Aquaculture 2022

February 28 - March 4, 2022

San Diego, California

DIRECT COMPARISON OF FECAL AND GUT MICROBIOTA IN THE BLUE MUSSEL Mytilus edulis DISCOURAGES FECAL SAMPLING AS A PROXY FOR RESIDENT GUT COMMUNITY

 Tyler W. Griffin*, Julia G. Baer, J. Evan Ward

 

 Department of Marine Sciences

 University of Connecticut

 Groton, CT 06340

 tyler.griffin@uconn.edu

 



Bivalves have ecological and economic importance but information regarding their associated microbiomes is lacking. As suspension-feeders, bivalves capture and ingest a myriad of particles, and their digestive organs have a high throughput of particle-associated microbiota. To better understand the complement of transient and resident microbial communities, standard methods need to be developed. For example, fecal sampling could represent a convenient proxy for the gut microbiome and is simple, nondestructive, and allows for sampling of individuals through time. The goal of this study was to evaluate fecal sampling as a reliable proxy for gut microbiome assessment in the blue mussel (Mytilus edulis ). Mussels were collected from the natural environment and placed into individual sterilized microcosms for six hours to allow for fecal egestion. Feces and gut homogenates from the same individuals were sampled and subjected to 16S rRNA gene amplicon sequencing. Fecal communities of different mussels resembled each other but did not resemble gut communities. Fecal communities were significantly more diverse, in terms of amplicon sequence variant (ASV) richness and evenness, than gut communities. Results suggested a mostly transient nature for fecal microbiota. Nonetheless, mussels retained a distinct resident microbial community in their gut after fecal egestion that was dominated by ASVs belonging to Mycoplasma. The use of fecal sampling as a nondestructive substitute for direct sampling of the gut is strongly discouraged. Experiments that aim to study solely resident bivalve gut microbiota should employ an egestion period prior to gut sampling to allow time for voidance of transient microbes.