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Diagnostic Performance of rep-PCR as a Rapid Subtyping Method for Listeria monocytogenes
Previously pulsed field gel electrophoresis-typed Listeria monocytogenes isolates ( N = 95) were tested by repetitive element sequence-based PCRs (rep-PRCs). A combined rep-PCR typing approach showed 95 % repeatability, 0.98 discriminatory power, 95.5 % sensitivity, 75 % specificity, 91.2 % predict...
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Published in: | Food analytical methods 2013-06, Vol.6 (3), p.868-871 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Previously pulsed field gel electrophoresis-typed
Listeria monocytogenes
isolates (
N
= 95) were tested by repetitive element sequence-based PCRs (rep-PRCs). A combined rep-PCR typing approach showed 95 % repeatability, 0.98 discriminatory power, 95.5 % sensitivity, 75 % specificity, 91.2 % predictive positive value, and 85.7 % predictive negative value. Hence, rep-PCR represents an efficient and rapid subtyping method for
L. monocytogenes
. |
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ISSN: | 1936-9751 1936-976X |
DOI: | 10.1007/s12161-012-9496-1 |