Evolved populations of Listeria monocytogenes related to biofilm formation and biocide stress in the context of food production environment niches

TL;DR

This study explores how Listeria monocytogenes adapts to harsh food production environments by forming biofilms and becoming resistant to disinfectants.

Contribution

The study identifies specific genetic mutations linked to biofilm persistence and biocide resistance in Listeria monocytogenes.

Findings

Mutations in genes related to metal homeostasis, stress response, and pyrimidine biosynthesis were found in evolved Listeria populations.

Reduced susceptibility to benzalkonium chloride arose through multiple mutations in the fepRA operon.

Fixed mutations in biofilm lineages were identified in loci like ykoK, pyrimidine synthesis operon, and rsbU.

Abstract

Cleaning and disinfection of food production environments (FPE) are fundamental components of food safety programmes designed to control microbial pathogens and prevent food contamination. Yet, FPE can still harbour foodborne pathogens, including Listeria monocytogenes, a significant concern to food manufacturers and health authorities due to the high mortality rate associated with invasive listeriosis. Mechanisms contributing to L. monocytogenes persistence in FPE include biofilm formation and reduced susceptibility to biocides, such as benzalkonium chloride (BC), for which several mechanisms are known. We hypothesized that prolonged exposure to disinfectants and other FPE-associated stressors would drive L. monocytogenes adaptation, resulting in the accumulation of genetic mutations linked to biofilm formation and reduced biocide susceptibility. To test this, we developed a biofilm persistence model, which studied 30 consecutive passages of biofilm-associated cells grown on stainless steel under sub-inhibitory BC concentrations. Whole-genome sequencing of evolved populations identified mutations that were associated with biofilm lineages and/or BC exposure. Non-synonymous mutations were identified in genes and pathways involved in metal homeostasis, stress response and pyrimidine biosynthesis. In addition, reduced susceptibility to BC arose through multiple independent mutations within the fepRA operon, encoding FepR transcriptional repressor and FepA MATE efflux pump. These mutations were observed across both planktonic and biofilm lifestyles, resulting in a comparable level of reduced susceptibility to BC in both states. Several loci with fixed mutations associated with biofilm lineages were identified, including the ykoK riboswitch leader, the pyrimidine synthesis operon and the stress response-related gene rsbU. Collectively, these findings provide new insights into the genetic mechanisms underlying L. monocytogenes biofilm persistence and reduced biocide susceptibility in the context of FPE and reveal novel targets potentially exploited by L. monocytogenes to establish and maintain niches in unfavourable environments.

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