Methods and compositions for rapidly detecting and quantifying viable
Methods and compositions detect and quantify viable Legionella . Dip-slides that include an absorbent medium, growth promoting, and growth selective substances are useful in rapid detection and quantification of microcolonies of Legionella . Most probable number method of detection and quantification of Legionella are disclosed.
1. A method of rapidly quantifying viable Legionella bacteria and total heterotrophic aerobic bacteria in a sample, the method comprising:
(a) providing a dip-slide comprising an absorbent medium, wherein the absorbent medium comprises nutrients for culturing Legionella and separately at least one agent to selectively inhibit the growth of non- Legionella microorganisms;
(b) contacting the dip-slide with the sample for a predetermined amount of time, wherein the dip-slide is calibrated to absorb a predetermined amount of the sample;
(c) incubating the dip-slide at a temperature in the range of 30° C. to about 45° C. for a period of 6-93 hours, less than required for the standard method, which takes at least 10 days;
(d) detecting growth of Legionella bacteria on the dip-slide with a detection reagent, wherein the detection agent selectively identifies Legionella ; and
(e) quantifying the amount of viable Legionella bacteria and total heterotrophic aerobic bacteria in the sample.
2. The method of claim 1 , wherein the absorbent medium comprises agarose in a range of about 0.5 wt % to about 10.0 wt %.
3. The method of claim 1 , wherein the detection reagent is selected from the group consisting of an antibody, a mixture of antibodies, a probe, and combinations thereof.
4. The method of claim 3 , wherein the antibody is specific for Legionella selected from the group consisting of Legionella pneumophila serogroups 1-15 , L. longbeachae, L. bozemanii, L. micdadei, L. dumoffii, L. feeleii, L. wadsworthii , and L. anisa.
5. The method of claim 3 , wherein the probe is selected from the group consisting of a dye, a color enhancing dye, a phase contrast dye, a labeled probe, a fluorescent probe, a colorimetric probe, a nucleic acid probe, and combinations thereof.
6. The method of claim 1 , wherein the detection of Legionella is by an ultraviolet light source.
7. The method of claim 1 , wherein the absorbent medium is calibrated to absorb about 0.3 ml of the sample in about 60 seconds.
8. The method of claim 1 , wherein the detection reagent increases contrast for imaging the growth of Legionella.
9. The method of claim 1 , wherein the detection reagent kills Legionella.
10. The method of claim 9 , wherein the detection reagent comprises an antimicrobial compound.
11. The method of claim 10 , wherein the antimicrobial compound is selected from the group consisting of isothiazolone, glutaraldehyde, formaldehyde, ammonium quaternary compounds, dibromonitrilopropionamide, β-bromonitrostyrene, carbamate antimicrobials, tris-nitromethane antimicrobials, sodium benzoate, organic acids, ethanol, isopropanol, chlorhexidine gluconate, chlorhexicline diacetate, and o-phenyl phenol.
12. The method of claim 1 , wherein the growth of Legionella is detected as a microcolony, wherein the microcolony is about 10-500 microns in diameter.
13. The method of claim 1 , wherein the growth of Legionella is detected as a microcolony under a magnification in the order of about 2× to about 10×.
14. The method of claim 1 wherein the dip-slide is incubated for at least 24 hours.
15. The method of claim 14 wherein the dip-slide is incubated for at least 42 hours.
16. The method of claim 15 wherein the dip-slide is incubated for at least 48 hours.
17. The method of claim 16 , wherein the dip-slide is incubated for about 92 hours.
18. The method of claim 1 wherein the agent is selected from the group consisting of dyes, glycine, vancomycin, and polymyxin (DGVP); an inorganic or an organic acid; cephalothin, colistin, vancomycin and cycloheximide (CCVC); and combinations thereof.