WO2008157384A2 - Method of detection of microorganisms with enhanced bacteriophage amplification - Google Patents
Method of detection of microorganisms with enhanced bacteriophage amplification Download PDFInfo
- Publication number
- WO2008157384A2 WO2008157384A2 PCT/US2008/066962 US2008066962W WO2008157384A2 WO 2008157384 A2 WO2008157384 A2 WO 2008157384A2 US 2008066962 W US2008066962 W US 2008066962W WO 2008157384 A2 WO2008157384 A2 WO 2008157384A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- bacteriophage
- fatty acid
- substance
- sample
- medium
- Prior art date
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/569—Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
- G01N33/56911—Bacteria
Definitions
- the invention relates generally to the field of identification of microscopic living organisms, and more particularly to the identification of microorganisms using bacteriophage.
- Bacteriophage amplification has been suggested as a method to accelerate microorganism identification. See, for example, U.S. Patents No. 5,985,596 issued November 16, 1999 and No. 6,461 ,833 B1 issued October 8, both to Stuart Mark Wilson; U.S. Patent No. 4,861 ,709 issued August 29, 1989 to Ulitzur et al.; U.S. Patent No. 5,824,468 issued October 20, 1998 to Scherer et al.; U.S. Patent No. 5,656,424 issued August 12, 1997 to Jurgensen et al.; U.S. Patent No. 6,300,061 B1 issued October 9, 2001 to Jacobs, Jr. et al.; U.S. Patent No.
- Bacteriophage are viruses that have evolved in nature to use bacteria as a means of replicating themselves. A bacteriophage (or phage) does this by attaching itself to a bacterium and injecting its genetic material into that bacterium, inducing it to replicate the phage from tens to thousands of times.
- lytic bacteriophage rupture the host bacterium releasing the progeny phage into the environment to seek out other bacteria.
- the total incubation time for infection of a bacterium by parent phage, phage multiplication (amplification) in the bacterium to produce progeny phage, and release of the progeny phage after lysis can take as little as an hour depending on the phage, the bacterium, and the environmental conditions.
- bacteriophage amplification in combination with a test for bacteriophage or a bacteriophage marker may be able to significantly shorten the assay time as compared to a traditional substrate-based identification.
- a single infected bacterium may produce 10 1 - 10 4 progeny bacteriophage, and each bacteriophage particle may contain 10 1 - 10 3 copies of capsid or other structural proteins.
- Signal amplifications of 10 2 - 10 7 from each infected bacterium therefore, are possible, given an appropriate method of detecting progeny bacteriophage, bacteriophage nucleic acids, or bacteriophage proteins.
- Many methods known to the art are suitable for detection, including but not limited to, PCR, mass spectrometry, antibody or aptamer-based binding assays, and plaque assays.
- samples potentially containing target bacteria are incubated with bacteriophage specific for those bacteria.
- the bacteriophage infect and replicate in the bacteria resulting in the production of a measurable signal indicating the presence of the target bacteria.
- Some methods utilize the detection of progeny phage released from infected target bacteria as a means of detection and identification. In this case, progeny phage are not produced if the parent phage do not successfully infect the target bacteria.
- Still other methods rely on the detection of phage replication products rather than whole progeny phage. For example, luciferase reporter bacteriophage produce luciferase when they successfully infect target bacteria.
- the luciferase then produces light that, if detected, indicates the presence of target bacteria in the sample.
- Other methods rely on the detection of bacterial debris that is released following a successful lytic infection of target bacteria by a specific bacteriophage.
- Still other methods rely only on the ability of bacteriophage to attach to the bacteria and do not employ amplification.
- To accurately identify the target bacteria each of these phage- based diagnostic methods demands that the bacteriophage have both high sensitivity for the target bacteria and high specificity to avoid replication in non-target strains or species of bacteria. Finding or developing bacteriophage with those characteristics is very challenging.
- Bacteriophage with acceptable sensitivity often lack sufficient specificity, i.e., they cross react with too many non-target bacteria. This lack of acceptable sensitivity in combination with sufficient specificity is a critical problem in commercializing bacteriophage diagnostic processes.
- the invention provides an advancement of the art and overcomes the above problems by the adding one or more substances to the bacteriophage-exposed sample, which substances enhance bacteriophage amplification without reducing specificity or sensitivity. It has been found, for example, that the expression of toxic shock proteins, as well as a variety of other S. aureus exoproteins, is suppressed by the presence of sub-lethal concentration of fatty acids and related compounds in the growth medium. We find that addition of fatty acids, conjugated fatty acids, fatty acid esters, or fatty acid amides to growth media significantly enhances the performance and utility of bactehophage-based tests in detecting, identifying, and characterizing bacterial hosts for diagnostic and research purposes.
- pyruvate in any of its various forms, such as pyruvic acid and sodium pyruvate.
- pyruvic acid and sodium pyruvate For example, the addition of 10 mmol/L (millimoles per liter) to 50 mmol/L of sodium pyruvate to a wide variety of S. aureus strains was found to significantly increase phage sensitivity.
- the addition of from 12 mmol/L to 37 mmol/L of sodium pyruvate was found to increase phage sensitivity in these strains from about 78% to between 87% and 92%. In the range of concentrations of from 15 mmol/L to 31 mmol/L, the sensitivity increased to above 90%.
- the most preferred concentration was 27 mmol/L, at which concentration the sensitivity was increased about 15% over sensitivities without sodium pyruvate.
- the mean amplification of the bacteriophage was increased significantly in a range from about 10 mmol/L to 60 mmol/L sodium pyruvate.
- the mean amplification increased from about 92 without sodium pyruvate to 150 at about 30 mmol/L of sodium pyruvate.
- the invention provides a method of determining the presence or absence of a target microorganism in a sample to be tested, the method comprising: combining with the sample an amount of bacteriophage capable of attaching to the target microorganism to create a bactehophage-exposed sample; providing conditions to the bactehophage-exposed sample sufficient to allow the bacteriophage to infect the microorganism; and assaying the bactehophage-exposed sample to detect the presence or absence of a bacteriophage marker to determine the presence or absence of the target microorganism; the method characterized by the combining, including combining with the bacteriophage and the target microorganism a substance which enhances bacteriophage amplification in the target organism or bacteriophage sensitivity to the target microorganism.
- the invention also provides a medium for determining the presence or absence of a target microorganism in a sample to be tested, the medium comprising bacteriophage and characterized in that the medium includes a substance that enhances the replication of the bacteriophage in the target microorganism or enhances bacteriophage sensitivity to the target organism.
- the microorganism is a bacterium and the assaying comprises detecting the bacteriophage marker as an indication of the presence of the target bacterium in the sample.
- the substance suppresses a bacterial virulence factor.
- the virulence factor is a toxic shock protein.
- the substance is a fatty acid compound.
- the fatty acid compound is lauric acid.
- the substance is selected from the group consisting of a fatty acid, a conjugated fatty acid, a fatty acid ester, and a fatty acid amide.
- the substance comprises pyruvate.
- the substance comprises sodium pyruvate.
- the method further comprises inhibiting phage replication in a potentially cross-reactive, non-target microorganism.
- the inhibiting comprises selectively removing potential cross-reactive bacteria from the sample using selective binding agents attached to a support, or selectively destroying potentially cross-reactive bacteria.
- the invention solves the problem of enhancing the sensitivity of the bacteriophage amplification process while at the same time maintaining or enhancing the selectivity of a bacteriophage.
- FIG. 1 is a graph indicating the addition of lauric acid improves amplification on poor or restrictive S. aureus hosts
- FIG. 2 is a graph indicating lauric acid increases bacteriophage amplification on permissive S. aureus hosts
- FIG. 3 is a graph indicating lauric acid relieves suppression of phage amplification by cefoxitin in MRSA strains
- FIG. 4 is a graph showing bacteriophage sensitivity in percent versus concentration of sodium pyruvate in mmol/L.
- FIG. 5 is a graph showing bacteriophage mean amplification versus concentration of sodium pyruvate in mmol/L.
- the invention relates to the use of bacteriophage to detect microorganisms.
- Bacteriophage are viruses that have evolved in nature to use bacteria as a means of replicating themselves. A phage does this by attaching itself to a bacterium and injecting its DNA (or RNA) into that bacterium and inducing it to replicate the phage hundreds or even thousands of times. This is referred to as phage amplification. As summarized in the Background of the Invention above, there is much literature based on the idea that phage amplification can potentially provide a marker indicative of the bacterium that can be detected more easily and more rapidly than the bacterium itself.
- a fundamental principle that allows particular bacteria to be detected via bacteriophage amplification followed by an assay of a bacteriophage marker is that a particular bacteriophage will infect only a particular bacterium. That is, the bacteriophage is specific to the bacteria. Thus, if a particular bacteriophage that is specific to particular bacteria is introduced into a sample, and later the bacteriophage has been found to have multiplied, the bacteria to which the bacteriophage is specific must have been present in the sample. In this way, the prior art teaches that bacteriophage amplification can be used to identify specific bacteria present in a sample. However, bacteriophage that are 100% specific to a single bacteria species that it is desired to detect are not present in nature.
- bacteriophage found in nature also are not 100% sensitive to the bacteria that it is desired to detect. Because the bacteriophage found in nature are imperfect as to these desired qualities, a commercially viable bacteria detection process has been much more difficult to arrive at than was at first hoped.
- This application discloses systems and processes that enhance bacteriophage amplification and bacteriophage sensitivity and, thus, lead for the first time to the possibility of a commercially viable process.
- the invention provides substances and processes that enhance bacteriophage amplification without reducing specificity or sensitivity. In fact, as will be shown below, the substances and processes of the invention not only enhance amplification but increase sensitivity.
- bacteriophage and “phage” include bacteriophage, phage, mycobactehophage (such as for TB and paraTB), mycophage (such as for fungi), mycoplasma phage or mycoplasmal phage, and any other term that refers to a virus that can invade living bacteria, fungi, mycoplasmas, protozoa, yeasts, and other microscopic living organisms and uses them to replicate itself.
- microscopic means that the largest dimension is one millimeter or less.
- a bacteriophage marker is any biological or organic element that can be associated with the presence of a bacteriophage. Without limitation, this may be the bacteriophage itself, a lipid incorporated into the phage structure, a protein associated with the bacteriophage, RNA or DNA associated with the bacteriophage, or any portion of any of the foregoing.
- a bacterial marker is any biological or organic element that is released when a bacterium is lysed by a bacteriophage, including cell wall components, bacterial nucleic acids, proteins, enzymes, small molecules, or any portion of the foregoing.
- each symbol, such as 12, represents an independent clinical isolate of S. aureus.
- Clinical isolates of S. aureus were grown in BacTec Aerobic F/10 broth charged with 20% blood at 35° to a density of approximately 10 8 cfu/ml. An aliquot of these cultures was then diluted 1 :250 into a test mixture of Tryptic Soy Broth containing bacteriophage strains MP1 12 and MP1 15, each at 10 7 pfu/ml, and varying concentrations of lauric acid. The cultures were grown for four hours at 35°, then diluted and plated on bacterial lawns using the top agar method.
- the set of isolates used in FIG. 1 is known from previous experiments to be resistant to bacteriophage infection or to amplify bacteriophage poorly after infection.
- the 28 strains in this study were chosen from a collection of 202 clinical isolates as the poorest hosts for bacteriophage amplification. Given that these strains represent -14% of the collection, it is plausible that most or all are TSS-positive; and lauric acid enhances phage amplification through suppression of TSS gene expression. However, we find that lauric acid, and by extension other fatty acids, generally promotes bacteriophage amplification in nearly all hosts tested. This novel result indicates that TSS suppression is not sufficient to explain the effect of fatty acids on bacteriophage amplification.
- the effect of lauric acid on good bacteriophage hosts is shown in FIG. 2.
- the results for these isolates with no lauric acid are shown at 42; the results for a concentration of 5 ⁇ g/ml of lauric acid are shown at 45; the results for a concentration of 10 ⁇ g/ml of lauric acid are shown at 48; the results for a concentration of 15 ⁇ g/ml of lauric acid are shown at 52; the results for a concentration of 20 ⁇ g/ml of lauric acid are shown at 56; and the results for a concentration of 30 ⁇ g/ml of lauric acid are shown at 59.
- the average amplification in this group increases from 69-fold to over 100-fold with the addition of lauric acid.
- the average level of amplification is shown by the solid line, such as 49, in each of the columns. To date, more than 80% of S. aureus strains tested show stimulation of bacteriophage amplification in response to lauric acid.
- Lauric acid, other fatty acids, and their derivatives ameliorate the effects of ⁇ - lactam antibiotics on phage amplification in methicillin-resistant S. aureus (MRSA) hosts, as shown in FIG. 3.
- MRSA methicillin-resistant S. aureus
- FIG. 3 This property enhances the performance and utility of bactehophage-based tests in detecting, classifying, and distinguishing MRSA from methicillin-susceptible S. aureus (MSSA).
- MSSA methicillin-susceptible S. aureus
- each symbol represents a clinical MRSA (methicillin-resistant S. aureus) isolate able to grow in the presence of ⁇ -lactam antibiotics such as cefoxitin.
- the first column 62 (circles) indicates amplification by MRSA strains with no cefoxitin and no lauric acid.
- the second column 64 (squares) indicates amplification with added cefoxitin. Note the suppression of phage amplification.
- the third column 66 (diamonds) indicates amplification with added lauric acid.
- the fourth column 70 (x's) indicate amplification with added lauric acid and cefoxitin. This shows that lauric acid relieves suppression of phage amplification by cefoxitin in MRSA strains.
- fatty acid compounds that positively stimulate bacteriophage amplification include saturated fatty acids: caproic acid, caprylic acid, capric acid, and myristic acid; conjugated fatty acids: glycerol monolaurate; and unsaturated fatty acids: oleic acid and linoleic acid.
- saturated fatty acids caproic acid, caprylic acid, capric acid, and myristic acid
- conjugated fatty acids glycerol monolaurate
- unsaturated fatty acids oleic acid and linoleic acid.
- oleic acid and linoleic acid unsaturated fatty acids
- FIGS. 4 and 5 show the effect of medium supplementation by sodium pyruvate.
- FIG. 4 is a graph showing a curve 80 of measured bacteriophage sensitivity in percent versus concentration of sodium pyruvate in mmol/L. A panel of 32 S.
- aureus strains was grown in charged BacTec SA blood culture medium to mid-log phase, and then diluted into growth medium containing bacteriophage and the indicated concentrations of sodium pyruvate in mmol/L. After 4 hours of incubation at 35°, the cultures were tested for bacteriophage amplification by standard microbiological methods. Strains showing significant amplification, defined as > 8-fold over input bacteriophage, were scored as positive. Sensitivity is defined as the number of positive strains as a percentage of all strains tested.
- FIG. 5 is a graph showing a curve 90 of measured bacteriophage mean amplification versus concentration of sodium pyruvate in mmol/L.
- the mean amplification of the bacteriophage was increased significantly in a range of from about 10 mmol/L to 60 mmol/L.
- the mean amplification increased from about 92 without sodium pyruvate to 150 at about 30 mmol/L of sodium pyruvate.
- the methods and substances that enhance bacteriophage amplification are preferably used in combination with substances and methods that inhibit replication in potentially cross-reactive, non-target bacteria, and use this inhibition to increase the selectivity of the phage-based diagnostic process.
- These embodiments are intended to be illustrative, though the invention is not limited to these embodiments. Other methods with the same results can be contemplated by those skilled in the arts.
- Inhibition of potentially cross-reactive bacteria can be accomplished using methods common to microbiological detection.
- substances such as sodium chloride (in high concentration), Polymyxin B, Polymyxin E, other Polymyxins, and metal compounds, such as potassium tellurite, inhibit the growth of some coagulase negative Staphylococcus (CNS) while allowing the growth of S. aureus.
- CNS coagulase negative Staphylococcus
- These compounds can also significantly inhibit or retard replication of bacteriophage in CNS while minimally affecting replication in S. aureus.
- the usage of selective media to differentially affect the efficiency and timing of phage replication is a novel method for improving the specificity of bacteriophage-based bacterial diagnostic methods.
- Removal of non-target bacteria may be accomplished using antibodies, bacteriophage selective for the non-target bacteria, or other compounds that selectively bind to non-target bacteria. For an S. aureus test, removal of CNS species can be beneficial. Binding of these compounds to non-target bacteria may be sufficient to block the binding of bacteriophage to those bacteria, preventing successful infection and replication. Alternatively, these compounds may be attached to other substrate such as micro-particles, magnetic beads, or solid substrates. When incubated with a sample, potential non-target bacteria will selectively bind to the substrate. The substrate then can be physically removed from the sample. Separation methods include centhfugation for micro-particles or by the application of a magnetic field for magnetic beads.
- Non-target bacteria can be accomplished using antibacterial compounds that selectively destroy non-target bacteria such that they are not susceptible to phage infection while leaving target bacteria largely unharmed and susceptible to phage infection.
- antibacterial compounds include: a) selective antibiotics, and b) bacteriophage that selectively bind to and/or infect potentially cross-reactive, non- target bacteria.
- the latter are complementary bacteriophage to the primary bacteriophage used to selectively infect the target bacteria in the sample.
- Complementary bacteriophage can destroy non-target bacteria by successfully infecting and lysing those non-target bacteria such that phage infection by the primary bacteriophage is eliminated or significantly reduced.
- Complementary bacteriophage can also be used to destroy non-target bacteria by a process known as lysis from without. Lysis from without refers to the destruction of a bacterium when hundreds or thousands of phage particles bind to its cell wall. This process can be utilized in this invention by adding a high concentration of complementary phage to the sample such that large numbers of complementary phage quickly and selectively bind to potentially cross-reactive bacteria. Under pressure of multiple phage binding, the cross-reactive bacteria can be made to burst, eliminating them as a locus for phage infection by the prime bacteriophage.
- bacteriophage can be used to detect bacteria simply using the property that phage attach to the bacteria, that is, without the amplification step.
- This application also discloses how bacteriophage can be used to determine the antibiotic susceptibility or antibiotic resistance of a microorganism. It is contemplated by the invention that the materials and processes described herein can also be used to advantage in any of the foregoing processes and systems. Many other phage-based methods and apparatus used to identify the microorganism and/or to determine the antibiotic resistance test or antibiotic susceptibility can be enhanced by the method and apparatus of the invention.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Immunology (AREA)
- Engineering & Computer Science (AREA)
- Urology & Nephrology (AREA)
- Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Hematology (AREA)
- Medicinal Chemistry (AREA)
- Analytical Chemistry (AREA)
- Biotechnology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Virology (AREA)
- Food Science & Technology (AREA)
- Microbiology (AREA)
- Physics & Mathematics (AREA)
- Cell Biology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Pathology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2690809A CA2690809A1 (en) | 2007-06-15 | 2008-06-13 | Method of detection of microorganisms with enhanced bacteriophage amplification |
EP08771055A EP2158490A2 (en) | 2007-06-15 | 2008-06-13 | Method of detection of microorganisms with enhanced bacteriophage amplification |
AU2008265989A AU2008265989B8 (en) | 2007-06-15 | 2008-06-13 | Method of detection of microorganisms with enhanced bacteriophage amplification |
CN200880024912A CN101802615A (en) | 2007-06-15 | 2008-06-13 | Utilize the enhancing bacteriophage to increase and detect method of microorganism |
US12/663,686 US8455186B2 (en) | 2007-06-15 | 2008-06-13 | Method of detection of microorganisms with enhanced bacteriophage amplification |
JP2010512392A JP5150856B2 (en) | 2007-06-15 | 2008-06-13 | Microbial detection method with improved bacteriophage amplification |
US12/402,337 US20090286225A1 (en) | 2004-02-13 | 2009-03-11 | Method and apparatus for bacteriophage-based diagnostic assays |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US93478107P | 2007-06-15 | 2007-06-15 | |
US60/934,781 | 2007-06-15 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US11/933,083 Continuation-In-Part US20080241819A1 (en) | 2004-02-13 | 2007-10-31 | Method and apparatus for enhanced bacteriophage-based diagnostic assays by selective inhibition of potential cross-reactive organisms |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2008157384A2 true WO2008157384A2 (en) | 2008-12-24 |
WO2008157384A3 WO2008157384A3 (en) | 2009-02-12 |
Family
ID=39765225
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2008/066962 WO2008157384A2 (en) | 2004-02-13 | 2008-06-13 | Method of detection of microorganisms with enhanced bacteriophage amplification |
Country Status (7)
Country | Link |
---|---|
US (1) | US8455186B2 (en) |
EP (1) | EP2158490A2 (en) |
JP (1) | JP5150856B2 (en) |
CN (1) | CN101802615A (en) |
AU (1) | AU2008265989B8 (en) |
CA (1) | CA2690809A1 (en) |
WO (1) | WO2008157384A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10881792B2 (en) | 2017-01-13 | 2021-01-05 | Bigfoot Biomedical, Inc. | System and method for adjusting insulin delivery |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9481903B2 (en) | 2013-03-13 | 2016-11-01 | Roche Molecular Systems, Inc. | Systems and methods for detection of cells using engineered transduction particles |
ES2780827T3 (en) | 2013-03-13 | 2020-08-27 | Geneweave Biosciences Inc | Non-replicative transduction particles and reporter systems based on transduction particles |
WO2015000079A1 (en) * | 2013-07-03 | 2015-01-08 | Qvella Corporation | Methods of targeted antibiotic susceptibility testing |
US9540675B2 (en) | 2013-10-29 | 2017-01-10 | GeneWeave Biosciences, Inc. | Reagent cartridge and methods for detection of cells |
US10351893B2 (en) | 2015-10-05 | 2019-07-16 | GeneWeave Biosciences, Inc. | Reagent cartridge for detection of cells |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1471329A (en) | 1973-09-04 | 1977-04-21 | Ajinomoto Kk | Method of inhibiting bacteriophage activity |
US4861709A (en) | 1985-05-31 | 1989-08-29 | Technicon Research A.G. | Detection and/or identification of microorganisms in a test sample using bioluminescence or other exogenous genetically-introduced marker |
WO1992002633A1 (en) | 1990-08-09 | 1992-02-20 | Amersham International Plc | Methods for rapid microbial detection |
US5656424A (en) | 1995-02-15 | 1997-08-12 | Albert Einstein College Of Medicine, A Division Of Yeshiva University | Identification of mycobacterium tuberculosis complex species |
US5824468A (en) | 1995-05-18 | 1998-10-20 | Merck Patent Gesellschaft Mit Beschrankkter Haftung | Detection of listeria by means of recombinant bacteriophages |
US5888725A (en) | 1992-09-22 | 1999-03-30 | The Secretary Of State For The Minister Of Agriculture Fisheries And Food In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Method for identifying target bacteria |
US5985596A (en) | 1995-12-15 | 1999-11-16 | Biotec Laboratories Limited | Method to detect bacteria |
US6300061B1 (en) | 1992-02-07 | 2001-10-09 | Albert Einstein College Of Medicine Of Yeshiva University | Mycobacterial species-specific reporter mycobacteriophages |
US6436661B1 (en) | 2000-04-13 | 2002-08-20 | 3M Innovative Properties Company | Bacteria and bacteriophage detection using immobilized enzyme substrates |
US6461833B1 (en) | 1995-12-15 | 2002-10-08 | Biotec Laboratories Limited | Method to detect bacteria |
US6544729B2 (en) | 2001-07-20 | 2003-04-08 | University Of Tennessee | Bioluminescent biosensor device |
US6555312B1 (en) | 1999-02-22 | 2003-04-29 | Matsushita Electric Industrial Co., Ltd. | Method for detecting bacteria with bacteriaphage |
US20040224359A1 (en) | 2002-04-12 | 2004-11-11 | Madonna Angelo J. | Method for detecting low concentrations of a target bacterium that uses phages to infect target bacterial cells |
WO2006125319A1 (en) | 2005-05-26 | 2006-11-30 | Gangagen Life Sciences Inc. | Bacterial management in animal holding systems |
Family Cites Families (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3843776A (en) * | 1971-05-06 | 1974-10-22 | Leo Ab | Diagnostic method and means therefor |
US4104126A (en) * | 1976-01-29 | 1978-08-01 | Nichols Institute Of Endocrinology, Inc. | Non-isotopic substrate assay employing bacteriolysis products |
US4797363A (en) * | 1984-03-19 | 1989-01-10 | Board Of Trustees, University Of Illinois | Bacteriophages as recognition and identification agents |
GB2181542A (en) | 1984-03-19 | 1987-04-23 | Marius Constantin Teodorescu | Bacteriophages as recognition and identification agents |
CA1277931C (en) | 1984-06-05 | 1990-12-18 | Shimon Ulitzur | Detection and/or identification of microorganisms in a test sample usingbioluminescence or other exogenous genetically-introduced marker |
FR2590675B1 (en) | 1985-11-27 | 1990-10-12 | Transia | MIXTURE OF SPECIFIC ANTIBODIES OF LACTIC BACTERIOPHAGES AND ITS APPLICATIONS TO THE DETECTION AND NEUTRALIZATION OF SAID BACTERIOPHAGES |
US5085982A (en) * | 1986-06-12 | 1992-02-04 | City Of Hope | Method of detecting specific substances by selective growth of living cells |
CA1313111C (en) | 1986-12-01 | 1993-01-26 | William J. Hubbard | Method of identifying unknown organisms |
US5620845A (en) | 1988-06-06 | 1997-04-15 | Ampcor, Inc. | Immunoassay diagnostic kit |
EP0439354A3 (en) | 1990-01-24 | 1992-06-17 | Amoco Corporation | Signal generating moiety and method for use |
JP2913419B2 (en) * | 1990-06-15 | 1999-06-28 | 日水製薬株式会社 | Medium for growth and detection of coliform bacteria |
US5168037A (en) | 1990-08-02 | 1992-12-01 | Phyllis Entis | Method for the preparation of a labelled virus without the inactivation of viral binding sites and method of assay utilizing said labelled virus |
JPH04117299A (en) * | 1990-09-05 | 1992-04-17 | Duskin Co Ltd | Detection of bacteria |
GB2255561B (en) | 1991-04-20 | 1995-06-21 | Agricultural & Food Res | Lysins from bacteriophages |
WO1993017129A1 (en) | 1992-02-28 | 1993-09-02 | Judkins Paul W | Method and diagnostic kit for determination of bacteria |
GB9220027D0 (en) | 1992-09-22 | 1992-11-04 | Mini Agriculture & Fisheries | Method and kits for detection of bacteria |
US5679510A (en) | 1993-04-27 | 1997-10-21 | Hybridon, Inc. | Quantitative detection of specific nucleic acid sequences using lambdoid bacteriophages linked by oligonucleotides to solid support |
DE4314998A1 (en) | 1993-05-06 | 1994-11-10 | Max Delbrueck Centrum | Monoclonal antibodies against filamentous phages, their preparation and use for detecting and isolating the phages |
GB9317139D0 (en) | 1993-08-18 | 1993-10-06 | Miniser For Agriculture Fisher | Method and test kits for detection of bacteriophage |
US5658747A (en) | 1994-05-10 | 1997-08-19 | Biocontrol System, Inc. | Compositions and methods for control of reactivity between diagnostic reagents and microorganisms |
CA2130072C (en) | 1994-08-12 | 2003-02-18 | John W. Cherwonogrodzky | Method of detecting a pathogen using a virus |
US5476768A (en) | 1995-03-10 | 1995-12-19 | Becton, Dickinson And Company | Mycobacteriophage DSGA specific for the mycobacterium tuberculosis complex |
JP3270722B2 (en) * | 1996-09-27 | 2002-04-02 | オルガノ株式会社 | Bacteria detection method and detection device |
US5789174A (en) | 1996-10-11 | 1998-08-04 | Universite Laval | Detection of periodontal pathogens including bacteroides forsythus, porphyromonas gingivalis, prevotilla intermedia and prevotella nigrescens |
US5710005A (en) | 1996-10-29 | 1998-01-20 | Biocode, Inc. | Analyte detection with a gradient lateral flow device |
US7153651B1 (en) | 1996-10-31 | 2006-12-26 | Inverness Medical - Biostar, Inc. | Flow-through optical assay devices providing laminar flow of fluid samples, and methods of construction thereof |
US5958675A (en) | 1997-04-18 | 1999-09-28 | 3M Innovative Properties Company | Method for detecting bacteria using bacteriophage, contrast-coloring dye and precipitable dye |
IT1291913B1 (en) | 1997-05-22 | 1999-01-21 | Angeletti P Ist Richerche Bio | METHOD INVOLVING THE USE OF BACTERIOPHAGES FOR THE DETECTION OF THE PRESENCE OF MOLECULES OF INTEREST IN BIOLOGICAL SAMPLES |
TW552304B (en) | 1997-08-08 | 2003-09-11 | Food Industry Res & Dev Inst | Rapid identification of microorganisms |
EP1049798B1 (en) * | 1998-01-21 | 2006-06-14 | The Secretary of State for Defence | Antibiotic sensitivity testing |
GB9809414D0 (en) * | 1998-05-02 | 1998-07-01 | Scottish Crop Research Inst | Method |
US6037118A (en) | 1998-05-14 | 2000-03-14 | University Of Maryland Baltimore County | Viral characterization by direct detection of capsid proteins |
CA2333463A1 (en) | 1998-06-04 | 1999-12-09 | Microsens Biophage Limited | Analytical method using multiple virus labelling |
CA2340719C (en) | 1998-08-14 | 2011-02-08 | Biocontrol Systems, Inc. | Composition, formulae, devices and methods for control of specificity and inclusivity of microorganisms containing closely related antigen epitopes |
JP2000308486A (en) * | 1999-02-22 | 2000-11-07 | Matsushita Electric Ind Co Ltd | Detection of bacterium |
US6681230B1 (en) | 1999-03-25 | 2004-01-20 | Lucent Technologies Inc. | Real-time event processing system with service authoring environment |
US6482632B1 (en) * | 1999-03-29 | 2002-11-19 | Council Of Scientic And Industrial Research | Bacteriophage, a process for the isolation thereof, and a universal growth medium useful in the process thereof |
DK1198713T3 (en) * | 1999-07-30 | 2006-05-01 | Profos Ag | Detection and identification of bacterial strains |
US6737266B1 (en) * | 1999-10-01 | 2004-05-18 | 3M Innovative Properties Company | Devices and methods for microorganism detection |
DE19957542C2 (en) | 1999-11-30 | 2002-01-10 | Infineon Technologies Ag | Alternating phase mask |
US6528325B1 (en) * | 2000-10-13 | 2003-03-04 | Dexall Biomedical Labs, Inc. | Method for the visual detection of specific antibodies in human serum by the use of lateral flow assays |
ES2263598T3 (en) | 2001-02-01 | 2006-12-16 | Profos Ag | DETECTION AND IDENTIFICATION OF BACTERIA GROUPS. |
US20020192676A1 (en) * | 2001-06-18 | 2002-12-19 | Madonna Angelo J. | Method for determining if a type of bacteria is present in a mixture |
JP4554206B2 (en) * | 2001-09-27 | 2010-09-29 | ガンガゲン インコーポレーティッド | Neutralized whole cell immunogenic bacterial composition |
US20050003346A1 (en) * | 2002-04-12 | 2005-01-06 | Colorado School Of Mines | Apparatus and method for detecting microscopic living organisms using bacteriophage |
CA2501648A1 (en) * | 2002-10-15 | 2004-04-29 | Regents Of The University Of Minnesota | Assays to detect or quantify bacterial or viral pathogens and contaminants |
EP1789572A2 (en) | 2004-06-07 | 2007-05-30 | Microphage, Incorporated | Microorganism detection using bacteriophage amplification |
WO2006012371A1 (en) | 2004-07-20 | 2006-02-02 | Medtronic, Inc. | Concurrent delivery of treatment therapy with telemetry in an implantable medical device |
WO2006105504A1 (en) | 2005-03-31 | 2006-10-05 | Microphage Incorporated | Apparatus and method for detecting microorganisms using flagged bacteriophage |
JP4675669B2 (en) * | 2005-04-28 | 2011-04-27 | アサヒ飲料株式会社 | Medium for detecting thermophilic Clostridium bacteria, method for shortening detection period, and method for detecting bacteria |
MX2009000285A (en) | 2006-06-30 | 2009-06-08 | Schering Corp | Substituted piperidines that increase p53 activity and the uses thereof. |
WO2008064241A2 (en) | 2006-11-20 | 2008-05-29 | Microphage Incorporated | Method and apparatus for enhanced bacteriophage-based diagnostic assay |
-
2008
- 2008-06-13 US US12/663,686 patent/US8455186B2/en not_active Expired - Fee Related
- 2008-06-13 JP JP2010512392A patent/JP5150856B2/en not_active Expired - Fee Related
- 2008-06-13 CA CA2690809A patent/CA2690809A1/en not_active Abandoned
- 2008-06-13 AU AU2008265989A patent/AU2008265989B8/en not_active Ceased
- 2008-06-13 WO PCT/US2008/066962 patent/WO2008157384A2/en active Application Filing
- 2008-06-13 EP EP08771055A patent/EP2158490A2/en not_active Withdrawn
- 2008-06-13 CN CN200880024912A patent/CN101802615A/en active Pending
Patent Citations (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1471329A (en) | 1973-09-04 | 1977-04-21 | Ajinomoto Kk | Method of inhibiting bacteriophage activity |
US4861709A (en) | 1985-05-31 | 1989-08-29 | Technicon Research A.G. | Detection and/or identification of microorganisms in a test sample using bioluminescence or other exogenous genetically-introduced marker |
WO1992002633A1 (en) | 1990-08-09 | 1992-02-20 | Amersham International Plc | Methods for rapid microbial detection |
US5498525A (en) | 1990-08-09 | 1996-03-12 | Amersham International Plc | Methods for rapid microbial detection |
US6300061B1 (en) | 1992-02-07 | 2001-10-09 | Albert Einstein College Of Medicine Of Yeshiva University | Mycobacterial species-specific reporter mycobacteriophages |
US5888725A (en) | 1992-09-22 | 1999-03-30 | The Secretary Of State For The Minister Of Agriculture Fisheries And Food In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Method for identifying target bacteria |
US5656424A (en) | 1995-02-15 | 1997-08-12 | Albert Einstein College Of Medicine, A Division Of Yeshiva University | Identification of mycobacterium tuberculosis complex species |
US5824468A (en) | 1995-05-18 | 1998-10-20 | Merck Patent Gesellschaft Mit Beschrankkter Haftung | Detection of listeria by means of recombinant bacteriophages |
US5985596A (en) | 1995-12-15 | 1999-11-16 | Biotec Laboratories Limited | Method to detect bacteria |
US6461833B1 (en) | 1995-12-15 | 2002-10-08 | Biotec Laboratories Limited | Method to detect bacteria |
US6555312B1 (en) | 1999-02-22 | 2003-04-29 | Matsushita Electric Industrial Co., Ltd. | Method for detecting bacteria with bacteriaphage |
US6436661B1 (en) | 2000-04-13 | 2002-08-20 | 3M Innovative Properties Company | Bacteria and bacteriophage detection using immobilized enzyme substrates |
US6544729B2 (en) | 2001-07-20 | 2003-04-08 | University Of Tennessee | Bioluminescent biosensor device |
US20040224359A1 (en) | 2002-04-12 | 2004-11-11 | Madonna Angelo J. | Method for detecting low concentrations of a target bacterium that uses phages to infect target bacterial cells |
WO2006125319A1 (en) | 2005-05-26 | 2006-11-30 | Gangagen Life Sciences Inc. | Bacterial management in animal holding systems |
Non-Patent Citations (6)
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10881792B2 (en) | 2017-01-13 | 2021-01-05 | Bigfoot Biomedical, Inc. | System and method for adjusting insulin delivery |
Also Published As
Publication number | Publication date |
---|---|
CN101802615A (en) | 2010-08-11 |
CA2690809A1 (en) | 2008-12-24 |
AU2008265989B8 (en) | 2012-01-12 |
US8455186B2 (en) | 2013-06-04 |
AU2008265989B2 (en) | 2011-11-24 |
US20100196877A1 (en) | 2010-08-05 |
EP2158490A2 (en) | 2010-03-03 |
JP2010529861A (en) | 2010-09-02 |
JP5150856B2 (en) | 2013-02-27 |
WO2008157384A3 (en) | 2009-02-12 |
AU2008265989A1 (en) | 2008-12-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP4490112B2 (en) | A method for detecting low concentrations of target bacteria using phage to infect target bacterial cells | |
US8092990B2 (en) | Apparatus and method for detecting microscopic organisms using bacteriophage | |
US20090246752A1 (en) | Apparatus and method for detecting microscopic living organisms using bacteriophage | |
US8455186B2 (en) | Method of detection of microorganisms with enhanced bacteriophage amplification | |
AU2006292496B2 (en) | Method and apparatus for identification of microorganisms using bacteriophage | |
US8216780B2 (en) | Method for enhanced sensitivity in bacteriophage-based diagnostic assays | |
US20070178450A1 (en) | Method and apparatus for determining level of microorganisms using bacteriophage | |
US20080241819A1 (en) | Method and apparatus for enhanced bacteriophage-based diagnostic assays by selective inhibition of potential cross-reactive organisms | |
EP1613965A2 (en) | Apparatus and method for detecting microscopic living organisms using bacteriophage | |
JP2007523628A (en) | Apparatus and method for detecting microorganisms using bacteriophage | |
US20110097702A1 (en) | Methods and compositions for in situ detection of microorganisms on a surface | |
WO2006083292A2 (en) | Microorganism detection using bacteriophage amplification | |
CN101595229A (en) | The cross reaction biology that suppresses to exist by selectivity strengthens the method and apparatus based on the diagnostic assay of phage |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200880024912.5 Country of ref document: CN |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 08771055 Country of ref document: EP Kind code of ref document: A2 |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2690809 Country of ref document: CA Ref document number: 2008771055 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2010512392 Country of ref document: JP |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2008265989 Country of ref document: AU |
|
ENP | Entry into the national phase |
Ref document number: 2008265989 Country of ref document: AU Date of ref document: 20080613 Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 12663686 Country of ref document: US |