SUMMARYRestriction enzyme fingerprints were generated from purified plasmid DNA from 324 clinical isolates that belonged to 7 enterobacterial genera and 88 single plasmids in Escherichia coli K 12 according to the following strategy.Purified plasmid DNA was digested with PstI. The number of fragments detected in a 0-8 agarose gel was used to determine which 2 of 6 restriction enzymes including PstI was most likely to provide a fingerprint comprising sufficient fragments to ensure specificity but sufficiently few to allow easy visual assessment and minimize coincidental matching. When Pst I produced > 20 fragments, Eco RI and Hind III were used; when PstI generated < 6 fragments Bsp 1286 and AvaII were used and SmaI was employed when between 6 and 20 fragments were obtained from PstI digests. Using a minimum of 12 fragments from a combination of 2 enzymes as the criterion for characterizing a strain/plasmid, satisfactory 2-enzyme fingerprints were obtained from 87 % of the strains and plasmids studied using Pst I and no more than two additional enzymes per strain. Of the remaining 54 strains, 51 harboured only small plasmids (< 10 kb) and 3 produced satisfactory fingerprints when digested with a fourth enzyme.

Summary. Two hundred and eighty-seven coliform bacteria were isolated from 1 16 rectal swabs or faecal specimens obtained from 113 patients. By means of plasmid analysis and resistance transfer (R-transfer) Escherichia coli was found to differ from other enteric genera in plasmid distribution. Criteria were proposed that enabled invivo "R-transfer potential" and in-vivo "R-transfer rate" to be calculated. From each of 22 of the 1 13 patients numerous coliforms were isolated, of which at least one per patient contained one or more self-transmissible R-plasmids potentially transferable to 43 other coliforms. Evidence indicated that R-plasmid transfer had occurred in vivo on two of the 43 potential occasions. These results are discussed in the context of plasmid ecology in the human host.

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