Literature DB >> 27016756

Disruption of the sigS gene attenuates the local innate immune response to Staphylococcus aureus in a mouse mastitis model.

Vincent Peton1, Koen Breyne2, Lucie Rault1, Kristel Demeyere2, Nadia Berkova1, Evelyne Meyer2, Sergine Even1, Yves Le Loir3.   

Abstract

Staphylococcus aureus (S. aureus) is a major pathogen involved in ruminant mastitis and present worldwide. Clinical signs of S. aureus mastitis vary considerably and are largely dependent on strain-specific factors. A comparison of two S. aureus strains that reproducibly induced either severe (O11) or mild (O46) mastitis in ewes revealed that the transcriptional regulator sigS was mutated in O46 (Le Maréchal et al., 2011. PLoS One. 6 (11) e27354. doi:10.1371/journal.pone.0027354). In the present paper, we analysed the sigS sequence in 18 other S. aureus strains isolated from goat or ewe mastitis and found a 4-bp deletion similar to that of the O46 sigS gene in three strains associated with subclinical ewe mastitis. This sigS gene was disrupted in strain O11 (O11ΔsigS), so our aim was to investigate its involvement in the severity of infections in the context of mastitis. The wild type (wt) and mutant strains were then characterized in vitro to determine the involvement of sigS in the response S. aureus under various stress conditions, and assess its influence on the cytotoxicity of the pathogen, its invasive capacity and biofilm formation. The strains were compared in vivo in an experimental mouse mastitis model in which clinical signs and cytokine production were evaluated at 24h post-infection. While no significant differences in the effect on bacterial growth between O11 and O11ΔsigS were observed either in vitro or in vivo, a significantly weaker in vivo production of interleukin (IL)-1α, IL-1β, and Tumor Necrosis Factor (TNF)-α was measured in the mammary glands infected with the mutant strain, suggesting that infection with O11ΔsigS induced an attenuated local innate immune response. These results suggest an impact of sigS disruption on S. aureus pathogenesis in a ruminant mastitis context. This disruption is probably involved in, and may partly explain, the milder symptoms previously observed in S. aureus O46-induced mastitis in ewes.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Inflammatory response; Mastitis; Mouse model; Staphylococcus aureus; Transcriptional regulator; Virulence; σ factor

Mesh:

Substances:

Year:  2016        PMID: 27016756     DOI: 10.1016/j.vetmic.2016.02.014

Source DB:  PubMed          Journal:  Vet Microbiol        ISSN: 0378-1135            Impact factor:   3.293


  4 in total

1.  Identification of a unique transcriptional architecture for the sigS operon in Staphylococcus aureus.

Authors:  Halie K Miller; Whittney N Burda; Ronan K Carroll; Lindsey N Shaw
Journal:  FEMS Microbiol Lett       Date:  2018-06-01       Impact factor: 2.742

2.  Preconditioning with Lipopolysaccharide or Lipoteichoic Acid Protects against Staphylococcus aureus Mammary Infection in Mice.

Authors:  Koen Breyne; Jonas Steenbrugge; Kristel Demeyere; Tom Vanden Berghe; Evelyne Meyer
Journal:  Front Immunol       Date:  2017-07-24       Impact factor: 7.561

3.  Anti-inflammatory signaling by mammary tumor cells mediates prometastatic macrophage polarization in an innovative intraductal mouse model for triple-negative breast cancer.

Authors:  Jonas Steenbrugge; Koen Breyne; Kristel Demeyere; Olivier De Wever; Niek N Sanders; Wim Van Den Broeck; Cecile Colpaert; Peter Vermeulen; Steven Van Laere; Evelyne Meyer
Journal:  J Exp Clin Cancer Res       Date:  2018-08-15

4.  Staphylococcus aureus Extracellular Vesicles Elicit an Immunostimulatory Response in vivo on the Murine Mammary Gland.

Authors:  Natayme R Tartaglia; Koen Breyne; Evelyne Meyer; Chantal Cauty; Julien Jardin; Denis Chrétien; Aurélien Dupont; Kristel Demeyere; Nadia Berkova; Vasco Azevedo; Eric Guédon; Yves Le Loir
Journal:  Front Cell Infect Microbiol       Date:  2018-08-22       Impact factor: 5.293

  4 in total

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