Articles citing this article

The Citing articles tool gives a list of articles citing the current article.
The citing articles come from EDP Sciences database, as well as other publishers participating in CrossRef Cited-by Linking Program. You can set up your personal account to receive an email alert each time this article is cited by a new article (see the menu on the right-hand side of the abstract page).

Cited article:

SNPs ofCXCR1Gene and Its Associations with Somatic Cell Score in Chinese Holstein Cattle

Renjin Chen, Zhangping Yang, Dejun Ji, et al.
Animal Biotechnology 22 (3) 133 (2011)
https://doi.org/10.1080/10495398.2011.582804

Natural antibodies in bovine milk and blood plasma: Variability among cows, repeatability within cows, and relation between milk and plasma titers

T.C.W. Ploegaert, E. Tijhaar, T.J.G.M. Lam, et al.
Veterinary Immunology and Immunopathology 144 (1-2) 88 (2011)
https://doi.org/10.1016/j.vetimm.2011.07.008

Differential leucocyte count for ewe milk with low and high somatic cell count

Marzia Albenzio and Mariangela Caroprese
Journal of Dairy Research 78 (1) 43 (2011)
https://doi.org/10.1017/S0022029910000798

Composition, indigenous proteolytic enzymes and coagulating behaviour of ewe milk as affected by somatic cell count

Marzia Albenzio, Antonella Santillo, Mariangela Caroprese, et al.
Journal of Dairy Research 78 (4) 442 (2011)
https://doi.org/10.1017/S0022029911000525

Apoptosis and necrosis of polymorphonuclear leukocytes in goat milk with high and low somatic cell counts

Maiara G. Blagitz, Fernando N. Souza, Viviani Gomes and Alice M.M.P. Della Libera
Small Ruminant Research 100 (1) 67 (2011)
https://doi.org/10.1016/j.smallrumres.2011.05.005

First evidence of the presence of genomic islands in Escherichia coli P4, a mammary pathogen frequently used to induce experimental mastitis

D. Dufour, P. Germon, E. Brusseaux, Y. Le Roux and A. Dary
Journal of Dairy Science 94 (6) 2779 (2011)
https://doi.org/10.3168/jds.2010-3446

Serum concentration and mRNA expression in milk somatic cells of toll-like receptor 2, toll-like receptor 4, and cytokines in dairy cows following intramammary inoculation with Escherichia coli

J.L. Ma, Y.H. Zhu, L. Zhang, et al.
Journal of Dairy Science 94 (12) 5903 (2011)
https://doi.org/10.3168/jds.2011-4167

Udder pathogens and their resistance to antimicrobial agents in dairy cows in Estonia

Piret Kalmus, Birgit Aasmäe, Age Kärssin, Toomas Orro and Kalle Kask
Acta Veterinaria Scandinavica 53 (1) (2011)
https://doi.org/10.1186/1751-0147-53-4

Immune response of bovine milk somatic cells to endotoxin in healthy quarters with normal and very low cell counts

Olga Wellnitz, Amandine Baumert, Machabbat Saudenowa and Rupert M Bruckmaier
Journal of Dairy Research 77 (4) 452 (2010)
https://doi.org/10.1017/S0022029910000348

Molecular-Based Analysis of Changes in Indigenous Milk Microflora during the Grazing Period

Tatsuro HAGI, Miho KOBAYASHI and Masaru NOMURA
Bioscience, Biotechnology, and Biochemistry 74 (3) 484 (2010)
https://doi.org/10.1271/bbb.90470

Neutrophil recruitment in endotoxin-induced murine mastitis is strictly dependent on mammary alveolar macrophages

Sharon Elazar, Erez Gonen, Ayala Livneh-Kol, Ilan Rosenshine and Nahum Yehuda Shpigel
Veterinary Research 41 (1) 10 (2010)
https://doi.org/10.1051/vetres/2009058

Stimulated expression of TNF-α and IL-8, but not of lingual antimicrobial peptide reflects the concentration of pathogens contacting bovine mammary epithelial cells

Juliane Günther, Shuzhen Liu, Kathrin Esch, Hans-Joachim Schuberth and Hans-Martin Seyfert
Veterinary Immunology and Immunopathology 135 (1-2) 152 (2010)
https://doi.org/10.1016/j.vetimm.2009.11.004

Assessment of epithelial cells' immune and inflammatory response toStaphylococcus aureuswhen exposed to a macrolide

Maria Mazzilli and Alfonso Zecconi
Journal of Dairy Research 77 (4) 404 (2010)
https://doi.org/10.1017/S0022029910000531

A sentinel function for teat tissues in dairy cows: dominant innate immune response elements define early response to E. coli mastitis

Manuela Rinaldi, Robert W. Li, Douglas D. Bannerman, et al.
Functional & Integrative Genomics 10 (1) 21 (2010)
https://doi.org/10.1007/s10142-009-0133-z

Characterisation of the anti-microbial activity of bovine milk ribonuclease4 and ribonuclease5 (angiogenin)

Paul Harris, Kirsti M. Johannessen, Grant Smolenski, et al.
International Dairy Journal 20 (6) 400 (2010)
https://doi.org/10.1016/j.idairyj.2009.12.018

Characterisation of physiological and immunological responses in beef cows to abrupt weaning and subsequent housing

Eilish M Lynch, Bernadette Earley, Mark McGee and Sean Doyle
BMC Veterinary Research 6 (1) (2010)
https://doi.org/10.1186/1746-6148-6-37

The induction of lymphoid follicle-like structures in the ovine teat duct following experimental infection with Mannheimia haemolytica

I.A. Fragkou, M.P. Dagleish, N. Papaioannou, et al.
The Veterinary Journal 184 (2) 194 (2010)
https://doi.org/10.1016/j.tvjl.2009.01.025

High concentration of human lactoferrin in milk of rhLf-transgenic cows relieves signs of bovine experimental Staphylococcus chromogenes intramammary infection

Heli Simojoki, Paula Hyvönen, Toomas Orro and Satu Pyörälä
Veterinary Immunology and Immunopathology 136 (3-4) 265 (2010)
https://doi.org/10.1016/j.vetimm.2010.03.017

Factors associated with concentrations of select cytokine and acute phase proteins in dairy cows with naturally occurring clinical mastitis

J.R. Wenz, L.K. Fox, F.J. Muller, et al.
Journal of Dairy Science 93 (6) 2458 (2010)
https://doi.org/10.3168/jds.2009-2819

Proteomics, Genomics, and Pathway Analyses of Escherichia coli and Staphylococcus aureus Infected Milk Whey Reveal Molecular Pathways and Networks Involved in Mastitis

Eveline M. Ibeagha-Awemu, Aloysius E. Ibeagha, Serge Messier and Xin Zhao
Journal of Proteome Research 9 (9) 4604 (2010)
https://doi.org/10.1021/pr100336e

Ethyl pyruvate diminishes the endotoxin-induced inflammatory response of bovine mammary endothelial cells

C.M. Corl, H.R. Robinson, G.A. Contreras, et al.
Journal of Dairy Science 93 (11) 5188 (2010)
https://doi.org/10.3168/jds.2010-3250

REVIEW ARTICLE: An integrated view on how the management of the dry period length of lactating cows could affect mammary biology and defence

A. Pezeshki, A. V. Capuco, B. De Spiegeleer, et al.
Journal of Animal Physiology and Animal Nutrition 94 (5) e7 (2010)
https://doi.org/10.1111/j.1439-0396.2010.00991.x

Evaluation of the protective effect of bovine lactoferrin against lipopolysaccharides in a bovine mammary epithelial cell line

Chiara Pecorini, Davide Sassera, Raffaella Rebucci, et al.
Veterinary Research Communications 34 (3) 267 (2010)
https://doi.org/10.1007/s11259-010-9351-z

Effect of Panax ginseng on cytokine expression in bovine mammary glands at drying off

C. Baravalle, B.E. Dallard, H.H. Ortega, et al.
Veterinary Immunology and Immunopathology 138 (3) 224 (2010)
https://doi.org/10.1016/j.vetimm.2010.07.019

Analysis of key molecules of the innate immune system in mammary epithelial cells isolated from marker-assisted and conventionally selected cattle

B. Griesbeck-Zilch, M. Osman, Ch. Kühn, et al.
Journal of Dairy Science 92 (9) 4621 (2009)
https://doi.org/10.3168/jds.2008-1954

Transcriptome profiling of Streptococcus uberis-induced mastitis reveals fundamental differences between immune gene expression in the mammary gland and in a primary cell culture model

K.M. Swanson, K. Stelwagen, J. Dobson, et al.
Journal of Dairy Science 92 (1) 117 (2009)
https://doi.org/10.3168/jds.2008-1382

Gene network and pathway analysis of bovine mammary tissue challenged with Streptococcus uberis reveals induction of cell proliferation and inhibition of PPARγ signaling as potential mechanism for the negative relationships between immune response and lipid metabolism

Kasey M Moyes, James K Drackley, Dawn E Morin, et al.
BMC Genomics 10 (1) (2009)
https://doi.org/10.1186/1471-2164-10-542

The acute-phase protein serum amyloid A3 is expressed in the bovine mammary gland and plays a role in host defence

Adrian J. Molenaar, D. Paul Harris, Gillian H. Rajan, et al.
Biomarkers 14 (1) 26 (2009)
https://doi.org/10.1080/13547500902730714

Real-time polymerase chain reaction-based identification of bacteria in milk samples from bovine clinical mastitis with no growth in conventional culturing

S. Taponen, L. Salmikivi, H. Simojoki, M.T. Koskinen and S. Pyörälä
Journal of Dairy Science 92 (6) 2610 (2009)
https://doi.org/10.3168/jds.2008-1729

Heifer and quarter characteristics associated with periparturient blood and milk neutrophil apoptosis in healthy heifers and in heifers with subclinical mastitis

S. Piepers, G. Opsomer, E. Meyer, et al.
Journal of Dairy Science 92 (9) 4330 (2009)
https://doi.org/10.3168/jds.2009-2029

Technical note: Flow cytometric identification of bovine milk neutrophils and simultaneous quantification of their viability

S. Piepers, S. De Vliegher, K. Demeyere, et al.
Journal of Dairy Science 92 (2) 626 (2009)
https://doi.org/10.3168/jds.2008-1393

Osteopontin: an early innate immune marker of Escherichia coli mastitis harbors genetic polymorphisms with possible links with resistance to mastitis

Karin Alain, Niel A Karrow, Catherine Thibault, et al.
BMC Genomics 10 (1) (2009)
https://doi.org/10.1186/1471-2164-10-444

Effect of bovine lactoferrin on the internalization of coagulase-negative staphylococci into bovine mammary epithelial cells under in-vitro conditions

Paula Hyvönen, Sari Käyhkö, Suvi Taponen, Atte von Wright and Satu Pyörälä
Journal of Dairy Research 76 (2) 144 (2009)
https://doi.org/10.1017/S0022029908003774

Cell population, viability, and some key immunomodulatory molecules in different milk somatic cell samples in dairy cows

Amandine Baumert, Rupert M. Bruckmaier and Olga Wellnitz
Journal of Dairy Research 76 (3) 356 (2009)
https://doi.org/10.1017/S0022029909004129

Assessment of the immune capacity of mammary epithelial cells: comparison with mammary tissue after challenge withEscherichia coli

Juliane Günther, Dirk Koczan, Wei Yang, et al.
Veterinary Research 40 (4) 31 (2009)
https://doi.org/10.1051/vetres/2009014

Mastitis detection: current trends and future perspectives

Caroline Viguier, Sushrut Arora, Niamh Gilmartin, Katherine Welbeck and Richard O’Kennedy
Trends in Biotechnology 27 (8) 486 (2009)
https://doi.org/10.1016/j.tibtech.2009.05.004

Dietary-induced negative energy balance has minimal effects on innate immunity during a Streptococcus uberis mastitis challenge in dairy cows during midlactation

K.M. Moyes, J.K. Drackley, J.L. Salak-Johnson, et al.
Journal of Dairy Science 92 (9) 4301 (2009)
https://doi.org/10.3168/jds.2009-2170

Immune components of bovine colostrum and milk1

K. Stelwagen, E. Carpenter, B. Haigh, A. Hodgkinson and T. T. Wheeler
Journal of Animal Science 87 (suppl_13) 3 (2009)
https://doi.org/10.2527/jas.2008-1377

Events of elevated somatic cell counts in high-producing dairy cows are associated with daily body weight loss in early lactation

M. van Straten, M. Friger and N.Y. Shpigel
Journal of Dairy Science 92 (9) 4386 (2009)
https://doi.org/10.3168/jds.2009-2204

Genetic analysis of lactoferrin content in bovine milk

V.M.-R. Arnould, H. Soyeurt, N. Gengler, et al.
Journal of Dairy Science 92 (5) 2151 (2009)
https://doi.org/10.3168/jds.2008-1255

Terminal differentiation of goat mammary tissue during pregnancy requires the expression of genes involved in immune functions

F. Faucon, E. Rebours, C. Bevilacqua, et al.
Physiological Genomics 40 (1) 61 (2009)
https://doi.org/10.1152/physiolgenomics.00032.2009

Imunidade inata da glândula mamária bovina: resposta à infecção

Deolinda Maria Vieira Filha Carneiro, Paulo Francisco Domingues and Adil Knackfuss Vaz
Ciência Rural 39 (6) 1934 (2009)
https://doi.org/10.1590/S0103-84782009005000106

Effect of a biological response modifier on expression of CD14 receptor and tumor necrosis factor-alpha in Staphylococcus aureus-infected mammary glands at drying off

B.E. Dallard, C. Baravalle, H.H. Ortega, et al.
Veterinary Immunology and Immunopathology 132 (2-4) 237 (2009)
https://doi.org/10.1016/j.vetimm.2009.05.004

The role of dietary selenium in bovine mammary gland health and immune function

S. Salman, A. Khol-Parisini, H. Schafft, et al.
Animal Health Research Reviews 10 (1) 21 (2009)
https://doi.org/10.1017/S1466252308001588

Metabolic factors affecting the inflammatory response of periparturient dairy cows

Lorraine M. Sordillo, G. A. Contreras and Stacey L. Aitken
Animal Health Research Reviews 10 (1) 53 (2009)
https://doi.org/10.1017/S1466252309990016

Neutrophils as one of the major haptoglobin sources in mastitis affected milk

I-Hsiang Lai, Jung Hsu Tsao, Yi Ping Lu, et al.
Veterinary Research 40 (3) 17 (2009)
https://doi.org/10.1051/vetres:2008055

Identification of immune genes and proteins involved in the response of bovine mammary tissue to Staphylococcus aureus infection

Ylva C Strandberg Lutzow, Laurelea Donaldson, Christian P Gray, et al.
BMC Veterinary Research 4 (1) (2008)
https://doi.org/10.1186/1746-6148-4-18

Escherichia coli, but notStaphylococcus aureustriggers an early increased expression of factors contributing to the innate immune defense in the udder of the cow

Wolfram Petzl, Holm Zerbe, Juliane Günther, et al.
Veterinary Research 39 (2) 18 (2008)
https://doi.org/10.1051/vetres:2007057

Identification and characterization of a new interleukin-8 receptor in bovine species

Hichem Lahouassa, Pascal Rainard, Alain Caraty and Céline Riollet
Molecular Immunology 45 (4) 1153 (2008)
https://doi.org/10.1016/j.molimm.2007.07.011

High Frequency of Mycobacterium bovis DNA in Colostra from Tuberculous Cattle Detected by Nested PCR

B. A. Serrano‐Moreno, T. A. Romero, C. Arriaga, et al.
Zoonoses and Public Health 55 (5) 258 (2008)
https://doi.org/10.1111/j.1863-2378.2008.01125.x

Genotype‐specific IL8RA gene expression in bovine neutrophils in response to Escherichia coli lipopolysaccharide challenge

I. Leyva‐Baca, G. Pighetti and N. A. Karrow
Animal Genetics 39 (3) 298 (2008)
https://doi.org/10.1111/j.1365-2052.2008.01711.x

Polymorphisms in the 5′ Upstream Region of the CXCR1 Chemokine Receptor Gene, and Their Association with Somatic Cell Score in Holstein Cattle in Canada

I. Leyva-Baca, F. Schenkel, J. Martin and N.A. Karrow
Journal of Dairy Science 91 (1) 407 (2008)
https://doi.org/10.3168/jds.2007-0142

Staphylococcus aureuslipoteichoic acid triggers inflammation in the lactating bovine mammary gland

Pascal Rainard, Angélina Fromageau, Patricia Cunha and Florence B. Gilbert
Veterinary Research 39 (5) 52 (2008)
https://doi.org/10.1051/vetres:2008034

Production of hydrogen peroxide by a small molecular mass compound in milk from Holstein cows with high and low milk somatic cell count

Senkiti Sakai, Eriko Nonobe, Takahiro Satow, Kazuhiko Imakawa and Kentaro Nagaoka
Journal of Dairy Research 75 (3) 335 (2008)
https://doi.org/10.1017/S0022029908003300

Bovine TLR2 and TLR4 properly transduce signals from Staphylococcus aureus and E. coli, but S. aureus fails to both activate NF-κB in mammary epithelial cells and to quickly induce TNFα and interleukin-8 (CXCL8) expression in the udder

Wei Yang, Holm Zerbe, Wolfram Petzl, et al.
Molecular Immunology 45 (5) 1385 (2008)
https://doi.org/10.1016/j.molimm.2007.09.004

Staphylococcus aureus and Escherichia coli Cause Deviating Expression Profiles of Cytokines and Lactoferrin Messenger Ribonucleic Acid in Mammary Epithelial Cells

B. Griesbeck-Zilch, H.H.D. Meyer, Ch. Kühn, M. Schwerin and O. Wellnitz
Journal of Dairy Science 91 (6) 2215 (2008)
https://doi.org/10.3168/jds.2007-0752

The toll-like receptor-4 (TLR-4) pathway and its possible role in the pathogenesis ofEscherichia colimastitis in dairy cattle

Stefanie De Schepper, Adelheid De Ketelaere, Douglas D. Bannerman, et al.
Veterinary Research 39 (1) 05 (2008)
https://doi.org/10.1051/vetres:2007044

The chemokine CXCL3 is responsible for the constitutive chemotactic activity of bovine milk for neutrophils

Pascal Rainard, Céline Riollet, Patricia Berthon, et al.
Molecular Immunology 45 (15) 4020 (2008)
https://doi.org/10.1016/j.molimm.2008.06.010

Platelet Activating Factor Production and Proinflammatory Gene Expression in Endotoxin-Challenged Bovine Mammary Endothelial Cells

C.M. Corl, J.C. Gandy and L.M. Sordillo
Journal of Dairy Science 91 (8) 3067 (2008)
https://doi.org/10.3168/jds.2008-1066

Proteomic Analysis of Differentially Expressed Proteins in Bovine Milk During Experimentally Induced Escherichia coli Mastitis

J.L. Boehmer, D.D. Bannerman, K. Shefcheck and J.L. Ward
Journal of Dairy Science 91 (11) 4206 (2008)
https://doi.org/10.3168/jds.2008-1297

Cumulative Physiological Events Influence the Inflammatory Response of the Bovine Udder to Escherichia coli Infections During the Transition Period

C. Burvenich, D.D. Bannerman, J.D. Lippolis, et al.
Journal of Dairy Science 90 E39 (2007)
https://doi.org/10.3168/jds.2006-696

Teat Lesions Predispose to Invasion of the Ovine Mammary Gland by Mannheimia haemolytica

I.A. Fragkou, N. Papaioannou, P.J. Cripps, C.M. Boscos and G.C. Fthenakis
Journal of Comparative Pathology 137 (4) 239 (2007)
https://doi.org/10.1016/j.jcpa.2007.08.002

Differential expression and secretion of α1-acid glycoprotein in bovine milk

Fabrizio Ceciliani, Vanessa Pocacqua, Cristina Lecchi, et al.
Journal of Dairy Research 74 (3) 374 (2007)
https://doi.org/10.1017/S0022029907002646

Bacterial lipopolysaccharide stimulates bovine neutrophil production of TNF-α, IL-1β, IL-12 and IFN-γ

Eun J. Sohn, Max J. Paape, Erin E. Connor, et al.
Veterinary Research 38 (6) 809 (2007)
https://doi.org/10.1051/vetres:2007033

Toll-like receptor 4 is needed to restrict the invasion of Escherichia coli P4 into mammary gland epithelial cells in a murine model of acute mastitis

Erez Gonen, Alexandra Vallon-Eberhard, Sharon Elazar, et al.
Cellular Microbiology 9 (12) 2826 (2007)
https://doi.org/10.1111/j.1462-5822.2007.00999.x

Morphometric analysis of proinflammatory cytokines in mammary glands of sows suggests an association between clinical mastitis and local production of IL-1beta, IL-6 and TNF-alpha

Yaohong Zhu, Caroline Fossum, Mikael Berg and Ulf Magnusson
Veterinary Research 38 (6) 871 (2007)
https://doi.org/10.1051/vetres:2007035

The bacterial flora in the teat duct of ewes can protect against and can cause mastitis

Ilectra A. Fragkou, Vasia S. Mavrogianni, Peter J. Cripps, Dimitris A. Gougoulis and George C. Fthenakis
Veterinary Research 38 (4) 525 (2007)
https://doi.org/10.1051/vetres:2007014

Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli

Hichem Lahouassa, Etienne Moussay, Pascal Rainard and Céline Riollet
Cytokine 38 (1) 12 (2007)
https://doi.org/10.1016/j.cyto.2007.04.006

Staphylococcus aureusleucotoxin LukM/F' is secreted and stimulates neutralising antibody response in the course of intramammary infection

Pascal Rainard
Veterinary Research 38 (5) 685 (2007)
https://doi.org/10.1051/vetres:2007026