P1-153 Yellowfin and Albacore Tuna Microbiomes: Using Metagenomics to Improve Our Understanding of Scombrotoxin Fish Poisoning

Monday, August 1, 2016
America's Center - St. Louis
Kristin Bjornsdottir-Butler, U.S. Food and Drug Administration, Gulf Coast Seafood Laboratory, Dauphin Island, AL
Andrea Ottesen, U.S. Food and Drug Administration, College Park, MD
Padmini Ramachandran, Oak Ridge Institue for Science and Education, Oak Ridge, TN
Ronald A. Benner, Jr, U.S. Food and Drug Administration, Gulf Coast Seafood Laboratory, Dauphin Island, AL
Introduction: Scombrotoxin fish poisoning (SFP) is the most common finfish-related illness in the US.  To design effective mitigation strategies for SFP, it is necessary to understand the composition and distribution of scombrotoxin-forming microbial species associated with fish microbiomes.

Purpose: The objective of this study was to provide a baseline description of culture independent and culture dependent microflora associated with two commercially important and widely consumed fish; yellowfin and albacore tuna.  A specific goal was the analysis of the anatomical incidence of histamine-producing bacterial species and co-occurring microbial community structure and diversity.

Methods: DNA was purified from gills, skin, and anal vent swabs of freshly caught yellowfin (n=3) and albacore (n=6) tuna.  16S rRNA gene amplicons were sequenced using the Illumina MiSeq V3 platform.  Data were analyzed using the QIIME pipeline (Quantitative Insights Into Microbial Ecology).  Enriched swab samples [48h at 25°C, Marine Broth (MB)+1% histidine] were analyzed for the presence of the histidine decarboxylase (hdc) gene using qPCR. 

Results: Principal component analyses of 16S rRNA gene amplicons showed distinct taxonomic profiles for the three sampling locations: gills, skin, and anal vent. The most abundant class/order/family in all sampling locations was Gammaproteobacteria/Vibrionales/Vibrionaceae.  Photobacterium was the most abundant genus (0.9%) observed in anal vent whereas only 0.1% of the OTUs from gills and skin were Photobacterium spp.  Other important histamine-producing bacteria (HPB) such as Citrobacter, Enterobacter, and Morganella spp. comprised a small fraction of the observed OTUs at all sampling locations or 2-9 x 106, 0.1-5.8 x 106, and 0.4-1.1 x 106%, respectively.   The hdc gene was only detected in anal vent enrichment samples from three albacore and two yellowfin tuna.

Significance: These data will be used to refine mitigation and detection strategies to control Photobacterium spp. and other histamine-producing bacteria in tuna and other fish species associated with SFP.