Abstract

ABSTRACTIn this study, we addressed different aspects regarding the implementation of quasimetagenomic sequencing as a hybrid surveillance method in combination with enrichment for early detection of Listeria monocytogenes in the food industry. Different experimental enrichment cultures were used, comprising seven L. monocytogenes strains of different sequence types (STs), with and without a background microbiota community. To assess whether the proportions of the different STs changed over time during enrichment, the growth and population dynamics were assessed using dapE colony sequencing and dapE and 16S rRNA amplicon sequencing. There was a tendency of some STs to have a higher relative abundance during the late stage of enrichment when L. monocytogenes was enriched without background microbiota. When coenriched with background microbiota, the population dynamics of the different STs was more consistent over time. To evaluate the earliest possible time point during enrichment that allows the detection of L. monocytogenes and at the same time the generation of genetic information that enables an estimation regarding the strain diversity in a sample, quasimetagenomic sequencing was performed early during enrichment in the presence of the background microbiota using Oxford Nanopore Technologies Flongle and Illumina MiSeq sequencing. The application of multiple displacement amplification (MDA) enabled detection of L. monocytogenes (and the background microbiota) after only 4 h of enrichment using both applied sequencing approaches. The MiSeq sequencing data additionally enabled the prediction of cooccurring L. monocytogenes strains in the samples.IMPORTANCE We showed that a combination of a short primary enrichment combined with MDA and Nanopore sequencing can accelerate the traditional process of cultivation and identification of L. monocytogenes. The use of Illumina MiSeq sequencing additionally allowed us to predict the presence of cooccurring L. monocytogenes strains. Our results suggest quasimetagenomic sequencing is a valuable and promising hybrid surveillance tool for the food industry that enables faster identification of L. monocytogenes during early enrichment. Routine application of this approach could lead to more efficient and proactive actions in the food industry that prevent contamination and subsequent product recalls and food destruction, economic and reputational losses, and human listeriosis cases.

Highlights

  • Background microbiota Listeria sppMF4030 MF8051 MF2618 MF6987 MF2623 Non-Listeria strains MF8071 MF8072 MF8068 MF5883 MF8070 MF8056 MF6692 MF5529 MF8054 MF8063L. innocua L. innocua L. ivanovii L. ivanovii L. welshimeriBacillus cereus group sp

  • Cultures containing the seven L. monocytogenes strains were analyzed to assess the proportion of each strain using two methods: (i) dapE colony PCR of colonies from Listeria-selective agar plates followed by Sanger sequencing and (ii) DNA extraction from culture pellets, dapE PCR, and Illumina MiSeq sequencing

  • Phylogenetic source tracking was possible using sequencing data obtained from enrichment cultures from 24 h onwards to 48 h of enrichment, giving the same result as Whole-genome sequencing (WGS) data from individual isolates obtained by classical culture techniques

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Summary

Objectives

We did not attempt to reconstruct any genomes or plasmids with our data, as our aim was primarily to detect L. monocytogenes and to predict cooccurring STs

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