Иммунологические аспекты борьбы с маститом коров

1. Jun 15; 10 (1). р. 9602.

2. 105.Bogni C. War against mastitis: current concepts on controlling bovine mastitis рathogens / C. Bogni, L. Odierno, C. Raspanti, J. Giraudo, A. Larriestra, E. Reinoso, M. Lasagno, M. Ferrari, E. Ducrós, C. Frigerio, S. Bettera, M. Pellegrino, I. Frola, S. Dieser, C. Vissio // In: Méndez-Vilas A. (ed). Science against microbial pathogens: communicating current research and technological advances. World Scientific, Singapore. 2011. p. 483-494.

3. 106.Bucher B. The effect of selective dry cow treatment on the udder health in Swiss dairy farms / B. Bucher, U. Bleul // Schweiz Arch Tierheilkd. 2019. Sep; 161 (9). р. 533-544.

4. 107.Burvenich C. Severity of E. coli mastitis is mainly determined by cow factors / C. Burvenich, V. Van Merris, J. Mehrzad, A. DiezFraile, L. Duchateau // Vet Res. 2003. Sep-Oct; 34 (5). р. 521-564.

5. 108.Caldeira M.O. Meloxicam affects the inflammatory responses of bovine mammary epithelial cells / M.O. Caldeira, R.M. Bruckmaier, O. Wellnitz // J Dairy Sci. 2019. Nov; 102 (11). р. 10277-10290.

6. 109.Collado R. Study of the efficacy of a Streptococcus uberis mastitis vaccine against an experimental intramammary infection with a heterologous strain in dairy cows / R. Collado, C. Montbrau, M. Sitjà, A. Prenafeta // J Dairy Sci. 2018. Nov; 101 (11). р. 10290-10302.

7. 110.Curone G. What we have lost: mastitis resistance in Holstein Friesians and in a local cattle breed / G. Curone, J. Filipe, P. Cremonesi, E. Trevisi, M. Amadori, C. Pollera, B. Castiglioni, L. Turin, V. Tedde, D. Vigo, P. Moroni, A. Minuti, V. Bronzo, M.F. Addis, F. Riva // Res Vet Sci. 2018. Feb; 116. р. 88-98.

8. 111.Dai H. Methionine and arginine supplementation alter inflammatory and oxidative stress responses during lipopolysaccharide challenge in bovine mammary epithelial cells in vitro / H. Dai, D.N. Coleman, L. Hu, I. Martinez-Cortés, M. Wang, C. Parys, X. Shen, J.J. Loor // J Dairy Sci. 2020. Jan; 103 (1). р. 676-689.

9. 112.Dalanezi F.M. Influence of pathogens causing clinical mastitis on reproductive variables of dairy cows / F.M. Dalanezi, S.F. Joaquim, F.F. Guimarães, S.T. Guerra, B.C. Lopes, E.M.S. Schmidt, R.L.A. Cerri, H. Langoni // J Dairy Sci. 2020. Apr; 103 (4). р. 3648-3655.

10. 113.Eisenberg S.W.F. Diurnal differences in milk composition and its influence on in vitro growth of Staphylococcus aureus and Escherichia coli in bovine quarter milk / S.W.F. Eisenberg, E.M. Boerhout, L. Ravesloot, A.J.J.M. Daemen, L. Benedictus, V.P.M.G. Rutten, A.P. Koets // J Dairy Sci. 2016. Jul; 99 (7). р. 5690-5700.

11. 114.Gill J.J. Efficacy and pharmacokinetics of bacteriophage therapy in treatment of subclinical Staphylococcus aureus mastitis in lactating

dairy cattle / J.J. Gill, J.C. Pacan, M.E. Carson, K.E. Leslie, M.W. Griffiths, P.M. Sabour // Antimicrob Agents Chemother. 2006. V. 50 (9). p. 2912.

• 115.Gomes F. Control of bovine mastitis: old and recent therapeutic approaches / F. Gomes, M. Henriques // Current Microbiology. 2016. Apr.; 72 (4). p. 377–382.

• 116.Grispoldi L. The relationship between S. aureus and branched-chain amino acids content in composite cow milk / L. Grispoldi, M. Karama, F. Ianni, A. La Mantia, L. Pucciarini, E. Camaioni, R. Sardella, P. Sechi, B. Natalini, B.T. Cenci-Goga // Animals (Basel). 2019. Nov 16; 9 (11). pii: E981.

• 117.Gross J.J. Metabolic status is associated with the recovery of milk somatic cell сount and milk secretion after lipopolysaccharideinduced mastitis in dairy cows / J.J. Gross, L. Grossen-Rösti, S.K. Wall, O. Wellnitz, R.M. Bruckmaier // J Dairy Sci. 2020. Jun; 103 (6). р. 5604-5615.

• 118.Gussmann M. Associations between udder health and culling in dairy cows / M. Gussmann, M. Denwood, C. Kirkeby, M. Farre, T. Halasa // Prev Vet Med. 2019. Nov 1; 171. р. 104751.

• 119.Hafez S.M. Development of new strategy for non-antibiotic therapy: bovine lactoferrin has a potent antimicrobial and immunomodulator effects / S.M. Hafez, A.B. Ismael, M.B. Mahmoud, A.A. Elaraby // Adv Infect Dis. 2013. V. 3. p. 185-192.

• 120.Hughes K. The mammary microenvironment in mastitis in humans, dairy ruminants, rabbits and rodents: a one health focus / K. Hughes, C.J. Watson // J Mammary Gland Biol Neoplasia. 2018. Jun; 23 (12). р. 27-41.

• 121.Hansen S. Dataset of the microbiome composition in skin lesions caused by lumpy skin disease virus via 16s rRNA massive parallel sequencing / S. Hansen, R. Pessôa, A. Nascimento, M. El-Tholoth, A. Abd El Wahed, S.S. Sanabani // Data Brief. 2019. Nov 6; 27. р. 104764.

• 122.Hogan J. Coliform mastitis / J. Hogan, K.L. Smith // Vet Res. 2003. Sep-Oct; 34 (5). р. 507-519.

• 123.Jia F. Matrine and baicalin inhibit apoptosis induced by PantonValentine leukocidin of Staphylococcus aureus in bovine mammary epithelial cells. F. Jia, W. Ma, X. Zhang, D. Wang, X. Zhou // J Dairy Sci. 2020. Jan; 15. p: S0022-0302(20)30042-4.

• 124.Kawai K. Dynamics of lingual antimicrobial peptide, lactoferrin concentrations and lactoperoxidase activity in the milk of cows treated for clinical mastitis / K. Kawai, K. Korematsu, K. Akiyama, M. Okita, Y. Yoshimura, N. Isobe // Anim Sci J. 2015. Feb; 86 (2). р.

153-158.

• 125.Keane O.M. Symposium review: intramammary infections - major pathogens and strain-associated complexity / O.M. Keane // J Dairy Sci. 2019. May; 102 (5). р. 4713-4726.

• 126.Khan M.Z. Significant genetic effects of JAK2 and DGAT1 mutations on milk fat content and mastitis resistance in Holsteins / M.Z. Khan, D. Wang, L. Liu, T. Usman, H. Wen, R. Zhang, S. Liu, L. Shi, S. Mi, W. Xiao, Y. Yu // J Dairy Res. 2019. Nov; 29. р. 1-6.

• 127.Kitano N. Concentration patterns of antibacterial factors and immunoglobulin A antibody in foremilk fractions of healthy cows / N. Kitano, N. Isobe, J. Noda, T. Takahashi // Anim Sci J. 2020. Jan; 91 (1). р. 13372.

• 128.Koba I.S. Prevention of mastitis in dairy cows on industrial farms / I.S. Koba, A.A. Lysenko, A.G. Koshchaev, A.K. Shantyz, I.M. Donnik, V.I. Dorozhkin, S.V. Shabunin // Journal of Pharmaceutical Sciences and Research. 2018. Т. 10. № 10. р. 2582-2585.

• 129.Kutila T. Lactoferrin and citrate concentrations at drying-off and during early mammary involution of dairy cows / T. Kutila, S. Pyörälä, L. Kaartinen, R. Isomäki, K. Vahtola, L. Myllykoski, H. Saloniemi // J Vet Med 2003. Series A. v. 50 (7). p. 350-353.

• 130.Laport M.S. Antimicrobial activity of marine sponges against coagulase-negative Staphylococci isolated from bovine mastitis / M.S. Laport, P.R. Marinho, O.C. Santos, P. de Almeida, M.T. Romanos, G. Muricy, M.A. Brito, M. Giambiagi-deMarval // Vet Microbiol. 2012. V. 155 (2-4). p. 362-368.

• 131.Lavon Y. Comparing effects of bovine Streptococcus and Escherichia coli mastitis on impaired reproductive performance / Y. Lavon, G. Leitner, Y. Kressel, E. Ezra, D. Wolfenson // J Dairy Sci. 2019. Nov; 102 (11). р. 10587-10598.

• 132.Lippolis J.D. Treatment of an intramammary bacterial infection with 25-hydroxyvitamin D(3) / J.D. Lippolis, T.A. Reinhardt, R.A. Sacco, B.J. Nonnecke, C.D. Nelson // PLoS One. 2011. 6 (10). р. 25479.

• 133.Malinowski E. The effect of low intensity laser irradiation of inflamed udders on the efficacy of antibiotic treatment of clinical mastitis in dairy cows / E. Malinowski, W. Krumrych, H. Markiewicz // Vet Ital. 2019. Sep. 30; 55 (3). р. 253-260.

• 134.Mee J.F. Assessing whether dairy cow welfare is 'better' in pasturebased than in confinement-based management systems / J.F. Mee, L. Boyle // N Z Vet J. 2020. Jan; 23. р. 1-24.

• 135.Mubarack H.M. Activity of some selected medicinal plant extracts against bovine mastitis pathogens / H.M. Mubarack, A.R. Doss, R.