Importance

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Abstract

The presence or absence of a target microbial analyte in a substance, such as a biological or environmental substance, is assayed by inoculating a sterile growth media with a sample of the substance. The media may be combined with a labeled analyte-specific material (LASM) which can migrate through the substrate and which is homogeneously distributed throughout the media. The LASM may be premixed with the media, or may be added to the media after inoculation with the substance. The nature of the media is such that it will support target analyte reproduction so as to form target analyte colonies in or on the media, and it will not allow the target analyte colonies to migrate within the media. After the sample to be assayed is added to the media, growth of the target analyte colonies in the sample will bind increasing quantities of the LASM, thereby creating localized intensely labeled areas in the media which can be visually or photometrically detected. As the target analyte colonies grow in the media they attract increasing quantities of the LASM which diffuses to the colonies through the media, causing the local target analyte colonies to become intensely labeled, which renders the colonies readily detectable. Each of the intensely labeled target analyte colonies in the media may also be surrounded by areas of lower intensity due to local depletion of the LASM in the regions of colony growth. The number of intensely labeled target analyte colonies in the media will be proportional to the amount of the target analyte present in the sample. In the event that the target analyte is absent from the sample, then there will be no localized labeled microbe colonies in the media.

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First Claim