Engineering a soluble high-affinity receptor domain that neutralizes staphylococcal enterotoxin C in rabbit models of disease

D. M. Mattis, A. R. Spaulding, O. N. Chuang-Smith, E. J. Sundberg, P. M. Schlievert, David M Kranz

Research output: Contribution to journalArticle

Abstract

Superantigens (SAgs) are a class of immunostimulatory exotoxins that activate large numbers of T cells, leading to overproduction of cytokines and subsequent inflammatory reactions and systemic toxicity. Staphylococcal enterotoxin C (SEC), a SAg secreted by Staphylococcus aureus, has been implicated in various illnesses including non-menstrual toxic shock syndrome (TSS) and necrotizing pneumonia. SEC has been shown to cause TSS illness in rabbits and the toxin contributes to lethality associated with methicillin-resistant S.aureus (MRSA) in a rabbit model of pneumonia. With the goal of reducing morbidity and mortality associated with SEC, a high-affinity variant of the extracellular variable domain of the T-cell receptor beta-chain for SEC (∼14 kDa) was generated by directed evolution using yeast display. This protein was characterized biochemically and shown to cross-react with the homologous (65% identical) SAg staphylococcal enterotoxin B (SEB). The soluble, high-affinity T-cell receptor protein neutralized SEC and SEB in vitro and also significantly reduced the bacterial burden of an SEC-positive strain of MRSA (USA400 MW2) in an infective endocarditis model. The neutralizing agent also prevented lethality due to MW2 in a necrotizing pneumonia rabbit model. These studies characterize a soluble high-affinity neutralizing agent against SEC, which is cross-reactive with SEB, and that has potential to be used intravenously with antibiotics to manage staphylococcal diseases that involve these SAgs.

Original languageEnglish (US)
Pages (from-to)133-142
Number of pages10
JournalProtein Engineering, Design and Selection
Volume26
Issue number2
DOIs
StatePublished - Feb 1 2013

Fingerprint

T-cells
Rabbits
Proteins
Superantigens
Antibiotics
Methicillin Resistance
Methicillin
Poisons
Yeast
Septic Shock
Toxicity
Display devices
Antigen Receptors, T-Cell, alpha-beta
Exotoxins
T-Cell Antigen Receptor
Endocarditis
staphylococcal enterotoxin C
Staphylococcus aureus
Pneumonia
Yeasts

Keywords

  • directed evolution
  • staphylococcal enterotoxin B (SEB)
  • staphylococcal enterotoxin C (SEC)
  • yeast display

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering
  • Biochemistry
  • Molecular Biology

Cite this

Engineering a soluble high-affinity receptor domain that neutralizes staphylococcal enterotoxin C in rabbit models of disease. / Mattis, D. M.; Spaulding, A. R.; Chuang-Smith, O. N.; Sundberg, E. J.; Schlievert, P. M.; Kranz, David M.

In: Protein Engineering, Design and Selection, Vol. 26, No. 2, 01.02.2013, p. 133-142.

Research output: Contribution to journalArticle

Mattis, D. M. ; Spaulding, A. R. ; Chuang-Smith, O. N. ; Sundberg, E. J. ; Schlievert, P. M. ; Kranz, David M. / Engineering a soluble high-affinity receptor domain that neutralizes staphylococcal enterotoxin C in rabbit models of disease. In: Protein Engineering, Design and Selection. 2013 ; Vol. 26, No. 2. pp. 133-142.
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