Method for detecting the presence of water born pathogens and indicator microorganism

Abstract

The present invention relates to a method for detecting the presence of water born pathogens and indicator microorganism including bacteria from water sample by selecting the target gene carried in template DNA by amplifying the target DNA using specific primers with biotinylated tag consist of all or a substantial part of 5′-CTGATCGAATGGCTGCCAGGCTCC-3′ and 5′-CAACCAGACGATAGTTATCACGCA-3′ and taq DNA polymerase to get desired biotinylated tagged probe followed by hybridization of biotinylated tagged probe with target gene in template DNA followed by enzyme coupled reaction.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

The following Detailed Description, given by way of example, but not intended to limit the invention to specific embodiments described, may be understood in conjunction with the accompanying drawings, in which:

FIG. 1 shows a glass slide protocol where the E.coli template has been mobilized on activated glass surface and assayed as been optimized for nylon membrane.

FIG. 2 shows an extension of glass-slide immobilization protocol where the template is immobilized on nylon membrane that can be easily detected by the presence of blue color.

Claims

1. A method for detecting the presence of water born pathogens and indicator microorganism including bacteria from water sample, wherein the said method comprising the steps of: a) providing water sample and concentrating into suitably sized concentrate of containing target indicator microorganisms in said water sample;b) isolating the template DNA from target cells obtained from step (a);c) selecting the target gene carried in said template DNA obtained from step (b) by amplifying the target DNA by using appropriate biotinylated tagged primers and taq DNA polymerase to get desired biotinylated tagged probe containing target gene;d) hybridizing the biotinylated tagged probe obtained from step (c) with target gene present in the said template DNA followed by enzyme coupled reaction as resulting by change in color wherein blue color indicates the presence of indicator microorganism in the test sample and absence of blue color indicates the absence of said microorganism in the test sample.

2. A method as claimed in claim 1, wherein the water sample is collected from a polluted source selected from any contaminated drinking water.

3. A method as claimed in claim 1, wherein the target cell used are selected from the group consisting of enteric bacteria such as E.coli, Salmonella, Vibrio etc.

4. A method as claimed in claim 1, wherein the said target gene used are selected from the group consisting of lamB gene of E.coli, InvA gene, PhoE gene, SpvA gene and SpvB gene of Salmonella and Ctx gene of Vibrio etc.

5. A method as claimed in claim 1, wherein the primer sequences used for detection of presence of enteric pathogens are selected from the group consisting of: a) Upper: 5′-CTGATCGAATGGCTGCCAGGCTCC-3′ (SEQ ID NO: 1) and Lower: 5′-CAACCAGACGATAGTTATCACGCA-3 (SEQ ID NO: 2) for detection of E-Coli based on target gene lamB;b) Upper: 5′-CCTGATCGCACTGAATATCGTACTG-3′(SEQ ID NO: 3) and Lower: 5′-GACCATCACCAATGGTCAGCAGG-3′(SEQ ID NO: 4) for detection of Salmonella based on target gene InvA;c) Upper: 5′-CTCAGACGGGATTTGTTAGGCACG-3′(SEQ ID NO: 5) and Lower: 5′-GATCTTGGAGCATTCCCACAACC-3′(SEQ ID NO: 6) for detection of Vibrio based on target gene CtxA;d) Upper: 5′-AGCGCCGCGGTACGGGCGATAAA-3′(SEQ ED NO: 7) and Lower: 5′-ATCATCGTCATTAATGCCTAACGT-3′(SEQ ID NO: 8 for detection of Salmonella based on target gene phoE;e) Upper: 5′-TGTATGTTGATACTAAATCC-3′(SEQ ID NO: 9) and Lower: 5′-CTGTCATGCAGTAACCAG-3′(SEQ ID NO: 10) for detection of Salmonella based on target gene spvA;f) Upper: 5′-ATGAATATGAATCAGACCACC-3′(SEQ ID NO: 11) and Lower: 5′-GGCGTATAGTCGGCGGTTTTC-3′(SEQ ID NO: 12) for detection of Salmonella based on target gene spvB;

6. A method as claimed in claim 1, wherein the template DNA is isolated from target cell by dipping the disc containing said cells in 0.5N NaOH solution for 2-5 minutes followed by similar treatment using Tris solution wherein the ratio of NaOH solution and Tris solution used 1:1.

7. A method as claimed in claim 1, wherein the template DNA used is isolated from commercially available strain Escherichia strain ATCC 35150.

8. A method as claimed in claim 1, wherein the target gene used is lamB gene, present in all species of the genera Escherichia.

9. A method as claimed in claim 1, wherein the primer sequence used is consist of all or a substantial part of 5′-CTGATCGAATGGCTGCCAGGCTCC-3′(SEQ ID NO: 1) and 5′-CAACCAGACGATAGTTATCACGCA-3′(SEQ ID NO: 2).

10. A method as claimed in claim 1, wherein the generated biotinylated tagged probe has a size of approximately 309 bp.

11. A method as claimed in claim 1, wherein the pre-hybridazation is carried out with hybridization buffer for 15 minutes at room temperature followed by hybridization wherein denatured lamB probe in sterilized distilled water is added in hybridization buffer.

12. A method as claimed in claim 1, wherein the denaturati on of lamB probe as claimed in claim 11 is carried out at about 95 degree C. for 5-6 minutes.

13. A method as claimed in claim 1, wherein non-specific signals is blocked by using blocking solution of BSA in TBS at about 55 degree C. for 10-15 minutes

14. A method as claimed in claim 1, wherein the signal is generated by diluting Streptavidin-Alkaline phosphatase in the ratio ranging from 1:2000 fold in BSA in TBS at room temperature with biotinylated-hybridized probe.

15. A method as claimed in claim 1, wherein excess and non-specifically bound Streptavidin-Alkaline phosphatase is removed by washing with Tris-NaCl SDS buffer at pH-8.0.

16. A method as claimed in claim 1, wherein signal amplification has been devised with substrate and amplifier for Streptavidin-Alkaline phosphatase as a powder is freshly mixed separately with dilution buffer.

17. A method as claimed in claim 1, wherein the substrate used is reduced nicotinamide adenine dinucleotide phosphate.

18. A method as claimed in claim 1, wherein the amplifiers used are selected from the group consisting of alcohol dehydrogenase and diaphorase

19. A method as claimed in claim 1, wherein the blue color is developed which indicates the presence of water born pathogens and indicator microorganism including bacteria wherein the said color is stabilized by using KOH and acetone in the ratio 5:3.

20. A method as claimed in claim 1, wherein an enzyme-coupled reaction with hybridization increases the sensitivity of the detection protocol.