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A species can benefit or be hurt by other species. For example, honeybees and flowering plants help each other to flourish, while lions and gazelles behave in ways that decrease each other’s populations. Understanding these relationships is important for controlling pests and diseases. Sometimes it is easiest to study such interactions by looking at simple ones that happen on a small scale. Amoebas are common soil organisms that have the same basic organization as human cells. They are much larger and more complex than the bacteria that also live in the soil. How exactly the amoebas and bacteria interact in the soil is an important question, particularly as some of the bacteria can also live inside amoebas. Does this intimate relationship help or harm the amoeba? Shu, Brock, Geist et al. studied the relationship between a widely studied species of social amoeba and two species of bacteria that can live inside it. Some of the amoebas naturally contained one of the bacteria species, and others were infected with the bacteria in experiments. Throughout the entire life cycle of the amoebas, the bacteria lived inside them. During one part of the life cycle, amoebas form so-called fruiting bodies, which release spores that can develop into new amoebas. Shu et al. found that both types of bacteria alter the structure of the fruiting bodies in ways that reduce how well the spores disperse. One of the bacteria species, called Burkholderia hayleyella, harmed the amoebas a lot. It caused most harm to amoebas that do not naturally host the bacteria. This indicates that the amoebas that do host this species may have evolved to avoid its worst effects. The amoebas have many similarities to the white blood cells that clear bacteria from the human body. Certain bacteria can get inside white blood cells, causing diseases such as tuberculosis. Understanding how bacteria harm amoebas might be useful for understanding such diseases, and developing treatments for them. Though the bacteria Shu et al. studied are not toxic to humans, they are closely related to bacteria that are harmful. It is therefore possible that some bacteria that infect humans first evolve to infect amoebas.
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Costs of being a diet generalist for the protist predator Dictyostelium discoideum
Consumers range from specialists that feed on few resources to generalists that feed on many. Generalism has the clear advantage of having more resources to exploit, but the costs that limit generalism are less clear. We explore two understudied costs of generalism in a generalist amoeba predator,Dictyostelium discoideum, feeding on naturally co-occurring bacterial prey. Both involve costs of combining prey that are suitable on their own. First, amoebas exhibit a reduction in growth rate when they switched to one species of prey bacteria from another compared to controls that experience only the second prey. The effect was consistent across all six tested species of bacteria. These switching costs typically disappear within a day, indicating adjustment to new prey bacteria. This suggests that these costs are physiological. Second, amoebas usually grow more slowly on mixtures of prey bacteria compared to the expectation based on their growth on single prey. There were clear mixing costs in three of the six tested prey mixtures, and none showed significant mixing benefits. These results support the idea that, although amoebas can consume a variety of prey, they must use partially different methods and thus must pay costs to handle multiple prey, either sequentially or simultaneously.
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- Award ID(s):
- 2237266
- PAR ID:
- 10572057
- Publisher / Repository:
- NAS
- Date Published:
- Journal Name:
- Proceedings of the National Academy of Sciences
- Volume:
- 121
- Issue:
- 14
- ISSN:
- 0027-8424
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1073/pnas.2313203121
