update on the annual reporting of vtec in the eu and on ... · pdf filefor e. coli in the eu...
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9th Annual Workshop of the NRLs for E. coli in the EU Rome, 20-21 October 2014
Update on the annual reporting of VTEC in the EU and on EFSA activities for molecular typing data collection for food ad animal isolates
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NEW EFSA STRUCTURE
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AGENDA
Update on the annual reporting of VTEC in the EU
EFSA activities for molecular typing data collection for food ad animal isolates
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VEROTOXIGENIC ESCHERICHIA COLI
• 21 MSs and one non-MSs reported data on VTEC in
food
• 11 MSs reported data on VTEC in animals
• Different investigations are not necessarily directly comparable owing to differences in sampling strategies and the analytical methods applied
o The most widely used analytical method, ISO 16654/2001, aims to detect only VTEC O157,
o Fewer investigations have been conducted with analytical methods aiming at detecting all VTEC or selected non-O157 serotypes of VTEC (e.g. ISO/PRF TS 13136:2012)
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In 2012, nine MSs reported data on VTEC in fresh bovine meat out of 4,603 units tested: 1.3% VTEC-positive and 0.1% VTEC O157-positive
VEROTOXIGENIC ESCHERICHIA COLI
N pos % pos N pos % pos
Austria fresh at retail single 25 g 56 1 1.8 0 0
O51:H49 eae positive
vtx1 negative vtx2
positive
carcase at
slaughterhouse,
carcase swab
single 1,600 cm2 453 4 0.9 1 0.2
fresh at processing batch 25 g 374 2 0.5 2 0.5
Czech Republic
carcase at
slaughterhouse,
carcase swab
batch 400 cm2 622 8 1.3 0 0
O103 eae positive vtx2
positive (1), O103 eae
positive vtx1 positive
(1), O104 (3), O145
eae positive vtx1
positive (1), O145 (2)
France fresh at processing single 25 g 1,923 7 0.4 3 0.2
O103:H2 eae positive
and stx1 positive (2),
O26:H11 eae positive
and stx2 positive (2),
O157:H7 eae positive,
stx1 and stx2 positive
(2), O157:H7 eae
positive and stx2
positive (1)
Germany
carcase at
slaughterhouse,
carcase swab
single 25 g 315 18 5.7 0 0
Hungary fresh at processing single 25 g 77 0 0 0 0
Netherlands fresh at retail single 25 g 555 18 3.2 0 0
Polandfresh at unspecified
sampling levelbatch 25 g 25 0 0 0 0
Romania
carcase - chilled at
slaughterhouse,
carcase swab
batch 100 cm2 203 0 0 0 0
Total (9 MSs) 4,603 58 1.3 6 0.1
Country DescriptionSample
unitN
VTEC VTEC O157VTEC serogroups
Sample
weight
Belgium
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In 2012, seven MSs reported data on VTEC in cattle out of 7,843 units tested: 7.4% VTEC-positive and 1.8% VTEC O157-positive
VEROTOXIGENIC ESCHERICHIA COLI
N pos % pos N pos % pos
adult cattle over 2 years at
slaughterhouse,
recto-anal swab
animal 56 18 32.1 0 0
eae negative vtx1 negative vtx2 positive: O113:H21 (2), O178:HNM (1),
O39:H48 (1), O113:H4 (1), O46:H2 (1), O43:Hrough (1), O178:H19 (1),
ONT:H21 (1)
eae negative vtx1 positive vtx2 positive: O183:H18 (2), O91:H21 (1),
Orough:H28 (1), O178:H19 (1), O179:HNM (1), O15:H2 (1), Orough:H2 (1)
eae positive vtx1 positive vtx2 negative: O129:HNM (1)
young cattle (1-2 years) at
slaughterhouse,
recto-anal swab
animal 56 20 35.7 1 1.8
eae negative vtx1 negative vtx2 positive: Orough:H21 (1), O91:H10 (1),
O91:H21 (1), O179:H8 (2), O39:H48 (2), ONT:Hrough (1), O36:Hrough (1),
O179:Hrough (1), O109:H16 (1), O113:H4 (1)
eae negative vtx1 positive vtx2 negative: O168:H8 (2)
eae negative vtx1 positive vtx2 positive: O15:HNM (1), O91:H21 (1),
O178:H12 (1), O22:H8 (2), Orough:HNM (1), O185:H5 (1), O36:H2 (1)
eae positive vtx1 positive vtx2 negative: O103:H2 (1), O26:HNM (3)
eae positive vtx1 positive vtx2 positive: O157:HNM (1)
Denmark at slaughterhouse, faeces animal 25 g 251 21 8.4 21 8.4
Estonia at slaughterhouse, hide animal cm2 246 13 5.3 13 5.3
Finland at slaughterhouse, faeces animal 10 g 1,553 27 1.7 27 1.7
at farm, domestic animal 925 127 13.7 2 0.2 VTEC O103 (2), VTEC O26 (1), VTEC O91 (1)
at farm, domestic herd 709 101 14.2 2 0.3 VTEC O103 (2), VTEC O26 (1), VTEC O91 (1)
calves (under 1 year) at farm,
domesticanimal 542 12 2.2 2 0.4 VTEC O103 (2), VTEC O26 (1)
calves (under 1 year) at
slaughterhouse, caecum,
domestic
animal 25 g 325 78 24.0 0 0
calves (under 1 year) at farm,
domesticherd 692 89 12.9 2 0.3 VTEC O103 (2), VTEC O26 (1)
Italy at slaughterhouse, domestic animal g 112 2 1.8 2 1.8
Swedenat slaughterhouse, faeces,
domesticanimal 2,376 73 3.1 73 3.1 VTEC O157:H (73)
Total (7 MSs) 7,843 581 7.4 145 1.8
Country DescriptionSample
unitN
VTEC VTEC O157VTEC serogroups
Sample
weight
Austria
Germany
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With regards to the data reported on VTEC isolates from food and animal samples, it is evident that the analytical method used to detect the bacteria has a major influence on the number of positive samples observed.
Human pathogenic VTEC strains were detected by the reporting MSs from fresh bovine meat occasionally and at low levels. The human pathogenic VTEC serogroups isolated from bovine meat and cattle samples included VTEC O157, O26, O91, O103 and O145.
VEROTOXIGENIC ESCHERICHIA COLI
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The importance of bovine meat as a source of human VTEC infections in humans is confirmed by the reported food-borne outbreak data from 2012. Overall, 41 outbreaks caused by human pathogenic E. coli were reported. Out of the total, 12 were supported by strong-evidence. 9 outbreaks were due to VTEC O157, 1 to VTEC O113:H4, 1
to ‘other’ VTEC serogroups, and 1 to non-grouped E. coli positive for LT genes.
Six of them were linked to bovine meat and products thereof. Moreover, 10 strong-evidence VTEC waterborne outbreaks were reported, all by Ireland, and seven were reported to be linked to private water supplies or wells.
VEROTOXIGENIC ESCHERICHIA COLI
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AGENDA
Update on the annual reporting of VTEC in the EU
EFSA activities for molecular typing data collection for food ad animal isolates
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MOLECULAR TYPING DATA COLLECTION IN THE EU
• The Standing Committee on Food Chain and Animal Health
(representing all EU Member States) approved in December 2012
Vision paper on the development of databases for molecular testing of food-borne pathogens in view of outbreak
preparedness
• The paper was prepared by the EU Commission in consultation with ECDC, EFSA and the EU Reference Laboratories (EURLs).
• The purpose is to encourage collection of molecular typing data to allow integration of data on isolates from human cases, food and animals.
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• Regular joint analyses of the data by ECDC, EFSA and EURLs – integration at the EU level
o ECDC to collect molecular typing data from food-borne pathogens isolated from human cases
o EFSA to collect similar data from food, feed and animal isolates, in close collaboration with relevant EURLs
• Ownership of the data
o The reporting Member States
o EU Commission if it has financed EURL’s typing or other research projects
• The data collection to cover initially Salmonella, VTEC and Listeria with PFGE and MLVA (S. Typhimurium) methods
• Other methods and pathogens can be taken aboard later on
MOLECULAR TYPING DATA COLLECTION IN THE EU
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MOLECULAR TYPING DATA COLLECTION IN THE EU
In particular, EFSA is requested:
1. to develop and manage a database on the above specified isolates from food and animals; access to the database will at all times require the agreement of EFSA, except for national data which should remain accessible for the respective national institutes;
2. to develop, jointly with the ECDC and in consultation of the relevant EURL, a data dictionary with harmonised parameters for the data fields and terminology to be used, when appropriate, in both the database on food and animals isolates and in the database developed by ECDC on human isolates;
3. to develop tools for the uploading of data by the EURL, the respective food/feed NRLs and other official control laboratories;
Terms of Reference
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MOLECULAR TYPING DATA COLLECTION IN THE EU
In particular, EFSA is requested:
4. to develop a tool allowing relevant EURL to be involved in the curation of the incoming molecular testing data and the regular verification of database consistency; the involvement of the EURL will be part of their work programme financed by the EU;
5. when considered necessary, to update, jointly with ECDC and in consultation with the relevant EURL, scientific parameters (experiment settings, terminology) included in the database;
6. to regularly provide scientific analyses of the data in collaboration with ECDC and the relevant EURL.
Terms of Reference
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MOLECULAR TYPING DATA COLLECTION IN THE EU
EFSA has set up a Working Group:
Objectives:
To define the structure of the data collection system and integration with the human data
To guarantee compatible data collection systems for human, food, feed and animal isolates, based on:
Common nomenclature
Common data dictionaries
Experts from:
ECDC
EURL Salmonella
EURL Listeria
EURL E. coli
National reference laboratories
WG Meetings: 10 meetings held
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MOLECULAR TYPING DATA COLLECTION IN THE EU
EFSA has launched three procurements for assistance related to establishing molecular typing data collection for isolates from food, feed and animals.
• Objectives:
– To produce Standard Operating Procedures for molecular testing of Salmonella, Listeria and VTEC isolates and interpretation of molecular typing data
• Procurements signed with the relevant EURLs:
– Salmonella,
– Listeria,
– E. coli
• Meetings: 4 meetings held
• Deliverables: Final SOPs (under final approval)
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STRUCTURE OF THE MOLECULAR TYPING SYSTEM
Laboratories from
food/veterinary side
TESSy server
Human reference
laboratories
curators
· Data curation
· Reference data typing
· Joint cluster analysis
· Web interface
Joint
EFSA-
ECDC
database
EFSA environment ECDC environment
EFSA Server
EFSA
molecular
typing
database
Selective
data transfer
Typing Data and
Limited set of Epidemiological Data
Data retrieval
Curated data
Reference type
Curator’s comments
Cluster code
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Users and their roles in the Joint ECDC-EFSA database
User Role for food/feed/ animal data Role for human data
Users at MS level
Nominated users for food/veterinary side Data Provider -
Nominated users for Public Health side - Data Provider
Curators
EURL Data Curator / Data analyst -
ECDC curator - Data Curator / Data analyst
European bodies
EFSA Data manager/ Data analyst Data analyst
ECDC Data analyst Data manager/ Data analyst
1
MOLECULAR TYPING DATA COLLECTION
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MOLECULAR TYPING DATA COLLECTION
NOTE: Data should be provided at result-based level according to the Standard Sample Description version 2 (SSD2).
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MOLECULAR TYPING DATA COLLECTION
Data providers shall guarantee the uniqueness of the identifiers for each submitted PFGE image, result, isolate, sample taken at the national level. If one country has several data providers collecting data, it shall coordinate internally to guarantee the uniqueness of the codes at national level. The responsibility to guarantee uniqueness is completely on MS side and each country can freely adopt any approach to coordinate laboratories in order to satisfy the requirement of having unique ids.
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• Epidemiological Data: data about an isolate in terms of sampling time and place, origin (food/ animal type, country of origin, producer) etc. - partly sensitive data
• Typing Data: the results of typing experiments performed on an isolate. e.g. serotype, PFGE pattern, antimicrobial susceptibility results, MLVA results – non sensitive data
MOLECULAR TYPING DATA COLLECTION
EPIDEMIOLOGICAL DATA (PARTLY SENSITIVE) TYPING DATA (NOT SENSITIVE BY ITSELF)
ID Country Animal/Food
Type
Area in the
country
Date of
Sample Serotype PFGE_XbaI AST_NAL
EFSA-001 BE Smoked salmon X 2012-06-01 STANLEY S
EFSA-002 HU Turkey Y 2012-07-01 STANLEY R
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MOLECULAR TYPING DATA COLLECTION
Accessibility to the joint database
The access to joint EFSA-ECDC database depends on the type of data (sensitive and non-sensitive) and the users.
Use of data
In line with the orientations provided in the Vision paper, a Collaboration Agreement will be signed by all parties to define data ownership, access, use, publication, procedures and confidentiality.
‘Data owners are always consulted for their permission before
any written or oral publication and/or communication of the data which have not yet been published’
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STATUS OF PROGRESS
WG activities
No other meeting of the WG are scheduled.
The technical requirements for the pilot phase have been agreed.
The technical report will be published by end of the year.
Procurements (SOPs for molecular testing and interpretation)
Final reports are under final approval and will be published on the EFSA website.
Trilateral meeting with EC and ECDC
Discussion on policy for data access, cluster analysis, collaboration agreement, Steering Committee.
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NEXT STEPS
A Collaboration Agreement is under preparation to ensure a common understanding and approach between all the parties involved with regard to:
data ownership, availability, access, use, publication, procedures, confidentiality.
A Steering Committee will be set up to:
Monitor and evaluate the pilot phase
Identify needs for revision of the data collection system
Develop standard operating procedures for scientific data analyses
It will be a joint Committee composed by staff members from ECDC and EFSA, the relevant EURLs and ECDC’s curators.
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Contacts in EFSA [email protected]
http://www.efsa.europa.eu/en/contact/askefsa.htm
All our reports are on www.efsa.europa.eu