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A genomic amplification affecting a carboxylesterase gene cluster confers organophosphate resistance in the mosquito Aedes aegypti : from genomic characterization to high-throughput field detection

https://doi.org/10.1101/2020.06.08.139741

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What this work says

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

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Gene amplification and insecticide resistance

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Fitness costs associated with insecticide resistance

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Action of Esterase B1 on Chlorpyrifos in Organophosphate-Resistant Culex Mosquitos

inferredcites →https://doi.org/10.1007/978-94-010-0585-2_18openalex-snapshot

Insecticide resistance in the mosquito Culex pipiens: What have we learned about adaptation?

inferredcites →https://doi.org/10.1007/s00436-015-4898-9openalex-snapshot

Insecticide resistance and its molecular basis in urban insect pests

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Resistance to the organophosphate temephos: Mechanisms, evolution and reversion in an Aedes aegypti laboratory strain from Brazil

inferredcites →https://doi.org/10.1016/j.cois.2017.04.011openalex-snapshot

Does resistance really carry a fitness cost?

inferredcites →https://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?

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Insecticide resistance: a silent base prediction

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Neofunctionalization of Duplicated P450 Genes Drives the Evolution of Insecticide Resistance in the Brown Planthopper

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The molecular basis of insecticide resistance in mosquitoes

inferredcites →https://doi.org/10.1016/j.ibmb.2016.05.007openalex-snapshot

Functional and immunohistochemical characterization of CCEae3a, a carboxylesterase associated with temephos resistance in the major arbovirus vectors Aedes aegypti and Ae. albopictus

inferredcites →https://doi.org/10.1016/j.pestbp.2012.05.008openalex-snapshot

Insecticide resistance in the major dengue vectors Aedes albopictus and Aedes aegypti

inferredcites →https://doi.org/10.1016/j.tig.2012.03.002openalex-snapshot

Exploring the role of copy number variants in human adaptation

inferredcites →https://doi.org/10.1016/j.tig.2013.04.005openalex-snapshot

Properties and rates of germline mutations in humans

inferredcites →https://doi.org/10.1016/j.ygeno.2015.11.004openalex-snapshot

Identification of a major Quantitative Trait Locus determining resistance to the organophosphate temephos in the dengue vector mosquito Aedes aegypti

inferredcites →https://doi.org/10.1016/s0169-5347(03)00033-8openalex-snapshot

Evolution by gene duplication: an update

inferredcites →https://doi.org/10.1023/a:1013300108134openalex-snapshot

Insecticide resistance in the mosquito Culex pipiens: what have we learned about adaptation?

inferredcites →https://doi.org/10.1038/hdy.1995.51openalex-snapshot

The same esterase B1 haplotype is amplified in insecticide-resistant mosquitoes of the Culex pipiens complex from the Americas and China

inferredcites →https://doi.org/10.1038/ng2054openalex-snapshot

Mutational and selective effects on copy-number variants in the human genome

inferredcites →https://doi.org/10.1038/npre.2010.4282.2openalex-snapshot

Differential expression analysis for sequence count data

inferredcites →https://doi.org/10.1038/sj.hdy.6885370openalex-snapshot

Quantitative variation and selection of esterase gene amplification in Culex pipiens

inferredcites →https://doi.org/10.1038/srep14529openalex-snapshot

An ace-1 gene duplication resorbs the fitness cost associated with resistance in Anopheles gambiae, the main malaria mosquito

inferredcites →https://doi.org/10.1073/pnas.84.8.2113openalex-snapshot

Overproduction of detoxifying esterases in organophosphate-resistant Culex mosquitoes and their presence in other insects.

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/10.1093/nar/29.9.e45openalex-snapshot

A new mathematical model for relative quantification in real-time RT-PCR

inferredcites →https://doi.org/10.1098/rspb.2012.1108openalex-snapshot

Gene duplication as a mechanism of genomic adaptation to a changing environment

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.189225.115openalex-snapshot

Identifying genomic changes associated with insecticide resistance in the dengue mosquito Aedes aegypti by deep targeted sequencing

inferredcites →https://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

inferredcites →https://doi.org/10.1111/eva.12867openalex-snapshot

Combining genetic crosses and pool targeted DNA‐seq for untangling genomic variations associated with resistance to multiple insecticides in the mosquito Aedes aegypti

inferredcites →https://doi.org/10.1111/j.1365-2583.1998.00077.xopenalex-snapshot

Polymorphisms and fluctuations in copy number of amplified esterase genes in Culex pipiens mosquitoes

inferredcites →https://doi.org/10.1111/jnc.13990openalex-snapshot

Natural genomic amplification of cholinesterase genes in animals

inferredcites →https://doi.org/10.1111/mec.13855openalex-snapshot

Relating fitness to long‐term environmental variations in natura

inferredcites →https://doi.org/10.1126/science.2950591openalex-snapshot

Construction of a General Human Chromosome Jumping Library, with Application to Cystic Fibrosis

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/10.1186/1471-213x-13-29openalex-snapshot

Stage-specific transcription during development of Aedes aegypti

inferredcites →https://doi.org/10.1186/1471-2164-10-494openalex-snapshot

Exploring the molecular basis of insecticide resistance in the dengue vector Aedes aegypti: a case study in Martinique Island (French West Indies)

inferredcites →https://doi.org/10.1186/gb-2010-11-10-r106openalex-snapshot

Differential expression analysis for sequence count data

inferredcites →https://doi.org/10.1186/s40249-017-0254-xopenalex-snapshot

Levels of insecticide resistance to deltamethrin, malathion, and temephos, and associated mechanisms in Aedes aegypti mosquitoes from the Guadeloupe and Saint Martin islands (French West Indies)

inferredcites →https://doi.org/10.1371/journal.pgen.1000998openalex-snapshot

Copy Number Variation and Transposable Elements Feature in Recent, Ongoing Adaptation at the Cyp6g1 Locus

inferredcites →https://doi.org/10.1371/journal.pntd.0002743openalex-snapshot

Identification of Carboxylesterase Genes Implicated in Temephos Resistance in the Dengue Vector Aedes aegypti

inferredcites →https://doi.org/10.1371/journal.pntd.0004226openalex-snapshot

Deltamethrin Resistance Mechanisms in Aedes aegypti Populations from Three French Overseas Territories Worldwide

inferredcites →https://doi.org/10.1371/journal.pntd.0005526openalex-snapshot

In the hunt for genomic markers of metabolic resistance to pyrethroids in the mosquito Aedes aegypti: An integrated next-generation sequencing approach

inferredcites →https://doi.org/10.1371/journal.pntd.0005533openalex-snapshot

Carboxylesterase gene amplifications associated with insecticide resistance in Aedes albopictus: Geographical distribution and evolutionary origin

inferredcites →https://doi.org/10.1371/journal.pntd.0005625openalex-snapshot

Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans

inferredcites →https://doi.org/10.1371/journal.pntd.0006822openalex-snapshot

Alternative strategies for mosquito-borne arbovirus control

inferredcites →https://doi.org/10.1371/journal.pntd.0007615openalex-snapshot

Management of insecticide resistance in the major Aedes vectors of arboviruses: Advances and challenges

inferredcites →https://doi.org/10.1371/journal.pntd.0007852openalex-snapshot

Distribution of insecticide resistance and mechanisms involved in the arbovirus vector Aedes aegypti in Laos and implication for vector control

inferredcites →https://doi.org/10.1371/journal.pntd.0007890openalex-snapshot

Repurposing the antimalarial pyronaridine tetraphosphate to protect against Ebola virus infection

inferredcites →https://doi.org/10.1371/journal.pone.0030989openalex-snapshot

Insecticide Resistance in the Dengue Vector Aedes aegypti from Martinique: Distribution, Mechanisms and Relations with Environmental Factors

inferredcites →https://doi.org/10.1385/1-59259-192-2:365openalex-snapshot

Primer3 on the WWW for General Users and for Biologist Programmers

inferredcites →https://doi.org/10.1590/0037-8682-1727-2013openalex-snapshot

Spatial distribution and esterase activity in populations of Aedes (Stegomyia) aegypti (Linnaeus) (Diptera: Culicidae) resistant to temephos

inferredcites →https://doi.org/10.1603/me10121openalex-snapshot

Energetic Cost of Insecticide Resistance in Culex pipiens Mosquitoes

inferredcites →https://doi.org/10.1603/me12064openalex-snapshot

Insecticide Resistance in Two Aedes aegypti (Diptera: Culicidae) Strains From Costa Rica

inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot

R: A Language and Environment for Statistical Computing

What points at this work

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

inferred← citeshttps://doi.org/10.24072/pci.evolbiol.100114openalex-snapshot

Identification of a gene cluster amplification associated with organophosphate insecticide resistance: from the diversity of the resistance allele complex to an efficient field detection assay

inferred← citeshttps://doi.org/10.70675/5ffea2f6z4961z4f2fza940z0bc2078e4d73openalex-snapshot

Résistance du moustique Anopheles gambiae à Fludora® Fusion, une nouvelle combinaison d’insecticides à double mode d’action utilisable en pulvérisation intra domiciliaire. Réponse adaptative et interactions gènes-environnement

inferred← citeshttps://doi.org/10.70675/8a150e43z6dadz4bd2z8a4ez6db71df79890openalex-snapshot

Étude du potentiel des biomarqueurs sérologiques pour évaluer le risque de transmission de la dengue dans le nord-est de la Thaïlande

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