Abstract

SUMMARYThe effects of various environmental conditions on the viability and growth of normal Escherichia coli and Staphylococcus aureus cells, and of cells of these species which had been damaged by exposure to phenol, o‐cresol and p‐chloro‐m‐cresol, have been examined.With normal cells none of the conditions tried had any effect on the initial counts, but sometimes, more often with Staph. aureus, the bulk of growth eventually obtained in broth media was larger, especially when the medium had been made with pyridine extracted peptone, or when it had been treated with 0·1% of Norit charcoal or 0·02% of FeCl3.In contrast, damaged cells of both species were very sensitive to their environment. At room temperature, 0·1% of Norit added to tap water adsorbed more than 80% of the cells and the initial count was increased. Nevertheless the cells died thereafter. Damaged cells inoculated into broth also died, but when Norit was present both the rate and the extent of death were markedly reduced, though few cells were adsorbed. The addition of FeCl3 (0·02 or 0·03%) had no effect. At 37° damaged cells died faster than at room temperature, but the protective effect of Norit was still evident. In nephelometric studies of cultures growing in Norit treated broth the times to turbidity were shorter than those of control cultures in untreated broth, but broth treated with FeCl3 often gave longer times than the controls.In a comparison of broths prepared with peptone and/or Lab‐Lemco which had been extracted with pyridine to remove suspected toxic substances, the initial counts of treated cells were highest when only the peptone had been extracted. With media containing extracted Lab‐Lemco, or with both ingredients extracted, the counts were smaller but were still generally higher than in normal broth. The results of nephelometric studies were consonant with these findings: broths prepared with extracted ingredients generally gave shorter turbidity times than normal broth, especially with E. coli.The addition to broth of cations, especially Mg2+ (10–3 M), favoured the survival of damaged E. coli but did not influence that of Staph. aureus. But with both species, five times that concentration of Mg2+ was as effective as 0·1% of Norit, which was shown to adsorb lead, tin, copper, zinc, silver and cobalt from broth.Temperatures above 37° were unfavourable to the survival of damaged cells of both species, 44° often being completely inhibitory for Staph. aureus, but this effect was not due to traces of phenol in the inoculum. At 25° damaged E. coli recovered less well than at 30° and 37°, but damaged Staph. aureus did better at 25° and 30° than at 37°.

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