Prevention of false positive binding during immunofluorescence of Staphylococcus aureus infected tissue biopsies

J Immunol Methods. 2012 Oct 31;384(1-2):111-7. doi: 10.1016/j.jim.2012.07.015. Epub 2012 Jul 31.

Abstract

Immunofluorescence is a fundamental tool used to analyse tissue and cell samples with a wide variety of available antibodies targeting specific proteins or molecules. Staphylococcal surface protein A is used both in clinical, research and industrial settings for its ability to bind mammalian immunoglobulin G. Spurious binding between protein A and IgG antibodies can lead to false-positive fluorescence and misleading results. Here we demonstrate this occurring in formalin-fixed patient samples that harbour Staphylococcus aureus infection, and characterise methods to overcome this issue. Specifically the use of F(ab') fragment antibodies or blocking with human IgG is shown to prevent antibody-protein A interaction in formalin-fixed S. aureus smears, biopsies obtained from infected patients, and experimentally infected tissue samples.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • Epithelium / immunology
  • Epithelium / metabolism
  • Epithelium / pathology
  • False Positive Reactions
  • Fluorescent Antibody Technique, Indirect / methods*
  • Formaldehyde
  • Humans
  • Immunoglobulin Fab Fragments / immunology
  • Immunoglobulin Fab Fragments / metabolism
  • Immunoglobulin G / immunology*
  • Immunoglobulin G / metabolism
  • Protein Binding / immunology
  • Reproducibility of Results
  • Staphylococcal Infections / immunology*
  • Staphylococcal Infections / metabolism
  • Staphylococcal Infections / pathology
  • Staphylococcal Protein A / immunology*
  • Staphylococcal Protein A / metabolism
  • Staphylococcus aureus / immunology*
  • Staphylococcus aureus / metabolism
  • Tissue Fixation

Substances

  • Immunoglobulin Fab Fragments
  • Immunoglobulin G
  • Staphylococcal Protein A
  • Formaldehyde