References
- Adkins P.R.F., Dufour S., Spain J.N., Calcutt M.J., Reilly T.J., Stewart G.C., Middleton J.R.: Molecular characterization of non-aureus Staphylococcus spp. from heifer intramammary infections and body sites. J Dairy Sci 2018, 101, 5388–5403.
- Albenzio M., Santillo A., Kelly A.L., Caroprese M., Marino R., Sevi A.: Activities of indigenous proteolytic enzymes in caprine milk of different somatic cell counts. J Dairy Sci 2015, 98, 7587– 7594.
- Alluwaimi A.M., Cullor J.S.: Cytokines gene expression patterns of bovine milk during middle and late stages of lactation. J Vet Med B Infect Dis Vet Public Health 2002, 49, 105–110.
- Durilova M., Stechova K., Petruzelkova L. Stavikova V., Ulmannova T., Nevoral J.: Is there any relationship between cytokine spectrum of breast milk and occurrence of eosinophilic colitis? Acta Paediatr 2010, 99, 1666–1670.
- Fang W., Pyörälä S.: Mastitis-causing Escherichia coli serum sensitivity and susceptibility to selected antibacterials in milk. J Dairy Sci 1996, 79, 76–82.
- Isobe N.: Control mechanisms for producing antimicrobial factors in ruminant mammary gland. Anim Sci J 2017, 88, 937–943.
- Jeurink P.V., van Bergenhenegouwen J., Jimenez E., Knippels L.M., Fernandez L., Garssen J., Knol J., Rodriguez J.M., Martin R.: Human milk: a source of more life than we imagine. Benef Microbes. 2013, 4, 417–430.
- Kai K., Komine Y., Komine K., Asai K., Kuroishi T., Kozutsumi T., Itagaki M., Ohta M., Kumagai K.: Effects of bovine lactoferrin by the intramammary infusion in cows with staphylococcal mastitis during the early non-lactating period. J Vet Med Sci 2002, 64, 873–878.
- Lasagno M., Ortiz M., Vissio C., Yaciuk R., Bonetto C., Pellegrino M., Bogni C., Odierno L., Raspanti C.: Pathogenesis and inflammatory response in experimental caprine mastitis due to Staphylococcus chromogenes Microb Pathog 2018, 116, 146–152.
- Martín R., Langa S., Reviriego C., Jiménez E., Olivares M., Boza J., Jiménez J., Fernández L., Xaus J., Rodríguez M.: The commensal microflora of human milk: new perpectives for food bacteriotherapy and probiotics. Trends Food Sci Technol 2004, 15, 121–127.
- Maeda Y., Ohtsuka H., Tomioka M., Oikawa M.: Effect of progesterone on Th1/Th2/Th17 and Regulatory T cell-related genes in peripheral blood mononuclear cells during pregnancy in cows. Vet Res Commun 2012, 37, 43–49.
- Metzger S.A., Hernandez L.L., Skarlupka J.H., Suen G., Walker T.M., Ruegg P.L.: Influence of sampling technique and bedding type on the milk microbiota: results of a pilot study. J Dairy Sci 2018, 101, 6346–6356.
- Murdough P.A., Deitz K.E., Pankey J.W.: Effects of freezing on the viability of nine pathogens from quarters with subclinical mastitis. J Dairy Sci 1996, 79, 334–336.
- Pawlik A., Sender G., Korwin-Kossakowska A.: Bovine lactoferrin gene polymorphism and expression in relation to mastitis resistance - a review. Anim Sci Pap Rep 2009, 27, 263–271.
- Pyörälä S., Jousimies-Somer H., Mero M.: Clinical, bacteriological and therapeutic aspects of bovine mastitis caused by aerobic and anaerobic pathogens. Br Vet J 1992, 148, 54–62.
- Rainard P., Riollet C.: Mobilization of neutrophils and defense of the bovine mammary gland. Reprod Nutr Dev 2003, 43, 439–457.
- Sakemi Y., Tamura Y., Hagiwara K.: Interleukin-6 in quarter milk as a further prediction marker for bovine subclinical mastitis. J Dairy Res 2011, 78, 118–121.
- Sordillo L.M., Streicher K.L.: Mammary gland immunity and mastitis susceptibility. J Mammary Gland Biol Neoplasia 2002, 7, 135–146.
- Špaková T., Elečko J., Vasil M., Legáth J., Pristaš P., Javorský P.: Limited genetic diversity of Aerococcus viridans strains isolated from clinical and subclinical cases of bovine mastitis in Slovakia. Pol J Vet Sci 2012, 15, 329–335.
- Thornberry N.A., Lazebnik Y.: Caspases: enemies within. Science 1998, 281, 1312–1316.
- Untergasser A., Cutcutache I., Koressaar T., Ye J., Faircloth B.C., Remm M. Rozen S.G.: Primer3–new capabilities and interfaces. Nucleic Acids Res. 2012, 40, 15:e115.
- Vorbach C., Capecchi M.R., Penninger J.M.: Evolution of the mammary gland from the innate immune system? Bio Essays 2006, 28, 606–616.
- Ward C., Chilvers E.R., Lawson M.F., Pryde J.G., Fujihara S., Farrow S.N., Haslett C., Rossi A.G.: NF-kappaB activation is a critical regulator of human granulocyte apoptosis in vitro J Biol Chem 1999, 274, 4309–4318.
- Wesson C.A., Deringer J., Liou L.E., Bayles K.W., Bohach G.A., Trumble W.R.: Apoptosis induced by Staphylococcus aureus in epithelial cells utilizes a mechanism involving caspases 8 and 3. Infect Immun 2000, 68, 2998–3001.
- Wirestam L., Enocsson H., Skogh T., Eloranta M.L., Rönnblom L., Sjöwall C., Wetterö J.: Interferon-α coincides with suppressed levels of pentraxin-3 (PTX3) in systemic lupus erythematosus and regulates leucocyte PTX3 in vitro Clin Exp Immun 2017, 189, 83–91.
- Wu H., Zhang G., Minton J.E., Ross C.R., Blecha F.: Regulation of cathelicidin gene expression: induction by lipopolysaccharide, interleukin-6, retinoic acid, and Salmonella enterica serovar Typhimurium infection. Infect Immun 2000, 68, 5552–5558.