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Can a Modified Latency-to-Lie Test be Used to Validate Gait-Scoring Results in Commercial Broiler Flocks?

Published online by Cambridge University Press:  11 January 2023

C Berg*
Affiliation:
Department of Animal Environment and Health, Swedish University of Agricultural Sciences, PO Box 234, SE-532 23 Skara, Sweden
G S Sanotra
Affiliation:
Department of Animal Science and Animal Health, The Royal Veterinary and Agricultural University, Grønnegårdsvej 8, DK-1870 Frederiksberg C, Copenhagen, Denmark
*
* Contact for correspondence and requests for reprints: [email protected]
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Abstract

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Bodily contact with water is a novel and aversive experience for broiler chickens, and this has been used when designing the Latency to Lie (LTL) test. The original testing procedure, in which the birds are tested in groups, involves a certain settling period, which makes the test time-consuming to carry out on commercial broiler farms. Our modifications of the LTL test for on-farm use mean that a) the birds are tested individually without visual contact with other birds; and b) the water tub is already filled with water when the birds are placed in it. The results from the LTL tests can then be compared with the scores achieved for each individual bird on the commonly used ‘gait scoring’ procedure. At 14 farms participating in a larger survey, we used three birds of each gait score from 0 to 4 (when available) for LTL testing. The time spent standing before making the first attempt to lie down was recorded. The results show a clear negative correlation (r = -0.86, P < 0.001) between time spent standing and gait score. The mean LTL values for the different gait scores were all significantly (P < 0.01) different. There was no significant difference in LTL results between flocks. The method described appears to be well suited for on-farm use. If further developed, it could become a useful tool in monitoring programmes for the ongoing efforts aiming at decreasing the levels of leg weakness in modern broiler production.

Type
Research Article
Copyright
© 2003 Universities Federation for Animal Welfare

References

Anonymous 2000 The welfare of chickens kept for meat production (broilers). Report of the Scientific Committee on Animal Health and Animal Welfare. European Commission, Health and Consumer Protection Directorate-General: Brussels, BelgiumGoogle Scholar
Butterworth, A 1999 Infectious components of broiler lameness: a review. World's Poultry Science Journal 55: 327352CrossRefGoogle Scholar
Clayton, D A 1978 Socially facilitated behaviour. The Quarterly Review of Biology 53: 373392CrossRefGoogle Scholar
Kestin, S C, Knowles, T G, Tinch, A E and Gregory, N G 1992 Prevalence of leg weakness in broiler chickens and its relationship with genotype. Veterinary Record 131: 190194CrossRefGoogle ScholarPubMed
Kestin, S C, Su, G and Sørensen, P 1999 Different commercial broiler crosses have different susceptibilities to leg weakness. Poultry Science 78(8): 10851090CrossRefGoogle ScholarPubMed
Lynch, M, Thorp, B H and Whitehead, C C 1992 Avian tibial dyschondroplasia as a cause of bone deformity. Avian Pathology 2: 275CrossRefGoogle Scholar
Rennie, J S and Whitehead, C C 1996 The effectiveness of dietary 25- and 1-hydroxy cholecalciferol in preventing tibial dyschondroplasia in broiler chickens. British Poultry Science 37: 413421CrossRefGoogle Scholar
Sanotra, G S, Lawson, L G, Vestergaard, K S and Gaardbo Thomsen, M 2001 Influence of stocking density on tonic immobility, lameness, and tibial dyschondroplasia in broilers. Journal of Applied Animal Welfare Science 4: 7187CrossRefGoogle Scholar
SAS Stat User's Guide 1990 Version 6, Edn 4. SAS Institute Inc: Cary NC, USAGoogle Scholar
Su, G, Sørensen, P and Kestin, S C 1999 Meal feeding is more effective than early feed restriction at reducing the prevalence of leg weakness in broiler chickens. Poultry Science 78: 949955CrossRefGoogle ScholarPubMed
Su, G, Sørensen, P and Kestin, S C 2000 A note on the effects of perches and litter substrate on leg weakness in broiler chickens. Poultry Science 79: 12591263CrossRefGoogle ScholarPubMed
Thorp, B H, Whitehead, C C, Cick, L, Bradbury, J M, Jones, R C and Wood, A 1993 Proximal femoral degeneration in growing broiler fowl. Avian Pathology 22: 325342CrossRefGoogle ScholarPubMed
Vestergaard, K S and Sanotra, G S 1999 Relationships between leg disorders and changes in the behaviour of broiler chickens. Veterinary Record 144: 205209CrossRefGoogle ScholarPubMed
Weeks, C A 2001 Development of a new method for quantitatively assessing lameness in broilers. British Poultry Science 42: S79S80Google Scholar
Weeks, C A, Danbury, T S, Davies, H C, Hunt, P and Kestin, S C 2000 The behaviour of broiler chickens and its modification by lameness. Applied Animal Behaviour Science 67: 111125CrossRefGoogle ScholarPubMed
Weeks, C A, Kerr, A E and Tilbrook, T 2001 Effect of settling period on the LTL test for lameness in broilers. British Poultry Science 42: S80S81Google Scholar
Weeks, C A, Knowles, T G, Gordon, R G, Kerr, A E, Peyton S T And Tilbrook, N T 2002 New method for objectively assessing lameness in broiler chickens. Veterinary Record 151: 762764Google ScholarPubMed