Loop-mediated isothermal amplification (LAMP) based assay for detecting microbes

Patent metadata

Field	Value
Publication number	US-12037650-B2
Application number	US-202217708169-A
Country	US
Kind code	B2
Filing date	Mar 30, 2022
Priority date	Jan 2, 2018
Publication date	Jul 16, 2024
Grant date	Jul 16, 2024

Abstract

A method and system are disclosed for detecting microbial pathogens in a sample suspected of containing the pathogens. The method includes combining loop-mediated isothermal amplification (LAMP) reagents and a polymer gel, such as a hydrogel, together with the sample to form a mixture. The gel polymerizes over a short time to immobilize the viral particles within the mixture. If target DNA/RNA are present in the sample, amplicons are produced. The target microorganisms are detected by visually detecting the presence or absence of the amplicons. The target microorganism concentrations may be determined based on the number of fluorescent amplicon dots after the reaction using a smartphone or a fluorescent microscope. The method may be employed for rapidly and inexpensively quantifying microbial pathogens in environmental water samples with high sensitivity.

First claim

What is claimed is:

1. A method of detecting a target microorganism in a sample suspected of containing the target microorganism, comprising:
combining loop mediated isothermal amplification (LAMP) reagents comprising a plurality of primers including a fluorophore labeled primer, a polyethylene glycol (PEG) hydrogel at a concentration of about 10% (w/v) of the total amount of LAMP reagents and hydrogel, and the sample to form a mixture, the hydrogel for immobilizing the microorganisms within the mixture, wherein the PEG hydrogel is formed through Michael addition between a four-arm PEG acrylate and a thiol-PEG-thiol at a mole ratio of about 1:2, and wherein the crosslinking of the PEG hydrogel is tuned to form a predetermined mesh size and a predetermined molecular weight between crosslinkers in the PEG hydrogel that restricts diffusion of DNA/RNA templates of the target microorganism within the PEG hydrogel while allowing free diffusion within the PEG hydrogel of molecules having a MW<100 kDa; and
detecting the presence or absence of one or more amplicons that are produced as a result of a LAMP reaction amplifying the DNA/RNA of the target microorganism if the target microorganism is present in the mixture, wherein the presence of the amplicons is indicative of the presence of the target microorganism in the sample and the absence of the amplicons is indicative of the absence of the target microorganism in the sample.

2. The method of claim 1 , further comprising:
quantifying a virus concentration in the sample based on the number of detected amplicons present after the LAMP reaction.

3. The method of claim 1 , wherein each of the target microorganism corresponds to one amplicon.

4. The method of claim 1 , wherein the microorganism is a virus, a bacteriophage, a coliphage, a protozoa, or a bacteria.

5. The method of claim 1 , further comprising:
allowing the polymer gel to polymerize in the mixture at a predetermined temperature for a predetermined time period; and
incubating the mixture following the polymer gel polymerization step.

6. The method of claim 1 , further comprising:
adding a primer-dye and primer-quencher duplex to the mixture.

7. The method of claim 1 , further comprising:
staining the mixture with a dye.

8. The method of claim 1 , wherein the sample is selected from the group consisting of environmental water, soil, feces, urine, blood, and any combination of the foregoing.

9. A method of detecting bacteriophage in a sample suspected of containing the bacteriophage, the method comprising:
combining loop mediated isothermal amplification (LAMP) reagents comprising a plurality of primers including a fluorophore labeled primer, a polyethylene glycol (PEG) hydrogel at a concentration of about 10% (w/v) of the total amount of LAMP reagents and hydrogel, and the sample to form a mixture, the hydrogel for immobilizing the bacteriophage within the mixture, wherein the PEG hydrogel is formed through Michael addition between a four-arm PEG acrylate and a thiol-PEG-thiol at a mole ratio of about 1:2, and wherein the crosslinking of the PEG hydrogel is tuned to form a predetermined mesh size and a predetermined molecular weight between crosslinkers in the PEG hydrogel that restricts diffusion of DNA/RNA templates of the target microorganism within the PEG hydrogel while allowing free diffusion within the PEG hydrogel of molecules having a MW<100 kDa;
incubating the mixture; and
detecting the presence or absence of one or more amplicons that are produced as a result of a LAMP reaction amplifying the DNA/RNA of the bacteriophage if the bacteriophage are present in the mixture, wherein the presence of the amplicons is indicative of the presence of the bacteriophage in the sample and the absence of the amplicons is indicative of the absence of the bacteriophage in the sample.

10. The method of claim 9 , wherein the bacteriophage is coliphage MS2 infecting Escherichia coli.

11. The method of claim 9 , wherein the sample is selected from the group consisting of environmental water, soil, feces, urine, blood, and any combination of the foregoing.

12. The method of claim 9 , further comprising:
allowing the polymer gel to polymerize in the mixture at a predetermined temperature for a predetermined time period; and
incubating the mixture following the polymer gel polymerization step.

13. The method of claim 9 , further comprising:
adding a primer-dye and primer-quencher duplex to the mixture.

14. The method of claim 1 , wherein the four-arm PEG acrylate has a molecular weight (MW) of 10K.

15. The method of claim 1 , wherein the thiol-PEG-thiol has a molecular weight (MW) of 3.4K.

16. The method of claim 9 , wherein the four-arm PEG acrylate has a molecular weight (MW) of 10K.

17. The method of claim 9 , wherein the thiol-PEG-thiol has a molecular weight (MW) of 3.4K.

Assignees

• California Inst Of Techn

Inventors

• Huang Xiao
• Hoffmann Michael R

Classifications

• C12Q1/6844

  Nucleic acid amplification reactions · CPC title

• C12Q1/70

  involving virus or bacteriophage {(immunoassay for viruses G01N33/56983)} · CPC title

• G02B21/16

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G02B21/34

  Microscope slides, e.g. mounting specimens on microscope slides · CPC title

• C12Q1/689 Primary

  for bacteria · CPC title