AbstractBackgroundConventional biochemical tests are the standard for the identification of Mycobacterium species, but molecular identifications are becoming more prevalent. The rpoB gene encodes the β-subunit of RNA polymerase and is utilized for the identification of Mycobacterium species. In the present study, a stepwise Mycobacterium species identification algorithm using the 16S rRNA encoding gene and rpoB analysis was evaluated for its effectiveness.MethodsA total of 172 clinical Mycobacterium isolates were tested, and concordant results were obtained with 108 strains by using the conventional method and molecular methods (AccuProbe or DDH method).ResultsIn these 108 strains, 4 strains were identified by 16S rRNA gene analysis, but rp...
A total of 0.3 to 0.4 kb of the promoter region of the 16S rRNA genes from Mycobacterium tuberculosi...
AbstractIndividuals suffering from fibrocystic disease may acquire non-tuberculous mycobacteria as c...
Previous studies have indicated that the conventional tests used for the identification of mycobacte...
AbstractBackgroundConventional biochemical tests are the standard for the identification of Mycobact...
PCR-restriction fragment length polymorphism analysis (PRA) using the novel region of the rpoB gene ...
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...
Objectives. To evaluate the resolution and reliability of the rpsA gene, encoding ribosomal protein ...
In the Netherlands, clinical isolation of nontuberculous mycobacteria (NTM) has increased over the p...
International audienceIn order to evaluate the suitability of 16S rRNA nucleotide sequence similarit...
The rapid and reliable identification of clinically significant Mycobacterium species is a challenge...
The identification of Mycobacteria in the species level has great medical importance. Biochemical te...
The identification of Mycobacteria in the species level has great medical importance. Biochemical te...
Background: Nontuberculous mycobacteria (NTM) are a heterogeneous group of microorganisms with dist...
AIMS: To develop a real-time PCR method for rapid differential identification of many clinically imp...
A total of 0.3 to 0.4 kb of the promoter region of the 16S rRNA genes from Mycobacterium tuberculosi...
AbstractIndividuals suffering from fibrocystic disease may acquire non-tuberculous mycobacteria as c...
Previous studies have indicated that the conventional tests used for the identification of mycobacte...
AbstractBackgroundConventional biochemical tests are the standard for the identification of Mycobact...
PCR-restriction fragment length polymorphism analysis (PRA) using the novel region of the rpoB gene ...
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...
Objectives. To evaluate the resolution and reliability of the rpsA gene, encoding ribosomal protein ...
In the Netherlands, clinical isolation of nontuberculous mycobacteria (NTM) has increased over the p...
International audienceIn order to evaluate the suitability of 16S rRNA nucleotide sequence similarit...
The rapid and reliable identification of clinically significant Mycobacterium species is a challenge...
The identification of Mycobacteria in the species level has great medical importance. Biochemical te...
The identification of Mycobacteria in the species level has great medical importance. Biochemical te...
Background: Nontuberculous mycobacteria (NTM) are a heterogeneous group of microorganisms with dist...
AIMS: To develop a real-time PCR method for rapid differential identification of many clinically imp...
A total of 0.3 to 0.4 kb of the promoter region of the 16S rRNA genes from Mycobacterium tuberculosi...
AbstractIndividuals suffering from fibrocystic disease may acquire non-tuberculous mycobacteria as c...
Previous studies have indicated that the conventional tests used for the identification of mycobacte...