EFSA statement on the requirements for whole genome sequence analysis of microorganisms intentionally used in the food chain

• Published in: EFSA journal Vol. 19; no. 7; pp. e06506 - n/a
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.07.2021; John Wiley and Sons Inc; Wiley
• Subjects: Antimicrobial agents; Councils; Data analysis; Enzymes; Food additives; food chain; Food chains; Fungi; Genetic modification; Genetically altered foods; Genetically engineered microorganisms; Genomes; intentional use; Metabolites; Microorganisms; Nucleotide sequence; Nutrition; Organisms; Quality control; Regulation; Resistance factors; Risk assessment; Software; Statement; Strains (organisms); Taxonomy; Virulence; Virulence factors; whole genome sequence‐based data; food chain; intentional use; whole genome sequence‐based data; microorganisms
• ISSN: 1831-4732; 1831-4732
• DOI: 10.2903/j.efsa.2021.6506

Microorganisms, genetically modified or not, may be used in the food chain as such or as production organisms of substances of interest. The placement of such microorganisms or derived substances/products in the European market may be subject to a pre‐market authorisation process. The authorisation process defines the need to perform a risk assessment to establish the safety and/or the efficacy of the microorganisms when used in the food chain as such or as production strains of substances of interest. In order to perform a risk assessment, the microorganism/s subject to the application for authorisation need/s to be characterised. In this regard, data obtained from whole genome sequence analysis can provide information on the unequivocal taxonomic identification of the strains and on the characterisation of their potential functional traits of concern which may include virulence factors, resistance to antimicrobials of clinical relevance for humans and animals, production of known toxic metabolites. In fact, in some areas of the regulated products, the use of whole genome sequence‐based data has been established as a requirement for the risk assessment. This document provides recommendations to applicants on how to describe the process and results which should be provided to the risk assessor in the context of an application for market authorisation of a regulated product. Indications are given on how to perform WGS and the quality criteria/thresholds that should be reached as well as the data and relevant information that need to be sent along whenever such kind of data is required.