Detection and identification of multiple mycobacterial pathogens by DNA amplification in a single tube

PCR Methods Appl. 1992 May;1(4):269-73. doi: 10.1101/gr.1.4.269.

Abstract

A comparison of the DNA sequence of the 16S rRNA revealed a region in which there was a minor variation between the species of mycobacteria. This information was used to develop a multiplex amplification system that could identify the genus Mycobacterium and then distinguish between M. avium and M. intracellulare, two commonly encountered mycobacteria other than tuberculosis. The combination of these rRNA gene primers together with primers aimed at the MPB70 gene of M. tuberculosis complex organisms permits the detection and identification of clinically significant mycobacteria in a single tube. An amplification product of 1030 bp is indicative of the genus Mycobacterium and smaller fragments of 850, 372, and 180 bp are the positive signals for M. intracellulare, M. tuberculosis complex, and M. avium, respectively.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA, Bacterial / analysis*
  • DNA, Ribosomal / analysis*
  • Genes, Bacterial
  • Molecular Sequence Data
  • Mycobacterium avium / genetics
  • Mycobacterium avium / isolation & purification*
  • Mycobacterium avium Complex / genetics
  • Mycobacterium avium Complex / isolation & purification*
  • Polymerase Chain Reaction* / instrumentation
  • RNA, Bacterial / genetics*
  • RNA, Ribosomal, 16S / genetics*
  • Sequence Analysis, DNA* / instrumentation
  • Species Specificity

Substances

  • DNA, Bacterial
  • DNA, Ribosomal
  • RNA, Bacterial
  • RNA, Ribosomal, 16S