Bristol Hospitals, Bristol, England, and $ Statens Seruminstitut, DK 2300 Copenhagen S., Denmark COAGULASE-NEGATIVE Micrococcaceae isolated from the skin and fur of farm and zoo animals are in general much less active against a range of lipid substrates than are coagulasenegative strains from various human sources (Alder et al., 1973). This could be attributed either to biochemical differences resulting from adaptation of similar strains to different habitats, or to type differences between the strains acquired by the two groups. To investigate this problem, strains were classified by the system of biotyping devised by Baird-Parker (1963).
MATERIALS A N D METHODSThe sources of strains and the methods of sampling are described by Alder et al. (1973).Representatives of each colonial type of catalase-positive, Gram-positive coccus obtained in primary culture were enumerated separately. Strains were again tested for coagulase production by the slide test for bound coagulase (Cadness-Graves et al., 1943) and in doubtful cases by the tube test of Gillespie (1943). They were classified by the methods described by Baird-Parker (1963), with the few minor modifications given below.The glucose oxidation-fermentation (0-F) test used to classify strains as staphylococci or micrococci was carried out in Subcommittee (1965) medium distributed in 150-mm x 13-mm tubes which were two-thirds filled with medium. The agar concentration was increased slightly to 0~3 %~ as this appeared to ensure a more certain and even inoculation of those strains that were very adherent to the wire loop. Tubes were heavily stab-inoculated to the bottom from overnight cultures on nutrient agar or blood agar, and incubated at 37°C for 7 days without a paraffin seal. Organisms that produced acid at the surface of the agar column only, or that failed to produce acid, were classified as micrococci, while those that produced acid throughout the column were classified as staphylococci.The novobiocin resistance of strains was determined by the disk-agar plate method, with 5-pg novobiocin disks (Mast). Resistance was indicated by an inhibition zone less than 17 mm in diameter (Churcher, 1968; Corse and Williams, 1968). Novobiocin-sensitive strains were provisionally regarded as staphylococci, and resistant strains as micrococci (Mitchell and Baird-Parker, 1967). If there was disagreement between the results of the glucose 0-F and novobiocin tests, the glucose 0-F test was repeated, if necessary several times, after subculturing the organism on nutrient agar containing 1% glucose. The eventual classification was decided on the result of the glucose 0-F test.Acid production from lactose, mannitol and L-arabinose was tested in Subcommittee (1965) basal medium, incorporating each carbohydrate at 1 % (w/v) final concentration.Short columns of media were stab-inoculated and incubated at 37°C for 7 days. For the phosphatase reaction, phenolphthalein diphosphate (Oxoid) was incorporated at 0.01% (w/v) final concentration in nutrient agar. A maximum of five strains ...