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EDITORIAL article

Front. Mar. Sci., 08 January 2024
Sec. Aquatic Microbiology
This article is part of the Research Topic Symbiotic Interactions of Algae and Microorganisms: Physiology and Industrial Applications View all 5 articles

Editorial: Symbiotic interactions of algae and microorganisms: physiology and industrial applications

  • 1Department of Biology, Skidmore College, Saratoga Springs, NY, United States
  • 2Patel College of Global Sustainability, University of South Florida, Tampa, FL, United States
  • 3Department of Biosciences and Bioengineering, Indian Institute of Technology Roorkee, Uttarakhand, India
  • 4Centre for Nanotechnology, Indian Institute of Technology Roorkee, Uttarakhand, India

Algae (micro- and macro) are one of the most diverse groups of species, representing a considerable part of terrestrial and aquatic ecosystems. The diversity of algae enables tailoring of the biomass for a spectrum of bioproducts, including pigments, biofertilizers, ink, nutraceuticals, fish feed, lubricating oils, food supplements, and cosmetics (Arora and Philippidis, 2023). Macroalgae, or seaweeds, are a vital part of aquaculture in addition to being a sustainable source of several marketed bioactive compounds. Interactions of seaweeds with microorganisms in natural ecosystems significantly impact their composition, metabolic activities, response to climate change, pollution, and anthropogenic activities, ultimately determining the suitability of their usage. The surface of seaweeds is a highly active interface, perfect for harboring a consortium of microorganisms, including bacteria, fungi, protozoa, and diatoms. Elucidation and understanding of interactions between algae and microorganisms are crucial from both an ecological and industrial standpoint (Ren et al., 2022). Moreover, a fundamental understanding of the changes in the microbial community in response to biotic and abiotic stress is necessary for optimizing the yield of the target bioactive compounds and controlling detrimental invaders.

Another important aspect of algae-microbial symbiosis is harnessing algae-based technologies for developing sustainable and cost-effective strategies for waste water remediation, biofuels, and bioproducts. One of the critical barriers to the successful translation of technology from research to market is the high cost of cultivating and harvesting algal biomass. Symbiotic interactions of algae with other microorganisms such as bacteria, yeast, and fungi could potentially enhance biomass productivity and quality, in addition to easing harvesting and reducing culture crashes by outcompeting invaders (Arora et al., 2019). Moreover, co-cultures of algae with other beneficial microorganisms alter the metabolism of the algae, which can be leveraged for improving or augmenting the yield of the desired bioproduct (Caudal et al., 2022). The added advantage of using mixed cultures is that they may enhance nutrient availability, reduce the consumption of nutrients, and prevent the accumulation of auto-inhibitors in the culture, thus enabling the recycling of the culture medium.

In this Research Topic, “Symbiotic Interactions of Algae and Microorganisms: Physiology and Industrial Applications,” the published research articles focus on underpinning the complex interplay between the algae and microbes to aid a better understanding of the interactions. For instance, Nguyen et al. characterized the succession of microbial communities associated with Ulva fasciata, a green macroalga playing a pivotal role in brackish and marine ecosystems, significantly affecting the growth of the alga. The authors utilized an integrated multi-trophic aquaculture (IMTA) system to monitor the temporal dynamics of the microbial communities cultivated in seawater effluents of fish (grey mullet) ponds to identify key biomarker. Co-culturing fish with seaweeds using IMTA systems is reported to reduce the load of pollutants in the effluents as the nutrients are taken up by algae for their growth. Notably, the microbial community present on the surface of the alga was comprised of 11 different bacterial phyla, with Proteobacteria, Bacteroidetes, Planctomycetes, and Deinococcus-Thermus accounting for >95% of the total population. Interestingly, Deinococcus-Thermus was first detected in this study, indicating its role in enhancing resilience to extreme environments. Overall, four families—Saprospiraceae, Thiohalorhabdaceae, Sphingomonadaceae, and Rhodobacteraceae—were identified as prominent biomarkers whose relative abundance significantly differed over time, contributing to the knowledge about microbial communities associated with Ulva fasciata.

In another study, Xu et al. explored the seasonal diversity of microbial (eukaryotic and bacterial) communities of economically important seaweeds: Neoporphyra haitanensis (monoculture, zone P), mixed cultures of Gracilaria lemaneiformis, and Saccharina japonica (zone G) as compared to seaweeds collected from Fujian Province’s largest mariculture bases in south China. For the eukaryotic community, the enriched phyla were Bacillariophyta, Chlorophyta, and Cnidaria; but their proportions differed among the three study zones, with the highest diversity occurring in December (highest salinity levels) and the lowest in May (lowest salinity levels). For the bacterial community, Proteobacteria was the most dominant phylum among all the zones. The study evidenced that zone P resulted in maximum release of dissolved organic carbon, resulting in the dominance of Flavobacteriaceae, which can degrade fucoidan (sulfated fucose-containing polysaccharides), in addition to utilizing sugars such as lactose, sucrose, and inositol and reducing nitrates to nitrites.

In addition, the study by Steinrücken et al. analyzed the bacterial community composition in three Phaeodactylum (Diatom) strains during batch cultivations (start, linear phase, and stationary phase) to optimize algal biomass and quality. The most dominant bacterial genera present in the microalgal cultures (>97%) belonged to the classes Alphaproteobacteria, Gammaproteobacteria (phylum Proteobacteria), and Bacteroidia (phylum Bacteroidetes), indicating that the microalgae to some degree have an influence on the development of the bacterial communities in different settings.

On another aspect, Ma et al. research provided molecular insights into the nutritional adaptation mechanism of mixotrophic flagellate Poterioochromonas malhamensis feeding on microalgal prey. The flagellate is widely distributed in aquatic ecosystems, and is considered a potential biocontrol for cyanobacterial blooms due to its unique capacity to degrade microcystin. However, this characteristic also makes it a potential invader in microalgal cultivation systems, especially Chlorella. The predator, P. malhamensis, cultivated in autotrophy fed with digestible (GT-1) green microalgae, Chlorella sorokiniana, showed upregulation of pigment and photosynthesis biosynthesis genes but downregulation of light harvesting complex genes, reducing the overall photosynthesis efficiency. On the contrary, mixotrophic cultures showed upregulation of carbon and nitrogen metabolism, indicating switching of the metabolism towards β-1,3-glucan. Moreover, feeding P. malhamensis with indigestible (CMBB-146) algae revealed downregulation of lysosome enzymes and upregulation of apoptosis and necrosis genes, resulting in the death of the flagellate.

In conclusion, the published research articles provided a fundamental understanding of the different aspects of algal-microbiome interactions and how these can be exploited for the restoration of ecosystems in response to global changes as well as for the development of sustainable bioproducts.

Author contributions

NA: Conceptualization, Validation, Writing – original draft, Writing – review & editing. KP: Conceptualization, Validation, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. KP acknowledge the receipt of SERB-STAR grant (STR/2022/000008) from Science and Engineering Research Board (SERB), India.

Acknowledgments

We would like to thank our co-guest editor Dr. Seema Rawat, all authors and reviewers who have contributed to this Research Topic.

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.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Arora N., Patel A., Mehtani J., Pruthi P. A., Pruthi V., Poluri K. M. (2019). Co-culturing of oleaginous microalgae and yeast: paradigm shift towards enhanced lipid productivity. Environ. Sci. pollut. Res. 26, 16952–16973. doi: 10.1007/s11356-019-05138-6

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Arora N., Philippidis G. P. (2023). The prospects of algae-derived vitamins and their precursors for sustainable cosmeceuticals. Processes 11, 587. doi: 10.3390/pr11020587

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Caudal F., Tapissier-Bontemps N., Edrada-Ebel R. A. (2022). Impact of co-culture on the metabolism of marine microorganisms. Mar. Drugs 20, 153. doi: 10.3390/md20020153

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Keywords: algae, biofuels, bioproducts, symbiotic, seaweed

Citation: Arora N and Poluri KM (2024) Editorial: Symbiotic interactions of algae and microorganisms: physiology and industrial applications. Front. Mar. Sci. 10:1345329. doi: 10.3389/fmars.2023.1345329

Received: 27 November 2023; Accepted: 05 December 2023;
Published: 08 January 2024.

Edited and Reviewed by:

Michael Rappe, University of Hawaii at Manoa, United States

Copyright © 2024 Arora and Poluri. 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: Neha Arora, nehaarora@skidmore.edu; nehaarora@usf.edu; Krishna Mohan Poluri, krishna.poluri@bt.iitr.ac.in; mohanpmmk@gmail.com

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.