Prevalence of susceptibility to Cryptosporidium spp. among dairy calves with different feeding regimens with an emphasis on the feeding of transition milk

Background and Aim: Colostrum composition and importance for newborn organisms were repeatedly studied. However, the interest in transitional milk usefulness is weak and recommendations concerning transition milk intake are not developed. The aim of this study was to evaluate whether transition milk intake after colostrum consumption affects the chances of calf infection with Cryptosporidium spp. Materials and Methods: We collected data for Cryptosporidium spp. infection from calves (n=425) divided into three groups: The first group – supervised colostrum and transition milk intake; the second group – supervised colostrum and whole milk intake; and the third group – not supervised colostrum and whole milk intake. To detect oocysts of Cryptosporidium spp. in feces, the flotation method was used, and slides were stained using the modified Ziehl-Neelsen method. Generalized linear mixed modeling was conducted to determine whether the explanatory variable – the management of colostrum and transition milk feeding with three categories (three research groups) – was related to the probability of calves incurring infection with Cryptosporidium spp. Results: In the first group, 26.1% of calves were positive for the presence of Cryptosporidium spp. oocysts, in the second – 37.2%, and in the third – 44.1%. Statistical data analysis showed that calves who did not receive transition milk after colostrum consumption had increased chances of having Cryptosporidium spp. (by 1.90-2.47 times on average). The main results showed that the management of colostrum and transition milk feeding is related to Cryptosporidium spp. infection, indicating that both colostrum and transitional milk play a significant role in controlling pathogenic infections. Conclusion: The most effective management of colostrum and transition milk feeding against Cryptosporidium spp. infection is the timely intake of an adequate amount of colostrum followed by transitional milk consumption for at least 2 weeks before weaning from the dam.

[1]  M. Nielen,et al.  A Scoping Review of On-Farm Colostrum Management Practices for Optimal Transfer of Immunity in Dairy Calves , 2021, Frontiers in Veterinary Science.

[2]  Michael Brunauer,et al.  Prevalence of Worldwide Neonatal Calf Diarrhoea Caused by Bovine Rotavirus in Combination with Bovine Coronavirus, Escherichia coli K99 and Cryptosporidium spp.: A Meta-Analysis , 2021, Animals : an open access journal from MDPI.

[3]  M. Ghaffari,et al.  Extended transition milk feeding for 3 weeks improves growth performance and reduces the susceptibility to diarrhea in newborn female Holstein calves. , 2020, Animal : an international journal of animal bioscience.

[4]  L. Hooper,et al.  Systematic review of modifiable risk factors shows little evidential support for most current practices in Cryptosporidium management in bovine calves , 2020, Parasitology Research.

[5]  M. Steele,et al.  Corrigendum to “Invited Review: Nutritional regulation of gut function in dairy calves: From colostrum to weaning” (Appl. Anim. Sci. 35:498–510) , 2020 .

[6]  M. Zolovs,et al.  Effect of immunoglobulin G concentration in dairy cow colostrum and calf blood serum on Cryptosporidium spp. invasion in calves , 2020, Veterinary world.

[7]  Grzegorz Grodkowski,et al.  Composition and Factors Affecting Quality of Bovine Colostrum: A Review , 2019, Animals : an open access journal from MDPI.

[8]  C. Villot,et al.  Invited Review: Nutritional regulation of gut function in dairy calves: From colostrum to weaning , 2019, Applied Animal Science.

[9]  K. Hertogs,et al.  477 Oligosaccharide and IgG concentrations throughout the first week of lactation in multiparous and primiparous Holstein dairy cattle. , 2018, Journal of Animal Science.

[10]  M. Steele,et al.  PSI-37 The effects of delaying initial colostrum feeding on gastrointestinal tract growth of neonatal bull dairy calves. , 2018, Journal of Animal Science.

[11]  D. Haines,et al.  342 The effects of extended colostrum feeding on gastrointestinal tract growth of the neonatal dairy calf. , 2018, Journal of Animal Science.

[12]  T. Orro,et al.  Molecular epidemiology of Cryptosporidium spp. in calves in Estonia: high prevalence of Cryptosporidium parvum shedding and 10 subtypes identified , 2018, Parasitology.

[13]  D. Haines,et al.  Effect of delaying colostrum feeding on passive transfer and intestinal bacterial colonization in neonatal male Holstein calves. , 2018, Journal of dairy science.

[14]  N. Mabbott,et al.  Bovine cryptosporidiosis: impact, host-parasite interaction and control strategies , 2017, Veterinary Research.

[15]  M. Steele,et al.  From pre- to postweaning: Transformation of the young calf's gastrointestinal tract. , 2017, Journal of dairy science.

[16]  P. Fox,et al.  Composition and properties of bovine colostrum: a review , 2016 .

[17]  G. Opsomer,et al.  Advances in prevention and therapy of neonatal dairy calf diarrhoea: a systematical review with emphasis on colostrum management and fluid therapy , 2014, Acta Veterinaria Scandinavica.

[18]  J. Murphy,et al.  Effect of feeding colostrum at different volumes and subsequent number of transition milk feeds on the serum immunoglobulin G concentration and health status of dairy calves. , 2014, Journal of dairy science.

[19]  Robert W. Li,et al.  Characterization of the rumen microbiota of pre-ruminant calves using metagenomic tools. , 2012, Environmental microbiology.

[20]  R. Chalmers,et al.  Zoonotic cryptosporidiosis in the UK – challenges for control , 2010, Journal of applied microbiology.

[21]  D. Ebert,et al.  Intensive Farming: Evolutionary Implications for Parasites and Pathogens , 2010, Evolutionary Biology.

[22]  A. Viltrop,et al.  Eimeria and Cryptosporidium in Estonian dairy farms in regard to age, species, and diarrhoea. , 2009, Veterinary parasitology.

[23]  B. Lassen,et al.  Eimeria and Cryptosporidium in Lithuanian cattle farms. , 2009 .

[24]  T. Matsuo,et al.  Detection of a small number of Cryptosporidium parvum oocysts by sugar flotation and sugar centrifugation methods. , 2006, The Journal of veterinary medical science.

[25]  H. Lindmark-Månsson,et al.  Immunoglobulins, growth factors and growth hormone in bovine colostrum and the effects of processing , 2002 .

[26]  V. Jansen,et al.  HOST LIFE HISTORY AND THE EVOLUTION OF PARASITE VIRULENCE , 2001, Evolution; international journal of organic evolution.

[27]  H. Hammon,et al.  Colostrum effects on the gastrointestinal tract, and on nutritional, endocrine and metabolic parameters in neonatal calves , 2000 .

[28]  J. Goff,et al.  Strategies for the control of Cryptosporidium parvum infection in calves. , 1998, Journal of dairy science.

[29]  Martin A. Nowak,et al.  Coinfection and the evolution of parasite virulence , 1995, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[30]  L. Robertson,et al.  Survival of Cryptosporidium parvum oocysts under various environmental pressures , 1992, Applied and environmental microbiology.

[31]  J. Pohlenz,et al.  Staining of Cryptosporidia by a Modified Ziehl-Neelsen Technique , 1981, Acta Veterinaria Scandinavica.