Sequencing of the gene coding for 16S rRNA (16S rDNA) is a well-established method used to identify bacteria, particularly mycobacteria. Unique sequences allow identification of a particular genus and species. If more than one 16S rDNA is present on one mycobacterial genome, their sequences are assumed to be strictly or almost identical. We have isolated a slowly growing Mycobacterium strain, "X", identified by conventional biochemical tests as Mycobacterium terrae. Identification by amplification and direct sequencing of 16S rDNA yielded ambiguous results in two variable regions, suggesting the presence of different copies of the sequenced gene. Total DNA was digested by restriction enzymes and hybridized after Southern blotting to a probe...
Variable region analysis of 16S rRNA gene sequences is the most common tool in bacterial taxonomic s...
Members of the Mycobacterium terrae complex are slow-growing, non-chromogenic acid-fast bacilli foun...
DNAs from nine mycobacteria cleaved with restriction endonucleases were hybridized with cDNA probes ...
Sequencing of the gene coding for 16S rRNA (16S rDNA) is a well-established method used to identify ...
Direct sequencing of the 16S rRNA gene (16S rDNA) of Mycobacterium celatum isolates showed ambiguiti...
Nontuberculous mycobacteria (NTM) can carry two or more 16S rRNA gene copies that are, in some insta...
International audienceIn order to evaluate the suitability of 16S rRNA nucleotide sequence similarit...
The 16S rRNA gene-based phylogenetic tree clearly distinguishes Mycobacterium grouping based on the ...
It is difficult to distinguish between clinically significant slowly-growing, non-pigmented mycobact...
A total of 0.3 to 0.4 kb of the promoter region of the 16S rRNA genes from Mycobacterium tuberculosi...
Two rapidly growing mycobacteria with identical 16S rRNA gene sequences were the subject of a polyph...
A novel genus-specific PCR for mycobacteria with simple identification to the species level by restr...
The nucleotide sequences of partial 16S rRNA and bacterial RNA polymerase ß-subunit (rpoB) gen...
Variable region analysis of 16S rRNA gene sequences is the most common tool in bacterial taxonomic s...
AbstractPhylogenetic knowledge of the genus Mycobacterium is based on comparative analysis of their ...
Variable region analysis of 16S rRNA gene sequences is the most common tool in bacterial taxonomic s...
Members of the Mycobacterium terrae complex are slow-growing, non-chromogenic acid-fast bacilli foun...
DNAs from nine mycobacteria cleaved with restriction endonucleases were hybridized with cDNA probes ...
Sequencing of the gene coding for 16S rRNA (16S rDNA) is a well-established method used to identify ...
Direct sequencing of the 16S rRNA gene (16S rDNA) of Mycobacterium celatum isolates showed ambiguiti...
Nontuberculous mycobacteria (NTM) can carry two or more 16S rRNA gene copies that are, in some insta...
International audienceIn order to evaluate the suitability of 16S rRNA nucleotide sequence similarit...
The 16S rRNA gene-based phylogenetic tree clearly distinguishes Mycobacterium grouping based on the ...
It is difficult to distinguish between clinically significant slowly-growing, non-pigmented mycobact...
A total of 0.3 to 0.4 kb of the promoter region of the 16S rRNA genes from Mycobacterium tuberculosi...
Two rapidly growing mycobacteria with identical 16S rRNA gene sequences were the subject of a polyph...
A novel genus-specific PCR for mycobacteria with simple identification to the species level by restr...
The nucleotide sequences of partial 16S rRNA and bacterial RNA polymerase ß-subunit (rpoB) gen...
Variable region analysis of 16S rRNA gene sequences is the most common tool in bacterial taxonomic s...
AbstractPhylogenetic knowledge of the genus Mycobacterium is based on comparative analysis of their ...
Variable region analysis of 16S rRNA gene sequences is the most common tool in bacterial taxonomic s...
Members of the Mycobacterium terrae complex are slow-growing, non-chromogenic acid-fast bacilli foun...
DNAs from nine mycobacteria cleaved with restriction endonucleases were hybridized with cDNA probes ...