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

https://doi.org/10.1002/ps.5369
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1 of the 60 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-21): 10.1186/s13071-017-2089-5 (notice 2022-07-22).

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What this work says

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

inferredcites →https://doi.org/10.1002/352760197x.app1openalex-snapshot
Annex: Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 Concerning the Placing of Biocidal Products on the Market
inferredcites →https://doi.org/10.1002/ps.3511openalex-snapshot
Area‐wide management of Aedes albopictus. Part 2: Gauging the efficacy of traditional integrated pest control measures against urban container mosquitoes
inferredcites →https://doi.org/10.1002/ps.4315openalex-snapshot
Not in my backyard: effectiveness of outdoor residual spraying from hand‐held sprayers against the mosquito Aedes albopictus in Rome, Italy
inferredcites →https://doi.org/10.1002/ps.4840openalex-snapshot
First evidence of resistance to pyrethroid insecticides in Italian Aedes albopictus populations 26 years after invasion
inferredcites →https://doi.org/10.1007/s00204-011-0726-xopenalex-snapshot
Molecular mechanisms of pyrethroid insecticide neurotoxicity: recent advances
inferredcites →https://doi.org/10.1007/s00436-015-4717-3openalex-snapshot
Studies on insecticide susceptibility of Aedes aegypti (Linn) and Aedes albopictus (Skuse) vectors of dengue and chikungunya in Andaman and Nicobar Islands, India
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.pestbp.2012.05.008openalex-snapshot
Insecticide resistance in the major dengue vectors Aedes albopictus and Aedes aegypti
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/10.1016/j.pt.2010.08.004openalex-snapshot
Pyrethroid resistance in African anopheline mosquitoes: what are the implications for malaria control?
inferredcites →https://doi.org/10.1016/j.pt.2015.11.010openalex-snapshot
Insecticide Resistance in African Anopheles Mosquitoes: A Worsening Situation that Needs Urgent Action to Maintain Malaria Control
inferredcites →https://doi.org/10.1016/s0140-6736(07)61779-6openalex-snapshot
Infection with chikungunya virus in Italy: an outbreak in a temperate region
inferredcites →https://doi.org/10.1017/s0007485315000103openalex-snapshot
An entomological review of invasive mosquitoes in Europe
inferredcites →https://doi.org/10.1038/hdy.2016.35openalex-snapshot
Population genetics of the Asian tiger mosquito Aedes albopictus, an invasive vector of human diseases
inferredcites →https://doi.org/10.1038/srep24707openalex-snapshot
The Cytochrome P450 gene CYP6P12 confers pyrethroid resistance in kdr-free Malaysian populations of the dengue vector Aedes albopictus
inferredcites →https://doi.org/10.1089/vbz.2006.0562openalex-snapshot
Spread of The Tiger: Global Risk of Invasion by The Mosquito Aedes albopictus
inferredcites →https://doi.org/10.1089/vbz.2011.0814openalex-snapshot
A Review of the Invasive Mosquitoes in Europe: Ecology, Public Health Risks, and Control Options
inferredcites →https://doi.org/10.1093/jme/tjw231openalex-snapshot
Baseline Insecticide Susceptibility Screening Against Six Active Ingredients for Culex and Aedes (Diptera: Culicidae) Mosquitoes in the United States
inferredcites →https://doi.org/10.1093/jme/tjx198openalex-snapshot
Insecticide Susceptibility Screening Against Culex and Aedes (Diptera: Culicidae) Mosquitoes From the United States
inferredcites →https://doi.org/10.1093/nar/gku1117openalex-snapshot
VectorBase: an updated bioinformatics resource for invertebrate vectors and other organisms related with human diseases
inferredcites →https://doi.org/10.1111/1469-0691.12189openalex-snapshot
Public health significance of invasive mosquitoes in Europe
inferredcites →https://doi.org/10.1111/j.1948-7134.2011.00158.xopenalex-snapshot
Frequency of pyrethroid resistance in Aedes aegypti and Aedes albopictus (Diptera: Culicidae) in Thailand
inferredcites →https://doi.org/10.1111/j.1948-7134.2012.00199.xopenalex-snapshot
Seasonal pattern of daily activity of Aedes caspius, Aedes detritus, Culex modestus, and Culex pipiens in the Po Delta of northern Italy and significance for vector-borne disease risk assessment
inferredcites →https://doi.org/10.1146/annurev.ento.45.1.371openalex-snapshot
Insecticide Resistance in Insect Vectors of Human Disease
inferredcites →https://doi.org/10.1155/2018/3098575openalex-snapshot
Insecticide Resistance Associated withkdrMutations inAedes albopictus: An Update on Worldwide Evidences
inferredcites →https://doi.org/10.1186/1756-3305-4-79openalex-snapshot
Insecticide susceptibility of Aedes aegypti and Aedes albopictus in Central Africa
inferredcites →https://doi.org/10.1186/1756-3305-6-253openalex-snapshot
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 Thailand
inferredcites →https://doi.org/10.1186/1756-3305-7-299openalex-snapshot
Insecticide resistance in disease vectors from Mayotte: an opportunity for integrated vector management
inferredcites →https://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
inferredcites →https://doi.org/10.1186/s13071-016-1501-xopenalex-snapshot
Enhancement of Aedes albopictus collections by ovitrap and sticky adult trap
inferredcites →https://doi.org/10.1186/s13071-016-1887-5openalex-snapshot
Susceptibility profile and metabolic mechanisms involved in Aedes aegypti and Aedes albopictus resistant to DDT and deltamethrin in the Central African Republic
inferredcites →https://doi.org/10.1186/s13071-017-2089-5openalex-snapshot
RETRACTED ARTICLE: First report of the Phe1534Cyskdr mutation in natural populations of Aedes albopictusfrom Brazil
inferredcites →https://doi.org/10.1186/s13071-017-2224-3openalex-snapshot
International workshop on insecticide resistance in vectors of arboviruses, December 2016, Rio de Janeiro, Brazil
inferredcites →https://doi.org/10.1186/s13071-017-2364-5openalex-snapshot
Insecticide susceptibility of Aedes albopictus and Ae. aegypti from Brazil and the Swiss-Italian border region
inferredcites →https://doi.org/10.1186/s13071-017-2408-xopenalex-snapshot
Temporal distribution and insecticide resistance profile of two major arbovirus vectors Aedes aegypti and Aedes albopictus in Yaoundé, the capital city of Cameroon
inferredcites →https://doi.org/10.1186/s40249-016-0125-xopenalex-snapshot
First identification of kdr allele F1534S in VGSC gene and its association with resistance to pyrethroid insecticides in Aedes albopictus populations from Haikou City, Hainan Island, China
inferredcites →https://doi.org/10.1303/aez.2010.275openalex-snapshot
Point mutations in domain II of the voltage-gated sodium channel gene in deltamethrin-resistant Aedes aegypti (Diptera: Culicidae)
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.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.0004226openalex-snapshot
Deltamethrin Resistance Mechanisms in Aedes aegypti Populations from Three French Overseas Territories Worldwide
inferredcites →https://doi.org/10.1371/journal.pntd.0004463openalex-snapshot
Assessment of the Effectiveness of a Seasonal-Long Insecticide-Based Control Strategy against Aedes albopictus Nuisance in an Urban Area
inferredcites →https://doi.org/10.1371/journal.pntd.0004696openalex-snapshot
Multi-country Survey Revealed Prevalent and Novel F1534S Mutation in Voltage-Gated Sodium Channel (VGSC) Gene in Aedes albopictus
inferredcites →https://doi.org/10.1371/journal.pntd.0005054openalex-snapshot
Tracking Insecticide Resistance in Mosquito Vectors of Arboviruses: The Worldwide Insecticide resistance Network (WIN)
inferredcites →https://doi.org/10.1371/journal.pntd.0005302openalex-snapshot
Pyrethroid Resistance in Malaysian Populations of Dengue Vector Aedes aegypti Is Mediated by CYP9 Family of Cytochrome P450 Genes
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.0049181openalex-snapshot
Effectiveness of Ultra-Low Volume Nighttime Applications of an Adulticide against Diurnal Aedes albopictus, a Critical Vector of Dengue and Chikungunya Viruses
inferredcites →https://doi.org/10.1371/journal.pone.0101992openalex-snapshot
Insecticide Resistance Status of United States Populations of Aedes albopictus and Mechanisms Involved
inferredcites →https://doi.org/10.2807/1560-7917.es.2016.21.21.30240openalex-snapshot
Autochthonous dengue outbreak in Nîmes, South of France, July to September 2015
inferredcites →https://doi.org/10.2807/1560-7917.es.2017.22.39.17-00646openalex-snapshot
Detection of a chikungunya outbreak in Central Italy, August to September 2017
inferredcites →https://doi.org/10.2807/ese.16.09.19805-enopenalex-snapshot
Autochthonous dengue fever in Croatia, August–September 2010
inferredcites →https://doi.org/10.2807/esw.12.47.03313-enopenalex-snapshot
Chikungunya in north-eastern Italy: a summing up of the outbreak
inferredcites →https://doi.org/10.2987/17-6636r.1openalex-snapshot
First Data on Resistance to Pyrethroids in Wild Populations of Aedes albopictus from Spain
inferredcites →https://doi.org/10.2987/moco-31-04-346-352.1openalex-snapshot
Establishment of Diagnostic Doses of Five Pyrethroids for Monitoring Physiological Resistance inAedes Albopictusin Thailand
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.4081/fe.2009.92openalex-snapshot
LE ZANZARE ITALIANE: GENERALITÀ E IDENTIFICAZIONE DEGLI ADULTI (DIPTERA, CULICIDAE)
inferredcites →https://doi.org/10.4103/0972-9062.154174openalex-snapshot
Status of DDT and pyrethroid resistance in Indian Aedes albopictus and absence of knockdown resistance (kdr) mutation
inferredcites →https://doi.org/10.4103/0972-9062.184837openalex-snapshot
Spatial distribution and insecticide susceptibility status of Aedes aegypti and Aedes albopictus in dengue affected urban areas of Rawalpindi, Pakistan
inferredcites →https://doi.org/10.5372/1905-7415.0701.150openalex-snapshot
Susceptibility of Aedes albopictus skuse (Diptera: Culicidae) to permethrin in Kuala Lumpur, Malaysia
inferredcites →https://doi.org/10.7554/elife.08347openalex-snapshot
The global distribution of the arbovirus vectors Aedes aegypti and Ae. albopictus
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.

inferred← citeshttps://doi.org/10.1186/s13071-024-06635-5zenodo-depositor-declared
Consequences of insecticide overuse in Hungary: assessment of pyrethroid resistance in Culex pipiens and Aedes albopictus mosquitoes
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/ece3.71009openalex-snapshot
Population Structure of the Invasive Asian Tiger Mosquito, Aedes albopictus, in Europe
inferred← citeshttps://doi.org/10.1002/ps.5643openalex-snapshot
A bacterium against the tiger: preliminary evidence of fertility reduction after release of Aedes albopictus males with manipulated Wolbachia infection in an Italian urban area
inferred← citeshttps://doi.org/10.1002/ps.7495openalex-snapshot
A bacterium against the tiger: further evidence of the potential of noninundative releases of males with manipulated Wolbachia infection in reducing fertility of Aedes albopictus field populations in Italy
inferred← citeshttps://doi.org/10.1016/j.cois.2020.03.009openalex-snapshot
Mosquito surveillance and disease outbreak risk models to inform mosquito-control operations in Europe
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.meegid.2024.105634openalex-snapshot
Detection and population genetic analysis of Aedes albopictus (Diptera: Culicidae) based on knockdown resistance (kdr) mutations in the Yangtze River basin of China
inferred← citeshttps://doi.org/10.1038/s41598-020-75780-5openalex-snapshot
Knowledge on exotic mosquitoes in Germany, and public acceptance and effectiveness of Bti and two self-prepared insecticides against Aedes japonicus japonicus
inferred← citeshttps://doi.org/10.1080/07391102.2021.1904004openalex-snapshot
A review targeting the infection by CHIKV using computational and experimental approaches
inferred← citeshttps://doi.org/10.1093/gbe/evag039openalex-snapshot
Metabolic resistance of the tiger mosquito to pyrethroid insecticides in La Réunion Island likely results from local adaptation
inferred← citeshttps://doi.org/10.1093/jme/tjac085openalex-snapshot
Insecticide Resistance in Alabama Populations of the Mosquito Aedes albopictus
inferred← citeshttps://doi.org/10.1093/jme/tjae005openalex-snapshot
Diversity and distribution of sodium channel mutations in Aedes albopictus (Diptera: Culicidae)
inferred← citeshttps://doi.org/10.1111/mve.12573openalex-snapshot
First evidence of pyrethroid resistance in Italian populations of West Nile virus vector Culex pipiens
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1126/sciadv.abq7345openalex-snapshot
Discovery of super–insecticide-resistant dengue mosquitoes in Asia: Threats of concomitant knockdown resistance mutations
inferred← citeshttps://doi.org/10.1186/s13071-020-04204-0openalex-snapshot
Bioassay and molecular monitoring of insecticide resistance status in Aedes albopictus populations from Greece, to support evidence-based vector control
inferred← citeshttps://doi.org/10.1186/s13071-022-05407-3openalex-snapshot
Geographic distribution of the V1016G knockdown resistance mutation in Aedes albopictus: a warning bell for Europe
inferred← citeshttps://doi.org/10.1186/s13071-025-07083-5openalex-snapshot
Molecular characterization of invasive Aedes albopictus (Diptera: Culicidae) populations in northwest Iran: Insights into origin, insecticide resistance, and Wolbachia infection
inferred← citeshttps://doi.org/10.1186/s13071-025-07116-zopenalex-snapshot
Development and application of a PCR–RFLP assay revealing widespread distribution of the pyrethroid resistance-associated VGSC V1016G mutation in Aedes albopictus from Guangyuan City, Sichuan Province of China
inferred← citeshttps://doi.org/10.1186/s13071-025-07130-1openalex-snapshot
Tracking pyrethroid resistance in arbovirus mosquito vectors: mutations I1532T and F1534C in Aedes albopictus across Europe
inferred← citeshttps://doi.org/10.1186/s40249-020-0635-4openalex-snapshot
Population dynamics, pathogen detection and insecticide resistance of mosquito and sand fly in refugee camps, Greece
inferred← citeshttps://doi.org/10.1371/journal.pntd.0007554openalex-snapshot
Complex interplay of evolutionary forces shaping population genomic structure of invasive Aedes albopictus in southern Europe
inferred← citeshttps://doi.org/10.1371/journal.pntd.0008350openalex-snapshot
Tracing temporal and geographic distribution of resistance to pyrethroids in the arboviral vector Aedes albopictus
inferred← citeshttps://doi.org/10.1371/journal.pntd.0009698openalex-snapshot
Aedes albopictus bionomics data collection by citizen participation on Procida Island, a promising Mediterranean site for the assessment of innovative and community-based integrated pest management methods
inferred← citeshttps://doi.org/10.1371/journal.pone.0217860openalex-snapshot
Phenotypic insecticide resistance in arbovirus mosquito vectors in Catalonia and its capital Barcelona (Spain)
inferred← citeshttps://doi.org/10.3390/insects12010079openalex-snapshot
A Novel Allele Specific Polymerase Chain Reaction (AS-PCR) Assay to Detect the V1016G Knockdown Resistance Mutation Confirms Its Widespread Presence in Aedes albopictus Populations from Italy
inferred← citeshttps://doi.org/10.3390/insects14050457openalex-snapshot
Integrated Plan of Insecticide Resistance Surveillance in Mosquito Vectors in France
inferred← citeshttps://doi.org/10.3390/insects16020204openalex-snapshot
Widespread Distribution of chs-1 Mutations Associated with Resistance to Diflubenzuron Larvicide in Culex pipiens Across Italy, Reaching Virtual Fixation in the Venetian Lagoon
inferred← citeshttps://doi.org/10.4103/apjtm.apjtm_438_25openalex-snapshot
Pyrethroid resistance in Aedes albopictus in Pudong New Area, Shanghai China
inferred← citeshttps://doi.org/10.46471/gigabyte.185openalex-snapshot
Tracking kdr alleles associated with pyrethroid resistance in Aedes albopictus across Italy: a nationwide genotypic dataset by MosqIRIT network
inferred← citeshttps://doi.org/10.6084/m9.figshare.11998971openalex-snapshot
Additional file 1 of Population dynamics, pathogen detection and insecticide resistance of mosquito and sand fly in refugee camps, Greece
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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