期刊
JOURNAL OF RAPID METHODS AND AUTOMATION IN MICROBIOLOGY
卷 17, 期 2, 页码 195-213出版社
WILEY
DOI: 10.1111/j.1745-4581.2009.00170.x
关键词
-
资金
- EU FP6 [NACBO-CT-2004-500804]
The aim of our work was to develop a new molecular method for the simultaneous detection of Salmonella spp., Listeria monocytogenes and Escherichia coli O157 directly in milk samples. Three specific target sequences were chosen for a multiplex polymerase chain reaction (PCR) assay: a 155-bp region of the Salmonella spp. tetrathionate reductase (ttr) locus; a 173-bp region of the L. monocytogenes listeriolysin O gene (hlyA); a 217-bp region of the E. coli O157 lipopolysaccharide gene (rfbE). An internal amplification control was also included to detect PCR inhibition. In addition, a magnetic-based extraction method was also developed to isolate PCR-ready DNA from milk. The assay was able to detect, whether alone or mixed, also with a difference of 2 log units, as few as 10(2) cells of each pathogen per 10 mL of spiked milk.
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