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Journal of Clinical Microbiology, September 1998, p. 2404-2407, Vol. 36, No. 9
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.

Study of the Relatedness of Isolates of Shigella flexneri and Shigella sonnei Obtained in 1986 and 1987 and in 1994 and 1995 from Hong Kong

E. T. S. Houang,1,* Y.-W. Chu,1 T.-K. Ng,2 and A. F. B. Cheng1

Department of Microbiology, Chinese University of Hong Kong, Prince of Wales Hospital,1 and Princess Margaret Hospital,2 Hong Kong

Received 17 December 1997/Returned for modification 5 May 1998/Accepted 29 May 1998

We used pulsed-field gel electrophoresis (PFGE) to study the genetic relatedness of 235 isolates of Shigella flexneri and Shigella sonnei collected in Hong Kong (97 isolates from 1986 and 1987 and 138 isolates from 1994 and 1995). Altogether, 13 gels were run with bacteriophage lambda ladder DNA (Pharmacia) as an external reference in every sixth lane, standardized reagents and methods, and isolates randomized for species and years. For quantitative illustration of the relationships within a large body of isolates, computer-generated dendrograms were used to determine the number of isolates in pulsotypes at Dice coefficients of similarity of 75% (PT75) and 50% (PT50). For S. flexneri, there was a significant difference in the distribution of isolates collected during the two periods in both PT75 and PT50, with 68% of isolates collected in 1994 and 1995 sharing a coefficient of similarity of >= 68%. For S. sonnei, a significant difference was observed in PT50 only. We also used Upholt's formula for an approximation of the fraction of nucleotide difference between isolates and Molecular Evolutionary Genetics Analysis to determine relative genetic distances. For both species, the relative genetic distances between isolates of the earlier collection period were significantly greater (P < 0.0001), i.e., they were further apart and therefore more diverse than those of the later period. We conclude that it is possible for a typical clinical laboratory to analyze a large amount of PFGE information on Shigella isolates obtained under controlled conditions. Such data analysis should enhance surveillance capabilities and give indications of further work to be done on various aspects of bacterial pathogenicity of the species.


* Corresponding author. Mailing address: Department of Microbiology, Chinese University of Hong Kong, Prince of Wales Hospital, Shatin N.T., Hong Kong. Phone: (852) 2632 3333. Fax: (852) 2647 3227. E-mail: ehouang{at}cuhk.edu.hk.


Journal of Clinical Microbiology, September 1998, p. 2404-2407, Vol. 36, No. 9
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.



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