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Changes in milk L-lactate, lactate dehydrogenase, serum albumin, and IgG during milk ejection and their association with somatic cell count

Published online by Cambridge University Press:  03 December 2014

Mirjam Lehmann
Affiliation:
Veterinary Physiology, Vetsuisse Faculty University of Bern, Bremgartenstrasse 109a, CH-3001 Bern, Switzerland
Samantha K Wall
Affiliation:
Veterinary Physiology, Vetsuisse Faculty University of Bern, Bremgartenstrasse 109a, CH-3001 Bern, Switzerland
Olga Wellnitz
Affiliation:
Veterinary Physiology, Vetsuisse Faculty University of Bern, Bremgartenstrasse 109a, CH-3001 Bern, Switzerland
Rupert M Bruckmaier*
Affiliation:
Veterinary Physiology, Vetsuisse Faculty University of Bern, Bremgartenstrasse 109a, CH-3001 Bern, Switzerland
*
*For correspondence; e-mail: rupert.bruckmaier@vetsuisse.unibe.ch

Abstract

In both conventional and automatic milking systems (AMS), sensitive and reliable mastitis detection is important for profitable milk production. Mastitis detection parameters must be able to detect mastitis when the somatic cell count (SCC) is only slightly elevated. Owing to the pre-milking teat cleaning process in AMS, sampling cannot take place before the occurrence of alveolar milk ejection and importantly, this can affect the ability of parameters to detect mastitis. The aim of the present study was to examine the effect of alveolar milk ejection on l-lactate, lactate dehydrogenase (LDH), serum albumin (SA) and immunoglobulin G (IgG) compared with SCC, a commonly used indicator of mastitis. In this experiment, milk samples were collected every 20 s from one quarter during a 120-s manual teat stimulation in ten cows. Samples were analysed for SCC, l-lactate, LDH, SA and IgG. Quarters were grouped by low (<5·0 log10 cells/ml), mid (5·0–5·7 log10 cells/ml), and high (>5·7 log10 cells/ml) SCC using the sample at t=0 s. Neither l-lactate nor LDH could statistically differentiate between low and mid-SCC quarters, but there were a significant difference in levels between the high-SCC quarters and low and mid-SCC quarters. SA could not differentiate between the low and mid-SCC quarters, but the SA levels for the high SCC quarters remained statistically different compared with low and mid-SCC quarters throughout the experiment. IgG could statistically differentiate between low and mid-SCC, although the high-SCC quarters were not statistically different from the mid-SCC quarters after 60 s. In the high-SCC quarters, a decrease was shown in all parameters during milk ejection, after t=60 s. In conclusion, alveolar milk ejection reduces the effectiveness of detection parameters when compared with SCC. With the exception of IgG, the ability of other tested parameters was not satisfactory to differentiate between quarters with low to mid-SCC levels

Type
Research Article
Copyright
Copyright © Proprietors of Journal of Dairy Research 2014 

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References

Biggadike, HJ, Ohnstad, I, Laven, RA & Hillerton, JE 2002 Evaluation of measurements of the conductivity of quarter milk samples for the early diagnosis of mastitis. Veterinary Record 150 655658Google Scholar
Bogin, E, Ziv, G, Avidar, J, Rivertz, B, Gordin, S & Saran, A 1977 Distribution of lactate dehydrogenase isoenzymes in normal and inflamed bovine udders and milk. Research in Veterinary Science 22 198200CrossRefGoogle ScholarPubMed
Bruckmaier, RM & Blum, JW 1998 Oxytocin release and milk removal in ruminants. Journal of Dairy Science 81 939949CrossRefGoogle ScholarPubMed
Bruckmaier, RM & Hilger, M 2001 Milk ejection in dairy cows at different degrees of udder filling. Journal of Dairy Research 68 369376Google Scholar
Bruckmaier, RM, Weiss, D, Wiedemann, M, Schmitz, S & Wendl, G 2004 Changes of physicochemical indicators during mastitis and the effects of milk ejection on their sensitivity. Journal of Dairy Research 71 316321CrossRefGoogle ScholarPubMed
Burton, JL & Erksine, RJ 2003 Immunity and mastitis. Some new ideas for an old disease. Veterinary Clinics of North America Food Animal Practice 19 145Google Scholar
Chagunda, MGG, Larsen, T, Bjerring, M & Ingvartsen, KL 2006 L-lactate dehydrogenase and N-acetyl-beta D-glucosaminidase activities in bovine milk as indicators of non-specific mastitis. Journal of Dairy Research 73 431440Google Scholar
Davis, SR, Farr, VC, Prosser, CG, Nicholas, GD, Turner, S, Lee, J & Hart, AL 2004 Milk L-lactate concentration is increased during mastitis. Journal of Dairy Research 71 175181Google Scholar
Dzidic, A, Macuhova, J & Bruckmaier, RM 2004a Effects of cleaning duration and water temperature on oxytocin release and milk removal in an automatic milking system. Journal of Dairy Science 87 41634169Google Scholar
Dzidic, A, Weiss, D & Bruckmaier, RM 2004b Oxytocin release, milk ejection and milking characteristics in a single stall automatic milking system. Livestock Production Science 86 6168CrossRefGoogle Scholar
Harmon, RJ 1994 Physiology of mastitis and factors affecting somatic cell counts. Journal of Dairy Science 77 21032112Google Scholar
Hillerton, JE 1999 Redefining mastitis based on somatic cell count. IDF Bulletin 345 46Google Scholar
Hiss, S, Mueller, U, Neu-Zahren, A & Sauerwein, H 2007 Haptoglobin and lactate dehydrogenase measurements in milk for the identification of subclinically diseased udder quarters. Veterinary Medicine-Czech 52 245252CrossRefGoogle Scholar
Hovinen, M & Pyörälä, S 2010 Invited review: udder health of dairy cows in automatic milking. Journal of Dairy Science 94 547562Google Scholar
Hovinen, M, Aisla, A-M & Pyörälä, S 2006 Accuracy and reliability of mastitis detection with electrical conductivity and milk colour measurement in automatic milking. Acta Agriculturae Scandinavica, Section A 56 121127Google Scholar
IDF 1971 A monograph on bovine mastitis. International Dairy Federation Bull. Standard No. 60. Brussels, BelgiumGoogle Scholar
Kato, K, Mori, K & Katoh, N 1989 Contribution of leukocytes to the origin of lactate dehydrogenase isozymes in milk of bovine mastitis. Journal of Veterinary Medical Science-Japan 51 530539Google Scholar
Lehmann, M, Wellnitz, O & Bruckmaier, RM 2013 Concomitant lipopolysaccarhide-induced transfer of blood-derived components including immunoglobulins into milk. Journal of Dairy Science 96 889896CrossRefGoogle ScholarPubMed
Milner, P, Page, KL & Hillerton, JE 1997 The effects of early antibiotic treatment following diagnosis of mastitis detected by a change in the electrical conductivity of milk. Journal of Dairy Science 80 859863CrossRefGoogle ScholarPubMed
Morr, CV, Harper, WJ & Gould, IA 1957 Some organic acids in raw and heated skim milk. Journal of Dairy Science 40 964972Google Scholar
Nickerson, SC & Pankey, JW 1983 Cytologic observations of the bovine teat end. American Journal of Veterinary Research 44 14331441Google Scholar
Ontsouka, CE, Bruckmaier, RM & Blum, JW 2003 Fractionized milk composition during removal of colostrum and mature milk. Journal of Dairy Science 86 20052011Google Scholar
Sarikaya, H & Bruckmaier, RM 2006 Importance of the sampled milk fraction for the prediction of total quarter somatic cell count. Journal of Dairy Science 86 42464250Google Scholar
Schalm, OW & Noorlander, DO 1957 Experiments and observations leading to the development of the California mastitis test. Journal of the American Veterinary Medical Association 130 199204Google Scholar
Smith, KL 1996 Standards for somatic cells in milk: physiological and regulatory. In IDF Mastitis Newsletter 144/21:7–9Google Scholar
Stelwagen, K, Politis, I, White, JH, Zavizion, B, Prosser, CG, Davis, SR & Farr, VC 1994 Effect of milking frequency and somatotropin on the activity of plasminogen activator, plasminogen, and plasma in bovine milk. Journal of Dairy Science 77 35773583Google Scholar
Symons, DBA & Wright, LJ 1974 Changes in bovine mammary gland permeability after intramammary exotoxin infusion. Journal of Comparative Pathology 84 917Google Scholar