Genetic relatedness of selected clinical Vibrio cholerae O139 isolates from the southern coastal area of China over a 20-year period

Epidemiol Infect. 2016 Sep;144(12):2679-87. doi: 10.1017/S0950268816001059. Epub 2016 Jun 16.

Abstract

Vibrio cholerae O139 emerged as a causative agent of epidemic cholera in 1992 in India and Bangladesh, and was subsequently reported in China in 1993. The genetic relatedness and molecular characteristics of V. cholerae O139 in Guangdong Province, located in the southern coastal area of China, remains undetermined. In this study, we investigated 136 clinical V. cholerae O139 isolates from 1993 to 2013 in Guangdong. By conventional PCR, 123 (90·4%) isolates were positive for ctxB, ace and zot. Sequencing of the positive amplicons indicated 113 (91·7%) isolates possessed the El Tor allele of ctxB (genotype 3); seven carried the classical ctxB type (genotype 1) and three harboured a novel ctxB type (genotype 5). With respect to tcpA, 123 (90·4%) isolates were positive for the El Tor allele. In addition, pulsed-field gel electrophoresis (with NotI digestion) differentiated the isolates into clusters A and B. Cluster A contained seven of the non-toxigenic isolates from 1998 to 2000; another six non-toxigenic isolates (from 1998 and 2007) and all of the toxigenic isolates formed cluster B. Our results suggest that over a 20-year period, the predominant O139 clinical isolates have maintained a relatively tight clonal structure, although some genetic variance and shift has occurred. Our data highlight the persistence of toxigenic V. cholerae O139 in clinical settings in the southern coastal area of China.

Keywords: Bacterial typing; Vibrio cholerae; clinical microbiology; epidemics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • China / epidemiology
  • Cholera / epidemiology*
  • Cholera / microbiology
  • Cholera Toxin / chemistry
  • Cholera Toxin / genetics*
  • Cholera Toxin / metabolism
  • Electrophoresis, Gel, Pulsed-Field
  • Genetic Variation*
  • Genotype
  • Phylogeny
  • Polymerase Chain Reaction
  • Sequence Alignment
  • Vibrio cholerae O139 / genetics*

Substances

  • Cholera Toxin