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Habitat structure and the evolution of diffusible siderophores in bacteria
Abstract
Bacteria typically rely on secreted metabolites, potentially shareable at the community level, to scavenge resources from the environment. The evolution of diffusible, shareable metabolites is, however, difficult to explain because molecules can get lost, or be exploited by cheating mutants. A key question is whether natural selection can act on molecule structure to control loss and shareability. We tested this possibility by collating information on diffusivity properties of 189 secreted iron‐scavenging siderophores and the natural habitats occupied by the siderophore‐producing species. In line with evolutionary theory, we found that highly diffusible siderophores have preferentially evolved in species living in structured habitats, such as soil and hosts, because structuring can keep producers and their shareable goods together. Poorly diffusible siderophores, meanwhile, have preferentially evolved in species living in unstructured habitats, such as seawater, indicating that these metabolites are less shareable and more likely provide direct benefits to the producers.
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“This insight furthers the possibility that certain classes of siderophores might not strictly play exclusionary roles in iron acquisition within microbial communities but might, in fact, be utilized and shared in a structured relationship across various microbial phyla (Amin et al. , 2012a; Kümmerli et al. , 2014), potentially involving beneficial associations (Amin et al. , 2009, 2012b).”
From Silicate minerals as a direct source of limiting nutrients: Siderophore synthesis and uptake promote ferric iron bioavailability from olivine and microbial growth (2021) · cites this paper as Kümmerli et al. , 2014
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Cited by
Bacterial siderophores in community and host interactions
Kramer, J., Özkaya, Ö., & Kümmerli, R. (2020) · Nature Reviews Microbiology · doi:10.1038/s41579-019-0284-4 · Cited by 998
Self-citationExploiting rRNA operon copy number to investigate bacterial reproductive strategies
Roller, B. R. K., Stoddard, S. F., & Schmidt, T. M. (2016) · Nature Microbiology · doi:10.1038/nmicrobiol.2016.160 · Cited by 591
Oleńska, E., Małek, W., Wójcik, M., Swiecicka, I., Thijs, S., & Vangronsveld, J. (2020) · Science of The Total Environment · doi:10.1016/j.scitotenv.2020.140682 · Cited by 555
Competition for iron drives phytopathogen control by natural rhizosphere microbiomes
Gu, S., Wei, Z., Shao, Z., Friman, V.-P., Cao, K., Yang, T., Kramer, J., Wang, X., Li, M., Mei, X., et al. (2020) · Nature Microbiology · doi:10.1038/s41564-020-0719-8 · Cited by 544
Self-citationDewar, A. E., Thomas, J. L., Scott, T. W., Wild, G., Griffin, A. S., West, S. A., & Ghoul, M. (2021) · Nature Ecology & Evolution · doi:10.1038/s41559-021-01573-2 · Cited by 44
Metadata
- Authors
- Kümmerli, R., Schiessl, K. T., Waldvogel, T., McNeill, K., & Ackermann, M.
- Affiliations
- Environmental Microbiology Swiss Federal Institute of Aquatic Science and Technology Überlandstrasse 133 Dübendorf 8600 Switzerland
- Department of Environmental Systems Science Institute of Biogeochemistry and Pollutant Dynamics Swiss Federal Institute of Technology Universitätsstrasse 16 Zürich 8092 Switzerland
- Venue
- Ecology Letters
- Publisher
- Wiley
- Published
- 2014-09-23
- Volume
- 17
- Issue
- 12
- Pages
- 1536-1544
- ISSN
- 1461-023X
- 1461-0248
- Cited by
- 119
- References
- 3
- Language
- en
- Funders
- Swiss National Science Foundation (PZ00P3_126337)
- European Commission (256435)
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- Kümmerli, R., Schiessl, K. T., Waldvogel, T., McNeill, K., & Ackermann, M. (2014). Habitat structure and the evolution of diffusible siderophores in bacteria. Ecology Letters. https://doi.org/10.1111/ele.12371
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