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Microbiology 146 (2000), 2613-2626
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Microbiology (2000), 146, 2613-2626.
© 2000 Society for General Microbiology


Systematics and Evolution

Genetic relationships between clinical and environmental Vibrio cholerae isolates based on multilocus enzyme electrophoresis

M. Farfán1, D. Miñana1, M. C. Fusté1 and J. G. Lorén1

Departament de Microbiologia i Parasitologia Sanitàries, Divisió de Ciències de la Salut, Facultat de Farmàcia, Universitat de Barcelona, Avda Joan XXIII s/n, 08028 Barcelona, Spain1

Author for correspondence: J. G. Lorén. Tel: +34 93 402 44 97. Fax: +34 93 402 18 96. e-mail: loren{at}farmacia.far.ub.es

A total of 107 isolates of Vibrio cholerae, including 29 strains belonging to serogroup O139, were studied using multilocus enzyme electrophoresis (MLEE) to determine allelic variation in 15 housekeeping enzyme loci. All loci were polymorphic and 99 electrophoretic types (ETs) were identified from the total sample. No significant clustering of isolates was detected in the dendrogram generated from a matrix of coefficients of distances with respect to serogroup, biotype or country of isolation. The mean genetic diversity of this V. cholerae population (H=0·50) was higher than reported previously. Linkage disequilibrium analysis of the MLEE data showed a clonal structure for the entire population, but not in some of the population subgroups studied. This suggests an epidemic population structure. The results showed that the O139 strains were not clustered in a unique ET, in contrast to previous MLEE studies. This higher genetic variation of the O139 serogroup is concordant with ribotyping studies. The results also confirm that the O139 and O1 ElTor isolates are genetically more closely related to each other than to all the other subpopulations of V. cholerae studied.

Keywords: MLEE, linkage disequilibrium, cholera, population genetics, electrophoretic types

Abbreviations: AFLP, amplified fragment length polymorphism; ET, electrophoretic type; MLEE, multilocus enzyme electrophoresis; RAPD, random amplified polymorphic DNA




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