The complement in milk and defense of the bovine mammary gland against infections
Vet. Res., 34 5 (2003) 647-670
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):
The mammary gland is intolerant to bacterial intrusion
Pascal RainardExploration of Immunology 59 (2024)
https://doi.org/10.37349/ei.2024.00128
373 (2024)
https://doi.org/10.1007/978-981-99-2718-0_11
Different Immune Control of Gram-Positive and Gram-Negative Mammary Infections in Dairy Cows
Giulio Curone, Joel Filipe, Alessia Inglesi, Valerio Bronzo, Claudia Pollera, Stefano Comazzi, Susanna Draghi, Renata Piccinini, Gianluca Ferlazzo, Alda Quattrone, Daniele Vigo, Massimo Amadori and Federica RivaVeterinary Sciences 11 (4) 166 (2024)
https://doi.org/10.3390/vetsci11040166
Ruminant livestock TR V(D)J genes and CDR3 repertoire
Fengli Wu, Yunlan Deng, Xinsheng Yao and Jun LiVeterinary Immunology and Immunopathology 277 110829 (2024)
https://doi.org/10.1016/j.vetimm.2024.110829
Complement in breast milk modifies offspring gut microbiota to promote infant health
Dongqing Xu, Siyu Zhou, Yue Liu, Alan L. Scott, Jian Yang and Fengyi WanCell 187 (3) 750 (2024)
https://doi.org/10.1016/j.cell.2023.12.019
Complement-ary protection for all ages
Geongoo Han and Shipra VaishnavaImmunity 57 (3) 411 (2024)
https://doi.org/10.1016/j.immuni.2024.02.010
93 (2024)
https://doi.org/10.1002/9781394204007.ch10
New Insights on Nucleotide Sequence Variants and mRNA Levels of Candidate Genes Assessing Resistance/Susceptibility to Mastitis in Holstein and Montbéliarde Dairy Cows
Bothaina Essa, Mona Al-Sharif, Mohamed Abdo, Liana Fericean and Ahmed AteyaVeterinary Sciences 10 (1) 35 (2023)
https://doi.org/10.3390/vetsci10010035
Comparative Label-Free Liquid Chromatography–Mass Spectrometry Milk Proteomic Profiles Highlight Putative Differences between the Autochthon Teramana and Saanen Goat Breeds
Alessio Di Luca, Francesca Bennato, Andrea Ianni, et al.Animals 13 (14) 2263 (2023)
https://doi.org/10.3390/ani13142263
Immune defences of the mammary gland in dairy ruminants
Pierre Germon and Rodrigo Prado MartinsReproduction in Domestic Animals 58 (S2) 4 (2023)
https://doi.org/10.1111/rda.14372
Comparative secretome analysis of Staphylococcus aureus strains with different within-herd intramammary infection prevalence
M. Filippa Addis, Salvatore Pisanu, Valentina Monistero, et al.Virulence 13 (1) 174 (2022)
https://doi.org/10.1080/21505594.2021.2024014
Vaccination against Bacterial Mastitis in Sheep
Natalia G. C. Vasileiou, Daphne T. Lianou, Charalambia K. Michael, George C. Fthenakis and Vasia S. MavrogianniVaccines 10 (12) 2088 (2022)
https://doi.org/10.3390/vaccines10122088
Progress towards the Elusive Mastitis Vaccines
Pascal Rainard, Florence B. Gilbert, Rodrigo P. Martins, Pierre Germon and Gilles FoucrasVaccines 10 (2) 296 (2022)
https://doi.org/10.3390/vaccines10020296
Transcriptome profiling of the nonlactating mammary glands of dairy goats reveals the molecular genetic mechanism of mammary cell remodeling
Rong Xuan, Tianle Chao, Xiaodong Zhao, et al.Journal of Dairy Science 105 (6) 5238 (2022)
https://doi.org/10.3168/jds.2021-21039
Complement component 3 haplotypes influence serum complement activity and milk production traits in Chinese Holstein cattle
Yonghui Wang, Junyu Zhai, Chunhong Yang, et al.PLOS ONE 17 (6) e0268959 (2022)
https://doi.org/10.1371/journal.pone.0268959
Shielding Effect of Escherichia coli O-Antigen Polysaccharide on J5-Induced Cross-Reactive Antibodies
Pascal Rainard, Maryline Repérant-Ferter, Christophe Gitton, Pierre Germon and Drusilla L. BurnsmSphere 6 (1) (2021)
https://doi.org/10.1128/mSphere.01227-20
Quantitative analysis of differentially expressed milk fat globule membrane proteins between donkey and bovine colostrum based on high-performance liquid chromatography with tandem mass spectrometry proteomics
Mohan Li, Kexin Zheng, Wanying Song, et al.Journal of Dairy Science 104 (12) 12207 (2021)
https://doi.org/10.3168/jds.2021-20471
Bovine Immunology: Implications for Dairy Cattle
Anastasia N. Vlasova and Linda J. SaifFrontiers in Immunology 12 (2021)
https://doi.org/10.3389/fimmu.2021.643206
High-Resolution Mass Spectrometer–Based Ultra-Deep Profile of Milk Whey Proteome in Indian Zebu (Sahiwal) Cattle
Alka Chopra, Syed Azmal Ali, Shveta Bathla, et al.Frontiers in Nutrition 7 (2020)
https://doi.org/10.3389/fnut.2020.00150
DIA proteomics reveals hypotensive and immune-enhancing constituents in buffalo whey from different altitudes
Fulan Zhang, Jinhui Pu, Zhaobing Gu and Huaming MaoInternational Journal of Biological Macromolecules 164 4146 (2020)
https://doi.org/10.1016/j.ijbiomac.2020.08.213
Viral Evasion of the Complement System and Its Importance for Vaccines and Therapeutics
Jack Mellors, Tom Tipton, Stephanie Longet and Miles CarrollFrontiers in Immunology 11 (2020)
https://doi.org/10.3389/fimmu.2020.01450
Lipopolysaccharide triggers different transcriptional signatures in taurine and indicine cattle macrophages: Reactive oxygen species and potential outcomes to the development of immune response to infections
Raquel Morais de Paiva Daibert, Carlos Alberto Oliveira de Biagi Junior, Felipe de Oliveira Vieira, et al.PLOS ONE 15 (11) e0241861 (2020)
https://doi.org/10.1371/journal.pone.0241861
Analyzing the genomic and transcriptomic architecture of milk traits in Murciano-Granadina goats
Dailu Guan, Vincenzo Landi, María Gracia Luigi-Sierra, et al.Journal of Animal Science and Biotechnology 11 (1) (2020)
https://doi.org/10.1186/s40104-020-00435-4
The role of O-polysaccharide chain and complement resistance of Escherichia coli in mammary virulence
Hagit Salamon, Einat Nissim-Eliraz, Oded Ardronai, Israel Nissan and Nahum Y. ShpigelVeterinary Research 51 (1) (2020)
https://doi.org/10.1186/s13567-020-00804-x
Anti-inflammatory mechanism of ginsenoside Rg1: Proteomic analysis of milk from goats with mastitis induced with lipopolysaccharide
Yuemin Wang, Yong Zhang, Xiaoqing Chi, et al.International Immunopharmacology 71 382 (2019)
https://doi.org/10.1016/j.intimp.2019.03.048
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
Mammary Defences and Immunity against Mastitis in Sheep
Angeliki I. Katsafadou, Antonis P. Politis, Vasia S. Mavrogianni, Mariana S. Barbagianni, Natalia G. C. Vasileiou, George C. Fthenakis and Ilektra A. FragkouAnimals 9 (10) 726 (2019)
https://doi.org/10.3390/ani9100726
Inclusion of grape marc in dairy cattle rations alters the bovine milk proteome
Richard A. Scuderi, David B. Ebenstein, Ying-Wai Lam, Jana Kraft and Sabrina L. GreenwoodJournal of Dairy Research 86 (2) 154 (2019)
https://doi.org/10.1017/S0022029919000372
Genomic and Transcriptomic Analysis of Escherichia coli Strains Associated with Persistent and Transient Bovine Mastitis and the Role of Colanic Acid
John D. Lippolis, Devin B. Holman, Brian W. Brunelle, et al.Infection and Immunity 86 (1) (2018)
https://doi.org/10.1128/IAI.00566-17
Control of bovine mastitis in the 21st century: Immunize or tolerize?
Massimo AmadoriResearch in Veterinary Science 121 1 (2018)
https://doi.org/10.1016/j.rvsc.2018.09.010
Comparative proteomics analysis of human and ruminant milk serum reveals variation in protection and nutrition
Jing Lu, Shuwen Zhang, Lu Liu, et al.Food Chemistry 261 274 (2018)
https://doi.org/10.1016/j.foodchem.2018.04.065
Transcriptome profiling of Staphylococci-infected cow mammary gland parenchyma
Ewa M Kosciuczuk, Paweł Lisowski, Justyna Jarczak, et al.BMC Veterinary Research 13 (1) (2017)
https://doi.org/10.1186/s12917-017-1088-2
Complement component 3: characterization and association with mastitis resistance in Egyptian water buffalo and cattle
NERMIN EL-HALAWANY, ABD-EL-MONSIF A. SHAWKY, AHMED F. M. AL-TOHAMY, et al.Journal of Genetics 96 (1) 65 (2017)
https://doi.org/10.1007/s12041-017-0740-8
Immuno-Detection of C3a, a C3 Complement Activated Product in Mastitis Milk, a Potential Diagnostic Marker
Thanislass Jacob, Gangasudan Subramani, Prathiba Sivaprakasam, Antony Xavier and Hirak MukhopadhyayVeterinary Sciences 4 (1) 13 (2017)
https://doi.org/10.3390/vetsci4010013
Immunopathology in Toxicology and Drug Development
Catherine A. Picut, Darlene Dixon and Eveline P. C. T. de RijkMolecular and Integrative Toxicology, Immunopathology in Toxicology and Drug Development 541 (2017)
https://doi.org/10.1007/978-3-319-47385-7_11
Escherichia coli mastitis strains: In vitro phenotypes and severity of infection in vivo
Perrine Roussel, Adeline Porcherie, Maryline Répérant-Ferter, et al.PLOS ONE 12 (7) e0178285 (2017)
https://doi.org/10.1371/journal.pone.0178285
Transformation of serum-susceptible Escherichia coli O111 with p16Slux plasmid to allow for real-time monitoring of complement-based inactivation of bacterial growth in bovine milk
S. Maye, C. Stanton, G.F. Fitzgerald and P.M. KellyJournal of Dairy Science 99 (1) 112 (2016)
https://doi.org/10.3168/jds.2015-10244
Nutritional strategies to optimize dairy cattle immunity
L.M. SordilloJournal of Dairy Science 99 (6) 4967 (2016)
https://doi.org/10.3168/jds.2015-10354
Genomic Analysis Reveals the Molecular Basis for Capsule Loss in the Group B Streptococcus Population
Roberto Rosini, Edmondo Campisi, Matteo De Chiara, et al.PLOS ONE 10 (5) e0125985 (2015)
https://doi.org/10.1371/journal.pone.0125985
The rapid increase of circulating adiponectin in neonatal calves depends on colostrum intake
J. Kesser, M. Hill, J.F.L. Heinz, et al.Journal of Dairy Science 98 (10) 7044 (2015)
https://doi.org/10.3168/jds.2015-9726
The economic impact of subclinical ketosis at the farm level: Tackling the challenge of over-estimation due to multiple interactions
D. Raboisson, M. Mounié, E. Khenifar and E. MaignéPreventive Veterinary Medicine 122 (4) 417 (2015)
https://doi.org/10.1016/j.prevetmed.2015.07.010
A Genome-Wide Association Study for Clinical Mastitis in First Parity US Holstein Cows Using Single-Step Approach and Genomic Matrix Re-Weighting Procedure
Francesco Tiezzi, Kristen L. Parker-Gaddis, John B. Cole, John S. Clay and Christian MalteccaPLOS ONE 10 (2) e0114919 (2015)
https://doi.org/10.1371/journal.pone.0114919
Combining Genome Wide Association Studies and Differential Gene Expression Data Analyses Identifies Candidate Genes Affecting Mastitis Caused by Two Different Pathogens in the Dairy Cow
Xing Chen, Zhangrui Cheng, Shujun Zhang, Dirk Werling and D. Claire WathesOpen Journal of Animal Sciences 05 (04) 358 (2015)
https://doi.org/10.4236/ojas.2015.54040
Characterization of persistent and transient Escherichia coli isolates recovered from clinical mastitis episodes in dairy cows
Julie-Hélène Fairbrother, Simon Dufour, John Morris Fairbrother, et al.Veterinary Microbiology 176 (1-2) 126 (2015)
https://doi.org/10.1016/j.vetmic.2014.12.025
Selenium Inhibits LPS-Induced Pro-inflammatory Gene Expression by Modulating MAPK and NF-κB Signaling Pathways in Mouse Mammary Epithelial Cells in Primary Culture
Wen Zhang, Runxiang Zhang, Tiancheng Wang, et al.Inflammation 37 (2) 478 (2014)
https://doi.org/10.1007/s10753-013-9761-5
Effect of pasture availability and genotype on welfare, immune function, performance and meat characteristics of growing rabbits
Cecilia Mugnai, Alessandro Dal Bosco, Raffaella Cardinali, et al.World Rabbit Science 22 (1) 29 (2014)
https://doi.org/10.4995/wrs.2014.1342
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
Fine-tuned characterization of Staphylococcus aureus Newbould 305, a strain associated with mild and chronic mastitis in bovines
Vincent Peton, Damien S Bouchard, Sintia Almeida, et al.Veterinary Research 45 (1) (2014)
https://doi.org/10.1186/s13567-014-0106-7
Genotyping and virulence factors assessment of bovine mastitis Escherichia coli
Shlomo E. Blum and Gabriel LeitnerVeterinary Microbiology 163 (3-4) 305 (2013)
https://doi.org/10.1016/j.vetmic.2012.12.037
The complement system of the goat: Haemolytic assays and isolation of major proteins
Isabel Moreno-Indias, Alister W Dodds, Anastasio Argüello, Noemi Castro and Robert B SimBMC Veterinary Research 8 (1) (2012)
https://doi.org/10.1186/1746-6148-8-91
Three novel single-nucleotide polymorphisms of complement component 4 gene (C4A) in Chinese Holstein cattle and their associations with milk performance traits and CH50
Yue Yang, Qiuling Li, Zhihua Ju, et al.Veterinary Immunology and Immunopathology 145 (1-2) 223 (2012)
https://doi.org/10.1016/j.vetimm.2011.11.010
The relationship between the variants of the bovine MBL2 gene and milk production traits, mastitis, serum MBL-C levels and complement activity
Xinju Wang, Zhihua Ju, Jinming Huang, et al.Veterinary Immunology and Immunopathology 148 (3-4) 311 (2012)
https://doi.org/10.1016/j.vetimm.2012.06.017
Host-defence-related proteins in cows’ milk
T.T. Wheeler, G.A. Smolenski, D.P. Harris, et al.Animal 6 (3) 415 (2012)
https://doi.org/10.1017/S1751731111002151
Anaphylatoxin C5a-induced toll-like receptor 4 signaling in bovine neutrophils
M.G.H. Stevens, M. Van Poucke, L.J. Peelman, et al.Journal of Dairy Science 94 (1) 152 (2011)
https://doi.org/10.3168/jds.2010-3358
Immunopathology of Mastitis: Insights into Disease Recognition and Resolution
Stacey L. Aitken, Christine M. Corl and Lorraine M. SordilloJournal of Mammary Gland Biology and Neoplasia 16 (4) 291 (2011)
https://doi.org/10.1007/s10911-011-9230-4
Quantitative milk proteomics – Host responses to lipopolysaccharide‐mediated inflammation of bovine mammary gland
Marianne Danielsen, Marius C. Codrea, Klaus L. Ingvartsen, et al.PROTEOMICS 10 (12) 2240 (2010)
https://doi.org/10.1002/pmic.200900771
Antibody and cell-mediated immune responses to Staphylococcus aureus small colony variants and their parental strains associated with bovine mastitis
Heba Atalla, Bruce Wilkie, Carlton Gyles, et al.Developmental & Comparative Immunology 34 (12) 1283 (2010)
https://doi.org/10.1016/j.dci.2010.07.005
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 ZhaoJournal of Proteome Research 9 (9) 4604 (2010)
https://doi.org/10.1021/pr100336e
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
Effects of intramammary infusion of cis–urocanic acid on mastitis-associated inflammation and tissue injury in dairy cows
Douglas D. Bannerman, Manuela Rinaldi, Bryan T. Vinyard, Jarmo Laihia and Lasse LeinoAmerican Journal of Veterinary Research 70 (3) 373 (2009)
https://doi.org/10.2460/ajvr.70.3.373
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
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
Proteomic Changes in Escherichia coli When Grown in Fresh Milk versus Laboratory Media
John D. Lippolis, Darrell O. Bayles and Timothy A. ReinhardtJournal of Proteome Research 8 (1) 149 (2009)
https://doi.org/10.1021/pr800458v
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
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
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 in Post‐Partum Dairy Cows
S PyöräläReproduction in Domestic Animals 43 (s2) 252 (2008)
https://doi.org/10.1111/j.1439-0531.2008.01170.x
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
Lactation performance of transgenic goats expressing recombinant human butyryl-cholinesterase in the milk
Hernan Baldassarre, Duncan K. Hockley, Monique Doré, et al.Transgenic Research 17 (1) 73 (2008)
https://doi.org/10.1007/s11248-007-9137-4
Activation of Immune Cells in Bovine Mammary Gland Secretions by Zymosan-Treated Bovine Serum
K. Kimura, J.P. Goff, M.J. Schmerr, et al.Journal of Dairy Science 91 (5) 1852 (2008)
https://doi.org/10.3168/jds.2007-0895
Identification of a bovine mastitis Escherichia coli subset
S. Blum, E.D. Heller, O. Krifucks, et al.Veterinary Microbiology 132 (1-2) 135 (2008)
https://doi.org/10.1016/j.vetmic.2008.05.012
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. WellnitzJournal of Dairy Science 91 (6) 2215 (2008)
https://doi.org/10.3168/jds.2007-0752
The effects of diet and age on serum complement system activity in goat kids
N. Castro, F. Acosta, T. Niño, et al.Livestock Science 119 (1-3) 102 (2008)
https://doi.org/10.1016/j.livsci.2008.03.004
The xMAP™ technique can be used for detection of the inflammatory cytokines IL-1β, IL-6 and TNF-α in bovine samples
Johanna Dernfalk, Karin Persson Waller and Anders JohannissonVeterinary Immunology and Immunopathology 118 (1-2) 40 (2007)
https://doi.org/10.1016/j.vetimm.2007.04.004
Innate immune response of bovine mammary gland to pathogenic bacteria responsible for mastitis
Javier Oviedo-Boyso, Juan J. Valdez-Alarcón, Marcos Cajero-Juárez, et al.Journal of Infection 54 (4) 399 (2007)
https://doi.org/10.1016/j.jinf.2006.06.010
Innate immunity of the bovine mammary gland
Pascal Rainard and Céline RiolletVeterinary Research 37 (3) 369 (2006)
https://doi.org/10.1051/vetres:2006007
Factors affecting mammary gland immunity and mastitis susceptibility
Lorraine M. SordilloLivestock Production Science 98 (1-2) 89 (2005)
https://doi.org/10.1016/j.livprodsci.2005.10.017
Development of a monoclonal blocking ELISA for the detection of antibody to Mycoplasma bovis in dairy cattle and comparison to detection by PCR
Ali Ghadersohi, Zahra Fayazi and Robert G. HirstVeterinary Immunology and Immunopathology 104 (3-4) 183 (2005)
https://doi.org/10.1016/j.vetimm.2004.11.008
Effect of Carprofen Treatment Following Experimentally Induced Escherichia coli Mastitis in Primiparous Cows
F. Vangroenweghe, L. Duchateau, P. Boutet, et al.Journal of Dairy Science 88 (7) 2361 (2005)
https://doi.org/10.3168/jds.S0022-0302(05)72914-3
Influence of 17β-Estradiol, Progesterone, and Dexamethasone on Diapedesis and Viability of Bovine Blood Polymorphonuclear Leukocytes
I. Lamote, E. Meyer, L. Duchateau and C. BurvenichJournal of Dairy Science 87 (10) 3340 (2004)
https://doi.org/10.3168/jds.S0022-0302(04)73470-0
Increase of Escherichia coli Inoculum Doses Induces Faster Innate Immune Response in Primiparous Cows
F. Vangroenweghe, P. Rainard, M. Paape, L. Duchateau and C. BurvenichJournal of Dairy Science 87 (12) 4132 (2004)
https://doi.org/10.3168/jds.S0022-0302(04)73556-0