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1.
Med Vet Entomol ; 33(4): 443-452, 2019 12.
Article in English | MEDLINE | ID: mdl-31361038

ABSTRACT

Mosquito-borne diseases resulting from the expansion of two key vectors, Aedes aegypti and Aedes albopictus (Diptera: Culicidae), continue to challenge whole regions and continents around the globe. In recent years there have been human cases of disease associated with Chikungunya, dengue and Zika viruses. In Europe, the expansion of Ae. albopictus has resulted in local transmission of Chikungunya and dengue viruses. This paper considers the risk that Ae. aegypti and Ae. albopictus represent for the U.K. and details the results of mosquito surveillance activities. Surveillance was conducted at 34 points of entry, 12 sites serving vehicular traffic and two sites of used tyre importers. The most common native mosquito recorded was Culex pipiens s.l. (Diptera: Culicidae). The invasive mosquito Ae. albopictus was detected on three occasions in southern England (September 2016, July 2017 and July 2018) and subsequent control strategies were conducted. These latest surveillance results demonstrate ongoing incursions of Ae. albopictus into the U.K. via ground vehicular traffic, which can be expected to continue and increase as populations in nearby countries expand, particularly in France, which is the main source of ex-continental traffic.


Subject(s)
Aedes , Animal Distribution , Introduced Species , Mosquito Vectors , Animals , Chikungunya virus , Dengue Virus , Mosquito Control , United Kingdom
2.
Insect Mol Biol ; 23(2): 199-215, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24299217

ABSTRACT

The mosquito Aedes aegypti is the main vector of Dengue and Yellow Fever flaviviruses. The organophosphate insecticide temephos is a larvicide that is used globally to control Ae. aegypti populations; many of which have in turn evolved resistance. Target site alteration in the acetylcholine esterase of this species has not being identified. Instead, we tracked changes in transcription of metabolic detoxification genes using the Ae. aegypti 'Detox Chip' microarray during five generations of temephos selection. We selected for temephos resistance in three replicates in each of six collections, five from Mexico, and one from Peru. The response to selection was tracked in terms of lethal concentrations. Uniform upregulation was seen in the epsilon class glutathione-S-transferase (eGST) genes in strains from Mexico prior to laboratory selection, while eGSTs in the Iquitos Peru strain became upregulated after five generations of temephos selection. While expression of many carboxyl/cholinesterase esterase (CCE) genes increased with selection, no single esterase was consistently upregulated and this same pattern was noted in the cytochrome P450 monooxygenase (CYP) genes and in other genes involved in reduction or oxidation of xenobiotics. Bioassays using glutathione-S-transferase (GST), CCE and CYP inhibitors suggest that various CCEs instead of GSTs are the main metabolic mechanism conferring resistance to temephos. We show that temephos-selected strains show no cross resistance to permethrin and that genes associated with temephos selection are largely independent of those selected with permethrin in a previous study.


Subject(s)
Aedes/genetics , Insecticide Resistance , Insecticides/pharmacology , Selection, Genetic , Temefos/pharmacology , Aedes/drug effects , Aedes/growth & development , Aedes/metabolism , Animals , Gene Expression Profiling , Larva/drug effects , Larva/genetics , Larva/metabolism , Mexico , Oligonucleotide Array Sequence Analysis , Peru , Real-Time Polymerase Chain Reaction , Transcription, Genetic
3.
Insect Mol Biol ; 21(1): 61-77, 2012 Feb.
Article in English | MEDLINE | ID: mdl-22032702

ABSTRACT

Changes in gene expression before, during and after five generations of permethrin laboratory selection were monitored in six strains of Aedes aegypti: five F(2)-F(3) collections from the Yucatán Peninsula of Mexico and one F(2) from Iquitos, Peru. Three biological replicate lines were generated for each strain. The response to selection was measured as changes in the lethal and knockdown permethrin concentrations (LC(50), KC(50)) and in the frequency of the Ile1,016 substitution in the voltage-gated sodium channel (para) gene. Changes in expression of 290 metabolic detoxification genes were measured using the 'Aedes Detox' microarray. Selection simultaneously increased the LC(50), KC(50) and Ile1,016 frequency. There was an inverse relationship between Ile1,016 frequency and the numbers of differentially transcribed genes. The Iquitos strain lacked the Ile1,016 allele and 51 genes were differentially transcribed after selection as compared with 10-18 genes in the Mexican strains. Very few of the same genes were differentially transcribed among field strains but 10 cytochrome P(450) genes were upregulated in more than one strain. Laboratory adaptation to permethrin in Ae. aegypti is genetically complex and largely conditioned by geographic origin and pre-existing target site insensitivity in the para gene. The lack of uniformity in the genes that responded to artificial selection as well as differences in the direction of their responses challenges the assumption that one or a few genes control permethrin metabolic resistance. Attempts to identify one or a few metabolic genes that are predictably associated with permethrin adaptation may be futile.


Subject(s)
Aedes/metabolism , Insecticides , Permethrin , Selection, Genetic , Aedes/genetics , Animals , Female , Gene Expression Profiling , Inactivation, Metabolic/genetics , Insecticide Resistance/genetics , Male , Oligonucleotide Array Sequence Analysis , Transcription, Genetic
4.
Trans R Soc Trop Med Hyg ; 103(11): 1139-45, 2009 Nov.
Article in English | MEDLINE | ID: mdl-18829056

ABSTRACT

Pyrethroid insecticide resistance in Anopheles gambiae sensu stricto is a major concern to malaria vector control programmes. Resistance is mainly due to target-site insensitivity arising from a single point mutation, often referred to as knockdown resistance (kdr). Metabolic-based resistance mechanisms have also been implicated in pyrethroid resistance in East Africa and are currently being investigated in West Africa. Here we report the co-occurrence of both resistance mechanisms in a population of An. gambiae s.s. from Nigeria. Bioassay, synergist and biochemical analysis carried out on resistant and susceptible strains of An. gambiae s.s. from the same geographical area revealed >50% of the West African kdr mutation in the resistant mosquitoes but <3% in the susceptible mosquitoes. Resistant mosquitoes synergized using pyperonyl butoxide before permethrin exposure showed a significant increase in mortality compared with the non-synergized. Biochemical assays showed an increased level of monooxygenase but not glutathione-S-transferase or esterase activities in the resistant mosquitoes. Microarray analysis using the An. gambiae detox-chip for expression of detoxifying genes showed five over-expressed genes in the resistant strain when compared with the susceptible one. Two of these, CPLC8 and CPLC#, are cuticular genes not implicated in pyrethroid metabolism in An. gambiae s.s, and could constitute a novel set of candidate genes that warrant further investigation.


Subject(s)
Anopheles/genetics , Insecticide Resistance/genetics , Larva/genetics , Point Mutation/genetics , Animals , Anopheles/drug effects , Insecticides/pharmacology , Larva/drug effects , Malaria/genetics , Malaria/transmission , Mosquito Control , Nigeria , Oligonucleotide Array Sequence Analysis , Pyrethrins/pharmacology
5.
Insect Mol Biol ; 15(4): 523-30, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16907839

ABSTRACT

The diverse habitats and diets encountered during the life cycle of an Anopheles mosquito have necessitated the development of extensive families of detoxification enzymes. Expansion of the three detoxification enzyme families (cytochrome P450s, carboxylesterases and glutathione transfereases), has occurred in mosquitoes compared with Drosophila, however, very little is known regarding the developmental expression of theses genes. Using a custom made microarray we determined the expression profile of the detoxification genes in adults, larvae and pupae of the malaria vector A. gambiae. The expression of approximately one quarter of these genes was developmentally regulated. The expression profile of each of these genes and the information this data provides on putative functions of the mosquito detoxification enzymes is discussed.


Subject(s)
Anopheles/genetics , Gene Expression , Insect Proteins/metabolism , Insect Vectors/genetics , Life Cycle Stages/physiology , Animals , Anopheles/metabolism , Carboxylic Ester Hydrolases/metabolism , Cytochrome P-450 Enzyme System/metabolism , Gene Expression Profiling , Glutathione Transferase/metabolism , Insect Vectors/metabolism , Life Cycle Stages/genetics , Microarray Analysis
6.
Insect Mol Biol ; 14(6): 591-7, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16313559

ABSTRACT

AnoBase (http://www.anobase.org) is an integrated, relational database of basic biological and genetic data on anopheline species, with a particular emphasis on Anopheles gambiae. It has been designed as an information source and research support tool for the broad vector biology community. Although AnoBase is not a primary genomic database that develops and provides tools to access the genome of the malaria mosquito, it nevertheless contains several sections that offer data of genomic interest such as in situ hybridization images, an integrated gene tool and direct online access to AnoXcel, the proteomic database of An. gambiae. Moreover, AnoBase also contains information on non-gambiae mosquito species and a novel section on studies related to insecticide resistance.


Subject(s)
Anopheles/genetics , Anopheles/physiology , Databases, Factual , Databases, Genetic , Genes, Insect/genetics , Animals , Anopheles/classification , Insecticide Resistance/genetics , Internet
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