18 results on '"VOEGTLIN, D. J."'
Search Results
2. Biocontrol for everyman: public participation in a weed project.
- Author
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Wiedenmann, R. N., primary, Post, S. L., additional, Jeffords, M. R., additional, and Voegtlin, D. J., additional
- Published
- 2007
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3. Identification of a new species of Aphis (Hemiptera: Aphididae) based on distinct morphology rather than DNA barcoding
- Author
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Lagos-Kutz, Doris, Voegtlin, D. J., and Hartman, Glen
- Subjects
Hemiptera ,Insecta ,Arthropoda ,Aphididae ,Animalia ,Biodiversity ,Taxonomy - Abstract
Lagos-Kutz, Doris, Voegtlin, D. J., Hartman, Glen (2017): Identification of a new species of Aphis (Hemiptera: Aphididae) based on distinct morphology rather than DNA barcoding. Insecta Mundi 2017 (535): 1-11, DOI: http://doi.org/10.5281/zenodo.5353418, {"references":["Blackman, R. L., and V. F. Eastop. 2006. Aphids on the World's Herbaceous Plants and Shrubs. Vols 1 and 2. Wiley, Chichester (UK) and New York. 1439 p. (Available at ~ http://www.aphidsonworldsplants.info. Last accessed December 2016.)","Brown, P. A. 1989. Keys to the alate Aphis (Homoptera) of northern Europe. British Museum (Natural History), London. Systematic Entomology 5: 1-29.","Carletto, J., A. Blin, and F. Vanlerberghe-Masutti. 2009. DNA-based discrimination between the sibling species Aphis gossypii Glover and Aphis frangulae Kaltenbach. Systematic Entomology 34 (2): 307-314.","Coeur d'acier, A., A. Cruaud, E. Artige, G. Genson, A-L. Clamens, E. Pierre, S. Hudaverdian, J-C. Simmon, A. E. Jousselin, and J. Y. Rasplus. 2014. DNA Barcoding and the Associated PhylAphidB@se Website for the Identification of European Aphids (Insecta: Hemiptera: Aphididae). PLoS ONE 9(6): e97620. (Available at ~ http://journals.plos.org/plosone/article?id=10.1371/journal. pone.0097620. Last accessed December 2016.)","Cook, E. F. 1984. Aphis (Homoptera: Aphididae) recorded from compositae in North America, with a key to the species East of the Rocky Mountains and comments on synonymy and redescriptions of some little known forms. Annals of the Entomological Society of America 77: 442-449.","DeSalle, R. 2006. Species Discovery versus Species Identification in DNA Barcoding Efforts: Response to Rubinoff. Conservation Biology 20(5): 1545-1547.","Favret, C., and G. L. Miller. 2011. The neotype of the cotton aphid (Hemiptera: Aphididae: Aphis gossypii Glover 1877. Proceedings of the Entomological Society of Washington 113(2): 119-126.","Foottit, R. G., H. E. L. Maw, C. D. von Dohlen, and P. D. N. Hebert. 2008. Species identification of aphids (Insecta:Hemiptera:Aphididae) through DNA barcodes. Molecular Ecology Resources 8: 1189-1201.","Garcia Prieto, F., A. Tinaut Ranera, N. Perez Hidalgo, and J. M. Nieto Nafria. 2005. Genero Aphis Linnaeus, 1788. p. 30-173. In: J. M. Nieto Nafria, M. P. Mier Durante, F. Garcia Prieto, and N. Perez Hidalgo (eds.). Hemiptera Aphididae III. Fauna Iberica, Vol. 28. Museo Nacional de Ciencias Naturales. CSIC; Madrid. 364 p.","Gillette, C. P. 1927. Notes on a few aphid species and the genus Illinoia Wilson. Annals of the Entomological Society of America 20(3): 344-348.","Harley, R. M., S. Atkins, A. L. Budantsev, P. D. Cantino, B. J. Conn, R. J. Grayer, M. M. Harley, R. P. J. de Kok, T. V. Krestovskaja, R. Morales, A. J. Paton, and P. O. Ryding. 2004. Labiatae. p. 167-275. In: K. Kubitzki (ed.). The Families and Genera of Vascular Plants, Vol. 7. Springer-Verlag; Berlin, Germany. 275 p.","Heie, O. 1986. The Aphidoidea (Hemiptera) of Fennoscandia and Denmark. III Family Aphididae: subfamily Pterocommatinae and tribe Aphidini of subfamily Aphidinae. Fauna Entomologica Scandinavica 3(17). 314 p.","Hottes, F. C., and T. H. Frison. 1931. The plant lice, or Aphiidae, of Illinois. Bull. Illinois Natural History Survey 19: 121-447.","Kim, H., and S. Lee. 2008. A molecular phylogeny of the tribe Aphidini (Insecta: Hemiptera: Aphididae) based on the mitochondrial tRNA/COII, 12S/16S and the nuclear EF1-α genes. Systematic Entomology 33(4): 711-721.","Kimura, M. 1980. A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution 16(2): 111-120.","Komazaki, S., T. Shigehara, and S. Toda. 2010. Diversity of Japanese Aphis gossypii and comparison with other Aphis species based on the mitochondrial cytochrome oxidase I sequence. Annals of the Entomological Society of America 103(6): 916-924. (Available at http://dx.doi.org/10.1603/ AN10085. Last accessed January 2017.)","Lagos, D. M., B. Puttler, R. Giordano, and D. J. Voegtlin. 2012. A new species of Aphis (Hemiptera:Aphididae) in Missouri on St. John's Wort, Hypericum kalmianum, and re-description of Aphis hyperici Monell. Zootaxa 3478: 81-92.","Lagos, D. M., D. J. Voegtlin, A. Coeur d'acier, and R. Giordano. 2014. Aphis (Hemiptera:Aphididae) species groups found in the Midwestern United States and their contribution to the phylogenetic knowledge of the genus. Insect Science 21: 1-18.","Lagos-Kutz, D., C. Favret, R. Giordano, and D. J. Voegtlin. 2014. Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49-72.","Lagos-Kutz, D., C. Favret, R. Giordano, and D. J. Voegtlin. 2016. The status of the members of the Aphis asclepiadis species group (Hemiptera, Aphididae) in the United States of America. Annals of the Entomological Society of America, 109(4), 585-594.","Lee, W., Y. Lee, H. Kim, S. Akimoto, and S. Lee. 2014. Developing a new molecular marker for aphid species identification. Evaluation of eleven candidate genes with species-level sampling. Journal of Asia-Pacific Entomology 17: 617-627.","Massimino Cocuzza, G.E., and V. Cavalieri. 2014. Identification of aphids of Aphis frangulae-group living on Lamiaceae species through DNA barcode. Molecular Ecology Resources 14: 447-457.","Meier, R. 2008. DNA sequences in taxonomy opportunities and challenges. p. 95-127. In: Q. D. Wheeler (eds.). The new taxonomy. The systematics association special volume, Vol. 76. CRC Press; Boca Raton, FL. 256 p.","Oestlund, O. W. 1887. Synopsis of the Aphididae of Minnesota. Bull. of the Geological and Natural History Survey of Minnesota. 14: 17-56.","Palmer, M. 1952. Aphids of the Rocky Mountain Region, Vol. 5. Thomas Say Foundation, Denver, Colorado. 452 p.","Stroyan, H. L. G. 1984. Aphids-Pterocommatinae and Aphidinae (Aphidini). Handbooks for the Identification of British Insects, Vol. 6. Royal Entomological Society of London, 41 Queen's Gate, London. 232 p.","Swofford, D. L. 2001. PAUP*: Phylogenetic Analysis Using Parsimony (*and other methods), version 4. Sinauer Associates, Sunderland, Massachusetts.","USDA-NRCS. 2015. The plants database National Plant Data Center, Baton Rouge, LA 70874-4490 USA. (Available at ~ http://plants.usda.gov. Last accessed October 2016.).","Voegtlin, D. J., S. E. Halbert, and G-X. Qiao. 2004. A guide to separating Aphis glycines Matsumura and morphologically similar species that share its hosts. Annals of the Entomological Society of America 97(2): 227-232.","Wang, J-F., L-Y. Jiang, and G-X. Qiao. 2011. Use of mitochondrial COI sequence to identify species of subtribe Aphidina. Zookeys 122: 1-17."]}
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- 2017
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4. Aphis elena Lagos-Kutz and Voegtlin 2017, sp. nov
- Author
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Lagos-Kutz, Doris, Voegtlin, D. J., and Hartman, Glen
- Subjects
Hemiptera ,Aphis elena ,Insecta ,Arthropoda ,Aphididae ,Animalia ,Biodiversity ,Aphis ,Taxonomy - Abstract
Aphis elena Lagos-Kutz and Voegtlin sp. nov. Diagnosis. Apterous viviparae similar to A. gossypii. Distinguished by the ratio of the length of siphunculus to the length of the cauda (SIPH/CA), 1–1.6 for A. elena and 1.3–2.5 for A. gossypii. Alate viviparae with few secondary sensoria in straight line restricted to antennal segments III (5–6) and IV (1–2). Distance from the base of antennal segment III to the first secondary sensorium (DBIII) 0.07–0.09. Forewing with median vein once-forked. Dark hind coxa. Cauda paler than siphunculus, with 6–7 setae. Ratio SIPH/CA=1–1.3. Marginal sclerites dusky. Description. Apterous viviparae (n=22) (Table 1 and Figures 1–8). Color in life (Figure 18): Head, thorax and abdomen dark green, covered with white wax. Color of cleared specimens: Head: dark. Six antennal segments, rarely five (not included in morphometry): first, second, fifth and base of last antennal segment dusky; the remainder pale or slightly dusky. Ultimate rostral segment (URS) reaches the hind coxae. Thorax: Coxae dusky. Trochanters paler than coxae. Femora slightly dusky on distal half, basal tips pale. Tibiae pale, darkening near distal tip. Tarsi dusky. Abdomen: Cauda dusky and slightly spoon-shaped with inward curled setae. Siphunculi dark, imbricated with flange. Pre and post-siphuncular sclerite absent. Marginal sclerites pale. Marginal tubercles on abdominal II, III, and IV absent. Dorsum of abdomen without sclerites, cuticle with reticulation. Sub-genital plate dusky and complete. Alate viviparae (n=6) (Table 1 and Figures 9–17). Color of cleared specimens: Head: Head and thorax dark. First and second antennal segments darker than other segments. Secondary sensoria restricted to antennal segments III and IV, arranged in a single row. URS reaches hind coxae, with 2 accessory setae. Thorax: Fore and middle femora dusky throughout. Hind femora dark except on pale base. Coxae dark. Trochanters paler than coxae. Tibiae pale, darkening near distal tip. Tarsi dusky or dark. Forewing with median vein once-forked. Abdomen: Cauda dusky, slightly spoon-shaped. Siphunculi dark, imbricated with flange. Marginal sclerites dusky. Pre-siphuncular sclerite absent. Postsiphuncular sclerite dusky. Marginal tubercles on abdominal II, III, and IV absent. Dorsum of abdomen with small transverse sclerites on VI, and VII and large transverse sclerite on VIII. Subgenital plate dusky and complete. Type material. HOLOTYPE. Apterous vivipara. USA; Illinois; Lake County; Middlefork Savanna County Forest Preserve; on Pycnanthemum virginianum (L.) T. Dur. & B.D. Jacks. ex B.L. Rob. & Fernald 42.2620° N x 87.8962° W; 20.vi.2010; D. Lagos-Kutz. (INHS Insect Collection 511,252). Paratypes: 4 alate viviparae, 25 apterous viviparae, 511,243-510,259, Middlefork Savanna County Forest Preserve, 42.2620° N x 87.8962° W, Lake County, IL, 20.vi. 2010, on Pycnanthemum virginianum, D. Lagos-Kutz; 1 apterous vivipara, 511,363, Middlefork Savanna County Forest Preserve, 42.2620° N x 87.8962° W, Lake County, IL, 28.vi.2008, on Pycnanthemum virginianum, D. Voegtlin. Biology. Two collections of alate and apterous viviparae females of A. elena were found in the summer (late June) of 2008 and 2010 on Pycnanthemum virginianum in Middlefork Savanna Forest Preserve, Lake Forest, Lake County, Illinois. The sexual morph was not found. It is likely that because the host plant is perennial, this aphid overwinters on the same host plant. Further observations need to be done to learn more about the biology of A. elena. Etymology. This species is named after the first author’s daughter’s middle name, Katherine Elena. Dichotomous keys to apterous and alate viviparous females of the Aphis that feed on Lamiaceae in the North American Midwest. The dichotomous key presented below is based on specimens from collections made in the Midwest (may not be reliable in other geographic regions), and molecular data for specimens from these collections support our morphologically based identifications. Morphological data for these species is shown in Lagos et al. (2014), Lagos-Kutz et al. (2014), and Blackman and Eastop (2006). For some comparative morphometric data of European specimens of A. fabae, A. gossypii and A. nasturtii see Stroyan (1984), Heie (1986), Brown (1989) and García Prieto et al. (2005)., Published as part of Lagos-Kutz, Doris, Voegtlin, D. J. & Hartman, Glen, 2017, Identification of a new species of Aphis (Hemiptera: Aphididae) based on distinct morphology rather than DNA barcoding, pp. 1-11 in Insecta Mundi 2017 (535) on pages 2-3, DOI: 10.5281/zenodo.5353418, {"references":["Lagos, D. M., D. J. Voegtlin, A. Coeur d'acier, and R. Giordano. 2014. Aphis (Hemiptera: Aphididae) species groups found in the Midwestern United States and their contribution to the phylogenetic knowledge of the genus. Insect Science 21: 1 - 18.","Lagos-Kutz, D., C. Favret, R. Giordano, and D. J. Voegtlin. 2014. Molecular and morphological differentiation between Aphis gossypii Glover (Hemiptera, Aphididae) and related species, with particular reference to the North American Midwest. ZooKeys 459: 49 - 72.","Blackman, R. L., and V. F. Eastop. 2006. Aphids on the World's Herbaceous Plants and Shrubs. Vols 1 and 2. Wiley, Chichester (UK) and New York. 1439 p. (Available at ~ http: // www. aphidsonworldsplants. info. Last accessed December 2016.)","Stroyan, H. L. G. 1984. Aphids-Pterocommatinae and Aphidinae (Aphidini). Handbooks for the Identification of British Insects, Vol. 6. Royal Entomological Society of London, 41 Queen's Gate, London. 232 p.","Heie, O. 1986. The Aphidoidea (Hemiptera) of Fennoscandia and Denmark. III Family Aphididae: subfamily Pterocommatinae and tribe Aphidini of subfamily Aphidinae. Fauna Entomologica Scandinavica 3 (17). 314 p.","Brown, P. A. 1989. Keys to the alate Aphis (Homoptera) of northern Europe. British Museum (Natural History), London. Systematic Entomology 5: 1 - 29.","Garcia Prieto, F., A. Tinaut Ranera, N. Perez Hidalgo, and J. M. Nieto Nafria. 2005. Genero Aphis Linnaeus, 1788. p. 30 - 173. In: J. M. Nieto Nafria, M. P. Mier Durante, F. Garcia Prieto, and N. Perez Hidalgo (eds.). Hemiptera Aphididae III. Fauna Iberica, Vol. 28. Museo Nacional de Ciencias Naturales. CSIC; Madrid. 364 p."]}
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- 2017
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5. A New Species of Aphis in Minnesota (Hemiptera: Aphididae) on Narrow-Leaved Purple Coneflower, Echinacea Angustifolia
- Author
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Lagos, D. M, primary and Voegtlin, D. J, additional
- Published
- 2018
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6. Identifi cation of a new species of Aphis (Hemiptera: Aphididae) based on distinct morphology rather than DNA barcoding
- Author
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Lagos-Kutz, Doris, Voegtlin, D. J., Hartman, Glen, Lagos-Kutz, Doris, Voegtlin, D. J., and Hartman, Glen
- Abstract
Aphis elena Lagos-Kutz and Voegtlin, sp. nov. (Hemiptera: Aphididae), is described from specimens collected in Illinois, USA, on the North American native plant, Pycnanthemum virginianum (L.) T. Dur. & B.D. Jacks. ex B.L. Rob. & Fernald (Family: Lamiaceae). Both apterous and alate viviparae are described and illustrated, and a dichotomous key is provided to apterous and alate viviparae of the six species of Aphis that have been recorded on plants in the family Lamiaceae in North America. Neighbor-joining analysis of cytochrome oxidase 1 (Cox1) indicated a close relationship of the new species with Aphis monardae Oestlund, which also feeds on a member of Lamiaceae. The range of pair-wise distances for DNA barcoding of these species is 0.17–0.33%. The newly described Aphis elena is morphologically more similar to Aphis gossypii Glover than it is to Aphis monardae.
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- 2017
7. The Status of the Members of theAphis asclepiadisSpecies Group (Hemiptera: Aphididae) in the United States of America
- Author
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Lagos-Kutz, D., primary, Favret, C., additional, Giordano, R., additional, and Voegtlin, D. J., additional
- Published
- 2016
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8. The Status of the Members of the Aphis asclepiadis Species Group (Hemiptera: Aphididae) in the United States of America.
- Author
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Lagos-Kutz, D., Favret, C., Giordano, R., and Voegtlin, D. J.
- Subjects
APHIS ,HEMIPTERA ,INSECT host plants ,INSECT phylogeny ,INSECT morphology ,CYTOCHROME oxidase - Abstract
In North America, there is a morphologically defined group of Aphis species that use Cornus spp. as primary host plants and also are associated with plants in the fam ily Apiaceae. We refer to them collectively as the Aphis asclepiadis species group and attempt to elucidate the taxonomic status of its members using sequences of mitochondrial cytochrome oxidase 1 (Cox7) and nuclear elongation factor 1-a (EF7a7) genes. The Bayesian phylogenetic analyses of the combined data of these two genes strongly supported a clade composed of the A. asclepiadis species group. This group includes the fo llow in g North American native species: A. asclepiadis, A. carduella, A. decepta, A. impatientis, A. neogillettei, A. nigratibialis, A. saniculae, A. thaspii, and A. viburniphila, and the related exotic species, A. salicariae. Bayesian phylogenetic and Maximum Parsimony Network nested all the collections that match the diagnostic characters described for A. asclepiadis and A. carduella, and the ones described for A. nigratibialis. Moreover, the range of pair-wise distances between collections of A. asclepiadis and A. carduella are 0.00-0.73 and 0.00-0.87% for Coxl and EFlcc 7, respectively. Therefore, we conclude that A. asclepiadis Fitch 1851 is a senior synonym of A. carduella Walsh 1863, syn. nov. In addition, all the sequences of species morphologically identified as A. impatientis matched almost 100%. Biological studies showed that Aphis impatientis is a heteroecious species that alternates between Cornus and Impatiens. We also found that morphological characterization of the sexual morph is useful to differentiate species that feed on Cornus spp. as primary host plants. [ABSTRACT FROM AUTHOR]
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- 2016
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9. Forecasting Seasonal Population Growth of Aphis glycines (Hemiptera: Aphididae) in Soybean in Illinois
- Author
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Onstad, D. W., primary, Fang, S., additional, and Voegtlin, D. J., additional
- Published
- 2005
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10. SamplingAphis glycines(Homoptera: Aphididae) in Soybean Fields in Illinois
- Author
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Onstad, D. W., primary, Fang, S., additional, Voegtlin, D. J., additional, and Just, M. G., additional
- Published
- 2005
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11. Migratory Aphid (Hemiptera: Aphididae) Habitat Selection in Agricultural and Adjacent Natural Habitats
- Author
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Favret, C., primary and Voegtlin, D. J., additional
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- 2001
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12. Occurrence and Distribution of Aphis glycines on Soybeans in Illinois in 2000 and Its Potential Control
- Author
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Hartman, G. L., primary, Domier, L. L., additional, Wax, L. M., additional, Helm, C. G., additional, Onstad, D. W., additional, Shaw, J. T., additional, Solter, L. F., additional, Voegtlin, D. J., additional, D'Arcy, C. J., additional, Gray, M. E., additional, Steffey, K. L., additional, Isard, S. A., additional, and Orwick, P. L., additional
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- 2001
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13. Solanaceous Weeds as Possible Sources of Cucumber mosaic virus in Southern Illinois for Aphid Transmission to Pepper
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Hobbs, H. A., primary, Eastburn, D. M., additional, D'Arcy, C. J., additional, Kindhart, J. D., additional, Masiunas, J. B., additional, Voegtlin, D. J., additional, Weinzierl, R. A., additional, and McCoppin, N. K., additional
- Published
- 2000
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14. Detection of Buchnera, the primary prokaryotic endosymbiont of aphids, using the polymerase chain reaction
- Author
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Rouhbakhsh, D., primary, Moran, N. A., additional, Baumann, L., additional, Voegtlin, D. J., additional, and Baumann, P., additional
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- 1994
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15. Evidence for the establishment of aphid-eubacterium endosymbiosis in an ancestor of four aphid families
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Munson, M A, primary, Baumann, P, additional, Clark, M A, additional, Baumann, L, additional, Moran, N A, additional, Voegtlin, D J, additional, and Campbell, B C, additional
- Published
- 1991
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16. Observations on the biology ofCinara ponderosae(Williams) (Homoptera: Aphididae) in the westside forests of the Sierra Nevada
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Voegtlin, D. J., primary and Dahlsten, D. L., primary
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- 1982
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17. Sampling Aphis glycines (Homoptera: Aphididae) in Soybean Fields in Illinois
- Author
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Onstad, D. W., Fang, S., Voegtlin, D. J., and Just, M. G.
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- 2005
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18. The tryptophan biosynthetic pathway of aphid endosymbionts (Buchnera): genetics and evolution of plasmid-associated anthranilate synthase (trpEG) within the aphididae.
- Author
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Rouhbakhsh D, Lai CY, von Dohlen CD, Clark MA, Baumann L, Baumann P, Moran NA, and Voegtlin DJ
- Subjects
- Amino Acid Sequence, Animals, Bacteria metabolism, Base Sequence, Biological Evolution, Conserved Sequence, Escherichia coli genetics, Molecular Sequence Data, Mutagenesis, Phylogeny, Plasmids genetics, Replication Origin, Sequence Homology, Amino Acid, Tryptophan Synthase genetics, Anthranilate Synthase genetics, Aphids microbiology, Bacteria genetics, Symbiosis genetics, Tryptophan biosynthesis
- Abstract
The bacterial endosymbionts (Buchnera) from the aphids Rhopalosiphum padi, R. maidis, Schizaphis graminum, and Acyrthosiphon pisum contain the genes for anthranilate synthase (trpEG) on plasmids made up of one or more 3.6-kb units. Anthranilate synthase is the first as well as the rate-limiting enzyme in the tryptophan biosynthetic pathway. The amplification of trpEG on plasmids may result in an increase of enzyme protein and overproduction of this essential amino acid, which is required by the aphid host. The nucleotide sequence of trpEG from endosymbionts of different species of aphids is highly conserved, as is an approximately 500-bp upstream DNA segment which has the characteristics of an origin of replication. Phylogenetic analyses were performed using trpE and trpG from the endosymbionts of these four aphids as well as from the endosymbiont of Schlechtendalia chinensis, in which trpEG occurs on the chromosome. The resulting phylogeny was congruent with trees derived from sequences of two chromosome-located bacterial genes (part of trpB and 16S ribosomal DNA). In turn, trees obtained from plasmid-borne and bacterial chromosome-borne sequences were congruent with the tree resulting from phylogenetic analysis of three aphid mitochondrial regions (portions of the small and large ribosomal DNA subunits, as well as cytochrome oxidase II). Congruence of trees based on genes from host mitochondria and from bacteria adds to previous support for exclusively vertical transmission of the endosymbionts within aphid lineages. Congruence with trees based on plasmid-borne genes supports the origin of the plasmid-borne trpEG from the chromosomal genes of the same lineage and the absence of subsequent plasmid exchange among endosymbionts of different species of aphids.
- Published
- 1996
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