Live Bioload detection using microparticles
The present invention provides methods to concentrate cells onto microparticles, to concentrate the microparticles, and to detect the cells. The present invention also includes unitary sample preparation and detection devices to be used in accordance with the methods.
1. A method of detecting one or more living cells in a liquid sample, the method comprising:
providing a cell concentration agent, a hydrogel comprising a cell extractant and a liquid sample suspected of containing one or more living cells;
contacting the liquid sample and the cell concentration agent for a period of time and forming a first mixture comprising the cell concentration agent;
isolating the cell concentration agent from at least a portion of the first mixture comprising the cell concentration agent;
forming a second liquid mixture comprising the isolated cell concentration agent and the hydrogel, wherein the cell extractant is released from the hydrogel into the second liquid mixture; and
detecting ATP in the second liquid mixture;
wherein said detecting ATP in the second liquid mixture comprises quantifying an amount of ATP in the second liquid mixture;
wherein the amount of ATP in the second liquid mixture is quantified at two or more time points;
wherein the amount of ATP in the second liquid mixture detected at a first time point of the two or more time points is compared to the amount of ATP in the second liquid mixture detected at a second time point of the two or more time points, wherein the second time point happens after the first time point;
wherein an increase in the amount of ATP detected at the second time point compared to the first time point is an indication of the presence of said one or more live cells in the liquid sample.
2. The method of claim 1 , wherein said one or more live cells are live microbial cells and the cell extractant selectively releases ATP from said live microbial cells.
3. The method of claim 1 , wherein the second time point happens about 1.5 seconds to about 540 seconds after said forming the second liquid mixture.
4. A method of detecting one or more live cells in a sample, the method comprising:
providing a sample suspected of containing one or more live cells; a cell concentration agent; a hydrogel comprising a cell extractant; a detection article comprising a housing with two or more receptacles comprising an upper receptacle and a lower receptacle and an opening configured to receive the sample; and means for isolating and transferring the cell concentration agent from the upper receptacle to the lower receptacle in the housing;
contacting in a liquid medium the sample with the cell concentration agent in the upper receptacle of the housing and forming a first liquid mixture comprising the cell concentration agent and the sample;
isolating and transferring the cell concentration agent from the first liquid mixture to the lower receptacle in the housing;
forming a second liquid mixture comprising the isolated cell concentration agent and the hydrogel, wherein the cell extractant is released from the hydrogel into the second liquid mixture; and
detecting ATP in the second liquid mixture;
wherein said detecting ATP in the second liquid mixture comprises quantifying an amount of ATP in the second liquid mixture;
wherein the amount of ATP in the second liquid mixture is quantified at two or more time points;
wherein the amount of ATP in the second liquid mixture detected at a first time point of the two or more time points is compared to the amount of ATP in the second liquid mixture detected at a second time point of the two or more time points, wherein the second time point happens after the first time point;
wherein an increase in the amount of ATP detected at the second time point compared to the first time point is an indication of the presence of said one or more live cells in the sample.
5. The method of claim 4 , wherein the second time point happens about 1.5 seconds to about 540 seconds after said forming the second liquid mixture.
6. A method of detecting one or more live cells in a sample, the method comprising:
providing a sample suspected of containing one or more live cells; a detection article comprising a housing with an opening configured to receive the sample, an upper receptacle containing a cell concentration agent, and a lower receptacle containing a hydrogel comprising a cell extractant; means for isolating the cell concentration agent from at least a portion of a liquid sample; and means for transferring the cell concentration agent from the upper receptacle to the lower receptacle in the housing;
contacting in a liquid medium the sample and the cell concentration agent in the upper receptacle and forming a first liquid mixture comprising the cell concentration agent and the sample;
isolating and transferring the cell concentration agent from the first liquid mixture to the lower receptacle;
forming a second liquid mixture comprising the isolated cell concentration agent and the hydrogel, wherein the cell extractant is released from the hydrogel into the second liquid mixture; and
detecting ATP in the second liquid mixture;
wherein said detecting ATP in the second liquid mixture comprises quantifying an amount of ATP in the second liquid mixture;
wherein the amount of ATP in the second liquid mixture is quantified at two or more time points;
wherein the amount of ATP in the second liquid mixture detected at a first time point of the two or more time points is compared to the amount of ATP in the second liquid mixture detected at a second time point of the two or more time points, wherein the second time point happens after the first time point;
wherein an increase in the amount of ATP detected at the second time point compared to the first time point is an indication of the presence of said one or more live cells in the sample.
7. The method of claim 6 , wherein the second time point happens about 1.5 seconds to about 540 seconds after said forming the second liquid mixture.