SUMMARY. A group of faecal isolates of Proteus vulgaris and P. mirabilis was studied for the presence of possible virulence factors such as growth rates in urine and broth, haemolysin production, hydrophobicity, sensitivity to the bactericidal activity of human serum and cell invasiveness. Differences were found in haemolysin production, cell invasiveness and experimental virulence in a mouse model. These differences might explain why P. mirabilis is much more common in human urinary-tract infections than P. vulgaris.
INTRODUCTIONProteus vulgaris and P. mirabilis are common inhabitants of the human gut; Krikler (1953) reported prevalences of 17% for P. mirabilis and 5% for P. vulgaris in the faeces of healthy persons. Urinary pathogens are thought to originate mainly from the gut and it is interesting that P. mirabilis is disproportionately more frequently isolated from patients with urinary-tract infections than P. vulgaris. Senior (1 979), for example, isolated 258 strains of P. mirabilis from infected urines against only four strains of P. vulgaris, two of which were isolated together with P. mirabilis. These epidemiological data suggest that P. mirabilis is more likely to cause urinary-tract infections than P. vulgaris. As both species are very similar, genetically and biochemically (Brenner et al., 1978), a comparative study of isolates of both species could yield valuable information about bacterial properties important in the pathogenesis of urinary-tract infections. Therefore, we have compared faecal isolates of both species, isolated from the same population, with regard to several properties: experimental virulence in a mouse model, growth rates in urine and broth, haemolysin production, hydrophobicity, sensitivity to the bactericidal activity of human serum, cell invasiveness and serotype.
MATERIALS AND METHODSIsolation of Proteus strains from faeces. Stool samples were obtained from patients seen in general practice. Most samples had been submitted for examination for occult blood or for suspected parasitic infestation. A suspension of the sample in phosphate-buffered saline (PBS) was inoculated in the centre of a fresh nutrient-agar plate (Oxoid). The plates were incubated for ~ ~