Devices and methods for detecting norovirus on surfaces

Patent metadata

Field	Value
Publication number	US-10209256-B2
Application number	US-201415526939-A
Country	US
Kind code	B2
Filing date	Nov 27, 2014
Priority date	Nov 27, 2014
Publication date	Feb 19, 2019
Grant date	Feb 19, 2019

Abstract

Lateral-flow assay and time-resolved fluorescence technologies provide a sensitive tool for detecting norovirus particles in a sample. A flow-through assay device employs norovirus and norovirus G2 antibodies. The lateral-flow assay includes a conjugate pad having conjugated probes. The conjugated probes are particles modified with a binding member that is configured to bind with a norovirus. The particles also have a fluorescent label. A general method of detecting the virus includes (i) preparing a sample with contaminants, (ii) processing the sample and depositing it onto the assay device, and (iii) measuring the fluorescence signal.

First claim

What is claimed is:

1. A method for detecting a presence of norovirus residing in a test sample, said method comprising:
i) providing a flow-through assay device that comprises a porous membrane in fluid communication with a conjugate pad, the conjugate pad comprising conjugated probes having particles modified with a binding member configured to bind with the norovirus and containing a fluorescent label, wherein the fluorescent label has a fluorescence emission lifetime of greater than about 1 microsecond; and
wherein the porous membrane defines a detection zone comprising a test line within which is immobilized a norovirus antibody configured to bind with the norovirus, and a control line positioned downstream from the test line, wherein the control line has immobilized within a norovirus G2 antibody configured to bind with the conjugated probes;
ii) contacting the conjugate pad with the test sample and allowing the particles to flow to the detection zone;
iii) subjecting the test line to pulses of illumination to generate a detection signal and, after a certain period of time has elapsed following a pulse, measuring an intensity of the detection signal, wherein a fluorescence reader is employed to provide an illumination and measure the intensity of the detection signal,
iv) subjecting the control line to pulses of illumination to generate a calibration signal and after a certain period of time has elapsed following a pulse, measuring an intensity of the calibration signal; and
v) comparing the intensity of the detection signal to the intensity of the calibration signal, wherein the amount of the norovirus within the test sample is proportional to the intensity of the detection signal as calibrated by the calibration signal.

2. The method of claim 1 wherein the test sample comprises at least 10 5 to 10 9 norovirus particles in a running buffer.

3. The method of claim 1 wherein the test sample comprises at least 2.5×10 5 norovirus particles in a running buffer.

4. The method of claim 2 wherein the running buffer comprises:
10 mM 2-[4-(2-Hydroxyethyl)-1-piperazinyl]ethanesulfonic acid;
3% by weight S9 surfactant; and
1% by weight bovine serum albumin.

5. The method of claim 1 , wherein the binding member is selected from the group consisting of biotin and avidin; biotin and streptavidin; antibody-binding protein A and antibodies, carbohydrates and lectins; antibody-binding protein G and antibodies, carbohydrates and lectins; complementary nucleotide sequences; and complementary peptide sequences.

6. The method of claim 1 , wherein the binding member comprises a monoclonal antibody.

7. The method of claim 5 wherein the binding member is an analog having at least one epitope in common with the norovirus.

8. The method of claim 1 , wherein the fluorescent label comprises a lanthanide chelate of samarium, dysprosium, europium, terbium, or combinations thereof.

9. The method of claim 1 , wherein the fluorescent label is europium chelate.

10. A flow-through assay device for detecting norovirus in a sample, the device comprising:
a porous membrane in fluid communication with a conjugate pad, the conjugate pad comprising conjugated probes having particles modified with a binding member configured to bind with the norovirus and containing a fluorescent label, wherein the fluorescent label has a fluorescence emission lifetime of greater than about 1 microsecond; and
wherein the porous membrane defines a detection zone having a test line within which is immobilized a norovirus antibody configured to bind with the norovirus, and a control line positioned downstream from the test line, wherein the control line has immobilized within a norovirus G2 antibody configured to bind with the conjugated probes.

11. The flow-through assay device of claim 10 , wherein the binding member comprises a monoclonal antibody.

12. The flow-through assay device of claim 10 wherein the particles are mixed with a lanthanide chelate compound.

13. The flow-through assay device of claim 10 wherein the porous membrane is a nitrocellulose membrane having a flow rate or 90 to 200 seconds per 40 mm test sample.

14. The flow-through assay device of claim 10 wherein the porous membrane is a nitrocellulose membrane having a pore size ranging from 5 to 10 micrometers.

15. The flow-through assay device of claim 10 wherein the porous membrane is a nitrocellulose membrane having a thickness of 125 to 200 micrometers.

Assignees

• Kimberly Clark Co

Inventors

• Do Bao Trong
• Hofmekler Jonathan
• Morales Cesar A
• Koenig David W
• Huang Yang
• He Aimin

Classifications

• G01N2469/10

  Detection of antigens from microorganism in sample from host · CPC title

• G01N33/558

  using diffusion or migration of antigen or antibody {(immunochromatographic test strips G01N33/54387)} · CPC title

• G01N2333/08

  RNA viruses · CPC title

• G01N33/56983 Primary

  Viruses · CPC title

• G01N33/54388

  based on lateral flow · CPC title