Abstract
Bacterial symbionts may be used as vehicles for expressing foreign genes in arthropods. Expression of selected genes can render an arthropod incapable of transmitting a second microorganism that is pathogenic for humans and is an alternative approach to the control of arthropod-borne diseases. We discuss the rationale for this alternative approach, its potential applications and limitations, and the regulatory concerns that may arise from its use in interrupting disease transmission in humans and animals.
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- Aksoy S., Pourhosseini A. A., Chow A. Mycetome endosymbionts of tsetse flies constitute a distinct lineage related to Enterobacteriaceae. Insect Mol Biol. 1995 Feb;4(1):15–22. doi: 10.1111/j.1365-2583.1995.tb00003.x. [DOI] [PubMed] [Google Scholar]
- Azad A. F., Beard C. B. Rickettsial pathogens and their arthropod vectors. Emerg Infect Dis. 1998 Apr-Jun;4(2):179–186. doi: 10.3201/eid0402.980205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Azad A. F., Sacci J. B., Jr, Nelson W. M., Dasch G. A., Schmidtmann E. T., Carl M. Genetic characterization and transovarial transmission of a typhus-like rickettsia found in cat fleas. Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):43–46. doi: 10.1073/pnas.89.1.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beard C. B., Benedict M. Q., Primus J. P., Finnerty V., Collins F. H. Eye pigments in wild-type and eye-color mutant strains of the African malaria vector Anopheles gambiae. J Hered. 1995 Sep-Oct;86(5):375–380. doi: 10.1093/oxfordjournals.jhered.a111606. [DOI] [PubMed] [Google Scholar]
- Beard C. B., Cornel A. J., Collins F. H. The polyubiquitin gene of the mosquito Anopheles gambiae: structure and expression. Insect Mol Biol. 1996 May;5(2):109–117. doi: 10.1111/j.1365-2583.1996.tb00045.x. [DOI] [PubMed] [Google Scholar]
- Beard C. B., Mason P. W., Aksoy S., Tesh R. B., Richards F. F. Transformation of an insect symbiont and expression of a foreign gene in the Chagas' disease vector Rhodnius prolixus. Am J Trop Med Hyg. 1992 Feb;46(2):195–200. doi: 10.4269/ajtmh.1992.46.195. [DOI] [PubMed] [Google Scholar]
- Benedict M. Q., Levine B. J., Ke Z. X., Cockburn A. F., Seawright J. A. Precise limitation of concerted evolution to ORFs in mosquito Hsp82 genes. Insect Mol Biol. 1996 Feb;5(1):73–79. doi: 10.1111/j.1365-2583.1996.tb00042.x. [DOI] [PubMed] [Google Scholar]
- Benedict M. Q., Salazar C. E., Collins F. H. A new dominant selectable marker for genetic transformation; Hsp70-opd. Insect Biochem Mol Biol. 1995 Dec;25(10):1061–1065. doi: 10.1016/0965-1748(95)00061-5. [DOI] [PubMed] [Google Scholar]
- Benedict M. Q., Scott J. A., Cockburn A. F. High-level expression of the bacterial opd gene in Drosophila melanogaster: improved inducible insecticide resistance. Insect Mol Biol. 1994 Nov;3(4):247–252. doi: 10.1111/j.1365-2583.1994.tb00173.x. [DOI] [PubMed] [Google Scholar]
- Besansky N. J., Lehmann T., Fahey G. T., Fontenille D., Braack L. E., Hawley W. A., Collins F. H. Patterns of mitochondrial variation within and between African malaria vectors, Anopheles gambiae and An. arabiensis, suggest extensive gene flow. Genetics. 1997 Dec;147(4):1817–1828. doi: 10.1093/genetics/147.4.1817. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boman H. G. Antibacterial peptides: key components needed in immunity. Cell. 1991 Apr 19;65(2):205–207. doi: 10.1016/0092-8674(91)90154-q. [DOI] [PubMed] [Google Scholar]
- Boyle L., O'Neill S. L., Robertson H. M., Karr T. L. Interspecific and intraspecific horizontal transfer of Wolbachia in Drosophila. Science. 1993 Jun 18;260(5115):1796–1799. doi: 10.1126/science.8511587. [DOI] [PubMed] [Google Scholar]
- Braig H. R., Guzman H., Tesh R. B., O'Neill S. L. Replacement of the natural Wolbachia symbiont of Drosophila simulans with a mosquito counterpart. Nature. 1994 Feb 3;367(6462):453–455. doi: 10.1038/367453a0. [DOI] [PubMed] [Google Scholar]
- Christensen B., Fink J., Merrifield R. B., Mauzerall D. Channel-forming properties of cecropins and related model compounds incorporated into planar lipid membranes. Proc Natl Acad Sci U S A. 1988 Jul;85(14):5072–5076. doi: 10.1073/pnas.85.14.5072. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Coates C. J., Jasinskiene N., Miyashiro L., James A. A. Mariner transposition and transformation of the yellow fever mosquito, Aedes aegypti. Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3748–3751. doi: 10.1073/pnas.95.7.3748. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Collins F. H., Sakai R. K., Vernick K. D., Paskewitz S., Seeley D. C., Miller L. H., Collins W. E., Campbell C. C., Gwadz R. W. Genetic selection of a Plasmodium-refractory strain of the malaria vector Anopheles gambiae. Science. 1986 Oct 31;234(4776):607–610. doi: 10.1126/science.3532325. [DOI] [PubMed] [Google Scholar]
- Durvasula R. V., Gumbs A., Panackal A., Kruglov O., Aksoy S., Merrifield R. B., Richards F. F., Beard C. B. Prevention of insect-borne disease: an approach using transgenic symbiotic bacteria. Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3274–3278. doi: 10.1073/pnas.94.7.3274. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eggleston P. The 1990 Balfour lecture. The control of insect-borne disease through recombinant DNA technology. Heredity (Edinb) 1991 Apr;66(Pt 2):161–172. doi: 10.1038/hdy.1991.21. [DOI] [PubMed] [Google Scholar]
- Higgins J. A., Azad A. F. Use of polymerase chain reaction to detect bacteria in arthropods: a review. J Med Entomol. 1995 May;32(3):213–222. doi: 10.1093/jmedent/32.3.213. [DOI] [PubMed] [Google Scholar]
- James A. A., Blackmer K., Marinotti O., Ghosn C. R., Racioppi J. V. Isolation and characterization of the gene expressing the major salivary gland protein of the female mosquito, Aedes aegypti. Mol Biochem Parasitol. 1991 Feb;44(2):245–253. doi: 10.1016/0166-6851(91)90010-4. [DOI] [PubMed] [Google Scholar]
- Jasinskiene N., Coates C. J., Benedict M. Q., Cornel A. J., Rafferty C. S., James A. A., Collins F. H. Stable transformation of the yellow fever mosquito, Aedes aegypti, with the Hermes element from the housefly. Proc Natl Acad Sci U S A. 1998 Mar 31;95(7):3743–3747. doi: 10.1073/pnas.95.7.3743. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kambhampati S., Rai K. S., Verleye D. M. Frequencies of mitochondrial DNA haplotypes in laboratory cage populations of the mosquito, Aedes albopictus. Genetics. 1992 Sep;132(1):205–209. doi: 10.1093/genetics/132.1.205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Klemenz R., Weber U., Gehring W. J. The white gene as a marker in a new P-element vector for gene transfer in Drosophila. Nucleic Acids Res. 1987 May 26;15(10):3947–3959. doi: 10.1093/nar/15.10.3947. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lehmann T., Besansky N. J., Hawley W. A., Fahey T. G., Kamau L., Collins F. H. Microgeographic structure of Anopheles gambiae in western Kenya based on mtDNA and microsatellite loci. Mol Ecol. 1997 Mar;6(3):243–253. doi: 10.1046/j.1365-294x.1997.00177.x. [DOI] [PubMed] [Google Scholar]
- Loukeris T. G., Livadaras I., Arcà B., Zabalou S., Savakis C. Gene transfer into the medfly, Ceratitis capitata, with a Drosophila hydei transposable element. Science. 1995 Dec 22;270(5244):2002–2005. doi: 10.1126/science.270.5244.2002. [DOI] [PubMed] [Google Scholar]
- O'Brochta D. A., Atkinson P. W. Recent developments in transgenic insect technology. Parasitol Today. 1997 Mar;13(3):99–104. doi: 10.1016/s0169-4758(97)01006-5. [DOI] [PubMed] [Google Scholar]
- Olson K. E., Higgs S., Gaines P. J., Powers A. M., Davis B. S., Kamrud K. I., Carlson J. O., Blair C. D., Beaty B. J. Genetically engineered resistance to dengue-2 virus transmission in mosquitoes. Science. 1996 May 10;272(5263):884–886. doi: 10.1126/science.272.5263.884. [DOI] [PubMed] [Google Scholar]
- Powers A. M., Kamrud K. I., Olson K. E., Higgs S., Carlson J. O., Beaty B. J. Molecularly engineered resistance to California serogroup virus replication in mosquito cells and mosquitoes. Proc Natl Acad Sci U S A. 1996 Apr 30;93(9):4187–4191. doi: 10.1073/pnas.93.9.4187. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Southwood T. R., Khalaf S., Sinden R. E. The micro-organisms of tsetse flies. Acta Trop. 1975;32(3):259–266. [PubMed] [Google Scholar]
- Turelli M., Hoffmann A. A. Rapid spread of an inherited incompatibility factor in California Drosophila. Nature. 1991 Oct 3;353(6343):440–442. doi: 10.1038/353440a0. [DOI] [PubMed] [Google Scholar]
- Vernick K. D., Collins F. H., Gwadz R. W. A general system of resistance to malaria infection in Anopheles gambiae controlled by two main genetic loci. Am J Trop Med Hyg. 1989 Jun;40(6):585–592. doi: 10.4269/ajtmh.1989.40.585. [DOI] [PubMed] [Google Scholar]
- Wade D., Boman A., Wåhlin B., Drain C. M., Andreu D., Boman H. G., Merrifield R. B. All-D amino acid-containing channel-forming antibiotic peptides. Proc Natl Acad Sci U S A. 1990 Jun;87(12):4761–4765. doi: 10.1073/pnas.87.12.4761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Warren A. M., Crampton J. M. Mariner: its prospects as a DNA vector for the genetic manipulation of medically important insects. Parasitol Today. 1994 Feb;10(2):58–63. doi: 10.1016/0169-4758(94)90394-8. [DOI] [PubMed] [Google Scholar]
- Werren J. H., Hurst G. D., Zhang W., Breeuwer J. A., Stouthamer R., Majerus M. E. Rickettsial relative associated with male killing in the ladybird beetle (Adalia bipunctata). J Bacteriol. 1994 Jan;176(2):388–394. doi: 10.1128/jb.176.2.388-394.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
