LRUE Fièvre Aphteuse

URL: 
https://eurl-fmd.anses.fr
Background type: 
color
Intro [EN]: 

The European Union Reference Laboratory organises Proficiency Tests (PTs) on detection and typing of Foot-and-Mouth disease virus in accordance with the Regulation (EU) No 2017/625.

PT panels for FMDV and SVDV detection are established for virus isolation, RT-PCR, Antigen-ELISA and VP1 sequencing. PT panels for FMD antibody detection are established for FMDV NSP antibodies, FMDV SP antibodies and SVDV antibodies detection by ELISAs or/and virus neutralisation test.

The proficiency test (PT) for FMD virus and SVD virus and antibody detection is organised annually. All EU national reference laboratories (NRLs) and other official laboratories of the network are invited to participate.

Intro [EN]: 

The European Union Reference Laboratory yearly organizes a workshop, especially intended for the EU national reference laboratories (NRLs) and other official laboratories of the network.

The purpose of these workshops is to inform the participants about the activities of the EURL, to present and discuss the results of the PT, to present and discuss scientific research projects and to exchange information on EU legislation, methods and other relevant subjects.

 

 Registration to the next workshop

Intro [EN]: 

The EURL for FMD, among other missions, gathers data and information on the methods of diagnosis and differential diagnosis used in the different National Laboratories.

A list of methods inspired by the WOAH official methods is available on this website.

Intro [EN]: 

The EURL for FMD supports the functions of National Laboratories by storing and supplying reagents and materials for use in diagnosis of foot-and-mouth disease such as virus and/or inactivated antigens, standardised sera, cell lines and other reference reagents.

A list of reagents and material is available on this website.

Display Name: 
Foot-and-Mouth disease
Title [FR]: 
Méthodes
Title [EN]: 
Methods
Title [FR]: 
Réactifs disponibles et matériaux de référence
Title [EN]: 
Available reagents and reference materials
Methods Background: 
Materiau Background: 
Code AT Internet: 
603911
Nom page d'accueil (AT): 
Accueil LRUE FA
Intro [EN]: 

The European Union Reference Laboratory organizes each year trainings specifically intended for the EU national reference laboratories (NRLs) and other official laboratories of the network.

The purpose of these sessions is to implement the further training of experts in laboratory diagnosis with the goal to harmonize the diagnostic techniques at the European and International levels.

Registration to the next training

Presentation - Worshop 2021

Workshop 2021

Annual Workshop of Foot-and-Mouth Disease

From 14 October 2021 to 14 October 2021

 

 

The FMD EURL team would like to thank you for your presence and participation to the 2021 FMD Workshop. The online webinar was a success.

 

 

Please, find here :

Presentations of the event

Certificate of attendance 2021 available until 07 december 2021.

 

The workshop report is available below.

 

The EURL team remains at your disposal for any further information.

 

The EURL Team

You must be logged in for downloading the report, click on the button below to proceed

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Scientific meeting of GFRA 2021

The next Scientific meeting of the Global Foot and Mouth disease Research Alliance will be held 1 - 3 November 2021 as a virtual edition due to the COVID-19 pandemic :

https://www.gfra2021.com/home-site/

WOAH Terrestrial Manual 2022

 

All methods used for FMD detection, including commercial kits, must be WOAH-based methods validated according to international standards.

You will find attached the most recent version of the WOAH terrestrial manual chapter regarding foot-and-mouth disease.

 

FDMV detection and typing - Decision tree

 

Diagnostic methods for FMD detection and typing are described in the WOAH Terrestrial Manual.

This document sums up the diagnostic strategy as a decision tree describing the workflow for implementation of the different methods prescribed. 

All methods used, including commercial kits, must be WOAH-based methods validated according to international standards and used successfully in the annual PT.