Determination of changes in bovine plasma and milk proteins during naturally occurring Escherichia coli mastitis by comparative proteomic analysis
Yongxin Yang A , Suizhong Cao B C , Xiaowei Zhao A , Dongwei Huang A , Huiling Zhao A and Guanglong Cheng A DA Institute of Animal Science and Veterinary Medicine, Anhui Academy of Agricultural Sciences, Hefei 230031, China.
B College of Veterinary Medicine, Sichuan Agricultural University, Ya’an 625014, China.
C College of Veterinary Medicine, Michigan State University, East Lansing, MI 48824, USA.
D Corresponding author. Email: cgl0126@126.com
Animal Production Science 56(11) 1888-1896 https://doi.org/10.1071/AN14901
Submitted: 27 July 2013 Accepted: 22 May 2015 Published: 15 September 2015
Abstract
The aim of this study was to investigate changes in plasma and milk proteins in response to Escherichia coli infection in cows. Plasma and milk were collected from healthy cows, cows suffering from mild E. coli mastitis, and cows suffering from severe E. coli mastitis. Protein composition was examined by two-dimensional gel electrophoresis coupled with mass spectrometry. Plasma haptoglobin and α-1 acid glycoprotein demonstrated greater expression in mastitic cows compared with controls, but there were no difference between mildly and severely mastitic cows. Milk from mildly mastitic cows showed increased albumin and casein variants. Severely mastitic cows showed lower casein levels and increased anti-microbial and acute phase proteins. Milk α-1 acid glycoprotein and cathelicidins were associated with severe mastitis. A greater number of β-casein fragments that corresponded to β-casein isoforms were found in milk from mildly mastitic cows. These results suggest that caseins levels decreased and the concentrations of anti-microbial and acute phase proteins increased corresponding to the degree of E. coli mastitis. Nevertheless, further studies are needed to determine whether cathelicidin could serve as a diagnostic marker for mastitis.
Additional keywords: dairy cows, proteome.
References
Alonso-Fauste I, Andrés M, Iturralde M, Lampreave F, Gallart J, Álava MA (2012) Proteomic characterization by 2-DE in bovine serum and whey from healthy and mastitis affected farm animals. Journal of Proteomics 75, 3015–3030.| Proteomic characterization by 2-DE in bovine serum and whey from healthy and mastitis affected farm animals.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38Xntlejtr0%3D&md5=05169933766f5a32436964da12692889CAS | 22193514PubMed |
Baeker R, Haebel S, Schlatterer K, Schlatterer B (2002) Lipocalin-type prostaglandin D synthase in milk: a new biomarker for bovine mastitis. Prostaglandins & Other Lipid Mediators 67, 75–88.
| Lipocalin-type prostaglandin D synthase in milk: a new biomarker for bovine mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xls1CrtA%3D%3D&md5=e21e5b75c6fb8d6d5e7b3e9b6c0d2f4cCAS |
Bannerman DD, Kauf AC, Paape MJ, Springer HR, Goff JP (2008) Comparison of Holstein and Jersey innate immune responses to Escherichia coli intramammary infection. Journal of Dairy Science 91, 2225–2235.
| Comparison of Holstein and Jersey innate immune responses to Escherichia coli intramammary infection.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXmsVWmt7g%3D&md5=cbf615c32890ec3dafbdbdaddccf74caCAS | 18487645PubMed |
Boehmer JL, Bannerman DD, Shefcheck K, Ward JL (2008) Proteomic analysis of differentially expressed proteins in bovine milk during experimentally induced Escherichia coli mastitis. Journal of Dairy Science 91, 4206–4218.
| Proteomic analysis of differentially expressed proteins in bovine milk during experimentally induced Escherichia coli mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtlajtL7M&md5=738046b0c1075de47ffa4f88261e6891CAS | 18946125PubMed |
Boehmer JL, Ward JL, Peters RR, Shefcheck KJ, McFarland MA, Bannerman DD (2010) Proteomic analysis of the temporal expression of bovine milk proteins during coliform mastitis and label-free relative quantification. Journal of Dairy Science 93, 593–603.
| Proteomic analysis of the temporal expression of bovine milk proteins during coliform mastitis and label-free relative quantification.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXht1CjtL0%3D&md5=63f18b82001094aca3408f27452be023CAS | 20105531PubMed |
Burvenich C, Van Merris V, Mehrzad J, Diez-Fraile A, Duchateau L (2003) Severity of E. coli mastitis is mainly determined by cow factors. Veterinary Research 34, 521–564.
| Severity of E. coli mastitis is mainly determined by cow factors.Crossref | GoogleScholarGoogle Scholar | 14556694PubMed |
Candiano G, Bruschi M, Musante L, Santucci L, Ghiggeri GM, Carnemolla B, Orecchia P, Zardi L, Righetti PG (2004) Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis. Electrophoresis 25, 1327–1333.
| Blue silver: a very sensitive colloidal Coomassie G-250 staining for proteome analysis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXks12ht7c%3D&md5=f6ebcc82622378541c0864b0258e4df8CAS | 15174055PubMed |
Cooray R, Waller KP, Venge P (2007) Haptoglobin comprises about 10% of granule protein extracted from bovine granulocytes isolated from healthy cattle. Veterinary Immunology and Immunopathology 119, 310–315.
| Haptoglobin comprises about 10% of granule protein extracted from bovine granulocytes isolated from healthy cattle.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXhtVWht7fF&md5=c9053b2a9e4531a4f0d52d2c2dcf56a9CAS | 17681384PubMed |
Danielsen M, Codrea MC, Ingvartsen KL, Friggens NC, Bendixen E, Røntved CM (2010) Quantitative milk proteomics–host responses to lipopolysaccharide-mediated inflammation of bovine mammary gland. Proteomics 10, 2240–2249.
| Quantitative milk proteomics–host responses to lipopolysaccharide-mediated inflammation of bovine mammary gland.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXns1CrtL0%3D&md5=66a92b8ab969731e50d81dc00ad8d0d2CAS | 20352626PubMed |
Dufour D, Jameh N, Dary A, Le Roux Y (2009) Short communication: can the mammopathogenic Escherichia coli P4 strain have a direct role on the caseinolysis of milk observed during bovine mastitis? Journal of Dairy Science 92, 1398–1403.
| Short communication: can the mammopathogenic Escherichia coli P4 strain have a direct role on the caseinolysis of milk observed during bovine mastitis?Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXjvFamsbY%3D&md5=175ada9576dcdfc3a43c4da1c2abe131CAS | 19307620PubMed |
Eckersall PD, Young FJ, McComb C, Hogarth CJ, Safi S, Weber A, McDonald T, Nolan AM, Fitzpatrick JL (2001) Acute phase proteins in serum and milk from dairy cows with clinical mastitis. The Veterinary Record 148, 35–41.
| Acute phase proteins in serum and milk from dairy cows with clinical mastitis.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD3Mzlt12qsw%3D%3D&md5=5454bc9ba28e60748290b91d7ef7959cCAS | 11202551PubMed |
Günther J, Koczan D, Yang W, Nürnberg G, Repsilber D, Schuberth HJ, Park Z, Maqbool N, Molenaar A, Seyfert HM (2009) Assessment of the immune capacity of mammary epithelial cells: comparison with mammary tissue after challenge with Escherichia coli. Veterinary Research 40, 31
| Assessment of the immune capacity of mammary epithelial cells: comparison with mammary tissue after challenge with Escherichia coli.Crossref | GoogleScholarGoogle Scholar | 19321125PubMed |
Günther J, Petzl W, Zerbe H, Schuberth HJ, Koczan D, Goetze L, Seyfert HM (2012) Lipopolysaccharide priming enhances expression of effectors of immune defence while decreasing expression of pro-inflammatory cytokines in mammary epithelia cells from cows. BMC Genomics 13, 17
| Lipopolysaccharide priming enhances expression of effectors of immune defence while decreasing expression of pro-inflammatory cytokines in mammary epithelia cells from cows.Crossref | GoogleScholarGoogle Scholar | 22235868PubMed |
Haddadi K, Moussaoui F, Hebia I, Laurent F, Le Roux Y (2005) E. coli proteolytic activity in milk and casein breakdown. Reproduction, Nutrition, Development 45, 485–496.
| E. coli proteolytic activity in milk and casein breakdown.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXhtVCjtrrO&md5=a8184f5bf03df4a404f07cc1c68fc941CAS | 16045896PubMed |
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
| The host defense proteome of human and bovine milk.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXls1Snu7s%3D&md5=c921b29f0d0d359744ec0e6b93af54afCAS | 21556375PubMed |
Hinz K, Larsen LB, Wellnitz O, Bruckmaier RM, Kelly AL (2012) Proteolytic and proteomic changes in milk at quarter level following infusion with Escherichia coli lipopolysaccharide. Journal of Dairy Science 95, 1655–1666.
Hirvonen J, Eklund K, Teppo AM, Huszenicza G, Kulcsar M, Saloniemi H, Pyörälä S (1999) Acute phase response in dairy cows with experimentally induced Escherichia coli mastitis. Acta Veterinaria Scandinavica 40, 35–46.
Hiss S, Mielenz M, Bruckmaier RM, Sauerwein H (2004) Haptoglobin concentrations in blood and milk after endotoxin challenge and quantification of mammary Hp mRNA expression. Journal of Dairy Science 87, 3778–3784.
| Haptoglobin concentrations in blood and milk after endotoxin challenge and quantification of mammary Hp mRNA expression.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXptVOksb4%3D&md5=6d1dcca292d2b41099e027575da3e435CAS | 15483161PubMed |
Hogarth CJ, Fitzpatrick JL, Nolan AM, Young FJ, Pitt A, Eckersall PD (2004) Differential protein composition of bovine whey: a comparison of whey from healthy animals and from those with clinical mastitis. Proteomics 4, 2094–2100.
| Differential protein composition of bovine whey: a comparison of whey from healthy animals and from those with clinical mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXlslKjurs%3D&md5=fef610b17f7e29b94a3f4fce08ea5aa1CAS | 15221770PubMed |
Ibeagha-Awemu EM, Ibeagha AE, Messier S, Zhao X (2010) Proteomics, genomics, and pathway analyses of Escherichia coli and Staphylococcus aureus infected milk whey reveal molecular pathways and networks involved in mastitis. Journal of Proteome Research 9, 4604–4619.
| Proteomics, genomics, and pathway analyses of Escherichia coli and Staphylococcus aureus infected milk whey reveal molecular pathways and networks involved in mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXhtVSmsL3N&md5=c025aaa6832aa2ba59f7250cb7f57ed1CAS | 20704270PubMed |
Kaartinen L, Veijalainen K, Kuosa PL, Pyörälä S, Sandholm M (1988) Endotoxin-induced mastitis. Inhibition of casein synthesis and activation of the caseinolytic system. Zentralblatt fur Veterinarmedizin. Reihe B. 35, 353–360.
Koskinen MT, Holopainen J, Pyörälä S, Bredbacka P, Pitkälä A, Barkema HW, Bexiga R, Roberson J, Sølverød L, Piccinini R, Kelton D, Lehmusto H, Niskala S, Salmikivi L (2009) Analytical specificity and sensitivity of a real-time polymerase chain reaction assay for identification of bovine mastitis pathogens. Journal of Dairy Science 92, 952–959.
| Analytical specificity and sensitivity of a real-time polymerase chain reaction assay for identification of bovine mastitis pathogens.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1MXivVakt7s%3D&md5=8cfa44b7577d4397d4955cbd1678cf76CAS | 19233788PubMed |
Lai IH, Tsao JH, Lu YP, Lee JW, Zhao X, Chien FL, Mao SJ (2009) Neutrophils as one of the major haptoglobin sources in mastitis affected milk. Veterinary Research 40, 17
| Neutrophils as one of the major haptoglobin sources in mastitis affected milk.Crossref | GoogleScholarGoogle Scholar | 19094922PubMed |
Lee KH, Lee JW, Wang SW, Liu LY, Lee MF, Chuang ST, Shy YM, Chang CL, Wu MC, Chi CH (2008) Development of a novel biochip for rapid multiplex detection of seven mastitis-causing pathogens in bovine milk samples. Journal of Veterinary Diagnostic Investigation 20, 463–471.
| Development of a novel biochip for rapid multiplex detection of seven mastitis-causing pathogens in bovine milk samples.Crossref | GoogleScholarGoogle Scholar | 18599851PubMed |
Lehtolainen T, Røntved C, Pyörälä S (2004) Serum amyloid A and TNF alpha in serum and milk during experimental endotoxin mastitis. Veterinary Research 35, 651–659.
| Serum amyloid A and TNF alpha in serum and milk during experimental endotoxin mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXmt1Wksw%3D%3D&md5=9e8837abb7199febeb4c4cd8632817a2CAS | 15535955PubMed |
Linde A, Ross CR, Davis EG, Dib L, Blecha F, Melgarejo T (2008) Innate immunity and host defense peptides in veterinary medicine. Journal of Veterinary Internal Medicine 22, 247–265.
| Innate immunity and host defense peptides in veterinary medicine.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1c3htVOltQ%3D%3D&md5=cbc284301fa370a27050a83a479858efCAS | 18312280PubMed |
Lutzow YCS, Donaldson L, Gray CP, Vuocolo T, Pearson RD, Reverter A, Byrne KA, Sheehy PA, Windon R, Tellam RL (2008) Identification of immune genes and proteins involved in the response of bovine mammary tissue to Staphylococcus aureus infection. BMC Veterinary Research 4, 18
| Identification of immune genes and proteins involved in the response of bovine mammary tissue to Staphylococcus aureus infection.Crossref | GoogleScholarGoogle Scholar |
Massart-Leën A-M, Burvenich C, Massart DL (1994) Triacylglycerol fatty acid composition of milk from periparturient cows during acute Escherichia coli mastitis. The Journal of Dairy Research 61, 191–199.
| Triacylglycerol fatty acid composition of milk from periparturient cows during acute Escherichia coli mastitis.Crossref | GoogleScholarGoogle Scholar | 8063965PubMed |
Mehrzad J, Desrosiers C, Lauzon K, Robitaille G, Zhao X, Lacasse P (2005) Proteases involved in mammary tissue damage during endotoxin-induced mastitis in dairy cows. Journal of Dairy Science 88, 211–222.
| Proteases involved in mammary tissue damage during endotoxin-induced mastitis in dairy cows.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2MXms12m&md5=9694f3f7904ff9f373b353b6b1cd854cCAS | 15591384PubMed |
Molhoek EM, van Dijk A, Veldhuizen EJA, Dijk-Knijnenburg H, Mars-Groenendijk RH, Boele LCB, Kaman-van Zanten WE, Haagsman HP, Bikker FJ (2010) Chicken cathelicidin-2-derived peptides with enhanced immunomodulatory and antibacterial activities against biological warfare agents. International Journal of Antimicrobial Agents 36, 271–274.
| Chicken cathelicidin-2-derived peptides with enhanced immunomodulatory and antibacterial activities against biological warfare agents.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3cXptVSrsLg%3D&md5=0a264d753f7044ae25f6a1643d8305d1CAS | 20630709PubMed |
Mookherjee N, Wilson HL, Doria S, Popowych Y, Falsafi R, Yu JJ, Li Y, Veatch S, Roche FM, Brown KL, Brinkman FS, Hokamp K, Potter A, Babiuk LA, Griebel PJ, Hancock RE (2006) Bovine and human cathelicidin cationic host defense peptides similarly suppress transcriptional responses to bacterial lipopolysaccharide. Journal of Leukocyte Biology 80, 1563–1574.
| Bovine and human cathelicidin cationic host defense peptides similarly suppress transcriptional responses to bacterial lipopolysaccharide.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28XhtlSisb7N&md5=e3be4c3881e3d47653f9d719b91a9dc6CAS | 16943385PubMed |
Nakajima Y, Mikami O, Yoshioka M, Motoi Y, Ito T, Ishikawa Y, Fuse M, Nakano K, Yasukawa K (1997) Elevated levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) activities in the sera and milk of cows with naturally occurring coliform mastitis. Research in Veterinary Science 62, 297–298.
| Elevated levels of tumor necrosis factor-alpha (TNF-alpha) and interleukin-6 (IL-6) activities in the sera and milk of cows with naturally occurring coliform mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2sXmt1Wrtbo%3D&md5=706dea0062bd18f8b2cd0472359acb04CAS | 9300553PubMed |
Napoli A, Aiello D, Di Donna L, Prendushi H, Sindona G (2007) Exploitation of endogenous protease activity in raw mastitic milk by MALDI-TOF/TOF. Analytical Chemistry 79, 5941–5948.
| Exploitation of endogenous protease activity in raw mastitic milk by MALDI-TOF/TOF.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXntVCqsbo%3D&md5=2d37d18d8952bc4bb408552ff0bb90f7CAS | 17602500PubMed |
Olde Riekerink RG, Barkema HW, Kelton DF, Scholl DT (2008) Incidence rate of clinical mastitis on Canadian dairy farms. Journal of Dairy Science 91, 1366–1377.
| Incidence rate of clinical mastitis on Canadian dairy farms.Crossref | GoogleScholarGoogle Scholar | 1:STN:280:DC%2BD1c7ptVOgsw%3D%3D&md5=5f6194df0a939427a0884cc94887a015CAS | 18349229PubMed |
Olson NC, Hellyer PW, Dodam JR (1995) Mediators and vascular effects in response to endotoxin. The British Veterinary Journal 151, 489–522.
| Mediators and vascular effects in response to endotoxin.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DyaK2MXovVWrtLk%3D&md5=e42ee2899556125e145eb2496b3ebd3fCAS | 8556312PubMed |
Pyörälä S (2003) Indicators of inflammation in the diagnosis of mastitis. Veterinary Research 34, 565–578.
| Indicators of inflammation in the diagnosis of mastitis.Crossref | GoogleScholarGoogle Scholar | 14556695PubMed |
Rahman MM, Miranda-Ribera A, Lecchi C, Bronzo V, Sartorelli P, Franciosi F, Ceciliani F (2008) Alpha(1)-acid glycoprotein is contained in bovine neutrophil granules and released after activation. Veterinary Immunology and Immunopathology 125, 71–81.
| Alpha(1)-acid glycoprotein is contained in bovine neutrophil granules and released after activation.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhtVWitrjJ&md5=b0d20582a8e4842736869982304d9dd3CAS | 18584879PubMed |
Raulo SM, Sorsa T, Tervahartiala T, Latvanen T, Pirilä E, Hirvonen J, Maisi P (2002) Increase in milk metalloproteinase activity and vascular permeability in bovine endotoxin-induced and naturally occurring Escherichia coli mastitis. Veterinary Immunology and Immunopathology 85, 137–145.
| Increase in milk metalloproteinase activity and vascular permeability in bovine endotoxin-induced and naturally occurring Escherichia coli mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD38Xis1OqsLY%3D&md5=edb3df28268330a752870dd83d74d49fCAS | 11943315PubMed |
Rinaldi M, Ceciliani F, Lecchi C, Moroni P, Bannerman DD (2008) Differential effects of alpha1-acid glycoprotein on bovine neutrophil respiratory burst activity and IL-8 production. Veterinary Immunology and Immunopathology 126, 199–210.
| Differential effects of alpha1-acid glycoprotein on bovine neutrophil respiratory burst activity and IL-8 production.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD1cXhsVWmtbbI&md5=fc2ed33902b3de8cd387193f634f5a3aCAS | 18692908PubMed |
Sears PM, Gonzalez RN, Wilson DJ, Han HR (1993) Procedures for mastitis diagnosis and control. The Veterinary Clinics of North America. Food Animal Practice 9, 445–468.
Smolenski G, Haines S, Kwan FY, Bond J, Farr V, Davis SR, Stelwagen K, Wheeler TT (2007) Characterisation of host defence proteins in milk using a proteomic approach. Journal of Proteome Research 6, 207–215.
| Characterisation of host defence proteins in milk using a proteomic approach.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD28Xht12lsLbE&md5=107acd96b313ddf88a3acc67b57355e8CAS | 17203965PubMed |
Smolenski GA, Wieliczko RJ, Pryor SM, Broadhurst MK, Wheeler TT, Haigh BJ (2011) The abundance of milk cathelicidin proteins during bovine mastitis. Veterinary Immunology and Immunopathology 143, 125–130.
| The abundance of milk cathelicidin proteins during bovine mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC3MXpvFymurg%3D&md5=006a5f3fc585ae94f0b010b34127de0bCAS | 21774993PubMed |
Suojala L, Orro T, Järvinen H, Saatsi J, Pyörälä S (2008) Acute phase response in two consecutive experimentally induced E. coli intramammary infections in dairy cows. Acta Veterinaria Scandinavica 50, 18
| Acute phase response in two consecutive experimentally induced E. coli intramammary infections in dairy cows.Crossref | GoogleScholarGoogle Scholar | 18554387PubMed |
Swanson K, Gorodetsky S, Good L, Davis S, Musgrave D, Stelwagen K, Farr V, Molenaar A (2004) Expression of a beta-defensin mRNA, lingual antimicrobial peptide, in bovine mammary epithelial tissue is induced by mastitis. Infection and Immunity 72, 7311–7314.
| Expression of a beta-defensin mRNA, lingual antimicrobial peptide, in bovine mammary epithelial tissue is induced by mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXhtVGls7jK&md5=f53dc13a01a021eda100d3bd96704927CAS | 15557657PubMed |
Theilgaard-Mönch K, Jacobsen LC, Nielsen MJ, Rasmussen T, Udby L, Gharib M, Arkwright PD, Gombart AF, Calafat J, Moestrup SK, Porse BT, Borregaard N (2006) Haptoglobin is synthesized during granulocyte differentiation, stored in specific granules, and released by neutrophils in response to activation. Blood 108, 353–361.
| Haptoglobin is synthesized during granulocyte differentiation, stored in specific granules, and released by neutrophils in response to activation.Crossref | GoogleScholarGoogle Scholar | 16543473PubMed |
Thielen MA, Mielenz M, Hiss S, Zerbe H, Petzl W, Schuberth HJ, Seyfert HM, Sauerwein H (2007) Short communication: cellular localization of haptoglobin mRNA in the experimentally infected bovine mammary gland. Journal of Dairy Science 90, 1215–1219.
| Short communication: cellular localization of haptoglobin mRNA in the experimentally infected bovine mammary gland.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXitlWntb0%3D&md5=913cccec839ab1bfe0fbad82426fd1d9CAS | 17297097PubMed |
Turk R, Piras C, Kovačić M, Samardžija M, Ahmed H, De Canio M, Urbani A, Meštrić ZF, Soggiu A, Bonizzi L, Roncada P (2012) Proteomics of inflammatory and oxidative stress response in cows with subclinical and clinical mastitis. Journal of Proteomics 75, 4412–4428.
| Proteomics of inflammatory and oxidative stress response in cows with subclinical and clinical mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XosVejt7Y%3D&md5=a232d5c64a760591758a6c8af21fbba0CAS | 22634041PubMed |
Vangroenweghe F, Duchateau L, Burvenich C (2004) Moderate inflammatory reaction during experimental Escherichia coli mastitis in primiparous cows. Journal of Dairy Science 87, 886–895.
| Moderate inflammatory reaction during experimental Escherichia coli mastitis in primiparous cows.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2cXivFyrurc%3D&md5=8cfef9a26f52c65ef30207c3317bac38CAS | 15259223PubMed |
Vanselow J, Yang W, Herrmann J, Zerbe H, Schuberth HJ, Petzl W, Tomek W, Seyfert HM (2006) DNA-remethylation around a STAT5-binding enhancer in the alphaS1-casein promoter is associated with abrupt shutdown of alphaS1-casein synthesis during acute mastitis. Journal of Molecular Endocrinology 37, 463–477.
| DNA-remethylation around a STAT5-binding enhancer in the alphaS1-casein promoter is associated with abrupt shutdown of alphaS1-casein synthesis during acute mastitis.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BD2sXmslersA%3D%3D&md5=0336cc823e72d21cf0d758b59937dea5CAS | 17170087PubMed |
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, 415–422.
| Host-defence-related proteins in cows’ milk.Crossref | GoogleScholarGoogle Scholar | 1:CAS:528:DC%2BC38XhsFCit78%3D&md5=11ed67d4db0873a54ae2fc2c9a5583cdCAS | 22436220PubMed |
Zanetti M (2004) Cathelicidins, multifunctional peptides of the innate immunity. Journal of Leukocyte Biology 75, 39–48.
| Cathelicidins, multifunctional peptides of the innate immunity.Crossref | GoogleScholarGoogle Scholar | 12960280PubMed |