Process and materials for the rapid detection of streptococcus pneumoniae employing purified antigen-specific antibodies
Disclosed is a cell wall C-polysaccharide antigen of Streptococcus pneumoniae which contains not more than 10% by weight of protein, and preferably less which has been purified with 0.1N NaOH prior to deproteinizing. Also disclosed are polyvalent antibodies raised against Streptococcus pneumoniae which have been affinity purified by passing them over a chromatographic affinity matrix to which is coupled the purified and at least partially deproteinized antigen to render them antigen-specific.
1 . A cell wall C-polysaccharide antigen of Streptococcus pneumoniae which contains not more than 10% by weight of protein which has been obtained by
a) subjecting a culture of S. pneumoniae to a treatment which kills the bacterial cells,
b) separating the killed bacteria cells as a cell pellet of weakly alkaline pH in the order of from about 7.0 to 7.4,
c) subjecting the pellet of step (b) to incubation with a sufficient quantity of 0.1 N NaOH to elevate its pH to a value in excess of 12.0 for a period of at least 45 minutes,
d) deproteinizing the mixture, and
e) separating out a purified cell wall C-polysaccharide antigen containing not more than about 10% by weight of protein.
2 . A cell wall C-polysaccharide antigen of Streptococcus pneumoniae according to claim 1 containing from 5 to 8% by weight of protein wherein the bacterial cells in step (a) were killed by a sodium azide treatment.
3 . Polyvalent antibodies raised in an animal against Streptococcus pneumoniae bacteria or their cell wall C-polysaccharide antigen which have been affinity purified and thereby rendered antigen specific by passing them over a chromatographic affinity column on which the affinity gel is wholly comprised of a non-ion exchange material to which has been coupled the cell wall C-polysaccharide antigen of claim 1 .
4 . Polyvalent antibodies raised in an animal against Streptococcus pneumoniae bacteria or their cell wall C-polysaccharide antigen which have been affinity purified and thereby rendered antigen specific by passing them over a chromatographic affinity column on which the affinity gel is wholly comprised of a non-ion exchange material to which has been coupled the cell C-polysaccharide antigen of claim 2 .