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Laboratory selection of Aedes aegypti field populations with the organophosphate malathion: Negative impacts on resistance to deltamethrin and to the organophosphate temephos

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

inferredcites →no DOI in the source recordopenalex-snapshot
Staphylococcal nasal carriage of health care workers.
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Effect of the synergist, piperonyl butoxide, on the development of deltamethrin resistance in yellow fever mosquito, Aedes aegypti L. (Diptera: Culicidae)
inferredcites →https://doi.org/10.1002/arch.940290402openalex-snapshot
Characterization of a novel esterase conferring insecticide resistance in the mosquito Culex tarsalis
inferredcites →https://doi.org/10.1002/ps.1547openalex-snapshot
Chitin synthesis inhibitor effect on Aedes aegypti populations susceptible and resistant to organophosphate temephos
inferredcites →https://doi.org/10.1007/978-3-319-31800-4openalex-snapshot
Advances in Insect Control and Resistance Management
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Advances in Insect Control and Resistance Management: An Overview
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Laboratory development of permethrin resistance and cross-resistance pattern of Culex quinquefasciatus to other insecticides
inferredcites →https://doi.org/10.1016/0169-5347(89)90088-8openalex-snapshot
The evolution of insecticide resistance: Have the insects won?
inferredcites →https://doi.org/10.1016/j.actatropica.2010.09.005openalex-snapshot
Characterization of insecticide resistance in Trinidadian strains of Aedes aegypti mosquitoes
inferredcites →https://doi.org/10.1016/j.bjid.2017.02.004openalex-snapshot
Yellow fever outbreak in Brazil, 2017
inferredcites →https://doi.org/10.1016/j.ibmb.2004.03.018openalex-snapshot
The molecular basis of insecticide resistance in mosquitoes
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.2008.01.004openalex-snapshot
Cross-induction of detoxification genes by environmental xenobiotics and insecticides in the mosquito Aedes aegypti: Impact on larval tolerance to chemical insecticides
inferredcites →https://doi.org/10.1016/j.vaccine.2015.05.010openalex-snapshot
The dengue vaccine pipeline: Implications for the future of dengue control
inferredcites →https://doi.org/10.1016/s0167-4781(01)00344-xopenalex-snapshot
Analysis of the promoters for the β-esterase genes associated with insecticide resistance in the mosquito Culex quinquefasciatus
inferredcites →https://doi.org/10.1038/nm.4253openalex-snapshot
A chikungunya fever vaccine utilizing an insect-specific virus platform
inferredcites →https://doi.org/10.1042/0264-6021:3570065openalex-snapshot
Glutathione S-transferases as antioxidant defence agents confer pyrethroid resistance in Nilaparvata lugens
inferredcites →https://doi.org/10.1046/j.1365-2915.1998.00064.xopenalex-snapshot
Cross‐resistance to malathion in Cuban Culex quinquefasciatus induced by larval selection with deltamethrin
inferredcites →https://doi.org/10.1046/j.1365-2915.1998.00082.xopenalex-snapshot
Mosquito carboxylesterases: a review of the molecular biology and biochemistry of a major insecticide resistance mechanism
inferredcites →https://doi.org/10.1046/j.1365-2915.1998.00120.xopenalex-snapshot
Pyrethroid resistance in Culex quinquefasciatus from West Africa
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/10.1098/rspb.1994.0138openalex-snapshot
Life-history costs associated with the evolution of insecticide resistance
inferredcites →https://doi.org/10.1099/jgv.0.001033openalex-snapshot
Genomic and structural features of the yellow fever virus from the 2016–2017 Brazilian outbreak
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/10.1111/j.1365-2583.2011.01113.xopenalex-snapshot
Transcription of detoxification genes after permethrin selection in the mosquito 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/mve.12241openalex-snapshot
Insecticide resistance, associated mechanisms and fitness aspects in two B razilian S tegomyia aegypti (= A edes aegypti ) populations
inferredcites →https://doi.org/10.1146/annurev.ento.45.1.371openalex-snapshot
Insecticide Resistance in Insect Vectors of Human Disease
inferredcites →https://doi.org/10.1146/annurev.ento.51.110104.151104openalex-snapshot
Molecular Mechanisms of Metabolic Resistance to Synthetic and Natural Xenobiotics
inferredcites →https://doi.org/10.1155/2016/6803098openalex-snapshot
Dengue Fever: Causes, Complications, and Vaccine Strategies
inferredcites →https://doi.org/10.1155/2016/8603263openalex-snapshot
Resistance Status to the Insecticides Temephos, Deltamethrin, and Diflubenzuron in BrazilianAedes aegyptiPopulations
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/10.1186/1756-3305-6-297openalex-snapshot
The susceptibility of Aedes aegypti populations displaying temephos resistance to Bacillus thuringiensis israelensis: a basis for management
inferredcites →https://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
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.0005625openalex-snapshot
Contemporary status of insecticide resistance in the major Aedes vectors of arboviruses infecting humans
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/10.1371/journal.pone.0039439openalex-snapshot
Expression Profile of Genes during Resistance Reversal in a Temephos Selected Strain of the Dengue Vector, Aedes aegypti
inferredcites →https://doi.org/10.1371/journal.pone.0060878openalex-snapshot
Assessing the Effects of Aedes aegypti kdr Mutations on Pyrethroid Resistance and Its Fitness Cost
inferredcites →https://doi.org/10.1371/journal.pone.0092424openalex-snapshot
Undesirable Consequences of Insecticide Resistance following Aedes aegypti Control Activities Due to a Dengue Outbreak
inferredcites →https://doi.org/10.1371/journal.pone.0130719openalex-snapshot
The Impact of Selection with Diflubenzuron, a Chitin Synthesis Inhibitor, on the Fitness of Two Brazilian Aedes aegypti Field Populations
inferredcites →https://doi.org/10.1371/journal.ppat.1001000openalex-snapshot
Insecticide Control of Vector-Borne Diseases: When Is Insecticide Resistance a Problem?
inferredcites →https://doi.org/10.1590/0074-02760150409openalex-snapshot
Spatial and temporal country-wide survey of temephos resistance in Brazilian populations of Aedes aegypti
inferredcites →https://doi.org/10.1590/0074-02760160332openalex-snapshot
First detection of natural infection of Aedes aegypti with Zika virus in Brazil and throughout South America
inferredcites →https://doi.org/10.1590/0074-02760170134openalex-snapshot
Genome analysis of yellow fever virus of the ongoing outbreak in Brazil reveals polymorphisms
inferredcites →https://doi.org/10.1590/s0037-86822000000400003openalex-snapshot
Comparação entre pesquisa larvária e armadilha de oviposição, para detecção de Aedes aegypti
inferredcites →https://doi.org/10.1590/s0074-02762004000200015openalex-snapshot
Aedes aegypti resistance to temephos during 2001 in several municipalities in the states of Rio de Janeiro, Sergipe, and Alagoas, Brazil
inferredcites →https://doi.org/10.1590/s0074-02762005000400016openalex-snapshot
Evaluation of methoprene effect on Aedes aegypti (Diptera: Culicidae) development in laboratory conditions
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/s0074-02762007000800001openalex-snapshot
Association of insecticide use and alteration on Aedes aegypti susceptibility status
inferredcites →https://doi.org/10.1590/s0074-02762009000500001openalex-snapshot
Development of physiological resistance and its stage specificity in Culex quinquefasciatus after selection with deltamethrin in Assam, India
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/10.1603/me10152openalex-snapshot
Early History of Laboratory Breeding of Aedes aegypti (Diptera: Culicidae) Focusing on the Origins and Use of Selected Strains
inferredcites →https://doi.org/10.1603/me12064openalex-snapshot
Insecticide Resistance in Two Aedes aegypti (Diptera: Culicidae) Strains From Costa Rica
inferredcites →https://doi.org/10.1603/me12254openalex-snapshot
Resistance to Malathion and Deltamethrin inAedes aegypti(Diptera: Culicidae) From Western Venezuela
inferredcites →https://doi.org/10.2307/3495526openalex-snapshot
The Molecular Genetics of Resistance: Resistance as a Response to Stress
inferredcites →https://doi.org/10.2987/14-6431.1openalex-snapshot
Insecticide Resistance and Metabolic Mechanisms Involved in Larval and Adult Stages ofAedes aegyptiInsecticide-Resistant Reference Strains from Cuba
inferredcites →https://doi.org/10.2987/8756-971x(2006)21[437:pisoaa]2.0.co;2openalex-snapshot
PYRETHROID INSECTICIDE-RESISTANT STRAIN OF AEDES AEGYPTI FROM CUBA INDUCED BY DELTAMETHRIN SELECTION
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/10.5123/s1679-49742007000200006openalex-snapshot
Aedes aegypti: histórico do controle no Brasil
inferredcites →https://doi.org/10.5860/choice.34-1529openalex-snapshot
The Biology of disease vectors

What points at this work

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

inferred← citeshttps://doi.org/10.1590/s1984-4689.v41.e23016zenodo-depositor-declared
Insecticide resistance of Stegomyia aegypti (Diptera: Culicidae) population from Paranaguá a port city in southern Brazil
inferred← citeshttps://doi.org/10.1007/978-3-030-81953-8_5openalex-snapshot
Toxic Effects of Pesticides or Herbicide on the Environment and Environmental Species: Wildlife, Including Insects, Aquatic Animals, and Plants
inferred← citeshttps://doi.org/10.1007/s40475-025-00357-zopenalex-snapshot
From Eradication to Resistance: The Evolution of Chemical Control of Aedes aegypti in Argentina
inferred← citeshttps://doi.org/10.1007/s42690-021-00727-wopenalex-snapshot
In-silico interactions of eugenol and temephos with metabolic detoxifying enzymes of Aedes aegypti (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1016/j.toxrep.2021.11.013openalex-snapshot
Gradual reduction of susceptibility and enhanced detoxifying enzyme activities of laboratory-reared Aedes aegypti under exposure of temephos for 28 generations
inferred← citeshttps://doi.org/10.1038/s41598-024-79988-7openalex-snapshot
Larvicidal and enzyme inhibition effects of Phoenix pusilla derived Methyl oleate and malathion on Aedes aegypti strains
inferred← citeshttps://doi.org/10.1093/jme/tjab045openalex-snapshot
Insecticide Resistance Patterns and Mechanisms in Aedes aegypti (Diptera: Culicidae) Populations Across Abidjan, Côte d’Ivoire Reveal Emergent Pyrethroid Resistance
inferred← citeshttps://doi.org/10.1093/jme/tjz161openalex-snapshot
Action of Metarhizium brunneum (Hypocreales: Clavicipitaceae) Against Organophosphate- and Pyrethroid-Resistant Aedes aegypti (Diptera: Culicidae) and the Synergistic Effects of Phenylthiourea
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Experimental evolution of insect resistance to two pesticide classes reveals mechanistic diversity and context-dependent fitness costs
inferred← citeshttps://doi.org/10.1101/2025.10.31.685655openalex-snapshot
The contribution of transposable element insertions to genetic diversity in Aedes aegypti populations
inferred← citeshttps://doi.org/10.11591/ijphs.v12i3.22843openalex-snapshot
Insecticide resistance of Aedes aegypti in Indonesia: a systematic review
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/10.1371/journal.pntd.0008154openalex-snapshot
Evidence for both sequential mutations and recombination in the evolution of kdr alleles in Aedes aegypti
inferred← citeshttps://doi.org/10.1590/0074-02760180544openalex-snapshot
Resistance to temephos and deltamethrin in Aedes aegypti from Brazil between 1985 and 2017
inferred← citeshttps://doi.org/10.1590/0074-02760200313openalex-snapshot
Spatiotemporal multiple insecticide resistance in Aedes aegypti populations in French Guiana: need for alternative vector control
inferred← citeshttps://doi.org/10.3390/insects12080710openalex-snapshot
Colonization and Authentication of the Pyrethroid-Resistant Anopheles gambiae s.s. Muleba-Kis Strain; an Important Test System for Laboratory Screening of New Insecticides
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Elevated Activity of Acetylcholinesterase and Glutathione S-Transferase in Temephos-Resistant Aedes aegypti L
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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/10.7554/elife.65655openalex-snapshot
The need for practical insecticide-resistance guidelines to effectively inform mosquito-borne disease control programs
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