Please use this identifier to cite or link to this item: http://hdl.handle.net/2381/14799
Title: Development of a new, combined rapid method using phage and PCR for detection and identification of viable Mycobacterium paratuberculosis bacteria within 48 hours.
Authors: Stanley, EC
Mole, RJ
Smith, RJ
Glenn, SM
Barer, MR
McGowan, M
Rees, CE
First Published: Mar-2007
Citation: APPL ENVIRON MICROBIOL, 2007, 73 (6), pp. 1851-1857
Abstract: The FASTPlaqueTB assay is an established diagnostic aid for the rapid detection of Mycobacterium tuberculosis from human sputum samples. Using the FASTPlaqueTB assay reagents, viable Mycobacterium avium subsp. paratuberculosis cells were detected as phage plaques in just 24 h. The bacteriophage used does not infect M. avium subsp. paratuberculosis alone, so to add specificity to this assay, a PCR-based identification method was introduced to amplify M. avium subsp. paratuberculosis-specific sequences from the DNA of the mycobacterial cell detected by the phage. To give further diagnostic information, a multiplex PCR method was developed to allow simultaneous amplification of either M. avium subsp. paratuberculosis or M. tuberculosis complex-specific sequences from plaque samples. Combining the plaque PCR technique with the phage-based detection assay allowed the rapid and specific detection of viable M. avium subsp. paratuberculosis in milk samples in just 48 h.
DOI Link: 10.1128/AEM.01722-06
ISSN: 0099-2240
Links: http://hdl.handle.net/2381/14799
Type: Journal Article
Appears in Collections:Published Articles, Dept. of Infection, Immunity and Inflammation

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