Literature DB >> 7505291

Genotypic identification of mycobacteria by nucleic acid sequence determination: report of a 2-year experience in a clinical laboratory.

P Kirschner1, B Springer, U Vogel, A Meier, A Wrede, M Kiekenbeck, F C Bange, E C Böttger.   

Abstract

Clinical isolates of Mycobacterium spp. were identified by direct sequence determination of 16S rRNA gene fragments amplified by polymerase chain reaction. Identification was based on a hypervariable region within the 16S rRNA gene in which mycobacterial species are characterized by species-specific nucleotide sequences. A manually aligned data base including the signature sequences of 52 species of mycobacteria easily allowed rapid and correct identification. The results of this study demonstrate that polymerase chain reaction-mediated direct sequence determination can be used as a rapid and reliable method for the identification of mycobacteria in the clinical laboratory. In addition, the prompt recognition of previously undescribed species is now feasible.

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Year:  1993        PMID: 7505291      PMCID: PMC266149          DOI: 10.1128/jcm.31.11.2882-2889.1993

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  38 in total

1.  Infection with a novel, unidentified mycobacterium.

Authors:  E C Böttger
Journal:  N Engl J Med       Date:  1990-12-06       Impact factor: 91.245

2.  The division between fast- and slow-growing species corresponds to natural relationships among the mycobacteria.

Authors:  D A Stahl; J W Urbance
Journal:  J Bacteriol       Date:  1990-01       Impact factor: 3.490

Review 3.  Bacterial evolution.

Authors:  C R Woese
Journal:  Microbiol Rev       Date:  1987-06

4.  Rapid determination of bacterial ribosomal RNA sequences by direct sequencing of enzymatically amplified DNA.

Authors:  E C Böttger
Journal:  FEMS Microbiol Lett       Date:  1989-11       Impact factor: 2.742

5.  Isolation and direct complete nucleotide determination of entire genes. Characterization of a gene coding for 16S ribosomal RNA.

Authors:  U Edwards; T Rogall; H Blöcker; M Emde; E C Böttger
Journal:  Nucleic Acids Res       Date:  1989-10-11       Impact factor: 16.971

6.  An improved method for directly sequencing PCR amplified material using dimethyl sulphoxide.

Authors:  P R Winship
Journal:  Nucleic Acids Res       Date:  1989-02-11       Impact factor: 16.971

7.  Detection and identification of mycobacteria by amplification of rRNA.

Authors:  B Böddinghaus; T Rogall; T Flohr; H Blöcker; E C Böttger
Journal:  J Clin Microbiol       Date:  1990-08       Impact factor: 5.948

8.  Direct identification of Mycobacterium tuberculosis, Mycobacterium avium, and Mycobacterium intracellulare from amplified primary cultures in BACTEC media using DNA probes.

Authors:  E M Peterson; R Lu; C Floyd; A Nakasone; G Friedly; L M de la Maza
Journal:  J Clin Microbiol       Date:  1989-07       Impact factor: 5.948

9.  Mycobacterium cookii sp. nov.

Authors:  J Kazda; E Stackebrandt; J Smida; D E Minnikin; M Daffe; J H Parlett; C Pitulle
Journal:  Int J Syst Bacteriol       Date:  1990-07

10.  Phylogenetic analysis and identification of different serovars of Mycobacterium intracellulare at the molecular level.

Authors:  B Böddinghaus; J Wolters; W Heikens; E C Böttger
Journal:  FEMS Microbiol Lett       Date:  1990-07       Impact factor: 2.742

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  179 in total

1.  Comparison of MB/BacT and BACTEC 460 TB systems for recovery of mycobacteria in a routine diagnostic laboratory.

Authors:  A Roggenkamp; M W Hornef; A Masch; B Aigner; I B Autenrieth; J Heesemann
Journal:  J Clin Microbiol       Date:  1999-11       Impact factor: 5.948

2.  Disseminated Mycobacterium lentiflavum infection in a human immunodeficiency virus-infected patient.

Authors:  S N Niobe; C M Bebear; M Clerc; J L Pellegrin; C Bebear; J Maugein
Journal:  J Clin Microbiol       Date:  2001-05       Impact factor: 5.948

Review 3.  Tuberculosis: 7. Laboratory aspects of diagnosis.

Authors:  A Laszlo
Journal:  CMAJ       Date:  1999-06-15       Impact factor: 8.262

4.  Sequence-based identification of Mycobacterium species using the MicroSeq 500 16S rDNA bacterial identification system.

Authors:  J B Patel; D G Leonard; X Pan; J M Musser; R E Berman; I Nachamkin
Journal:  J Clin Microbiol       Date:  2000-01       Impact factor: 5.948

5.  Species identification of mycobacteria by PCR-restriction fragment length polymorphism of the rpoB gene.

Authors:  H Lee; H J Park; S N Cho; G H Bai; S J Kim
Journal:  J Clin Microbiol       Date:  2000-08       Impact factor: 5.948

6.  Identification of 54 mycobacterial species by PCR-restriction fragment length polymorphism analysis of the hsp65 gene.

Authors:  F Brunello; M Ligozzi; E Cristelli; S Bonora; E Tortoli; R Fontana
Journal:  J Clin Microbiol       Date:  2001-08       Impact factor: 5.948

7.  Identification of Mycobacterium spp. by using a commercial 16S ribosomal DNA sequencing kit and additional sequencing libraries.

Authors:  J L Cloud; H Neal; R Rosenberry; C Y Turenne; M Jama; D R Hillyard; K C Carroll
Journal:  J Clin Microbiol       Date:  2002-02       Impact factor: 5.948

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

Authors:  C Y Turenne; L Tschetter; J Wolfe; A Kabani
Journal:  J Clin Microbiol       Date:  2001-10       Impact factor: 5.948

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

Authors:  Jean-Noël Dauendorffer; Isabelle Guillemin; Alexandra Aubry; Chantal Truffot-Pernot; Wladimir Sougakoff; Vincent Jarlier; Emmanuelle Cambau
Journal:  J Clin Microbiol       Date:  2003-03       Impact factor: 5.948

10.  Evaluation of the MicroSeq system for identification of mycobacteria by 16S ribosomal DNA sequencing and its integration into a routine clinical mycobacteriology laboratory.

Authors:  Leslie Hall; Kelly A Doerr; Sherri L Wohlfiel; Glenn D Roberts
Journal:  J Clin Microbiol       Date:  2003-04       Impact factor: 5.948

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