Safety/Hazard Cont: Improved Identification of Listeria Spp
Feb 14 2006
This innovative chromogenic medium detects B-glucosidase activity common to all Listeria species, resulting in distinct blue colonies. Selective agents within the medium inhibit other organisms that possess this enzyme, such as enterococci, in addition to background flora that may be present in the sample.
The addition of lecithin to the medium permits the further differentiation of L. monocytogenes and pathogenic L. ivanovii, both of which have the ability to produce the phospholipase enzyme, lecithinase (PCPLC). The activity of this enzyme produces a clearly visible, opaque white halo around L. monocytogenes and pathogenic L. ivanovii colonies.
The presence of PCPLC and another phospholipase enzyme (PIPLC) are required for virulence, although detection of one is sufficient for the identification of pathogenicity.
L. monocytogenes is the most common pathogenic Listeria spp. and has been found in humans and animals. Pathogenic strains of L. ivanovii (those that possess lecithinase activity) are primarily found in animals but have also been shown to cause infection in humans.
In This Edition Chromatography - Optimising Viral Vector Purification Strategies with Multimodal Chromatography - Key UHPLC Characteristics Required for High throughput LC-MS - New Low Volu...
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