Alexey Potekhin
Andrey O. Plotnikov
Natalia Gogoleva
Bettina Sonntag- 1Research Department for Limnology, Mondsee, University of Innsbruck, Mondsee, Austria
- 2Institute for Cellular and Intracellular Symbiosis of the UrB RAS, Orenburg Federal Research Center, Orenburg, Russia
- 3Laboratory of Environmental Metagenomics, Institute of Fundamental Medicine and Biology, Kazan Federal University, Kazan, Russia
Editorial on the Research Topic
Microbial associations formed and hosted by protists, algae, and fungi
Microbial associations hosted by protists, algae, and fungi remain out of the research mainstream. Prokaryotic and eukaryotic microorganisms share the same environments, form complex communities, and are inseparable in nature. However, there is an artificial gap in human knowledge between microbiology and protistology, which undoubtedly will be closed in the future due to emerging interest in microbial communities. The microbiomes of unicellular eukaryotes probably play an important role in the environmental adaptation and survival of both hosts and associates, a role that still has to be elucidated. The surface of multicellular algae provides generous substrates for different microorganisms, whose functional role in host biology needs to be figured out. This Research Topic provides new insights into different aspects of the structure and functions of the microbiomes associated with protists and algae.
Some members of the microbiomes of protists can be professional symbionts (Lanzoni et al., 2019; Husnik et al., 2021), but the majority of the prokaryotic associates of protists are, likely, occasional (Plotnikov et al., 2019; Zhang et al., 2023), and, thus, should be considered as provisional symbionts. Giddings et al. recorded for the first time slime mold Stemonitis sp. in acid rock drainage. Metagenomic sequencing and FISH showed that these amoebae hosted Dyella terrae (Xanthomonadales), which is known to be an acid-tolerant and metal-resistant free-living bacterium. The bacteria were also present outside of the host, the non-reduced bacterial genome also indirectly witnessed that the symbiosis was facultative. The bacteria had type IV secretion system genes that could aid in their ability to colonize amoeba cells and to resist Stemonitis predation. The bacteria could find shelter inside amoeba cells, while the host could benefit either from metabolites and nutrients provided by the occasional symbionts in the poor extreme environment or simply maintain them as a “symbiotic farm” and consume upon starvation.
The other protist that is known to settle a “food farm” on the cell surface is a ciliate Kenthrophoros flavus. This astomatous ciliate possesses thiotrophic ectosymbionts (“Ca. Kentron”, Gammaproteobacteria) that are used as a food source by the ciliate (Seah et al., 2017). By PacBio sequencing of the cloned 16S rRNA genes, Bi et al. detected a major symbiont of Kenthrophoros, a new species of “Ca. Kentron”, and another bacterium from the family Muribaculaceae (Bacteroidales), whose members are known from mouse and human gut microbiomes (Lagkouvardos et al., 2019). This bacterium called MLAKF was present stably and in big numbers on the surface of the ciliate host cells together with “Ca. Kentron”. The authors hypothesize a tripartite symbiosis, suggesting that MLAKF could supply “Ca. Kentron” ectobionts limited in their ability to fix CO2 with extra organic carbon produced by degrading carbohydrates, and both bacteria could be used by the ciliate as a preferential food under diverse conditions.
Sometimes the unicellular hosts' fitness depends on their microbiomes. Himi et al. demonstrated that Paramecium bursaria, a ciliate that maintains unicellular green algae in its cytoplasm and is able to survive consuming only the sugars produced by the photosynthetic symbionts, harbors a taxonomically rich bacterial community. The host fitness decreased significantly under non-lethal treatment with antibiotics, confirming that the microbiomes were essential for the ciliates. The sublines of the P. bursaria strain that was for several years maintained in the absence of exogenous bacterial food were examined by the 16S rRNA gene metabarcoding. Interestingly, the sets of associated bacteria were quite different among well- and poorly proliferating lines, while the lines of the same proliferation mode manifested a highly similar composition of their bacterial communities. Thus, the disrupted microbiome of ciliates could be the reason for differences in their fitness.
Le Reun et al. investigated the microbiome associated with the marine diatom Actinocyclus sp. The authors used co-cultivation to examine the growth-promoting capabilities of 15 bacterial isolates of different taxa from the bacterial community associated with this diatom. The diatoms were shown to grow differently in association with this or that particular member of their microbiome. The diatom growth was enhanced by several bacterial strains from the associated community, but the beneficial effects of different associates were observed in different time periods. Probably, the dynamics of the microbiome followed the changes in the pool of chemicals released by the diatom, similar to the dynamics of microbial community during phytoplankton blooms (Jung et al., 2021).
Currently not only the complete genomes of all partners in symbiotic association can be obtained and assembled from one metagenomic dataset, but the metabolic abilities of the microbial community can also be predicted. Wang et al. described that differences in the predicted functional profiles of the epiphytic bacterial communities on the surface of the marine macroalga Sargassum thunbergii male and female specimens and their receptacles were accompanied by differences in the structure of the microbiomes. Representatives of numerous bacterial taxa formed a core microbiome of S. thunbergii as they were always found in all analyzed microbiomes. Probably, it is mainly the nutrient cycling between algae and bacteria that shapes this core community and serves as a basis for a long and stable relationship between algae and bacteria (Christie-Oleza et al., 2017). However, the physiology of the communities associated with male and female specimens and their receptacles was different. Some specific associates exploited metabolic differences of the colonized hosts and their organs, responding positively to the phenolic compounds that are more abundant in the tissues of the female algae. Thus, the sex of the host alga influences the microbiome. Not all of the microbiome members were beneficial for the host, and the functions of bacteria with low abundances might also be important in the community, adding complexity to the relations between the host and its microbiome.
All articles included in this Research Topic provide some evidence that the microbiomes of protists and algae play significant roles in the biology of their hosts. These roles include, but are not limited to, being a food source for the host, providing metabolic aid and compensation, host protection, and community maintenance. The articles clearly point the perspective for methods of protist and algae microbiomes management to enhance the harvest of hosts in laboratories and biotechnology plants.
Author contributions
AP: Writing—original draft. AOP: Writing—review & editing. NG: Writing—review & editing. BS: Writing—review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Acknowledgments
We are grateful to the authors who contributed to the Research Topic and provided the insightful articles. We are especially grateful to the reviewers who spent their time and efforts doing their best to help improving the manuscripts.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.
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References
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Keywords: microbiome, protists, algae, microbial communities, 16S rRNA gene metabarcoding, microbiome function, symbiosis, prokaryotic symbionts
Citation: Potekhin A, Plotnikov AO, Gogoleva N and Sonntag B (2024) Editorial: Microbial associations formed and hosted by protists, algae, and fungi. Front. Microbiol. 14:1341058. doi: 10.3389/fmicb.2023.1341058
Received: 19 November 2023; Accepted: 08 December 2023;
Published: 05 January 2024.
Edited and reviewed by: Zhiyong Li, Shanghai Jiao Tong University, China
Copyright © 2024 Potekhin, Plotnikov, Gogoleva and Sonntag. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Alexey Potekhin, YWFwb3Rla2hpbiYjeDAwMDQwO2dtYWlsLmNvbQ==