Purpose: FDACS Bureau of Food Laboratories (BFL) has applied current technologies to develop an internal genomics pipeline to pinpoint possible foodborne outbreaks. This study demonstrates BFL’s ability to compare genomic data from clinical, food, and environmental Listeria monocytogenes isolates to deduce SNP-based relationships.
Methods: FL DOH genomic data from eight clinical L. monocytogenes isolates was compared against BFL’s L. monocytogenes phylogenic tree, containing approximately 700 Florida food and environmental isolates. Internal isolates were sequenced on a MiSeq using the Nextera XT and MiSeq V2 500-Cycle chemistry kits. An in-house developed pipeline consisting of kSNP3, FastTree2, and FigTree was used to establish preliminary sequence comparisons. The internally applied CFSAN SNP pipeline was used to detect hqSNPs amongst the cluster of interest. Lastly, FastTree2 was reincorporated along with FigTree to identify SNP distances and produce a phylogenetic tree.
Results: A cluster containing food and environmental isolates was found to be the closest to seven of the eight clinical samples. However, hqSNP analysis for this group showed that there were between 6,400 and 6,500 SNPs separating the clinical and food and environmental isolates. There were 1 to 4 SNPs identified within the cluster of seven clinical isolates.
Significance: BFL’s usage of an in-house SNP pipeline quickly disproved a possible correlation eight clinical L. monocytogenes isolates had to current food and environmental isolates within Florida. This highlights the BFL’s capability to promptly identify in-state foodborne outbreaks using a high resolution hqSNP-based approach.