Staphylococcus aureus lipoteichoic acid triggers inflammation in the lactating bovine mammary gland
Vet. Res., 39 5 (2008) 52
Published online: 2008-07-03
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):
Heat stress induces specific methylation, transcriptomic and metabolic pattern in dairy cows and their female progeny
Kathrin Halli, Tong Yin, Christian Koch, Stefan Krebs and Sven KönigScientific Reports 15 (1) (2025)
https://doi.org/10.1038/s41598-025-01082-3
DNA methylation and gene expression changes in mouse mammary tissue during successive lactations: part I – the impact of inflammation
E. Ivanova, C. Hue-Beauvais, A. Chaulot-Talmon, J. Castille, J Laubier, C De Casanove, A. Aubert-Frambourg, P. Germon, H. Jammes and F. Le ProvostEpigenetics 18 (1) (2023)
https://doi.org/10.1080/15592294.2023.2215633
RNA-seq reveals the role of miR-223 in alleviating inflammation of bovine mammary epithelial cells
Yan-Xia Li, Peng Jiao, Xing-Ping Wang, Jin-Peng Wang, Fen Feng, Bin-Wu Bao, Yi-Wen Dong, Zhuo-Ma Luoreng and Da-Wei WeiResearch in Veterinary Science 159 257 (2023)
https://doi.org/10.1016/j.rvsc.2023.04.012
Traditional and emerging Fusarium mycotoxins disrupt homeostasis of bovine mammary cells by altering cell permeability and innate immune function
Ran Xu, Umesh K. Shandilya, Alexandros Yiannikouris and Niel A. KarrowAnimal Nutrition 12 388 (2023)
https://doi.org/10.1016/j.aninu.2022.10.007
Effects of lipoteichoic and arachidonic acids on the immune-regulatory mechanism of bovine mammary epithelial cells using multi-omics analysis
Weitao Dong, Yan Chen, Quanwei Zhang, et al.Frontiers in Veterinary Science 9 (2022)
https://doi.org/10.3389/fvets.2022.984607
Mastitis: Impact of Dry Period, Pathogens, and Immune Responses on Etiopathogenesis of Disease and its Association with Periparturient Diseases
Ashley F. Egyedy and Burim N. AmetajDairy 3 (4) 881 (2022)
https://doi.org/10.3390/dairy3040061
Immune defenses of the mammary gland epithelium of dairy ruminants
Pascal Rainard, Florence B. Gilbert and Pierre GermonFrontiers in Immunology 13 (2022)
https://doi.org/10.3389/fimmu.2022.1031785
Ochratoxin A and Citrinin Differentially Modulate Bovine Mammary Epithelial Cell Permeability and Innate Immune Function
Ran Xu, Umesh K. Shandilya, Alexandros Yiannikouris and Niel A. KarrowToxins 14 (9) 640 (2022)
https://doi.org/10.3390/toxins14090640
Early effects of lipoteichoic acid from Staphylococcus aureus on milk production-related signaling pathways in mouse mammary epithelial cells
Ken Kobayashi, Naoki Omatsu, Liang Han, Lu Shan-Ni and Takanori NishimuraExperimental Cell Research 420 (1) 113352 (2022)
https://doi.org/10.1016/j.yexcr.2022.113352
Maintaining Optimal Mammary Gland Health and Prevention of Mastitis
František Zigo, Milan Vasil', Silvia Ondrašovičová, et al.Frontiers in Veterinary Science 8 (2021)
https://doi.org/10.3389/fvets.2021.607311
Identification of candidate genes affecting chronic subclinical mastitis in Norwegian Red cattle: combining genome‐wide association study, topologically associated domains and pathway enrichment analysis
E. Kirsanova, B. Heringstad, A. Lewandowska‐Sabat and I. OlsakerAnimal Genetics 51 (1) 22 (2020)
https://doi.org/10.1111/age.12886
Expression analysis of candidate genes for chronic subclinical mastitis in Norwegian Red cattle
E. Kirsanova, P. Boysen, G.M. Johansen, B. Heringstad, A. Lewandowska-Sabat and I. OlsakerJournal of Dairy Science 103 (10) 9142 (2020)
https://doi.org/10.3168/jds.2020-18170
Matrine alleviates Staphylococcus aureus lipoteichoic acid-induced endometritis via suppression of TLR2-mediated NF-κB activation
Kangfeng Jiang, Shuai Guo, Jing Yang, et al.International Immunopharmacology 70 201 (2019)
https://doi.org/10.1016/j.intimp.2019.02.033
The Effect of Lipopolysaccharide-Induced Experimental Bovine Mastitis on Clinical Parameters, Inflammatory Markers, and the Metabolome: A Kinetic Approach
Carl-Fredrik Johnzon, Josef Dahlberg, Ann-Marie Gustafson, et al.Frontiers in Immunology 9 (2018)
https://doi.org/10.3389/fimmu.2018.01487
Experimentally induced subclinical mastitis: are lipopolysaccharide and lipoteichoic acid eliciting similar pain responses?
Annalisa Elena Jolanda Giovannini, Bart Henricus Philippus van den Borne, Samantha Kay Wall, et al.Acta Veterinaria Scandinavica 59 (1) (2017)
https://doi.org/10.1186/s13028-017-0306-z
Mastitis Pathogens with High Virulence in a Mouse Model Produce a Distinct Cytokine Profile In Vivo
Carl-Fredrik Johnzon, Karin Artursson, Robert Söderlund, et al.Frontiers in Immunology 7 (2016)
https://doi.org/10.3389/fimmu.2016.00368
Innate and Adaptive Immunity Synergize to Trigger Inflammation in the Mammary Gland
Pascal Rainard, Patricia Cunha, Florence B. Gilbert and Emanuele BurattiPLOS ONE 11 (4) e0154172 (2016)
https://doi.org/10.1371/journal.pone.0154172
The cell wall component lipoteichoic acid of Staphylococcus aureus induces chemokine gene expression in bovine mammary epithelial cells
Yoshio KIKU, Yuya NAGASAWA, Fuyuko TANABE, et al.Journal of Veterinary Medical Science 78 (9) 1505 (2016)
https://doi.org/10.1292/jvms.15-0706
Lipoteichoic acids as a major virulence factor causing inflammatory responses via Toll-like receptor 2
Seok-Seong Kang, Ju-Ri Sim, Cheol-Heui Yun and Seung Hyun HanArchives of Pharmacal Research 39 (11) 1519 (2016)
https://doi.org/10.1007/s12272-016-0804-y
Location-specific expression of chemokines, TNF-α and S100 proteins in a teat explant model
Monique Lind, Anja S Sipka, Hans-Joachim Schuberth, Andreas Blutke, Rüdiger Wanke, Carola Sauter-Louis, Katarzyna A Duda, Otto Holst, Pascal Rainard, Pierre Germon, Holm Zerbe and Wolfram PetzlInnate Immunity 21 (3) 322 (2015)
https://doi.org/10.1177/1753425914539820
Neutrophil dynamics in the blood and milk of crossbred cows naturally infected with Staphylococcus aureus
Dilip K. Swain, Mohar Singh Kushwah, Mandheer Kaur and Ajay K. DangVeterinary World 8 (3) 336 (2015)
https://doi.org/10.14202/vetworld.2015.336-345
The CD markers of camel (Camelus dromedarius) milk cells during mastitis: The LPAM-1 expression is an indication of possible mucosal nature of the cellular trafficking
Roqaya A. Al-Ashqar, Khadim M. Al-Mohammad Salem, Abdul Kareem M. Al Herz, Amal I. Al-Haroon and Ahmed M. AlluwaimiResearch in Veterinary Science 99 77 (2015)
https://doi.org/10.1016/j.rvsc.2015.01.011
Oral administration of LPS and lipoteichoic acid prepartum modulated reactants of innate and humoral immunity in periparturient dairy cows
Summera Iqbal, Qendrim Zebeli, Dominik A Mansmann, Suzanna M Dunn and Burim N AmetajInnate Immunity 20 (4) 390 (2014)
https://doi.org/10.1177/1753425913496125
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
The crosstalk between Dectin1 and TLR4 via NF-κB subunits p65/RelB in mammary epithelial cells
Wei Zhu, Naishuo Zhu, Dou Bai, Jinfeng Miao and Sixiang ZouInternational Immunopharmacology 23 (2) 417 (2014)
https://doi.org/10.1016/j.intimp.2014.09.004
275 (2013)
https://doi.org/10.1007/978-1-4614-4714-6_9
Short communication: Differential immunoglobulin transfer during mastitis challenge by pathogen-specific components
O. Wellnitz, E.T. Arnold, M. Lehmann and R.M. BruckmaierJournal of Dairy Science 96 (3) 1681 (2013)
https://doi.org/10.3168/jds.2012-6150
Validation of RNA isolated from milk fat globules to profile mammary epithelial cell expression during lactation and transcriptional response to a bacterial infection
P. Brenaut, R. Bangera, C. Bevilacqua, et al.Journal of Dairy Science 95 (10) 6130 (2012)
https://doi.org/10.3168/jds.2012-5604
Repertoire of Escherichia coli agonists sensed by innate immunity receptors of the bovine udder and mammary epithelial cells
Adeline Porcherie, Patricia Cunha, Angelina Trotereau, et al.Veterinary Research 43 (1) (2012)
https://doi.org/10.1186/1297-9716-43-14
Genetic susceptibility to S. aureus mastitis in sheep: differential expression of mammary epithelial cells in response to live bacteria or supernatant
Cécile M. D. Bonnefont, Pascal Rainard, Patricia Cunha, et al.Physiological Genomics 44 (7) 403 (2012)
https://doi.org/10.1152/physiolgenomics.00155.2011
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
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
Lactobacillus plantarum Lipoteichoic Acid Alleviates TNF-α-Induced Inflammation in the HT-29 Intestinal Epithelial Cell Line
Hangeun Kim, Bong Jun Jung, Ji Hae Jung, Joo Yun Kim, Sung Kyun Chung and Dae Kyun ChungMolecules and Cells 33 (5) 479 (2012)
https://doi.org/10.1007/s10059-012-2266-5
Lipopolysaccharide and lipoteichoic acid induce different immune responses in the bovine mammary gland
O. Wellnitz, E.T. Arnold and R.M. BruckmaierJournal of Dairy Science 94 (11) 5405 (2011)
https://doi.org/10.3168/jds.2010-3931
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
Staphylococcal-associated molecular patterns enhance expression of immune defense genes induced by IL-17 in mammary epithelial cells
Salim Bougarn, Patricia Cunha, Florence B. Gilbert, et al.Cytokine 56 (3) 749 (2011)
https://doi.org/10.1016/j.cyto.2011.09.020
Purified Staphylococcus aureus leukotoxin LukM/F′ does not trigger inflammation in the bovine mammary gland
Angélina Fromageau, Patricia Cunha, Florence B. Gilbert and Pascal RainardMicrobial Pathogenesis 51 (6) 396 (2011)
https://doi.org/10.1016/j.micpath.2011.09.005
Lipoteichoic acid from Staphylococcus aureus exacerbates respiratory disease in porcine respiratory coronavirus-infected pigs
Kalina Atanasova, Steven Van Gucht, Filip Barbé, Luc Duchateau and Kristien Van ReethThe Veterinary Journal 188 (2) 210 (2011)
https://doi.org/10.1016/j.tvjl.2010.03.001
The bovine milk proteome: cherishing, nourishing and fostering molecular complexity. An interactomics and functional overview
Angelo D'Alessandro, Lello Zolla and Andrea ScaloniMol. BioSyst. 7 (3) 579 (2011)
https://doi.org/10.1039/C0MB00027B
Cattle and chemokines: evidence for species‐specific evolution of the bovine chemokine system
S. Widdison and T. J. CoffeyAnimal Genetics 42 (4) 341 (2011)
https://doi.org/10.1111/j.1365-2052.2011.02200.x
The bovine milk proteome: cherishing, nourishing and fostering molecular complexity. An interactomics and functional overview
Angelo D'Alessandro, Lello Zolla and Andrea ScaloniMol. BioSyst. 7 (3) 579 (2011)
https://doi.org/10.1039/c0mb00027b
Binding of the Staphylococcus aureus leucotoxin LukM to its leucocyte targets
Angélina Fromageau, Florence B. Gilbert, Gilles Prévost and Pascal RainardMicrobial Pathogenesis 49 (6) 354 (2010)
https://doi.org/10.1016/j.micpath.2010.07.002
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
Expression of bovine granulocyte chemotactic protein-2 (GCP-2) in neutrophils and a mammary epithelial cell line (MAC-T) in response to various bacterial cell wall components
Chi Yu, Zhao-Ru Shi, Chun-Yen Chu, et al.The Veterinary Journal 186 (1) 89 (2010)
https://doi.org/10.1016/j.tvjl.2009.07.012
Muramyl Dipeptide Synergizes with Staphylococcus aureus Lipoteichoic Acid To Recruit Neutrophils in the Mammary Gland and To Stimulate Mammary Epithelial Cells
Salim Bougarn, Patricia Cunha, Abdallah Harmache, et al.Clinical and Vaccine Immunology 17 (11) 1797 (2010)
https://doi.org/10.1128/CVI.00268-10