Literature DB >> 8573508

Semantide- and chemotaxonomy-based analyses of some problematic phenotypic clusters of slowly growing mycobacteria, a cooperative study of the International Working Group on Mycobacterial Taxonomy.

L G Wayne1, R C Good, E C Böttger, R Butler, M Dorsch, T Ezaki, W Gross, V Jonas, J Kilburn, P Kirschner, M I Krichevsky, M Ridell, T M Shinnick, B Springer, E Stackebrandt, I Tarnok, Z Tarnok, H Tasaka, V Vincent, N G Warren, C A Knott, R Johnson.   

Abstract

During previous cooperative numerical taxonomic studies of slowly growing mycobacteria, the International Working Group on Mycobacterial Taxonomy described a number of strains whose taxonomic status was ambiguous. A new study of DNA, RNA, and proteins from 66 of these organisms was performed to correlate their properties with phenotypic clustering behavior; the results of this study permitted 51 of the strains studied to be assigned to known species. The methods used to characterize the semantides included nucleotide sequencing and assessment of levels of semantide relatedness by affinity binding techniques, including whole DNA-DNA hybridization, probe hybridization, and antibody binding. There was good overall agreement between the phenotypic and chemotaxonomic clusters and the groups of organisms identified by semantide analyses. Our results supported the conclusion that we should continue to rely on polyphasic taxonomy to provide satisfactory systematic resolution of members of the genus Mycobacterium. We identified no single 16S rRNA interstrain nucleotide sequence difference value that unequivocally defined species boundaries. DNA-DNA hybridization remains the gold standard, but common resources are needed to permit DNA-DNA hybridization analyses to be made available to laboratories that are not prepared to use this technology. One of the large novel clusters which we studied corresponds to the recently described species Mycobacterium interjectum, a pathogen that resembles the nonpathogen Mycobacterium gordonae phenotypically. We also identified strains that appear to represent ribovars of Mycobacterium intracellulare which do not react with the commercial diagnostic probes that are currently used for identification of this species. Other branches or clusters consisted of too few strains to permit a decision about their taxonomic status to be made.

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Year:  1996        PMID: 8573508     DOI: 10.1099/00207713-46-1-280

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


  30 in total

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2.  Necessity of quality-controlled 16S rRNA gene sequence databases: identifying nontuberculous Mycobacterium species.

Authors:  C Y Turenne; L Tschetter; J Wolfe; A Kabani
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Review 3.  Search and discovery strategies for biotechnology: the paradigm shift.

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4.  Occurrence of nontuberculous mycobacteria in environmental samples.

Authors:  T C Covert; M R Rodgers; A L Reyes; G N Stelma
Journal:  Appl Environ Microbiol       Date:  1999-06       Impact factor: 4.792

5.  Identification of mycobacterial species by PCR sequencing of quinolone resistance-determining regions of DNA gyrase genes.

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Review 6.  Impact of 16S rRNA gene sequence analysis for identification of bacteria on clinical microbiology and infectious diseases.

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7.  Evaluation of the GenoType Mycobacterium Assay for identification of mycobacterial species from cultures.

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8.  Evolution of Mycobacterium ulcerans and other mycolactone-producing mycobacteria from a common Mycobacterium marinum progenitor.

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9.  Identification of Mycobacterium species by secA1 sequences.

Authors:  Adrian M Zelazny; Leslie B Calhoun; Li Li; Yvonne R Shea; Steven H Fischer
Journal:  J Clin Microbiol       Date:  2005-03       Impact factor: 5.948

10.  Assessment of partial sequencing of the 65-kilodalton heat shock protein gene (hsp65) for routine identification of Mycobacterium species isolated from clinical sources.

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