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Discovery of super–insecticide-resistant dengue mosquitoes in Asia: Threats of concomitant knockdown resistance mutations

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What this work says

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

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Automated docking using a Lamarckian genetic algorithm and an empirical binding free energy function

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Comparative Protein Structure Modeling Using Modeller

inferredcites →https://doi.org/10.1002/arch.21686openalex-snapshot

Chronology of sodium channel mutations associated with pyrethroid resistance in Aedes aegypti

inferredcites →https://doi.org/10.1002/cpbi.3openalex-snapshot

Comparative Protein Structure Modeling Using MODELLER

inferredcites →https://doi.org/10.1002/cpps.20openalex-snapshot

Comparative Protein Structure Modeling Using MODELLER

inferredcites →https://doi.org/10.1002/jps.2600600940openalex-snapshot

Probit Analysis

inferredcites →https://doi.org/10.1002/ps.4771openalex-snapshot

Voltage‐sensitive sodium channel mutations S989P + V1016G in Aedes aegypti confer variable resistance to pyrethroids, DDT and oxadiazines

inferredcites →https://doi.org/10.1002/ps.5369openalex-snapshot

Phenotypic and genotypic pyrethroid resistance of Aedes albopictus , with focus on the 2017 chikungunya outbreak in Italy

inferredcites →https://doi.org/10.1002/ps.5763openalex-snapshot

The F1534C voltage‐sensitive sodium channel mutation confers 7‐ to 16‐fold resistance to pyrethroid insecticides in Aedes aegypti

inferredcites →https://doi.org/10.1002/ps.6324openalex-snapshot

A first, naturally occurring substitution at the second pyrethroid receptor of voltage‐gated sodium channel of Aedes aegypti

inferredcites →https://doi.org/10.1007/bf01731581openalex-snapshot

A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences

inferredcites →https://doi.org/10.1007/bf02173204openalex-snapshot

Identification of mutations in the housefly para -type sodium channel gene associated with knockdown resistance ( kdr ) to pyrethroid insecticides

inferredcites →https://doi.org/10.1007/s004389670007openalex-snapshot

Cloning and sequencing of the para-type sodium channel gene from susceptible and kdr-resistant German cockroaches (Blattella germanica) and house fly (Musca domestica)

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Dengue in a changing climate

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A sodium channel mutation identified in Aedes aegypti selectively reduces cockroach sodium channel sensitivity to type I, but not type II pyrethroids

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Molecular biology of insect sodium channels and pyrethroid resistance

inferredcites →https://doi.org/10.1016/j.neuro.2016.06.009openalex-snapshot

Alanine to valine substitutions in the pore helix IIIP1 and linker-helix IIIL45 confer cockroach sodium channel resistance to DDT and pyrethroids

inferredcites →https://doi.org/10.1016/j.pestbp.2016.03.005openalex-snapshot

Pyrethroid resistance in Aedes aegypti and Aedes albopictus: Important mosquito vectors of human diseases

inferredcites →https://doi.org/10.1038/nature12060openalex-snapshot

The global distribution and burden of dengue

inferredcites →https://doi.org/10.1038/nrmicro2968openalex-snapshot

Beyond insecticides: new thinking on an ancient problem

inferredcites →https://doi.org/10.1038/s41586-019-1407-9openalex-snapshot

Incompatible and sterile insect techniques combined eliminate mosquitoes

inferredcites →https://doi.org/10.1038/s41587-020-0471-xopenalex-snapshot

Efficient production of male Wolbachia-infected Aedes aegypti mosquitoes enables large-scale suppression of wild populations

inferredcites →https://doi.org/10.1038/s41598-017-11357-zopenalex-snapshot

Contributions of cuticle permeability and enzyme detoxification to pyrethroid resistance in the major malaria vector Anopheles gambiae

inferredcites →https://doi.org/10.1038/s41598-019-49660-6openalex-snapshot

Transgenic Aedes aegypti Mosquitoes Transfer Genes into a Natural Population

inferredcites →https://doi.org/10.1038/srep46549openalex-snapshot

Detection of a new pyrethroid resistance mutation (V410L) in the sodium channel of Aedes aegypti: a potential challenge for mosquito control

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/10.1073/pnas.1305118110openalex-snapshot

Molecular evidence for dual pyrethroid-receptor sites on a mosquito sodium channel

inferredcites →https://doi.org/10.1073/pnas.1618558114openalex-snapshot

Climate variation drives dengue dynamics

inferredcites →https://doi.org/10.1093/jme/tjaa238openalex-snapshot

Novel CONCOMITANT mutations L932F and I936V in the Voltage-Gated Sodium Channel and Its Association With Pyrethroid Resistance inCulex quinquefasciatus(Diptera: Culicidae)

inferredcites →https://doi.org/10.1093/molbev/msy096openalex-snapshot

MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms

inferredcites →https://doi.org/10.1111/imb.12206openalex-snapshot

Overcoming super‐knock down resistance ( super‐kdr ) mediated resistance: multi‐halogenated benzyl pyrethroids are more toxic to super‐kdr than kdr house flies

inferredcites →https://doi.org/10.1111/imb.12605openalex-snapshot

Conservation of the voltage‐sensitive sodium channel protein within the Insecta

inferredcites →https://doi.org/10.1111/j.1365-3156.2010.02717.xopenalex-snapshot

Can piperonyl butoxide enhance the efficacy of pyrethroids against pyrethroid‐resistant Aedes aegypti?

inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot

CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP

inferredcites →https://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

inferredcites →https://doi.org/10.1111/mve.12580openalex-snapshot

Detection of pyrethroid resistance mutations and intron variants in the voltage‐gated sodium channel of Aedes (Stegomyia) aegypti and Aedes (Stegomyia) albopictus mosquitoes from Lao People's Democratic Republic

inferredcites →https://doi.org/10.1126/science.1138878openalex-snapshot

Genome Sequence of Aedes aegypti , a Major Arbovirus Vector

inferredcites →https://doi.org/10.1126/science.287.5462.2474openalex-snapshot

Insect Population Control Using a Dominant, Repressible, Lethal Genetic System

inferredcites →https://doi.org/10.1126/science.aau2596openalex-snapshot

Structural basis for the modulation of voltage-gated sodium channels by animal toxins

inferredcites →https://doi.org/10.1155/2021/8874092openalex-snapshot

Voltage‐Gated Sodium Channel (Vgsc) Mutation‐Based Pyrethroid Resistance in Aedes aegypti Populations of Three Endemic Dengue Risk Areas of Sri Lanka

inferredcites →https://doi.org/10.1177/1010539517753876openalex-snapshot

Resistance of Aedes aegypti (Diptera: Culicidae) Populations to Deltamethrin, Permethrin, and Temephos in Cambodia

inferredcites →https://doi.org/10.1186/1756-3305-3-67openalex-snapshot

Cuticle thickening associated with pyrethroid resistance in the major malaria vector Anopheles funestus

inferredcites →https://doi.org/10.1186/s13071-017-2096-6openalex-snapshot

Combined target site (kdr) mutations play a primary role in highly pyrethroid resistant phenotypes of Aedes aegypti from Saudi Arabia

inferredcites →https://doi.org/10.1186/s13071-018-2899-0openalex-snapshot

Pyrethroid resistance in the dengue vector Aedes aegypti in Southeast Asia: present situation and prospects for management

inferredcites →https://doi.org/10.1186/s13071-019-3472-1openalex-snapshot

Enzymatic and molecular characterization of insecticide resistance mechanisms in field populations of Aedes aegypti from Selangor, Malaysia

inferredcites →https://doi.org/10.1186/s13071-020-04090-6openalex-snapshot

Distribution and pyrethroid resistance status of Aedes aegypti and Aedes albopictus populations and possible phylogenetic reasons for the recent invasion of Aedes aegypti in Nepal

inferredcites →https://doi.org/10.1186/s13071-022-05156-3openalex-snapshot

Monitoring insecticide resistance of adult and larval Aedes aegypti (Diptera: Culicidae) in Phnom Penh, Cambodia

inferredcites →https://doi.org/10.1186/s41182-021-00321-3openalex-snapshot

Phenotypic and haplotypic profiles of insecticide resistance in populations of Aedes aegypti larvae (Diptera: Culicidae) from central Lao PDR

inferredcites →https://doi.org/10.1371/journal.pgen.1009606openalex-snapshot

Permethrin resistance in Aedes aegypti: Genomic variants that confer knockdown resistance, recovery, and death

inferredcites →https://doi.org/10.1371/journal.pntd.0000391openalex-snapshot

Nationwide Investigation of the Pyrethroid Susceptibility of Mosquito Larvae Collected from Used Tires in Vietnam

inferredcites →https://doi.org/10.1371/journal.pntd.0000527openalex-snapshot

Widespread Distribution of a Newly Found Point Mutation in Voltage-Gated Sodium Channel in Pyrethroid-Resistant Aedes aegypti Populations in Vietnam

inferredcites →https://doi.org/10.1371/journal.pntd.0002948openalex-snapshot

Mechanisms of Pyrethroid Resistance in the Dengue Mosquito Vector, Aedes aegypti: Target Site Insensitivity, Penetration, and Metabolism

inferredcites →https://doi.org/10.1371/journal.pntd.0003032openalex-snapshot

Co-occurrence of Point Mutations in the Voltage-Gated Sodium Channel of Pyrethroid-Resistant Aedes aegypti Populations in Myanmar

inferredcites →https://doi.org/10.1371/journal.pntd.0003085openalex-snapshot

A Single Crossing-Over Event in Voltage-Sensitive Na+ Channel Genes May Cause Critical Failure of Dengue Mosquito Control by Insecticides

inferredcites →https://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

inferredcites →https://doi.org/10.1371/journal.pntd.0008154openalex-snapshot

Evidence for both sequential mutations and recombination in the evolution of kdr alleles in Aedes aegypti

inferredcites →https://doi.org/10.1371/journal.pntd.0009549openalex-snapshot

Levels of cross-resistance to pyrethroids conferred by the Vssc knockdown resistance allele 410L+1016I+1534C in Aedes aegypti

inferredcites →https://doi.org/10.1371/journal.pone.0232192openalex-snapshot

Genetic analysis of Aedes aegypti captured at two international airports serving to the Greater Tokyo Area during 2012–2015

inferredcites →https://doi.org/10.1371/journal.pone.0233669openalex-snapshot

High diversity of mosquito vectors in Cambodian primary schools and consequences for arbovirus transmission

inferredcites →https://doi.org/10.1371/journal.ppat.1008433openalex-snapshot

Multiple Wolbachia strains provide comparative levels of protection against dengue virus infection in Aedes aegypti

inferredcites →https://doi.org/10.1584/jpestics.10.141openalex-snapshot

Pyrethroid Resistance: Importance of the kdr-Type Mechanism

inferredcites →https://doi.org/10.2807/1560-7917.es.2019.24.5.1700847openalex-snapshot

First detection of a Vssc allele V1016G conferring a high level of insecticide resistance in Aedes albopictus collected from Europe (Italy) and Asia (Vietnam), 2016: a new emerging threat to controlling arboviral diseases

inferredcites →https://doi.org/10.3201/eid2512.181193openalex-snapshot

Predicting Dengue Outbreaks in Cambodia

inferredcites →https://doi.org/10.3390/insects12050469openalex-snapshot

Sterile Insect Technique: Successful Suppression of an Aedes aegypti Field Population in Cuba

inferredcites →https://doi.org/10.3390/insects6030658openalex-snapshot

Association between Three Mutations, F1565C, V1023G and S996P, in the Voltage-Sensitive Sodium Channel Gene and Knockdown Resistance in Aedes aegypti from Yogyakarta, Indonesia

inferredcites →https://doi.org/10.7883/yoken.64.217openalex-snapshot

First Detection of a Putative Knockdown Resistance Gene in Major Mosquito Vector, Aedes albopictus

What points at this work

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

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Understanding the Global Dynamics of Pyrethroid Resistance-related kdr mutations in Aedes (Stegomyia) aegypti (Linnaeus, 1762) (Diptera: Culicidae).

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Insecticide resistance status of Aedes aegypti in border areas of Yunnan Province

inferred← citeshttps://doi.org/10.1002/ps.8139openalex-snapshot

Pseudomonas mosselii: a potential alternative for managing pyrethroid‐resistant Aedes aegypti

inferred← citeshttps://doi.org/10.1007/978-981-97-4406-0_8openalex-snapshot

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inferred← citeshttps://doi.org/10.1016/j.actatropica.2025.107736openalex-snapshot

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Larvicidal activity, oviposition deterrence, enzymatic test and docking of essential oil of Laurencia dendroidea (Rhodophyta, Ceramiales) for control of the mosquito Aedes aegypti L.

inferred← citeshttps://doi.org/10.1016/j.antiviral.2025.106139openalex-snapshot

Broad-spectrum antiviral ferruginol analog affects the viral proteins translation and actin remodeling during dengue virus infection

inferred← citeshttps://doi.org/10.1016/j.aspen.2025.102421openalex-snapshot

Comparing organophosphate and pyrethroid resistance levels of Aedes aegypti (Diptera: Culicidae) in frequent and infrequent application areas of Taiwan

inferred← citeshttps://doi.org/10.1016/j.cois.2024.101178openalex-snapshot

Recent advances in the study of knockdown resistance mutations in Aedes mosquitoes with a focus on several remarkable mutations

inferred← citeshttps://doi.org/10.1016/j.cois.2025.101384openalex-snapshot

Genomics of urban adaptation and exaptation in mosquitoes and consequences for vectorial capacity

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inferred← citeshttps://doi.org/10.1016/j.ibmb.2024.104214openalex-snapshot

A Unique Mechanism of Transfluthrin Action Revealed by Mapping its Binding Sites in the Mosquito Sodium Channel

inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2025.139455openalex-snapshot

Role of mutation G255A in modulating pyrethroid sensitivity in insect sodium channels

inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105422openalex-snapshot

Concomitant knockdown resistance allele, L982W + F1534C, in Aedes aegypti has the potential to impose fitness costs without selection pressure

inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105490openalex-snapshot

Leucine to tryptophane substitution in the pore helix IIP1 confer sodium channel resistance to pyrethroids and DDT

inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106748openalex-snapshot

Characterization of the mechanism of action of a re-engineered spider toxin acting on insect voltage-gated sodium channels

inferred← citeshttps://doi.org/10.1016/j.pt.2025.03.007openalex-snapshot

Aedes aegypti (Yellow fever mosquito)

inferred← citeshttps://doi.org/10.1038/s41467-024-49792-yopenalex-snapshot

Global, asynchronous partial sweeps at multiple insecticide resistance genes in Aedes mosquitoes

inferred← citeshttps://doi.org/10.1038/s41598-024-64007-6openalex-snapshot

Uncovering the genetic diversity in Aedes aegypti insecticide resistance genes through global comparative genomics

inferred← citeshttps://doi.org/10.1038/s41598-025-13427-zopenalex-snapshot

Context-dependent effects of carbon dioxide on cross-modal integration during mosquito flight

inferred← citeshttps://doi.org/10.1080/21505594.2026.2723655openalex-snapshot

Advances in mosquito gut microbiota: Mechanisms of regulating pathogen transmission and applications in vector control

inferred← citeshttps://doi.org/10.1093/jme/tjag032openalex-snapshot

Impact of niche shift on the spread of Aedes aegypti (Diptera: Culicidae) to and within Japan

inferred← citeshttps://doi.org/10.1101/2023.03.29.534712openalex-snapshot

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inferred← citeshttps://doi.org/10.1101/2024.02.29.582728openalex-snapshot

Uncovering the genetic diversity in Aedes aegypti insecticide resistance genes through global comparative genomics

inferred← citeshttps://doi.org/10.1101/2024.04.09.588653openalex-snapshot

Global, asynchronous partial sweeps at multiple insecticide resistance genes in Aedes mosquitoes

inferred← citeshttps://doi.org/10.1101/2024.12.03.626538openalex-snapshot

Trehalose supports the growth of Aedes aegypti cells and modifies gene expression and dengue virus replication

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

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Four-year monitoring of the malaria vector Anopheles funestus in central-west Cameroon reveals an escalation of pyrethroid resistance combined with high malaria transmission

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Fine-scale monitoring of insecticide resistance in Aedes aegypti (Diptera: Culicidae) from Sri Lanka and modeling the phenotypic resistance using rational approximation

inferred← citeshttps://doi.org/10.1186/s13071-024-06481-5openalex-snapshot

Review of dengue vectors in Cambodia: distribution, bionomics, vector competence, control and insecticide resistance

inferred← citeshttps://doi.org/10.1186/s13071-025-06817-9openalex-snapshot

Global distribution and impact of knockdown resistance mutations in Aedes aegypti on pyrethroid resistance

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Pyrethroid resistance in Aedes aegypti: genetic mechanisms worldwide, and recommendations for effective vector control

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Pyrethroid insecticide resistance of Aedes albopictus and Aedes aegypti (Diptera: Culicidae) across the Hawaiian Islands

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A next generation targeted amplicon sequencing method to screen for insecticide resistance mutations in Aedes aegypti populations reveals a rdl mutation in mosquitoes from Cabo Verde

inferred← citeshttps://doi.org/10.1371/journal.pntd.0012768openalex-snapshot

First detection of the S989P+V1016G+D1763Y haplotype and expansion of voltage-gated sodium channel mutations in Aedes aegypti in Taiwan in 2016–2023

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/10.1371/journal.pntd.0013792openalex-snapshot

Insecticide resistance levels, spatial distribution, and kdr mutations in the dengue vector Aedes albopictus of Hong Kong

inferred← citeshttps://doi.org/10.1371/journal.pntd.0014222openalex-snapshot

Establishment and characterization of a Wolbachia (wAlbB)-infected Aedes aegypti line (Tw-Kao) for dengue control

inferred← citeshttps://doi.org/10.1371/journal.pntd.0014393openalex-snapshot

Discovery of two novel mutations, R52H and N868D, in the voltage-gated sodium channel of Aedes aegypti associated with pyrethroid resistance

inferred← citeshttps://doi.org/10.1371/journal.pntd.0014670openalex-snapshot

Mitochondrial phylogeography and insecticide resistance of Aedes aegypti in Kenya

inferred← citeshttps://doi.org/10.1371/journal.pone.0285883openalex-snapshot

Reconsideration of importance of the point mutation L982W in the voltage-sensitive sodium channel of the pyrethroid resistant Aedes aegypti (L.)(Diptera: Culicidae) in Vietnam

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inferred← citeshttps://doi.org/10.1371/journal.ppat.1012795openalex-snapshot

Trehalose supports the growth of Aedes aegypti cells and modifies gene expression and dengue virus type 2 replication

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First Report on the Molecular Phylogenetics and Population Genetics of Aedes Lineatopennis (Ludlow) in the World

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

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T7-Synthesized Double-Stranded RNA Mimicking miR-71 Induces Termite RNAi and Increases Fungal Efficacy

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Metabolic Resistance and Not Voltage-Gated Sodium Channel Gene Mutation Is Associated with Pyrethroid Resistance of Aedes albopictus (Skuse, 1894) from Cambodia

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Synergistic Larvicidal and Pupicidal Effects of Monoterpene Mixtures Against Aedes aegypti with Low Toxicity to Guppies and Honeybees

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Larvicidal and Oviposition Activity of Commercial Essential Oils of Abies sibirica Ledeb., Pogostemon cablin (Blanco) Benth., Juniperus communis L. and Their Combinations Against Aedes aegypti

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Targeting Aedes aegypti Metabolism with Next-Generation Insecticides

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Action publique et responsabilité individuelle face aux risques épidémiques en France

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Pyrethroid Resistance in Aedes aegypti L. across Southeast Asia: Mechanisms and Implications for Vector Control

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Additional file 1 of Fine-scale monitoring of insecticide resistance in Aedes aegypti (Diptera: Culicidae) from Sri Lanka and modeling the phenotypic resistance using rational approximation

inferred← citeshttps://doi.org/10.6084/m9.figshare.26666890openalex-snapshot

Additional file 2 of Fine-scale monitoring of insecticide resistance in Aedes aegypti (Diptera: Culicidae) from Sri Lanka and modeling the phenotypic resistance using rational approximation

inferred← citeshttps://doi.org/10.6084/m9.figshare.26666893openalex-snapshot

Additional file 3 of Fine-scale monitoring of insecticide resistance in Aedes aegypti (Diptera: Culicidae) from Sri Lanka and modeling the phenotypic resistance using rational approximation

inferred← citeshttps://doi.org/10.64898/2026.05.21.726856openalex-snapshot

Pyrethroid Resistance Status and Multiple kdr Mutations (F1534C/L) in Aedes aegypti Populations from Zika-prone Areas in Lamu County, Kenya

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