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:

Comparative analysis of Streptococcus agalactiae serotypes Ia and II isolates from China and Pakistan in a murine model: A focus on pathogenesis and immune response

Ambreen Leghari, Rabia Sabir, Sheereen Laghari, Faiz Muhammad Khand, Muhammad Ali Chandio, Abdul Samad Magsi, Khaliq ur Rehman Bhutto, Mohammad Farooque Hassan, Shakeel Ahmed Lakho, Huixing Lin and Hongjie Fan
Microbial Pathogenesis 191 106675 (2024)
https://doi.org/10.1016/j.micpath.2024.106675

Impact of a teat disinfectant based on Lactococcus cremoris on the cow milk proteome

Maria Filippa Addis, Elisa Margherita Maffioli, Alessandra Gazzola, Federica Santandrea, Gabriella Tedeschi and Renata Piccinini
BMC Veterinary Research 20 (1) (2024)
https://doi.org/10.1186/s12917-024-04014-x

Retained Placenta as a Potential Source of Mastitis Pathogens in Dairy Cows

Diana Ribeiro, Susana Astiz, Aitor Fernandez-Novo, Gisele Margatho and João Simões
Applied Sciences 14 (12) 4986 (2024)
https://doi.org/10.3390/app14124986

Cytokine inflammatory response in dairy cows with mastitis caused by Streptococcus agalactiae

Mariola Bochniarz, Agata Hahaj-Siembida, Monika Krajewska-Wędzina, Marcelina Osińska, Anna Tracz, Aleksandra Trościańczyk, Piotr Brodzki, Leszek Krakowski, Urszula Kosior-Korzecka and Aneta Nowakiewicz
Journal of Veterinary Research 68 (1) 115 (2024)
https://doi.org/10.2478/jvetres-2024-0002

Intramammary calcitriol treatment of mastitis alters profile of milk somatic cells and indicators of redox activity in milk

Teri L. Wells, Michael B. Poindexter, Mercedes F. Kweh, Jeff Gandy and Corwin D. Nelson
Veterinary Immunology and Immunopathology 266 110679 (2023)
https://doi.org/10.1016/j.vetimm.2023.110679

Immunological and Oxidative Biomarkers in Bovine Serum from Healthy, Clinical, and Sub-Clinical Mastitis Caused by Escherichia coli and Staphylococcus aureus Infection

Asmaa Sadat, Alshimaa M. M. Farag, Driss Elhanafi, et al.
Animals 13 (5) 892 (2023)
https://doi.org/10.3390/ani13050892

FABP4-mediated lipid droplet formation in Streptococcus uberis-infected macrophages supports host defence

Zhixin Wan, Shaodong Fu, Zhenglei Wang, et al.
Veterinary Research 53 (1) (2022)
https://doi.org/10.1186/s13567-022-01114-0

Association of Milk Somatic Cell Count with Bacteriological Cure of Intramammary Infection—A Review

Jenna Williamson, Todd Callaway, Emmanuel Rollin and Valerie Ryman
Agriculture 12 (9) 1437 (2022)
https://doi.org/10.3390/agriculture12091437

In-vitroanalysis of Interleukin-10 expression in cell cultures of Crossbred cattle, Tharparkar cattle and Murrah buffalo in response to mastitis causing antigens derived fromStaphylococcus aureusandEscherichia coli

Sourabh Sulabh, Manjit Panigrahi, Rajat Varshney, et al.
Biological Rhythm Research 53 (2) 197 (2022)
https://doi.org/10.1080/09291016.2019.1628407

Environmental Bovine Mastitis Pathogens: Prevalence, Antimicrobial Susceptibility, and Sensitivity to Thymus vulgaris L., Thymus serpyllum L., and Origanum vulgare L. Essential Oils

Dragana Tomanić, Biljana Božin, Nebojša Kladar, Jovan Stanojević, Ivana Čabarkapa, Nebojša Stilinović, Jelena Apić, Dragana D. Božić and Zorana Kovačević
Antibiotics 11 (8) 1077 (2022)
https://doi.org/10.3390/antibiotics11081077

Immune response variations and intestinal flora changes in mastitis induced by three Streptococcus uberis strains

Shaodong Fu, Yuanyuan Zhou, Yawei Qiu, et al.
Microbiology and Immunology 66 (3) 113 (2022)
https://doi.org/10.1111/1348-0421.12955

Diverging in vitro inflammatory responses toward Streptococcus uberis in mouse macrophages either preconditioned or continuously treated with β-hydroxybutyrate

T.H. Swartz, B.J. Bradford and L.K. Mamedova
JDS Communications 2 (3) 142 (2021)
https://doi.org/10.3168/jdsc.2020-0038

Invited review: A critical appraisal of mastitis vaccines for dairy cows

Pascal Rainard, Florence B. Gilbert, Pierre Germon and Gilles Foucras
Journal of Dairy Science 104 (10) 10427 (2021)
https://doi.org/10.3168/jds.2021-20434

Going further post-RNA-seq: In silico functional analyses revealing candidate genes and regulatory elements related to mastitis in dairy cattle

Hyago Passe Pereira, Lucas Lima Verardo, Mayara Morena Del Cambre Amaral Weller, et al.
Journal of Dairy Research 88 (3) 286 (2021)
https://doi.org/10.1017/S0022029921000571

Inhibition of PI3K/Akt/mTOR pathway by ammonium chloride induced apoptosis and autophagy in MAC-T cell

Luping Feng, Hang Liao, Jingsong Liu, et al.
Research in Veterinary Science 136 622 (2021)
https://doi.org/10.1016/j.rvsc.2021.01.020

Integrative Analysis of miRNA and mRNA Expression Profiles in Mammary Glands of Holstein Cows Artificially Infected with Staphylococcus aureus

Xiaolong Wang, Yongliang Fan, Yifan He, Ziyin Han, Zaicheng Gong, Yalan Peng, Yining Meng, Yongjiang Mao, Zhangping Yang and Yi Yang
Pathogens 10 (5) 506 (2021)
https://doi.org/10.3390/pathogens10050506

Haematological findings in 158 cows with acute toxic mastitis with a focus on the leukogram

Ueli Braun, Christian Gerspach, Barbara Riond, et al.
Acta Veterinaria Scandinavica 63 (1) (2021)
https://doi.org/10.1186/s13028-021-00576-0

Genome-wide methylation and transcriptome of blood neutrophils reveal the roles of DNA methylation in affecting transcription of protein-coding genes and miRNAs in E. coli-infected mastitis cows

Zhihua Ju, Qiang Jiang, Jinpeng Wang, et al.
BMC Genomics 21 (1) (2020)
https://doi.org/10.1186/s12864-020-6526-z

Concentrations of Acute-Phase Proteins in Milk from Cows with Clinical Mastitis Caused by Different Pathogens

Felipe M. Dalanezi, Elizabeth M. S. Schmidt, Sâmea F. Joaquim, Felipe F. Guimarães, Simoni T. Guerra, Bruna C. Lopes, Ronaldo L. A. Cerri, Christopher Chadwick and Hélio Langoni
Pathogens 9 (9) 706 (2020)
https://doi.org/10.3390/pathogens9090706

Investigations on cytokines and proteins in lactating cows with and without naturally occurring mastitis

Tabasum Shaheen, Sheikh Bilal Ahmad, Muneeb U. Rehman, et al.
Journal of King Saud University - Science 32 (6) 2863 (2020)
https://doi.org/10.1016/j.jksus.2020.07.009

Characterization of bovine mammary gland dry secretions and their proteome from the end of lactation through day 21 of the dry period

Timothy A. Reinhardt and John D. Lippolis
Journal of Proteomics 223 103831 (2020)
https://doi.org/10.1016/j.jprot.2020.103831

Immunophenotyping and cytokine gene expression in experimental intramammary infection with staphylococcal species in mice

P KRISHNAMOORTHY, M L SATYANARAYANA, B R SHOME and P ROY
The Indian Journal of Animal Sciences 89 (5) (2019)
https://doi.org/10.56093/ijans.v89i5.89999

Minthostachys verticillata essential oil activates macrophage phagocytosis and modulates the innate immune response in a murine model of Enterococcus faecium mastitis

Ivana Dalila Montironi, Elina Beatriz Reinoso, Valentina Croce Paullier, et al.
Research in Veterinary Science 125 333 (2019)
https://doi.org/10.1016/j.rvsc.2019.07.015

Therapeutic effect of ginsenoside Rg1 on mastitis experimentally induced by lipopolysaccharide in lactating goats

Y.M. Wang, Y.Q. Ma, S.C. Bi, et al.
Journal of Dairy Science 102 (3) 2443 (2019)
https://doi.org/10.3168/jds.2018-15280

Isolated perfused udder model for transcriptome analysis in response toStreptococcus agalactiae

Mayara M. D. C. A. Weller, Isabela Fonseca, Ana P. Sbardella, et al.
Journal of Dairy Research 86 (3) 307 (2019)
https://doi.org/10.1017/S0022029919000451

Genome-wide association study identifies loci associated with milk leukocyte phenotypes following experimental challenge with Streptococcus uberis

Lydia Siebert, Margaret E. Staton, Susan Headrick, et al.
Immunogenetics 70 (9) 553 (2018)
https://doi.org/10.1007/s00251-018-1065-3

Invited review: Low milk somatic cell count and susceptibility to mastitis

P. Rainard, G. Foucras, D. Boichard and R. Rupp
Journal of Dairy Science 101 (8) 6703 (2018)
https://doi.org/10.3168/jds.2018-14593

Supplementation of linoleic acid (C18:2n-6) or α-linolenic acid (C18:3n-3) changes microbial agonist-induced oxylipid biosynthesis

V.E. Ryman, N. Packiriswamy, B. Norby, et al.
Journal of Dairy Science 100 (3) 1870 (2017)
https://doi.org/10.3168/jds.2016-11599

TRIENNIAL LACTATION SYMPOSIUM/BOLFA: Pathogen-specific immune response and changes in the blood–milk barrier of the bovine mammary gland1

R. M. Bruckmaier and O. Wellnitz
Journal of Animal Science 95 (12) 5720 (2017)
https://doi.org/10.2527/jas2017.1845

Pathological changes in experimental intramammary infection with different Staphylococcus species in Mice

P. Krishnamoorthy, M.L. Satyanarayana, B.R. Shome and H. Rahman
Journal of Microscopy and Ultrastructure (2017)
https://doi.org/10.1016/j.jmau.2017.05.001

Streptococcus uberis strains isolated from the bovine mammary gland evade immune recognition by mammary epithelial cells, but not of macrophages

Juliane Günther, Anna Czabanska, Isabel Bauer, et al.
Veterinary Research 47 (1) (2016)
https://doi.org/10.1186/s13567-015-0287-8

Addition of meloxicam to the treatment of clinical mastitis improves subsequent reproductive performance

S. McDougall, E. Abbeloos, S. Piepers, et al.
Journal of Dairy Science 99 (3) 2026 (2016)
https://doi.org/10.3168/jds.2015-9615

Apoptosis of Endothelial Cells by 13-HPODE Contributes to Impairment of Endothelial Barrier Integrity

Valerie E. Ryman, Nandakumar Packiriswamy and Lorraine M. Sordillo
Mediators of Inflammation 2016 1 (2016)
https://doi.org/10.1155/2016/9867138

Mastitomics, the integrated omics of bovine milk in an experimental model of Streptococcus uberis mastitis: 1. High abundance proteins, acute phase proteins and peptidomics

Funmilola Clara Thomas, William Mullen, Riccardo Tassi, et al.
Molecular BioSystems 12 (9) 2735 (2016)
https://doi.org/10.1039/C6MB00239K

Correlation of hypothetical virulence traits of two Streptococcus uberis strains with the clinical manifestation of bovine mastitis

Riccardo Tassi, Tom N. McNeilly, Anja Sipka and Ruth N. Zadoks
Veterinary Research 46 (1) (2015)
https://doi.org/10.1186/s13567-015-0268-y

Role of endothelial cells in bovine mammary gland health and disease

Valerie E. Ryman, Nandakumar Packiriswamy and Lorraine M. Sordillo
Animal Health Research Reviews 16 (2) 135 (2015)
https://doi.org/10.1017/S1466252315000158

The association between occurrence and severity of subclinical and clinical mastitis on pregnancies per artificial insemination at first service of Holstein cows

M.J. Fuenzalida, P.M. Fricke and P.L. Ruegg
Journal of Dairy Science 98 (6) 3791 (2015)
https://doi.org/10.3168/jds.2014-8997

Gene expression profile in zebu dairy cows (Bos taurus indicus) with mastitis caused by Streptococcus agalactiae

I. Fonseca, F.F. Cardoso, R.H. Higa, et al.
Livestock Science 180 47 (2015)
https://doi.org/10.1016/j.livsci.2015.07.012

Development of an improved Streptococcus uberis experimental mastitis challenge model using different doses and strains in lactating dairy cows

Manouchehr Khazandi, Patricia Eats, Darren Trott, et al.
Journal of Dairy Research 82 (4) 470 (2015)
https://doi.org/10.1017/S0022029915000321

TRIENNIAL LACTATION SYMPOSIUM: Nutrient partitioning during intramammary inflammation: A key to severity of mastitis and risk of subsequent diseases?1

K. M. Moyes
Journal of Animal Science 93 (12) 5586 (2015)
https://doi.org/10.2527/jas.2015-8945

MicroRNA Regulation of Bovine Monocyte Inflammatory and Metabolic Networks in an In Vivo Infection Model

Nathan Lawless, Timothy A Reinhardt, Kenneth Bryan, et al.
G3 Genes|Genomes|Genetics 4 (6) 957 (2014)
https://doi.org/10.1534/g3.113.009936

Dairy cows produce cytokine and cytotoxic T cell responses following vaccination with an antigenic fraction from Streptococcus uberis

D. Neil Wedlock, Bryce M. Buddle, John Williamson, et al.
Veterinary Immunology and Immunopathology 160 (1-2) 51 (2014)
https://doi.org/10.1016/j.vetimm.2014.03.012

The Immunology of Mammary Gland of Dairy Ruminants between Healthy and Inflammatory Conditions

Mohamed Ezzat Alnakip, Marcos Quintela-Baluja, Karola Böhme, et al.
Journal of Veterinary Medicine 2014 1 (2014)
https://doi.org/10.1155/2014/659801

Effect of cooling during the dry period on immune response after Streptococcus uberis intramammary infection challenge of dairy cows

I.M.T. Thompson, S. Tao, A.P.A. Monteiro, K.C. Jeong and G.E. Dahl
Journal of Dairy Science 97 (12) 7426 (2014)
https://doi.org/10.3168/jds.2013-7621

Changes in various metabolic parameters in blood and milk during experimental Escherichia coli mastitis for primiparous Holstein dairy cows during early lactation

Kasey M Moyes, Torben Larsen, Peter Sørensen and Klaus L Ingvartsen
Journal of Animal Science and Biotechnology 5 (1) (2014)
https://doi.org/10.1186/2049-1891-5-47

Strain-specific pathogenicity of putative host-adapted and nonadapted strains of Streptococcus uberis in dairy cattle

R. Tassi, T.N. McNeilly, J.L. Fitzpatrick, et al.
Journal of Dairy Science 96 (8) 5129 (2013)
https://doi.org/10.3168/jds.2013-6741

Relationship between previous history ofStreptococcus uberisinfection and response to a challenge model

Sally-Anne Turner, John H Williamson, S Jane Lacy-Hulbert and J Eric Hillerton
Journal of Dairy Research 80 (3) 360 (2013)
https://doi.org/10.1017/S0022029913000289

Early host response in the mammary gland after experimental Streptococcus uberis challenge in heifers

Astrid de Greeff, Ruth Zadoks, Lisette Ruuls, et al.
Journal of Dairy Science 96 (6) 3723 (2013)
https://doi.org/10.3168/jds.2012-6320

Single Intramammary Infusion of Recombinant Bovine Interleukin-8 at Dry-Off Induces the Prolonged Secretion of Leukocyte Elastase, Inflammatory Lactoferrin-Derived Peptides, and Interleukin-8 in Dairy Cows

Atsushi Watanabe, Jiro Hirota, Shinya Shimizu, Shigeki Inumaru and Kazuhiro Kimura
Veterinary Medicine International 2012 1 (2012)
https://doi.org/10.1155/2012/172072

Value of microbiology study in congenital nasolacrimal duct obstruction

Yasser H. Al-Faky, Tahir Naeem, Nora Al-Sobaie, et al.
Saudi Journal of Ophthalmology 26 (2) 223 (2012)
https://doi.org/10.1016/j.sjopt.2012.03.001

The bovine CXCR1 gene is highly polymorphic

Gina M. Pighetti, Cheryl J. Kojima, Leszek Wojakiewicz and Magdalena Rambeaud
Veterinary Immunology and Immunopathology 145 (1-2) 464 (2012)
https://doi.org/10.1016/j.vetimm.2011.09.012

Quantotypic Properties of QconCAT Peptides Targeting Bovine Host Response to Streptococcus uberis

Stine L. Bislev, Ulrike Kusebauch, Marius C. Codrea, et al.
Journal of Proteome Research 11 (3) 1832 (2012)
https://doi.org/10.1021/pr201064g

Taurine attenuates Streptococcus uberis-induced mastitis in rats by increasing T regulatory cells

Jinfeng Miao, Jinqiu Zhang, Liuhai Zheng, et al.
Amino Acids 42 (6) 2417 (2012)
https://doi.org/10.1007/s00726-011-1047-3

Characterization of the bovine innate immune response in milk somatic cells following intramammary infection with Streptococcus dysgalactiae subspecies dysgalactiae

C. Beecher, M. Daly, R.P. Ross, et al.
Journal of Dairy Science 95 (10) 5720 (2012)
https://doi.org/10.3168/jds.2012-5338

The “Other” Gram-Negative Bacteria in Mastitis

Ynte Schukken, Matt Chuff, Paolo Moroni, et al.
Veterinary Clinics of North America: Food Animal Practice 28 (2) 239 (2012)
https://doi.org/10.1016/j.cvfa.2012.04.001

Estimation of (co)variances for genomic regions of flexible sizes: application to complex infectious udder diseases in dairy cattle

Lars P Sørensen, Luc Janss, Per Madsen, Thomas Mark and Mogens S Lund
Genetics Selection Evolution 44 (1) (2012)
https://doi.org/10.1186/1297-9686-44-18

Host-response patterns of intramammary infections in dairy cows

Ynte H. Schukken, J. Günther, J. Fitzpatrick, et al.
Veterinary Immunology and Immunopathology 144 (3-4) 270 (2011)
https://doi.org/10.1016/j.vetimm.2011.08.022

Assessment of bacterial diversity in the cattle tick Rhipicephalus (Boophilus) microplusthrough tag-encoded pyrosequencing

Renato Andreotti, Adalberto A Pérez de León, Scot E Dowd, et al.
BMC Microbiology 11 (1) (2011)
https://doi.org/10.1186/1471-2180-11-6

Innate immune response in experimentally induced bovine intramammary infection with Staphylococcus simulans and S. epidermidis

Heli Simojoki, Tiina Salomäki, Suvi Taponen, Antti Iivanainen and Satu Pyörälä
Veterinary Research 42 (1) 49 (2011)
https://doi.org/10.1186/1297-9716-42-49

Mastitis impact on technological properties of milk and quality of milk products—a review

Caroline Le Maréchal, Richard Thiéry, Eric Vautor and Yves Le Loir
Dairy Science & Technology 91 (3) 247 (2011)
https://doi.org/10.1007/s13594-011-0009-6

Comparative Kinetics of Escherichia coli - and Staphylococcus aureus -Specific Activation of Key Immune Pathways in Mammary Epithelial Cells Demonstrates That S. aureus Elicits a Delayed Response Dominated by Interleukin-6 (IL-6) but Not by IL-1A or Tumor Necrosis Factor Alpha

Juliane Günther, Kathrin Esch, Norbert Poschadel, et al.
Infection and Immunity 79 (2) 695 (2011)
https://doi.org/10.1128/IAI.01071-10

Gene Polymorphisms: The Keys for Marker Assisted Selection and Unraveling Core Regulatory Pathways for Mastitis Resistance

Gina M. Pighetti and A. A. Elliott
Journal of Mammary Gland Biology and Neoplasia 16 (4) 421 (2011)
https://doi.org/10.1007/s10911-011-9238-9

Streptococcus uberis-specific T cells are present in mammary gland secretions of cows and can be activated to kill S. uberis

Michel Denis, S. Jane Lacy-Hulbert, Bryce M. Buddle, John H. Williamson and D. Neil Wedlock
Veterinary Research Communications 35 (3) 145 (2011)
https://doi.org/10.1007/s11259-011-9462-1

Molecular Epidemiology of Mastitis Pathogens of Dairy Cattle and Comparative Relevance to Humans

Ruth N. Zadoks, John R. Middleton, Scott McDougall, Jorgen Katholm and Ynte H. Schukken
Journal of Mammary Gland Biology and Neoplasia 16 (4) 357 (2011)
https://doi.org/10.1007/s10911-011-9236-y

In Vivo Activation of the Intracrine Vitamin D Pathway in Innate Immune Cells and Mammary Tissue during a Bacterial Infection

Corwin D. Nelson, Timothy A. Reinhardt, Donald C. Beitz, John D. Lippolis and Derya Unutmaz
PLoS ONE 5 (11) e15469 (2010)
https://doi.org/10.1371/journal.pone.0015469

Differential levels of mRNA transcripts encoding immunologic mediators in mammary gland secretions from dairy cows with subclinical environmental Streptococci infections

Daniela R. Bruno, Paul V. Rossitto, Ralph.G.S. Bruno, et al.
Veterinary Immunology and Immunopathology 138 (1-2) 15 (2010)
https://doi.org/10.1016/j.vetimm.2010.06.009

Consequences of Interference of Milk with Chemoattractants for Enzyme-Linked Immunosorbent Assay Quantifications

P. Rainard
Clinical and Vaccine Immunology 17 (5) 848 (2010)
https://doi.org/10.1128/CVI.00447-09

Greater expression of TLR2, TLR4, and IL6 due to negative energy balance is associated with lower expression of HLA-DRA and HLA-A in bovine blood neutrophils after intramammary mastitis challenge with Streptococcus uberis

Kasey M. Moyes, James K. Drackley, Dawn E. Morin and Juan J. Loor
Functional & Integrative Genomics 10 (1) 53 (2010)
https://doi.org/10.1007/s10142-009-0154-7

Mammary gene expression profiles during an intramammary challenge reveal potential mechanisms linking negative energy balance with impaired immune response

Kasey M. Moyes, James K. Drackley, Dawn E. Morin, et al.
Physiological Genomics 41 (2) 161 (2010)
https://doi.org/10.1152/physiolgenomics.00197.2009

Sortase anchored proteins ofStreptococcus uberisplay major roles in the pathogenesis of bovine mastitis in dairy cattle

James A. Leigh, Sharon A. Egan, Philip N. Ward, Terence R. Field and Tracey J. Coffey
Veterinary Research 41 (5) 63 (2010)
https://doi.org/10.1051/vetres/2010036

Expression of innate resistance factors in mammary secretion from periparturient dairy heifers and their association with subsequent infection status

Chris W.R. Compton, Ray T.M. Cursons, Catherine M.E. Barnett and Scott McDougall
Veterinary Immunology and Immunopathology 127 (3-4) 357 (2009)
https://doi.org/10.1016/j.vetimm.2008.10.331

Effect of treatment with the nonsteroidal antiinflammatory meloxicam on milk production, somatic cell count, probability of re-treatment, and culling of dairy cows with mild clinical mastitis

S. McDougall, M.A. Bryan and R.M. Tiddy
Journal of Dairy Science 92 (9) 4421 (2009)
https://doi.org/10.3168/jds.2009-2284

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

Somatic cell scores and clinical signs following experimental intramammary infection of dairy cows with a Staphylococcus aureus small colony variant (S. aureus SCV) in comparison to other bovine strains

Heba Atalla, Carlton Gyles, Bruce Wilkie, Ken Leslie and Bonnie Mallard
Veterinary Microbiology 137 (3-4) 326 (2009)
https://doi.org/10.1016/j.vetmic.2009.01.027

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

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 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

Administration of a live culture ofLactococcus lactisDPC 3147 into the bovine mammary gland stimulates the local host immune response, particularlyIL-1β andIL-8gene expression

Christine Beecher, Mairéad Daly, Donagh P Berry, et al.
Journal of Dairy Research 76 (3) 340 (2009)
https://doi.org/10.1017/S0022029909004154

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

Vaccines against bovine mastitis in the New Zealand context: What is the best way forward?

M Denis, DN Wedlock, SJ Lacy-Hulbert, JE Hillerton and BM Buddle
New Zealand Veterinary Journal 57 (3) 132 (2009)
https://doi.org/10.1080/00480169.2009.36892

Pathogen-dependent induction of cytokines and other soluble inflammatory mediators during intramammary infection of dairy cows1

D. D. Bannerman
Journal of Animal Science 87 (suppl_13) 10 (2009)
https://doi.org/10.2527/jas.2008-1187

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

Expression of macrophage CD14 receptor in the course of experimental inflammatory responses induced by lipopolysaccharide and muramyl dipeptide

Z. Sladek and D. Rysanek
Veterinární medicína 53 (7) 347 (2008)
https://doi.org/10.17221/1991-VETMED

Pathogen-Specific Effects of Quantitative Trait Loci Affecting Clinical Mastitis and Somatic Cell Count in Danish Holstein Cattle

L.P. Sørensen, B. Guldbrandtsen, J.R. Thomasen and M.S. Lund
Journal of Dairy Science 91 (6) 2493 (2008)
https://doi.org/10.3168/jds.2007-0583

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

Interleukin-1β infusion in bovine mammary glands prior to challenge with Streptococcus uberis reduces bacterial growth but causes sterile mastitis

D. Neil Wedlock, Michel Denis, Jane Lacy-Hulbert and Bryce M. Buddle
Veterinary Research Communications 32 (6) 439 (2008)
https://doi.org/10.1007/s11259-008-9044-z

Molecular analysis of the bovine anaphylatoxin C5a receptor

Sailasree Nemali, Daniel W Siemsen, Laura K Nelson, Peggy L Bunger, Craig L Faulkner, Pascal Rainard, Katherine A Gauss, Mark A Jutila and Mark T Quinn
Journal of Leukocyte Biology 84 (2) 537 (2008)
https://doi.org/10.1189/jlb.0208142

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

The response of HEK293 cells transfected with bovine TLR2 to established pathogen-associated molecular patterns and to bacteria causing mastitis in cattle

Katja Farhat, Kay-Sara Sauter, Marija Brcic, et al.
Veterinary Immunology and Immunopathology 125 (3-4) 326 (2008)
https://doi.org/10.1016/j.vetimm.2008.05.026

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