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Proceedings of the 10th International Colloquium on Paratuberculosis

Proceedings of the 10th International Colloquium on Paratuberculosis

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#200<br />

Use <str<strong>on</strong>g>of</str<strong>on</strong>g> multiple tests to determine <str<strong>on</strong>g>the</str<strong>on</strong>g> status <str<strong>on</strong>g>of</str<strong>on</strong>g> UK dairy herds with respect to Mycobacterium<br />

avium subsp. paratuberculosis<br />

Alasdair Cook, Alberto Vidal-Diez, Mark Arnold, Robin Sayers, George Caldow, Adrian McGoldrick,<br />

John D<strong>on</strong>aghy, Samuel Strain, Ian Gardner<br />

Veterinary Laboratory Agency, DEFRA, United Kingdom; Scottish Agricultural College, United Kingdom; Agri-Food<br />

and Biosciences Institute, United Kingdom; University <str<strong>on</strong>g>of</str<strong>on</strong>g> California, USA<br />

A random sample <str<strong>on</strong>g>of</str<strong>on</strong>g> 136 UK dairy herds was recruited to a survey to estimate <str<strong>on</strong>g>the</str<strong>on</strong>g> proporti<strong>on</strong> <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g>se that were<br />

infected with Mycobacterium avium subsp. paratuberculosis (MAP). Three tests were employed: firstly, heparinised<br />

blood samples were collected from all female cattle over three years old and sera were tested using a<br />

commercial ELISA test (Pourquier); sec<strong>on</strong>dly, individual faecal samples were collected from <str<strong>on</strong>g>the</str<strong>on</strong>g>se cows and<br />

combined into pools <str<strong>on</strong>g>of</str<strong>on</strong>g> five which were inoculated into a liquid media system (Trek ESP II) for culture for MAP<br />

and finally, bulk milk samples were collected and tested for presence <str<strong>on</strong>g>of</str<strong>on</strong>g> MAP DNA by PCR targeting <str<strong>on</strong>g>the</str<strong>on</strong>g> IS900<br />

inserti<strong>on</strong> sequence. These tests are all imperfect and <str<strong>on</strong>g>the</str<strong>on</strong>g>re is no “Gold Standard”. They were applied at different<br />

levels – to individual animals, to groups <str<strong>on</strong>g>of</str<strong>on</strong>g> 5 animals or to <str<strong>on</strong>g>the</str<strong>on</strong>g> entire herd. Each herd was categorised as<br />

positive (at least <strong>on</strong>e positive sample) or negative for each test. Bayesian approaches have been proposed<br />

(eg Branscum et al 2004; 2005) for data from two or more imperfect tests and we applied an integrated multilevel<br />

Bayesian model to <str<strong>on</strong>g>the</str<strong>on</strong>g> data to estimate <str<strong>on</strong>g>the</str<strong>on</strong>g> herd-level sensitivity and specificity <str<strong>on</strong>g>of</str<strong>on</strong>g> each test. The median<br />

herd level sensitivity (HSe) and specificity (HSp) and 95% credibility intervals were estimated for each test as<br />

follows: ELISA HSe 95%-100% and HSp 47%-53%; pooled faecal liquid culture HSe 54%-69% and HSp 98%-<br />

100%; bulk milk PCR HSe 13%-51% and HSp 57%-82%. Bayesian analysis incorporates prior estimates <str<strong>on</strong>g>of</str<strong>on</strong>g> parameter<br />

values based <strong>on</strong> existing knowledge and results can be sensitive to <str<strong>on</strong>g>the</str<strong>on</strong>g>se assumpti<strong>on</strong>s. We undertook<br />

a sensitivity analysis by varying <str<strong>on</strong>g>the</str<strong>on</strong>g> prior values that were used in our model. This showed that prior assumpti<strong>on</strong>s<br />

<str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> individual level specificity <str<strong>on</strong>g>of</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> ELISA test had a limited impact <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g> results described above.<br />

160

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