Microbial Interactions in the Phycosphere

A special issue of Phycology (ISSN 2673-9410).

Deadline for manuscript submissions: 30 March 2027 | Viewed by 5637

Editor


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Guest Editor
Laboratory of Phycosphere Microbiology, Zhejiang Ocean University, Zhoushan, China
Interests: phycosphere microbiology; phycosphere microbiota; algae–bacteria interactions; phycobiont

Special Issue Information

Dear Colleagues,

The phycosphere represents one of the most dynamic and ecologically critical microenvironments in aquatic ecosystems. As primary producers, algae form the base of aquatic food webs, and their interactions with co-occurring associated microbes (including bacteria, archaea, viruses, fungi, and protozoa) shape diverse processes, ranging from global biogeochemical cycling to phytoplankton bloom dynamics, as well as the ecological health of marine and freshwater habitats. Despite decades of research, the complex nature of these interactions—their molecular mechanisms, ecological consequences, and responses to environmental changes—remains incompletely resolved. It is within this context that we are launching this Special Issue, “Microbial Interactions in the Phycosphere”.

Aims:

The primary aims of this Special Issue are as follows:

  1. Advance Mechanistic Understanding: To synthesize and publish research that uncovers the molecular, physiological, and ecological mechanisms driving interactions in the phycosphere. This can include, but is not limited to, nutrient exchange, signaling pathways, and symbiotic or antagonistic relationships.
  2. Bridge Scales of Inquiry: To connect microscale interactions (e.g., cell-to-cell signaling) to macroscale ecological outcomes (e.g., bloom formation, carbon export to the deep ocean). By integrating studies across spatial (from nanometers to ecosystems) and temporal (from hours to seasonal) scales, this Special Issue aims to resolve gaps in how phycosphere dynamics can be scaled up to influence aquatic biogeochemistry and food web structures.
  3. Address Global Change Impacts: To highlight research exploring how anthropogenic stressors—such as ocean warming, acidification, eutrophication, and pollution—alter phycosphere interactions. Understanding these responses is critical in predicting shifts in aquatic ecosystem function (e.g., changes in primary productivity, increased harmful algal blooms) under a changing climate.

Scope:

To achieve these aims, this Special Issue will encompass a broad range of topics, approaches, and aquatic systems, including the following:

  • Key Organism Interactions: Studies investigating pairwise or multi-species interactions involving phytoplankton (e.g., diatoms, dinoflagellates, cyanobacteria) and associated microbes (e.g., heterotrophic bacteria of the Roseobacter clade, viruses, protozoan grazers). We will consider work on both beneficial interactions (e.g., mutualistic nutrient cycling) and detrimental ones (e.g., viral lysis, algicidal bacterial activity).
  • Methodological Advancements: Contributions showcasing innovative techniques to study the phycosphere, such as meta-omics (metagenomics, metatranscriptomics, metabolomics), single-cell imaging (e.g., fluorescence in situ hybridization, atomic force microscopy), microfluidic systems (to mimic phycosphere microenvironments), and stable isotope probing (to trace nutrient flow).
  • Aquatic Ecosystem Diversity: Research conducted in diverse aquatic habitats, including marine (coastal, open ocean), freshwater (lake, river), and brackish (estuary) systems. This breadth reflects the universality of the phycosphere while highlighting ecosystem-specific variations in interaction dynamics (e.g., nutrient limitation in oligotrophic oceans vs. eutrophic lakes).
  • Theoretical and Applied Perspectives: In addition to empirical research, this Special Issue will include review articles synthesizing current knowledge, perspective pieces proposing new hypotheses (e.g., "the phycosphere as a hub for horizontal gene transfer"), and applied studies (e.g., leveraging phycosphere interactions for bioremediation, sustainable aquaculture, or the mitigation of harmful algal blooms).

By bringing together these diverse perspectives, this Special Issue will serve as a definitive resource for researchers, students, and practitioners in phycosphere microbial ecology, aquatic biology, biogeochemistry, and climate science, ultimately advancing our collective understanding of the phycosphere as a driver of aquatic ecosystem health and global biogeochemical cycles.

Dr. Qiao Yang
Guest Editor

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Keywords

  • phycosphere
  • algae–bacteria interactions
  • interaction between bacteria and algae
  • relationship between bacteria and algae
  • interaction between diatoms and bacteria
  • microbial interactions
  • phytoplankton–bacteria relationships
  • phytoplankton–bacteria interactions
  • host–microbe interactions
  • phycosphere microbiology
  • mutualistic interactions
  • symbiotic interactions
  • bacteria–dinoflagellate interactions
  • interaction between microalgae and phycosphere bacteria
  • diatom–bacterium interactions
  • phycosphere microbes
  • phycosphere microbiota
  • phycosphere bacteria
  • algal–bacteria consortia
  • phycosphere microbial diversity
  • algae–bacteria symbiotic system
  • bacteria–algae symbiotic system
  • quorum sensing
  • algicidal bacteria
  • microalgae growth-promoting bacteria
  • phycosphere holobiont
  • chemotaxis
  • auxin signaling
  • aquatic ecosystems
  • biogeochemical cycling
  • molecular mechanisms
  • harmful algal blooms
  • phytoplankton bloom
  • phycoremediation
  • wastewater treatment
  • extracellular polymeric substances
  • aquatic ecosystems
  • marine food web
  • microbial loop
  • exopolysaccharide
  • indole-3-acetic acid

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Published Papers (6 papers)

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Research

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19 pages, 3443 KB  
Article
Growth Promotion of Chlamydomonas reinhardtii by Cupriavidus oxalaticus MEYA8
by Xinyan Wu, Xin Li, Mengya Song, Jie Yu, Yuanpei Jin, Yunhao Wang and Bo Xie
Phycology 2026, 6(3), 89; https://doi.org/10.3390/phycology6030089 - 6 Aug 2026
Viewed by 233
Abstract
Microalgal growth-promoting bacteria (MGPBs) represent a promising strategy to enhance biomass productivity, yet the mechanistic basis of these mutualistic interactions remains poorly understood. Here, we isolated a new MGPB, Cupriavidus oxalaticus MEYA8, and characterized its mutualistic interaction with the model microalga Chlamydomonas reinhardtii [...] Read more.
Microalgal growth-promoting bacteria (MGPBs) represent a promising strategy to enhance biomass productivity, yet the mechanistic basis of these mutualistic interactions remains poorly understood. Here, we isolated a new MGPB, Cupriavidus oxalaticus MEYA8, and characterized its mutualistic interaction with the model microalga Chlamydomonas reinhardtii. Co-cultivation at an optimal MEYA8: Chlamydomonas ratio greatly enhanced microalgal cell density and chlorophyll content, which reached 2.1-fold and 1.6-fold those of the control, respectively, with markedly improved photosynthetic efficiency across both photosystems. Transwell assays confirmed that this promotion is mediated by diffusible metabolites rather than direct cell contact. Metabolites and multi-omics analyses revealed that MEYA8 can produce compounds similar to indole-3-acetic acid (IAA) and is adapted to the microalgal phycosphere by preferentially utilizing organic acids and amino acid derivatives. In response, Chlamydomonas upregulated proteins involved in photosynthetic electron transport, energy metabolism, and nitrogen assimilation, consistent with the observed enhancement in photosynthetic performance. These findings suggest a metabolically reciprocal interaction model: MEYA8 supplies diffusible growth-promoting factors such as IAA-like compounds to enhance Chlamydomonas photosynthesis and growth, while Chlamydomonas provides organic substrates that sustain bacterial proliferation. Our work provides new insights into algal–bacterial mutualism and may provide a new microbial resource for engineering microalgal and beneficial bacterial consortia. Full article
(This article belongs to the Special Issue Microbial Interactions in the Phycosphere)
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17 pages, 5663 KB  
Article
Algae-Enriched Bacterial Community Composition Varies with Stress Response Patterns in Antarctic Algal Enrichment Cultures
by Bradley Krzysiak and Rachael M. Morgan-Kiss
Phycology 2026, 6(3), 71; https://doi.org/10.3390/phycology6030071 - 2 Jul 2026
Viewed by 342
Abstract
Perennially ice-covered lakes in the McMurdo Dry Valleys, Antarctica, are shaped by permanent stratification, extreme oligotrophy, and salinity gradients, yet these features are vulnerable to climate-driven hydrologic change. Because phytoplankton and associated bacteria regulate carbon flow and nutrient cycling, understanding how algal–bacterial consortia [...] Read more.
Perennially ice-covered lakes in the McMurdo Dry Valleys, Antarctica, are shaped by permanent stratification, extreme oligotrophy, and salinity gradients, yet these features are vulnerable to climate-driven hydrologic change. Because phytoplankton and associated bacteria regulate carbon flow and nutrient cycling, understanding how algal–bacterial consortia respond to disturbance is key to predicting ecosystem change. We used enrichment cultures from Lakes Bonney and Fryxell to test responses to nutrient deprivation and salinity alteration, two perturbations relevant to climate-driven changes in hydrologic connectivity and expansion of open water moats. Autotrophic enrichments lacking added organic carbon were used to enrich algal–bacterial consortia dependent on photosynthetically derived substrates. Community responses were assessed with 16S rRNA amplicon sequencing of size-fractionated samples, allowing comparison of particle-associated and planktonic communities. Short-term nutrient limitation produced only limited shifts in community composition, indicating resistance to transient nutrient stress. However, bacterial communities were strongly structured by size fraction: particle-associated assemblages separated clearly from planktonic communities and were enriched in taxa linked to algal surfaces and polysaccharide-rich microhabitats, including Flavobacteriales, Sphingobacteriales, Rhizobiales, and Rhodobacterales. Salinity perturbation drove stronger restructuring of bacterial communities, with shallow Lake Bonney enrichments showing greater sensitivity than deeper communities. These findings suggest that algae-associated bacterial communities help structure Antarctic algal enrichment cultures and may influence microbial responses to climate-linked disturbance. Full article
(This article belongs to the Special Issue Microbial Interactions in the Phycosphere)
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16 pages, 2695 KB  
Article
Vitamin K1 Can Effectively Promote the Photosynthesis and Lipid Production of Chlorella pyrenoidosa
by Yixin Yan, Wanchuan Xing, Yaming Ge, Xiaoling Zhang, Ye Chen and Junzhi Liu
Phycology 2026, 6(2), 62; https://doi.org/10.3390/phycology6020062 - 3 Jun 2026
Cited by 1 | Viewed by 534
Abstract
Whether exogenous vitamin K1 (VK1) promotes microalgal growth is unknown. This study reports for the first time that Bacillus megaterium can promote the growth of Chlorella pyrenoidosa, an effect possibly mediated by VK1. To confirm this finding and clarify the corresponding mechanism, [...] Read more.
Whether exogenous vitamin K1 (VK1) promotes microalgal growth is unknown. This study reports for the first time that Bacillus megaterium can promote the growth of Chlorella pyrenoidosa, an effect possibly mediated by VK1. To confirm this finding and clarify the corresponding mechanism, the effects of exogenous VK1 on the growth and lipid production of C. pyrenoidosa were studied. The results showed that the microalgal cell density, chlorophyll a content, lipid content, and lipid productivity increased by 117%, 90%, 291%, and 247%, respectively, following the addition of 0.3 g/L exogenous VK1. Additionally, the microalgal Fv/Fo, Fv/Fm, and Fm/Fo were also improved by the VK1, indicating that VK1 promoted microalgae growth by increasing microalgal photosynthesis activities. The microalgal genes of lipid synthesis, including the acetyl-CoA carboxylase gene, malonyl-transferase gene, 3-oxoacylsynthase I gene, and 3-oxoacyl-[acyl-carrier-protein] synthase II gene, were all up-regulated by VK1 at the transcript level, revealing the promotion mechanism of VK1 on microalgal lipid production. Moreover, the total phosphorus utilization of the C. pyrenoidosa reached nearly 100%, indicating its excellent phosphorus utilization ability. The results are beneficial for exploring a more effective technology of utilizing C. pyrenoidosa for biofuel production and provide a new perspective on understanding the interaction mechanism between bacteria and microalgae. Full article
(This article belongs to the Special Issue Microbial Interactions in the Phycosphere)
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12 pages, 2581 KB  
Article
Getting Attached: A Heterotrophic Nanoflagellate Mingling with Centric Diatoms
by Gabrielle Corradino and Astrid Schnetzer
Phycology 2026, 6(1), 20; https://doi.org/10.3390/phycology6010020 - 1 Feb 2026
Viewed by 800
Abstract
Heterotrophic nanoflagellates (HNANs) are central components of the microbial loop, transferring carbon from bacteria to higher trophic levels and facilitating nutrient recycling. While many HNANs are free-swimming, some exhibit enhanced feeding efficiency when attached to surfaces, including diatom frustules. Here, we describe the [...] Read more.
Heterotrophic nanoflagellates (HNANs) are central components of the microbial loop, transferring carbon from bacteria to higher trophic levels and facilitating nutrient recycling. While many HNANs are free-swimming, some exhibit enhanced feeding efficiency when attached to surfaces, including diatom frustules. Here, we describe the attachment behavior of a novel interception-feeding HNAN affiliated with the order Bicosoecida to centric diatoms common in North Carolina coastal waters. Using growth experiments, live observations, and time-lapse microscopy, we quantified attachment frequency and assessed its influence on diatom growth for three diatom species: Coscinodiscus sp., Odontella sp., and Rhizosolenia sp. HNAN attachment differed significantly among diatom taxa: Coscinodiscus sp. hosted the highest and most sustained numbers per frustule, whereas after normalizing for surface area, Rhizosolenia sp. exhibited the highest attachment efficiency. Diatom peak growth was 1.2 to 2.1-fold higher and occurred earlier in HNAN co-cultures than in controls, indicating microbial recycling by the HNAN stimulated growth. These findings highlight the nuanced ecological role attached HNANs might play as they exploit diatom-associated boundary layers to enhance bacterial encounter rates. The growth trajectories in our lab experiments suggests that attachment behavior in situ can play a role in driving diatom bloom dynamics and, therefore, play an important role for carbon cycling. Full article
(This article belongs to the Special Issue Microbial Interactions in the Phycosphere)
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Review

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24 pages, 1264 KB  
Review
Occurrence and Ecological Significance of Microalgae Species Associated with Egg Clutches of Aquatic Animals
by Wiktoria Pisarska, Marcelina Ochab, Zuzanna Opalińska and Sylwia Śliwińska
Phycology 2026, 6(3), 93; https://doi.org/10.3390/phycology6030093 - 10 Aug 2026
Viewed by 189
Abstract
The association of microalgae with aquatic animal egg masses plays an important role in the reproductive ecology of several species. The first descriptions of this phenomenon were reported in 1888 for the egg masses of the spotted salamander Ambystoma maculatum. The microalgae [...] Read more.
The association of microalgae with aquatic animal egg masses plays an important role in the reproductive ecology of several species. The first descriptions of this phenomenon were reported in 1888 for the egg masses of the spotted salamander Ambystoma maculatum. The microalgae most commonly associated with animal egg masses are green algae belonging to the genus Oophila. For many years, Oophila sp. was considered the only known intracellular endosymbiont in vertebrates; however, subsequent research has expanded the list of microorganisms capable of forming such associations. Here, we reviewed 69 English-language scientific publications on the occurrence of microalgae in the egg clutches of aquatic animals. This clearly indicates that current knowledge of these organisms remains incomplete and requires further investigation. This review presents a general characterization of the occurrence of microalgae in aquatic animal egg clutches, summarizes the locations where this phenomenon has been documented, describes both the animal hosts and the microalgae involved, examines the benefits resulting from the presence of photosynthetic microorganisms within egg masses, and highlights future research directions, including potential practical applications of these associations. Full article
(This article belongs to the Special Issue Microbial Interactions in the Phycosphere)
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30 pages, 4919 KB  
Review
Algal–Bacterial Interactions: Mechanisms, Ecological Significance, and Biotechnological Implications
by Domenico Prisa, Aristidis Matsoukis, Aftab Jamal, Damiano Spagnuolo and Lorenzo Maria Ruggeri
Phycology 2026, 6(2), 50; https://doi.org/10.3390/phycology6020050 - 11 May 2026
Cited by 3 | Viewed by 1684
Abstract
Algae rarely occur as solitary phototrophs in nature or engineering; instead, they are embedded in complex bacterial consortia that control their physiology, productivity and ecological performance. The phycosphere, a microscale niche rich in algal exudates, promotes extensive metabolic exchange and chemical signaling, defining [...] Read more.
Algae rarely occur as solitary phototrophs in nature or engineering; instead, they are embedded in complex bacterial consortia that control their physiology, productivity and ecological performance. The phycosphere, a microscale niche rich in algal exudates, promotes extensive metabolic exchange and chemical signaling, defining these associations. Bacteria capitalize on the dissolved organic carbon released by algae, providing growth supporting molecules such as vitamins, trace metals, and siderophores, as well as regenerated inorganic nutrients. Bidirectional beneficial interactions range from obligate mutualism to facultative commensalism and antagonism, depending on environmental context and community membership. Bacterial partners can stimulate algal growth, morphogenesis, and stress tolerance, as well as modulating defense and programmed cell death during the decline and bloom succession of algae resulting from algicidal taxa. Metabolic cooperation, QS signaling, extracellular enzyme activity, and chemically induced gene expression produce the exometabolome in the phycosphere, which in turn reprograms gene expression in all partners. Recent advances in multi-omics toolboxes, single-cell isotopic analyses, and microfluidics have greatly enhanced our understanding of the functional and spatiotemporal orientation of algal microbiomes. Ecologically, algal–bacterial interactions manage the phytoplankton community structure, control HABs, and modulate carbon and nutrient fluxes in both marine and freshwater realms. Biotechnologically, engineered algal–bacterial consortia are a promising tool for enhancing biomass production, stabilizing large-scale cultivation, improving wastewater treatment, and upgrading biofuels and fine chemicals. Despite these notable research advances, the context- and species-dependent complexity of multispecies interactions remains a major obstacle to their practical modeling and scalable implementation. Integrative research frameworks that combine molecular, ecological, and bioengineering approaches are urgently needed to unlock the full potential of sustainable applications in the future. Full article
(This article belongs to the Special Issue Microbial Interactions in the Phycosphere)
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