Neutrophil extracellular traps in sheep mastitis

Veterinary Research

Volumn 46, Issue 1, 2015, Pages

  Pisanu, Salvatore ^a   Cubeddu, Tiziana ^b   Pagnozzi, Daniela ^a   Rocca, Stefano ^b   Cacciotto, Carla ^b   Alberti, Alberto ^b   Marogna, Gavino ^c   Uzzau, Sergio ^a   Addis, Maria Filippa ^a  

^a Porto Conte Ricerche Srl   (Italy)

^b UNIVERSITY OF SASSARI   (Italy)

^c Istituto Zooprofilattico Sperimentale G   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALIA; BACTERIA (MICROORGANISMS); OVIS ARIES; STREPTOCOCCUS UBERIS;

ANIMAL; CYTOLOGY; EXTRACELLULAR TRAP; FEMALE; HUMAN; IMMUNOLOGY; MASTITIS; METABOLISM; MICROBIOLOGY; MILK; NEUTROPHIL; PATHOLOGY; PHYSIOLOGY; SHEEP; SHEEP DISEASE; STREPTOCOCCUS; STREPTOCOCCUS INFECTION; UDDER; VETERINARY;

ANIMALS; EXTRACELLULAR TRAPS; FEMALE; HUMANS; MAMMARY GLANDS, ANIMAL; MASTITIS; MILK; NEUTROPHILS; SHEEP; SHEEP DISEASES; STREPTOCOCCAL INFECTIONS; STREPTOCOCCUS;

EID: 84935858179     PISSN: 09284249     EISSN: 12979716     Source Type: Journal    
DOI: 10.1186/s13567-015-0196-x     Document Type: Article

References (45)

1. Bergonier D, De Crémoux R, Rupp R, Lagriffoul G, Berthelot X (2003) Mastitis of dairy small ruminants. Vet Res 34:689-716
2. Contreras A, Sierra D, Sánchez A, Corrales JC, Marco JC, Paape MJ, Gonzalo C (2007) Mastitis in small ruminants. Small Rumin Res 68:145-153
3. Marogna G, Rolesu S, Lollai S, Tola S, Leori G (2010) Clinical findings in sheep farms affected by recurrent bacterial mastitis. Small Rumin Res 88:119-125
4. Corrales JC, Esnal A, De la Fe C, Sánchez A, Assunçao P, Poveda JB, Contreras A (2007) Contagious agalactia in small ruminants. Small Rumin Res 68:154-166
5. Riollet C, Rainard P, Poutrel B (2000) Cells and cytokines in inflammatory secretions of bovine mammary gland. Adv Exp Med Biol 480:247-158
6. Paape MJ, Wiggans GR, Bannerman DD, Thomas DL, Sanders AH, Contreras A, Moroni P, Miller RH (2007) Monitoring goat and sheep milk somatic cell counts. Small Rumin Res 68:114-125
7. Turin L, Pisoni G, Giannino ML, Antonini M, Rosati S, Ruffo G, Moroni P (2005) Correlation between milk parameters in CAEV seropositive and negative primiparous goats during an eradication program in Italian farm. Small Rumin Res 57:73-79
8. Leitner G, Shoshani E, Krifucks O, Chaffer M, Saran A (2000) Milk leucocyte population patterns in bovine udder infection of different aetiology. J Vet Med B Infect Dis Vet Public Health 47:581-589
9. Strandberg Y, Gray C, Vuocolo T, Donaldson L, Broadway M, Tellam R (2005) Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells. Cytokine 31:72-86
10. Lahouassa H, Moussay E, Rainard P, Riollet C (2007) Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli. Cytokine 38:12-21
11. Günther J, Koczan D, Yang W, Nürnberg G, Repsilber D, Schuberth H-J, Park Z, Maqbool N, Molenaar A, Seyfert H-M (2009) Assessment of the immune capacity of mammary epithelial cells: comparison with mammary tissue after challenge with Escherichia coli. Vet Res 40:31
12. Elazar S, Gonen E, Livneh-Kol A, Rosenshine I, Shpigel NY (2010) Essential role of neutrophils but not mammary alveolar macrophages in a murine model of acute Escherichia coli mastitis. Vet Res 41:53
13. Paape MJ, Bannerman DD, Zhao X, Lee J-W (2003) The bovine neutrophil: Structure and function in blood and milk. Vet Res 34:597-627
14. Mehrzad J, Dosogne H, Vangroenweghe F, Burvenich C (2001) A comparative study of bovine blood and milk neutrophil functions with luminol-dependent chemiluminescence. Luminescence 16:343-356
15. Schukken YH, Günther J, Fitzpatrick J, Fontaine MC, Goetze L, Holst O, Leigh J, Petzl W, Schuberth H-J, Sipka A, Smith DGE, Quesnell R, Watts J, Yancey R, Zerbe H, Gurjar A, Zadoks RN, Seyfert H-M (2011) Host-response patterns of intramammary infections in dairy cows. Vet Immunol Immunopathol 144:270-289
16. Brinkmann V, Reichard U, Goosmann C, Fauler B, Uhlemann Y, Weiss DS, Weinrauch Y, Zychlinsky A (2004) Neutrophil extracellular traps kill bacteria. Science 303:1532-1535
17. Wartha F, Beiter K, Normark S, Henriques-Normark B (2007) Neutrophil extracellular traps: casting the NET over pathogenesis. Curr Opin Microbiol 10:52-56
18. Phillipson M, Kubes P (2011) The neutrophil in vascular inflammation. Nat Med 17:1381-1390
19. Wang Y, Li M, Stadler S, Correll S, Li P, Wang D, Hayama R, Leonelli L, Han H, Grigoryev SA, Allis CD, Coonrod SA (2009) Histone hypercitrullination mediates chromatin decondensation and neutrophil extracellular trap formation. J Cell Biol 184:205-213
20. Von Köckritz-Blickwede M, Nizet V (2009) Innate immunity turned inside-out: antimicrobial defense by phagocyte extracellular traps. J Mol Med (Berl) 87:775-783
21. Lu T, Kobayashi SD, Quinn MT, Deleo FR (2012) A NET Outcome. Front Immunol 3:365
22. Lippolis JD, Reinhardt TA, Goff JP, Horst RL (2006) Neutrophil extracellular trap formation by bovine neutrophils is not inhibited by milk. Vet Immunol Immunopathol 113:248-255
23. Reinhardt TA, Sacco RE, Nonnecke BJ, Lippolis JD (2013) Bovine milk proteome: quantitative changes in normal milk exosomes, milk fat globule membranes and whey proteomes resulting from Staphylococcus aureus mastitis. J Proteomics 82:141-154
24. Addis MF, Pisanu S, Marogna G, Cubeddu T, Pagnozzi D, Cacciotto C, Campesi F, Schianchi G, Rocca S, Uzzau S (2013) Production and release of antimicrobial and immune defense proteins by mammary epithelial cells following Streptococcus uberis infection of sheep. Infect Immun 81:3182-3197
25. Addis MF, Pisanu S, Ghisaura S, Pagnozzi D, Marogna G, Tanca A, Biosa G, Cacciotto C, Alberti A, Pittau M, Roggio T, Uzzau S (2011) Proteomics and pathway analyses of the milk fat globule in sheep naturally infected by Mycoplasma agalactiae provide indications of the in vivo response of the mammary epithelium to bacterial infection. Infect Immun 79:3833-4385
26. Pisanu S, Ghisaura S, Pagnozzi D, Biosa G, Tanca A, Roggio T, Uzzau S, Addis MF (2011) The sheep milk fat globule membrane proteome. J Proteomics 350-358
27. Pisanu S, Ghisaura S, Pagnozzi D, Falchi G, Biosa G, Tanca A, Roggio T, Uzzau S, Addis MF (2012) Characterization of sheep milk fat globule proteins by two-dimensional polyacrylamide gel electrophoresis/mass spectrometry and generation of a reference map. Int Dairy J 24:78-86
28. Pisanu S, Marogna G, Pagnozzi D, Piccinini M, Leo G, Tanca A, Roggio AM, Roggio T, Uzzau S, Addis MF (2013) Characterization of size and composition of milk fat globules from Sarda and Saanen dairy goats. Small Rumin Res 109:141-151
29. Tanca A, Biosa G, Pagnozzi D, Addis MF, Uzzau S (2013) Comparison of detergent-based sample preparation workflows for LTQ-Orbitrap analysis of the Escherichia coli proteome. Proteomics 13:2597-2607
30. Wis̈niewski JR, Zougman A, Nagaraj N, Mann M (2009) Universal sample preparation method for proteome analysis. Nat Methods 6:359-362
31. Wis̈niewski JR, Zielinska DF, Mann M (2011) Comparison of ultrafiltration units for proteomic and N-glycoproteomic analysis by the filter-aided sample preparation method. Anal Biochem 410:307-309
32. Tanca A, Palomba A, Deligios M, Cubeddu T, Fraumene C, Biosa G, Pagnozzi D, Addis MF, Uzzau S (2013) Evaluating the impact of different sequence databases on metaproteome analysis: insights from a lab-assembled microbial mixture. PLoS One 8:e82981
33. Old WM, Meyer-Arendt K, Aveline-Wolf L, Pierce KG, Mendoza A, Sevinsky JR, Resing KA, Ahn NG (2005) Comparison of label-free methods for quantifying human proteins by shotgun proteomics. Mol Cell Proteomics 4:1487-1502
34. Zybailov B, Mosley AL, Sardiu ME, Coleman MK, Florens L, Washburn MP (2006) Statistical analysis of membrane proteome expression changes in Saccharomyces cerevisiae. J Proteome Res 5:2339-2347
35. Pham TV, Piersma SR, Warmoes M, Jimenez CR (2010) On the beta-binomial model for analysis of spectral count data in label-free tandem mass spectrometry-based proteomics. Bioinformatics 26:363-369
36. Yousefi S, Mihalache C, Kozlowski E, Schmid I, Simon HU (2009) Viable neutrophils release mitochondrial DNA to form neutrophil extracellular traps. Cell Death Differ 16:1438-1444
37. Yousefi S, Gold JA, Andina N, Lee JJ, Kelly AM, Kozlowski E, Schmid I, Straumann A, Reichenbach J, Gleich GJ, Simon HU (2008) Catapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense. Nat Med 14:949-953
38. Remijsen Q, Kuijpers TW, Wirawan E, Lippens S, Vandenabeele P, Vanden Berghe T (2011) Dying for a cause: NETosis, mechanisms behind an antimicrobial cell death modality. Cell Death Differ 18:581-588
39. György B, Tóth E, Tarcsa E, Falus A, Buzás EI (2006) Citrullination: a posttranslational modification in health and disease. Int J Biochem Cell Biol 38:1662-1677
40. Hagiwara T, Hidaka Y, Yamada M (2005) Deimination of histone H2A and H4 at arginine 3 in HL-60 granulocytes. Biochemistry 44:5827-5834
41. Wang Y, Wysocka J, Sayegh J, Lee Y-H, Perlin JR, Leonelli L, Sonbuchner LS, McDonald CH, Cook RG, Dou Y, Roeder RG, Clarke S, Stallcup MR, Allis CD, Coonrod SA (2004) Human PAD4 regulates histone arginine methylation levels via demethylimination. Science 306:279-283
42. Raijmakers R, van Beers JJBC, El-Azzouny M, Visser NFC, Božič B, Pruijn GJM, Heck AJR (2012) Elevated levels of fibrinogen-derived endogenous citrullinated peptides in synovial fluid of rheumatoid arthritis patients. Arthritis Res Ther 14:R114
43. Tripathi A, Lammers KM, Goldblum S, Shea-Donohue T, Netzel-Arnett S, Buzza MS, Antalis TM, Vogel SN, Zhao A, Yang S, Arrietta M-C, Meddings JB, Fasano A (2009) Identification of human zonulin, a physiological modulator of tight junctions, as prehaptoglobin-2. Proc Natl Acad Sci U S A 106:16799-16804
44. Li P, Li M, Lindberg MR, Kennett MJ, Xiong N, Wang Y (2010) PAD4 is essential for antibacterial innate immunity mediated by neutrophil extracellular traps. J Exp Med 207:1853-1862
45. Gupta AK, Joshi MB, Philippova M, Erne P, Hasler P, Hahn S, Resink TJ (2010) Activated endothelial cells induce neutrophil extracellular traps and are susceptible to NETosis-mediated cell death. FEBS Lett 584:3193-3197