The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
Sexual acquisition of beneficial symbionts in aphids
Open accessAbstract
A noted cost of mating is the risk of acquiring sexually transmitted infections that are detrimental to the recipient. But many microbial associates of eukaryotes are mutualistic, raising the possibility that sexual contact provides the opportunity to acquire symbionts that are beneficial. In aphids, facultative bacterial symbionts, which benefit hosts by conferring resistance to natural enemies or to heat, are transmitted maternally with high fidelity and are maintained stably throughout hundreds of parthenogenetic generations in the laboratory. Data from field populations indicate that horizontal transfer of these facultative symbionts is frequent, and transfections are readily achieved by microinjection or ingestion in artificial diet. However, no natural mechanism for the horizontal transfer of these symbionts has been identified. Here we demonstrate that during sexual reproduction, male-borne symbionts can be acquired by females and subsequently transferred to sexually and parthenogenetically produced progeny, establishing stable, maternally transmitted associations. In our experiments, sexually transmitted symbionts resulted in ( i ) infection of previously uninfected matrilines, ( ii ) a double infection in a matriline already bearing a different symbiont, and ( iii ) replacement of the maternal symbiont. We also observed some cases in which maternal symbionts failed to become established in sexually produced progeny. Microscopy indicated that symbionts were abundant in the male reproductive system, which demonstrates a natural route of nonmaternal transfer of insect symbionts. Because such transfer can generate coinfections, thereby creating opportunities for symbiont competition and recombination, paternal inheritance has major consequences for expectations regarding symbiont evolution.
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Cites
Facultative bacterial symbionts in aphids confer resistance to parasitic wasps
Oliver, K. M., Russell, J. A., Moran, N. A., & Hunter, M. S. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0335320100 · Cited by 1,264
Self-citationEndosymbiosis of Animals with Plant Microorganisms
Batra, L. R., & Buchner, P. (1968) · Mycologia · doi:10.2307/3757184 · Cited by 1,245
Wolbachia Pipientis: Microbial Manipulator of Arthropod Reproduction
Stouthamer, R., Breeuwer, J. A. J., & Hurst, G. D. D. (1999) · Annual Review of Microbiology · doi:10.1146/annurev.micro.53.1.71 · Cited by 1,236
Endosymbiosis of animals with plant microorganisms
Brooks, M. A. (1966) · Journal of Invertebrate Pathology · doi:10.1016/0022-2011(66)90065-6 · Cited by 1,106
BIOLOGY OF BACTERIOCYTE-ASSOCIATED ENDOSYMBIONTS OF PLANT SAP-SUCKING INSECTS
Baumann, P. (2005) · Annual Review of Microbiology · doi:10.1146/annurev.micro.59.030804.121041 · Cited by 1,050
Aphid Protected from Pathogen by Endosymbiont
Scarborough, C. L., Ferrari, J., & Godfray, H. C. J. (2005) · Science · doi:10.1126/science.1120180 · Cited by 750
Facultative bacterial endosymbionts benefit pea aphids Acyrthosiphon pisum under heat stress
Montllor, C. B., Maxmen, A., & Purcell, A. H. (2002) · Ecological Entomology · doi:10.1046/j.1365-2311.2002.00393.x · Cited by 709
Variation in resistance to parasitism in aphids is due to symbionts not host genotype
Oliver, K. M., Moran, N. A., & Hunter, M. S. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0506131102 · Cited by 601
Self-citationHost Plant Specialization Governed by Facultative Symbiont
Tsuchida, T., Koga, R., & Fukatsu, T. (2004) · Science · doi:10.1126/science.1094611 · Cited by 542
Russell, J. A., & Moran, N. A. (2005) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2005.3348 · Cited by 502
Self-citation
Cited by
Genomics and Evolution of Heritable Bacterial Symbionts
Moran, N. A., McCutcheon, J. P., & Nakabachi, A. (2008) · Annual Review of Genetics · doi:10.1146/annurev.genet.41.110306.130119 · Cited by 1,737
Self-citationA complex journey: transmission of microbial symbionts.
Bright, M., & Bulgheresi, S. (2010) · Nature Reviews Microbiology · doi:10.1038/nrmicro2262 · Cited by 894
The diversity of reproductive parasites among arthropods: Wolbachiado not walk alone
Duron, O., Bouchon, D., Boutin, S., Bellamy, L., Zhou, L., Engelstädter, J., & Hurst, G. D. (2008) · BMC Biology · doi:10.1186/1741-7007-6-27 · Cited by 733
Bacterial symbionts in insects or the story of communities affecting communities
Ferrari, J., & Vavre, F. (2011) · Philosophical Transactions of the Royal Society B: Biological Sciences · doi:10.1098/rstb.2010.0226 · Cited by 334
The evolution of host-symbiont dependence
Fisher, R. M., Henry, L. M., Cornwallis, C. K., Kiers, E. T., & West, S. A. (2017) · Nature Communications · doi:10.1038/ncomms15973 · Cited by 316
Metadata
- Authors
- Moran, N. A., & Dunbar, H. E.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2006-08-22
- Volume
- 103
- Issue
- 34
- Pages
- 12803-12806
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2010440202
- Cited by
- 271
- References
- 27
- FWCI
- 14.93
- Type
- journal article
- Language
- en
- Open access
- green
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