“…1), was shipped to the United States, preserved with 1% glutaraldehyde, and treated with antibodies specific to A. anophagefferens (19,24,27) and A. lagunensis (this study) in order to quickly identify the causative organism. As further verification, bloom water was pelleted and frozen, and a culture was established and preserved for molecular analysis as described previously by Gobler et al (15). Culture isolates were obtained by serially diluting bloom water into polystyrene cell culture plates containing GSe culture medium (21), and an antibiotic-antimycotic solution (Mediatech, Inc., Herndon, VA) was added at a 1% concentration (final concentrations of 100 IU ml Ϫ1 penicillin, 100 g ml Ϫ1 streptomycin, and 0.25 g ml Ϫ1 amphotericin B) to ensure that cultures remained free of bacteria and fungi.…”