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An experimental test of the influence of microbial manipulation on sugar kelp (Saccharina latissima) supports the core influences host function hypothesis

Jungsoo Park, Evan Kohn, Siobhan Schenk, Katherine Davis, Jennifer Clark, Laura Wegener Parfrey

Posted on: 15 April 2025

Preprint posted on 28 February 2025

Bring bacteria back: The influence of microbial manipulation on sugar kelp development

Selected by Jasmine Talevi

Categories: ecology

Background

The ability to grow food and resources has become imperative for our expanding population. The cultivation of sugar kelp (Saccharina latissimi) has gained popularity in the Northern Hemisphere as a potential source for biofuels, livestock feed, and as a component of integrated multi-trophic aquaculture. Like most other forms of cultivation, kelp growers experience challenges when it comes to increasing growth and yield, which appear to be linked to microbial communities.

In kelp aquaculture, it is standard practice to remove microbes and reduce microbial growth to limit disease and biofouling pressure. However, these processes also remove beneficial microbes. Recent research highlights the importance of symbiotic bacteria for host development, survival, and overall fitness. With this knowledge, growers have an opportunity to manipulate the microbial environment of kelp during cultivation to potentially increase production while still limiting disease and fouling pressure.

While the microbial community can be quite diverse, it is generally assumed that microbes more consistently associated with sugar kelp, referred to as core bacteria, will have more influence on its functioning. Thus, identifying and manipulating these core bacteria during the cultivation process may be most impactful.

Park et al., (2025) investigated this in the study highlighted here. They began by sampling the sugar kelp microbiome across space and time, and then compared it to the surrounding environment to identify the core microbes. Once identified, these core microbes were isolated and co-cultured with sugar kelp to assess their influence on kelp development. Lastly, the kelp was outplanted at several ocean farms, where development was tracked over a six-month period.

Key Findings

1) The microbiome of wild sugar kelp is different to that of its surrounding environment and cultivated (hatchery and out planted) kelp.

The microbiome composition of wild sugar kelp was significantly different to the microbiome of the surrounding water and rocks. Additionally, the microbiome of wild, nursery, and outplanted cultivated sugar kelp were all significantly different from one another (Fig. 1). However, the core bacteria found on wild kelp were also observed on the outplanted cultivated kelp after 12 months, suggesting that core bacteria can be recruited onto cultivated kelp over time (Fig. 1).

Figure 1. NMDS plots using Bray-Curtis dissimilarities and a taxa-plot were made to compare the microbiota found on different Saccharina populations and on surrounding abiotic substrates. A. Bacterial community composition on Saccharina compared to rocky substrate and seawater in the surrounding environment. B. Bacterial community composition on Saccharina samples collected from wild populations through the year in comparison to samples from cultivated Saccharina in the nursery and ocean farm sites. Figure is made available under a CC-BY-NC-ND 4.0 International license.

 

2) Culturing sugar kelp with microbes from wild sugar kelp increased development most of the time.

Across all trials, 87% of the bacterial isolates had a significant positive impact on gametophyte coverage and 85% of bacterial isolates had a positive impact on sporophyte number (Fig. 2).

Figure 2. Volcano plot depicting the effect of bacterial inoculants on Saccharina across all four trials. The x-axis depicts the log2 fold change for each bacterial isolate compared to the control groups in each experimental trial on (A) gametophyte percent cover and (B) the number of sporophytes produced. The y-axis displays log10 Bonferroni-corrected p-value from two tailed t-tests comparing the control group to co-culture treatments with each bacterial isolate. Isolates are colored by co-culture trial, and grey if their effect was not significant. Figure is made available under a CC-BY-NC-ND 4.0 International license.

 

3) Bacterial genera more strongly associated with sugar kelp are more likely to increase development.

There was a significantly positive relationship between the strength of association between bacteria with sugar kelp and the number of sporophytes produced as well as gametophyte coverage (Fig. 3).

Figure 3. The relationship between strength of association with wild Saccharina (IndVal statitistic) and effects of bacterial inoculation on Saccharina development. The y-axis displays the log2 fold changes for each bacterial isolate compared to the control groups in each experimental trial, for (A) gametophyte coverage % and (B) the number of sporophytes. Points and trend lines are colored co-culture trial, while black trend-lines represent the relationship across all trials. Figure is made available under a CC-BY-NC-ND 4.0 International license.

Why I highlight this preprint

This preprint is well written and reports unique findings that can be implemented to benefit kelp growers. Additionally, the focus on the microbiome I found particularly compelling. While microbiomes are commonly discussed in the context of human health, typically regarding the importance of a balanced gut ecosystem, it is intriguing to see this concept extended to marine organisms like kelp. This broader application highlights the fundamental role microbiomes play across diverse biological systems.

Questions for the authors

1) Was there a consistent relationship between the bacteria isolates that had a negative impact on gametophyte coverage and sporophyte number, and can these be removed for future experimentation?

2) How do the increased sporophyte numbers and gametophyte coverage seen with added microbes in the hatchery compare to those found in wild kelp?

Tags: bacterial isolation, kelp cultivation, microbial ecology, microbial manipulation, saccharina latissima

doi: https://doi.org/10.1242/prelights.40201

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Author's response

Jungsoo Park shared

1) Negative effects were relatively uncommon overall, but we did observe some isolates that had negative impacts on kelp development. While most isolates were only tested once, limiting our ability to assess consistency, Vibrio 2Man3 stood out as having a repeatedly negative effect, particularly on sporophyte development. This suggests that some strains may consistently inhibit growth and could be considered for exclusion in future trials, especially if confirmed in more replicates. Identifying such inhibitory taxa is valuable for refining microbial applications in kelp cultivation.

2) This is difficult to compare directly, as we did not quantify gametophyte coverage or early sporophyte numbers in wild kelp. Our study focused on controlled co-culture experiments simulating hatchery conditions, where sporophytes were counted manually and gametophyte coverage was estimated under the microscope using a gridded field of view. This method worked well, though future studies could benefit from image-based quantification tools like ImageJ for greater objectivity.

We focused on the hatchery stage because it is the only phase in cultivation where microbial manipulation is currently feasible, particularly in most countries, including Canada, where adding microbes in the open ocean is not permitted. Since wild kelp is typically sampled at the mature sporophyte stage, early developmental comparisons are not available. For now, I believe that the hatchery provides the best opportunity to explore microbial influences on kelp development.

Comment from the authors

The concept of a core microbiome has become popular in microbial ecology, but it remains mostly hypothetical and sometimes receives criticism. While some symbiotic bacteria are consistently found on hosts, these associations are not always beneficial. In fact, in some plant systems, consistently present microbes can be parasitic. Despite this complexity, the logic behind the core microbiome still makes sense from an evolutionary and ecological perspective. Consistent associations between hosts and microbes can be the result of long-term interactions shaped by selection. We saw this as a testable idea rather than a claim to be accepted.

Kelp is a great system to test this hypothesis because it has a distinctive microbiome that is different from the surrounding environment. Our study is significant because we brought this question into a laboratory cultivation setting, allowing us to experimentally evaluate whether microbes that are consistently associated with kelp in nature actually influence its growth and development.

Behind the scenes, introducing and defining the core microbiome was a real challenge. The definition is inherently variable, and we wanted to avoid assuming the core concept is universally valid. Instead, we framed the hypothesis in a neutral way, as a tool for identifying potentially meaningful associations that can be tested functionally.

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