Open session of the standing technical committee of the EUFMD- 2004

Page 455

Appendix 72 Using NSP ELISA (Chekit-FMD-3ABC Bommeli-Intervet) as a Tool for FMDV Serosurveillance in Bulgaria Georgi Georgiev*¹, Emiliya Veleva¹, Liliyana Polihronova¹ and Alessandro Rossi² 1 National Diagnostic and Research Veterinary Medical Institute – Sofia, Bulgaria 2 Bommeli Diagnostics, Stationsstrasse 12, 3097 Liebefeld-Bern, CH Abstract: Bulgaria has adopted a non-vaccination strategy for the control of FMD since 1993 and is free country from the disease since 1996. For us is deeply important to have a high sensitive and exact laboratory method for early detection of FMDV infection and for serumsurveillance purposes. Therefore Bulgaria has more 300 km. common border with Turkey which use vaccination policy against FMDV in Thrace and a couple of FMD outbreaks caused by more than one and often some exotic FMDV strains each year have been reported in Anatolia. So, each serum sample should be tested minimum against 3 or 4 different serum types of FMDV currently circulating in the neighbouring countries. The commercial 3ABC NSP ELISA tests are available since 2001 on the market. We performed Bommeli-Intervet CHEKIT-FMD-3ABC ELISA test bov-ov in Bulgaria during 2 years period (2002-2003). On this paper we are going to summaries the results of evaluation of the test's sensitivity on the basis of the investigated serum samples. The CHEKIT-FMD-3ABC ELISA was used according to the manufacturers instruction (SOP), accompanied the testkit 4797 serum samples in 2002 and 5754 serum samples in 2003 have been tested using CHEKIT-FMD-3ABC ELISA Bommeli according to the Bulgarian National monitoring and surveillance FMDV program. Only 4 serum samples from cattle origin have been determined as NSP FMDV antibody positive on the basis of estimation of OD % value and confirming the results using additional NSP ELISA tests. The correlation between the number of non-conclusive and positive evaluated samples have been shown. CHEKITFMD-3ABC ELISA Bommeli-Intervet is easy to perform, reproducible and specific. The final result can be obtain in real time and the test can be use with success as a tool in FMDV surveillance programs in FMDV free countries bordering with endemic regions. The nonconclusive serum samples have to be retested using the same or the second confirmation test up to the full determination. Introduction Foot-and-mouth disease (FMD) is highly contagious viral and economically devastating disease of cloven-hoofed animals. The causative agent is aphtovirus belonging to the Picornaviridae family for which seven serum types have been described. The detection of antibodies to the nonstructural 3ABC poly protein is the single most reliable indicator of the infection and confirmation of serum conversion of these antibodies is evidence of infection with wild FMD virus (FMDV) (3, 4). Antibodies directed to the capsid proteins of FMDV are induced by both – inactivated (from vaccines) and live viruses (infection, carrier animals) therefore it is not possible to differemtiate the origin of the antibodies using routine Liquid Phase (LPBL) or Solid Phase ELISA tests. The non-structural proteins (NSP) of FMDV have received considerable attention in recent years with a search for improved serological tests for FMDV (5). For countries using vaccination in their strategy for the control of FMD outbreaks, it is of a great importance to differentiate post vaccine from post infection derived antibodies in order to discriminate FMDV which is circulated in the field (1). Bulgaria has adopted a non vaccination strategy for the control of FMD since 1993 and has a free country status from the disease since 1996. For us is important to have a high sensitive and exact laboratory method for early detection of FMDV infection and for serumsurveillance needs. Moreover Bulgaria has more than 300 km. common border with Turkey, which use vaccination policy against FMD in Thrace and each year reported of a couple of FMD outbreaks caused by more than one and often some exotic FMD viral strains. There also reports for presence of NSP FMDV serum positives in Thrace as a result of low, but still circulation of wild FMDV in that part of the country (1). The commercial 3ABC NSP ELISA tests are available on the market since 2001. In this paper we present the results of use of Bommeli FMDV 3 ABC NSP ELISA CHEKIT-test (bov-ov) as a tool for FMDV serum – surveillance programs in Bulgaria during 2 years period (2002-2003). We also would like to summary the results of evaluation of the test specificity.

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Appendix 82

17min
pages 492-500

Appendix 77

22min
pages 468-476

Appendix 78

25min
pages 477-484

Appendix 79

14min
pages 485-489

Appendix 81

1min
page 491

Appendix 80

1min
page 490

Appendix 76

12min
pages 464-467

Appendix 75

1min
page 463

Appendix 64

10min
pages 412-414

Appendix 72

13min
pages 455-460

Appendix 73

1min
page 461

Appendix 65

1min
page 415

Appendix 67

1min
page 424

Appendix 63

34min
pages 401-411

Appendix 62

2min
page 400

Appendix 54

8min
pages 361-363

Appendix 61

15min
pages 394-399

Appendix 55

11min
pages 364-366

Appendix 59

1min
page 385

Appendix 60

20min
pages 386-393

Appendix 56

1min
page 367

Appendix 42

21min
pages 270-276

Appendix 52

10min
pages 350-352

Appendix 50

21min
pages 330-339

Appendix 46

2min
page 307

Appendix 37

7min
pages 241-243

Appendix 38

7min
pages 244-246

Appendix 41

2min
page 269

Appendix 40

15min
pages 255-268

Appendix 36

16min
pages 236-240

Appendix 35

15min
pages 231-235

Appendix 34

25min
pages 224-230

Appendix 28

2min
page 198

Appendix 31

10min
pages 212-215

Appendix 29

16min
pages 199-203

Appendix 33

3min
pages 221-223

Appendix 27

1min
page 197

Appendix 26

27min
pages 188-196

Appendix 25

12min
pages 182-187

Appendix 23

8min
pages 168-171

Appendix 22

28min
pages 158-167

Appendix 15

2min
page 113

Appendix 16

7min
pages 114-116

Appendix 20 EMEA paper extract - Recommendations for tests for induction of antibodies to NSP antigens by FMD vaccines

4min
pages 144-145

Appendix 19

18min
pages 136-143

Appendix 14

4min
page 112

Appendix 13

10min
pages 107-111

Appendix 5

2min
page 64

Appendix 12

9min
pages 104-106

Appendix 3

9min
pages 47-49

Appendix 4

26min
pages 50-63

Appendix 8

12min
pages 77-80

Appendix 2

8min
pages 43-46

Open Session

6min
pages 39-42

Closed Session

2min
pages 37-38

Item 11 – Persistent and subclinical infections – diagnostic and surveillance issues

3min
page 33

Item 15 – Managing the decision-making process in control of FMD and in the priority setting of research and development

3min
page 36

Item 14 – Regulatory compliance

2min
page 35

Item 10 – International issues

3min
page 32

Item 9 – Novel vaccines

3min
page 31

Item 7 – Optimisation of conventional vaccines

3min
page 29

Item 4 – Managing diagnostic demands

3min
page 27

Item 8 – Regulatory issues affecting FMD vacine selection and use

3min
page 30

Item 3 – Transmission and its control

3min
page 26

3.4.2 Post-vaccination serosurveillance (PVS) for presence of FMD infected animals

3min
page 16

Item 1 – Recent findings in molecular epidemiology of FMDV

3min
page 24

Item 2 – Surveillance: for what purpose and how much is enough?

3min
page 25

4.2 Collection of sera/specimens for validation of DIVA tests for detection of animals received from SAT virus infection

3min
page 20
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