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

Page 224

Appendix 34

Influence of Exposure Intensity on Efficiency and Speed of FMD Transmission Soren Alexandersen1,2*, Melvyn Quan1, Ciara M Murphy1, Zhidong Zhang1 and Stephanie Durand1 1 Pirbright Laboratory, Institute for Animal Health, Ash Rd, Woking, Surrey, GU24 0NF, UK. 2 Current address: Danish Institute for Food and Veterinary Research, Department of Virology, Lindholm, DK-4771 Kalvehave, Denmark. Abstract FMDV can be spread by a variety of mechanisms including direct animal-to-animal contact, indirect contact facilitated by contaminated materials or airborne spread. The rate of spread, the incubation period until developing clinical signs of disease, as well as the severity of disease depends on many variables, including the dose received, the route of introduction, the virus strain, the animal species and the conditions under which the animals are kept. We previously presented data modelling infection in pigs directly inoculated with virus and also presented some experiments with varied intensity of contact among infected and susceptible pigs. Much more knowledge in regards to these variables is needed if model predictions are to be used in practical disease control. Here we extend our previous findings with more detailed studies in pigs exposed by contact to facilitate a better assessment of transmission risks. We used groups of pigs inoculated with the FMDV O UKG 34/2001 strain and an experimental set-up that allowed the infectiousness and intensity of contact among pigs to be varied. Experiments with other strains of FMDV and experiments using sheep are also briefly mentioned. Virus replicated rapidly in inoculated pigs and when exposed by direct contact the mean incubation period was from 1-10 days for pig-to-pig transmission depending on the infectiousness of the source and the intensity of contact. These differences confirm our previous notion that a strong correlation exists between dose (i.e. infectiousness of source and intensity of contact) and length of incubation period, severity of clinical disease and efficiency of spread. Clearly, local conditions are of immense importance in determining efficiency and speed of FMD transmission and can be an important determinant for the outcome of an initial outbreak and a considerable source of inaccuracy if not truthfully accounted for in mathematical models of epidemiological spread. Introduction FMDV can be spread by a variety of mechanisms and the rate of spread and the incubation period as well as the severity of disease depends on many variables. These variables include the dose received, the route of introduction, the virus strain, the animal species and the conditions under which the animals are kept. We have previously presented data modelling infection in pigs directly inoculated with virus and also presented some experiments with varied intensity of contact among infected and susceptible pigs. Here we extend our previous findings with more detailed studies in pigs exposed by contact to facilitate a better assessment of transmission risks. Much more knowledge about these variables is needed if model predictions are to be used in practical disease control. Materials and Methods Animals and virus One hundred and fifty four Landrace cross-bred Large White pigs weighing between 20 and 30 kg were used and inoculation was by heel pad injection or by contact as described previously (Alexandersen et al., 2001; Alexandersen et al., 2002a; Alexandersen et al., 2003b; Alexandersen & Donaldson, 2002). These pigs were part of experiments conducted for several purposes and the descriptions and results described in the present paper are directed towards describing transmission aspects. Twelve sheep were housed and inoculated in the coronary band or kept as contacts as described previously (Alexandersen et al., 2002b; Alexandersen et al., 2003b; Alexandersen & Donaldson, 2002).The usual dose for inoculation was approximately 0.25-0.5 ml of a 1:10 dilution of virus stock containing 105.6-5.9 TCID50 (BTY) of O UK 34/2001 virus (first pig passage). Contact pigs where kept in direct contact with inoculated (donor) pigs for various periods of time and in various numbers as described for the individual experiments. The progression of disease were assessed daily using a subjective scoring system (Alexandersen et al., 2003b; Quan et al., 2004). Body temperatures were recorded daily and blood and swab samples collected as needed. Animals

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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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