I N comparison with the vast literature concerning group-A streptococci, our knowledge of group-F streptococci is very meagre and there is little published work concerning them. This report documents a series of 22 strains isolated from children and puerperal women during about 4 years and discusses their significance in human disease.
MATERIALS AND METHODSPrimary cultures were inoculated on horse-blood agar (BBL Columbia Base; Becton, Dickinson and Co., Canada, Ltd, Mississauga, Ontario) and incubated at 37°C under aerobic and anaerobic conditions for up to 48 h. Haemolytic colonies were examined microscopically and Gram-positive cocci were inoculated into Todd-Hewitt Broth (BBL). These cultures were incubated at 37°C overnight and used for preparing antigen by the method of Rantz and Randall (1955). Lancefield groups were determined by the microprecipitin technique (Lancefield, 1938) with grouping sera purchased from Burroughs Wellcome Ltd, Beckenham, Kent.Sensitivity to bacitracin (Maxted, 1953) was tested with standard bacitracin disks (BBL Tax0 A) and Columbia horse-blood agar. Some strains were inoculated on to aesculin-bileagar slopes (Difco Aesculin Bile Agar, Difco Laboratories, Detroit, USA) or aesculin-agar slopes.
RESULTSDuring the period 1971-74 inclusive, some 3500 strains of haemolytic streptococci were subjected to Lancefield grouping. Of these, 22 strains isolated from 22 different patients belonged to Lancefield's group F. Eight of the strains were from peritoneal-cavity swabs taken at operation, in seven for acute appendicitis and in one for ruptured jejunum; five strains were from the vagina of puerperal women; two isolates were from urine, and one from the perineum of one of these patients was presumably related to the infection of the urine. One strain came from an abscess in the neck of a patient who had a history of dental infection, one from an ear swab from a child with cerebrospinal fluid (CSF) leaking from the ear, and one from a maxillary sinus.All group-F organisms were isolated from mixed cultures and since they were selected for further study because they were haemolytic on horse-blood agar, non-haemolytic strains would not have been recognised. Eight strains were quite fastidious anaerobes, two were microaerophilic, and 12 grew readily and were easily recognised on aerobic culture.Colonial morphology was variable. Nine of the strains grew very slowly, producing the classically described pinpoint colonies and attracting attention because of their haemolysis (Long and Bliss, 1934) but 13 strains produced colonies that were easily visible after overnight incubation. One strain was isolated repeatedly in pure culture from the urine and perineum of a patient who had undergone a renal transplant. Several strains, including this one, grew so slowly in Todd-Hewitt broth that incubation for 5-7 days was required before growth was adequate for the production of grouping antigen. All strains gave clear precipitin