Identification and characterization of a neutralizing monoclonal antibody against botulinum neurotoxin serotype F, following vaccination with active toxin

Hybridoma. 1997 Oct;16(5):447-56. doi: 10.1089/hyb.1997.16.447.

Abstract

Clostridium botulinum may produce any of seven known serotypes of neurotoxin (BoNT/A-/G), which are the most toxic bacterial proteins known. Efforts to develop a second-generation vaccine to these toxins would benefit from the isolation of hybridomas producing neutralizing monoclonal antibodies (MAbs). We hypothesized that previous efforts to isolate neutralizing MAbs against various BoNTs failed due to use of toxoided, chemically altered antigens. We employed a novel vaccination regimen employing native, active, single-chain BoNT/E (scBoNT/E). A number of the BoNT/E immunized mice were further vaccinated with lethal doses of fully active BoNT/F. MAb 7F8 consistently neutralized BoNT/F in three different assays: in vivo neutralization, passive neutralization, and neutralization of regional paralysis. There was no detectable recognition and essentially no neutralization of scBoNT/E. The epitope recognized by this MAb was denatured when treated with formalin, urea, guanidine chloride, or sodium dodecyl sulfate. Preliminary epitope mapping studies indicate that the MAb bound to a conformational epitope.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / chemistry*
  • Antibodies, Monoclonal / immunology
  • Botulinum Toxins / immunology*
  • Epitope Mapping
  • Formaldehyde / pharmacology
  • Hybridomas / metabolism
  • Immunoglobulin Heavy Chains / chemistry
  • Immunoglobulin Heavy Chains / isolation & purification
  • Immunoglobulin Light Chains / chemistry
  • Immunoglobulin Light Chains / isolation & purification
  • Mice
  • Mice, Inbred BALB C
  • Protein Denaturation
  • Vaccination

Substances

  • Antibodies, Monoclonal
  • Immunoglobulin Heavy Chains
  • Immunoglobulin Light Chains
  • Formaldehyde
  • Botulinum Toxins
  • botulinum toxin type F