Department of Biology, University of Central Arkansasgrid.266128.9, Conway, Arkansas, USA.
Department of Biomedical Informatics, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Appl Environ Microbiol. 2022 Sep 22;88(18):e0128522. doi: 10.1128/aem.01285-22. Epub 2022 Aug 31.
The relationship between the social amoeba Dictyostelium discoideum and its endosymbiotic bacteria provides a model system for studying the development of symbiotic relationships. Laboratory experiments have shown that any of three species of the symbiont allow D. discoideum food bacteria to persist through the amoeba life cycle and survive in amoeba spores rather than being fully digested. This phenomenon is termed "farming," as it potentially allows spores dispersed to food-poor locations to grow their own. The occurrence and impact of farming in natural populations, however, have been a challenge to measure. Here, we surveyed natural D. discoideum populations and found that only one of the three symbiont species, Paraburkholderia agricolaris, remained prevalent. We then explored the effect of on the amoeba microbiota, expecting that by facilitating bacterial food carriage, it would diversify the microbiota. Contrary to our expectations, tended to infectiously dominate the D. discoideum microbiota, in some cases decreasing diversity. Similarly, we found little evidence for facilitating the carriage of particular food bacteria. These findings highlight the complexities of inferring symbiont function in nature and suggest the possibility that could be playing multiple roles for its host. The functions of symbionts in natural populations can be difficult to completely discern. The three bacterial farming symbionts of the social amoeba Dictyostelium discoideum have been shown in the laboratory environment to allow the amoebas to carry, rather than fully digest, food bacteria. This potentially provides a fitness benefit to the amoebas upon dispersal to food-poor environments, as they could grow their food. We expected that meaningful food carriage would manifest as a more diverse microbiota. Surprisingly, we found that tended to infectiously dominate the D. discoideum microbiota rather than diversifying it. We determined that only one of the three symbionts has increased in prevalence in natural populations in the past 20 years, suggesting that this symbiont may be beneficial, however. These findings suggest that may have an alternative function for its host, which drives its prevalence in natural populations.
黏菌与其内共生菌之间的关系为研究共生关系的发展提供了一个模型系统。实验室实验表明,三种共生体中的任何一种都可以使 D. discoideum 食细菌在变形虫生命周期中持续存在,并在变形虫孢子中存活而不被完全消化。这种现象被称为“养殖”,因为它有可能使分散到食物匮乏的地方的孢子能够自行生长。然而,在自然种群中,养殖的发生和影响一直是一个难以衡量的问题。在这里,我们调查了自然 D. discoideum 种群,发现只有三种共生体中的一种,即 Paraburkholderia agricolaris,仍然普遍存在。然后,我们探讨了对变形虫微生物群的影响,预计通过促进细菌食物携带,它会使微生物群多样化。与我们的预期相反,感染性地主导了 D. discoideum 微生物群,在某些情况下降低了多样性。同样,我们几乎没有证据表明促进了特定食物细菌的携带。这些发现强调了在自然环境中推断共生体功能的复杂性,并表明共生体可能在其宿主身上扮演着多种角色。在自然种群中,共生体的功能很难完全辨别。在实验室环境中,已经表明黏菌的三种细菌养殖共生体允许变形虫携带而不是完全消化食物细菌。这可能为变形虫在分散到食物匮乏的环境中提供了一种适应性优势,因为它们可以生长自己的食物。我们预计,有意义的食物携带将表现为微生物群更加多样化。令人惊讶的是,我们发现,感染性地主导了 D. discoideum 微生物群,而不是使其多样化。我们确定,在过去的 20 年里,三种共生体中的一种在自然种群中的流行率有所增加,这表明这种共生体可能是有益的。这些发现表明,对其宿主可能有替代功能,这导致了它在自然种群中的流行。