Literature DB >> 8573484

16S rRNA and 16S to 23S internal transcribed spacer sequence analyses reveal inter- and intraspecific Bifidobacterium phylogeny.

N Leblond-Bourget1, H Philippe, I Mangin, B Decaris.   

Abstract

In the last few years many attempts have been made to differentiate more than 20 Bifidobacterium species. It has been recognized that identification of bifidobacterial species is problematic because of phenetic and genetic heterogeneities. In order to contribute to our understanding of Bifidobacterium taxonomy, we studied Bifidobacterium phylogeny by performing both 16S rRNA and 16S to 23S (16S-23S) internally transcribed spacer (ITS) sequence analyses. In this study, we determined 16S rRNA sequences of five Bifidobacterium strains representing four species, and compared them with the sequences available in the GenBank database, and used them to construct a distance tree and for a bootstrap analysis. Moreover, we determined the ITS sequences of 29 bifidobacterial strains representing 18 species and compared these sequences with each other. We constructed a phylogenetic tree based on these sequence data and compared this tree with the tree based on 16S rRNA sequence data. We found that the two trees were similar topologically, suggesting that the two types of molecules provided the same kind of phylogenetic information. However, while 16S rRNA sequences are a good tool to infer interspecific links, the 16S-23S rDNA spacer data allowed us to determine intraspecific relationships. Each of the strains was characterized by its own ITS sequence; hence, 16S-23S rRNA sequences are a good tool for strain identification. Moreover, a comparison of the ITS sequences allowed us to estimate that the maximum level of ITS divergence between strains belonging to the same species was 13%. Our data allowed us to confirm the validity of most of the Bifidobacterium species which we studied and to identify some classification errors. Finally, our results showed that Bifidobacterium strains have no tRNA genes in the 16S-23S spacer region.

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Year:  1996        PMID: 8573484     DOI: 10.1099/00207713-46-1-102

Source DB:  PubMed          Journal:  Int J Syst Bacteriol        ISSN: 0020-7713


  40 in total

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2.  Resolution of Prochlorococcus and Synechococcus ecotypes by using 16S-23S ribosomal DNA internal transcribed spacer sequences.

Authors:  Gabrielle Rocap; Daniel L Distel; John B Waterbury; Sallie W Chisholm
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Review 3.  The bifidobacterial and Lactobacillus microflora of humans.

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Journal:  Clin Rev Allergy Immunol       Date:  2002-06       Impact factor: 8.667

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Journal:  Appl Environ Microbiol       Date:  2000-09       Impact factor: 4.792

5.  Cyanobacterial ecotypes in different optical microenvironments of a 68 degrees C hot spring mat community revealed by 16S-23S rRNA internal transcribed spacer region variation.

Authors:  Mike J Ferris; Michael Kühl; Andrea Wieland; David M Ward
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6.  Quantification of human fecal bifidobacterium species by use of quantitative real-time PCR analysis targeting the groEL gene.

Authors:  Jana Junick; Michael Blaut
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7.  Critical evaluation of two primers commonly used for amplification of bacterial 16S rRNA genes.

Authors:  Jeremy A Frank; Claudia I Reich; Shobha Sharma; Jon S Weisbaum; Brenda A Wilson; Gary J Olsen
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8.  Nuclear ribosomal spacer regions in plant phylogenetics: problems and prospects.

Authors:  Péter Poczai; Jaakko Hyvönen
Journal:  Mol Biol Rep       Date:  2009-07-21       Impact factor: 2.316

9.  Bifidobacteria in feces and environmental waters.

Authors:  Regina Lamendella; Jorge W Santo Domingo; Catherine Kelty; Daniel B Oerther
Journal:  Appl Environ Microbiol       Date:  2007-11-09       Impact factor: 4.792

10.  Use of Bifidobacterium dentium as an indicator of the origin of fecal water pollution.

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Journal:  Appl Environ Microbiol       Date:  2003-05       Impact factor: 4.792

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