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Journal of Clinical Microbiology, 11 1997, 2915-2917, Vol 35, No. 11
Copyright © 1997 by the American Society for Microbiology. All rights reserved.

Culture of the causative organism of donovanosis (Calymmatobacterium granulomatis) in HEp-2 cells [In Process Citation]

J Carter, S Hutton, KS Sriprakash, DJ Kemp, G Lum, J Savage and FJ Bowden
Menzies School of Health Research, Darwin, Northern Territory, Australia.

We report successful culture of Calymmatobacterium granulomatis by standard cell culture methods. Swabs were obtained from lesions in three patients with a clinical diagnosis of donovanosis. For two patients, there was histological confirmation of the disease (i.e., the presence of Donovan bodies in Giemsa-stained smears). Specimens were inoculated onto cycloheximide-treated HEp-2 cell monolayers in RPMI 1640 medium (supplemented with fetal calf serum, NaHCO3, vancomycin hydrochloride, and benzylpenicillin). At 48 h, organisms resembling Donovan bodies were identified in monolayer cultures from all three specimens. The organisms appeared as pleomorphic bacilli with characteristic bipolar staining and "safety pin" appearance. Using a PCR designed to differentiate C. granulomatis from the Klebsiella species (which have a high degree of molecular homology), we were able to demonstrate that the cultured organisms produced a PCR product identical to that obtained from the original swab specimens. It is now possible to test in vitro susceptibility of C. granulomatis to antibiotics and to provide a ready source of DNA and antigenic material to enable the development of serological tests and, possibly in the future, a vaccine.

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