Literature DB >> 12628544

Staphylococcus aureus strains isolated from bovine mastitis: virulence, antibody production and protection from challenge in a mouse model.

G Leitner1, O Krifucks, A Glickman, A Younis, A Saran.   

Abstract

Septic arthritis in mice was used as a model to evaluate the virulence of Staphylococcus aureus and coagulase-negative staphylococci (CNS) isolated from cases of bovine mastitis. In addition, the model was used to evaluate the cross protection elicited by heterologous antibodies. Mice were intramuscularly inoculated with serial bacterial doses of different strains of S. aureus or CNS, for virulence determination; they were monitored for arthritis, gangrene or death up to 20 days. Antibody response, cross reactivity and resistance to challenge were tested by subcutaneous inoculation with a low dose of one of the S. aureus or CNS strains followed by challenge with two S. aureus strains. S. aureus alpha-hemolysin isolate was the most virulent, followed by alpha+beta-hemolysin and beta-hemolysin isolates. The least virulent isolates were the non-hemolytic S. aureus strains but even they were more virulent than the CNS strains tested. Antibodies against three different S. aureus antigens were detected by the ELISA in all mice that were inoculated with the S. aureus strains but not in any of those with the CNS strains. Immunoblot test against various S. aureus strains as antigens showed high cross-reactivity among the S. aureus strains but only a slight similarity, restricted to the bands above 36 kDa, with the CNS sera. Low-dose inoculation of alpha or alpha+beta strains before challenge with homologous and heterologous strains protected the mice, whereas the two beta strains provided only partial protection. The inoculations of non-hemolytic S. aureus or the CNS strains did not elicit any protection. Our findings demonstrate that pre-exposure of mice to a low dose of certain S. aureus strains could provide protection and that the antibodies produced could have an important protective role.

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Year:  2003        PMID: 12628544     DOI: 10.1016/S0928-8244(02)00458-3

Source DB:  PubMed          Journal:  FEMS Immunol Med Microbiol        ISSN: 0928-8244


  5 in total

1.  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

2.  Use of 5-Enolpyruvylshikmate-3-Phosphate Synthase Encoding Gene for Typing of Staphylococcus aureus Isolated from Skin and Urinary Tract Infections of Human.

Authors:  Reza Talebi-Satlou; Malahat Ahmadi; Farokh Ghavam; Habib Dastmalchi Saei
Journal:  Iran J Basic Med Sci       Date:  2012-07       Impact factor: 2.699

3.  Molecular correlates of host specialization in Staphylococcus aureus.

Authors:  Lisa Herron-Olson; J Ross Fitzgerald; James M Musser; Vivek Kapur
Journal:  PLoS One       Date:  2007-10-31       Impact factor: 3.240

4.  Mastitis Pathogens with High Virulence in a Mouse Model Produce a Distinct Cytokine Profile In Vivo.

Authors:  Carl-Fredrik Johnzon; Karin Artursson; Robert Söderlund; Bengt Guss; Elin Rönnberg; Gunnar Pejler
Journal:  Front Immunol       Date:  2016-09-22       Impact factor: 7.561

5.  Pathological Changes in Experimental Intramammary Infection with Different Staphylococcus Species in Mice.

Authors:  P Krishnamoorthy; M L Satyanarayana; B R Shome; H Rahman
Journal:  J Microsc Ultrastruct       Date:  2018 Apr-Jun
  5 in total

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