Mapping of resistance to vegetable polyphenols among Aedes taxa (Diptera, Culicidae) on a molecular phylogeny.

To recover some evolutionary aspects of the interaction between culicine larvae and dietary polyphenols of the vegetation surrounding mosquito breeding sites, we constructed a phylogeny of the most common French Aedes species, chosen as reference species. We also evaluated the differential resistance of these larval taxa to the polyphenols of leaf litter from the riparian vegetation used as a food source. Mitochondrial DNA sequence analysis was performed among 14 different taxa and ecotypes (Aedes aegypti, Ae. albopictus, Ae. cantans, Ae. caspius, Ae. cataphylla, Ae. cinereus, Ae. detritus, Ae. geniculatus, Ae. mariae, Ae. pullatus, Ae. punctor, Ae. rusticus, Ae. sticticus, and Ae. vexans) through direct sequencing of a 763-base segment of the cytochrome oxidase subunit I gene. Phylogenetic analysis, based on nucleotide and amino acid sequences, was conducted by means of parsimony and distance methods. The differential tolerance of larvae to vegetable leaf litter was comparatively tested by use of 10-month-old alder leaf litter as an experimental standard. The absence of correlation between resistance to polyphenols and molecular phylogeny suggests that larval adaptation to polyphenol-rich vegetable breeding sites is a labile character. The acquisition of such resistance appears not to be ancestrally inherited, but rather to be a dynamic adaptation to the environment. Molecular data also support the classical morphological classification within the Aedes genus.

[1]  J. David,et al.  Comparative sensitivity of larval mosquitoes to vegetable polyphenols versus conventional insecticides , 2001 .

[2]  J. David,et al.  Toxicity of vegetable tannins on crustacea associated with alpine mosquito breeding sites. , 2000, Ecotoxicology and Environmental Safety.

[3]  J. David,et al.  Comparative ability to detoxify alder leaf litter in field larval mosquito collections. , 2000, Archives of insect biochemistry and physiology.

[4]  J. David,et al.  Role of vegetable tannins in habitat selection among mosquito communities from the Alpine hydrosystems. , 2000, Comptes rendus de l'Academie des sciences. Serie III, Sciences de la vie.

[5]  A. Paterson,et al.  Phylogeny of "Oxycanus" lineages of hepialid moths from New Zealand inferred from sequence variation in the mtDNA COI and II gene regions. , 1999, Molecular phylogenetics and evolution.

[6]  B. Emerson,et al.  MtDNA phylogeography and recent intra-island diversification among Canary Island Calathus beetles. , 1999, Molecular phylogenetics and evolution.

[7]  Jaeger,et al.  Evolution of oviposition strategies and speciation in the globeflower flies Chiastocheta spp. (Anthomyiidae) , 1999 .

[8]  M. Pautou,et al.  Histopathological effects of tannic acid on the midgut epithelium of some aquatic Diptera larvae. , 1999, Journal of invertebrate pathology.

[9]  W. Black,et al.  An estimate of phylogenetic relationships among culicine mosquitoes using a restriction map of the rDNA cistron , 1998, Insect molecular biology.

[10]  I. Kitching,et al.  Phylogeny and classification of the Culicidae (Diptera) , 1998 .

[11]  E. Guilvard,et al.  DESCRIPTION D'AEDES (OCHLEROTATUS) COLUZZII N. SP. (DIPTERA, CULICIDAE), ESPECE JUMELLE A DU COMPLEXE DETRITUS , 1998 .

[12]  J. Pasteels,et al.  THE EVOLUTION OF HOST‐PLANT USE AND SEQUESTRATION IN THE LEAF BEETLE GENUS PHRATORA (COLEOPTERA: CHRYSOMELIDAE) , 1998, Evolution; international journal of organic evolution.

[13]  D. -. Zhang,et al.  Assessment of the universality and utility of a set of conserved mitochondrial COI primers in insects , 1997, Insect molecular biology.

[14]  N. Besansky,et al.  Utility of the white gene in estimating phylogenetic relationships among mosquitoes (Diptera: Culicidae). , 1997, Molecular biology and evolution.

[15]  A. Austin,et al.  Evidence for AT-Transversion Bias in Wasp (Hymenoptera: Symphyta) Mitochondrial Genes and Its Implications for the Origin of Parasitism , 1997, Journal of Molecular Evolution.

[16]  E. Walker,et al.  Feeding behavior of aquatic insects: Case studies on black fly and mosquito larvae , 1996 .

[17]  G. Hewitt,et al.  Phylogeny of the Coleoptera based on mitochondrial cytochrome oxidase I sequence data , 1995, Insect molecular biology.

[18]  B. Crespi,et al.  Evolution, weighting, and phylogenetic utility of mitochondrial gene sequences and a compilation of conserved polymerase chain reaction primers , 1994 .

[19]  John C. Avise,et al.  Molecular Markers, Natural History and Evolution , 1993, Springer US.

[20]  C H Porter,et al.  Sequence and secondary structure comparisons of ITS rDNA in mosquitoes (Diptera: Culicidae). , 1992, Molecular phylogenetics and evolution.

[21]  P. Bartlein,et al.  Global Changes During the Last 3 Million Years: Climatic Controls and Biotic Responses , 1992 .

[22]  W. Black,et al.  Random amplified polymorphic DNA of mosquito species and populations (Diptera: Culicidae): techniques, statistical analysis, and applications. , 1992, Journal of medical entomology.

[23]  K. S. Rai,et al.  VARIATION IN MITOCHONDRIAL DNA OF AEDES SPECIES (DIPTERA: CULICIDAE) , 1991, Evolution; international journal of organic evolution.

[24]  R. DeSalle,et al.  FOUNDER EFFECTS AND THE RATE OF MITOCHONDRIAL DNA EVOLUTION IN HAWAIIAN DROSOPHILA , 1988, Evolution; international journal of organic evolution.

[25]  Brian D. Farrell,et al.  The Phylogenetic Study of Adaptive Zones: Has Phytophagy Promoted Insect Diversification? , 1988, The American Naturalist.

[26]  N. Saitou,et al.  The neighbor-joining method: a new method for reconstructing phylogenetic trees. , 1987, Molecular biology and evolution.

[27]  J. Felsenstein CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP , 1985, Evolution; international journal of organic evolution.

[28]  Tibor Jermy,et al.  Evolution of Insect/Host Plant Relationships , 1984, The American Naturalist.

[29]  Joseph Felsenstein,et al.  DISTANCE METHODS FOR INFERRING PHYLOGENIES: A JUSTIFICATION , 1984, Evolution; international journal of organic evolution.

[30]  F. Rohlf Congruence or Larval and Adult Classifications in Aedes (Diptera: Culicidae) , 1963 .

[31]  W. S. Abbott,et al.  A method of computing the effectiveness of an insecticide. 1925. , 1925, Journal of the American Mosquito Control Association.

[32]  J. David,et al.  Differential toxicity of leaf litter to dipteran larvae of mosquito developmental sites. , 2000, Journal of invertebrate pathology.

[33]  Han Olff,et al.  Herbivores Between Plants and Predators , 1999 .

[34]  J. Conn,et al.  Systematics of mosquito disease vectors (Diptera, Culicidae): impact of molecular biology and cladistic analysis. , 1997, Annual review of entomology.

[35]  D. Rey,et al.  Composés phénoliques chez Alnus glutinosa et contrôle des populations larvaires de Culicidae , 1996 .

[36]  J. Miller,et al.  Ecological Characters and Phylogeny , 1995 .

[37]  J. N. Thompson,et al.  Phylogeny of Greya (Lepidoptera: Prodoxidae), based on nucleotide sequence variation in mitochondrial cytochrome oxidase I and II: congruence with morphological data. , 1994, Molecular biology and evolution.

[38]  R. Crozier,et al.  The mitochondrial genome of the honeybee Apis mellifera: complete sequence and genome organization. , 1993, Genetics.

[39]  R. Brust,et al.  Morphological and Genetic Characterization of the Aedes (Ochlerotatus) communis Complex (Diptera: Culicidae) in North America , 1992 .

[40]  P. Cranston,et al.  Keys to the adults, male hypopygia, fourth-instar larvae, and pupae of the British mosquitoes (Culicidae) : with notes on their ecology and medical importance , 1987 .

[41]  K. Knight,et al.  A catalog of the mosquitoes of the world (Diptera : Culicidae) , 1977 .