Journal of Clinical Microbiology, March 2001, p. 1190-1194, Vol. 39, No. 3
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.3.1190-1194.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Department of Microbiology, The University of Hong Kong, University Pathology Building, Queen Mary Hospital,1 and HKU-Pasteur Research Centre,2 Hong Kong, Republic of China
Received 17 October 2000/Returned for modification 12 December 2000/Accepted 8 January 2001
We report the isolation and characterization of a member of the
family Enterobacteriaceae isolated from the gallbladder pus of a food handler. Conventional biochemical tests suggested
Salmonella enterica serotype Typhi, but the isolate
agglutinated with poly(O), 2O, 9O, and Vi Salmonella
antisera but not with poly(H) or any individual H
Salmonella antisera. 16S rRNA gene sequencing showed that
there were two base differences between the isolate and
Salmonella enterica serotype Montevideo, four base
differences between the isolate and serotype Typhi, five base
differences between the isolate and Salmonella enterica
serotype Typhimurium, and six base differences between the isolate and
Salmonella enterica serotype Dublin, indicating that the
isolate was a strain of S. enterica. Electron microscopy
confirmed that the isolate was aflagellated. The flagellin gene
sequence of the isolate was 100% identical to that of the H1-d
flagellin gene of serotype Typhi. Sequencing of the rfbE
gene, which encoded the CDP-tyvelose epimerase of the isolate, showed
that there was a point mutation at position +694 (G
T), leading to an
amino acid substitution (Gly
Cys). This may have resulted in a
protein of reduced catalytic activity and hence the presence of both 2O
and 9O antigens. We therefore concluded that the isolate was a variant
of serotype Typhi. Besides antibiotic therapy and cholecystectomy,
removal of all stones in the biliary tree was performed for
eradication of the carrier state.
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