Microbiome Population Dynamics of Cold-Smoked Sockeye Salmon during Refrigerated Storage and after Culture Enrichment

Author:

JARVIS KAREN G.1ORCID,HSU CHIUN-KANG1,PETTENGILL JAMES B.2,IHRIE JOHN2,KARATHIA HIREN3,HASAN NUR A.4,GRIM CHRISTOPHER J.1

Affiliation:

1. Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, Laurel, Maryland 20708

2. Center for Food Safety and Applied Nutrition, U.S. Food and Drug Administration, College Park, Maryland 20742

3. Cancer Data Science Laboratory, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892

4. Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland 20742, USA

Abstract

ABSTRACT Cold-smoked salmon is a ready-to-eat seafood product of high commercial importance. The processing and storage steps facilitate the introduction, growth, and persistence of foodborne pathogens and spoilage bacteria. The growth of commensal bacteria during storage and once the product is opened also influence the quality and safety of cold-smoked salmon. Here we investigated the microbial community through targeted 16S rRNA gene and shotgun metagenomic sequencing as means to better understand the interactions among bacteria in cold-smoked salmon. Cold-smoked salmon samples were tested over 30 days of aerobic storage at 4°C and cultured at each time point in a buffered Listeria enrichment broth (BLEB) commonly used to detect Listeria in foods. The microbiomes were composed of Firmicutes and Proteobacteria, namely, Carnobacterium, Brochothrix, Pseudomonas, Serratia, and Psychrobacter. Pseudomonas species were the most diverse species, with 181 taxa identified. In addition, we identified potential homologs to 10 classes of bacteriocins in microbiomes of cold-smoked salmon stored at 4°C and corresponding BLEB culture enrichments. The findings presented here contribute to our understanding of microbiome population dynamics in cold-smoked salmon, including changes in bacterial taxa during aerobic cold storage and after culture enrichment. This may facilitate improvements to pathogen detection and quality preservation of this food. HIGHLIGHTS

Publisher

International Association for Food Protection

Subject

Microbiology,Food Science

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