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dc.creatorKatsafadou A.I., Politis A.P., Mavrogianni V.S., Barbagianni M.S., Vasileiou N.G.C., Fthenakis G.C., Fragkou I.A.en
dc.date.accessioned2023-01-31T08:33:16Z
dc.date.available2023-01-31T08:33:16Z
dc.date.issued2019
dc.identifier10.3390/ani9100726
dc.identifier.issn20762615
dc.identifier.urihttp://hdl.handle.net/11615/74596
dc.description.abstractThe objectives of this review paper are to present udder defences, including teat of the udder, mammary epithelial cells, leucocytes, immunoglobulins, complement systemand chemical antibacterial agents, to describe cooperation and interactions between them and to elaborate on potentials regarding their significance inmammary immunisation strategies. The teat of the udder provides initial protection to the mammary gland. The mammary epithelial cells synthesise antibacterial proteins and the leucocytes produce various inflammation mediators (cytokines or chemokines), phagocytose bacteria and recognise antigenic structures. In themammary gland, four immunoglobulins (IgG1, IgG2, IgMand IgA) have important roles against bacterial pathogens. The complement systemis a collection of proteins, participating in the inflammatory process through various pathways. Other components contributing to humoral mammary defence include lactoferrin, lysozyme and the lactoperoxidase/myeloperoxidase systems, as well as oligosaccharides, gangliosides, reactive oxygen species, acute phase proteins (e.g., haptoglobin and serum amyloid A), ribonucleases and a wide range of antimicrobial peptides. Management practices, genetic variations and nutrition can influence mammary defences and should be taken into account in the formulation of prevention strategies against ovine mastitis. © 2019 by the authors. Licensee MDPI, Basel, Switzerland.en
dc.language.isoenen
dc.sourceAnimalsen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85073466733&doi=10.3390%2fani9100726&partnerID=40&md5=0232abf9e3227bea816ae9dc088b83fd
dc.subjectacute phase proteinen
dc.subjectamyloid A proteinen
dc.subjectantiinfective agenten
dc.subjectchemokineen
dc.subjectcomplementen
dc.subjectcytokineen
dc.subjectgamma interferonen
dc.subjectgangliosideen
dc.subjectgranulocyte colony stimulating factoren
dc.subjectgranulocyte macrophage colony stimulating factoren
dc.subjecthaptoglobinen
dc.subjectimmunoglobulinen
dc.subjectimmunoglobulin Aen
dc.subjectimmunoglobulin G1en
dc.subjectimmunoglobulin G2en
dc.subjectimmunoglobulin Men
dc.subjectinterleukin 1en
dc.subjectinterleukin 2en
dc.subjectinterleukin 8en
dc.subjectlactoferrinen
dc.subjectlactoperoxidaseen
dc.subjectlysozymeen
dc.subjectmyeloperoxidaseen
dc.subjectoligosaccharideen
dc.subjectpolypeptide antibiotic agenten
dc.subjectreactive oxygen metaboliteen
dc.subjectribonucleaseen
dc.subjectserum amyloid Aen
dc.subjecttoll like receptor 2en
dc.subjecttumor necrosis factoren
dc.subjectactive immunizationen
dc.subjectadaptive immunityen
dc.subjectbacterium adherenceen
dc.subjectbovine mastitisen
dc.subjectbreast epithelium cellen
dc.subjectCD4+ T lymphocyteen
dc.subjectCD8+ T lymphocyteen
dc.subjectcomplement systemen
dc.subjectcytoskeletonen
dc.subjectEscherichia colien
dc.subjecteween
dc.subjectgenetic variationen
dc.subjecthumanen
dc.subjecthumoral immunityen
dc.subjectimmune responseen
dc.subjectimmunityen
dc.subjectimmunizationen
dc.subjectimmunomodulationen
dc.subjectinfectious agenten
dc.subjectinflammationen
dc.subjectintestine floraen
dc.subjectleukocyteen
dc.subjectlymphocyteen
dc.subjectmacrophageen
dc.subjectmammary glanden
dc.subjectmastitisen
dc.subjectmatrix assisted laser desorption ionization time of flight mass spectrometryen
dc.subjectmicrofloraen
dc.subjectneutrophilen
dc.subjectnippleen
dc.subjectnonhumanen
dc.subjectnutritionen
dc.subjectphagocytosisen
dc.subjectphenotypeen
dc.subjectproteomicsen
dc.subjectReviewen
dc.subjectsheepen
dc.subjectStaphylococcus aureusen
dc.subjectStreptococcus uberisen
dc.subjectudderen
dc.subjectvaccinationen
dc.subjectMDPI AGen
dc.titleMammary defences and immunity against mastitis in sheepen
dc.typeotheren


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