Molecular Epidemiology of Newly Emerged V. cholerae O139 in Taiwan
CHEIN-SHENG LIN1, TIEN-KWEI WANG1, CHIH-LUNG LEE1*, TZU-MING PAN2, JIN-LAI TSAI1, SU-ING HO1 AND CHENG-HSIUNG LU1
1. Bacteriology Division, Center of Disease Control, Department of Health, Executive Yuan, 161, Kuen Yang Street, NanKang 115, Taipei, Taiwan, R.O.C.
2. Department of Agricultural Chemistry, National Taiwan University, DaAn 106, Taipei, Taiwan, R.O.C.
(Received: January 30, 2001; Accepted: July 9, 2001)
ABSTRACT
A Vibrio cholerae O139 strain was isolated from a cholera patient in August 1997 in Kaohsiung County, Taiwan. This was the first case of V. cholerae O139 emerging in Taiwan. An epidemiological study showed that the infectious source was turtle eggs. One clinical isolate and fourteen isolates from environmental specimens of the turtle farm were collected. From all isolates, the genes encoded for cholera toxin (ctxA and ctxB) and for toxin-coregulated pili genes (tcpA and tcpI) were specifically amplified by polymerase chain reactions. In pulsed-field gel electrophoresis (PFGE) studies, these isolates were categorized to five subtypes using SfiI restriction digestion; whereas three distinct subtypes were identified when NotI was used for digestion. The banding pattern of the clinical isolate in PFGE only differed by 1-3 bands from those of the environmental isolates regardless of the restriction enzyme used. The Dice coefficients were found to be in the range of 0.88-1.0 and 0.87-1.0, respectively, by using SfiI and NotI for the subtyping. When these isolates were analyzed by plasmid profile analysis, the profile pattern of the clinical strain was identical to 12 of the 14 environmental strains. Based on these results, it was concluded that the fifteen strains studied were descended from the same origin, with the clinical isolate originated from the environmental isolates. The data suggests that the molecular subtyping is a powerful tool for tracing and verifying the infectious sources of V. cholerae cases.
Key words: Vibrio cholerae O139, polymerase chain reaction, pulsed-field gel electrophoresis, plasmid profile analysis, Dice coefficient