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欧洲食品安全局关于食物链中有意使用的微生物全基因组序列分析要求的声明。

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

出版信息

EFSA J. 2021 Jul 28;19(7):e06506. doi: 10.2903/j.efsa.2021.6506. eCollection 2021 Jul.

Abstract

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.

摘要

微生物,无论是否经过基因改造,都可以直接用于食物链,或作为生产相关物质的生物。此类微生物或其衍生物质/产品在欧洲市场的投放可能需要经过上市前授权程序。授权程序规定需要进行风险评估,以确定微生物在直接用于食物链或作为相关物质的生产菌株时的安全性和/或有效性。为了进行风险评估,需要对申请授权的微生物进行特性描述。在这方面,全基因组序列分析获得的数据可以提供有关菌株明确分类鉴定的信息,以及其潜在关注功能特性的表征,这些特性可能包括毒力因子、对人类和动物临床相关抗菌药物的耐药性、已知有毒代谢产物的产生。事实上,在受监管产品的某些领域,使用基于全基因组序列的数据已被确定为风险评估的一项要求。本文档就如何描述应在受监管产品上市授权申请中提供给风险评估人员的过程和结果向申请人提供建议。说明了如何进行全基因组测序以及应达到的质量标准/阈值,以及每当需要此类数据时需要一并发送的数据和相关信息。

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