Utility of Whole Genome Sequencing To Describe the Persistence and Evolution of Listeria monocytogenes Strains within Crabmeat Processing Environments Linked to Two Outbreaks of Listeriosis

Author:

ELSON RICHARD12,AWOFISAYO-OKUYELU ADEDOYIN2,GREENER TREVOR3,SWIFT CRAIG1,PAINSET ANAÏS12,AMAR CORINNE FRANCOISE LAURENCE1,NEWTON AUTILIA4,AIRD HEATHER5,SWINDLEHURST MARK5,ELVISS NICOLA5,FOSTER KIRSTY6,DALLMAN TIMOTHY J.12,RUGGLES RUTH1,GRANT KATHIE12

Affiliation:

1. Public Health England, National Infection Service, 61 Colindale Avenue, London NW9 5EQ, UK

2. National Institute for Health Research Health Protection Research Unit (NIHR HPRU) in Gastrointestinal Infections, University of Liverpool, Liverpool L3 5TR, UK

3. North Tyneside Council, Public Protection Services, The Silverlink North, Cobalt Business Park, North Tyneside NE27 0BY, UK

4. Public Health England UKOT Program IHR, 133-135, Wellington Road, London SE1 8UG, UK

5. Public Health England, National Infection Service, Food, Water and Environmental Microbiology Laboratory, National Agri-Food Innovation Campus, Block 10, Sand Hutton, York YO41 1LZ, UK

6. Public Health England, North East PHE Centre, Floor 2 Citygate, Gallowgate, Newcastle-upon-Tyne NE1 4WH, UK

Abstract

ABSTRACT This article describes the identification and investigation of two extended outbreaks of listeriosis in which crabmeat was identified as the vehicle of infection. Comparing contemporary and retrospective typing data of Listeria monocytogenes isolates from clinical cases and from food and food processing environments allowed the detection of cases going back several years. This information, combined with the analysis of routinely collected enhanced surveillance data, helped to direct the investigation and identify the vehicle of infection. Retrospective whole genome sequencing (WGS) analysis of isolates provided robust microbiological evidence of links between cases, foods, and the environments in which they were produced and demonstrated that for some cases and foods, identified by fluorescent amplified fragment length polymorphism, the molecular typing method in routine use at the time, were not part of the outbreak. WGS analysis also showed that the strains causing illness had persisted in two food production environments for many years and in one producer had evolved into two strains over a period of around 8 years. This article demonstrates the value of reviewing L. monocytogenes typing data from clinical cases together with that from foods as a means of identifying potential vehicles and sources of infection in outbreaks of listeriosis. It illustrates the importance of reviewing retrospective L. monocytogenes typing alongside enhanced surveillance data to characterize extended outbreaks and inform control measures. Also, this article highlights the advantages of WGS analysis for strain discrimination and clarification of evolutionary relationships that refine outbreak investigations and improve our understanding of L. monocytogenes in the food chain.

Publisher

International Association for Food Protection

Subject

Microbiology,Food Science

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