AU2013203143B2 - Materials and methods for capture of pathogens and removal of aurintricarboxylic acid from a sample - Google Patents

Abstract

The present invention concerns methods and materials for extracting infectious pathogens from a sample, such as blood, comprising the steps of creating a fibrin aggregate confining the pathogens and introducing a fibrin lysis reagent to expose the pathogens for analysis. The fibrin lysis reagent is preferably composed of plasminogen and streptokinase frozen in coincident relation until the fibrin lysis reagent is needed whereby streptokinase enzymatically reacts with plasminogen to form plasmin upon thawing. Preferably, the plasminogen is suspended in an aqueous salt solution prior to freezing including NaCI and Na3PO4. The subject invention also concerns materials and methods for efficiently removing ATA from a sample comprising nucleic acid composition. The subject methods provide a nucleic acid composition sufficiently free of ATA such that a RT-PCR reaction and other reactions involving reverse transcriptase can be performed.

Description

2013203143 09 Apr 2013 AUSTRALIA Patents Act 1990

Regulation 3.2

Complete Specification Standard Patent

APPLICANT: University of South Florida Invention Title: MATERIALS AND METHODS FOR CAPTURE AND REMOVAL OF AURINTRICARBOXYLIC SAMPLE

OF PATHOGENS ACID FROM A

The following statement is a full description of this invention, including performing it known to me: the best method of 2013203143 09 Apr 2013 1

DESCRIPTION MATERIALS AND METHODS FOR CAPTURE OF PATHOGENS AND REMOVAL OF AURINTRICARBOXYLIC ACID FROM A SAMPLE 5

Cross-Reference to Related Applications

This application claims the benefit of U.S. application Serial No. 10/604,779, filed August 15, 2003, and U.S. Provisional application Serial No. 60/481,892, filed January 14, 2004, the disclosure of each of which is incorporated herein by reference in its entirety. 10

Background of the Invention

The threat of bioterrorism (BT) and biological warfare presents challenges for the clinical setting that are best met with rapid and sensitive technologies to detect BT agents. Peripheral blood samples could contribute to early and specific clinical and epidemiological 15 management of a biological attack if detection could take place when the concentration of the infecting organism is still very low. The worried well and recently infected patients would benefit, both psychologically and physically, from early pharmacological intervention.

Infection with Bacillus anfhracis or Yersinia pesds often present initially as a nonspecific febrile or flu-like illness. The mediastinitis associated with inhalational anthrax 20 ultimately results in bacilli entering the blood once the efferent lymphatics become laden with organisms. When bacteremia (the presence of bacteria in the blood) and sepsis (the invasion of bodily tissue by pathogenic bacteria) have initiated, the number of bacilli may increase quickly, doubling every 48 minutes, most often resulting in death of the patient.

It has been reported that microbiological studies on pafienfblood samples arc useful 25 for diagnosing pneumonic plague. The potential for Yersinia pestis bacilli to be present in peripheral circulating blood suggests that a PCR assay would make a useful diagnostic tool. Testing for pneumonic plague or inhalational anthrax would be effective when healthy patients present with ’’flu-like” symptoms (malaise, fever, cough, chest pain and shortness of breath) that may accompany other nonspecific symptoms. However, in order to maximize 2 2013203143 09 Apr 2013 the probability of successful, detection of the infecting organism must take place early in the disease process, when the concentration of circulating bacteria is very low.

Extraction of pathogen DNA from whole blood typically requires between 200μ1 to 500μ1 of patient sample for each preparation event. Detection of early bacteremia is 5 improved by using an entire 6 ml tube of patient blood for a single sample preparation event. Prior art literature describes a single tube blood culture system exploiting the selective lysis of blood elements, followed by centrifugation to pellet bacteria for plating on solid media. The technique has been examined thoroughly in conjunction with microbiological testing.

Fibrin is an insoluble protein precipitated from blood that forms a network of fibers, 10 In vivo, this process is central to blood clotting. Fibrin is created by the proteolytic cleavage of terminal peptides in fibrinogen. In the laboratory analysis of blood, an aggregate (pellet) of fibrin collects at the bottom of a tube when blood is centrifuged. Within the fibrin aggregate, pathogens are trapped. The analysis of these pathogens is highly desirable. However, like coins embedded in a slab of concrete, the captured pathogens are substantially 15 hidden from analysis, trapped in the fibrin aggregate, For individuals potentially exposed to dangerous pathogens, time is of the essence and rapid identification of the captured pathogens is paramount.

Plasmin is a substance in blood capable of converting fibrin to fibrinogen monomers. Plasminogen is a precursor of plasmin in the blood. Streptokinase is an enzyme that activates 20 plasminogen to form plasmin. The combination of plasminogen and streptokinase in the presence of the fibrin aggregate containing blood elements and bacteria (formally present in peripheral circulation) allows the conversion of the fibrin aggregate to a liquid state.

This conversion facilitates rapid and efficient pathogen analysis through blood - culture, antibody based testing, or nucleic-acid sequence based testing (Reverse Transcription 25 PCR, PCR, NASBA, TMA or the like).

The addition of DNAse (a DNA nuclease) to the above-described reaction provides for the conversion of human DNA into short fragments. This conversion of human DNA into short fragments contributes to a more rapid and efficient protein hydrolysis process during DNA extraction. This conversion of human DNA into short fragments is done while the 30 bacterial DNA is protected. The short fragment human DNA is carried less efficiently through the DNA extraction process and hence represents a smaller proportion of total DNA product. As a result, the reduced human DNA level presents less of an inhibitory component to the nucleic acid sequence based reactions. 2013203143 09 Apr 2013 3

Aurintricarboxylic acid (ATA) is a polymeric anion that has been demonstrated in the literature to be a potent ribonuclease inhibitor. The compound has been described previously as an additive to sample lysis buffers where the objective is to extract RNA species from tissue samples. The nucleic acid extract derived from such procedures has been shown to be 5 suitable for hybridization and gel electrophoresis analysis. However, ATA is a potent inhibitor of reverse transcriptase, which is essential for the polymerase chain reaction (PCR) detection of RNA species. Published procedures to remove ATA from nucleic acid containing compositions have revolved around chromatographic procedures that eliminate or remove only a portion of the ATA. 10 The use of ATA in a proteinase K lysis buffer is potentially superior to 1) chaothrophic salts (since they tend to reduce the efficiency of proteinase K driven protein hydrolysis as evidenced by PCR results); 2) protein based ribonuclease inhibitors (since these inhibitors would be broken down by proteinase K); and 3) EDTA (which only indirectly inhibits nucleases via chelation of the divalent cations used by those nucleases). In fact, divalent 15 cations must be added to RNA preparations where enzymatic DNA hydrolysis is conducted. What has not been demonstrated in prior art is a method where, once added, the complete downstream removal of ATA from nucleic acid extracts can be achieved to the point that down stream reverse transcriptase PCR (RT-PCR) will function.

Also not previously described in the art is a way to utilize ATA in a lyses buffer to 20 treat a large volume (l-10ml) whole blood sample and after several reagents addition steps move directly to RNA array hybridization using the entire blood sample for one analysis event hence bypassing RNA extraction and amplification.

Also not previously described in the art is a way to use blood samples treated with —ATA containing mixtures in combination with pathogen capture using bioaetive peptides 25 functionalized on hyaluronic acid detailed in U.S. application number 10/604,779 where the hyaluronic acid in turn acts as a polymeric waveguide.

Also not previously described in the art is a way to cause a calcium release at the site of pathogen capture via bioactive peptide or annealing of RNA species so as to trigger the conversion of reporter molecule labeled fibrinogen to insoluble fibrin at the site of pathogen 30 capture via bioactive peptide or annealing of RNA species upon the matrix of the hyaluronic acid polymeric waveguide. ATA also serves an important function in the protection of bacterial DNA when that bacteria is present in a blood sample processed with reagents containing high levels (>I00 4 U/ml) of DNase I as is used in various embodiments contained within U.S. application number 10/604,779. In order to achieve RNA detection capabilities that are superior to what can be achieved with technology described in U.S. application number 10/604,779, and to do so without additional steps or requirements, the present invention is utilized in combination with blood sample treatment technology described in U.S. application number 10/604,779 and prior art nucleic acid extraction methods that utilize chaotrophic salts such as guanidine thiocyanate in the presence of capture matrices such as silica or methods that utilize precipitation methods to concentrate nucleic acids out of crude samples.

Accordingly, there remains a need in the art for: 1) a method of destroying and making soluble the spectrum of blood element components (erythrocytes, leukocytes, nuclear membranes, fibrin, and host nucleic acid) without damaging analyte particles (bacteria, virus, fungi, toxin, metabolic markers, disease state markers, or chemical agents) in order to expose and rapidly concentrate (via centrifugation, filtration, or capture) the analyte particles from large volumes of blood, 2) removal of the host DNA and the matrix associated biomass present in the large volume blood sample using a single step enzyme detergent cocktail that is amenable to automation and portable systems, and 3) an analyte particle concentration method that can be coupled to existing manual or automated processes for nucleic acid extraction, biosensor testing, or liquid chromatography separation and mass spectrometry analysis.

Brief Summary of the Invention

The present invention concerns methods and materials for extracting infectious pathogens from a volume of a sample, such as blood, and includes the steps of creating a fibrin aggregate confining the pathogens and introducing a fibrin lysis reagent to expose the pathogens for analysis and DNAse to facilitate DNA extraction. The fibrin lysis reagents may be composed of DNAse, plasminogen and streptokinase frozen in coincident relation until the fibrin lysis reagent is needed whereby streptokinase enzymatically reacts with plasminogen to form plasmin upon thawing and introduction into the fibrin sample. Preferably, the plasminogen is suspended in an aqueous salt solution prior to freezing including NaCl and NaaPO.). The fibrin lysis reagent is preferably composed of DNAse and Phospholipase A2. The DNAse enzyme is used to facilitate the chemical and physical disruption of pelleted blood elements that result from the previously described protocol. 5

Phospholipase hi is used to help human DNA digestion by destroying phospholipid bilayers and, hence, destruction of the nuclear membrane.

The subject invention concerns materials and methods for efficiently removing ATA from a sample, such as a sample consisting of a nucleic acid composition. The subject methods provide a nucleic acid composition sufficiently free of ATA such that a RT-PCR reaction and other reactions involving reverse transcriptase can be performed.

The subject invention also concerns materials and methods for a mixture of ATA, magnesium chloride, potassium phosphate, and sodium chloride that is dried and combined with other dried components such as those described herein.

The subject invention also concerns materials and methods for heating a solution of urea, diethylenetriaminepentaacetate (DTPA), optionally containing EDTA, sodium citrate, and sodium chloride, to at least 6000 C for 4 hours followed by drying and combination with proteinase K and optionally Methyl 6-0- (N-heptylcarbamoyl)-(X-D-glucopyranoside and the use of this reagent to allow ATA removal from nucleic acid extracts made with existing prior art methods based on chaotrophic salts or nucleic acid precipitation followed by centrifugation or methods described herein to allow downstream hybridization of RNA species directly out of treated whole blood samples.

The subject invention also concerns the urea/DTPA reagent that was heat treated to above 600 0 C for 4 hours during production and used in sample treatment as described above followed by the combination of urease to break down the urea followed by RNA array analysis.

The subject invention also concerns materials and methods for pathogen capture using bioactive peptides functionalized on hyaluronic acid as described herein where the hyaluronic acid in turn acts as a polymeric waveguide. ___ _ _

The subject invention also concerns methods to cause a calcium release at the site of pathogen capture via bioactive peptide or annealing of RNA species so as to trigger the conversion of reporter molecule labeled fibrinogen to insoluble fibrin at the site of pathogen capture via bioactive peptide or annealing of RNA species upon the matrix of the hyaluronic acid polymeric waveguide.

The subject invention also concerns materials and methods where the hyaluronic acid matrix that is cross linked utilizing biotin and strepavidin and functionalized with bioactive peptides, such as those described herein, can be subsequently broken down with hyaluronidase in order to facilitate pathogen elution. 2013203143 09 Apr 2013 6

Brief Description of the Drawings

Figure 1 is a diagrammatic view of the method according to the invention according to the invention.

Figure 2 is a diagrammatic view of the preparation of the fibrin lysis reagent 5 according to Protocol 1 of the invention.

Figure 3 is a table providing data on Bacillus anthracis blood protocol.

Figure 4 is a table providing data on a comparison of two blood samples from different individuals.

Figure 5 is a table providing data on an evaluation of the present method by a 10 Department of Health laboratorian.

Figure 6 is a table providing data on Yersinia pestis blood protocol.

Figure 7 is a diagrammatic view of the setup of extraction reagents according to Protocol 1 of the invention.

Figures 7-9 are diagrammatic views of bacterial recovery and fibrin lysis according to 15 Protocoll of the invention.

Figure 10-13 are diagrammatic views of bacterial lysis and nucleic acid extraction according to Protocol 1 of the invention.

Figure 14a is a diagrammatic view of the steps of extracting reagents according to Protocol 2 of the invention. 20 Figure 14b is a diagrammatic view of the steps of extracting reagents according to

Protocol 2 of the invention.

Figure 15 is a diagrammatic view of the steps of extracting reagents according to Protocol 3 of the invention. — -Figure16a is a-diagrammatic view-of the steps of extracting reagents according to 25 Protocol 4 of the invention.

Figure 16b is a diagrammatic view of the steps of extracting reagents according to Protocol 4 of the invention.

Figure 17 is a table providing data on noise band crossing points for blood samples spiked with B. anthracis and processed with plasminogen, streptokinase, phospholipase A2, 30 DNase I, and lipase with centrifugation or filtration.

Figure 18 shows sedimentation and solublization of tissue aggregates from 6 ml blood samples exposed to various detergent and enzyme treatments. 2013203143 09 Apr 2013 7

Figure 19 shows filtration characteristics of 6 ml blood samples exposed, to various detergent and enzyme treatments.

Detailed Disclosure of the Invention 5 The present invention concerns methods of extracting infectious pathogens from a biological sample, such as a volume of blood, and includes the steps of creating a fibrin aggregate confining the pathogens and introducing a fibrin lysis reagent to expose the pathogens for analysis and DNAse to facilitate DNA extraction. The fibrin lysis reagents may be composed of DNAse, plasminogen and streptokinase frozen in coincident relation 10 until the fibrin lysis reagent is needed whereby streptokinase enzymatically reacts with plasminogen to form plasmin upon thawing and introduction into the fibrin sample, Preferably, the plasminogen is suspended in an aqueous salt solution prior to freezing including NaCl and NasPO^. The fibrin lysis reagent is preferably composed of DNAse and Phospholipase A2. The DNAse enzyme is used to facilitate the chemical and physical 15 disruption of pelleted blood elements that result from the previously described protocol. Phospholipase A2 is used to help human DNA digestion by destroying phospholipid bilayers and, hence, destruction of the nuclear membrane.

The present invention utilizes resuspension of the dried enzymes in a buffer solution using Potassium Phosphate as an aide to blood element solublization. It is imperative that the 20 streptokinase and plasminogen are not mixed with the buffer solution until immediately prior to the addition of the blood sample. The Potassium Phosphate pH range is about 7.8 to 8.0, which is different from prior art that claims an effective pH range of 7.2 to 7.6. Prior art uses phosphate ion solutions with lower pH to act as a true buffer; however, the current method — allows for optimal Phospholipase A2activity and Magnesium solubility. Magnesium is 25 present in the buffer solution as the divalent cation driving the activity of Phospholipase A2 in the presence of DNase. Prior art uses calcium as the classic divalent cation for driving Phospholipase A2 activity, however, calcium is not compatible with the phosphate ions essential for blood element solublization.

An embodiment of the present invention includes concentrating and extracting 30 particles such as prions, toxins, metabolic markers, cancerous matter, disease state markers, bacteria, virus, and fungi from a volume of blood by introducing an enzyme-detergent combination to expose pathogens in the blood sample and analyzing the blood sample for the particles now readily identifiable via the extraction. The enzyme-detergent may be a fibrin 2013203143 09 Apr 2013 8 lysis reagent comprising plasminogen and streptokinase. The plasminogen and streptokinase may be frozen in coincident relation until the fibrin lysis reagent is needed. The streptokinase then reacts with the plasminogen to form plasmin upon thawing. The plasminogen may be suspended in an aqueous salt solution prior to freezing. Suitable salt solutions may include 5 NaCl, NaPOi or the like. To enhance analysis, the particles may be replicated via polymerase chain reactions (PCR).

By introducing DNase, the process is facilitated by the conversion of DNA into short fragments thereby contributing to a more rapid and efficient protein hydrolysis process during DNA extraction and lowering the burden of inhibitory human DNA. Similarly, introduction 10 of Endonuclease produces a similar advantage.

As an alternative to freezing, the enzyme-detergent may include dried streptokinase and dried plasminogen as the fibrin lysis reagents, The dried reagents may then be mixed and distributed into disposable test containers. This embodiment may be particularly useful for field-testing in locations where sophisticated laboratory equipment and controls are 15 unavailable.

The plasminogen may be combined with Phospholipase A2. DNase, Endonuclease, Lipase, and combinations thereof. The dried enzyme-detergent combination may be suspended in pellets of trehalose buffer and packaged into tubes as a dry reagent. The dried reagents may then be resuspended in a buffer, added to a l-10ml volume of blood and 20 incubated for about 5-20 minutes at room temperature. More specifically, the dried reagent is comprised of about 1,500-4,500 KU Phospholipase A2, about 5,000-10,000 U Streptokinase, about 2-10 U Plasminogen, about 200-3,650 U DNase, about 200-4,000 U Endonuclease, and about 10,000-100,000 Lipase.

The solution may be centrifuged for approximately 20 minutes at 5,000-5,500 x g at a 25 temperature of 10-20°C, the supernatant decanted, and the pellet washed. The pellet may be washed three times with a 10-20 mM solution of Ecotine/20 mM HEPES ph 7.7 and/or a 10-20 mM solution of sucrose/20 mM HEPES ph 7.7, The resultant sample may then be applied to a commercially available nucleic acid extraction method.

Digesting the sample may include lysis and DNase inactivation or lysis and 30 Endonuclease inactivation. 12.5-25 mg proteinase K, 1-105% SDS (sodium dodecyl sulfate), 10-200 mM aurintricarboxylic acid, and 10- 20mM sodium citrate buffer pH 7.8-8.4 may be utilized, the solution allowed to incubate at room temperature for 10 minutes. The sample may then be filtered with a 0.22-0.45 μτη filter unit, washed with a 10-200 mM 2013203143 09 Apr 2013 9

Aurintricarboxylic Acid, digested with lysis and DNase inactivation and/or Endonuclease inactivation, and purified.

Digesting the sample may include the steps of combining 12.5-25 mg proteinease K, 1-1.5% SDS, 10-200 raM aurintricarboxylic acid, and 10-20 mM sodium citrate buffer, 5 incubating at room temperature for 10 minutes, and eluting the lysate from the filter surface by addition of 3.5-4.2 M guanidine isothiocyanate pH 6.4.

The solutions may be applied directly to a biosensor device wherein, responsive to the presence of the pathogens in the blood sample, the patient develops pathogenic or native disease state markers that allow for the capture and detection of these markers by the 10 biosensor device. Alternatively, the solution may be applied directly to a liquid chromatography mass spectrometry device whereby, responsive to the presence of the pathogens in the blood sample, the patient develops pathogenic or native disease state markers that allow for the detection of mass signatures associated with the structural components of the pathogens using the mass spectrometry device. 15 The buffer can comprise detergent and salts. This may be achieved by aiding blood element solublization by introducing 10-30 mM Potassium Phosphate at a pH range of 7.8 to 8.0, driving Phospholipase A2 activity by adding 10-80 mM Magnesium Chloride as the divalent cation, adding 20-150 mM Sodium Chloride, and including 10-200 mM Aurintricarboxylic Acid during the DNase incubation process. The buffer may also include 20 1.0-1.2% Triton X-100. Additional steps may include combining 20-35 mM methyl 6-0-(N- heptylcarbamoyl)-a-D-glucopyranoside and 0.05-0.1% Saponin; and storing the enzymes by using a trehalose buffer. Storing the enzymes is accomplished by using a trehalose buffer in combination with methyl 6-0-(N-heptylcarbamoyl)-a-D-glucopyranoside. The trehalose storage buffer comprises 10 mM Potassium Phosphate. 0.01-0.04% Triton X-100, 1-5 mM 25 Dithiothreitol, and 0.3-0.5 M Trehalose.

In Figure 1, a blood draw 30 is performed on a patient. A solution of PBS, pH 7.4 and 1.2% Triton X-100 is added, the blood is vortexed and centrifuged 40 creating pellet 60 in a 15 ml tube 50. Preferably, resins, metal hydroxides, and/or nano materials may be added with the PBS/Triton X-100 solution to capture particles such as bacteria, virus, fungi, 30 cancerous cells, prions, toxins and the like to contribute greater density to these particles. The increase in particle density allows lower speeds to run during centrifugation.

The supernatant is decanted leaving a fibrin aggregate. A fibrin lysis reagent 70 of the invention is added to tube 50 dissolving the fibrin aggregate and leaving pathogens 65 2013203143 09 Apr 2013 10 exposed for analysis, Pathogens 65 are vortexed, centrifuged, and subject to lysis to extract the pathogen DNA. The DNA is then replicated 90 and analyzed 100 for the identity of the suspected pathogen.

In an alternative embodiment of the invention, a device would be used to obviate the 5 need for a centrifuge. The device will use flexible electrodes similar to a fish gill to collect particles (such as bacteria, virus, cancerous cells, prions, or toxins). The electrodes will also be used to collect resins and nano materials that have these particles attached to them. The device will resemble a bubble on a surface. An electrical potential will be used to accelerate pathogen capture, The device can be compressed to allow efficient removal of the contents. 10 The device would preferably have the following properties: (1) a rigid base layer and flexible top layer; (2) flexible gills to be mounted on either the top or bottom layer; (3) Strepavidin and hyaluronic acid strands functionalized with bioactive peptides, antibodies, aptomers, molecular imprinted polymers, or metals that attract particles such as bacteria, virus, fungi, toxins, metabolic markers, disease state markers, or chemical agents are to be deposited on 15 the flexible gill electrodes; (4) the flexible layer will have electrodes deposited on it; (5) counter electrodes for the gill electrodes will reside on the opposite side; (6) the average dead volume of the device is 300 micro liters - it is preferred that there is to be no residual material in the device after squeezing out the material from the device; and (7) polyimide will form the flexible portion and the electrodes will be made of Pt, Au, or carbon. The device is 20 preferably used as follows: (1) flow liquid into the device and apply voltage at this time; (2) add chemicals and heat the device; and (3) squeeze out the device to remove all contents. The device is used to prepare a sample for analysis of particles (such as bacteria, virus, cancerous cells, prions, or toxins) using spectrophotometric, mass spectroscopy, antibodies, culture, or nucleic acid (e.g, PCR, NASBA, TMA) based detection systems. _ 25 A filtering device may be used to filter out the particles from blood treated with the

Triton X-100 / PBS/ magnesium solutions with enzymes selected from the group of streptokinase, plasminogen, phospholipase A2, DNase, and lipase. A filtering device may also be used to filter out the particles from blood treated with a combination of methyl 6-0-(N-heptylcarbamoyl)-a-D-glucopyranoside, Saponin, and PBS / magnesium plus enzymes 30 selected from the group of streptokinase, plasminogen, phospholipase A2, DNase, and lipase. After washing away the enzyme and detergent treatment reagents and any residual broken down blood components, the particle is ready for analysis or further processing. 2013203143 09 Apr 2013 Π

The preparation of one embodiment of a fibrin lysis reagent is shown as Protocol i in Figure 2 wherein NaCl, MnCI, DTT, DNAse, and plasminogen are added to mixing tube 110. Sodium phosphate is then added to mixing tube 110 and the solution is distributed into 1.5 ml reagent tubes 120 placed on ice. The reagent tubes 120 are frozen to -75°C for approximately 5 20 minutes. Approximately 2,700 U of streptokinase 130 is added to the wall of reagent tubes 120 just above the frozen plasminogen solution.

Figures 3-6 provide PCR results derived from testing blood samples seeded with encapsulated vegetative avirulent Bacillus anlhracis were grown according to CDC protocol # CDC.DFA.1.2, stored in 15% glycerol TSB, and frozen at -75°C. Stocks of avirulent 10 Yersinia pestis grown in TSB at 37°C, frozen in 15% glycerol TSB, and frozen at -75°C. Bacterial counts were tested at the time of harvest and retested at the time of sample spike.

Figures for average Bacillus anthracis CFU per six ml of human blood are derived from post-freezing testing given the large standard deviation encountered in side-by-side post freezing dilution events. No significant cellular death is recognized or expected. A 30% 15 cellular death rate is the highest that is reasonably expected in the worst circumstances. A conservative approach would be to increase all calculated Bacillus anthracis CFU by 30%.

Figures for average Yersinia pestis CFU per six ml of blood are derived from prefreezing testing. The low standard deviation of pre-freezing count replicates and concordance with post-freezing testing allows use of the pre-freezing bacteria count numbers. This is a 20 conservative approach that can be utilized given the now predictable results that are derived from storing and diluting this organism.

The present invention reproducibly generates analyte DNA appropriate for PCR testing of pathogens, such as Bacillus anthracis, using patient blood samples that are up to 3 months old, Sensitivity is100% at <10 CFU / ml of human blood when using 6 ml of blood 25 collected in a Becton Dickinson Vacutainer (Tables 1 and 2), This protocol also allows detection of Yersinia pestis at 100% sensitivity at <10 CFU / ml for at least one of four oligo sets according to the more limited data gathered for this organism (Table 3), It should be noted that CDC does not consider samples positive for Y. pestis unless two oligo sets produce an acceptable PCR signal. 30 In accordance with Protocol 1, Figure 7 shows a preferred method of the setup of extraction reagents according to the invention. Figures 8-9 show a method of bacterial recovery and fibrin lysis according to the invention. Figures 10-13 show a preferred method of bacterial lysis and nucleic acid extraction according to the invention. 2013203143 09 Apr 2013 12

In an alternative embodiment, as shown in Figures 14-16b, the individual enzymes of streptokinase and plasminogen are made into dried powders, mixed, then distributed to disposable tubes. In another embodiment, Phospholipase A2, plasminogen, DNase or Endonuclease, and lipase are suspended and dried in pellets of trehalose buffer. Although 5 Phospholipase A2 is preferred, any enzyme that will destroy nuclear membrane while keeping bacterial cell wall or viral coats intact may also be used. Streptokinase is likewise suspended and dried in pellets of trehalose buffer. At least one pellet of the plasminogen and one pellet of the streptokinase are packaged into tubes as dried reagents.

Dried reagents of the invention can be resuspended in a 10 ml buffer solution 10 comprising about 10-30 mM Potassium Phosphate, about 10-SO mM Magnesium Chloride, about 20-150 mM Sodium Chloride, about 10-200 mM Aurintricarboxylic Acid and about 1.0-1.2% Triton X-100. Aurintricarboxylic Acid is evidenced to provide a level of protection to bacterial nucleic acid without impeding human DNA digestion. The use of Aurintricarboxylic Acid is not described in prior methods of human DNA digestion. Methyl 15 6-0-(N-heptylcarbamoyl)-a-D-gIucopyranoside and Saponin can be substituted for Triton X-100. In one embodiment, the methyl 6-0-(N-heptylcarbomoyI)-or-D-glucopyranoside is used at 20-35 mM and the saponin is used at 0.05-0.19 concentration. The methyl 6-0-(N-heptylcarbamoyl)-G!-D-glucopyranoside is stored with the phospholipase A2, plasminogen, DNase I, and lipase in a Trehalose storage buffer. Substitution of the Triton X-100 with the 20 methyl 6-0-(N-heptylcarbamoyl)-a-D-glucopyranoside and saponin solution allows for the efficient activity of Phospholipase A2, provides the action of breaking up protein aggregates without denaturation, and is more genial to bacterial walls than Triton X-100, Use of Saponin and methyl 6-0-(N-heptylcarbamoyl)-a-D-glucopyranoside in this combination is not described in the prior art. The Trehalose storage buffer can comprise 10 mM Potassium 25 Phosphate pH 7.4, 0.01-0.04% Triton X-100 or methyl 6-0-(N-heptylcarbamoyl)-a-D-glucopyranoside, 1-5 mM Dithiothreitol, and 0.3-0.5 Trehalose. The buffer and enzyme mix are then immediately combined with a 10 ml blood sample, which may be scaled down to 1 ml. The sample is then incubated at room temperature for 5-10 minutes. The aforementioned components aide blood element solublization through minimizing certain particulates that 30 would otherwise clog filters, impair biosensors or mass spectrometry devices, and impede nucleic acid extraction. Solublization occurs while human DNA is efficiently digested and as viral and/or bacterial DNA remain intact. 13

In accordance with Protocol 2 and 4, a preferred enzyme combination is comprised of Streptokinase, Plasminogen, DNase or Endonuclease, Phospholipase A2, and Lipase. Alternatively, enzyme combinations comprising of Streptokinase, Plasminogen, DNase or Endonuclease, and Phospholipase A2 may also be used. In another alternative combination, Streptokinase, Plasminogen, DNase or Endonuclease may be used, as well as, DNase or Endonuclease, Phospholipase A2 and Lipase. DNase or Endonuclease in combination with Phospholipase A2 is yet another alternative. The efficacy of the three latter combinations was found to be equal.

In accordance with Protocol 3, a preferred enzyme combination is comprised of Streptokinase, Plasminogen, DNase or Endonuclease, Phospholipase At , and Lipase. Alternatively, enzyme combinations comprising of Streptokinase, Plasminogen, DNase or Endonuclease, and Phospholipase A2 may also be used. In another alternative combination, Streptokinase, Plasminogen, DNase or Endonuclease may be used.

As shown in Figure 14 with Protocol 2, the sample is centrifuged for a period of about 20 minutes at 5,000-5,500 x g at a temperature between 10-22°C after incubation. The supernatant is then decanted and the pellet washed three times with a 10-20 mM solution of Ecotine/20 mM HEPES pH 7.7 and/or a 20-30 mM solution of Sucrose/20 mM HEPES pH 7.7.

Alternatively after incubation, the Protocol 2 sample is centrifuged in similar fashion and the supernatant decanted, followed by sample lysis and DNase or Endonuclease inactivation using about 12.5-25 mg Proteinase K, about 1-1.5% Sodium Dodecyl Sulfate (SDS), about 10-200 mM Aurintricarboxylic Acid and about 10-20 mM Sodium Citrate buffer pH 7.8-8.4. The sample is allowed to incubate at room temperature for about 10 minutes. The digested sample may then be applied to any commercially available nucleic acid extraction method, shown in Figure 14b.

Yet in another alternative, referred to as Protocol 3 and depicted in Figure 15, the sample is filtered with a 0.22-0.45 μτα filter unit and washed with 10-20 ml of about 10-200 mM Aurintricarboxylic Acid, followed by sample lysis and DNase or Endonuclease inactivation. Sample lysis and DNase or Endonuclease inactivation is accomplished by using about 12.5-25 mg Proteinase K, about 1-1.5% SDS, about 10-200 mM Aurintricarboxylic acid, and about 10-20 mM Sodium Citrate buffer. The sample is then incubated at room temperature for about 10 minutes. Addition of about 3.5-4.2 M Guanidine Isothiocyanate pH 2013203143 09 Apr 2013 14 6.4 is necessary to elute the lysate from the filter surface. The nucleic acid extract may then be further purified using a commercially available method.

Another alternative, referred to as Protocol 4 and shown as Figure 16a, applies the sample directly to a biosensor device that will capture and detect bacteria, virus, fungi, toxins, 5 prions, chemical agents, metabolic markers or native disease state markers developed by the patient’s own body in response to these pathogens and agents present in the blood sample.

In yet,another Protocol 4 alternative shown in Figure 16b, the sample is applied directly to a liquid chromatography mass spectrometry device that will detect mass signatures of structural components that comprise bacteria, virus, toxins, prions, and chemical agents 10 present in the blood sample or native disease state markers developed by the patients own body in response to these pathogens and agents present in the blood sample. It will be seen that the objects set forth above, and those made apparent from the foregoing description, are efficiently attained and since certain changes may be made in the above construction without departing from the scope of the invention, it is intended that all matters contained in the 15 foregoing description or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.

The subject invention concerns materials and methods that can be used for the selective removal of ATA from a sample, such as a blood sample containing nucleic acid. Typically, ATA is used in procedures for extracting and purifying RNA from cells, viruses, 20 etc., because of its activity as a ribonuclease inhibitor. In one embodiment of the claimed invention, the potent ribonuclease inhibitor ATA will be present during the portion of the nucleic acid extraction process where protein hydrolysis is allowed to proceed at optimal conditions (/>., with ATA and not chaotrophic salts such as guanidine thiocyanate). Compositions for removing ATA can be provided in either solution form or dry, solid form. 25 Preferably, compositions are provided in a dry solid form to which a liquid or fluid is subsequently added. In an exemplified embodiment, a composition of the invention is used in combination with the lysis reagents described herein.

In one embodiment, a method of the invention comprises contacting a sample that comprises ATA and, optionally, nucleic acid, with a urea/DTPA composition of the 30 invention, In one embodiment, the sample can comprise any combination of reagents as described in a lysis buffer of the invention. A urea/DTPA composition of the invention can be prepared by combining urea with DTPA and optionally EDTA, sodium citrate, and enough of a base, such as sodium hydroxide to achieve pH 8.0 as defined in Table 1, In one 2013203143 09 Apr 2013 15 embodiment, the mixture is heated to above about 600 0 C for about 4 hours, dried, ground to a powder, and optionally combined with proteinase K and methyl 6-0-(N-hcptylcarbamoyl)-α-D-glucopyranoside. The urea/DTPA reagent is preferably provided in a dried form so as to minimize the downstream sample volumes and obviate the procedure of having to add 5 proteinase K (PK) in a separate step (since PK is not stable for long periods of time in 6.0 to 7.5 M urea). The ground urea/DTPA reagent is dried under vacuum and added (at 360 mg / ml blood sample) to blood treated previously with lysis reagents described herein. The sample treated with urea/DTPA is incubated about 5-10 minutes at about 65 0 C. When samples treated with AT A and a urea/DTPA reagent of the invention are combined with prior 10 art nucleic acid extraction protocols where binding matrices such as silica or other materials that bind nucleic acids in the presence of chaotrophic salts or where precipitation and centrifugation is used, the ATA will not co-purify with the nucleic acid extract. In another embodiment, the proteinase K can be inactivated by exposure to temperatures above about 80 0 C for 5 - 10 or more minutes, the sample then cooled to below about 40 ° C, wherein urease 15 is then added to about 1,000 - 100,000 U / ml to break down the urea. The sample can then be applied directly to a nucleic acid array device.

Using the subject methods in conjunction with PCR, 10 CFU Bacillus anthracis per 10 ml of blood can be detected. Also, there was no difference in the RT-PCR kinetics derived from PBS samples where 1 ng of MS2 RNA was seeded into nucleic acid extracts 20 made with and without ATA. Also, 1,000 pfu polio sabin ΙΠ virus / 8 ml SPS whole blood was detected by RT-PCR when lysis reagents described herein were combined with the urea/DTPA reagent and protocol described above. By using a urea/DTPA reagent of the invention, ATA that was present prior to the proteinase K. digestion step did not have a -negative impact-on theJPCR kinetics Jising-the_nuclekLacid_extracts that were prepared using 25 the subject methods. 2013203143 09 Apr 2013 16

Table 1. Contents of powdered Urea/DTPA reagent (upon addition of 1 ml sample to 360 mg reagent__ Urea 6.0-7.5 M Methyl 6-0- (N-heptylcarbamoyl)-a-D-glucopyranoside 10 - 20 mg / ml Proteinase K 600 - 1,000 /rg / ml EDTA 20 - 70 mM DTPA 20 — 70 mM Sodium Citrate 120 mM Sodium Hydroxide add to pH 8.0

In another embodiment, if a sample is not processed with lysis reagents, such as those described herein, then a buffer comprising only ATA can be added to the cells as a first step 5 and subsequently treated as outlined above.

In another embodiment, urea can be added to about 6.0 - 7.5 M to an ATA containing sample, and then combined with prior art chaotrophic salt based binding buffers and silica binding matrices, conduct the protocol according to the literature citation or manufacturer specifications with the exception of heating the chaotrophic salt based binding and wash 10 buffer to about 55 - 65 ° C prior to use with the sample. The reaction of urea with the aurintricarboxylic acid (ATA) plus the combination of this solution with chaotrophic salt at about 55 - 65 ° C followed by application to a silica based nucleic acid capture matrix allows the selective binding of nucleic acid to the matrix and exclusion of ATA (passed out in the column flow through). It is the combination of reaction with urea and heat that provides for 15 the exclusion of ATA from the silica capture matrix while nucleic acid binds readily. The above described urca/DTPA reagent produced by heating above 600 ° C during production eliminates the need for this chaotrophic salt heat step and allows for more complete removal of the ATA.

In another embodiment, blood samples can be treated with ATA containing mixtures 20 described herein combination with pathogen capture using bioactive peptides functionalized on hyaluronic acid also as described herein where the hyaluronic acid in turn acts as a polymeric waveguide. The hyaluronic acid is labeled with biotin via carboxyl groups or amines and the excess unbound biotin is subsequently removed via dialysis. Strepavidin is cross-linked and the excess unbound cross linker is removed via dialysis. The cross-linked 2013203143 09 Apr 2013 17 strepavidin is added in 100 - 10,000 molar excess to the biotinylated hyaluronic acid and incubated about 4-10 hours with or without an applied electrophoretic or dielectrophoretic field. Alternatively, the strepavidin is added in the described ratios, incubated for about 1 - 4 hours with mixing, combined with a photo- activated cross-linking reagent, and cross-linked 5 within as lithography system in order to generate structures positioned within a sample flow path. In this system a calcium release at the site of pathogen capture via bioactive peptide or annealing of RNA species is in the presence of thrombin (about 10 - 500 /xg per milliliter) used to trigger the local conversion of reporter molecule labeled fibrinogen (about 10 - 500 μg per milliliter) to an insoluble fibrin aggregate at the site of pathogen capture via bioactive 10 peptide or annealing of RNA species upon the matrix of the hyaluronic acid polymeric waveguide. Reporter molecules can be any molecule that can be detected and include, for example, fluorescent molecules (fluorescein, etc.), radioactive molecules, enzymes, antigens, and the like. As used herein, bioactive peptides include native and modified non-specific virus binding peptides most optimally, such as lactoferrin or fatty acid modified lactoferrin, 15 and native and modified non-specific bacteria binding peptides, most optimally, such as Cecropin PI, but also including, for example, protamine, Buforin I, Buforin II, Defensin, D-Magainin Π, Cecrpin A, Cecropin B, Lectin PA-1, and Tritrpticin. The modified peptides may be altered in terms of amino acid content and include the salts, esters, amides, and acylated forms thereof. 20 In another embodiment, the bioactive peptides functionalized upon the hyaluronic acid (that is cross linked via biotin and strepavidin) act as pathogen capture moieties. Upon pathogen or biomarker capture, the hyaluronic acid is broken down using about 1,000 - 1,000,000 units of hyaluronidase / ml of sample within the device. _In another embodiment, the ATA. magnesium chloride, and potassium phosphate 25 components described in the lysis buffer of the present invention are combined, brought to about pH 9.2 - 10 in batches of 100 ml, and heated to boiling until a dry residue forms. The dry residue is ground up, dried further under vacuum, and added to the other enzyme, detergent, and Trehalose components, such as those described herein. 2013203143 09 Apr 2013 18

All patents, patent applications, provisional applications, and publications referred to or cited herein are incorporated by reference in their entirety, including all figures and tables, to the extent they are not inconsistent with the explicit teachings of this specification.

It should be understood that the examples and embodiments described herein are for 5 illustrative purposes only and that various modifications or changes in light thereof will be suggested to persons skilled in the art and are to be included within the spirit and purview of this application and the scope of the appended claims.

The reference to any prior art in this specification is not, and should not be taken as an acknowledgement or any form of suggestion that the referenced prior art forms part of the 10 common general knowledge in Australia.

In the specification the term “comprising” shall be understood to have a broad meaning similar to the term “including” and will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps. This definition also applies to variations on the term 15 “comprising” such as "comprise” and “comprises”.

Claims (23)

1. A method for capturing a particle from a biological sample including the particle, the method comprising: a. contacting the biological sample with: (i) 2 to 10 U plasminogen and 5,000 to 10,000 U streptokinase or plasmin produced by combining 2 to 10 U plasminogen and 5,000 to 10,000 U streptokinase, (ii) 200 to 3,650 U DNAse, (iii) 1,500 to 4,500 KU phospholipase A2, and (iv) a detergent; and; and b. capturing the particle, wherein the particle is a prion, a toxin, a metabolic marker, cancerous matter, a disease state marker, a bacterium, a virus, or a fungus.

2. The method of claim 1, wherein the particle is a bacterium.

3. The method of claims 1, wherein the particle is a fungus.

4. The method of claim 1 or 2, wherein the DNase is an endonuclease.

5. The method of any one of claims 1 to 4, wherein the method further comprises contacting the biological sample with 10,000 to 100,000 U lipase.

6. The method of any one of claims 1 to 5, wherein the capturing the particle comprises filtering the biological sample to extract the particle.

7. The method of claim 6, wherein the filtering comprises filtering the biological sample through a 0.22 to 0.45 mm filter unit.

8. The method of claim 7, wherein the filter unit is a Polyethersulfone (PES) filter unit.

9. The method of any one of claims 1 to 8, wherein the biological sample is blood.

10. The method of any one of claims 1 to 8, wherein the biological sample is a fibrin aggregate.

11. The method of claim 6, wherein the method further comprises: contacting the extracted particle with proteinase K, thereby producing a lysate; eluting the lysate from the filter surface; and extracting a nucleic acid from the lysate.

12. The method of claim 11, wherein the method further comprises: amplifying the nucleic acid by polymerase chain reaction (PCR).

13. The method of claim 1, wherein the capturing the particle comprises centrifuging the biological sample to extract the particle.

14. A container comprising a biological sample with added proteins prepared by adding to a biological sample:; (a) 2 to 10 U of an isolated plasminogen; (b) 5,000 to 10,000 U of an isolated streptokinase; (c) 200 to 3,650 U of an isolated DNAse; (d) 1,500 to 4,500 KU of a phospholipase A2; and (e) a detergent.

15. The container of claim 14, wherein the biological sample comprises a bacterium.

16. The container of claim 14, wherein the biological sample comprises a fungus.

17. The container of claim 14, wherein the DNase is an isolated endonuclease.

18. The container of claim 14, wherein the biological sample is further prepared by adding to the biological sample 10,000 to 100,000 U of an isolated lipase.

19. The container of any one of claims 14 to 17, wherein the biological sample is blood.

20. The container of any one of claims 14 to 17, wherein the biological sample is a fibrin aggregate.

21. A reagent composition, comprising: (a) 2 to 10 U of an isolated plasminogen; (b) 5,000 to 10,000 U of an isolated streptokinase; (c) 200 to 3,650 U of an isolated DNAse; (d) 1,500 to 4,500 KU of a phospholipase A2; and (e) a detergent.

22. The reagent composition of claim 20, wherein the DNase is an isolated endonuclease.

23. The reagent composition of claim 20 or 21, wherein the composition further comprises 10,000 to 100,000 U of an isolated lipase.