Normal serum cytotoxicity for P32-labeled smooth Enterobacteriaceae. 3. Isolation of a gammag normal antibody and characterization of other serum factors causing P32 loss

J Bacteriol. 1966 Jan;91(1):401-8. doi: 10.1128/jb.91.1.401-408.1966.

Abstract

Spitznagel, John K. (University of North Carolina School of Medicine, Chapel Hill). Normal serum cytotoxicity for P(32)-labeled smooth Enterobacteriaceae. III. Isolation of a gammaG normal antibody and characterization of other serum factors causing P(32) loss. J. Bacteriol. 91:401-408. 1966.-Gram-negative bacteria lost metabolically incorporated P(32) when suspended in serum only if the serum contained heat-labile in addition to heat-stable factors. Gram-positive bacteria labeled with P(32) and included for comparison lost P(32) in heat-inactivated as well as in fresh normal serum. Further investigation of gram-negative bacteria showed that a smooth Escherichia coli (O117:H27) lost P(32) only if suspended in serum containing complement fractions C'1, C'2, C'3, and C'4 "normal" antibody and lysozyme. The normal antibody was recovered by absorption on and subsequent elution from E. coli O117:H27 cell walls. Immunoelectrophoresis showed that it was a gammaG-globulin. Its P(32)-releasing activity was destroyed by 2-mercaptoethanol. Lysozyme was found to potentiate the P(32)-releasing action of normal antibody plus complement. Evidence was obtained suggesting that beta(1C) globulin was the component absorbed to zymosan during serum absorption at 15 C. Reduction of the beta(1C) level evidently upsets an important balance that exists in normal serum among complement, antibody, and lysozyme. This balance is essential for maximal P(32) release from labeled bacteria, or possibly for a maximal antibacterial effect from normal serum. The possible relationships of bactericidal, bacteriolytic, and opsonic action of normal serum are discussed.

MeSH terms

  • Animals
  • Bacteriolysis
  • Blood Bactericidal Activity
  • Blood*
  • Complement System Proteins
  • Escherichia coli / metabolism*
  • Guinea Pigs
  • Immunity*
  • Immunoelectrophoresis
  • In Vitro Techniques
  • Mercaptoethanol / pharmacology
  • Muramidase*
  • Opsonin Proteins
  • Phosphorus / metabolism*
  • Phosphorus Isotopes
  • gamma-Globulins*

Substances

  • Opsonin Proteins
  • Phosphorus Isotopes
  • gamma-Globulins
  • Phosphorus
  • Mercaptoethanol
  • Complement System Proteins
  • Muramidase