Bloom-forming marine gelatinous zooplankton, including the pelagic
tunicate Dolioletta gegenbauri, occur circumglobally and have the
potential to significantly influence the structure of pelagic marine
food webs and biogeochemical cycling through interactions with microbial
communities. Using targeted metabarcoding (16S rRNA genes recovering
Bacteria/Archaea) and qPCR approaches associated with laboratory-based
feeding experiments, we characterized patterns in doliolid gut
microbiomes and microbial communities associated with doliolid fecal
pellets and the surrounding seawater. The characterization of starved
doliolids provides the first description of the doliolid gut microbiome.
At the highest taxonomic levels, doliolid-associated bacterial
communities are characteristic of marine bacterioplankton communities
around the globe and were dominated by representatives of six major
bacterial groups including Gammaproteobacteria, Alphaproteobacteria,
Cyanobacteria, Planctomycetes, Bacteroidia and, Phycisphaerae.
Comparison between sample types, however, revealed distinct patterns in
diversity and biomass supporting the hypothesis that through their
presence and trophic activity, doliolids influence the structure of
pelagic food webs and biogeochemical cycling in subtropical continental
shelf systems where doliolid blooms are common. Bacteria associated with
starved doliolids (representative of the resident doliolid gut
microbiome) possessed distinct communities, supporting the hypothesis
that doliolids possess a unique but low diversity, low biomass
microbiome optimized to support a detrital trophic mode. Among potential
core microbiome taxa, the genera Pseudoalteromomas and
Shimia were the most abundant, similar to patterns observed in
other marine invertebrates. Exploratory bioinformatic analyses of
predicted functional genes suggest that doliolids, via their
interactions with bacterial communities, may affect important
biogeochemical processes including nitrogen, sulfur, and organic matter
cycling.