Method and device for combined detection of viral and bacterial infections
View Patent ↗A lateral flow assay detects and differentiates between viral and bacterial infections. A combined point of care diagnostic device tests markers for viral infection and markers for bacterial infection, to effectively assist in the rapid differentiation of viral and bacterial infections. In one preferred embodiment, the bacterial marker is CRP. In another preferred embodiment, the viral marker is MxA. In some embodiments, it is unnecessary to lyse the cells in the sample prior to applying it to the device.
1. A method of analyzing a sample for a presence of CRP and MxA, comprising the steps of:
a) collecting a sample;
b) transferring the sample to a sample analysis device comprising:
a reagent zone comprising:
at least one first reagent specific to CRP such that, when CRP present in the sample contacts the first reagent, a first labeled complex forms; and
at least one second reagent specific to MxA such that, when MxA present in the sample contacts the second reagent, a second labeled complex forms;
a lysis zone comprising at least one lysis agent comprising approximately 1% to 6% weight/volume CHAPS and approximately 0.5% to 2% weight/volume NP40, wherein the lysis agent lyses the sample on the device; and
a detection zone comprising a first binding partner which binds to the first labeled complex; and a second binding partner which binds to the second labeled complex; and
c) analyzing the sample for a presence of CRP and/or MxA;
wherein steps b) and c) are performed in approximately ten minutes or less.
2. The method of claim 1 , wherein the presence of MxA or CRP is indicated by a test line located in the detection zone visible to the naked eye.
3. The method of claim 2 , wherein the presence of MxA is indicated by a first test line located in the detection zone and the presence of CRP is indicated by a second test line located in the detection zone, wherein the first test line is spatially separate from the second test line on the sample analysis device.
4. The method of claim 3 , wherein the first test line displays a first color when positive and the second test line displays a second color different from the first color when positive.
5. The method of claim 2 , wherein the presence of MxA is indicated by a first color on a test line and the presence of CRP is indicated by the a second color located on the test line in the same space within the detection zone on the sample analysis device such that a third color is formed when both the first color and the second test line are positive on the test line.
6. The method of claim 1 , wherein the sample comprises leukocytes and the method further comprises the step of lysing leukocytes on the sample analysis device.
7. The method of claim 1 , wherein the sample is taken from a location selected from the group consisting of: peripheral blood, nasopharyngeal aspirates, tears, spinal fluid, and middle ear aspirates.
8. The method of claim 1 , wherein a threshold concentration of CRP in a sample that elicits a positive result is at least approximately 15 mg/L.
9. The method of claim 1 , wherein a threshold concentration of MxA in a sample that elicits a positive result is at least approximately 15 ng/ml.
10. The method of claim 1 , wherein the sample analysis device is a lateral flow chromatography test strip.
11. A method of analyzing a sample for a presence of CRP and MxA, comprising the steps of:
a) collecting a sample;
b) transferring the sample to a sample analysis device comprising:
a reagent zone comprising:
at least one first reagent specific to CRP such that, when CRP present in the sample contacts the first reagent, a first labeled complex forms; and
at least one second reagent specific to MxA such that, when MxA present in the sample contacts the second reagent, a second labeled complex forms;
a lysis zone comprising at least one lysis agent comprising 100 mM HEPES buffer (pH 8.0) including 5% CHAPS and 2% NP-40 with 150 mM Sodium Chloride, 0.1% BSA, and 0.1% Sodium Azide, wherein the lysis agent lyses the sample on the device; and
a detection zone comprising a first binding partner which binds to the first labeled complex; and a second binding partner which binds to the second labeled complex; and
c) analyzing the sample for a presence of CRP and/or MxA;
wherein steps b) and c) are performed in approximately ten minutes or less.
12. The method of claim 11 , wherein the presence of MxA or CRP is indicated by a test line located in the detection zone visible to the naked eye.
13. The method of claim 12 , wherein the presence of MxA is indicated by a first test line located in the detection zone and the presence of CRP is indicated by a second test line located in the detection zone, wherein the first test line is spatially separate from the second test line on the sample analysis device.
14. The method of claim 13 , wherein the first test line displays a first color when positive and the second test line displays a second color different from the first color when positive.
15. The method of claim 12 , wherein the presence of MxA is indicated by a first color on a test line and the presence of CRP is indicated by a second color located on the test line in the same space within the detection zone on the sample analysis device such that a third color is formed when both the first color and the second color are positive on the test line.
16. The method of claim 11 , wherein the sample comprises leukocytes and the method further comprises the step of lysing the leukocytes on the sample analysis device.
17. The method of claim 11 , wherein the sample is taken from a location selected from the group consisting of: peripheral blood, nasopharyngeal aspirates, tears, spinal fluid, and middle ear aspirates.
18. The method of claim 11 , wherein a threshold concentration of CRP in a sample that elicits a positive result is at least approximately 15 mg/L.
19. The method of claim 11 , wherein a threshold concentration of MxA in a sample that elicits a positive result is at least approximately 15 ng/ml.
20. The method of claim 11 , wherein the sample analysis device is a lateral flow chromatography test strip.