Sequencing of variable regions of the 16S rRNA gene for identification of lactic acid bacteria isolated from the intestinal microbiota of healthy salmonids

Abstract The aim of this study was to identify lactic acid bacteria (LAB) using polymerase chain reaction (PCR) amplification of variable regions of the 16S rRNA gene. Thirteen LAB strains were isolated from the intestinal microbiota of healthy salmonids. A ∼500-bp region of the highly conserved 16S...

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Veröffentlicht in:Comparative Immunology, Microbiology and Infectious Diseases Microbiology and Infectious Diseases, 2007-03, Vol.30 (2), p.111-118
Hauptverfasser: Balcázar, José Luis, de Blas, Ignacio, Ruiz-Zarzuela, Imanol, Vendrell, Daniel, Gironés, Olivia, Muzquiz, José Luis
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Sprache:eng
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Zusammenfassung:Abstract The aim of this study was to identify lactic acid bacteria (LAB) using polymerase chain reaction (PCR) amplification of variable regions of the 16S rRNA gene. Thirteen LAB strains were isolated from the intestinal microbiota of healthy salmonids. A ∼500-bp region of the highly conserved 16S rRNA gene was PCR-amplified and following this, a portion of the amplicon (272-bp) including the V1 and V2 variable regions was sequenced. The sequence containing both the V1 and V2 region provided strong evidence for the identification of LAB. The LAB strains were identified as Carnobacterium maltaromaticum , Lactobacillus curvatus , Lactobacillus sakei , Lactobacillus plantarum , Lactococcus lactis subsp. cremoris , Lactococcus lactis subsp. lactis , and Leuconostoc mesenteroides . The method described was found to be a very simple, rapid, specific, and low-cost tool for the identification of unknown strains of LAB.
ISSN:0147-9571
1878-1667
1365-2567
DOI:10.1016/j.cimid.2006.12.001