Resistance to Infectious Disease
Jesse P. Goff and Kayoko Kimura
Periparturient Diseases of Cattle Research Unit
National Animal Disease Center
USDA-Agricultural Research Service
Ames, IA
Introduction
The transition from pregnant, non-lactating to non-pregnant, lactating is too often a disastrous experience for the cow. Most of the metabolic diseases of dairy cows - milk fever, ketosis, retained placenta, and displacement of the abomasum - occur within the first 2 wk of lactation. In addition to metabolic disease, the majority of infectious disease experienced by the dairy cow, especially mastitis, but also diseases such as
Johne 's disease and Salmonellosis, become clinically apparent during the first 2 wk of lactation. This review will make two assumptions before reviewing studies correlating metabolic disease with changes in infectious disease resistance. One of those assumptions is that mammary gland infections are less likely in animals with a “strong” immune system and that periparturient immune suppression exists and predisposes cows to mastitis, and other infectious disease. This assumption helps explain why an animal that has harbored bacteria, within the udder or within the gut, for a long period without clinical disease suddenly breaks with the disease shortly after calving. The second assumption is that assays scientists have utilized to assess functional capacity and number of immune cells are reasonably accurate. The relative merit of the assays used in different labs will not be debated in this review. Excellent reviews are available which support these assumptions
(Sordillo, et al.,1997; Burvenich, et al., 1994; Kehrli and Shuster ,1994; Tyler et al.,
1993 ; Hogan et al., 1993 ; Senft and Neudecker, 1991). This review will examine the evidence that metabolic disease in cattle increases the susceptibility of the cow, particularly the periparturient cow, to
References: Boulay M, Scott ME, Conly SL, Stevenson MM, Koski KG. 1998. Dietary protein and zinc restrictions independently modify a Heligmosomoides polygyrus (Nematoda) Brand A. 1994. Role of the neutrophil leucocyte in the local and systemic reactions during experimentally induced E Christadoss P, Talal N, Lindstrom J, Fernandes G. 1984. Suppression of cellular and humoral immunity to T-dependent antigens by calorie restriction Doherty ML, Monaghan ML, Bassett HF, Quinn PJ, Davis WC. 1996. Effect of dietary restriction on cell-mediated immune responses in cattle infected with Mycobacterium Franklin ST, Young JW, Nonnecke BJ. 1991. Effects of ketones, acetate, butyrate, and glucose on bovine lymphocyte proliferation Goff JP, Horst RL, Jardon PW, Borelli C, Wedam J. 1996. Field trials of an oral calcium propionate paste as an aid to prevent milk fever in periparturient dairy cows Gregory R, McElveen J, Tattersall RB, Todd I. 1993. The effects of 3-hydroxybutyrate and glucose on human T cell responses to Candida albicans Gunnink, J. W. 1984. Pre-partum leucotytic activity and retained placenta. Vet. Q. 6: 52-54. Hoeben D, Heyneman R, Burvenich C. 1997. Elevated levels of beta-hydroxybutyric acid in periparturient cows and in vitro effect Horst, R. L., and N. A. Jorgensen. 1982. Elevated plasma cortisol during induced and spontaneous hypocalcemia in ruminants Ishikawa, H. 1987. Observation of lymphocyte function in perinatal cows and neonatal calves Kandefer-Szerszen M, Filar J, Szuster-Ciesielska A, Rzeski W. 1992. Suppression of interferon response of bovine leukocytes during clinical and subclinical ketosis in Kashiwazaki, Y., Y. Maede, and S. Namioka. 1985. Transformation of bovine peripheral blood lymphocytes in the perinatal period Kehrli, Jr., M. E., B. J. Nonnecke, and J. A. Roth. 1989a. Alterations in bovine neutrophil function during the periparturient period Kehrli, Jr., M. E., B. J. Nonnecke, and J. A. Roth. 1989b. Alterations in bovine lymphocyte function during the periparturient period Kehrli ME Jr, Goff JP. 1989. Periparturient hypocalcemia in cows: effects on peripheral blood neutrophil and lymphocyte function Kehrli ME Jr, Goff JP, Harp JA, Thurston JR, Norcross NL. 1990. Effects of preventing periparturient hypocalcemia in cows by parathyroid hormone administration on Kehrli ME Jr, Shuster DE. 1994. Factors affecting milk somatic cells and their role in health of the bovine mammary gland Kimura K, Goff JP, Kehrli ME Jr. 1999. Effects of the presence of the mammary gland on expression of neutrophil adhesion molecules and myeloperoxidase activity in Kimura, K, J. P. Goff, M. E. Kehrli, Jr., and T. A. Reinhardt. 2002 Decreased Neutrophil Function as a Cause of Retained Placenta in Dairy Cattle Kimura, K., Goff, JP, Reinhardt, TA. 2001. Parturition blunts calcium signals in immune cells Leiba A, Amital H, Gershwin ME, Shoenfeld Y. 2001. Diet and lupus. Lupus 10:246-8. Marquardt, J. P., R. L. Horst, and N. A. Jorgensen. 1977. Effect of parity on dry matter intake at parturition in dairy cattle Meijer GA, Van der Meulen J, Bakker JG, Van der Koelen CJ, Van Vuuren AM. 1995. Nonnecke BJ, Franklin ST, Young JW. 1992. Effects of ketones, acetate, and glucose on in vitro immunoglobulin secretion by bovine Oltenacu PA, Ekesbo I., 1994. Epidemiological study of clinical mastitis in dairy cattle. Peeler EJ, Otte MJ, Esslemont RJ. 1994. Inter-relationships of periparturient diseases in dairy cows Plank LD, Hill GL. 2000. Sequential metabolic changes following induction of systemic inflammatory response in patients with severe sepsis or major blunt trauma