SAMPLE PREPARATION AND SPECIFIC CAPTURE FOR MULTIPLEX DETECTION OF TARGET ANALYTES (i.e., BACTERIA, VIRUSES, ETC.)

Abstract

A method and apparatus for the rapid and reliable preparation of a sample for use in testing for target analytes such as bacteria, viruses, toxins and pathogenic agents in various products. A sample for testing the target analyte is collected from various sources. The method for sample preparation provides for an express process for preparing collected samples for testing. The collected sample may be concentrated by centrifugation, filtration, or other means suitable for sample concentration, homogenized with the addition of a broth and enriched for specified period of time. Immunomagnetic separation of the sample occurs with receptor-coated magnetic microspheres in different test-specific formulations (singleplex or multiplex). An automatic testing system is disclosed which includes a biological testing cassette, in which testing of the sample occurs using liquid crystal diagnostic methodologies.

Claims

1. A method for preparing a sample containing multiple target analytes of antigenic materials for detection of the analytes comprising: homogenizing and incubating the sample with an enrichment media; adding magnetic microspheres having different preselected formulations and a solution to the sample to form a mixture, the magnetic microspheres being structured and arranged to bind to specific preselected antigenic materials contained within the mixture; precipitating the antigenic materials out of the mixture when the antigenic materials becomes specifically bound to the magnetic microspheres to form a precipitate and a supernatant; discarding the supernatant; and isolating the precipitate to produce a prepared sample.

2. The method of claim 1, wherein the precipitating step further comprises the step of applying of a magnetic field to the precipitate.

3. The method of claim 1, further comprising the steps of: washing the prepared sample in a PBS or PBST solution to form a mixture with the magnetic microspheres; applying a magnetic field to the mixture to stabilize the magnetic microspheres; and collecting the antigen-containing materials to form an isolated prepared sample.

4. The method of claim 1, wherein the solution is a buffer solution.

5. The method of claim 1, wherein the mixture further comprises a surfactant.

6. The method of claim 5, wherein the surfactant is a nonionic surfactant.

7. The method of claim 1, wherein the magnetic microspheres are comprised of a material selected from the group consisting of iron, iron oxide, iron nitride, iron carbide, nickel and cobalt, and mixtures and alloys thereof.

8. The method of claim 1, wherein the magnetic microspheres are paramagnetic microspheres.

9. The method of claim 1, wherein the magnetic microspheres are non-functionalized microspheres.

10. The method of claim 9, wherein the magnetic microspheres are plain polystyrene beads

11. The method of claim 1, wherein the magnetic microspheres have an average diameter within the range of approximately 0.1 m to approximately 100 m.

12. The method of claim 1, wherein the magnetic microspheres have an average diameter within the range of approximately 1 m to approximately 50 m.

13. The method of claim 12, wherein the magnetic microspheres have an average diameter within the range of approximately 1 m to approximately 5 m.

14. The method of claim 1, wherein the antigenic materials are selected from the group consisting of immunoglobulins, proteins, (lipo)polysaccharides, or enzymes.

15. The method of claim 1, wherein the prepared sample is structured and arranged for use in liquid crystal diagnostics.

16. The method of claim 1, wherein the magnetic microspheres are functionalized microspheres.

17. The method of claim 16, wherein the functionalized microspheres are coated with an affinity ligand.

18. The method of claim 1, wherein the sample is a meat, produce, pet food, a swab/surface, rinse or fecal sample.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0012] FIG. 1.A. is an illustration of single antibody conjugated microspheres in accordance with an embodiment;

[0013] FIG. 1.B. is an illustration of the single antibody conjugated microspheres of FIG. 1.A. added to a test sample containing a potential target material in accordance with an embodiment;

[0014] FIG. 1.C. is an illustration of the aggregates formed by the antibody conjugated microspheres after binding to a targeted material in accordance with an embodiment;

[0015] FIG. 2 is a top cross-sectional view of a liquid crystal detection medium for detecting aggregates formed by antibody conjugated microspheres after binding to a targeted material in accordance with an embodiment;

[0016] FIG. 3.A. is an illustration of multiple, antibody conjugated microspheres of different preselected formulations in accordance with an embodiment;

[0017] FIG. 3.B. is an illustration of multiple different antibody conjugated microspheres of FIG. 3.A. added to a test sample containing a potential target material in accordance with an embodiment;

[0018] FIG. 3.C. is an illustration of the aggregates formed by the multiple different antibody conjugated microspheres after binding to a targeted material in accordance with an embodiment;

[0019] FIG. 4. is a graphical presentation of antibody detection of Escherichia coli O26 with one, two and three non-specific antibodies illustrating that the detection of an organism is not impeded by the combination of microspheres conjugated with different antibodies in accordance with the embodiments of the present invention;

[0020] FIG. 5.A. illustrates a format of a multiple antibody conjugated microsphere sample design having a first combination of antibody conjugated microspheres and a test sample distributed in a first panel of a multiplex microsphere test kit in accordance with an embodiment;

[0021] FIG. 5.B. illustrates a second panel of a multiplex microsphere test kit having a combination of antibody conjugated microspheres and a test sample distributed therein in accordance with an embodiment;

[0022] FIG. 5.C. illustrates a negative control panel of the multiplex microsphere test kit of FIGS. 5.A and 5.B in accordance with an embodiment; and

[0023] FIG. 6 is an example of a multiplex antibody conjugated test kit showing a bio-cassette and test sample containers in accordance with an embodiment.

DETAILED DESCRIPTION

[0024] Before proceeding with the detailed description, it is to be appreciated that the present teaching is by way of example only, not by limitation. The concepts herein are not limited to use or application with a specific type of apparatus, system or method for the detection of target analytes for rapid identification, diagnosis and treatment of contaminants in various materials. Thus, although the instrumentalities described herein are for the convenience of explanation, shown and described with respect to exemplary embodiments, it will be appreciated that the principles herein may be applied equally in other types of analyte detection apparatus, systems and methods without departing from the scope of the present invention.

[0025] Referring now to the drawings, the present invention comprises a method and an apparatus for preparation of a sample for use in testing for a wide range of harmful bacteria. A sample for testing analytes, such as E. coli O157:H7, non-O157 Shiga-toxin producing E. coli, Salmonella spp., or Listeria spp., is collected from various sources. The sources can include raw or cooked food, animal carcasses, pet food, or food production surface/environmental samples. The method for sample preparation provides an expedited process for preparing collected samples for testing. Certain samples may be concentrated via centrifugation or filtration before or after enrichment. Samples are homogenized with a stomacher blender or mixed by hand agitation of the containment vessel with the addition of an enrichment broth. The samples are enriched using media at a temperature that is optimal for the specific target bacteria (e.g., 46 C. prewarmed media added to enrich E. coli O157:H7), and then placed in a warming device to maintain a constant, optimized growth temperature (typically 30-42 C.). Once enriched to an optimal time, immunomagnetic separation of the sample occurs with plain magnetic polymer beads or microspheres, such as non-functionalized plain polystyrene beads. Alternatively, functionalized polymer beads, such as carboxyl polymer beads or affinity ligands (receptor-coated) (e.g., antibody, aptamer, bacteriophage, etc.) magnetic microspheres of a specific size appropriate for detection in a detection system such as the Crystal Diagnostics Xpress system may be used. By way of example and not of limitation, the functionalized or coated magnetic microspheres may be streptavidin or latex coated magnetic polymer beads to which surface a receptor is then chemically conjugated to act as a receptor for the intended target analyte. The plain or receptor-coated magnetic microspheres may be formulated for a single analyte target, a singleplex format as shown in FIGS. 1.A, 1.B and 1.C, or combined into an advanced formulation for detection of multiple targets, a multiplex format as shown in FIGS. 3.A, 3.B and 3.C.

[0026] It has been shown that the multiplex formulation of the receptor-coated magnetic microspheres does not impede the detection of the target analyte(s) as best illustrated by the antibody detection curves of FIG. 4). These curves plot the number of total aggregates (y-axis) vs. the number of microspheres per aggregate (x-axis) for the antibody detection of Escherichia coli O26 as a model organism under three different conditions: Plot A is the combination of Escherichia coli O26 antibody conjugated microspheres with two other non-specific antibody conjugated microspheres; Plot B is the combination of Escherichia coli O26 antibody conjugated microspheres with one other non-specific antibody conjugated microsphere; and Plot C is the Escherichia coli O26 antibody conjugated microspheres alone.

[0027] Returning again to the methodology of the instant invention, a biological testing cassette, in which testing of the sample will occur, is then prepared (or the receptor coated microspheres might be incorporated into the testing cassette). The cassette can be part of an automated testing system for testing of harmful bacteria in food, surface or environmental samples using the above-referenced platform, such as the microsphere test kit and its components shown in FIGS. 5.A, 5.B and 5.C and in FIG. 6. Examples of such automated testing systems are disclosed in U.S. patent application Ser. Nos. 12/373,051 and 12/398,144, both of which are hereby incorporated herein by reference.

Sample Collection

[0028] Food and surface/environmental samples from sources such as ground beef, produce (such as lettuce or spinach), pet food, food production surfaces and other environments can be collected for sample preparation according to the present invention. For example, in the case of testing ground beef for harmful bacteria, approximately 25-375 g of ground beef product is collected. In the case of testing a carcass, a food production surface, or an environment (e.g., machine (stainless steel), table (plastic), or floor (ceramic tile)), a sponge, swab or vacuum technique is utilized. After the sponge or swab contacts the surface, the sponge or swab is then directly enriched in an enrichment media, as will be described below in greater detail. Before or after sample enrichment, the sample can be concentrated by high-speed centrifugation or filtration to remove excess liquid. Up to approximately 500 ml of concentrated sample material, for example, can be used. Similarly, the sample from the carcass can be added to enrichment broth, and grown to detectable concentrations.

Enrichment

[0029] A range of 25-375 g of the collected sample is transferred into a sample bag for homogenization either using a stomacher or by hand mixing. Alternatively, a surface swab may be placed in a sample bag for mixing. The sample bag is preferably a filtered bag (e.g., from VWR International LLC or Nasco (Whirl-Pak)), which includes a filter membrane dividing the inside thereof into two compartments. Liquid can be extracted from the non-sample side of the compartment for division into aliquots. An enrichment broth (e.g., modified Trypticase Soy Broth plus Novobiocin (mTSB+n) for E. coli O157:H7) is added to the collected sample in the sample bag. In this embodiment, approximately 1 to 3 (and as many as 10) times of pre-warmed (e.g., 42-46 C.) enrichment media is added to 1 part of the collected sample in the sample bag (wt/wt, vol/wt or vol/vol, e.g., approximately 1000 mL mTSB+n to 325 g of raw ground beef). The sample bag is then pummeled in the stomacher blender (or by hand) for approximately 30 sec. and then incubated at approximately 42 C. for approximately 9 hours (enrichment time is dependent on sample size and ranges from 7 to 24 hours for 25 to 325 g samples, respectively) in an incubator. After enrichment, up to 50 mL of the liquid fraction from the bag is poured out of the sample bag and into a sterile conical tube (or pipetted directly to the microspheres for processing). The conical tube is then capped and left undisturbed for approximately 5-10 min. A similar process is used for surface/environmental samples (though a smaller volume of media (approximately 10-50 mL) is added to the sample swab and it can be enriched in various types of containers).

Immunomagnetic Separation Materials

[0030] The present invention utilizes paramagnetic microspheres (from this point forward, simply described as magnetic microspheres) to prepare the sample for testing. Referring now to FIGS. 1.A.-1.C., a method and apparatus for the detection of a single analyte target, also referred to herein as a singleplex format or singleplex method and apparatus 10, specific for one target, is shown. In the singleplex format, a plurality of single antibody conjugated paramagnetic microspheres 12 in FIGS. 1.A and 1.6 are prepared as described in greater detail below for the detection of a target material 14 (FIG. 1.B.). The magnetic microspheres may comprise iron, iron oxide, iron nitride, iron carbide, nickel and cobalt and mixtures and alloys thereof. In another embodiment, referred to herein as a multiplex format 20 depicted in FIGS. 3.A.-3.C., a plurality of magnetic microspheres, having different preselected formulations illustrated by exemplary, microspheres 22, 24 and 26, may be combined for detection of multiple analyte targets in the same sample.

[0031] In the singleplex format, the magnetic microspheres 12 detect and bind to the single target 14 (for example, bacteria, a virus or a pathogen) to form an aggregate 16, as shown in FIG. 1.C. The aggregate may be dispersed into and detected in a liquid crystal medium 18, as best shown in FIG. 2. In the multiplex detection format, as shown in FIGS. 3.A, 3.B and 3.C the magnetic microspheres 22, 24, and 26 combine with analyte targets 30 to form aggregates 32 (FIG. 3.C.). Dispersed in a liquid crystal medium 18 as discussed above with respect to the singleplex technique, the presence of aggregates 32 may be detected.

[0032] The magnetic microspheres may be prepared with a receptor (antibody, aptamer, etc.) in various ways. By way of example, and not of limitation, in an embodiment, approximately 100 to 200 l of suspended antibody microsphere-mixture, is added to a deep well plate, as is known in the art. The concentration of microspheres may range from 110.sup.6 to 110.sup.7 per target depending on kit and application). Approximately, 100 to 200 l of IgG-conjugated (e.g., purified goat IgG from Jackson ImmunoResearch Laboratories Inc.) and blocked (e.g., with bovine serum albumin) magnetic microspheres may be used for the negative microsphere control. For example, the magnetic microspheres discussed herein can be Dynal microspheres from ThermoFisher Scientific (Waltham, Mass.), or other manufacturer's microspheres having similar properties.

Immunomagnetic Separation

[0033] Using a pipette, for example, approximately 1-1.4 ml aliquots of supernatant (enriched collection sample) 38 are collected. For some sample types, collected aliquots can be centrifuged at 1000-5000g for the optimal time (40-120 sec). As shown in FIGS. 5.A., 5.B and 5.C., approximately 100-600 l of the supernatant is transferred to containers or receptacles 40, 42 and 44 in a deep-well plate (not shown). Preselected test antibody magnetic microspheres A, B and C are added to receptacle 40, (FIG. 5.A) and D, E and F are added to receptacle 42 (FIG. 5.B) respectively. Negative control antibody magnetic microspheres G are added to receptacle 44, as shown in FIG. 5.C. Alternatively, some sample types may require no centrifugation before addition to the antibody magnetic microspheres.

[0034] The deep-well plate with the enriched collection sample and magnetic microspheres is incubated on a microplate vortex mixer for approximately 5-30 min. at room temperature and at a slow mixing speed. The mixer may be a microplate vortex mixer from Thermo Scientific, Inc., for example.

[0035] The deep-well plate is then transferred to a 96-well plate bar magnet (e.g., V&P Scientific) for approximately 3 min. to permit the microspheres to be captured from the sample matrix. While the magnetic microspheres remain held at the inner wall by the magnet, the liquid in the deep-well plate is removed by a pipetting and replaced with 1000 l of wash buffer such as phosphate buffered saline (PBS) or PBST, i.e., PBS with Tween-20 (0.01-0.03%), for example.

[0036] The deep-well plate remains on the magnet and is permitted to rest for approximately 2 minutes, before the supernatant is again removed while the microspheres are retained. Alternatively, and depending on the sample matrix and the background microflora, the deep-well plate may be returned to the mixer for additional mixing with the wash buffer, or multiple exchanges of wash buffer may be incorporated.

[0037] After final collection of the magnetic microspheres on the magnet and removal of the entire volume of wash buffer, the deep-well plate is then removed from the magnet and the microspheres are resuspended in an appropriate volume (e.g., 20-100 l) depending on the desired concentration.

[0038] The sample is then transferred to appropriate strip micro-tubes or microplates for mixing with the detection medium for analysis.

Preparation for Crystal Diagnostics

[0039] Liquid crystal with a buffer solution (MilliQ water, Sterile DNA/RNA quality water, or similar) is mixed (vortexed) and allowed to rest for a prescribed period of time (e.g. 20 min) at 60 C. until fully dissolved. Then, the temperature of the liquid crystal in suspension is lowered to 40-45 C. Thereafter, it is ready for mixing with the magnetic microspheres. Approximately 20-100 l (5 l) of the solution is aliquoted to a separate 200 l tube, for example.

[0040] The immunomagnetic separated sample (washed magnetic microspheres), prepared as described above, is briefly mixed using pipette mixing to homogenize the sample and re-suspend the microspheres. Approximately 4-20 l of the sample is then added to the 20-100 l, respectively, of liquid crystal and buffer solution and pipette mixed.

[0041] As shown generally in FIG. 6, a cassette 60 is used to detect the analyte. The cassette includes a plurality of separate, mateable housings 62, forming multiple reservoirs 64 with respective inlets for receiving the sample. A second portion of the cassette includes multiple channels 66 with inlets 68 for receiving the sample, which are operatively connected to the receiving inlets. Specifically, each of the inlets is tapered so as to fit within the inlet of the other mateable housing, which forms a concave cavity sized and configured to receive the first inlet. Approximately 50 l of the liquid crystal-sample mixture is loaded into each reservoir desired for use.

[0042] The cassette is then inserted into a crystal diagnostic device, such as The Crystal Diagnostic Xpress Reader (not shown), containing a liquid crystal medium such as medium 18 illustrated in FIG. 2, to detect any analyte which may be in the sample using the diagnosis medium by methods described in U.S. patent application Ser. Nos. 12/373,051 and 12/398,144, for example.

General Interpretation of Terms

[0043] In understanding the scope of the present invention, the term comprising and its derivatives, as used herein, are intended to be open ended terms that specify the presence of the stated features, elements, components, groups, integers, and/or steps, but do not exclude the presence of other unstated features, elements, components, groups, integers and/or steps. The foregoing also applies to words having similar meanings such as the terms, including, having and their derivatives. Finally, terms of degree such as substantially, about and approximately as used herein mean a reasonable amount of deviation of the modified term such that the end result is not significantly changed. For example, these terms can be construed as including a deviation of at least 5% of the modified term if this deviation would not negate the meaning of the word it modifies.

[0044] It will be apparent to those skilled in the art from this disclosure that various changes and modifications can be made herein without departing from the scope of the invention as defined in the appended claims. Furthermore, the foregoing descriptions are provided for illustration only, and not for the purpose of limiting the invention as defined by the appended claims and their equivalents.