Analysis of 16S-23S rRNA gene internal transcribed spacer of Vibrio anguillarum and Vibrio ordalii strains isolated from fish

Fernandez, J; Avendano-Herrera, R

Abstract

The 16S-23S rRNA intergenic spacer (ITS) of Vibrio anguillarum and Vibrio ordalii were PCR amplified and cloned with TA vector pCR2.1. PCR amplification obtained five products ranging from 917 to 437 bp. Three clones were obtained and analysed from all fragments with the exception of 437 bp. These products were designated ITS-1, ITS-2, ITS-3 and ITS-4. ITS-1 contained genes for tRNAGlu(TTC), tRNALys(TTT), tRNAAla(TGC)and tRNAVal(TAC), while ITS-2 was almost the same as the ITS-1 sequence, but without tRNAVal(TAC). ITS-3 contained tRNAAla(TGC) and tRNAIle (GAT) and ITS-4, tRNAAla (GGC) or tRNA Glu(TTC). The number of copies of the ribosomal operon (rrn) in V. ordalii chromosome ranged from at least six to seven and V. anguillarum had at least seven rrn. The sequences ITS-1, ITS-2 and ITS-3 showed a high similarity among the V. anguillarum and V. ordalii sequences (97.2% to 100%). Little variation was found for ITS-4, which does not seem to be sufficient to distinguish these two closely related species. Based on the findings, we confirm a close genetic relationship among V. anguillarum and V. ordalii and that they may be descended from a common ancestor in the Vibrionaceae linage. © 2009 Federation of European Microbiological Societies. Published by Blackwell Publishing Ltd. All rights reserved.

Más información

Título según WOS: Analysis of 16S-23S rRNA gene internal transcribed spacer of Vibrio anguillarum and Vibrio ordalii strains isolated from fish
Título según SCOPUS: Analysis of 16S-23S rRNA gene internal transcribed spacer of Vibrio anguillarum and vibrio ordalii strains isolated from fish
Título de la Revista: FEMS MICROBIOLOGY LETTERS
Volumen: 299
Número: 2
Editorial: OXFORD UNIV PRESS
Fecha de publicación: 2009
Página de inicio: 184
Página final: 192
Idioma: English
URL: http://doi.wiley.com/10.1111/j.1574-6968.2009.01755.x
DOI:

10.1111/j.1574-6968.2009.01755.x

Notas: ISI, SCOPUS