Hostname: page-component-76c49bb84f-l6pkv Total loading time: 0 Render date: 2025-07-10T09:29:42.896Z Has data issue: false hasContentIssue false

Description of innate immunity and haematological changes in Holstein calves during the gradual weaning process

Published online by Cambridge University Press:  24 June 2025

Karen Nascimento Silva
Affiliation:
Department of Internal Medicine, College of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil
Karina Medici Madureira
Affiliation:
Department of Anatomy, Pathology and Internal Medicine, College of Veterinary Medicine and Animal Science, Federal University of Bahia, Salvador, Bahia, Brazil
Camila Cecília Martin
Affiliation:
Department of Internal Medicine, College of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil
Daniela Irlanda Castro Tardón
Affiliation:
Department of Internal Medicine, College of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil
Bianca Paola Santarosa
Affiliation:
Department of Internal Medicine, College of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil
David John Hurley
Affiliation:
Department of Infectious Diseases, College of Veterinary Medicine, University of Georgia, Athens, GA, USA
Viviani Gomes*
Affiliation:
Department of Internal Medicine, College of Veterinary Medicine and Animal Science, University of São Paulo, São Paulo, Brazil
*
Corresponding author: Viviani Gomes; Email: viviani.gomes@usp.br

Abstract

The weaning process negatively affects the haematological parameters and innate immune response of dairy calves, even when managed under an intensive milk program. Here we describe haematological and innate immunity changes in 47 Holstein calves aged 69-85 days subjected to a gradual weaning process. Blood samples were collected at six (D-6), four (D-4), and two (D-2) days before and on the weaning day (D0) for the phagocytosis assay and to measure the production of reactive oxygen species (ROS) after stimulation with Staphylococcus aureus, Escherichia coli, and Mannhemia haemolytica, in addition to total protein (TP), haptoglobin (Hp), and iron concentration. The highest mean neutrophil number was recorded at D-2. The absolute number of monocytes was initially high on D-6 and D-4 but declined as the calf progressed to weaning. The number of basophils decreased rapidly, reaching a low value on D-4, and remained low for the remainder of the study period. The TP, Hp, and Fe concentrations decreased. Overall, polymorphonuclear leukocyte phagocytosis activity induced by S. aureus and E. coli decreased from D-6 to D-2, indicating persistence of the low phagocytosis rate for S. aureus. ROS production was constant for all bacterial stimulations from D-6 to D-2, followed by an increase on D0. Phagocytosis and ROS production indicate that the weaning process dampens the innate immune response relative to exposure to these common pathogenic bacteria in dairy calves. Phagocytosis and the corresponding indicators of intracellular killing activities (ROS production and myeloperoxidase index) represent the most accepted core mechanisms for the early elimination of pathogenic microorganisms in calves. Despite a slow gradual weaning management system, the study concluded that intensive milk production programs contribute to innate immune response suppression during weaning.

Information

Type
Research Communication
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of Hannah Dairy Research Foundation.

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Article purchase

Temporarily unavailable

References

Ballou, MA (2012) Immune responses of Holstein and Jersey calves during the preweaning and immediate postweaned periods when fed varying planes of milk replacer. Journal of Dairy Science 95, 73197330.10.3168/jds.2012-5970CrossRefGoogle ScholarPubMed
Ballou, MA, Hanson, DL, Cobb, CJ, Obeidat, BS, Sellers, MD, Pepper-Yowell, AR, Carroll, JA, Earleywine, TJ and Lawhon, SD (2015) Plane of nutrition influences the performance, innate leukocyte responses, and resistance to an oral Salmonella enterica serotype Typhimurium challenge in Jersey calves. Journal of Dairy Science 98, 19721982.10.3168/jds.2014-8783CrossRefGoogle Scholar
Bittar, CMM, Gallo, MP, Silva, JT, De Paula, MR, Poczynek, M and Mourão, GB (2020) Gradual weaning does not improve performance for calves with low starter intake at the beginning of the weaning process. Journal of Dairy Science 103, 46724680.10.3168/jds.2019-17614CrossRefGoogle Scholar
Brun-Hansen, HC, Kampen, AH and Lund, A (2006) Hematologic values in calves during the first 6 months of life. Veterinary Clinical Pathology 35, 182187.10.1111/j.1939-165X.2006.tb00111.xCrossRefGoogle ScholarPubMed
Credille, BC, Capik, SF, Credille, A, Crossley, BM, Blanchard, P, Woolums, AR and Lehenbauer, TW (2023) Agreement of antimicrobial susceptibility testing of Pasteurella multocida and Mannheimia haemolytica isolates from preweaned dairy calves with bovine respiratory disease. American Journal of Veterinary Research 84, 102460.Google ScholarPubMed
Exel, C, Gerritsen, K, Spaninks, M, Duim, B, Koop, G and Benedictus, L (2023) Association of Staphylococcus aureus genotypes with milk or colonization of extramammary sites in Dutch dairy cattle indicates strain variation in reservoirs for intramammary infections. Research in Veterinary Science 154, 138144.10.1016/j.rvsc.2022.12.010CrossRefGoogle ScholarPubMed
Gomes, V, Barros, BP, Castro-Tardón, DI, Martin, CC, Santos, FCR, Knobl, T, Santarosa, BP, Padilha, LM and Hurley, DJ (2023) The role of anti-E. coli antibody from maternal colostrum on the colonization of newborn dairy calves’ gut with Escherichia coli and the development of clinical diarrhea. Journal of Animal - Open Space 2, 100037.10.1016/j.anopes.2023.100037CrossRefGoogle Scholar
Hulbert, LE, Cobb, CJ, Carroll, JA and Ballou, MA (2011) The effects of early weaning on innate immune responses of Holstein calves. Journal of Dairy Science 94, 25452556.10.3168/jds.2010-3983CrossRefGoogle ScholarPubMed
Hulbert, LE and Moisá, SJ (2016) Stress, immunity, and the management of calves. Journal of Dairy Science 99, 31993216.10.3168/jds.2015-10198CrossRefGoogle ScholarPubMed
Kim, ET, Lee, HG, Kim, DH, Son, JK, Kim, BW, Joo, SS, Park, DS, Park, YJ, Lee, SY and Kim, MH (2020) Hydrolyzed yeast supplementation in calf starter promotes innate immune responses in Holstein calves under weaning stress condition. Animals 10, 1468.10.3390/ani10091468CrossRefGoogle ScholarPubMed
Kim, MH, Yang, JY, Upadhaya, SD, Lee, HJ, Yun, CH and Ha, JK (2011) The stress of weaning influences serum levels of acute-phase proteins, iron-binding proteins, inflammatory cytokines, cortisol, and leukocyte subsets in Holstein calves. Journal of Veterinary Science 12, 151157.10.4142/jvs.2011.12.2.151CrossRefGoogle ScholarPubMed
Lynch, EM, Earley, B, McGee, M and Doyle, S (2010) Effect of abrupt weaning at housing on leukocyte distribution, functional activity of neutrophils, and acute phase protein response of beef calves. BMC Veterinary Research 6, 39.10.1186/1746-6148-6-39CrossRefGoogle ScholarPubMed
Martin, CC, Smfn, O, Costa, JFR, Baccili, CC, Silva, BT, Hurley, DJ and Gomes, V (2021) Influence of feeding fresh colostrum from the dam or frozen colostrum from a pool on indicator gut microbes and the inflammatory response in neonatal calves. Research in Veterinary Science 135, 355365.10.1016/j.rvsc.2020.10.017CrossRefGoogle ScholarPubMed
Morita, LM, Martin, CC, Silva, KN, Woolums, A, Hurley, DJ and Gomes, V (2022) Hematologic profiles and development of innate immune function in healthy Holstein calves during the pre-weaning period. Veterinary Clinical Pathology 51, 480490.10.1111/vcp.13155CrossRefGoogle ScholarPubMed
O'loughlin, A, McGee, M, Waters, SM, Doyle, S and Earley, B (2011) Examination of the bovine leukocyte environment using immunogenetic biomarkers to assess immunocompetence following exposure to weaning stress. BMC Veterinary Research 7, 45.10.1186/1746-6148-7-45CrossRefGoogle ScholarPubMed
Ramos, JS, Madureira, KM, Silva, KN, Bosco, KA, Morita, LM, Guimarães, JE and Gomes, V (2021) Haptoglobin and its association with naturally occurring diseases in Holstein heifer calves. Arquivo Brasileiro de Medicina Veterinária E Zootecnia 73, 15901678.10.1590/1678-4162-12159CrossRefGoogle Scholar
Santos, FCR, Santarosa, BP, Dal Más, FE, Silva, KN, Guirro, ECBP and Gomes, V (2023) Clinical physiological parameters of Holstein calves in the first month of life. Journal of Animal - Open Space 2, 100036.10.1016/j.anopes.2022.100036CrossRefGoogle Scholar
Supplementary material: File

Silva et al. supplementary material

Silva et al. supplementary material
Download Silva et al. supplementary material(File)
File 344.4 KB