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Localization of a biologically important epitope on toxic-shock-syndrome toxin-1

  • Brian G. Murphy
  • , Barry N. Kreiswirth
  • , Richard P. Novick
  • , Patrick M. Schlievert
  • , Patrick M. Schlievert
  • University of Minnesota Twin Cities
  • City University of New York

Research output: Contribution to journal › Article › peer-review

6 Scopus citations

Abstract

A monoclonal antibody, designated B-14, inhibits the nonspecific T lymphocyte mitoge- nicity of toxic-shock-syndrome toxin-1 (TSST-1), and the antibody binds to an internal cyanogen bromide (CNBr) fragment (Mr, 14 000) of the toxin. The epitope recognized by B-14 was further localized to include a decapeptide at the NH2-terminus of the CNBr fragment. The decapeptide inhibited the ELISA and western blot reactivity of B-14 with TSST-1, although it was -10 000-fold less effective than the native toxin. The peptide also inhibited the capacity of B-14 to block TSST-l-induced mitogenicity. A conjugate, consisting of decapeptide4-ovalbumin, was used to hyperimmunize three rabbits. Serum from these rabbits reacted specifically with intact TSST-1 in ELISA and western blots and partially neutralized toxin mitogenicity; however, the serum did not prevent fever and enhancement of susceptibility to endotoxin shock typically seen in rabbits after administration of TSST-1.

Original languageEnglish
Pages (from-to)549-555
Number of pages7
JournalJournal of Infectious Diseases
Volume158
Issue number3
DOIs
StatePublished - Sep 1988

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