The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
The microbial dimension in insect nutritional ecology
Abstract
1 Many insects derive nutritional advantage from persistent associations with microorganisms that variously synthesize essential nutrients or digest and detoxify ingested food. These persistent relationships are symbioses. 2 There is strong experimental evidence that symbiotic microorganisms provide plant sap-feeding insects with essential amino acids and contribute to the digestion of cellulose in some wood-feeding insects, including lower termites. Basic nutritional information is, however, lacking for many associations, including the relative roles of microbial and intrinsic sources of cellulose degradation in many insects and B-vitamin provisioning by microorganisms in blood-feeding insects. 3 Some nutritional interactions between insects and their symbiotic microorganisms vary among conspecifics and closely related species. This variation can, in principle, contribute to nutritional explanations for variation in the abundance and distribution of insects. For example, the plant utilization traits of phloem-feeding aphids and stinkbugs have been demonstrated to depend on the identity of microbial partners. Evidence that associations can evolve rapidly comes from the demonstration that the impact of the bacterium Wolbachia on natural populations of its insect host can change from deleterious to beneficial within two decades. 4 Developing genomic tools, especially massively parallel sequencing and metagenomic analyses, offer the opportunity to explore the metabolic capabilities of symbiotic microorganisms and their insect hosts, from which defined hypotheses of nutritional function can be constructed. Nutritional ecology provides the appropriate framework to test these hypotheses in the relevant ecological context.
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Cites
An obesity-associated gut microbiome with increased capacity for energy harvest
Turnbaugh, P. J., Ley, R. E., Mahowald, M. A., Magrini, V., Mardis, E. R., & Gordon, J. I. (2006) · Nature · doi:10.1038/nature05414 · Cited by 12,444
Human gut microbes associated with obesity
Ley, R. E., Turnbaugh, P. J., Klein, S., & Gordon, J. I. (2006) · Nature · doi:10.1038/4441022a · Cited by 8,785
Cited by
Multiorganismal Insects: Diversity and Function of Resident Microorganisms
Douglas, A. E. (2015) · Annual Review of Entomology · doi:10.1146/annurev-ento-010814-020822 · Cited by 1,315
Self-citationHost Biology in Light of the Microbiome: Ten Principles of Holobionts and Hologenomes
Bordenstein, S. R., & Theis, K. R. (2015) · PLOS Biology · doi:10.1371/journal.pbio.1002226 · Cited by 1,240
Bacteriophages encode factors required for protection in a symbiotic mutualism
Oliver, K. M., Degnan, P. H., Hunter, M. S., & Moran, N. A. (2009) · Science · doi:10.1126/science.1174463 · Cited by 481
Microbial Volatile Emissions as Insect Semiochemicals
Davis, T. S., Crippen, T. L., Hofstetter, R. W., & Tomberlin, J. K. (2013) · Journal of Chemical Ecology · doi:10.1007/s10886-013-0306-z · Cited by 470
Understanding insect life histories and senescence through a resource allocation lens
Boggs, C. L. (2009) · Functional Ecology · doi:10.1111/j.1365-2435.2009.01527.x · Cited by 448
Metadata
- Authors
- Douglas, A. E.
- Venue
- Functional Ecology
- Publisher
- Wiley
- Published
- 2009-01-16
- Volume
- 23
- Issue
- 1
- Pages
- 38-47
- ISSN
- 0269-8463 (ISSN-L)
- 1365-2435
- OpenAlex
- W2169641336
- Cited by
- 842
- References
- 2
- FWCI
- 29.12
- Type
- journal article
- Language
- en
- Open access
- closed
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