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-
1
Reinert JF, 2000. New classification for the composite genus Aedes (Diptera: Culicidae: Aedini), elevation of subgenus Ochlerotatus to generic rank, reclassification of the other subgenera, and notes on certain subgenera and species. J Am Mosq Control Assoc 16 :175–188.
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2
Thompson WH, Anslow RO, Hanson RP, DeFoliart GR, 1972. La Crosse virus isolations from mosquitoes in Wisconsin, 1964–1968. Am J Trop Med Hyg 21 :90–96.
-
3
Sinsko MJ, Craig GB Jr, 1979. Dynamics of an isolated population of Aedes triseriatus (Diptera: Culicidae) 1. Population size. J Med Entomol 15 :89–98.
-
4
Matthews TC, Craig GB Jr, 1980. Genetic heterozygosity in natural populations of the tree-hole mosquito Aedes triseriatus.Ann Entomol Soc Am 73 :739–743.
-
5
Avise JC, 1994. Molecular Markers, Natural History, and Evolution. New York: Chapman and Hall.
-
6
Mitchell SE, Narang SK, Cockburn AF, Seawright JA, Goldenthal M, 1992. Mitochondrial and ribosomal DNA variation among members of the Anopheles quadrimaculatus (Diptera: Culicidae) species complex. Genome 35 :939–950.
-
7
Caccone A, Garcia BA, Powell JR, 1996. Evolution of the mitochondrial DNA control region in the Anopheles gambiae complex. Insect Mol Biol 5 :51–59.
-
8
Besansky NJ, Lehman JA, Fahey GT, Fontenille D, Braack LEO, Hawley WA, Collins FH, 1997. Patterns of mitochondrial DNA variation within and between African malaria vectors, Anopheles gambiae and An. arabiensis, suggest extensive gene flow. Genetics 147 :1817–1828.
-
9
Conn JE, Mitchell SE, Cockburn AF, 1997. Mitochondrial DNA variation within and between two species of neotropical anopheline mosquitoes (Diptera: Culicidae). J Hered 88 :98–107.
-
10
Conn JE, Mitchell SE, Cockburn AF, 1998. Mitochondrial DNA analysis of the neotropical malaria vector Anopheles nuneztovari.Genome 41 :313–327.
-
11
De Merida AMP, Palmieri M, Yurrita MM, Molina A, Molina E, Black WC IV, 1999. Mitochondrial DNA variation among Anopheles albimanus populations. Am J Trop Med Hyg 61 :230–239.
-
12
Gorrochotegui-Escalante N, Munoz MD, Fernandez-Salas I, Beaty BJ, Black WC IV, 2000. Genetic isolation by distance among Aedes aegypti populations along the northeastern coast of Mexico. Am J Trop Med Hyg 62 :200–209.
-
13
Gorrochotegui-Escalante N, Gomez-Machorro C, Lozano-Fuentes S, Fernandez-Salas I, Munoz MD, Farfan-Ale JA, Garcia-Rejon J, Beaty BJ, Black WC IV, 2002. Breeding structure of Aedes aegypti populations in Mexico varies by region. Am J Trop Med Hyg 66 :213–222.
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14
Beaty BJ, Thompson WH, 1975. Emergence of La Crosse virus from endemic foci: fluorescent antibody studies of overwintered Aedes triseriatus.Am J Trop Med Hyg 24 :685–691.
-
15
Black WC IV, DuTeau NM, 1997. RAPD-PCR and SSCP analysis for insect population genetic studies. Crampton J, Beard CB, Louis C, eds. The Molecular Biology of Insect Disease Vectors: A Methods Manual. New York: Chapman and Hall, 361–373.
-
16
Lynd A, Ranson H, McCall PJ, Randle NP, Black WC IV, Walker ED, Donnelly MJ, 2005. A simplified high-throughput method for pyrethroid knock-down resistance (kdr) detection in Anopheles gambiae.Malaria J 4 :16–20.
-
17
Nei M, 1987. Molecular Evolutionary Genetics. New York: Columbia University Press.
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18
Excoffier L, Smouse PE, Quatro JM, 1992. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131 :479–491.
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19
Felsenstein J, 1993. Phylogeny Inference Package Version 3.5C. Seattle, WA: University of Washington.
-
20
Slatkin M, 1993. Isolation by distance in equilibrium and non-equilibrium populations. Evolution 47 :264–279.
-
21
Mantel N, 1967. The detection of disease clustering and a generalized regression approach. Cancer Res 27 :209–220.
-
22
Zar JH, 1999. Data Transformations. Snavely SL, Ryu T, eds. Biostatistical Analysis. Englewood Cliffs, NJ: Prentice-Hall, 273–281.
-
23
Rosenberg MS, 2000. Passage: Pattern Analysis, Spatial Statistics, and Geographic Exegesis. Version 1.0. Tempe, AZ: Department of Biology, Arizona State University.
-
24
Apostol BL, Black WC IV, Miller BR, Reiter P, Beaty BJ, 1993. Estimation of family numbers at an oviposition site using RAPD-PCR markers: applications to the mosquito Aedes aegypti.Theor Appl Genet 86 :991–1000.
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25
Apostol BL, Black WC IV, Reiter P, Miller BR, 1994. Use of RAPD-PCR markers to estimate the number of Aedes aegypti families at oviposition sites in San Juan, Puerto Rico. Am J Trop Med Hyg 51 :89–97.
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| Abstract Views | 255 | 225 | 7 |
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AN ANALYSIS OF GENE FLOW AMONG MIDWESTERN POPULATIONS OF THE MOSQUITO OCHLEROTATUS TRISERIATUS
ERIC T. BECK
ERIC T. BECK
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado; Division of Vector Control, La Crosse County Health Department, La Crosse, Wisconsin
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CHRISTOPHER F. BOSIO
CHRISTOPHER F. BOSIO
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado; Division of Vector Control, La Crosse County Health Department, La Crosse, Wisconsin
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DAVID A. GESKE
DAVID A. GESKE
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado; Division of Vector Control, La Crosse County Health Department, La Crosse, Wisconsin
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CAROL D. BLAIR
CAROL D. BLAIR
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado; Division of Vector Control, La Crosse County Health Department, La Crosse, Wisconsin
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BARRY J. BEATY
BARRY J. BEATY
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado; Division of Vector Control, La Crosse County Health Department, La Crosse, Wisconsin
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WILLIAM C. BLACK IV
WILLIAM C. BLACK IV
Arthropod-Borne and Infectious Diseases Laboratory, Department of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, Colorado; Division of Vector Control, La Crosse County Health Department, La Crosse, Wisconsin
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A population genetics study of the mosquito Ochlerotatus triseriatus was performed on 36 collections from adjoining regions of Iowa, Minnesota, and Wisconsin covering approximately 120 km2. Single nucleotide polymorphism analysis was used to estimate variation in the mitochondrial NADH dehydrogenase subunit 4 (ND4) gene. The heated oligonucleotide ligation assay was used to identify the ND4 haplotype of each mosquito. No evidence of genetic isolation by distance was found, nor did Interstate 90 or the Mississippi River serve as barriers to gene flow. The effective migration rate varied from 18 to 45 reproductive migrants/generation, which is similar to estimates from an earlier study. The collections belong to a single, large, panmictic population. However, within this panmictic population, local genetic drift arises, possibly due to one or a few females ovipositing in larval breeding containers. From generation to generation, there is sufficient gene flow to mix families arising from individual breeding sites and eliminate founder effects due to drift.
Author Notes
ProCite
RefWorks
Reference Manager
BibTeX
Zotero
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-
1
Reinert JF, 2000. New classification for the composite genus Aedes (Diptera: Culicidae: Aedini), elevation of subgenus Ochlerotatus to generic rank, reclassification of the other subgenera, and notes on certain subgenera and species. J Am Mosq Control Assoc 16 :175–188.
-
2
Thompson WH, Anslow RO, Hanson RP, DeFoliart GR, 1972. La Crosse virus isolations from mosquitoes in Wisconsin, 1964–1968. Am J Trop Med Hyg 21 :90–96.
-
3
Sinsko MJ, Craig GB Jr, 1979. Dynamics of an isolated population of Aedes triseriatus (Diptera: Culicidae) 1. Population size. J Med Entomol 15 :89–98.
-
4
Matthews TC, Craig GB Jr, 1980. Genetic heterozygosity in natural populations of the tree-hole mosquito Aedes triseriatus.Ann Entomol Soc Am 73 :739–743.
-
5
Avise JC, 1994. Molecular Markers, Natural History, and Evolution. New York: Chapman and Hall.
-
6
Mitchell SE, Narang SK, Cockburn AF, Seawright JA, Goldenthal M, 1992. Mitochondrial and ribosomal DNA variation among members of the Anopheles quadrimaculatus (Diptera: Culicidae) species complex. Genome 35 :939–950.
-
7
Caccone A, Garcia BA, Powell JR, 1996. Evolution of the mitochondrial DNA control region in the Anopheles gambiae complex. Insect Mol Biol 5 :51–59.
-
8
Besansky NJ, Lehman JA, Fahey GT, Fontenille D, Braack LEO, Hawley WA, Collins FH, 1997. Patterns of mitochondrial DNA variation within and between African malaria vectors, Anopheles gambiae and An. arabiensis, suggest extensive gene flow. Genetics 147 :1817–1828.
-
9
Conn JE, Mitchell SE, Cockburn AF, 1997. Mitochondrial DNA variation within and between two species of neotropical anopheline mosquitoes (Diptera: Culicidae). J Hered 88 :98–107.
-
10
Conn JE, Mitchell SE, Cockburn AF, 1998. Mitochondrial DNA analysis of the neotropical malaria vector Anopheles nuneztovari.Genome 41 :313–327.
-
11
De Merida AMP, Palmieri M, Yurrita MM, Molina A, Molina E, Black WC IV, 1999. Mitochondrial DNA variation among Anopheles albimanus populations. Am J Trop Med Hyg 61 :230–239.
-
12
Gorrochotegui-Escalante N, Munoz MD, Fernandez-Salas I, Beaty BJ, Black WC IV, 2000. Genetic isolation by distance among Aedes aegypti populations along the northeastern coast of Mexico. Am J Trop Med Hyg 62 :200–209.
-
13
Gorrochotegui-Escalante N, Gomez-Machorro C, Lozano-Fuentes S, Fernandez-Salas I, Munoz MD, Farfan-Ale JA, Garcia-Rejon J, Beaty BJ, Black WC IV, 2002. Breeding structure of Aedes aegypti populations in Mexico varies by region. Am J Trop Med Hyg 66 :213–222.
-
14
Beaty BJ, Thompson WH, 1975. Emergence of La Crosse virus from endemic foci: fluorescent antibody studies of overwintered Aedes triseriatus.Am J Trop Med Hyg 24 :685–691.
-
15
Black WC IV, DuTeau NM, 1997. RAPD-PCR and SSCP analysis for insect population genetic studies. Crampton J, Beard CB, Louis C, eds. The Molecular Biology of Insect Disease Vectors: A Methods Manual. New York: Chapman and Hall, 361–373.
-
16
Lynd A, Ranson H, McCall PJ, Randle NP, Black WC IV, Walker ED, Donnelly MJ, 2005. A simplified high-throughput method for pyrethroid knock-down resistance (kdr) detection in Anopheles gambiae.Malaria J 4 :16–20.
-
17
Nei M, 1987. Molecular Evolutionary Genetics. New York: Columbia University Press.
-
18
Excoffier L, Smouse PE, Quatro JM, 1992. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics 131 :479–491.
-
19
Felsenstein J, 1993. Phylogeny Inference Package Version 3.5C. Seattle, WA: University of Washington.
-
20
Slatkin M, 1993. Isolation by distance in equilibrium and non-equilibrium populations. Evolution 47 :264–279.
-
21
Mantel N, 1967. The detection of disease clustering and a generalized regression approach. Cancer Res 27 :209–220.
-
22
Zar JH, 1999. Data Transformations. Snavely SL, Ryu T, eds. Biostatistical Analysis. Englewood Cliffs, NJ: Prentice-Hall, 273–281.
-
23
Rosenberg MS, 2000. Passage: Pattern Analysis, Spatial Statistics, and Geographic Exegesis. Version 1.0. Tempe, AZ: Department of Biology, Arizona State University.
-
24
Apostol BL, Black WC IV, Miller BR, Reiter P, Beaty BJ, 1993. Estimation of family numbers at an oviposition site using RAPD-PCR markers: applications to the mosquito Aedes aegypti.Theor Appl Genet 86 :991–1000.
-
25
Apostol BL, Black WC IV, Reiter P, Miller BR, 1994. Use of RAPD-PCR markers to estimate the number of Aedes aegypti families at oviposition sites in San Juan, Puerto Rico. Am J Trop Med Hyg 51 :89–97.
| Past two years | Past Year | Past 30 Days | |
|---|---|---|---|
| Abstract Views | 255 | 225 | 7 |
| Full Text Views | 232 | 7 | 0 |
| PDF Downloads | 45 | 5 | 0 |