Innate immune response to intramammary infection with Serratia marcescens and Streptococcus uberis
Vet. Res., 35 6 (2004) 681-700
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:
This article has been cited by the following article(s):
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 FanMicrobial Pathogenesis 191 106675 (2024)
https://doi.org/10.1016/j.micpath.2024.106675
Retained Placenta as a Potential Source of Mastitis Pathogens in Dairy Cows
Diana Ribeiro, Susana Astiz, Aitor Fernandez-Novo, Gisele Margatho and João SimõesApplied Sciences 14 (12) 4986 (2024)
https://doi.org/10.3390/app14124986
The change in the number of somatic cells in cow’s milk during lactation
Anja Duvnjak, Ksenija Čobanović, Marija Pajić, Saša Krstović, Tamara Papović and Denis KučevićAgroReS 13 193 (2024)
https://doi.org/10.7251/ZARS2401193D
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 NowakiewiczJournal of Veterinary Research 68 (1) 115 (2024)
https://doi.org/10.2478/jvetres-2024-0002
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 PiccininiBMC Veterinary Research 20 (1) (2024)
https://doi.org/10.1186/s12917-024-04014-x
(2023)
https://doi.org/10.21203/rs.3.rs-3753736/v1
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. NelsonVeterinary 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
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
Association of Milk Somatic Cell Count with Bacteriological Cure of Intramammary Infection—A Review
Jenna Williamson, Todd Callaway, Emmanuel Rollin and Valerie RymanAgriculture 12 (9) 1437 (2022)
https://doi.org/10.3390/agriculture12091437
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
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 KovačevićAntibiotics 11 (8) 1077 (2022)
https://doi.org/10.3390/antibiotics11081077
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 YangPathogens 10 (5) 506 (2021)
https://doi.org/10.3390/pathogens10050506
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
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. MamedovaJDS 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 FoucrasJournal of Dairy Science 104 (10) 10427 (2021)
https://doi.org/10.3168/jds.2021-20434
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
Invited review: Mechanisms of hypophagia during disease
W.E. Brown and B.J. BradfordJournal of Dairy Science 104 (9) 9418 (2021)
https://doi.org/10.3168/jds.2021-20217
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
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
Large Animal Internal Medicine
Pamela L. Ruegg and Ronald J. ErskineLarge Animal Internal Medicine 1118 (2020)
https://doi.org/10.1016/B978-0-323-55445-9.00036-7
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 LangoniPathogens 9 (9) 706 (2020)
https://doi.org/10.3390/pathogens9090706
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. LippolisJournal 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 ROYThe Indian Journal of Animal Sciences 89 (5) (2019)
https://doi.org/10.56093/ijans.v89i5.89999
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
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
Symposium review: Intramammary infections—Major pathogens and strain-associated complexity
O.M. KeaneJournal of Dairy Science 102 (5) 4713 (2019)
https://doi.org/10.3168/jds.2018-15326
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. RuppJournal of Dairy Science 101 (8) 6703 (2018)
https://doi.org/10.3168/jds.2018-14593
A Critical Appraisal of Probiotics for Mastitis Control
Pascal Rainard and Gilles FoucrasFrontiers in Veterinary Science 5 (2018)
https://doi.org/10.3389/fvets.2018.00251
The importance of non-steroidal anti-inflammatory drugs (NSAIDs) in mastitis therapeutics
James BreenLivestock 22 (4) 182 (2017)
https://doi.org/10.12968/live.2017.22.4.182
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. WellnitzJournal of Animal Science 95 (12) 5720 (2017)
https://doi.org/10.2527/jas2017.1845
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
Pathological changes in experimental intramammary infection with different Staphylococcus species in Mice
P. Krishnamoorthy, M.L. Satyanarayana, B.R. Shome and H. RahmanJournal of Microscopy and Ultrastructure (2017)
https://doi.org/10.1016/j.jmau.2017.05.001
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
Apoptosis of Endothelial Cells by 13-HPODE Contributes to Impairment of Endothelial Barrier Integrity
Valerie E. Ryman, Nandakumar Packiriswamy and Lorraine M. SordilloMediators of Inflammation 2016 1 (2016)
https://doi.org/10.1155/2016/9867138
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
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
TRIENNIAL LACTATION SYMPOSIUM: Nutrient partitioning during intramammary inflammation: A key to severity of mastitis and risk of subsequent diseases?1
K. M. MoyesJournal of Animal Science 93 (12) 5586 (2015)
https://doi.org/10.2527/jas.2015-8945
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
Role of endothelial cells in bovine mammary gland health and disease
Valerie E. Ryman, Nandakumar Packiriswamy and Lorraine M. SordilloAnimal Health Research Reviews 16 (2) 135 (2015)
https://doi.org/10.1017/S1466252315000158
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. ZadoksVeterinary Research 46 (1) (2015)
https://doi.org/10.1186/s13567-015-0268-y
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. RueggJournal of Dairy Science 98 (6) 3791 (2015)
https://doi.org/10.3168/jds.2014-8997
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
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
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. DahlJournal of Dairy Science 97 (12) 7426 (2014)
https://doi.org/10.3168/jds.2013-7621
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
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 IngvartsenJournal of Animal Science and Biotechnology 5 (1) (2014)
https://doi.org/10.1186/2049-1891-5-47
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
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 HillertonJournal of Dairy Research 80 (3) 360 (2013)
https://doi.org/10.1017/S0022029913000289
The bovine CXCR1 gene is highly polymorphic
Gina M. Pighetti, Cheryl J. Kojima, Leszek Wojakiewicz and Magdalena RambeaudVeterinary Immunology and Immunopathology 145 (1-2) 464 (2012)
https://doi.org/10.1016/j.vetimm.2011.09.012
The innate immune response of the bovine mammary gland to bacterial infection
Olga Wellnitz and Rupert M. BruckmaierThe Veterinary Journal 192 (2) 148 (2012)
https://doi.org/10.1016/j.tvjl.2011.09.013
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 “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
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
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
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 KimuraVeterinary Medicine International 2012 1 (2012)
https://doi.org/10.1155/2012/172072
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 LundGenetics Selection Evolution 44 (1) (2012)
https://doi.org/10.1186/1297-9686-44-18
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
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. SchukkenJournal of Mammary Gland Biology and Neoplasia 16 (4) 357 (2011)
https://doi.org/10.1007/s10911-011-9236-y
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 PyöräläVeterinary Research 42 (1) 49 (2011)
https://doi.org/10.1186/1297-9716-42-49
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
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
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
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 WedlockVeterinary Research Communications 35 (3) 145 (2011)
https://doi.org/10.1007/s11259-011-9462-1
Gene Polymorphisms: The Keys for Marker Assisted Selection and Unraveling Core Regulatory Pathways for Mastitis Resistance
Gina M. Pighetti and A. A. ElliottJournal of Mammary Gland Biology and Neoplasia 16 (4) 421 (2011)
https://doi.org/10.1007/s10911-011-9238-9
Mastitis impact on technological properties of milk and quality of milk products—a review
Caroline Le Maréchal, Richard Thiéry, Eric Vautor and Yves Le LoirDairy Science & Technology 91 (3) 247 (2011)
https://doi.org/10.1007/s13594-011-0009-6
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. LoorFunctional & 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
Consequences of Interference of Milk with Chemoattractants for Enzyme-Linked Immunosorbent Assay Quantifications
P. RainardClinical and Vaccine Immunology 17 (5) 848 (2010)
https://doi.org/10.1128/CVI.00447-09
Mastitis associated transcriptomic disruptions in cattle
Manuela Rinaldi, Robert W. Li and Anthony V. CapucoVeterinary Immunology and Immunopathology 138 (4) 267 (2010)
https://doi.org/10.1016/j.vetimm.2010.10.005
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. CoffeyVeterinary Research 41 (5) 63 (2010)
https://doi.org/10.1051/vetres/2010036
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 UnutmazPLoS 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
Changing trends in mastitis
RN Zadoks and JL FitzpatrickIrish Veterinary Journal 62 (S4) (2009)
https://doi.org/10.1186/2046-0481-62-S4-S59
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
Pathogen-dependent induction of cytokines and other soluble inflammatory mediators during intramammary infection of dairy cows1
D. D. BannermanJournal of Animal Science 87 (suppl_13) 10 (2009)
https://doi.org/10.2527/jas.2008-1187
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 MallardVeterinary Microbiology 137 (3-4) 326 (2009)
https://doi.org/10.1016/j.vetmic.2009.01.027
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 BuddleNew Zealand Veterinary Journal 57 (3) 132 (2009)
https://doi.org/10.1080/00480169.2009.36892
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
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. TiddyJournal of Dairy Science 92 (9) 4421 (2009)
https://doi.org/10.3168/jds.2009-2284
Imunidade inata da glândula mamária bovina: resposta à infecção
Deolinda Maria Vieira Filha Carneiro, Paulo Francisco Domingues and Adil Knackfuss VazCiência Rural 39 (6) 1934 (2009)
https://doi.org/10.1590/S0103-84782009005000106
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
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
Genetic parameters for pathogen-specific mastitis resistance in Danish Holstein Cattle
L.P. Sørensen, P. Madsen, T. Mark and M.S. LundAnimal 3 (5) 647 (2009)
https://doi.org/10.1017/S1751731109003899
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 McDougallVeterinary Immunology and Immunopathology 127 (3-4) 357 (2009)
https://doi.org/10.1016/j.vetimm.2008.10.331
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
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
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. BuddleVeterinary Research Communications 32 (6) 439 (2008)
https://doi.org/10.1007/s11259-008-9044-z
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
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
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
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. LundJournal of Dairy Science 91 (6) 2493 (2008)
https://doi.org/10.3168/jds.2007-0583
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 QuinnJournal of Leukocyte Biology 84 (2) 537 (2008)
https://doi.org/10.1189/jlb.0208142
Identification and characterization of a new interleukin-8 receptor in bovine species
Hichem Lahouassa, Pascal Rainard, Alain Caraty and Céline RiolletMolecular Immunology 45 (4) 1153 (2008)
https://doi.org/10.1016/j.molimm.2007.07.011