenalex-snapshot
Frequency of Val1016Ile mutation in the voltage‐gated sodium channel gene of Aedes aegypti Brazilian populations
inferredcites →https://doi.org/10.1111/j.1558-5646.1998.tb01644.xopenalex-snapshot
EVOLUTION OF RESISTANCE INCULEX PIPIENS: ALLELE REPLACEMENT AND CHANGING ENVIRONMENT
inferredcites →https://doi.org/10.1126/science.1076781openalex-snapshot
Evolution of Supergene Families Associated with Insecticide Resistance
inferredcites →https://doi.org/10.1126/science.3755546openalex-snapshot
Amplification of an Esterase Gene Is Responsible for Insecticide Resistance in a California Culex Mosquito
inferredcites →https://doi.org/10.1186/1756-3305-4-5openalex-snapshot
Insecticide resistance in Aedes aegypti populations from Ceará, Brazil
inferredcites →https://doi.org/10.1242/jeb.205.5.575openalex-snapshot
Evolution of voltage-gated Na+ channels
inferredcites →https://doi.org/10.1371/journal.pntd.0000531openalex-snapshot
Recent Rapid Rise of a Permethrin Knock Down Resistance Allele in Aedes aegypti in México
inferredcites →https://doi.org/10.1371/journal.pntd.0001692openalex-snapshot
Gene Amplification, ABC Transporters and Cytochrome P450s: Unraveling the Molecular Basis of Pyrethroid Resistance in the Dengue Vector, Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pone.0002172openalex-snapshot
Evidence of Introgression of the ace-1R Mutation and of the ace-1 Duplication in West African Anopheles gambiae s. s
inferredcites →https://doi.org/10.1371/journal.pone.0031889openalex-snapshot
Effect of Insecticide Resistance on Development, Longevity and Reproduction of Field or Laboratory Selected Aedes aegypti Populations
inferredcites →https://doi.org/10.1590/s0074-02762005000400017openalex-snapshot
Monitoring of resistance to the pyrethroid cypermethrin in Brazilian Aedes aegypti (Diptera: Culicidae) populations collected between 2001 and 2003
inferredcites →https://doi.org/10.1590/s0074-02762009000100007openalex-snapshot
Effect of the chitin synthesis inhibitor triflumuron on the development, viability and reproduction of Aedes aegypti
inferredcites →https://doi.org/10.1590/s0074-02762012000400001openalex-snapshot
The classification of esterases: an important gene family involved in insecticide resistance - A review
inferredcites →https://doi.org/10.2307/2411080openalex-snapshot
Evolution of Resistance in Culex pipiens: Allele Replacement and Changing Environment
inferredcites →https://doi.org/10.4269/ajtmh.2003.68.329openalex-snapshot
RESISTANCE OF AEDES AEGYPTI TO ORGANOPHOSPHATES IN SEVERAL MUNICIPALITIES IN THE STATE OF RIO DE JANEIRO AND ESPiRITO SANTO, BRAZIL
inferredcites →https://doi.org/10.4269/ajtmh.2007.77.467openalex-snapshot
Insecticide Resistance Mechanisms of Brazilian Aedes aegypti Populations from 2001 to 2004
inferredcites →https://doi.org/10.4269/ajtmh.2009.81.108openalex-snapshot
Voltage-Gated Sodium Channel Polymorphism and Metabolic Resistance in Pyrethroid-Resistant Aedes aegypti from Brazil
inferredcites →https://doi.org/10.4269/ajtmh.2010.09-0623openalex-snapshot
Pyrethroid Resistance in Aedes aegypti from Grand Cayman
inferredcites →https://doi.org/10.5123/s1679-49742007000400007openalex-snapshot
Aedes aegypti: vigilância, monitoramento da resistência e alternativas de controle no Brasil
inferredcites →https://doi.org/10.5772/2446openalex-snapshot
Insecticides - Basic and Other Applications
inferredcites →https://doi.org/10.5772/30588openalex-snapshot
The Pyrethroid Knockdown Resistance

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4827982openalex-extracted
Glycine to Valine Substitution Enhances I1011m-Mediated Sodium Channel Resistance to Type I Pyrethroids, But Not Type Ii Pyrethroids
inferred← citeshttps://doi.org/10.6620/zs.2025.64-31zenodo-depositor-declared
Understanding the Global Dynamics of Pyrethroid Resistance-related kdr mutations in Aedes (Stegomyia) aegypti (Linnaeus, 1762) (Diptera: Culicidae).
inferred← citeshttps://doi.org/10.1002/arch.21686openalex-snapshot
Chronology of sodium channel mutations associated with pyrethroid resistance in Aedes aegypti
inferred← citeshttps://doi.org/10.1002/ps.6631openalex-snapshot
Perspectives on gene copy number variation and pesticide resistance
inferred← citeshttps://doi.org/10.1002/ps.8761openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00436-025-08538-5openalex-snapshot
Pyrethroid and organochlorine susceptibility in Aedes aegypti populations from eastern black sea region, Türkiye: traces in the kdr gene region of the species origin
inferred← citeshttps://doi.org/10.1016/j.actatropica.2015.04.026openalex-snapshot
Involvement of metabolic resistance and F1534C kdr mutation in the pyrethroid resistance mechanisms of Aedes aegypti in India
inferred← citeshttps://doi.org/10.1016/j.actatropica.2026.108331openalex-snapshot
A novel L932F mutation in the voltage-gated sodium channel associated with deltamethrin resistance in Aedes aegypti (Diptera: Culicidae) from Southern Taiwan
inferred← citeshttps://doi.org/10.1016/j.aquaculture.2025.743270openalex-snapshot
Nanopore sequencing reveals copy number variants (CNV) and single nucleotide polymorphisms (SNP) in the sea louse genome associated with drug resistance
inferred← citeshttps://doi.org/10.1016/j.aspen.2018.07.013openalex-snapshot
The characteristics of voltage-gated sodium channel and the association with lambda cyhalothrin resistance in Spodoptera exigua
inferred← citeshttps://doi.org/10.1016/j.bbrc.2015.06.085openalex-snapshot
A sodium channel variant in Aedes aegypti as a candidate pathogen sensor for viral-associated molecular patterns
inferred← citeshttps://doi.org/10.1016/j.cbpb.2016.10.006openalex-snapshot
Characterization of an insect heterodimeric voltage-gated sodium channel with unique alternative splicing mode
inferred← citeshttps://doi.org/10.1016/j.cois.2018.04.005openalex-snapshot
Copy number variation (CNV) and insecticide resistance in mosquitoes: evolving knowledge or an evolving problem?
inferred← citeshttps://doi.org/10.1016/j.pestbp.2015.01.004openalex-snapshot
Genotype to phenotype, the molecular and physiological dimensions of resistance in arthropods
inferred← citeshttps://doi.org/10.1016/j.pestbp.2019.03.008openalex-snapshot
Point mutations in the voltage-gated sodium channel gene associated with pyrethroid resistance in Iranian populations of the European red mite Panonychus ulmi
inferred← citeshttps://doi.org/10.1016/j.pestbp.2021.104851openalex-snapshot
Comparative characterization of two putative duplicated sodium channel genes in the red flour beetle, Tribolium castaneum
inferred← citeshttps://doi.org/10.1016/j.pestbp.2024.105994openalex-snapshot
Glycine to valine substitution in the short intracellular linkers of domain II enhances I1011M-mediated sodium channel resistance to Type I pyrethroids, but not Type II pyrethroids
inferred← citeshttps://doi.org/10.1038/s41598-017-06080-8openalex-snapshot
Detection and quantitation of copy number variation in the voltage-gated sodium channel gene of the mosquito Culex quinquefasciatus
inferred← citeshttps://doi.org/10.1038/s41598-020-70029-7openalex-snapshot
Kdr genotyping in Aedes aegypti from Brazil on a nation-wide scale from 2017 to 2018
inferred← citeshttps://doi.org/10.1038/s41598-022-08642-xopenalex-snapshot
Detection of sex in adults and larvae of Leptinotarsa decemlineata on principle of copy number variation
inferred← citeshttps://doi.org/10.1038/s41598-023-44430-xopenalex-snapshot
Genetic structure and kdr mutations in Aedes aegypti populations along a road crossing the Amazon Forest in Amapá State, Brazil
inferred← citeshttps://doi.org/10.1093/jme/tjab048openalex-snapshot
Molecular Analysis of Targeted Insecticide Resistance Gene Mutations in Field-Caught Mosquitos of Medical Importance From Saudi Arabia
inferred← citeshttps://doi.org/10.1093/jme/tjy037openalex-snapshot
Effect of Relaxation of Deltamethrin Pressure on Metabolic Resistance in a Pyrethroid-Resistant Aedes aegypti (Diptera: Culicidae) Strain Harboring Fixed P989P and G1016G kdr Alleles
inferred← citeshttps://doi.org/10.1093/jme/tjz035openalex-snapshot
V1016G Point Mutation: The Key Mutation in the Voltage-Gated Sodium Channel (Vgsc) Gene of Pyrethroid-Resistant Aedes aegypti (Diptera: Culicidae) in Indonesia.
inferred← citeshttps://doi.org/10.1101/2024.12.11.627862openalex-snapshot
Knockdown-resistance ( kdr ) mutations in Indian Aedes aegypti populations: lack of recombination among haplotypes bearing V1016G, F1534C, and F1534L kdr alleles
inferred← citeshttps://doi.org/10.1101/399568openalex-snapshot
Whole genome sequencing reveals high complexity of copy number variation at insecticide resistance loci in malaria mosquitoes
inferred← citeshttps://doi.org/10.1101/740829openalex-snapshot
A new knockdown resistance ( kdr ) mutation, F1534L, in the voltage-gated sodium channel of Aedes aegypti , co-occurring with F1534C, S989P and V1016G
inferred← citeshttps://doi.org/10.1101/gr.189225.115openalex-snapshot
Identifying genomic changes associated with insecticide resistance in the dengue mosquito Aedes aegypti by deep targeted sequencing
inferred← citeshttps://doi.org/10.1101/gr.245795.118openalex-snapshot
Whole-genome sequencing reveals high complexity of copy number variation at insecticide resistance loci in malaria mosquitoes
inferred← citeshttps://doi.org/10.1111/jvec.12298openalex-snapshot
Two novel mutations in the voltage-gated sodium channel associated with knockdown resistance (kdr) in the dengue vectorAedes aegyptiin Vietnam
inferred← citeshttps://doi.org/10.1155/2018/2410819openalex-snapshot
Levels of Resistance to Pyrethroid among DistinctkdrAlleles inAedes aegyptiLaboratory Lines and Frequency ofkdrAlleles in 27 Natural Populations from Rio de Janeiro, Brazil
inferred← citeshttps://doi.org/10.1155/2018/6257860openalex-snapshot
Insecticide Resistance and Fitness: The Case of Four Aedes aegypti Populations from Different Brazilian Regions
inferred← citeshttps://doi.org/10.1186/1756-3305-7-25openalex-snapshot
Distribution and dissemination of the Val1016Ile and Phe1534Cys Kdr mutations in Aedes aegypti Brazilian natural populations
inferred← citeshttps://doi.org/10.1186/s12915-023-01693-0openalex-snapshot
The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.1186/s12936-015-0599-1openalex-snapshot
Novel mutations on the ace-1 gene of the malaria vector Anopheles albimanus provide evidence for balancing selection in an area of high insecticide resistance in Peru
inferred← citeshttps://doi.org/10.1186/s13071-015-0797-2openalex-snapshot
Contrasting patterns of insecticide resistance and knockdown resistance (kdr) in the dengue vectors Aedes aegypti and Aedes albopictus from Malaysia
inferred← citeshttps://doi.org/10.1186/s13071-016-1346-3openalex-snapshot
Spatial variation of insecticide resistance in the dengue vector Aedes aegypti presents unique vector control challenges
inferred← citeshttps://doi.org/10.1186/s13071-020-04127-wopenalex-snapshot
Evaluation of resistance to pyrethroid and organophosphate adulticides and kdr genotyping in Aedes aegypti populations from Roraima, the northernmost Brazilian State
inferred← citeshttps://doi.org/10.1186/s13071-020-04201-3openalex-snapshot
A new knockdown resistance (kdr) mutation, F1534L, in the voltage-gated sodium channel of Aedes aegypti, co-occurring with F1534C, S989P and V1016G
inferred← citeshttps://doi.org/10.1186/s13071-026-07619-3openalex-snapshot
Insecticide susceptibility and knockdown resistance (Kdr) mutations (F1534C and V1016I) in Aedes aegypti populations from Dar es Salaam, Tanzania
inferred← citeshttps://doi.org/10.13057/biodiv/d240136openalex-snapshot
Bioassay and molecular detection of insecticides resistance of Aedes aegypti, vector of dengue in Central Java Province, Indonesia
inferred← citeshttps://doi.org/10.1371/journal.pntd.0005917openalex-snapshot
Local selection in the presence of high levels of gene flow: Evidence of heterogeneous insecticide selection pressure across Ugandan Culex quinquefasciatus populations
inferred← citeshttps://doi.org/10.1371/journal.pntd.0006227openalex-snapshot
The impact of insecticide applications on the dynamics of resistance: The case of four Aedes aegypti populations from different Brazilian regions
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007291openalex-snapshot
Voltage-gated sodium channel intron polymorphism and four mutations comprise six haplotypes in an Aedes aegypti population in Taiwan
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007818openalex-snapshot
High-throughput genotyping of a full voltage-gated sodium channel gene via genomic DNA using target capture sequencing and analytical pipeline MoNaS to discover novel insecticide resistance mutations
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008219openalex-snapshot
Evolution of kdr haplotypes in worldwide populations of Aedes aegypti: Independent origins of the F1534C kdr mutation
inferred← citeshttps://doi.org/10.1371/journal.pntd.0013126openalex-snapshot
Knockdown-resistance (kdr) mutations in Indian Aedes aegypti populations: Lack of recombination among haplotypes bearing V1016G, F1534C, and F1534L kdr alleles
inferred← citeshttps://doi.org/10.21203/rs.3.rs-28170/v1openalex-snapshot
Molecular Analysis of Targeted Insecticide Resistance Gene Mutations in field Aedes Aegypti and Culex Quinquefasciatus Mosquito Vectors of Arboviruses from Saudi Arabia
inferred← citeshttps://doi.org/10.21203/rs.3.rs-35782/v1openalex-snapshot
Molecular analysis of targeted insecticide resistance gene mutations in field Aedes aegypti and Culex quinquefasciatus mosquito vectors of arboviruses from Saudi Arabia
inferred← citeshttps://doi.org/10.21203/rs.3.rs-35782/v2openalex-snapshot
Molecular analysis of targeted insecticide resistance gene mutations in field Aedes aegypti and Culex quinquefasciatus mosquito vectors of arboviruses from Saudi Arabia
inferred← citeshttps://doi.org/10.24072/pcjournal.497openalex-snapshot
A genomic duplication spanning multiple P450s contributes to insecticide resistance in the dengue mosquito Aedes aegypti
inferred← citeshttps://doi.org/10.3390/insects11090584openalex-snapshot
The Midgut Microbiota of Colombian Aedes aegypti Populations with Different Levels of Resistance to the Insecticide Lambda-cyhalothrin
inferred← citeshttps://doi.org/10.47209/2317-5729.v.12.n.4.p.1-16openalex-snapshot
As mutações Kdr em Aedes aegypti e a prevalência da Dengue em Roraima pré e pós-pandemia da Covid-19
inferred← citeshttps://doi.org/10.5007/2175-7925.2020.e75366openalex-snapshot
An overview of the mitigating mechanisms of the fitness cost of mutations associated with pesticide resistance in arthropods
inferred← citeshttps://doi.org/10.51161/conbrapah2023/18512openalex-snapshot
MUTAÇÕES KDR EM AEDES AEGYPTI E A PREVALÊNCIA DA DENGUE NO EXTREMO NORTE DO BRASIL PRÉ E PÓS-PANDEMIA DA COVID-19
inferred← citeshttps://doi.org/10.6084/m9.figshare.12344981openalex-snapshot
Additional file 1 of Evaluation of resistance to pyrethroid and organophosphate adulticides and kdr genotyping in Aedes aegypti populations from Roraima, the northernmost Brazilian State
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617204openalex-snapshot
Additional file 1 of The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617207openalex-snapshot
Additional file 2 of The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.6084/m9.figshare.26617210openalex-snapshot
Additional file 3 of The dynamics of deltamethrin resistance evolution in Aedes albopictus has an impact on fitness and dengue virus type-2 vectorial capacity
inferred← citeshttps://doi.org/10.70675/738358caz5e8az4c8cza0c5z8eb894d1277eopenalex-snapshot
Influence de l’architecture génétique et des variations environnementales sur l’adaptation : la résistance aux insecticides chez les moustiques
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