Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A multiplex PCR for detection of knockdown resistance mutations, V1016G and F1534C, in pyrethroid-resistant Aedes aegypti.

Parasites & vectors - 10 Oct 2017

Saingamsook Jassada, Saeung Atiporn, Yanola Jintana, Lumjuan Nongkran, Walton Catherine, Somboon Pradya

Abstract excerpt

BACKGROUND: Mutation of the voltage-gated sodium channel (VGSC) gene, or knockdown resistance (kdr) gene, is an important resistance mechanism of the dengue vector Aedes aegypti mosquitoes against pyrethroids. In many countries in Asia, a valine to glycine substitution (V1016G) and a phenylalanine to cysteine substitution (F1534C) are common in Ae. aegypti populations. The G1016 and C1534 allele frequencies have...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aedes
Share to DNA Primers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Frequency

Share to Insecticide Resistance

Share to Insecticides

Share to Multiplex Polymerase Chain Reaction

Share to Potassium Channels, Voltage-Gated

Share to Pyrethrins

Source

Open in PubMed Open full text

Identifiers

PMID: 29017613
DOI: 10.1186/s13071-017-2416-x
PMCID: PMC5634894

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A multiplex PCR for detection of knockdown resistance mutations, V1016G and F1534C, in pyrethroid-resistant Aedes aegypti.PMID 29017613Read ↗

Multiplex PCR for simultaneous genotyping of kdr mutations V410L, V1016I and F1534C in Aedes aegypti (L.).Semantic proximity Read ↗

Establishment of an innovative and sustainable PCR technique for 1534 locus mutation of the knockdown resistance (kdr) gene in the dengue vector Aedes albopictus.Semantic proximity Read ↗

Multiplex PCR for simultaneous genotyping of kdr mutations V410L, V1,016I and F1,534C in Aedes aegypti (L.)Semantic proximity Read ↗

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

Multiplex PCR for simultaneous genotyping of kdr mutations V410L, V1,016I and F1,534C in <i>Aedes aegypti</i> (L.)Semantic proximity Read ↗

First report of V1016G and S989P knockdown resistant (kdr) mutations in pyrethroid-resistant Sri Lankan Aedes aegypti mosquitoesSemantic proximity Read ↗

Kdr genotyping in Aedes aegypti from Brazil on a nation-wide scale from 2017 to 2018.Semantic proximity Read ↗

Multi-country Survey Revealed Prevalent and Novel F1534S Mutation in Voltage-Gated Sodium Channel (VGSC) Gene in Aedes albopictus.Semantic proximity Read ↗

Detection of the V1016G mutation in the voltage-gated sodium channel gene of Aedes aegypti (Diptera: Culicidae) by allele-specific PCR assay, and its distribution and effect on deltamethrin resistance in ThailandSemantic proximity Read ↗

First detection of a putative knockdown resistance gene in major mosquito vector, Aedes albopictus.Semantic proximity Read ↗

A new knockdown resistance (kdr) mutation, F1534L, in the voltage-gated sodium channel of Aedes aegypti, co-occurring with F1534C, S989P and V1016G.Semantic proximity Read ↗

Knockdown resistance (kdr) mutations within seventeen field populations of Aedes albopictus from Beijing China: first report of a novel V1016G mutation and evolutionary origins of kdr haplotypesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.