Application of Silver Ion for Clinical Mastitis in Holstein Cows

임상형 유방염을 가진 홀스테인(Holstein) 소에 대한 은 이온의 적용 연구

  • Seol, Jae-Won (Center for Healthcare Technology Development, Bio-Safety Research Institute, College of Veterinary Medicine, Chonbuk National University) ;
  • Hur, Tai-Young (National Institute of Animal Science, Rural Development Administration) ;
  • Jung, Young-Hun (National Institute of Animal Science, Rural Development Administration) ;
  • Park, Sang-Youel (Center for Healthcare Technology Development, Bio-Safety Research Institute, College of Veterinary Medicine, Chonbuk National University) ;
  • Kang, Seog-Jin (National Institute of Animal Science, Rural Development Administration)
  • 설재원 (헬스케어 기술개발 사업단, 전북대학교 수의과대학 생체안전성 연구소) ;
  • 허태영 (농촌진흥청 국립축산과학원) ;
  • 정영훈 (농촌진흥청 국립축산과학원) ;
  • 박상열 (헬스케어 기술개발 사업단, 전북대학교 수의과대학 생체안전성 연구소) ;
  • 강석진 (농촌진흥청 국립축산과학원)
  • Accepted : 2010.04.12
  • Published : 2010.06.30

Abstract

Mastitis is an inflammation of the mammary gland that develops as a response to pathogenic microorganisms. Somatic cell count (SCC) and bacteriological analysis are the most accepted tools to determine udder health. This study evaluated the effects of intra-mammary gland infusion of silver ion against clinical mastitis in Holstein cows. Silver ion (20 ${\mu}g$/ml) was infused through the intra-mammary gland in quarters having clinical mastitis and milk was collected to determine SCC, and levels of lactoferrin and bovine serum albumin (BSA). Silver ion infusion decreased udder inflammation, firmness and swelling, and reduced clots, BSA, lactoferrin and SCC in milk. However, milk yield and circulating blood cells remained unchanged. The silver ion-mediated reductions of BSA and SCC indicate reduced inflammation and bacterial activity in silver ion-treated mammary glands in Holsteins with mastitis, which may be exploited in a curative strategy.

유방염은 병원성 미생물들에 의한 유선 내에 염증이 생기는 질환으로, 유방 조직과 우유 내 체세포수 (SCC)와 세균학적 분석이 유방염 진단을 위해서 사용된다. 본 연구에서는 임상형 유방염이 걸린 홀스테인 소의 유선 내로 은 이온(20 ${\mu}g$/ml)을 투입하고, 유방염의 임상 증상의 변화와 우유 내 somatic cell count, 소 혈청 알부민과 lactoferrin 등과 같은 유방염 관련 인자들을 조사하였다. 은 이온의 유선 내 투입은 유방의 부종과 견고함 등의 염증 증상을 완화시켰으며, 우유의 응고와 체세포수를 감소시켰다. 또한, 우유 내 소 혈청 알부민과 lactoferrin의 농도가 은 이온의 투입에 의해 감소되었다, 그러나 임상형 유방염이 걸린 소의 유선 내 은 이온의 투입은 착유된 우유의 양과 혈액 내 백혈구와 적혈구 수를 변화시키지는 않았다. 이러한 결과는 유방염이 걸린 소에 은 이온을 유선 내로 투입 함으로서 염증과 세균의 활성을 감소시킨다는 것을 보여주며, 은 이온을 임상형 유방염의 치료에 적용할 수 있는 가능성을 보여 주는 것이다.

Keywords

References

  1. Ahn BS, Jeong YK, Choi YL, Jeon BS, Kim HS, Suh KH, Kim JS. Estimation of environment and Sire effect for somatic cell score in different lactation period of hostein cattle. J Anim Sci & Tehcnol 2001; 43: 623-630.
  2. Baggiolini M, Hirsch JG, De Duve C. Further biochemical and morphological studies of granule fractions from rabbit heterophil leukocytes. J Cell Biol 1970; 45: 586-597. https://doi.org/10.1083/jcb.45.3.586
  3. Bannerman DD, Paape MJ, Hare WR, Sohn EJ. Increased levels of LPS-binding protein in bovine blood and milk following bacterial lipopolysaccharide challenge. J Dairy Sci 2003; 86: 3128-3137. https://doi.org/10.3168/jds.S0022-0302(03)73914-9
  4. Beaudeau F, Seegers H, Fourichon C, Hortet P. Association between milk somatic cell counts up to 400,000 cells/ml and clinical mastitis in French Holstein cows. Vet Rec 1998; 143: 685-687.
  5. Bechert T, Steinrucke P, Guggenbichler JP. A new method for screening anti-infective biomaterials. Nat Med 2000; 6: 1053-1056. https://doi.org/10.1038/79568
  6. Berger TJ, Spadaro JA, Chapin SE, Becker RO. Electrically generated silver ions: quantitative effects on bacterial and mammalian cells. Antimicrob Agents Chemother 1976; 9: 357-358. https://doi.org/10.1128/AAC.9.2.357
  7. Brock JH. Lactoferrin in human milk: its role in iron absorption and protection against enteric infection in the newborn infant. Arch Dis Child 1980; 55: 417-421. https://doi.org/10.1136/adc.55.6.417
  8. Daley MJ, Oldham ER. Lysostaphin: immunogenicity of locally administered recombinant protein used in mastitis therapy. Vet Immunol Immunopathol 1992; 31: 301-312. https://doi.org/10.1016/0165-2427(92)90017-K
  9. Furr JR, Russell AD, Turner TD, Andrews A. Antibacterial activity of Actisorb Plus, Actisorb and silver nitrate. J Hosp Infect 1994; 27: 201-208. https://doi.org/10.1016/0195-6701(94)90128-7
  10. Hagiwara S, Kawai K, Anri A, Nagahata H. Lactoferrin concentrations in milk from normal and subclinical mastitic cows. J Vet Med Sci 2003; 65: 319-323. https://doi.org/10.1292/jvms.65.319
  11. Harmon RJ, Schanbacher FL, Ferguson LC, Smith KL.Concentration of lactoferrin in milk of normal lactating cows and changes occurring during mastitis. Am J Vet Res 1975; 36: 1001-1007.
  12. Harmon RJ, Heald CW. Migration of polymorphonuclear leukocytes into the bovine mammary gland during experimentally induced Staphylococcus aureus mastitis. Am J Vet Res 1982; 43: 992-998.
  13. Harmon RJ. Physiology of mastitis and factors affecting somatic cell counts. J Dairy Sci 1994; 77: 2103-2112. https://doi.org/10.3168/jds.S0022-0302(94)77153-8
  14. Hotta M, Nakajima H, Yamamoto K, Aono M. Antibacterial temporary filling materials: the effect of adding various ratios of Ag-Zn-Zeolite. J Oral Rehabil 1998; 25: 485-489. https://doi.org/10.1046/j.1365-2842.1998.00265.x
  15. Hu S, Concha C, Johannisson A, Meglia G, Waller KP. Effect of subcutaneous injection of ginseng on cows with subclinical Staphylococcus aureus mastitis. J Vet Med B Infect Dis Vet Public Health 2001; 48: 519-528. https://doi.org/10.1046/j.1439-0450.2001.00470.x
  16. Inchaisri C, Waller KP, Johannisson A. Studies on the modulation of leucocyte subpopulations and immunoglobulins following intramammary infusion of beta 1,3-glucan into the bovine udder during the dry period. J Vet Med B Infect Dis Vet Public Health 2000; 47: 373-386. https://doi.org/10.1046/j.1439-0450.2000.00357.x
  17. Jain NC, Schalm OW, Lasmanis J. Experimentally induced coliform (Aerobacter aerogenes) mastitis in normal cows and in cows made neutropenic by an equine anti-bovine leukocyte serum. Am J Vet Res 1971; 32: 1929-1935.
  18. Kai K, Komine K, Asai K, Kuroishi T, Komine Y, Kozutsumi T, Itagaki M, Ohta M, Endo Y, Kumagai K. Antiinflammatory effects of intramammary infusions of glycyrrhizin in lactating cows with mastitis caused by coagulase-negative staphylococci. Am J Vet Res 2003; 64: 1213-1220. https://doi.org/10.2460/ajvr.2003.64.1213
  19. Kawai K, Nagahata H, Lee NY, Anri A, Shimazaki K. Effect of infusing lactoferrin hydrolysate into bovine mammary glands with subclinical mastitis. Vet Res Commun 2003; 27: 539-548. https://doi.org/10.1023/A:1026039522286
  20. Kehrli ME, Jr., Goff JP, Stevens MG, Boone TC. Effects of granulocyte colony-stimulating factor administration to periparturient cows on neutrophils and bacterial shedding. J Dairy Sci 1991; 74: 2448-2458. https://doi.org/10.3168/jds.S0022-0302(91)78420-8
  21. Knaapen AM, Seiler F, Schilderman PA, Nehls P, Bruch J, Schins RP, Borm PJ. Neutrophils cause oxidative DNA damage in alveolar epithelial cells. Free Radic Biol Med 1999; 27: 234-240. https://doi.org/10.1016/S0891-5849(98)00285-8
  22. Matsuura T, Abe Y, Sato Y, Okamoto K, Ueshige M, Akagawa Y. Prolonged antimicrobial effect of tissue conditioners containing silver-zeolite. J Dent 1997; 25: 373-377. https://doi.org/10.1016/S0300-5712(96)00050-4
  23. Menzies FD, McBride SH, McDowell SW, McCoy MA, McConnell W, Bell C. Clinical and laboratory findings in cases of toxic mastitis in cows in Northern Ireland. Vet Rec 2000; 147: 123-128. https://doi.org/10.1136/vr.147.5.123
  24. Ogata A, Nagahata H. Intramammary application of ozone therapy to acute clinical mastitis in dairy cows. J Vet Med Sci 2000; 62: 681-686. https://doi.org/10.1292/jvms.62.681
  25. Oka H, Tomioka T, Tomita K, Nishino A, Ueda S. Inactivation of enveloped viruses by a silver-thiosulfate complex. Met Based Drugs 1994; 1: 511. https://doi.org/10.1155/MBD.1994.511
  26. Oldham ER, Daley MJ. Lysostaphin: use of a recombinant bactericidal enzyme as a mastitis therapeutic. J Dairy Sci 1991; 74: 4175-4182. https://doi.org/10.3168/jds.S0022-0302(91)78612-8
  27. Reddy PG, Reddy DN, Pruiett SE, Daley MJ, Shirley JE, Chengappa MM, Blecha F. Interleukin 2 treatment of Staphylococcus aureus mastitis. Cytokine 1992; 4: 227-231. https://doi.org/10.1016/1043-4666(92)90060-5
  28. Seol JW, Kang SJ, Park SY. Silver ion treatment of primary cultured bovine mammary gland epithelial cell (BMEC) damage from Staphylococcus aureus-derived alpha-toxin. Vet Res Commun 34: 33-42.
  29. Shuster DE, Kehrli ME, Jr., Rainard P, Paape M. Complement fragment C5a and inflammatory cytokines in neutrophil recruitment during intramammary infection with Escherichia coli. Infect Immun 1997; 65: 3286-3292.
  30. Smith JA. Neutrophils, host defense, and inflammation: a double-edged sword. J Leukoc Biol 1994; 56: 672-686. https://doi.org/10.1002/jlb.56.6.672
  31. Somerfield SD, Brandwein S. Bee venom and adjuvant arthritis. J Rheumatol 1988; 15: 1878.
  32. Steeneveld W, Hogeveen H, Barkema HW, van den Broek J, Huirne RB. The influence of cow factors on the incidence of clinical mastitis in dairy cows. J Dairy Sci 2008; 91: 1391-1402. https://doi.org/10.3168/jds.2007-0705
  33. Varshney JP, Naresh R. Evaluation of a homeopathic complex in the clinical management of udder diseases of riverine buffaloes. Homeopathy 2004; 93: 17-20. https://doi.org/10.1016/j.homp.2003.11.007