Long-term study of Cryptosporidium prevalence on a lowland farm in the United Kingdom

• Published in: Veterinary parasitology Vol. 116; no. 2; pp. 97 - 113
• Main Authors: Sturdee, A.P., Bodley-Tickell, A.T., Archer, A., Chalmers, R.M.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 08.10.2003
• Subjects: Animals; Animals, Domestic - parasitology; Animals, Wild - parasitology; Cryptosporidiosis - epidemiology; Cryptosporidiosis - veterinary; Cryptosporidium - isolation & purification; Cryptosporidium parvum; Cryptosporidium parvum - isolation & purification; Feces - parasitology; Female; Livestock; Longitudinal survey; Male; Oocysts; Parasite Egg Count - veterinary; Prevalence; Rodents; Seasonal dynamics; Seasons; United Kingdom - epidemiology; Longitudinal survey; Livestock; Prevalence; Cryptosporidium parvum; Rodents; Seasonal dynamics
• ISSN: 0304-4017; 1873-2550
• DOI: 10.1016/S0304-4017(03)00261-9

A longitudinal sample survey testing for Cryptosporidium in livestock and small wild mammals conducted over 6 years (1992–1997) on a lowland farm in Warwickshire, England, has shown the parasite to be endemic and persistently present in all mammalian categories. Faecal samples were taken throughout the year and oocysts concentrated by a formal ether sedimentation method for detection by immunofluorescence staining using a commercially available genus specific monoclonal antibody. Cryptosporidium parvum was identified by morphology and measurement of modified Ziehl-Neelsen stained oocysts. C. muris was rarely found in wild mammals and C. andersoni oocysts were never detected in livestock. Faecal samples from 3721 individuals gave cumulative 6-year prevalences for C. parvum as follows: bull beef, 3.6%; dairy cows, 3.5%; ewes, 6.4%; horses, 8.9%; calves (home bred), 52%; calves (bought-in) 23.2%; lambs, 12.9%; small wild mammals (rodents) living in and around farm buildings, 32.8%; small wild mammals (mainly rodents) living in areas of pasture, 29.9%. Animal categories with the highest prevalences also shed the highest average oocyst numbers per gram of faeces (ranging from 1.4×10 3 for bull beef to 1.1×10 5 for calves). Analysis of annual and seasonal data for each animal category revealed that patterns of infection were variable and sporadic; this means that short-term sampling was never likely to provide a true or representative picture. Seasonally combined data for adult livestock, young livestock and small wild mammals showed all three categories tended to have the highest Cryptosporidium prevalences in the autumn. Calves were separated from their dams within 24 h of birth and yet showed high prevalence of infection in most years despite the low prevalence for the dairy herd. It is possible the coincidence of high autumn prevalence in mice with the main period for the rearing of calves contributed to the infection of the latter. The farming estate was used to teach students of agriculture and took pride in good land management and husbandry practices that produced well fed and healthy livestock. The data from this estate may represent, therefore, the baseline, the lowest possible levels to be expected, for Cryptosporidium infection and oocyst production on a lowland farm in the United Kingdom.