A peptidomic approach to biomarker discovery for bovine mastitis

Journal of Proteomics

Volumn 85, Issue , 2013, Pages 89-98

  Mansor, Rozaihan ^a,f   Mullen, William ^b   Albalat, Amaya ^b   Zerefos, Panagiotis ^b,c   Mischak, Harald ^b,d   Barrett, David C ^b,g   Biggs, Andrew ^e   Eckersall, P David ^a  

^a UNIVERSITY OF GLASGOW   (United Kingdom)

^b UNIVERSITY OF GLASGOW   (United Kingdom)

^c BIOMEDICAL RESEARCH FOUNDATION   (Greece)

^d Mosaiques Diagnostics   (Germany)

^e Vale Veterinary Laboratories   (United Kingdom)

^f UNIVERSITY PUTRA MALAYSIA   (Malaysia)

^g UNIVERSITY OF BRISTOL   (United Kingdom)

Author keywords

Biomarkers; Bovine mastitis; Capillary electrophoresis; E. coli; Peptidome; S. aureus

Indexed keywords

ALPHA CASEIN; ALPHA TUBULIN; BETA CASEIN; BETA LACTOGLOBULIN; BIOLOGICAL MARKER; INTERLEUKIN 4 RECEPTOR; LACTOPEROXIDASE; OSTEOPONTIN; RHO GUANINE NUCLEOTIDE BINDING PROTEIN; STAT1 PROTEIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BOVINE MASTITIS; CAPILLARY ELECTROPHORESIS; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; ESCHERICHIA COLI INFECTION; MASS SPECTROMETRY; MILK; NONHUMAN; PEPTIDOMICS; PRIORITY JOURNAL; PROTEIN ANALYSIS; SENSITIVITY AND SPECIFICITY; STAPHYLOCOCCUS INFECTION;

ANIMALS; BIOLOGICAL MARKERS; CATTLE; ESCHERICHIA COLI; ESCHERICHIA COLI INFECTIONS; FEMALE; MASTITIS, BOVINE; MILK PROTEINS; PROTEOMICS; STAPHYLOCOCCAL INFECTIONS; STAPHYLOCOCCUS AUREUS;

BACTERIA (MICROORGANISMS); BOVINAE; ESCHERICHIA COLI; NEGIBACTERIA; POSIBACTERIA; STAPHYLOCOCCUS AUREUS;

EID: 84878368603     PISSN: 18743919     EISSN: 18767737     Source Type: Journal    
DOI: 10.1016/j.jprot.2013.04.027     Document Type: Article

References (37)

1. Radostits O.M., Blood D.C., Gay C.C., Hinchkliff K.W. Veterinary medicine 2000, ELBS-Bailliere Tindal, London. 9th ed.
2. Contreras G.A., Rodriguez J.M. Mastitis: comparative etiology and epidemiology. J Mammary Gland Biol 2011, 16:339-356.
3. De Vliegher S., Fox L., Piepers S., McDougall S., Barkema H. Invited review: mastitis in dairy heifers: nature of the disease, potential impact, prevention, and control. J Dairy Sci 2012, 95:1025-1040.
4. Schukken Y.H., Guenther J., Fitzpatrick J., Fontaine M., Goetze L., Holst O., et al. Host-response patterns of intramammary infections in dairy cows. Vet Immunol Immunopathol 2011, 144:270-289.
5. Halasa T., Huijps K., Osteras O., Hogeveen H. Economic effects of bovine mastitis and mastitis management: a review. Vet Q 2007, 29:18-31.
6. Miller G.Y., Bartlett P.C., Lance S.E., Anderson J., Heider L.E. Costs of clinical mastitis and mastitis prevention in dairy herds. J Am Vet Med Assoc 1993, 202:1230-1236.
7. Biggs A. Mastitis in cattle 2009, Crowood Press, Marlborough, Wiltshire, UK.
8. Seegers H., Fourichon C., Beaudeau F. Production effects related to mastitis and mastitis economics in dairy cattle herds. Vet Res 2003, 34:475-491.
9. Wellnitz O., Bruckmaier R.M. The innate immune response of the bovine mammary gland to bacterial infection. Vet J 2012, 192:148-152.
10. Hogarth C.J., Fitzpatrick J.L., Nolan A., Young F.J., Pitt A., Eckersall P.D. Differential protein composition of bovine whey: a comparison of whey from healthy animals and from those with clinical mastitis. Proteomics 2004, 4:2094-2100.
11. Smolenski G., Haines S., Kwan F.Y.S., Bond J., Farr V., Davis S.R., et al. Characterisation of host defence proteins in milk using a proteomic approach. J Proteome Res 2007, 6:207-215.
12. Boehmer J.L., Bannerman D.D., Shefcheck K., Ward J.L. Proteomic analysis of differentially expressed proteins in bovine milk during experimentally induced Escherichia coli mastitis. J Dairy Sci 2008, 91:4206-4218.
13. Danielsen M., Codrea M.C., Ingvartsen K.L., Friggens N.C., Bendixen E., Rontved C.M. Quantitative milk proteomics-host responses to lipopolysaccharide-mediated inflammation of bovine mammary gland. Proteomics 2010, 10:2240-2249.
14. Ibeagha-Awemu E.M., Ibeagha A.E., Messier S., Zhao X. Proteomics, genomics, and pathway analyses of Escherichia coli and Staphylococcus aureus infected milk whey reveal molecular pathways and networks involved in mastitis. J Proteome Res 2010, 9:4604-4619.
15. Larsen T., Hinz K., Jorgensen A.L., Moller H.S., Wellnitz O., Bruckmaier R.M., et al. Proteomic and peptidomic study of proteolysis in quarter milk after infusion with lipoteichoic acid from Staphylococcus aureus. J Dairy Sci 2010, 93:5613-5626.
16. Good D.M., Zuerbig P., Argiles A., Bauer H.W., Behrens G., Coon J.J., et al. Naturally occurring human urinary peptides for use in diagnosis of chronic kidney disease. Mol Cell Proteomics 2010, 9(11):2424-2437.
17. Metzger J., Kirsch T., Schiffer E., Ulger P., Mentes E., Brand K., et al. Urinary excretion of twenty peptides forms an early and accurate diagnostic pattern of acute kidney injury. Kidney Int 2010, 78(12):1252-1262.
18. Delles C., Schiffer E., von zur Muhlen C., Peter K., Rossing P., Parving H.H., et al. Urinary proteomic diagnosis of coronary artery disease: identification and clinical validation in 623 individuals. J Hypertens 2010, 28(11):2316-2322.
19. Maahs D.M., Siwy J., Argiles A., Cerna M., Delles C., Dominiczak A.F., et al. Urinary collagen fragments are significantly altered in diabetes: a link to pathophysiology. PLoS One 2010, 5(9).
20. Siwy J., Mullen W., Golovko I., Franke J., Zuerbig P. Human urinary peptide database for multiple disease biomarker discovery. Proteomics Clin Appl 2011, 5:367-374.
21. Albalat A., Franke J., Gonzalez J., Mischak H., Zurbig P. Urinary proteomics based on capillary electrophoresis coupled to mass spectrometry in kidney disease. Methods Mol Biol 2013, 919:203-213.
22. Zurbig P., Schiffer E., Mischak H. Capillary electrophoresis coupled to mass spectrometry for proteomic profiling of human urine and biomarker discovery. Methods Mol Biol 2009, 564:105-121.
23. Neuhoff N.V., Kaiser T., Wittke S., Krebs R., Pitt A., Burchard A., et al. Mass spectrometry for the detection of differentially expressed proteins: a comparison of surface-enhanced laser desorption/ionization and capillary electrophoresis/mass spectrometry. Rapid Commun Mass Spectrom 2004, 18:149-156.
24. Kolch W., Neususs C., Peizing M., Mischak H. Capillary electrophoresis-mass spectrometry as a powerful tool in clinical diagnosis and biomarker discovery. Mass Spectrom Rev 2005, 24:959-977.
25. Wedholm A., Moller H.S., Stensballe A., Lindmark-Mansson H., Karlsson A.H., Andersson R., et al. Effect of minor milk proteins in chymosin separated whey and casein fractions on cheese yield as determined by proteomics and multivariate data analysis. J Dairy Sci 2008, 91:3787-3797.
26. Mullen W., Albalat A., Gonzalez J., Zerefos P., Siwy J., Franke J., et al. Performance of different separation methods interfaced in the same MS-reflection TOF detector: a comparison of performance between CE versus HPLC for biomarker analysis. Electrophoresis 2012, 33:567-574.
27. Verdi R.J., Barbano D.M., Dellavalle M.E., Senyk G.F. Variability in true protein, casein, nonprotein nitrogen, and proteolysis in high and low somatic-cell milks. J Dairy Sci 1987, 70:230-242.
28. Hinz K., Larsen L.B., Wellnitz O., Bruckmaier R.M., Kelly A.L. Proteolytic and proteomic changes in milk at quarter level following infusion with Escherichia coli lipopolysaccharide. J Dairy Sci 2012, 95:1655-1666.
29. Larsen L.B., McSweeney P.L.H., Hayes M.G., Andersen J.B., Ingvartsen K.L., Kelly A.L. Variation in activity and heterogeneity of bovine milk proteases with stage of lactation and somatic cell count. Int Dairy J 2006, 16:1-8.
30. O'Donnell R., Holland J.W., Deeth H.C., Alewood P. Milk proteomics. Int Dairy J 2004, 14:1013-1023.
31. Manso M.A., Leonil J., Jan G., Gagnaire V. Application of proteomics to the characterisation of milk and dairy products. Int Dairy J 2005, 15:845-855.
32. Bastian E.D., Brown R.J. Plasmin in milk and dairy products: an update. Int Dairy J 1996, 6:435-457.
33. Politis I., Lachance E., Block E., Turner J.D. Plasmin and plasminogen in bovine-milk-a relationship with involution. J Dairy Sci 1989, 72:900-906.
34. Boehmer J., Ward J., Peters R., Shefcheck K., McFarland M., Bannerman D. Proteomic analysis of the temporal expression of bovine milk proteins during coliform mastitis and label-free relative quantification. J Dairy Sci 2010, 93:593-603.
35. Xie B., Tassi E., Swift M.R., McDonnell K., Bowden E.T., Wang S.M., et al. Identification of the fibroblast growth factor (FGF)-interacting domain in a secreted FGF-binding protein by phage display. J Biol Chem 2006, 281:1137-1144.
36. Kawakami A., Hirayama K., Kawakami F., Kawakami H., Fujihara M., Ohtsuki K. Purification and biochemical characterization of a fibroblast growth factor-binding protein (FGF-BP) from the lactoferrin fraction of bovine milk. BBA-Gen Subj 2006, 1760:421-431.
37. Plath A., Einspanier R., Gabler C., Peters F., Sinowatz F., Gospodarowicz D., et al. Expression and localization of members of the fibroblast growth factor family in the bovine mammary gland. J Dairy Sci 1998, 81:2604-2613.