|
|
||||||||
Food Safety Center of Excellence, Department of Animal Science, The University of Tennessee, Knoxville 37996
Corresponding author: S. P. Oliver; e-mail: soliver{at}utk.edu.
The objective of this study was to develop a multiplex real-time polymerase chain reaction (PCR) method for simultaneous detection of Staphylococcus aureus, Streptococcus agalactiae, and Streptococcus uberis directly from milk. A genetic marker specific for Staph. aureus was used for primers and dual-labeled probe design. The target for Strep. agalactiae primers and dual-labeled probe was selected from the cfb gene encoding the Christie-Atkins-Munch-Petersen factor. The plasminogen activator gene was the target for primers and dual-labeled probe design for Strep. uberis. Quarter milk samples (n = 192) were analyzed by the multiplex real-time PCR assay and conventional microbiological methods. An additional 57 quarter milk samples were analyzed in a separate real-time PCR assay for Strep. agalactiae only. Using an overnight enrichment step, the real-time PCR technique correctly identified 96.4% of all quarter milk samples; 91.7% of Staph. aureus, 98.2% of Strep. agalactiae, and 100% of Strep. uberis. Results of conventional microbiological methods were used to determine the sensitivity and specificity of the multiplex real-time PCR procedure. The sensitivity of the procedure to correctly identify Staph. aureus, Strep. agalactiae, and Strep. uberis directly from milk was 95.5%, and the specificity was 99.6%. Results of this study indicate that the multiplex real-time PCR procedure has the potential to be a valuable diagnostic technique for simultaneous identification of Staph. aureus, Strep. agalactiae, and Strep. uberis directly from quarter milk samples.
Key Words: multiplex real-time polymerase chain reaction Staphylococcus aureus Streptococcus agalactiae Streptococcus uberis
Abbreviation key: ATCC = American Type Culture Collection, CAMP = Christie-Atkins-Munch-Petersen, CPS = coagulase-positive Staphylococcus, CT= cycle threshold
This article has been cited by other articles:
![]() |
M. T. Koskinen, J. Holopainen, S. Pyorala, P. Bredbacka, A. Pitkala, H. W. Barkema, R. Bexiga, J. Roberson, L. Solverod, R. Piccinini, et al. Analytical specificity and sensitivity of a real-time polymerase chain reaction assay for identification of bovine mastitis pathogens J Dairy Sci, March 1, 2009; 92(3): 952 - 959. [Abstract] [Full Text] [PDF] |
||||
![]() |
K.-H. Lee, J.-W. Lee, S.-W. Wang, L.-Y. Liu, M.-F. Lee, S.-T. Chuang, Y.-M. Shy, C.-L. Chang, M.-C. Wu, and C.-H. Chi Development of a novel biochip for rapid multiplex detection of seven mastitis-causing pathogens in bovine milk samples J Vet Diagn Invest, July 1, 2008; 20(4): 463 - 471. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Fernandez, B. del Rio, D. M. Linares, M. C. Martin, and M. A. Alvarez Real-time polymerase chain reaction for quantitative detection of histamine-producing bacteria: use in cheese production. J Dairy Sci, October 1, 2006; 89(10): 3763 - 3769. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |