Answers are grounded in this paper and cite their sources.
Summary Cell walls from “mouse-virulent” strains of Staphylococcus aureus were found to have “aggressin” activity; the addition of isolated cell walls to a dose of staphylococci that was too low to produce any lesion on subcutaneous injection alone led to the formation of a large necro-purulent lesion. Cell walls from “mouse non-virulent” strains did not enhance lesion production in this way. A method of isolating the lesion-enhancing material from the cell walls of mouse-virulent strains is described. This material consists mainly of mucopeptide with some protein but no teichoic acid. It is resistant to heating at 100°C for 10 min., to tryptic digestion, and to treatment with periodate or formaldehyde, but is rendered soluble and subsequently destroyed by lysozyme. The lesion-enhancing material, when injected subcutaneously into mice on a plug of cotton dust, inhibits the accumulation of oedema fluid at the site of injection. The corresponding cell-wall fraction isolated from mouse non-virulent strains not only failed to inhibit but even stimulated the exudation of oedema fluid.
No takes yet. Share an insight, caveat, or question.
M. J. Hill (1968) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: