Details
Title
Expression of anti-inflammatory markers IL-2, IL-10, TGF-β1, βDEF-2, βDEF-3 and Cathelicidin LL37 in dairy cattle milk with different health status of the udderJournal title
Polish Journal of Veterinary SciencesYearbook
2022Volume
vol. 25Issue
No 2Affiliation
Šerstņova, K. : The Institute of Anatomy and Anthropology, RSU, 9 Kronvalda bulvaris, Riga, Latvia ; Pilmane, M. : The Institute of Anatomy and Anthropology, RSU, 9 Kronvalda bulvaris, Riga, Latvia ; Vitenberga-Verza, Z. : The Institute of Anatomy and Anthropology, RSU, 9 Kronvalda bulvaris, Riga, Latvia ; Melderis, I. : The Institute of Anatomy and Anthropology, RSU, 9 Kronvalda bulvaris, Riga, Latvia ; Gontar, Ł. : Research and Innovation Centre Pro-Akademia, Innowacyjna 9/11, 95-050 Konstantynow Lodzki, Poland ; Kochański, M. : Research and Innovation Centre Pro-Akademia, Innowacyjna 9/11, 95-050 Konstantynow Lodzki, Poland ; Drutowska, A. : Research and Innovation Centre Pro-Akademia, Innowacyjna 9/11, 95-050 Konstantynow Lodzki, Poland ; Maróti, G. : Seqomics Biotechnology Ltd., Morahalom, Vallalkozak utja 7, Hungary ; Maróti, G. : Biological Research Center, Plant Biology Institute, Szeged, Temesvári krt. 62, Hungary ; Prieto-Simón, B. : Department of Electronic Engineering, Universitat Rovira i Virgili, C. de l’Escorxador, 43007 Tarragona, Spain ; Prieto-Simón, B. : ICREA, Pg. Lluís Companys 23, Barcelona, SpainAuthors
Keywords
cytokines ; interleukins ; mastitis ; bovine milkDivisions of PAS
Nauki Biologiczne i RolniczeCoverage
237-248Publisher
Polish Academy of Sciences Committee of Veterinary Sciences ; University of Warmia and Mazury in OlsztynBibliography
Addis MF, Bronzo V, Puggioni GMG, Cacciotto C, Tedde V, Pagnozzi D, Locatelli C, Casula A, Curone G, Uzzau S, Moroni P (2017) Relationship between milk cathelicidin abundance and microbiologic culture in clinical mastitis. J Dairy Sci 100: 2944-2953.
Addis MF, Tedde V, Puggioni GM, Pisanu S, Casula A, Locatelli C, Rota N, Bronzo V, Moroni P, Uzzau S (2016) Evaluation of milk cathelicidin for detection of bovine mastitis. J Dairy Sci 99: 8250-8258.
Alnakip EM, Quintela-Baluja M, Böhme K, Fernández-No I, Caamaño-Antelo S, Calo-Mata P, Barros-Velázquez J (2014) The Immunology of Mammary Gland of Dairy Ruminants between Healthy and Inflammatory Conditions. J Vet Med 2014: 659801.
Alluwaimi AM (2000) Detection of IL-2 and IFN-gamma m RNA expression in bovine milk cells at the late stage of the lactation period with RT-PCR. Res Vet Sci 69: 185-187.
Alluwaimi AM, Cullor JS (2002) Cytokines gene expression patterns of bovine milk during middle and late stages of lactation. J Vet Med B Infect Dis Vet Public Health 49: 105-110.
Alluwaimi AM, Leutenegger CM, Farver TB, Rossitto PV, Smith WL, Cullor JS (2003) The Cytokine Markers in Staphylococcus aureus Mastitis of Bovine Mammary Gland. J Vet Med50: 105-111.
Alhussien MN, Dang AK (2020) Sensitive and rapid lateral- -flow assay for early detection of subclinical mammary infection in dairy cows. Sci Rep Jul 10: 11161.
Anton K, Glod J (2017) Tumor-secreted factors that induce mesenchymal stromal cell chemotaxis. In: Mesenchymal stromal cells as tumor stromal modulators. Academic Press is an imprint of Elsevier, pp 193-214.
Azooz MF, El-Wakeel SA, Yousef HM (2020) Financial and economic analyses of the impact of cattle mastitis on the profitability of Egyptian dairy farms. Vet World 13: 1750-1759.
Bannerman DD (2009) Pathogen-dependent induction of cytokines and other soluble inflammatory mediators during intramammary infection of dairy cows. J Anim Sci 87 (13 Suppl): 10-25.
Bannerman DD, Paape MJ, Chockalingam A (2006) Staphylococcus aureus intramammary infection elicits increased production of trans-forming growth factor-alpha, beta1, and beta2. Vet Immunol Immunopathol 112: 309-315.
Bannerman DD, Springer HR, Paape MJ, Kauf AC, Goff JP (2008) Evaluation of breed-dependent differences in the innate immune re-sponses of Holstein and Jersey cows to Staphylococcus aureus intramammary infection. J Dairy Res 75: 291-301.
Bartee E, McFadden G (2013) Cytokine synergy: an underappreciated contributor to innate anti-viral immunity. Cytokine 63: 237-240.
Bochniarz M, Zdzisińska B, Wawron W, Szczubiał M, Dąbrowski R (2017) Milk and serum IL-4, IL-6, IL-10, and amyloid A concentrations in cows with subclinical mastitis caused by coagulase-negative staphylococci. J Dairy Sci 100: 9674-9680.
Britti D, Peli A, Massimini G, Polci A, Luciani A, Famigli-Bergamini P (2005) Evaluation of TNF-alpha, IL-8 and IL-10 transcriptional activity in milk from healthy dairy cows during lactation period. Vet Res Commun 29 (Suppl 2): 281-284.
Chockalingam A, Paape MJ, Bannerman DD (2005) Increased milk levels of transforming growth factor-alpha, beta1, and beta2 during Esch-erichia coli-induced mastitis. J Dairy Sci 88: 1986-1993.
Cheng G, Yu A, Malek TR (2011) T-cell tolerance and the multi-functional role of IL-2R signaling in T-regulatory cells. Immunol Rev 241: 63-76.
Cheng WN, Han SG (2020) Bovine mastitis: risk factors, therapeutic strategies, and alternative treatments - A review. Asian-Australas J Anim Sci 33: 1699-1713.
Commins S, Steinke JW, Borish L (2008) The extended IL-10 superfamily: IL-10, IL-19, IL-20, IL-22, IL-24, IL-26, IL-28, and IL-29. J Allergy Clin Immunol 121: 1108-1111.
Cubeddu T, Cacciotto C, Pisanu S, Tedde V, Alberti A, Pittau M, Dore S, Cannas A, Uzzau S, Rocca S, Addis MF (2017) Cathelicidin pro-duction and release by mammary epithelial cells during infectious mastitis. Vet Immunol Immunopathol 189: 66-70.
Dallas SL, Alliston T, Bonewald LF (2008) Transforming growth factor-β. In: Principles of bone biology. 2: 1145-1166.
De Vliegher S, Fox LK, Piepers S, McDougall S, Barkema HW (2012) Invited review: Mastitis in dairy heifers: nature of the disease, poten-tial impact, prevention, and control. J Dairy Sci 95:1025-1040.
Dooms H (2013) Interleukin-7: Fuel for the autoimmune attack. J Autoimmun 45 : 40-48.
Eckersall PD (2019) Proteomic approaches to control lactational parameters in dairy cows. Animal 13(S1): s82-s85.
Gauthier SF, Pouliot Y, Maubois JL (2006) Growth factors from bovine milk and colostrum: composition, extraction and biological activities. Lait 86: 99-125.
Gorelik L, Flavell RA (2002) Transforming growth factor- beta in T-cell biology. Nat Rev Immunol 2: 46-53.
Gulbe G, Pilmane M, Saulīte V, Doniņa S, Jermolajevs J, Peškova L, Valdovska A (2020) Cells and Cytokines in Milk of Subclinically Infected Bovine Mammary Glands after the Use of Immunomodulatory Composition GLP 810. Mediators Inflamm 2020: 8238029.
Hettinga K, van Valenberg H, de Vries S, Boeren S, van Hooijdonk T, van Arendonk J, Vervoort J (2011) The host defense proteome of human and bovine milk. PLoS One 6: e19433.
Isobe N, Nakamura J, Nakano H, Yoshimura Y (2009) Existence of functional lingual antimicrobial peptide in bovine milk. J Dairy Sci 92: 2691-2695.
Jiang Q, Li WQ, Aiello FB, Mazzucchelli R, Asefa B, Khaled AR, Durum SK (2005) Cell biology of IL-7, a key lymphotrophin. Cytokine Growth Factor Rev 16: 513-533.
Jakiel M, Jesiołkiewicz E, Ptak E (2011): Relationship between somatic cell score and daily milk yield traits of Polish HF cows. Roczniki Naukowe Polskiego Towarzystwa Zootechnicznego 7: 9-17.
Kawai K, Akamatsu H, Obayashi T, Nagahata H, Higuchi H, Iwano H, Oshida T, Yoshimura Y, Isobe N (2013) Relationship between con-centration of lingual antimicrobial peptide and somatic cell count in milk of dairy cows. Vet Immunol Immunopathol 153: 298-301.
Khan MZ, Khan A (2006) Basic facts of mastitis in dairy animals: A review. Pakistan Vet J 26: 204-208.
Kitano N, Isobe N, Noda J, Takahashi T (2020) Concentration patterns of antibacterial factors and immunoglobulin A antibody in foremilk fractions of healthy cows. Anim Sci J 91: e13372.
Komai T, Inoue M, Okamura T, Morita K, Iwasaki Y, Sumitomo S, Shoda H, Yamamoto K, Fujio K (2018) Transforming Growth Factor-β and Interleukin-10 Synergistically Regulate Humoral Immunity via Modulating Metabolic Signals. Front Immunol 9: 1364.
Krömker V, Leimbach S (2017) Mastitis treatment-Reduction in antibiotic usage in dairy cows. Reprod Domest Anim 52 (Suppl 3): 21-29.
Moore KW, de Waal Malefyt R, Coffman RL, O’Garra A (2001) Interleukin-10 and the interleukin-10 receptor. Annu. Rev Immunol 19: 683-765.
Opal SM, DePalo VA (2000) Anti-inflammatory cytokines. Chest 117: 1162-72.
Paudyal S, Pena G, Melendez P, Roman-Muniz IN, Pinedo PJ (2018) Relationships among quarter milk leukocyte proportions and cow and quarter-level variables under different intramammary infection statuses. Transl Anim Science 2: 231-240.
Pazgier M, Hoover DM, Yang D, Lu W, Lubkowski J (2006) Human beta-defensins. Cell Mol Life Sci 63: 1294-1313.
Petzl W, Zerbe H, Günther J, Yang W, Seyfert HM, Nürnberg G, Schuberth HJ (2008) Escherichia coli, but not Staphylococcus aureus trig-gers an early increased expression of factors contributing to the innate immune defense in the udder of the cow. Vet Res 39: 18.
Pongthaisong P, Katawatin S, Thamrongyoswittayakul C, Roytrakul S (2016) Milk protein profiles in response to Streptococcus agalactiae subclinical mastitis in dairy cows. Anim Sci J 87: 92-98.
Riollet C, Rainard P, Poutrel B (2000) Cells and cytokines in inflammatory secretions of bovine mammary gland. Adv Exp Med Biol 480: 247-158.
Saraiva M, O’Garra A (2010) The regulation of IL-10 production by immune cells. Nat Rev Immunol 10:170-181.
Schneider JJ, Unholzer A, Schaller M, Schäfer-Korting M, Korting HC (2005) Human defensins. J Mol Med (Berl) 83: 587-595.
Schukken YH, Günter J, Fitzpatrick J, Fontaine MC, Goetze L, Holst O, Leigh J, Petzl W, Schuberth HJ, Sipka A, Smith DG, Quesnell R, Watts J, Yancey R, Zerbe H, Gurjar A, Zadoks RN, Seyfert HM, members of the Pfizer mastitis research consortium (2011) Host- -response patterns of intramammary infections in dairy cows. Vet ImmunolImmunopathol 144: 270-289.
Stelwagen K, Carpenter E, Haigh B, Hodgkinson A, Wheeler TT (2009) Immune components of bovine colostrum and milk. J Anim Sci 87 (Suppl 13): 3-9.
Taylor A, Akdis M, Joss A, Akkoç T, Wenig R, Colonna M, Daigle I, Flory E, Blaser K, Akdis CA (2007) IL-10 inhibits CD28 and ICOS costimulations of T cells via src homology 2 domain-containing protein tyrosine phosphatase 1. J. Allergy Clin Immunol 120: 76-83.
Tzavlaki K, Moustakas A (2020) TGF-β Signaling. Biomolecules 10: 487.
Wheeler TT, Smolenski GA, Harris DP, Gupta SK, Haigh BJ, Broadhurst MK, Molenaar AJ, Stelwagen K (2012) Host-defence-related proteins in cows’ milk. Animal 6: 415-22.
Whelehan CJ, Barry-Reidy A, Meade KG, Eckersall PD, Chapwanya A, Narciandi F, Lloyd AT, Farrelly CO (2014) Characterisation and expression profile of the bovine cathelicidin gene repertoire in mammary tissue. BMC Genomics 15: 128.
Wollowski L, Heuwieser W, Kossatz A, Addis MF, Puggioni GMG, Meriaux L, Bertulat S (2021) The value of the biomarkers cathelicidin, milk amyloid A, and haptoglobin to diagnose and classify clinical and subclinical mastitis. J Dairy Sci 104: 2106-2122.