“…Strains of legionellae were cultured on buffered charcoal yeast extract agar [19] at 30" or 37°C in a moist chamber or, in the case of legionella-like amoebal pathogens (LLAPs), their amoebal host [16, 17, 201. Non-type strains of legionellae used in this study were divided into two sets: dataset I (52 strains) comprising well characterised strains and dataset I1 (46 strains) comprising recent clinical and environmental isolates. Strains assigned to dataset I were available either from type culture collections (NCTC or ATCC), or had been the subject of phylogenetic studies, such as 16s rRNA (gene) sequence analysis [16,17,20,21], DNA restriction fragment length polymorphism (RFLP) analysis [ l l ] , or DNA:DNA homology [18]; the identity of these strains was taken to be 'true'. Strains assigned to dataset I1 were identified in the RSIL by standard phenotypic techniques, including growth requirements, biochemical characteristics and serological tests with hyperimmune rabbit antisera [6, 71, or genotypic RFLP analysis [ l l ] .…”