4.6 Article

Interplay between the microalgae Micrasterias radians and its symbiont Dyadobacter sp. HH091

Journal

FRONTIERS IN MICROBIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fmicb.2022.1006609

Keywords

Dyadobacter sp; HH091; Micrasterias radians; microalgaebacteria interaction; synthetic early plant-bacteria system; symbiotic relations

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Based on previous research, an artificial plant-bacteria system was established to study the mutualistic collaboration between a microalga and its microbiome. The study focused on the mechanism of a type IX secretion system (T9SS) and its role in the attachment and invasion of the microalga by a bacterial isolate. Genome analysis revealed the presence of T9SS genes and other genes associated with gliding motility and protein secretion. The study proposed a model for the T9SS apparatus of the bacterial isolate and examined the bacterial colonization and penetration into the cell wall of the microalga.
Based on previous research, related to detailed insight into mutualistic collaboration of microalga and its microbiome, we established an artificial plant-bacteria system of the microalga Micrasterias radians MZCH 672 and the bacterial isolate Dyadobacter sp. HH091. The bacteria, affiliated with the phylum Bacteroidota, strongly stimulated growth of the microalga when it was added to axenic algal cultures. For further advances, we studied the isolate HH091 and its interaction with the microalga M. radians using transcriptome and extensive genome analyses. The genome of HH091 contains predicted polysaccharide utilizing gene clusters co-working with the type IX secretion system (T9SS) and conceivably involved in the algae-bacteria liaison. Here, we focus on characterizing the mechanism of T9SS, implementing the attachment and invasion of microalga by Dyadobacter sp. HH091. Omics analysis exposed T9SS genes: gldK, gldL, gldM, gldN, sprA, sprE, sprF, sprT, porU and porV. Besides, gld genes not considered as the T9SS components but required for gliding motility and protein secretion (gldA, gldB, gldD, gldF, gldG, gldH, gldI, gldJ), were also identified at this analysis. A first model of T9SS apparatus of Dyadobacter was proposed in a course of this research. Using the combination of fluorescence labeling of Dyadobacter sp. HH091, we examined the bacterial colonisation and penetration into the cell wall of the algal host M. radians MZCH 672.

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