Literature DB >> 19727872

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

Manuela Rinaldi1, Robert W Li, Douglas D Bannerman, Kristy M Daniels, Christina Evock-Clover, Marcos V B Silva, Max J Paape, Bernadette Van Ryssen, Christian Burvenich, Anthony V Capuco.   

Abstract

Escherichia coli intramammary infection elicits localized and systemic responses, some of which have been characterized in mammary secretory tissue. Our objective was to characterize gene expression patterns that become activated in different regions of the mammary gland during the acute phase of experimentally induced E. coli mastitis. Tissues evaluated were from Fürstenburg's rosette, teat cistern (TC), gland cistern (GC), and lobulo-alveolar (LA) regions of control and infected mammary glands, 12 and 24 h after bacterial (or control) infusions. The main networks activated by E. coli infection pertained to immune and inflammatory response, with marked induction of genes encoding proteins that function in chemotaxis and leukocyte activation and signaling. Genomic response at 12 h post-infection was greatest in tissues of the TC and GC. Only at 24 h post-infection did tissue from the LA region respond, at which time the response was the greatest of all regions. Similar genetic networks were impacted in all regions during early phases of intramammary infection, although regional differences throughout the gland were noted. Data support an important sentinel function for the teat, as these tissues responded rapidly and intensely, with production of cytokines and antimicrobial peptides.

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Year:  2009        PMID: 19727872     DOI: 10.1007/s10142-009-0133-z

Source DB:  PubMed          Journal:  Funct Integr Genomics        ISSN: 1438-793X            Impact factor:   3.410


  59 in total

Review 1.  Evolution and integration of innate immune recognition systems: the Toll-like receptors.

Authors:  Kiyoshi Takeda
Journal:  J Endotoxin Res       Date:  2005

Review 2.  Innate immunity of the bovine mammary gland.

Authors:  Pascal Rainard; Céline Riollet
Journal:  Vet Res       Date:  2006-02-23       Impact factor: 3.683

3.  Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells.

Authors:  Ylva Strandberg; Christian Gray; Tony Vuocolo; Laurelea Donaldson; Mary Broadway; Ross Tellam
Journal:  Cytokine       Date:  2005-07-07       Impact factor: 3.861

4.  Short communication: Cellular localization of haptoglobin mRNA in the experimentally infected bovine mammary gland.

Authors:  M A Thielen; M Mielenz; S Hiss; H Zerbe; W Petzl; H-J Schuberth; H-M Seyfert; H Sauerwein
Journal:  J Dairy Sci       Date:  2007-03       Impact factor: 4.034

5.  Determination of milk and blood concentrations of lipopolysaccharide-binding protein in cows with naturally acquired subclinical and clinical mastitis.

Authors:  R Zeng; B J Bequette; B T Vinyard; D D Bannerman
Journal:  J Dairy Sci       Date:  2009-03       Impact factor: 4.034

Review 6.  Nitric oxide and oxygen radicals in infection, inflammation, and cancer.

Authors:  H Maeda; T Akaike
Journal:  Biochemistry (Mosc)       Date:  1998-07       Impact factor: 2.487

Review 7.  Severity of E. coli mastitis is mainly determined by cow factors.

Authors:  Christian Burvenich; Valérie Van Merris; Jalil Mehrzad; Araceli Diez-Fraile; Luc Duchateau
Journal:  Vet Res       Date:  2003 Sep-Oct       Impact factor: 3.683

8.  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.

Authors:  K M Swanson; K Stelwagen; J Dobson; H V Henderson; S R Davis; V C Farr; K Singh
Journal:  J Dairy Sci       Date:  2009-01       Impact factor: 4.034

Review 9.  Cumulative physiological events influence the inflammatory response of the bovine udder to Escherichia coli infections during the transition period.

Authors:  C Burvenich; D D Bannerman; J D Lippolis; L Peelman; B J Nonnecke; M E Kehrli; M J Paape
Journal:  J Dairy Sci       Date:  2007-06       Impact factor: 4.034

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

Authors:  Wei Yang; Holm Zerbe; Wolfram Petzl; Ronald Marco Brunner; Juliane Günther; Christian Draing; Sonja von Aulock; Hans-Joachim Schuberth; Hans-Martin Seyfert
Journal:  Mol Immunol       Date:  2007-10-22       Impact factor: 4.407

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  18 in total

Review 1.  Immunopathology of mastitis: insights into disease recognition and resolution.

Authors:  Stacey L Aitken; Christine M Corl; Lorraine M Sordillo
Journal:  J Mammary Gland Biol Neoplasia       Date:  2011-09-22       Impact factor: 2.673

2.  Advances in genome studies: The PAG 2010 conference.

Authors:  R Appels; R Barrerro; G Keeble; M Bellgard
Journal:  Funct Integr Genomics       Date:  2010-03       Impact factor: 3.410

Review 3.  Functional adaptations of the transcriptome to mastitis-causing pathogens: the mammary gland and beyond.

Authors:  Juan J Loor; Kasey M Moyes; Massimo Bionaz
Journal:  J Mammary Gland Biol Neoplasia       Date:  2011-10-04       Impact factor: 2.673

4.  HDAC1/2-mediated regulation of JNK and ERK phosphorylation in bovine mammary epithelial cells in response to TNF-α.

Authors:  Samantha S Romanick; Kristen Morrill; Andrew Hostler; Levi W Evans; Yiqiu Shen; Allison Matsumura; Haleigh Piotrowski; Lorrayny G Silva; Antonio P Faciola; Bradley S Ferguson
Journal:  J Cell Physiol       Date:  2018-09-10       Impact factor: 6.384

5.  In depth analysis of genes and pathways of the mammary gland involved in the pathogenesis of bovine Escherichia coli-mastitis.

Authors:  Bart Buitenhuis; Christine M Røntved; Stefan M Edwards; Klaus L Ingvartsen; Peter Sørensen
Journal:  BMC Genomics       Date:  2011-02-28       Impact factor: 3.969

Review 6.  The Immunology of Mammary Gland of Dairy Ruminants between Healthy and Inflammatory Conditions.

Authors:  Mohamed Ezzat Alnakip; Marcos Quintela-Baluja; Karola Böhme; Inmaculada Fernández-No; Sonia Caamaño-Antelo; Pillar Calo-Mata; Jorge Barros-Velázquez
Journal:  J Vet Med       Date:  2014-11-10

7.  Antigen-Specific Mammary Inflammation Depends on the Production of IL-17A and IFN-γ by Bovine CD4+ T Lymphocytes.

Authors:  Pascal Rainard; Patricia Cunha; Marion Ledresseur; Christophe Staub; Jean-Luc Touzé; Florent Kempf; Florence B Gilbert; Gilles Foucras
Journal:  PLoS One       Date:  2015-09-16       Impact factor: 3.240

8.  Escherichia coli- and Staphylococcus aureus-induced mastitis differentially modulate transcriptional responses in neighbouring uninfected bovine mammary gland quarters.

Authors:  Kirsty Jensen; Juliane Günther; Richard Talbot; Wolfram Petzl; Holm Zerbe; Hans-Joachim Schuberth; Hans-Martin Seyfert; Elizabeth J Glass
Journal:  BMC Genomics       Date:  2013-01-16       Impact factor: 3.969

9.  Keratin and S100 calcium-binding proteins are major constituents of the bovine teat canal lining.

Authors:  Grant A Smolenski; Ray T Cursons; Brad C Hine; Thomas T Wheeler
Journal:  Vet Res       Date:  2015-09-25       Impact factor: 3.683

10.  Non-classical proIL-1beta activation during mammary gland infection is pathogen-dependent but caspase-1 independent.

Authors:  Koen Breyne; Steven K Cool; Dieter Demon; Kristel Demeyere; Tom Vandenberghe; Peter Vandenabeele; Harald Carlsen; Wim Van Den Broeck; Niek N Sanders; Evelyne Meyer
Journal:  PLoS One       Date:  2014-08-27       Impact factor: 3.240

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