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Microbiol Spectr
2023 Jun 15;113:e0051423. doi: 10.1128/spectrum.00514-23.
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Spatial Succession Underlies Microbial Contribution to Food Digestion in the Gut of an Algivorous Sea Urchin.
Masasa M
,
Kushmaro A
,
Nguyen D
,
Chernova H
,
Shashar N
,
Guttman L
.
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Dietary influence on the microbiome in algivorous sea urchins such as Tripneustes gratilla elatensis suggests a bacterial contribution to the digestion of fiber-rich seaweed. An ecological insight into the spatial arrangement in the gut bacterial community will improve our knowledge of host-microbe relations concerning the involved taxa, their metabolic repertoire, and the niches of activity. Toward this goal, we investigated the bacterial communities in the esophagus, stomach, and intestine of Ulva-fed sea urchins through 16S rRNA amplicon sequencing, followed by the prediction of their functional genes. We revealed communities with distinct features, especially those in the esophagus and intestine. The esophageal community was less diverse and was poor in food digestive or fermentation genes. In contrast, bacteria that can contribute to the digestion of the dietary Ulva were common in the stomach and intestine and consisted of genes for carbohydrate decomposition, fermentation, synthesis of short-chain fatty acids, and various ways of N and S metabolism. Bacteroidetes and Firmicutes were found as the main phyla in the gut and are presumably also necessary in food digestion. The abundant sulfate-reducing bacteria in the stomach and intestine from the genera Desulfotalea, Desulfitispora, and Defluviitalea may aid in removing the excess sulfate from the decomposition of the algal polysaccharides. Although these sea urchins were fed with Ulva, genes for the degradation of polysaccharides of other algae and plants were present in this sea urchin gut microbiome. We conclude that the succession of microbial communities along the gut obtained supports the hypothesis on bacterial contribution to food digestion. IMPORTANCE Alga grazing by the sea urchin Tripneustes gratilla elatensis is vital for nutrient recycling and constructing new reefs. This research was driven by the need to expand the knowledge of bacteria that may aid this host in alga digestion and their phylogeny, roles, and activity niches. We hypothesized alterations in the bacterial compositional structure along the gut and their association with the potential contribution to food digestion. The current spatial insight into the sea urchin's gut microbiome ecology is novel and reveals how distinct bacterial communities are when distant from each other in this organ. It points to keynote bacteria with genes that may aid the host in the digestion of the complex sulfated polysaccharides in dietary Ulva by removing the released sulfates and fermentation to provide energy. The gut bacteria's genomic arsenal may also help to gain energy from diets of other algae and plants.
FIG 1. Ecological indices of richness and diversity of the microbial assemblies in the gut of T. gratilla elatensis. (a and b) Richness (a) and Shannon diversity (b) indices are presented for the different gut regions of esophagus, stomach, and intestine. Box plots represent the variation between the five biological replicates within each examined gut region. Black diamonds mark mean values; medians and standard deviations (SD) are shown within and outside the box plots, respectively. (c) The dissimilarity between the microbial assemblies in the different examined gut regions is demonstrated by a principal-coordinate analysis (PCA) generated based on Bray-Curtis dissimilarity (n = 15).
FIG 2. Relative abundances of the various bacterial taxa in the gut assemblies of T. gratilla elatensis. For each taxon, mean relative abundance (in percent) was calculated for each gut region based on the five examined biological replicates (out of the total of 15 samples). The taxonomic classification of ASVs was set (at the highest taxonomic level).
FIG 3. Phylogenetic tree of T. gratilla elatensis gut microbial assembly. ASVs were colored based on their spatial niche specification in the gut as follows: the red ASVs were exclusive to the esophagus, the green ASVs were exclusive to the stomach, and the blue ASVs were exclusive to the intestine. Gray ASVs occurred in at least two different gut regions. The phylogenic tree of closeness between the various ASVs was constructed using the Interactive Tree of Life (iTOL) tool based on the weighted UniFrac indices. The branch was colored based on their bootstraps (1,000); the minimum was represented in blue, the midpoint in black, and the maximum in red.
FIG 4. A comparative analysis of the KOs in the gut microbial assemblies of T. gratilla elatensis. (a) A heatmap diagram of the KEGG orthologous genes in the three main gut regions of the esophagus, stomach, and intestine. Each gene orthologue is colored according to its number of KOs in each of the five biological replicates (for each gut region); color varies from dark blue (0) to dark red (20,098). (b) A principal-coordinate analysis demonstrates the dissimilarity between the microbial assemblies in the different gut regions regarding their potential functions based on the measured, weighted UniFrac indices (n = 15).
FIG 5. Microbial functional gene distribution in the different gut regions of T. gratilla elatensis. The rows represent the number of gene copies (log transformed) in each functional category (annotated by COG) in the esophagus (red), stomach (green), and intestine (blue). Values are means ± SDs (n = 15).
FIG 6. A heatmap diagram of selected KEGG orthologous genes of the microbial assemblies in the different gut regions of T. gratilla elatensis. The map highlights the occurrence and the cumulative number of copies after vector scaling in the microbial assembly of the esophagus, stomach, and intestine gut regions.
FIG 7. Hypothetical pathway for the starch and sucrose metabolism of the gut microbial assembly of T. gratilla elatensis. The metabolic mapping was performed according to KEGG. Purple boxes with red font represent the genes that have been identified, while purple boxes with black font represent other known genes in the hypothetical pathway of each compound (marked by circles). Arrows present the direction of the metabolic function.
FIG 8. Hypothetical pathway for the sulfur metabolism of the gut microbial assembly of T. gratilla elatensis. The metabolic mapping was performed according to KEGG. Purple boxes with red font represent the genes that have been identified, while purple boxes with black font represent other known genes in the hypothetical pathway of each compound (marked by circles). Arrows present the direction of the metabolic function. Abbreviations: APS, adenosine 5′-phosphosulfate; PAP, phosphoadenosine phosphate; PAPS, 3′-phosphoadenosine 5′-phosphosulfate; CoA, coenzyme A; CoM, coenzyme M; DMSO, dimethyl sulfoxide; DMSP, S-dimethylsulfonium propionic acid.
FIG 9. Hypothetical pathway for the nitrogen metabolism of the gut microbial assembly of T. gratilla elatensis. The metabolic mapping was performed according to KEGG. Purple boxes with red font represent the genes that have been identified, while purple boxes with black font represent other known genes in the hypothetical pathway of each compound (marked by circles). Arrows present the direction of the metabolic function.
FIG 10. Hypothetical pathway for the biosynthesis of fatty acids by the gut microbial assembly of T. gratilla elatensis. The metabolic mapping was performed according to KEGG. Purple boxes with red font represent the genes that have been identified, while purple boxes with black font represent other known genes in the hypothetical pathway of each compound (marked by circles). Arrows present the direction of the metabolic function. Abbreviations: ACP, acyl carrier protein; FAS, fatty acid synthase bacteria type; FASN, fatty acid synthase animal type; MECR, mitochondrial enoyl-[acyl-carrier protein] reductase.
FIG 11. Hypothetical pathway for the degradation of fatty acids by the gut microbial assembly of T. gratilla elatensis. The metabolic mapping was performed according to KEGG. Purple boxes with red font represent the genes that have been identified, while purple boxes with black font represent other known genes in the hypothetical pathway of each compound (marked by circles). Arrows present the direction of the metabolic function.
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