Method and device for rapid detection of microorganisms by changing the shape of micro-colonies
This invention describes a method of rapid detection of micro-colonies of microorganisms by changing their shape from a regular semi-sphere to a long and thin cylinder. Cells are trapped by filtration in long (diameter/length=1/10-1/100), cylindrical, parallel, micro-channels that are open from both sides, and attached to a filter from one side. A micro-channel plate houses a multiplicity of micro-channels (diameter of each channel=1 -20 μm, and length 100-1000 μm). The micro-channel plate with cells trapped on the surface of the filter is attached to a nutrient media agar block. Cells produce micro-colonies of a long and thin shape according the shape of the micro-channel. The growth of microorganisms in the micro-channels permits a change in the number of cells to accomplish light absorbance. Fewer cells need a shorter time to reproduce. Thus detection and counting of cells can be accomplished in a rapid fashion. The light absorbance can be enhanced by additional coloration of micro-colonies by cell dyes or artificial chromogenic or fluorogenic substrates.
1. A method for rapid detection of one or a multiplicity of cells comprising the steps of:
filtrating a sample comprising one or a multiplicity of cells through one or a multiplicity of micro-channels that are positioned adjacent to and above a filter so as to trap the one or multiplicity of cells with the one or a multiplicity of micro-channels, and wherein the one or multiplicity of micro-channels have a volume of about 1-500 picoliters, and wherein the ratio of the diameter to a length of the one or a multiplicity of micro-channels is between about 1:10 to 1:100,
growing the one or a multiplicity of cells inside the one or a multiplicity of microchannels into one or a multiplicity of micro-colonies, and
detecting the one or multiplicity of micro-colonies.
2. The method of claim 1 , wherein the filter is porous such that the pores are smaller than an average of a size of the one or a multiplicity of cells.
3. The method of claim 1 , wherein the filtrating step includes removing effluent that passes through the one or a multiplicity of micro-channels with a manifold.
4. The method of claim 1 , wherein the filtrating of the sample is aided with a pump.
5. The method of claim 1 , wherein the filtrating step further includes filtering the sample through a porous support, the porous support adjacent the filter opposite the one or a multiplicity of micro-channels.
6. The method of claim 1 , wherein the filtration step further includes adding the sample into a funnel, wherein the funnel directs the sample into the one or a multiplicity of micro-channels.
7. The method of claim 1 , wherein the filtration step includes adding the sample to the one or a multiplicity of micro-channels in the substantial absence of ambient air pressure.
8. The method of claim 7 , wherein the substantial absence of ambient air pressure is achieved by mounting a syringe to a top side of the one or a multiplicity of micro-channels.
9. The method of claim 1 , wherein the sample is selected from the group consisting of liquids and bioaerosols.
10. The method of claim 1 , wherein the micro-channels are substantially cylindrical.
11. The method of claim 1 , wherein the micro-colonies obtain cylindrical shape within the one or a multiplicity of micro-channels.
12. The method of claim 1 , wherein the growing step includes placing the one or a multiplicity of micro-channels and the filter on a nutrient media, the nutrient media adjacent to the filter opposite the micro-channels.
13. The method of claim 12 , wherein the filter and one or a multiplicity of micro-channels is removed from the nutrient media and an indicator is introduced to the micro-colonies by placing the one or a multiplicity of micro-channels and the filter on a surface containing the indicator, the surface adjacent the filter opposite the one or a multiplicity of micro-channels.
14. The method of claim 12 , wherein the nutrient media is selected from the group consisting of solid nutrient media or liquid nutrient media.
15. The method of claim 1 , wherein the number of the one or a multiplicity of cells in the sample is equal or less than 50% of the number of the multiplicity of micro-channels.
16. The method of claim 15 , wherein the number of the one or a multiplicity of cells in the sample is equal or less than 15% of the number of the multiplicity of micro-channels.
17. The method of claim 1 , further comprising the step of introducing an indicator to the micro-colonies subsequent to the growing step.
18. The method of claim 17 , wherein the indicator is introduced to the microcolonies by placing the one or a multiplicity of micro-channels and the filter on a surface containing the indicator, the surface adjacent the filter opposite the one or a multiplicity of micro-channels.
19. A method for cylindrically shaping one or a multiplicity of micro-colonies to create rapid detection of the one or a multiplicity of colonies, comprising the steps of:
introducing one or a multiplicity of cells into one or a multiplicity of substantially cylindrical micro-channels, wherein the substantially cylindrical micro-channels have a volume of about 1-500 picoliters, and wherein the ratio of the diameter to a length of the one or a multiplicity of micro-channels is between about 1:10 to 1:100
growing the one or a multiplicity of cells into the one or a multiplicity of microcolonies, such that the one or a multiplicity of micro-colonies have a substantially cylindrical shape inside the one or a multiplicity of substantially cylindrical microchannels, and
detecting visually the one or a multiplicity of micro-colonies.
20. The method of claim 19 , wherein the step of visually detecting the one or multiplicity of micro-colonies utilizes an indicator selected from the group consisting of: chromogenic substrates or absorbent dyes; fluorogenic substrate or fluorescent dyes; Tetrazolium salts; iron sulfide or potassium telluride in agar; and pH indicators for detecting microcolonies with changed pH.