Methods and compositions for in situ detection of microorganisms on a surface

• US 20110097702A1
• Filed: 03/30/2006
• Published: 04/28/2011
• Est. Priority Date: 03/31/2005
• Status: Abandoned Application

• Current Assignee: Colorado School of Mines
• Original Assignee: Colorado School of Mines
• Inventors: Voorhees, Kent J.
• Application Number:
  US11/395,485
• Publication Number:
  US 20110097702A1
• Time in Patent Office: Days
• US Class Current: 435/5
• CPC Class Codes: C12Q 1/04 Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor C12Q1/6897 takes precedence

Abstract

Compositions and methods for in situ detection of one or more target microorganisms on a surface and preferably on a hard surface. Compositions and methods of the invention are based on the specificity of certain bacteriophage for target microorganisms. Bacteriophage are modified to express detectable biomarkers in the presence of the target microorganism, the detectable markers being detectable on the surface being tested using a portable detection device. Only living microorganisms are detected using the methods and compositions of the invention.

Claims

1. A method for in situ detection of a target microorganism on a hard surface comprising:

preparing a detection composition wherein the detection composition comprises a non-volatile media impregnated with at least one bacteriophage having specificity for the target microorganism and wherein each of the at least one bacteriophage are modified to express a detectable marker when the target microorganism is present;

contacting the detection composition with the hard surface for a period of time sufficient to allow the modified bacteriophage to infect and express the detectable marker when the target microorganism is present and the target microorganism is alive; and

in situ detecting the presence of the detectable marker on the hard surface wherein presence of the detectable marker indicates presence of living target microorganism on the hard surface and absence of the detectable marker indicates absence of the target microorganism.

2. The method of claim 1 further comprising raising the temperature of an environment around the hard surface to facilitate target microorganism growth wherein enhanced target microorganism growth increases modified bacteriophage levels and detection marker production.

3. The method of claim 1 wherein the detectable marker is a fluorescent protein marker.

4. The method of claim 1 wherein the target microorganism is anthrax.

5. The method of claim 1 wherein the non-volatile media is a combination of glycerol and water.

6. The method of claim 1 wherein the non-volatile media is a combination of polyethylene glycol and water.

7. The method of claim 1 wherein the non-volatile media is a bacterial growth agar complementary for the target microorganism.

8. The method of claim 1 wherein the contacting of the detection composition and the hard surface is by spraying the detection composition onto the hard surface.

9. The method of claim 1 wherein the hard surface is located inside a building.

10. The method of claim 1 wherein the hard surface is located inside a vehicle.

11. A composition for in situ detection of a target microorganism on a hard surface comprising a non-volatile growth media impregnated with at least one genetically modified bacteriophage, the at least one genetically modified bacteriophage selective to the target microorganism wherein the genetically modified bacteriophage is capable of expressing a detectable marker if the bacteriophage contacts the target microorganism.

12. The composition of claim 11 wherein the non-volatile growth media is a combination of water and glycerol.

13. The compositions of claim 11 wherein the non-volatile growth media is a combination of water and polyethylene glycol.

14. The composition of claim 11 wherein the non-volatile growth media is a growth agar for the target microorganism.

15. The composition of claim 11 wherein the detectable marker is a fluorescent protein.

16. The composition of claim 11 wherein the target microorganism is anthrax.