Rapid identification of Mycobacterium bovis BCG by the detection of the RD1 deletion using a multiplex PCR technique

Citation
Am. Kearns et al., Rapid identification of Mycobacterium bovis BCG by the detection of the RD1 deletion using a multiplex PCR technique, INT J TUBE, 3(7), 1999, pp. 635-638
Citations number
10
Categorie Soggetti
Cardiovascular & Respiratory Systems
Journal title
INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE
ISSN journal
10273719 → ACNP
Volume
3
Issue
7
Year of publication
1999
Pages
635 - 638
Database
ISI
SICI code
1027-3719(199907)3:7<635:RIOMBB>2.0.ZU;2-W
Abstract
The BCG vaccine strain cannot, with confidence, be differentiated from othe r members of the Mycobacterium tuberculosis complex on phenotypic tests alo ne. Isolates from clinical sites not associated with vaccination may be con fused with M. tuberculosis. A characteristic of BCG strains is the deletion of the genomic region RD1; detection of this forms the basis of a multiple x polymerase chain reaction (PCR) assay to distinguish BCG strains. In this study, 28 M. tuberculosis complex strains were analysed by the PCR assay. A DNA sequence displaying the characteristic deletion was detected in all e leven of the BCG strains tested and was not found in representatives of oth er members of the complex, including M. bovis. Thus, the assay affords a ra pid, simple and effective method for the discrimination of the BCG vaccine strain from other members of the M. tuberculosis complex.