참고문헌
- Barkema, H. W., Y. H. Schukken, T. J. G. M. Lam, M. L. Beiboer, G. Benedictus and A. Brand. 1999. Management practices associated with the incidence rate of clinical mastitis. J. Dairy Sci. 82:1643-1654. https://doi.org/10.3168/jds.S0022-0302(99)75393-2
- Beckley, M. S. and T. Johnson. 1966. Five year study of a California mastitis test on a commercial dairy herd. J. Dairy Sci. 49:746.
- Blackburn, P. S. 1966. The variation in cell count of cow's milk throughout lactation and from one lactation to the next. J. Dairy Res. 33:193-198. https://doi.org/10.1017/S0022029900011857
- Boyso, J. O., J. J. V. Alrcon, M. C. Juarez, A. O. Zarzosa, J. E. L. Meza, A. B. Patino and V. M. B. Aguirre. 2007. Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis. J. Infect. 54:399-409. https://doi.org/10.1016/j.jinf.2006.06.010
- Bramley, A. J. 1992. Mastitis. In: Bovine Medicine - Diseases and Husbandry of Cattle (Ed. A. H. Andrews, R. W. Blowey, H. Boyd and R. G. Eddy). Blackwell Scientific Publications: Oxford, 289-300.
- Bytyqi, H., U. Zaugg, K. Sherifi, A. Hamidi, M. Gjonbalaj, S. Muji and H. Mehmeti. 2010. Influence of management and physiological factors on somatic cell count in raw milk in Kosova. Veterinarski Archiv, 80(2):173-183.
- Craven. N. and M. R. Williams. 1985. Defences of the bovine mammary gland against infection and prospects for the enhancement. Vet. Immunol. Immunopathol. 10:71. https://doi.org/10.1016/0165-2427(85)90039-X
- Dairyman's Digest 2009. What you should know about somatic cells. Winter issue.
- Dohoo, I. R. and A. H. Meek. 1982. Somatic cell counts in bovine milk. Can. Vet. J. 23(4):119-125.
- Dohoo, I. R., A. H. Meek and S. W. Martin. 1984. Somatic cell counts in bovine milk: relationships to production and clinical episodes of mastitis. Can. J. Comp. Med. 48:130-135.
- Fernandes, A. M., A. F. Oliveira and C. G. Lima. 2007. Effects of somatic cell counts in milk on physical and chemical characteristics of yoghurt. Int. Dairy J. 17:111-115. https://doi.org/10.1016/j.idairyj.2006.02.005
- Gallin, J. I., I. M. Goldstein and R. Snyderman. 1992. Inflammation: Basic Principles and Clinical Correlates. 2nd ed. Raven Press. New York, NY.
- Gonzalo, C., J. A. Baro, J. A. Carriedo and F. San Primitivo. 1993. Use of the Fossomatic method to determine somatic cell counts in sheep milk. J. Dairy Sci. 76:115-119. https://doi.org/10.3168/jds.S0022-0302(93)77330-0
- Gonzalo, C., J. R. Martinez, J. A. Carriedo and F. San Primitivo. 2003. Fossomatic cell-counting on ewe milk: comparison with direct microscopy and study of variation factors. J. Dairy Sci. 86:138-145. https://doi.org/10.3168/jds.S0022-0302(03)73593-0
- Hallen Sandgren, C., K. Persson Waller and U. Emanuelson. 2008. Therapeutic effects of systemic or intramammary antimicrobial treatment of bovine subclinical mastitis during lactation. Vet. J. 175:108-117. https://doi.org/10.1016/j.tvjl.2006.12.005
- Harmon, R. J. 1994. Physiology of mastitis and factors affecting somatic cell counts. J. Dairy Sci. 77:2103-2112. https://doi.org/10.3168/jds.S0022-0302(94)77153-8
- Harmon, R. J. 2001. Somatic cell counts: A primer. In: Proc. National Mastitis Council Annual Meeting. pp. 3-9.
- Hillerton, J. E. 1999. Redefining mastitis based on somatic cell count. IDF Bulletin 345:4-6.
- Hillerton, J. E., A. J. Bramley, R. T. Staker and C. H. McKinnon. 1995. Patterns of intramammary infection and clinical mastitis over a 5-year period in a closely monitored herd applying mastitis control measures. J. Dairy Res. 62:39-50. https://doi.org/10.1017/S0022029900033653
- Ingalls, W. 2001. Somatic cells: Function and relation to milk quality. December, 2001. http://www.milkproduction.com/Library/Articles/Somatic_Cells_Function_and_Relationship_to_Milk_Production.htm
- International Dairy Federation. 1997. Recommendations for presenting of mastitis related data. IDF Bulletin 321. Brussels, Belgium. pp. 7-25.
- International Dairy Federation. 1999. Suggested interpretation of mastitis terminology. IDF Bulletin 338. Brussels, Belgium. pp. 3-26.
- Jensen, D. L. and R. J. Eberhart. 1981. Total and differential cell counts in secretions of the nonlactating bovine mammary gland. Am. J. Vet. Res. 42(5):743-747.
- Khate, K. and B. R. Yadav. 2010. Incidence of mastitis in Sahiwal cattle and Murrah buffaloes of a closed organized herd. Indian J. Anim. Sci. 80(5):467-469.
- Lam, T. J. G. M., J. H. Van Vliet, Y. H. Schukken, F. J. Grommers, A. Van Velden-Russcher, H. W. Barkema and A. Brand. 1997b. The effect of discontinuation of postmilking teat disinfection in low somatic cell count herds. II. Dynamics of intramammary infections. Vet. Quart. 19:47-53.
- Lee, C. S., F. B. P. Wooding and P. Kemp. 1980. Identification properties, and differential counts of cell populations using electron microscopy of dry cows secretions, colostrum and milk from normal cows. J. Dairy Res. 47:39. https://doi.org/10.1017/S0022029900020860
- Ma, Y., C. Ryan, D. M. Barbano, D. M. Galton, M. A. Rudan and K. J. Boor. 2000. Effects of somatic cell count on quality and shelf life of pasteurized fluid milk. J. Dairy Sci. 83:264-274. https://doi.org/10.3168/jds.S0022-0302(00)74873-9
- Malinowski, E., H. Lassa, A. Kłossowska, H. Markiewicz, M. Kaczmarowski and S. Smulski. 2006. Relationship between mastitis agents and somatic cell count in foremilk samples. Bull. Vet. Inst. Pulawy. 50:349-352.
- McDonald, J. S. and A. J. Anderson. 1981. Total and differential somatic cell counts in secretions from noninfected bovine mammary glands; the peripartum period. Am. J. Vet. Res. 42:1366-1368.
- Meek, A. H., D. A. Barnum and F. H. S. Newbould. 1980. Use of total and differential somatic cell counts to differentiate potentially infected from potentially non-infected quarters and cows and between herds of various levels of infection. J. Food Prot. 43:10-14.
- Miller, R. H. and M. J. Paape. 1985. Relationship between milk somatic cell count and milk yield. In: Proc. Ann. Mtg. Natl. Mastitis Counc. p. 60.
-
Miller, R. H., M. J. Paape, R. R. Peters and M. D. Young, 1990. Total and differential cell counts and N-Acetyl-
${\beta}$ -Dglucosaminidase activity in mammary secretions during dry period. J. Dairy Sci. 73(7):1751-1755. https://doi.org/10.3168/jds.S0022-0302(90)78852-2 - Mullan, N. A., E. A. Carter and K. A. Nguyen. 1985. Phagocytic and bactericidal properties of bovine macrophages from non-lactating mammary glands. Res. Vet. Sci. 38:160-166.
- National Mastitis Council. 2001. National mastitis council recommended mastitis control.
- Nickerson, S. C. 2009. Control of heifer mastitis: Antimicrobial treatment- An overview. Vet. Microbiol. 134:128-135. https://doi.org/10.1016/j.vetmic.2008.09.019
- Nonnccke, B. J. and J. A. Harp. 1986. Effect of chronic staphylococcal mastitis on mitogenic responses of bovine lymphocytes. J. Dairy Sci. 68:3323.
- Oliver, S. P., B. M. Jayarao and R. A. Almeida. 2005. Foodborne pathogens, mastitis, milk quality, and dairy food safety. Proc. 44th NMC Annual Meeting. Orlando, FL, pp. 3-27.
- Opdebeeck, J. P. 1982. Mammary gland immunity. J. Am. Vet. Med. Assoc. 181:1061-1065.
- Park, Y. H., L. K. Fox, M. J. Hamilton and W. C. Davis. 1992. Bovine mononuclear leukocyte subpopulations in peripheral blood and mammary gland secretions during lactation. J. Dairy Sci. 75(4):998-1006. https://doi.org/10.3168/jds.S0022-0302(92)77842-4
- Reichmuth, J. 1975. Somatic cell counting - interpretation of results. In Proc. of Sem. on Mast. Cont., 1975 IDF Doc. 85. pp. 93-109.
- Rogers, G. W., G. Banos, U. Sander Nielsen and J. Philipsson. 1998. Genetic correlations among somatic cell scores, productive life, and type traits from the United States and udder health measures from Denmark and Sweden. J. Dairy Sci. 81:1445-1453. https://doi.org/10.3168/jds.S0022-0302(98)75708-X
- Schallibaum, M. 2001. Impact of SCC on the quality of fluid milk and cheese. National Mastitis Council, Inc. 40th Annual Meeting Proceedings. 38-46.
- Schalm, O. W., E. J. Carroll and N. C. Jain. 1971. Bovine Mmstitis. Lea & Febiger, Philadelphia, USA.
- Schepers, A. J., T. J. Lam, Y. H. Schukken, J. B. M. Wilmink and W. J. A. Hanekamp. 1997. Estimation of variance components for somatic cell counts to determine thresholds for uninfected quarters. J. Dairy Sci. 80:1833-1840. https://doi.org/10.3168/jds.S0022-0302(97)76118-6
- Sharif, A., M. Umer and G. Muhammad. 2009. Mastitis control in dairy production. J. Agric. Soc. Sci. 5:102-105.
- Sharma, N. and S. K. Maiti. 2005. Effect of dietary supplementation of vitamin E and selenium in sub clinical mastitis in dairy cows. Indian J. Vet. Med. 25(2):76-79.
- Sharma, N. and S. K. Maiti. 2009. Incidence, etiology and antibiogram of sub clinical mastitis in cows in Durg, Chhattisgarh. Indian J. Vet. Res. (In press).
- Sharma, N. 2003. Epidemiological investigation on subclinical mastitis in dairy animals: Role of vitamin E and selenium supplementation on its control. MVSc. Thesis, I.G.K.V.V., Raipur (C.G.) India.
- Sharma, N. 2007. Alternative approach to control intramammary infection in dairy cows- A review. Asian J. Anim. Vet. Adv. 2(2):50-62. https://doi.org/10.3923/ajava.2007.50.62
- Sharma, N. 2008. Foot and mouth disease - Mastitis cascade in dairy cattle: A field study. Int. J. Zoolog. Res. 4(1):64-67. https://doi.org/10.3923/ijzr.2008.64.67
- Sharma, N., A. Gautam, S. R. Upadhyay, K. Hussain, J. S. Soodan and S. K. Gupta. 2006. Role of antioxidants in udder health: a review. Indian J. Field Vet. 2(1):73-76.
- Sharma, N., S. K. Gupta, U. Sharma and K. Hussai. 2007. Treatment of clinical mastitis in buffalo-A case report. Buffalo Bull. 26(2):56-58.
- Sharma, N., S. K. Maiti and K. M. Koley. 2004. Studies on the incidence of sub clinical mastitis in buffaloes of Rajnandgaon district of Chhattisgarh state. Vet. Pract. 5(2):123-124.
- Sharma, N., S. K. Maiti and K. K. Sharma. 2007. Prevalence, etiology and antibiogram of microorganisms associated with Sub-clinical mastitis in buffaloes in Durg, Chhattisgarh State (India). Int. J. Dairy Sci. 2(2):145-151. https://doi.org/10.3923/ijds.2007.145.151
- Sharma, S. D. and P. Rai. 1977. Studies on the incidence of bovine mastitis in Uttar Pradesh. II. Subclinical mastitis. Indian Vet. J. 54(6):435-439.
- Sheldrake, R. F., R. J. T. Hoare and G. D. McGregor. 1983. Lactation stage, parity, and infection affecting somatic cells, electrical conductivity, and serum albumin in milk. J. Dairy Sci. 66:542-547. https://doi.org/10.3168/jds.S0022-0302(83)81823-2
- Shook, G. E. 1993. Genetic improvement of mastitis through selection on somatic cell count. Vet. Clin. North Am., Food Anim. Pract. 9:563-581.
- Singh, M. 2002. Somatic cell counts during lactation in bovines as a index of subclinical mastitis. In: Proc. All India dairy husbandry officers workshop NDRI, Karnal, 2002. pp. 64-77.
- Skrzypek, R., J. Wojtowski and R. D. Fahr. 2004. Factors affecting somatic cell count in cow bulk tank milk: A case study from Poland. J. Vet. Med. A. 51:127-131. https://doi.org/10.1111/j.1439-0442.2004.00611.x
- Smith, K. L., D. A. Todhunter and P. S. Schoenberger. 1985. Environmental mastitis: cause, prevalence, prevention. J. Dairy Sci. 68:1531. https://doi.org/10.3168/jds.S0022-0302(85)80993-0
- Stabel, J. R. 2005. Paratuberculosis and Crohn's disease. In: Proc. 44th NMC Annual Meeting. Orlando, FL, pp. 36-40.
- Tamime, A. Y. and R. Robinson. 1999. Yoghurt science and technology. 2nd ed. Woodhead Publishing Ltd., Cambridge, UK.
- Topel, A. 2004. Chemie und physik der milch. Behr's Verlag GmbH & Co. KG, Hamburg DE, 756, pp. 369-434.
- White, F. and E. A. S. Rattray. 1965. Diurnal variation in the cell content of cow's milk. J. Comp. Pathol. 75:253. https://doi.org/10.1016/0021-9975(65)90029-0
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- Milk somatic cell count-derived traits as new indicators to monitor udder health in dairy buffaloes vol.20, pp.1, 2011, https://doi.org/10.1080/1828051x.2021.1899856
- Maintaining Optimal Mammary Gland Health and Prevention of Mastitis vol.8, pp.None, 2011, https://doi.org/10.3389/fvets.2021.607311
- The value of the biomarkers cathelicidin, milk amyloid A, and haptoglobin to diagnose and classify clinical and subclinical mastitis vol.104, pp.2, 2011, https://doi.org/10.3168/jds.2020-18539
- Development of ELISA against milk haptoglobin for diagnosis of subclinical mastitis in goats vol.7, pp.2, 2011, https://doi.org/10.1016/j.heliyon.2021.e06314
- Comparative analyses of enteric methane emissions, dry matter intake, and milk somatic cell count in different residual feed intake categories of dairy cows vol.101, pp.1, 2011, https://doi.org/10.1139/cjas-2019-0085
- Effect of season, stage of lactation, parity and level of milk production on incidence of clinical mastitis in Karan Fries and Sahiwal cows vol.52, pp.4, 2021, https://doi.org/10.1080/09291016.2019.1621064
- Employee Management and Animal Care: A Comparative Ethnography of Two Large-Scale Dairy Farms in China vol.11, pp.5, 2011, https://doi.org/10.3390/ani11051260
- Subclinical Mastitis in Selected Bovine Dairy Herds in North Upper Egypt: Assessment of Prevalence, Causative Bacterial Pathogens, Antimicrobial Resistance and Virulence-Associated Genes vol.9, pp.6, 2011, https://doi.org/10.3390/microorganisms9061175
- Multiple Breeds and Countries’ Predictions of Mineral Contents in Milk from Milk Mid-Infrared Spectrometry vol.10, pp.9, 2011, https://doi.org/10.3390/foods10092235
- Prediction of Streptococcus uberis clinical mastitis treatment success in dairy herds by means of mass spectrometry and machine-learning vol.11, pp.1, 2011, https://doi.org/10.1038/s41598-021-87300-0
- Comparison of machine learning methods to predict udder health status based on somatic cell counts in dairy cows vol.11, pp.1, 2011, https://doi.org/10.1038/s41598-021-93056-4
- Oxidative Stress in Dairy Cows: Insights into the Mechanistic Mode of Actions and Mitigating Strategies vol.10, pp.12, 2011, https://doi.org/10.3390/antiox10121918
- Genome-Wide Association Study Candidate Genes on Mammary System-Related Teat-Shape Conformation Traits in Chinese Holstein Cattle vol.12, pp.12, 2021, https://doi.org/10.3390/genes12122020
- Milk Somatic Cell Count and Polymorphonuclear Cells in Healthy Quarters of Cows That Underwent Blanket and Selective Dry Therapy: An Italian Case Study vol.8, pp.12, 2011, https://doi.org/10.3390/vetsci8120298