Streptococcal beta protein has separate binding sites for human factor H and IgA-Fc

J Biol Chem. 2002 Apr 12;277(15):12642-8. doi: 10.1074/jbc.M112072200. Epub 2002 Jan 25.

Abstract

The group B streptococcus (GBS) is the most important cause of life-threatening bacterial infections in newborn infants. Protective immunity to GBS infection is elicited by several surface proteins, one of which, the beta protein, is known to bind human IgA-Fc. Here, we show that the beta protein also binds human factor H (FH), a negative regulator of complement activation. Absorption experiments with whole human plasma demonstrated binding of FH to a GBS strain expressing beta protein but not to an isogenic beta-negative mutant. This binding was due to a direct interaction between beta and FH, as shown by experiments with purified proteins. Inhibition tests and studies with beta fragments demonstrated that FH and IgA-Fc bind to separate and nonoverlapping regions in beta. Heparin, a known ligand for FH, specifically inhibited the binding between beta and FH, suggesting that FH has overlapping binding sites for beta and heparin. Bacteria-bound FH retained its complement regulatory activity, implying that beta-expressing GBS may use bound FH to evade complement attack. The finding that beta protein binds FH adds to a growing list of interactions between human pathogens and complement regulatory proteins, supporting the notion that these interactions are of general importance in bacterial pathogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / blood
  • Antigens, CD / metabolism*
  • Bacterial Proteins / metabolism*
  • Base Sequence
  • Binding Sites
  • Complement Factor H / metabolism*
  • DNA Primers
  • Humans
  • Receptors, Fc / blood
  • Receptors, Fc / metabolism*
  • Streptococcus / metabolism*

Substances

  • Antigens, CD
  • Bacterial Proteins
  • CFH protein, human
  • DNA Primers
  • Fc(alpha) receptor
  • Receptors, Fc
  • Complement Factor H