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Evidence for a Wolbachia symbiont in Drosophila melanogaster

Published online by Cambridge University Press:  14 April 2009

Peter Jones
Affiliation:
Departments of Biochemistry, University of Nottingham, Queens Medical Centre, Nottingham NG7 2UH England
John F. Y. Brookfield
Affiliation:
Genetics, University of Nottingham, Queens Medical Centre, Nottingham NG7 2UH England
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The bacterial cell division gene, ftsZ, was used as a specific probe to show the presence of a symbiotic bacterium in two wild type strains of Drosophila melanogaster. Under stringent hybridization conditions we have shown that the bacterium is transferred to the progeny of these strains from infected mothers and can be eradicated by treatment with the antibiotic tetracycline. We have characterized this bacterium, by amplifying and sequencing its 16S rRNA gene, as being a member of the genus Wolbachia, an organism that is known to parasitize a range of insects including Drosophila simulans. In a series of reciprocal crosses no evidence was found that the symbiont causes cytoplasmic incompatibility (CI) which is known to occur in infected strains of D. simulans. The implications of these findings are discussed.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1993

References

Ashburner, M. (1989). Drosophila: A Laboratory Handbook. New York: Cold Spring Harbor.Google Scholar
Curtis, C. F. (1992). Selfish genes in mosquitos. Nature 357, 450.CrossRefGoogle Scholar
Devereux, J., Haebert, M. & Smithies, O. (1984). A comprehensive set of sequence analysis programs for the VAX. Nucleic Acids Research 12, 387395.CrossRefGoogle ScholarPubMed
Glover, D. M., Raff, J., Karr, T., O'Neill, S. L., Lin, H. & Wolfner, M. F. (1990). Parasites in Drosophila embryos. Nature 348, 117.CrossRefGoogle ScholarPubMed
Hertig, M. (1936). The rickettsia Wolbachia pipientis(gen et sp n) and associated inclusions of the mosquito, Culex pipiens. Parasitology 28, 453486.CrossRefGoogle Scholar
Hoffmann, A. A. (1988). Partial cytoplasmic incompatibility between two Australian populations of Drosophila melanogaster. Entomologia Experimentalis et Applicata 48, 6167.CrossRefGoogle Scholar
Hoffmann, A. A., Turelli, M. & Simmons, G. M. (1986). Unidirectional incompatibility between populations of Drosophila simulans. Evolution 40, 692701.CrossRefGoogle ScholarPubMed
Holden, P. R., Brookfield, J. F. Y. & Jones, P. (1993). Cloning and characterization of an ftsZ homologue from a bacterial symbiont of Drosophila melanogaster. Molecular and General Genetics (in press).CrossRefGoogle ScholarPubMed
Hurst, G. D. D., Hurst, L. L. & Majerus, M. E. N. (1992). Selfish genes move sideways. Nature 356, 659660.CrossRefGoogle ScholarPubMed
Lipmann, D. J. & Pearson, W. R. (1985). Rapid and sensitive protein similarity searches. Science 227, 14351441.CrossRefGoogle Scholar
Louis, C. & Nigro, L. (1989). Ultrastructure evidence of Wolbachia rickettsales in Drosophila simulans and their relationship with unidirectional cross incompatibility. Journal of Invertebrate Pathology 54, 3944.CrossRefGoogle Scholar
Ochman, H. & Wilson, A. C. (1987). Evolutionary history of enteric bacteria. In: Neidhardt, FC (ed.) Escherichia coli and Salmonella typhimurium: Cellular and molecular biology. American Society for Microbiology, Washington DC, pp. 16491654.Google Scholar
O'Neill, S. L. & Karr, T. L. (1990). Bidirectional incompatibility between conspecific populations of Drosophila simulans. Nature 348, 178180.CrossRefGoogle ScholarPubMed
O'Neill, S. L., Giordano, R., Colbert, A. M. E., Karr, T. L. & Robertson, H. M. (1992). 16S rRNA phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic incompatibility in insects. Proceedings of the National Academy of Sciences USA 89, 26992702.CrossRefGoogle ScholarPubMed
Rousset, F., Vautrin, D. & Solignac, M. (1992). Molecular identification of Wolbachia, the agent of cytoplasmic incompatibility in Drosophila simulans, and variability in relation with host mitochondrial types. Proceedings of the Royal Society of London B 247, 163168.Google ScholarPubMed
Sambrook, J., Fritsch, E. F. & Maniatis, T. (1989). Molecular cloning: A laboratory manual. New York: Cold Spring Harbor.Google Scholar
Stevens, L. & Wade, M. J. (1990). Cytoplasmically inherited reproductive incompatibility in Tribolium flour beetles: The rate of spread and effect on population size. Genetics 124, 367372.CrossRefGoogle ScholarPubMed
Turelli, M. & Hoffmann, A. A. (1991). Rapid spread of an inherited incompatibility factor in California Drosophila. Nature 353, 440442.CrossRefGoogle ScholarPubMed
Wolstenholme, D. R. (1965). A DNA and RNA-containing cytoplasmic body in Drosophila melanogaster. Genetics 52, 949975.CrossRefGoogle ScholarPubMed