+

US20050181363A1 - Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith - Google Patents

Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith Download PDF

Info

Publication number
US20050181363A1
US20050181363A1 US10/500,435 US50043504A US2005181363A1 US 20050181363 A1 US20050181363 A1 US 20050181363A1 US 50043504 A US50043504 A US 50043504A US 2005181363 A1 US2005181363 A1 US 2005181363A1
Authority
US
United States
Prior art keywords
acid
heating
fast bacterium
gene
minutes
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US10/500,435
Inventor
Tatsuo Kamata
Yuji Izumizawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Arkray Inc
Original Assignee
Arkray Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Arkray Inc filed Critical Arkray Inc
Assigned to ARKRAY, INC. reassignment ARKRAY, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: IZUMIZAWA, YUJI, KAMATA, TATSUO
Publication of US20050181363A1 publication Critical patent/US20050181363A1/en
Priority to US11/656,575 priority Critical patent/US7935483B2/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/06—Lysis of microorganisms
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
    • C12N15/1003—Extracting or separating nucleic acids from biological samples, e.g. pure separation or isolation methods; Conditions, buffers or apparatuses therefor
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6806—Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844—Nucleic acid amplification reactions

Definitions

  • the present invention relates to a method of lysing acid-fast bacteria and to a method of performing gene amplification or gene detection using the same.
  • Tuberculosis still is a serious bacterial disease worldwide, and not only treatment methods but also diagnostic methods therefor are extremely important.
  • a final diagnosis as to the tuberculosis infection is made by carrying out a culture method.
  • tubercule bacilli have an extremely slow growth rate, the establishment of a preliminary diagnostic method to be performed prior to the culture method has been desired.
  • a method using a polymerase chain reaction (PCR) method is attracting attention.
  • a primer specific to a gene of a tubercule bacillus is used to amplify a gene of the tubercule bacillus, if any, so that it can be detected, thereby enabling the presence or absence of the tubercule bacillus to be determined.
  • a first lysis method of the present invention is a method of lysing an acid-fast bacterium to extract a gene from the acid-fast bacterium, including: heating the acid-fast bacterium in a liquid containing a non-ionic detergent at a temperature below a boiling point of the liquid.
  • a second lysis method of the present invention is a method of lysing an acid-fast bacterium to extract a gene from the acid-fast bacterium, including: causing lipolysis by treating the acid-fast bacterium with lipase, and heating the acid-fast bacterium in the presence of a non-ionic detergent.
  • a gene can be extracted sufficiently from an acid-fast bacterium by merely heating the acid-fast bacterium in a solution containing a non-ionic detergent, for example, at 96° C. for 10 minutes.
  • a method of amplifying or detecting the gene to be performed subsequently can be carried out easily.
  • the heating temperature is below the boiling point of the liquid, the method has the following advantages, for example. Since the bumping of the liquid is prevented, there is reduced concern that a sample might be scattered. Moreover, since the temperature can be controlled easily, a special heater is not necessary.
  • the inventors of the present invention achieved the second lysis method of the present invention by focusing on the fact that acid-fast bacteria have a high cell-wall lipid content. That is, in the second lysis method of the present invention, a cell wall of an acid-fast bacterium is weakened by the lipolysis and the acid-fast bacterium is lysed by the heating.
  • the first and second lysis methods of the present invention acid-fast bacteria can be lysed easily and in a short time without using any special reagent such as a chaotropic reagent or any special device such as an ultrasonic device. Besides, since the first and second lysis methods are chemical methods, they can be carried out safely with little risk that a sample might be scattered. Moreover, according to the first and the second lysis methods of the present invention, the gene extracted may be subjected to a gene amplification process or a gene detection process as it is without being purified. It is to be noted that the first and the second lysis methods of the present invention are applicable not only to a method of performing gene amplification or gene detection but also to other fields such as gene manipulation, for example.
  • FIG. 1 is a photograph showing the result of the electrophoresis performed to determine a lysing effect of one example of the present invention
  • FIG. 2 is a photograph showing the result of the electrophoresis performed to determine a lysing effect of another example of the present invention.
  • FIG. 3 is a photograph showing the result of the electrophoresis performed to determine a lysing effect of still another example of the present invention.
  • the heating temperature preferably is not less than 70° C. and less than 100° C., more preferably not less than 80° C. and less than 100° C., and most suitably 96° C. Furthermore, the heating is performed, for example, for 1 to 30 minutes, preferably for 10 minutes.
  • the pH of the liquid is, for example, in the range from 7.0 to 12.0, preferably 8.0.
  • the concentration of the non-ionic detergent in the liquid is, for example, 0.01 to 10 wt %, preferably 0.5 to 2.0 wt %, and more preferably 1.0 wt %.
  • non-ionic detergent examples include: D-sorbitol fatty acid esters such as Span 20, Span 40, Span 60, Span 65, Span 80, and Span 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol sorbitan alkyl esters such as Tween 20, Tween 21, Tween 40, Tween 60, Tween 65, Tween 80, Tween 81, and Tween 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol p-t-octylphenyl ethers such as Triton X-100 (manufactured by Nacalai Tesque, Inc., for example). These detergents may be used either alone or in combinations of two or more types. Among these, Triton X-100, Tween 20, and Tween 21 are preferable, and Triton X-100 is more preferable.
  • the liquid further contains a metal chelating agent.
  • the metal chelating agent serves to prevent a gene-degrading enzyme such as DNase contained in a sample from degrading the gene, for example.
  • the concentration of the metal chelating agent in the liquid is, for example, 0.1 to 100 mM, preferably 1.0 mM.
  • the metal chelating agent include ethylenediaminetetraacetic acid (EDTA), ethylene glycol bis( ⁇ -aminoethyl ether)—N, N, N′, N′-tetraacetic acid (EGTA), diaminocyclohexane tetraacetic acid, o-phenanthroline, and salicylic acid.
  • EDTA ethylenediaminetetraacetic acid
  • EGTA ethylene glycol bis( ⁇ -aminoethyl ether)—N, N, N′, N′-tetraacetic acid
  • Examples of an acid-fast bacterium to which the first lysis method of the present invention is applicable include M. avium, M. intracellularae, M. gordonae, M. tuberculosis, M. kansasii, M. fortuitum, M. chelonae, M. bovis, M. scrofulaceum, M. paratuberculosis, M. phlei, M. marinum, M. simiae, M. scrofulaceum, M. szulgai, M. leprae, M. xenopi, M. ulcerans, M. lepraemurium, M. flavescens, M. terrae, M. nonchromogenicum, M. malmoense, M. asiaticum, M. vaccae, M. gastri, M. triviale, M. haemophilum, M. africanum, M. thermoresistahle, and M. smegmatis.
  • examples of a biological sample containing an acid-fast bacterium include sputum, spinal fluid, feces, saliva, blood, tissues, and urine.
  • the first lysis method of the present invention can be carried out in the following manner, for example.
  • a metal chelating agent such as EDTA is added as necessary and a non-ionic detergent further is added, thus preparing a lysis reagent solution.
  • a buffer Tris-HCl buffer, HEPES buffer, MOPS buffer, HEPPS buffer, TAPS buffer, phosphate buffer, or the like may be used.
  • This lysis reagent solution preferably is sterilized by high-pressure steam in an autoclave.
  • a sample solution is prepared.
  • a sputum specimen that has been homogenized and sterilized by the N-acetyl-L-cysteine-NaOH method (NALC-NaOH method) or the like may be used as the sample solution.
  • the sample solution is centrifuged and the supernatant is removed.
  • the lysis reagent solution is added to the remaining precipitate (pellet).
  • a lysis treatment is carried out by heating the mixture at a temperature in the above-described predetermined range using a heating block or the like.
  • heating means other than the heating block include a water bath, a microwave oven, and an air bath.
  • the specimen thus lysed may be subjected to a gene amplification process or a gene detection process simply as it is or after being pretreated.
  • Examples of the method of performing the gene amplification or gene detection include a PCR method and modifications of the PCR method, such as a RT-PCR method.
  • examples of the gene to be analyzed include DNA and RNA.
  • the heating also serves to deactivate the lipase. This allows the lipase to be deactivated without performing any special process.
  • the possibility that the lipase might affect a process to be performed subsequent to the lysis treatment, such as a gene amplification process or a gene detection process, can be eliminated.
  • the lipolysis and the heating are performed in buffers, respectively. It is more preferable that the lipolysis and the heating are performed in the same buffer.
  • the type of the buffer is not particularly limited, and for example, Tris buffer, HEPES buffer, phosphate buffer, glycine buffer, McIlvaine buffer, and the like can be used. Among these, Tris buffer and HEPES buffer are preferable.
  • the lipolysis and the heating are performed in the same container as a closed system.
  • the lipolysis and the heating are performed in the same container as a closed system.
  • the heating may be performed after the lipolysis, or the lipolysis and the heating may be performed simultaneously.
  • the lipolysis is performed at a pH of 4 to 8 and at a temperature of 37° C. to 60° C. for 5 to 30 minutes, and the heating is performed at a temperature of 37° C. to 100° C. for 5 to 30 minutes.
  • the lipolysis is performed at a pH of 6 to 8 and at a temperature of 37° C. to 50° C. for 5 to 20 minutes, and the heating is performed at a temperature of 80° C. to 100° C. for 5 to 20 minutes.
  • the lipolysis is performed at a pH of 6.5 to 7.5 and at a temperature of 37° C. to 50° C. for 10 minutes, and the heating is performed at a temperature of 90° C. to 98° C. for 10 minutes.
  • the lipolysis and the heating are performed, for example, at a pH of 4 to 8 and at a temperature of 37° C. to 60° C. for 10 to 30 minutes; preferably at a pH of 6 to 8 and at a temperature of 37° C. to 50° C. for 10 to 20 minutes, and more preferably at a pH of 6.5 to 7.5 and at a temperature of 45° C. to 50° C. for 10 to 20 minutes.
  • the concentration of the lipase in the buffer is 10 to 10000 units/ml, preferably 100 to 2000 units/ml, and more preferably 200 to 1000 units/ml.
  • the lipase used is not particularly limited, and for example, products named Lipase R “AMANO” G, Lipase M “AMANO” 10, Lipase G “AMANO” 50, Lip ase AY “AMANO” 30G, Lip ase A “AMANO” 6 (all manufactured by Amano Pharmaceutical Co., Ltd.) and the like may be used. They may be used either alone or in combinations of two or more types. Among these, Lipase G “AMANO” 50 and Lipase AY “AMANO” 30G are preferable, and Lipase AY “AMANO” 30G is more preferable.
  • the concentration of the non-ionic detergent in the buffer is, for example, 0.01 to 10 wt %, preferably 0.1 to 2.0 wt %, and more preferably 0.5 to 1.0 wt %.
  • non-ionic detergent examples include: D-sorbitol fatty acid esters such as Span 20, Span 40, Span 60, Span 65, Span 80, and Span 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol sorbitan alkyl esters such as Tween 20, Tween 21, Tween 40, Tween 60, Tween 65, Tween 80, Tween 81, and Tween 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol p-t-octylphenyl ethers such as Triton X-100 (manufactured by Nacalai Tesque, Inc., for example). These detergents may be used either alone or in combinations of two or more types. Among these, Tween 20 and Triton X-100 are preferable, and Triton X-100 is more preferable.
  • the heating is performed in the presence of a metal chelating agent in addition to the non-ionic detergent.
  • the metal chelating agent serves to prevent a gene-degrading enzyme such as DNase contained in a sample from degrading the gene, for example.
  • concentration of the metal chelating agent in the liquid is, for example, 0.1 to 2.0 mM, preferably 0.5 to 1.0 mM.
  • the metal chelating agent include ethylenediaminetetraacetic acid (EDTA), glycol ether diaminetetraacetic acid (EGTA), and 1,2-cyclohexanediaminetetraacetic acid (CyDTA). These metal chelating agents may be used either alone or in combinations of two or more types. Among these, EDTA and EGTA are preferable, and EDTA is more preferable.
  • the second lysis method is applicable to the same acid-fast bacteria as the first lysis method. Furthermore, biological samples containing an acid-fast bacterium to be used in the second lysis method also are the same as those in the first lysis method.
  • the second method of the present invention can be carried out in the following manner, for example.
  • a buffer having a pH in the above-described predetermined range lipase and a non-ionic detergent are added, and a metal chelating agent such as EDTA is added as necessary, thus preparing a lysis reagent solution.
  • This lysis reagent solution preferably is sterilized by high-pressure steam in an autoclave.
  • a sample is added to this lysis reagent solution, and the resultant mixture is incubated at 45° C. for 10 minutes (the lipolysis), and then further incubated at 96° C. for 10 minutes (the heating).
  • a cell wall of the acid-fast bacterium is weakened by the former incubation, and the acid-fast bacterium is lysed and also the lipase is deactivated by the latter incubation.
  • Both of the incubations may be carried out using a heating block, a water bath, a thermal cycler, or the like.
  • the lipolysis and the heating may be performed simultaneously by adding the sample to the lysis reagent solution and then incubating the resultant mixture at a temperature of 37° C. to 50° C. for 10 to 20 minutes.
  • the sample may be prepared, for example, by homogenizing and sterilizing a sputum specimen by the N-acetyl-L-cysteine-NaOH method (NALC-NaOH method) or the like.
  • NALC-NaOH method N-acetyl-L-cysteine-NaOH method
  • the sample is centrifuged and the supernatant is removed. Thereafter, the lysis reagent solution is added to the remaining precipitate (pellet).
  • the specimen thus lysed may be subjected to a gene amplification process or a gene detection process simply as it is or after being pretreated.
  • Examples of the method of performing the gene amplification or gene detection include a PCR method and modifications of the PCR method, such as a RT-PCR method.
  • examples of the gene to be analyzed include DNA and RNA.
  • Examples 1-1, 1-2, 1-3, and 1-4 are directed to the first lysis method of the present invention, and Examples 2-1, 2-2, 2-3, and 2-4 are directed to the second lysis method of the present invention.
  • a clinical isolate of a tubercule bacillus was cultured in a product named MycoBroth (Kyokuto Pharmaceutical Industrial Co., Ltd.) at 37° C. until a turbidity corresponding to #1 of the McFarland turbidity standard was obtained. Then, the culture was diluted with phosphate buffer (pH 6.8) so as to achieve a series of 10-fold dilutions (10 2 -fold to 10 5 -fold), thus preparing test solutions containing the tubercule bacillus. Subsequently, 100 ⁇ l of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10000 g, 15 minutes) to prepare pellets.
  • the pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction.
  • a product named Triton X-100 (Nacalai Tesque, Inc.) was dissolved in TE buffer (10 mM EDTA and 25 mM Tris-HCl, pH 8.0) so that its concentration became 3 wt % to prepare a lysis reagent solution, and the lysis reagent solution was sterilized by high-pressure steam in an autoclave.
  • Example 1-1 To 37.5 ⁇ l of the thus-obtained lysed sample solutions of Example 1-1 and Comparative Example 1, 50 ⁇ l of a premixture of a product named AMPLICOR Amplification and Detection Kit (Nippon Roche K.K.) and 12.5 ⁇ l of 12 mM magnesium acetate were added. With regard to each of the mixtures obtained, amplification and detection by the PCR method were carried out in a COBAS AMPLICOR in accordance with the operating instructions of the kit.
  • AMPLICOR Amplification and Detection Kit Nippon Roche K.K.
  • Example 1-1 As a result of the above-described amplification and detection, it was found that, in both Example 1-1 and Comparative Example 1, the samples prepared from the test solutions with a dilution factor of up to 10 7 were judged as tuberculosis positive and those with a dilution factor of greater than 10 7 were judged as tuberculosis negative.
  • the lysis method according to Example 1-1 can achieve a sensitivity (lysis efficiency) equivalent to that of the conventional method (Comparative Example 1).
  • the lysis method according to Example 1-1 took only half the treatment period of the conventional method (Comparative Example 1).
  • a clinical isolate of a tubercule bacillus was cultured in a product named MycoBroth (Kyokuto Pharmaceutical Industrial Co., Ltd.) at 37° C. until a turbidity corresponding to #1 of the McFarland turbidity standard was obtained. Then, the culture was diluted with a non-tuberculous sputum that had been homogenized with a product named SUPTAZYME (Kyokuto Pharmaceutical Industrial Co., Ltd.) so as to achieve a series of 10-fold dilutions (10 0 -fold to 10 10 -fold). The resultant diluents were used as samples.
  • Triton X-100 (Nacalai Tesque, Inc.) was dissolved in TE buffer (10 mM EDTA and 25 mM Tris-HCl, pH 8.0) so that its concentration became 3 wt % to prepare a lysis reagent solution, and the lysis reagent solution was sterilized by high-pressure steam in an autoclave.
  • Example 1-2 To 37.5 ⁇ l of the thus-obtained lysed sample solutions of Example 1-2 and Comparative Example 2, 50 ⁇ l of a premixture of a product named AMPLICOR Amplification and Detection Kit (Nippon Roche K.K.) and 12.5 ⁇ l of 12 mM magnesium acetate were added. With regard to each of the mixtures obtained, amplification and detection by the PCR method were carried out in a COBAS AMPLICOR in accordance with the operating instructions of the kit.
  • AMPLICOR Amplification and Detection Kit Nippon Roche K.K.
  • Example 1-2 As a result of the above-described amplification and detection, it was found that, in both Example 1-2 and Comparative Example 2, the samples with a dilution factor of up to 10 4 were judged as tuberculosis positive and those with a dilution factor of greater than 10 4 were judged as tuberculosis negative.
  • the lysis method according to Example 1-2 can achieve a sensitivity (lysis efficiency) equivalent to that of the conventional method (Comparative Example 2) even under the influence of contaminants.
  • the lysis method according to Example 1-2 took only half the treatment period of the conventional method (Comparative Example 2).
  • a product named Triton X-100 (Nacalai Tesque, Inc.) was dissolved in TE buffer (10 mM EDTA and 25 mM Tris-HCl, pH 8.0) so that its concentration became 1 wt % to prepare a lysis reagent solution, and the lysis reagent solution was used after being sterilized by high-pressure steam in an autoclave. Specifically, 50 ⁇ l of the sterilized lysis reagent solution was added to the pellets obtained from the respective specimens to suspend the pellets. Then, a lysis treatment was carried out by heating the suspensions at 96° C. for 10 minutes in a heating block.
  • Comparative Example 3 samples (pellets) prepared in the same manner as in the above were lysed using a product named AMPLICOR Specimen Pretreatment Kit (Nippon Roche K.K.).
  • Example 3 To 12.5 ⁇ l of the thus-obtained lysed sample solutions of Example 1-3 and Comparative Example 3, 50 ⁇ l of a premixture of a product named AMPLICOR Amplification and Detection Kit (Nippon Roche K.K.) and 37.5 ⁇ l of 12 mM magnesium acetate were added. With regard to each of the mixtures obtained, amplification and detection by the PCR method were carried out in a COBAS AMPLICOR in accordance with the operating instructions of the kit. In addition, with regard to samples (pellets) prepared in the same manner as in the above, a culture test was carried out in the usual way.
  • AMPLICOR Amplification and Detection Kit Nippon Roche K.K.
  • the lysis method of the present invention can produce the lysing effect equivalent to that of the conventional method and can serve as a useful method in actual clinical tests.
  • the time required for the lysis treatment in the method of Example 1-3 was 30 minutes shorter than that in the method of Comparative Example 3.
  • a product named Lipase G “AMANO” 50 (Amano Pharmaceutical Co., Ltd.) and a product named Lipase AY “AMANO” 30G (Amano Pharmaceutical Co., Ltd.) were dissolved in 10 mM HEPES buffer (pH 7.0) to prepare lipase reagent solutions. Furthermore, a lysis reagent solution was prepared by adding a product named Triton X-100 (Nacalai Tesque, Inc.) to TE buffer (10 mM Tris and 1 mM EDTA, pH 8.0) and sterilizing the mixture by high-pressure steam in an autoclave (the thus-obtained lysis reagent solution is hereinafter referred to as “TE-Triton reagent”).
  • a culture of BCG used for preparing samples was prepared by culturing BCG in a liquid culture medium for growing acid-fast bacteria (a product named MycoBroth, manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd.) until the solution containing the BCG had a turbidity corresponding to #1 of the McFarland turbidity standard and then diluting the solution as necessary.
  • a liquid culture medium for growing acid-fast bacteria a product named MycoBroth, manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd.
  • the resultant solution containing the BCG was diluted gradually (10 ⁇ 4 , 10 ⁇ 3.5 , 10 ⁇ 3 , 10 ⁇ 2.5 , 10 ⁇ 2 ) with phosphate buffer (pH 6.8), thus preparing test solutions.
  • 100 ⁇ l of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10,000 g, 15 minutes) to prepare pellets.
  • the pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction.
  • the above-described lipase solutions were prepared so that the lipase concentrations became 100, 500, 1000, 2000, and 3000 (units/ml), respectively.
  • Example 1-4 the same procedures were carried out except that the lipase treatment was not performed.
  • PCR was carried out in the following manner: 94° C. for 1 minute to denature, followed by 30 thermal cycles, each cycle consisting of 94° C. for 30 seconds, 60° C. for 1 minute, and 72° C. for 1 minute.
  • the sequence of the primers and the composition of the reaction solutions are shown below.
  • the solution containing BCG obtained in the same manner as in the above was diluted gradually (10 ⁇ 4 , 10 ⁇ 3.5 , 10 ⁇ 3 , 10 ⁇ 2.5 ) with phosphate buffer (pH 6.8).
  • the resultant diluents were used as test solutions.
  • 100 ⁇ l of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10,000 g, 15 minutes) to prepare pellets.
  • the pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction.
  • Lipase AY “AMANO” 30G was added to the above-described TE-Triton solution so that its concentrations became 500 units/ml to prepare a lysis reagent solution.
  • 100 ⁇ l of the lysis reagent solution was added to the samples.
  • the resultant mixtures were mixed in a vortex mixer and then centrifuged slightly, followed by incubation at 45° C. The incubation was carried out for the following two different periods: 10 minutes and 30 minutes. Subsequently, a lysis treatment was carried out by heating the mixtures at 96° C. for 10 minutes (Example 2-2).
  • Example 2-3 the same procedures were carried out except that the lipase treatment and the heat treatment were performed simultaneously (45° C., 10 minutes).
  • Triton X-100 (Nacalai Tesque, Inc.) was added to TE buffer (10 mM Tris and 1 mM EDTA, pH 8.0) and to Tris buffer (10 mM Tris, pH 8.0) so that its concentration became 1%.
  • the resultant mixtures were sterilized in an autoclave, thus preparing a reagent containing EDTA and a reagent containing no EDTA.
  • these reagents are referred to as a TE-Triton reagent (containing EDTA) and a Tris-Triton reagent (containing no EDTA), respectively.
  • a culture of BCG used for preparing samples was prepared by culturing BCG in a liquid culture medium for growing acid-fast bacteria (a product named MycoBroth, manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd.) until the solution containing the BCG had a turbidity corresponding to #1 of the McFarland turbidity standard and then diluting the solution as necessary.
  • a liquid culture medium for growing acid-fast bacteria a product named MycoBroth, manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd.
  • the resultant solution containing BCG was diluted gradually (10 ⁇ 4.5 , 10 ⁇ 4 , 10 ⁇ 3.5 , 10 ⁇ 3 , 10 ⁇ 2.5 ) with phosphate buffer (pH 6.8), thus preparing test solutions.
  • 100 ⁇ l of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10,000 g, 15 minutes) to prepare pellets.
  • the pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction.
  • Lipase AY “AMANO” 30G was added to the above-described TE-Triton solution and to the Tris-Triton solution so that its concentrations became 500 units/ml.
  • the present invention provides a method of securely lysing acid-fast bacteria easily and in a short time without using any special device or special reagent. Therefore, by applying the method of the present invention to, for example, a pretreatment of a sample to be analyzed in an acid-fast bacterium test utilizing gene amplification and detection, the efficiency of the test can be improved easily.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Genetics & Genomics (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Biomedical Technology (AREA)
  • Biotechnology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Analytical Chemistry (AREA)
  • Microbiology (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Physics & Mathematics (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Plant Pathology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Immunology (AREA)
  • Mycology (AREA)
  • Medicinal Chemistry (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Virology (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Amplifiers (AREA)
  • Measurement Of Radiation (AREA)

Abstract

A method of effecting lysis of acid-fast bacteria, comprising heating acid-fast bacteria in a liquid containing a non-ionic surfactant at a temperature of below the boiling point of the liquid. This method enables accomplishing secure lysis of acid-fast bacteria in a simple manner within a short period of time without the use of special apparatus and agent and enables extracting genes. The heating is preferably conducted at 96° C. for 10 min. As the nonionic surfactant, use can be made of a d-sorbitol fatty acid ester, a polyoxyethylene glycol sorbitan alkyl ester, a polyoxyethylene glycol p-t-octylphenyl ether or the like. The pH value of the liquid is preferably 8, and the liquid preferably contains EDTA. It is also preferred that before the heating, the acid-fast bacteria be treated with lipase.

Description

    TECHNICAL FIELD
  • The present invention relates to a method of lysing acid-fast bacteria and to a method of performing gene amplification or gene detection using the same.
    • BACKGROUND ART
  • Tuberculosis still is a serious bacterial disease worldwide, and not only treatment methods but also diagnostic methods therefor are extremely important. A final diagnosis as to the tuberculosis infection is made by carrying out a culture method. However, since tubercule bacilli have an extremely slow growth rate, the establishment of a preliminary diagnostic method to be performed prior to the culture method has been desired. As such a preliminary diagnostic method, a method using a polymerase chain reaction (PCR) method is attracting attention. In this method, a primer specific to a gene of a tubercule bacillus is used to amplify a gene of the tubercule bacillus, if any, so that it can be detected, thereby enabling the presence or absence of the tubercule bacillus to be determined.
  • In the above-described preliminary diagnostic method using the PCR method, extracting the gene by lysing the tubercule bacillus is necessary as a pretreatment. Examples of conventional lysis methods include chemical methods using organic solvents or the like and physical methods using ultrasonic waves or repeating freezing and thawing. However, since tubercule bacilli have a high cell-wall lipid content, such conventional lysis methods cannot extract genes sufficiently. In order to achieve sufficient gene extraction, it is necessary to make the treatment conditions severer, which requires the use of a special device and/or a special reagent. Besides, this may result in a longer treatment period and a more complicated operation. Such problems with lysing are not specific to tubercule bacilli and relate to the entire acid-fast bacteria group including the tubercule bacilli.
    • DISCLOSURE OF INVENTION
  • Therefore, with the foregoing in mind, it is an object of the present invention to provide a method of lysing acid-fast bacteria easily and in a short time without using any special device or special reagent.
  • In order to achieve the above object, a first lysis method of the present invention is a method of lysing an acid-fast bacterium to extract a gene from the acid-fast bacterium, including: heating the acid-fast bacterium in a liquid containing a non-ionic detergent at a temperature below a boiling point of the liquid.
  • Furthermore, in order to achieve the above object, a second lysis method of the present invention is a method of lysing an acid-fast bacterium to extract a gene from the acid-fast bacterium, including: causing lipolysis by treating the acid-fast bacterium with lipase, and heating the acid-fast bacterium in the presence of a non-ionic detergent.
  • According to the first lysis method of the present invention, a gene can be extracted sufficiently from an acid-fast bacterium by merely heating the acid-fast bacterium in a solution containing a non-ionic detergent, for example, at 96° C. for 10 minutes. Thus, a method of amplifying or detecting the gene to be performed subsequently can be carried out easily. Furthermore, since the heating temperature is below the boiling point of the liquid, the method has the following advantages, for example. Since the bumping of the liquid is prevented, there is reduced concern that a sample might be scattered. Moreover, since the temperature can be controlled easily, a special heater is not necessary.
  • On the other hand, the inventors of the present invention achieved the second lysis method of the present invention by focusing on the fact that acid-fast bacteria have a high cell-wall lipid content. That is, in the second lysis method of the present invention, a cell wall of an acid-fast bacterium is weakened by the lipolysis and the acid-fast bacterium is lysed by the heating.
  • According to the first and second lysis methods of the present invention, acid-fast bacteria can be lysed easily and in a short time without using any special reagent such as a chaotropic reagent or any special device such as an ultrasonic device. Besides, since the first and second lysis methods are chemical methods, they can be carried out safely with little risk that a sample might be scattered. Moreover, according to the first and the second lysis methods of the present invention, the gene extracted may be subjected to a gene amplification process or a gene detection process as it is without being purified. It is to be noted that the first and the second lysis methods of the present invention are applicable not only to a method of performing gene amplification or gene detection but also to other fields such as gene manipulation, for example.
    • BRIEF DESCRIPTION OF DRAWINGS
  • FIG. 1 is a photograph showing the result of the electrophoresis performed to determine a lysing effect of one example of the present invention;
  • FIG. 2 is a photograph showing the result of the electrophoresis performed to determine a lysing effect of another example of the present invention; and
  • FIG. 3 is a photograph showing the result of the electrophoresis performed to determine a lysing effect of still another example of the present invention.
    • BEST MODE FOR CARRYING OUT THE INVENTION
  • Hereinafter, the first lysis method and the second lysis method according to the present invention will be described in further detail.
  • First, the first lysis method of the present invention will be described.
  • In the first lysis method of the present invention, the heating temperature preferably is not less than 70° C. and less than 100° C., more preferably not less than 80° C. and less than 100° C., and most suitably 96° C. Furthermore, the heating is performed, for example, for 1 to 30 minutes, preferably for 10 minutes. The pH of the liquid is, for example, in the range from 7.0 to 12.0, preferably 8.0. The concentration of the non-ionic detergent in the liquid is, for example, 0.01 to 10 wt %, preferably 0.5 to 2.0 wt %, and more preferably 1.0 wt %.
  • Examples of the non-ionic detergent include: D-sorbitol fatty acid esters such as Span 20, Span 40, Span 60, Span 65, Span 80, and Span 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol sorbitan alkyl esters such as Tween 20, Tween 21, Tween 40, Tween 60, Tween 65, Tween 80, Tween 81, and Tween 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol p-t-octylphenyl ethers such as Triton X-100 (manufactured by Nacalai Tesque, Inc., for example). These detergents may be used either alone or in combinations of two or more types. Among these, Triton X-100, Tween 20, and Tween 21 are preferable, and Triton X-100 is more preferable.
  • In the first lysis method of the present invention, it is preferable that the liquid further contains a metal chelating agent. The metal chelating agent serves to prevent a gene-degrading enzyme such as DNase contained in a sample from degrading the gene, for example. The concentration of the metal chelating agent in the liquid is, for example, 0.1 to 100 mM, preferably 1.0 mM. Examples of the metal chelating agent include ethylenediaminetetraacetic acid (EDTA), ethylene glycol bis(β-aminoethyl ether)—N, N, N′, N′-tetraacetic acid (EGTA), diaminocyclohexane tetraacetic acid, o-phenanthroline, and salicylic acid. These metal chelating agents may be used either alone or in combinations of two or more types. Among these, EDTA and EGTA are preferable, and EDTA is more preferable.
  • Examples of an acid-fast bacterium to which the first lysis method of the present invention is applicable include M. avium, M. intracellularae, M. gordonae, M. tuberculosis, M. kansasii, M. fortuitum, M. chelonae, M. bovis, M. scrofulaceum, M. paratuberculosis, M. phlei, M. marinum, M. simiae, M. scrofulaceum, M. szulgai, M. leprae, M. xenopi, M. ulcerans, M. lepraemurium, M. flavescens, M. terrae, M. nonchromogenicum, M. malmoense, M. asiaticum, M. vaccae, M. gastri, M. triviale, M. haemophilum, M. africanum, M. thermoresistahle, and M. smegmatis.
  • In the first lysis method of the present invention, examples of a biological sample containing an acid-fast bacterium include sputum, spinal fluid, feces, saliva, blood, tissues, and urine.
  • Next, the first lysis method of the present invention can be carried out in the following manner, for example. First, to a buffer having a pH in the above-described predetermined range, a metal chelating agent such as EDTA is added as necessary and a non-ionic detergent further is added, thus preparing a lysis reagent solution. As the buffer, Tris-HCl buffer, HEPES buffer, MOPS buffer, HEPPS buffer, TAPS buffer, phosphate buffer, or the like may be used. This lysis reagent solution preferably is sterilized by high-pressure steam in an autoclave. On the other hand, a sample solution is prepared. For example, a sputum specimen that has been homogenized and sterilized by the N-acetyl-L-cysteine-NaOH method (NALC-NaOH method) or the like may be used as the sample solution. The sample solution is centrifuged and the supernatant is removed. To the remaining precipitate (pellet), the lysis reagent solution is added. Thereafter, a lysis treatment is carried out by heating the mixture at a temperature in the above-described predetermined range using a heating block or the like. Examples of heating means other than the heating block include a water bath, a microwave oven, and an air bath.
  • The specimen thus lysed may be subjected to a gene amplification process or a gene detection process simply as it is or after being pretreated. Examples of the method of performing the gene amplification or gene detection include a PCR method and modifications of the PCR method, such as a RT-PCR method. Furthermore, examples of the gene to be analyzed include DNA and RNA.
  • Next, the second lysis method of the present invention will be described.
  • In the second lysis method of the present invention, it is preferable that the heating also serves to deactivate the lipase. This allows the lipase to be deactivated without performing any special process. In addition, the possibility that the lipase might affect a process to be performed subsequent to the lysis treatment, such as a gene amplification process or a gene detection process, can be eliminated.
  • In the second lysis method of the present invention, it is preferable that the lipolysis and the heating are performed in buffers, respectively. It is more preferable that the lipolysis and the heating are performed in the same buffer. The type of the buffer is not particularly limited, and for example, Tris buffer, HEPES buffer, phosphate buffer, glycine buffer, McIlvaine buffer, and the like can be used. Among these, Tris buffer and HEPES buffer are preferable.
  • In the second lysis method of the present invention, it is preferable that the lipolysis and the heating are performed in the same container as a closed system. By performing the lipolysis and the heating in the closed system, it is possible to prevent a sample from being scattered. Moreover, by performing the lipolysis and the heating in the same container, the processing efficiency can be improved.
  • In the second lysis method of the present invention, the heating may be performed after the lipolysis, or the lipolysis and the heating may be performed simultaneously. In the former case, for example, the lipolysis is performed at a pH of 4 to 8 and at a temperature of 37° C. to 60° C. for 5 to 30 minutes, and the heating is performed at a temperature of 37° C. to 100° C. for 5 to 30 minutes. Preferably, the lipolysis is performed at a pH of 6 to 8 and at a temperature of 37° C. to 50° C. for 5 to 20 minutes, and the heating is performed at a temperature of 80° C. to 100° C. for 5 to 20 minutes. More preferably, the lipolysis is performed at a pH of 6.5 to 7.5 and at a temperature of 37° C. to 50° C. for 10 minutes, and the heating is performed at a temperature of 90° C. to 98° C. for 10 minutes. On the other hand, in the latter case, the lipolysis and the heating are performed, for example, at a pH of 4 to 8 and at a temperature of 37° C. to 60° C. for 10 to 30 minutes; preferably at a pH of 6 to 8 and at a temperature of 37° C. to 50° C. for 10 to 20 minutes, and more preferably at a pH of 6.5 to 7.5 and at a temperature of 45° C. to 50° C. for 10 to 20 minutes.
  • The concentration of the lipase in the buffer is 10 to 10000 units/ml, preferably 100 to 2000 units/ml, and more preferably 200 to 1000 units/ml. The lipase used is not particularly limited, and for example, products named Lipase R “AMANO” G, Lipase M “AMANO” 10, Lipase G “AMANO” 50, Lip ase AY “AMANO” 30G, Lip ase A “AMANO” 6 (all manufactured by Amano Pharmaceutical Co., Ltd.) and the like may be used. They may be used either alone or in combinations of two or more types. Among these, Lipase G “AMANO” 50 and Lipase AY “AMANO” 30G are preferable, and Lipase AY “AMANO” 30G is more preferable.
  • The concentration of the non-ionic detergent in the buffer is, for example, 0.01 to 10 wt %, preferably 0.1 to 2.0 wt %, and more preferably 0.5 to 1.0 wt %.
  • Examples of the non-ionic detergent include: D-sorbitol fatty acid esters such as Span 20, Span 40, Span 60, Span 65, Span 80, and Span 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol sorbitan alkyl esters such as Tween 20, Tween 21, Tween 40, Tween 60, Tween 65, Tween 80, Tween 81, and Tween 85 (all manufactured by Nacalai Tesque, Inc., for example); polyoxyethyleneglycol p-t-octylphenyl ethers such as Triton X-100 (manufactured by Nacalai Tesque, Inc., for example). These detergents may be used either alone or in combinations of two or more types. Among these, Tween 20 and Triton X-100 are preferable, and Triton X-100 is more preferable.
  • Preferably, the heating is performed in the presence of a metal chelating agent in addition to the non-ionic detergent. The metal chelating agent serves to prevent a gene-degrading enzyme such as DNase contained in a sample from degrading the gene, for example. The concentration of the metal chelating agent in the liquid is, for example, 0.1 to 2.0 mM, preferably 0.5 to 1.0 mM. Examples of the metal chelating agent include ethylenediaminetetraacetic acid (EDTA), glycol ether diaminetetraacetic acid (EGTA), and 1,2-cyclohexanediaminetetraacetic acid (CyDTA). These metal chelating agents may be used either alone or in combinations of two or more types. Among these, EDTA and EGTA are preferable, and EDTA is more preferable.
  • The second lysis method is applicable to the same acid-fast bacteria as the first lysis method. Furthermore, biological samples containing an acid-fast bacterium to be used in the second lysis method also are the same as those in the first lysis method.
  • Next, the second method of the present invention can be carried out in the following manner, for example. First, to a buffer having a pH in the above-described predetermined range, lipase and a non-ionic detergent are added, and a metal chelating agent such as EDTA is added as necessary, thus preparing a lysis reagent solution. This lysis reagent solution preferably is sterilized by high-pressure steam in an autoclave. A sample is added to this lysis reagent solution, and the resultant mixture is incubated at 45° C. for 10 minutes (the lipolysis), and then further incubated at 96° C. for 10 minutes (the heating). A cell wall of the acid-fast bacterium is weakened by the former incubation, and the acid-fast bacterium is lysed and also the lipase is deactivated by the latter incubation. Both of the incubations may be carried out using a heating block, a water bath, a thermal cycler, or the like. Alternatively, the lipolysis and the heating may be performed simultaneously by adding the sample to the lysis reagent solution and then incubating the resultant mixture at a temperature of 37° C. to 50° C. for 10 to 20 minutes.
  • The sample may be prepared, for example, by homogenizing and sterilizing a sputum specimen by the N-acetyl-L-cysteine-NaOH method (NALC-NaOH method) or the like. The sample is centrifuged and the supernatant is removed. Thereafter, the lysis reagent solution is added to the remaining precipitate (pellet).
  • The specimen thus lysed may be subjected to a gene amplification process or a gene detection process simply as it is or after being pretreated. Examples of the method of performing the gene amplification or gene detection include a PCR method and modifications of the PCR method, such as a RT-PCR method. Furthermore, examples of the gene to be analyzed include DNA and RNA.
    • EXAMPLES
  • Hereinafter, examples of the present invention will be described along with comparative examples. Examples 1-1, 1-2, 1-3, and 1-4 are directed to the first lysis method of the present invention, and Examples 2-1, 2-2, 2-3, and 2-4 are directed to the second lysis method of the present invention.
    • (Example 1-1, Comparative Example 1)
  • A clinical isolate of a tubercule bacillus was cultured in a product named MycoBroth (Kyokuto Pharmaceutical Industrial Co., Ltd.) at 37° C. until a turbidity corresponding to #1 of the McFarland turbidity standard was obtained. Then, the culture was diluted with phosphate buffer (pH 6.8) so as to achieve a series of 10-fold dilutions (102-fold to 105-fold), thus preparing test solutions containing the tubercule bacillus. Subsequently, 100 μl of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10000 g, 15 minutes) to prepare pellets. The pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction. On the other hand, a product named Triton X-100 (Nacalai Tesque, Inc.) was dissolved in TE buffer (10 mM EDTA and 25 mM Tris-HCl, pH 8.0) so that its concentration became 3 wt % to prepare a lysis reagent solution, and the lysis reagent solution was sterilized by high-pressure steam in an autoclave.
  • Then, 50 μl of the above-described lysis reagent solution was added to the respective samples, and a lysis treatment was carried out by heating the resultant mixtures at 96° C. for 10 minutes in a heating block. Furthermore, as Comparative Example 1, samples prepared in the same manner as in the above were lysed using a product named AMPLICOR Specimen Pretreatment Kit (Nippon Roche K.K.).
  • To 37.5 μl of the thus-obtained lysed sample solutions of Example 1-1 and Comparative Example 1, 50 μl of a premixture of a product named AMPLICOR Amplification and Detection Kit (Nippon Roche K.K.) and 12.5 μl of 12 mM magnesium acetate were added. With regard to each of the mixtures obtained, amplification and detection by the PCR method were carried out in a COBAS AMPLICOR in accordance with the operating instructions of the kit.
  • As a result of the above-described amplification and detection, it was found that, in both Example 1-1 and Comparative Example 1, the samples prepared from the test solutions with a dilution factor of up to 107 were judged as tuberculosis positive and those with a dilution factor of greater than 107 were judged as tuberculosis negative. Thus, it can be said that the lysis method according to Example 1-1 can achieve a sensitivity (lysis efficiency) equivalent to that of the conventional method (Comparative Example 1). Moreover, the lysis method according to Example 1-1 took only half the treatment period of the conventional method (Comparative Example 1).
    • (Example 1-2, Comparative Example 2)
  • A clinical isolate of a tubercule bacillus was cultured in a product named MycoBroth (Kyokuto Pharmaceutical Industrial Co., Ltd.) at 37° C. until a turbidity corresponding to #1 of the McFarland turbidity standard was obtained. Then, the culture was diluted with a non-tuberculous sputum that had been homogenized with a product named SUPTAZYME (Kyokuto Pharmaceutical Industrial Co., Ltd.) so as to achieve a series of 10-fold dilutions (100-fold to 1010-fold). The resultant diluents were used as samples. On the other hand, a product named Triton X-100 (Nacalai Tesque, Inc.) was dissolved in TE buffer (10 mM EDTA and 25 mM Tris-HCl, pH 8.0) so that its concentration became 3 wt % to prepare a lysis reagent solution, and the lysis reagent solution was sterilized by high-pressure steam in an autoclave.
  • Then, 50 μl of the above-described lysis reagent solution was added to the respective samples (100 μl), and a lysis treatment was carried out by heating the resultant mixtures at 96° C. for 10 minutes in a heating block. Furthermore, as Comparative Example 2, samples prepared in the same manner as in the above were lysed using a product named AMPLICOR Specimen Pretreatment Kit (Nippon Roche K.K.).
  • To 37.5 μl of the thus-obtained lysed sample solutions of Example 1-2 and Comparative Example 2, 50 μl of a premixture of a product named AMPLICOR Amplification and Detection Kit (Nippon Roche K.K.) and 12.5 μl of 12 mM magnesium acetate were added. With regard to each of the mixtures obtained, amplification and detection by the PCR method were carried out in a COBAS AMPLICOR in accordance with the operating instructions of the kit.
  • As a result of the above-described amplification and detection, it was found that, in both Example 1-2 and Comparative Example 2, the samples with a dilution factor of up to 104 were judged as tuberculosis positive and those with a dilution factor of greater than 104 were judged as tuberculosis negative. Thus, it can be said the lysis method according to Example 1-2 can achieve a sensitivity (lysis efficiency) equivalent to that of the conventional method (Comparative Example 2) even under the influence of contaminants. Moreover, the lysis method according to Example 1-2 took only half the treatment period of the conventional method (Comparative Example 2).
    • (Example 1-3, Comparative Example 3)
  • 90 sputum specimens collected from patients were homogenized and sterilized by the NALC-NaOH method (“New Guideline for Tubercle Bacillus Test 2000” edited by The Japanese Society for Tuberculosis). Then, 100 μl of each of the treated sputum specimens was centrifuged at 13,000 g for 10 minutes. After removing the supernatant, the precipitate (pellet) was collected. On the other hand, a product named Triton X-100 (Nacalai Tesque, Inc.) was dissolved in TE buffer (10 mM EDTA and 25 mM Tris-HCl, pH 8.0) so that its concentration became 1 wt % to prepare a lysis reagent solution, and the lysis reagent solution was used after being sterilized by high-pressure steam in an autoclave. Specifically, 50 μl of the sterilized lysis reagent solution was added to the pellets obtained from the respective specimens to suspend the pellets. Then, a lysis treatment was carried out by heating the suspensions at 96° C. for 10 minutes in a heating block. On the other hand, as Comparative Example 3, samples (pellets) prepared in the same manner as in the above were lysed using a product named AMPLICOR Specimen Pretreatment Kit (Nippon Roche K.K.).
  • To 12.5 μl of the thus-obtained lysed sample solutions of Example 1-3 and Comparative Example 3, 50 μl of a premixture of a product named AMPLICOR Amplification and Detection Kit (Nippon Roche K.K.) and 37.5 μl of 12 mM magnesium acetate were added. With regard to each of the mixtures obtained, amplification and detection by the PCR method were carried out in a COBAS AMPLICOR in accordance with the operating instructions of the kit. In addition, with regard to samples (pellets) prepared in the same manner as in the above, a culture test was carried out in the usual way.
  • As a result, among the 90 sputum specimens, 41 specimens were judged as tuberculosis positive and 49 specimens were judged as tuberculosis negative when treated by the conventional method (Comparative Example 3). On the other hand, when treated by the first lysis method of the present invention (Example 1-3), 41 specimens were judged as tuberculosis positive and 49 specimens were judged as tuberculosis negative. Thus, the results obtained when treated by the method of Example 1-3 were in exact agreement with those obtained when treated by the conventional method (Comparative Example 3). Moreover, according to the culture test, 42 specimens were judged as tuberculosis positive and 48 specimens were judged as tuberculosis negative, and these results were in approximately 100% (97.8%) agreement with those obtained when treated by the methods of Example 1-3 and Comparative Example 3. Therefore, it can be said that the lysis method of the present invention can produce the lysing effect equivalent to that of the conventional method and can serve as a useful method in actual clinical tests. In addition, the time required for the lysis treatment in the method of Example 1-3 was 30 minutes shorter than that in the method of Comparative Example 3.
    • (Example 2-1, Example 1-4)
  • A product named Lipase G “AMANO” 50 (Amano Pharmaceutical Co., Ltd.) and a product named Lipase AY “AMANO” 30G (Amano Pharmaceutical Co., Ltd.) were dissolved in 10 mM HEPES buffer (pH 7.0) to prepare lipase reagent solutions. Furthermore, a lysis reagent solution was prepared by adding a product named Triton X-100 (Nacalai Tesque, Inc.) to TE buffer (10 mM Tris and 1 mM EDTA, pH 8.0) and sterilizing the mixture by high-pressure steam in an autoclave (the thus-obtained lysis reagent solution is hereinafter referred to as “TE-Triton reagent”). A culture of BCG used for preparing samples was prepared by culturing BCG in a liquid culture medium for growing acid-fast bacteria (a product named MycoBroth, manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd.) until the solution containing the BCG had a turbidity corresponding to #1 of the McFarland turbidity standard and then diluting the solution as necessary.
  • Thereafter, the resultant solution containing the BCG was diluted gradually (10−4, 10−3.5, 10−3, 10−2.5, 10−2) with phosphate buffer (pH 6.8), thus preparing test solutions. Subsequently, 100 μl of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10,000 g, 15 minutes) to prepare pellets. The pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction. The above-described lipase solutions were prepared so that the lipase concentrations became 100, 500, 1000, 2000, and 3000 (units/ml), respectively. 50 μl of each of the lipase solutions with the above-described concentrations was added to the samples. The resultant mixtures were mixed in a vortex mixer and then centrifuged slightly, followed by incubation at 37° C. for 30 minutes. Next, 50 μl of the TE-Triton reagent (Toriton concentration: 2%) was added to the mixtures, and a lysis treatment was carried out by heating the resultant mixtures at 96° C. for 20 minutes. On the other hand, as Example 1-4, the same procedures were carried out except that the lipase treatment was not performed.
  • Among 100 μl of each of the lysates obtained through the above-described procedures, 2 μl was used as a template to carry out PCR in order to confirm whether the cells were lysed. The PCR was carried out in the following manner: 94° C. for 1 minute to denature, followed by 30 thermal cycles, each cycle consisting of 94° C. for 30 seconds, 60° C. for 1 minute, and 72° C. for 1 minute. The sequence of the primers and the composition of the reaction solutions are shown below.
  • (Composition of PCR Reaction)
    10 × Ex-Taq Buffer 2.5 μl
    2.5 mM dNTP Mixture 2.0 μl
    100 μM Primer No. 1 0.125 μl (Sequence Number 1)
    100 μM Primer No. 2 0.125 μl (Sequence Number 2)
    Ex-Taq (5 u/μL) 0.125 μl
    D.W. 18.125 μl
    each lysed sample 2.0 μl
    Total 25.0 μl
  • With regard to 8 μl of each of the amplification reaction products, electrophoresis was carried out using 3% agarose gel. The results are shown in FIG. 1. The samples supplied to lanes (1) to (7) in FIG. 1 were as follows.
  • (Explanation of FIG. 1)
    • (1) The samples only heat-treated in the TE-Triton reagent.
    • (2) The samples treated with the Lipase G “AMANO” 50 and then heat-treated in the TE-Triton reagent. Lipase concentration: 100 units/ml
    • (3) The samples treated with the Lipase G “AMANO” 50 and then heat-treated in the TE-Triton reagent. Lipase concentration: 500 units/ml
    • (4) The samples treated with the Lipase G “AMANO” 50 and then heat-treated in the TE-Triton reagent. Lipase concentration: 1,000 units/ml
    • (5) The samples treated with the Lipase AY “AMANO” 30G and then heat-treated in the TE-Triton reagent. Lipase concentration: 100 units/ml
    • (6) The samples treated with the Lipase AY “AMANO” 30G and then heat-treated in the TE-Triton reagent. Lipase concentration: 500 units/ml
    • (7) The samples treated with the Lipase AY “AMANO” 30G and then heat-treated in the TE-Triton reagent. Lipase concentration: 1,000 units/ml
      • The mark “M” in FIG. 1 indicates a 100 bp ladder molecular weight marker.
      • In each of the regions (1) to (7), the dilution factors of the samples are 10−4, 10−3.5, 10−3, 10−2.5, and 10−2 from the left of the lane.
  • As can be seen from FIG. 1, although a sufficient lysing effect was obtained even when only the heat treatment in the TE-Triton reagent was performed ((1), Example 1-4), still improved lysing effect was obtained when the pretreatment with the lipase was performed ((2) to (7), Example 2-1).
    • (Example 2-2, Example 2-3)
  • The solution containing BCG obtained in the same manner as in the above was diluted gradually (10−4, 10−3.5, 10−3, 10−2.5) with phosphate buffer (pH 6.8). The resultant diluents were used as test solutions. Subsequently, 100 μl of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10,000 g, 15 minutes) to prepare pellets. The pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction. On the other hand, Lipase AY “AMANO” 30G was added to the above-described TE-Triton solution so that its concentrations became 500 units/ml to prepare a lysis reagent solution. 100 μl of the lysis reagent solution was added to the samples. The resultant mixtures were mixed in a vortex mixer and then centrifuged slightly, followed by incubation at 45° C. The incubation was carried out for the following two different periods: 10 minutes and 30 minutes. Subsequently, a lysis treatment was carried out by heating the mixtures at 96° C. for 10 minutes (Example 2-2). Furthermore, as Example 2-3, the same procedures were carried out except that the lipase treatment and the heat treatment were performed simultaneously (45° C., 10 minutes).
  • Among 100 μl of each of the lysates obtained through the above-described procedures, 2 μl was used as a template to carry out PCR in order to confirm whether the cells were lysed. The conditions for carrying out the PCR were the same as those in Example 2-1. With regard to 8 μl of each of the PCR amplification reaction products, whether the cells were lysed was confirmed by carrying out electrophoresis using 3% agarose gel. The results are shown in FIG. 2. The samples supplied to lanes (1) to (5) in FIG. 2 were as follows.
  • (Explanation of FIG. 2)
    • (1) The samples subjected to the lipase treatment and the heat treatment simultaneously in the mixed reagent containing the Lipase AY “AMANO” 30G and the TE-Triton reagent (Example 2-3).
    • (2) The samples treated with the mixed reagent containing the Lipase AY “AMANO” 30G and the TE-Triton reagent.
      45° C., 10 minutes→96° C., 10 minutes
    • (3) The samples treated with the mixed reagent containing the Lipase AY “AMANO” 30G and the TE-Triton reagent.
      45° C., 30 minutes→96° C., 10 minutes
    • (4) The samples treated with the Lipase AY “AMANO” 30G at 37° C. for 10 minutes and then heat-treated at 96° C. for 10 minutes after the addition of the TE-Triton reagent.
    • (5) The samples treated with the Lipase AY “AMANO” 30G at 37° C. for 10 minutes and then heat-treated at 96° C. for 10 minutes after the addition of the TE-Triton reagent.
    • The mark “M” in FIG. 2 indicates a 100 bp ladder molecular weight marker.
    • In each of the regions (1) to (7), the dilution factors of the samples are 10−4, 10−3.5, 10−3, and 10−2.5 from the left of the lane.
  • As can be seen from FIG. 2, a sufficient lysing effect was obtained even when the lipolysis treatment and the heat treatment were performed simultaneously (Example 2-3). On the other hand, when the lipolysis treatment and the heat treatment were performed separately (Example 2-2), still improved lysing effect was obtained. The time period for carrying out the incubation did not affect the lysing effect, and no problem arose by dissolving the non-ionic detergent and the lipase in the same buffer.
    • (Example 2-4)
  • Triton X-100 (Nacalai Tesque, Inc.) was added to TE buffer (10 mM Tris and 1 mM EDTA, pH 8.0) and to Tris buffer (10 mM Tris, pH 8.0) so that its concentration became 1%. The resultant mixtures were sterilized in an autoclave, thus preparing a reagent containing EDTA and a reagent containing no EDTA. Hereinafter, these reagents are referred to as a TE-Triton reagent (containing EDTA) and a Tris-Triton reagent (containing no EDTA), respectively. A culture of BCG used for preparing samples was prepared by culturing BCG in a liquid culture medium for growing acid-fast bacteria (a product named MycoBroth, manufactured by Kyokuto Pharmaceutical Industrial Co., Ltd.) until the solution containing the BCG had a turbidity corresponding to #1 of the McFarland turbidity standard and then diluting the solution as necessary.
  • Thereafter, the resultant solution containing BCG was diluted gradually (10−4.5, 10−4, 10−3.5, 10−3, 10−2.5) with phosphate buffer (pH 6.8), thus preparing test solutions. Subsequently, 100 μl of the test solutions with the above-described concentrations were poured into screw capped tubes, respectively, and then centrifuged (10,000 g, 15 minutes) to prepare pellets. The pellets obtained from the respective test solutions were used as samples to be subjected to a lysis reaction. Lipase AY “AMANO” 30G was added to the above-described TE-Triton solution and to the Tris-Triton solution so that its concentrations became 500 units/ml. Then, 100 μl of each of these solutions was added to the samples. The resultant mixtures were mixed in a vortex mixer and then centrifuged slightly, followed by incubation at 45° C. The incubation was carried out for the following two different periods: 10 minutes and 30 minutes. Subsequently, a heat treatment was carried out by heating the mixtures at 96° C. for 10 minutes.
  • Among 100 μl of each of the lysates obtained through the above-described procedures, 2 μl was used as a template to carry out PCR in order to confirm whether the cells were lysed. The conditions for carrying out the PCR were the same as those in Example 2-1. With regard to 8 μl of each of the PCR amplification reaction products, whether the cells were lysed was confirmed by carrying out electrophoresis using 3% agarose gel. The results are shown in FIG. 3. The samples supplied to lanes (1) to (6) in FIG. 3 were as follows.
  • (Explanation of FIG. 3)
    • (1) to (3): The samples treated with the mixed reagent containing the Lipase AY “AMANO” 30G and the TE-Triton reagent (in the presence of EDTA).
      45° C., 10 minutes→96° C., 10 minutes
    • (4) to (6): The samples treated with the mixed reagent containing the Lipase AY “AMANO” 30G and the Tris-triton reagent (in the absence of EDTA).
      45° C., 10 minutes→96° C., 10 minutes
    • The mark “M” in FIG. 3 indicates a 100 bp ladder molecular weight marker.
    • In each of the regions (1) to (7), the dilution factors of the samples are 10−4.5, 10−4, 10−3.5, 10−3, and 10−2.5 from the left of the lane.
  • As can be seen from FIG. 3, a sufficient lysing effect was obtained even when EDTA was not used ((4) to (6)). However, a still improved lysing effect was obtained by using EDTA ((1) to (3)).
    • INDUSTRIAL APPLICABILITY
  • As specifically described above, the present invention provides a method of securely lysing acid-fast bacteria easily and in a short time without using any special device or special reagent. Therefore, by applying the method of the present invention to, for example, a pretreatment of a sample to be analyzed in an acid-fast bacterium test utilizing gene amplification and detection, the efficiency of the test can be improved easily.

Claims (30)

1. A method of lysing an acid-fast bacterium to extract a gene from the acid-fast bacterium, comprising:
heating the acid-fast bacterium in a liquid containing a non-ionic detergent at a temperature below a boiling point of the liquid.
2. The method according to claim 1, wherein the heating temperature is not less than 70° C. and less than 100° C.
3. The method according to claim 1, wherein the heating is performed for 1 to 30 minutes.
4. The method according to claim 1, wherein the heating is performed at 96° C. for 10 minutes.
5. The method according to claim 1, wherein a pH of the liquid is in a range from 7.0 to 12.0.
6. The method according to claim 1, wherein a concentration of the non-ionic detergent in the liquid is 0.01 to 10 wt %.
7. The method according to claim 1, wherein the non-ionic detergent is at least one selected from the group consisting of D-sorbitol fatty acid esters, polyoxyethyleneglycol sorbitan alkyl esters, and polyoxyethyleneglycol p-t-octylphenyl ethers.
8. The method according to claim 1, wherein the liquid further contains a metal chelating agent.
9. The method according to claim 8, wherein a concentration of the metal chelating agent in the liquid is 0.1 to 100 mM.
10. The method according to claim 8, wherein the metal chelating agent is at least one selected from the group consisting of ethylenediaminetetraacetic acid (EDTA), ethylene glycol bis(β-aminoethyl ether)□N,N,N′,N′-tetraacetic acid (EGTA), diaminocyclohexane tetraacetic acid, o-phenanthroline, and salicylic acid.
11. The method according to claim 1, wherein the acid-fast bacterium to be lysed is at least one selected from the group consisting of M. avium, M. intracellularae, M. gordonae, M. tuberculosis, M. kansasii, M. fortuitum, M. chelonae, M. bovis, M. scrofulaceum, M. paratuberculosis, M. phlei, M. marinum, M. simiae, M. szulgai, M. leprae, M. xenopi, M. ulcerans, M. lepraemurium, M. flavescens, M. terrae, M. nonchromogenicum, M. malmoense, M. asiaticum, M. vaccae, M. gastri, M. triviale, M. haemophilum, M. africanum, M. thermoresistable, and M. smegmatis.
12. The method according to claim 1, wherein a biological sample containing the acid-fast bacterium is at least one selected from the group consisting of sputum, spinal fluid, feces, saliva, blood, tissues, and urine.
13. A method of amplifying or detecting a gene of an acid-fast bacterium specifically, comprising:
lysing an acid-fast bacterium by the method according to claim 1 to extract a gene of the acid-fast bacterium; and
amplifying or detecting the gene specifically using the extracted gene as a sample.
14. A method of lysing an acid-fast bacterium to extract a gene from the acid-fast bacterium, comprising:
causing lipolysis by treating the acid-fast bacterium with lipase, and
heating the acid-fast bacterium in the presence of a non-ionic detergent.
15. The method according to claim 14, wherein the heating also serves to deactivate the lipase.
16. The method according to claim 14, wherein the lipolysis and the heating are performed in a buffer.
17. The method according to claim 14, wherein the lipolysis and the heating are performed in a same container as a closed system.
18. The method according to claim 14, wherein the heating is performed after the lipolysis.
19. The method according to claim 18, wherein the lipolysis is caused at a pH of 4 to 8 and at a temperature of 37° C. to 60° C. for 5 to 30 minutes, and the heating is performed at a temperature of 37° C. to 100° C. for 5 to 30 minutes.
20. The method according to claim 14, wherein the lipolysis and the heating are performed simultaneously.
21. The method according to claim 20, wherein the lipolysis and the heating are performed at a pH of 4 to 8 and at a temperature of 37° C. to 60° C. for 5 to 30 minutes.
22. The method according to claim 16, wherein a concentration of the lipase in the buffer is 10 to 10000 units/ml.
23. The method according to claim 14, wherein the non-ionic detergent is at least one selected from the group consisting of D-sorbitol fatty acid esters, polyoxyethyleneglycol sorbitan alkyl esters, and polyoxyethyleneglycol p-t-octylphenyl ethers.
24. The method according to claim 16, wherein a concentration of the non-ionic detergent in the buffer is 0.01 to 10 wt %.
25. The method according to claim 14, wherein the heating is performed in the presence of a metal chelating agent in addition to the non-ionic detergent.
26. The method according to claim 25, wherein the metal chelating agent is at least one selected from the group consisting of ethylenediaminetetraacetic acid (EDTA), glycol ether diaminetetraacetic acid (EGTA), and 1,2-cyclohexanediaminetetraacetic acid (CyDTA).
27. The method according to claim 25, wherein a concentration of the metal chelating agent in the buffer is 0.1 to 2.0 mM.
28. The method according to claim 14, wherein the acid-fast bacterium to be lysed is at least one selected from the group consisting of M. avium, M. intracellularae, M. gordonae, M. tuberculosis, M. kansasii, M. fortuitum, M. chelonae, M. bovis, M. scrofulaceum, M. paratuberculosis, M. phlei, M. marinum, M. simiae, M. szulgai, M. leprae, M. xenopi, M. ulcerans, M. lepraemurium, M. flavescens, M. terrae, M. nonchromogenicum, M. malmoense, M. asiaticum, M. vaccae, M. gastri, M. triviale, M. haemophilum, M. africanum, M. thermoresistable, and M. smegmatis.
29. The method according to claim 14, wherein a biological sample containing the acid-fast bacterium is at least one selected from the group consisting of sputum, spinal fluid, feces, saliva, blood, tissues, swab, liquid obtained by gastrolavage, and urine.
30. A method of amplifying or detecting specifically a gene of an acid-fast bacterium, comprising:
lysing an acid-fast bacterium by the method according to claim 14 to extract a gene of the acid-fast bacterium; and
amplifying or detecting the gene specifically using the extracted gene as a sample.
US10/500,435 2002-05-21 2003-05-21 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith Abandoned US20050181363A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US11/656,575 US7935483B2 (en) 2002-05-21 2007-01-23 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2002146823 2002-05-21
JP2002-146823 2002-05-21
JP2002-183461 2002-06-24
JP2002183461 2002-06-24
PCT/JP2003/006321 WO2003097816A1 (en) 2002-05-21 2003-05-21 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US11/656,575 Division US7935483B2 (en) 2002-05-21 2007-01-23 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith

Publications (1)

Publication Number Publication Date
US20050181363A1 true US20050181363A1 (en) 2005-08-18

Family

ID=29552327

Family Applications (2)

Application Number Title Priority Date Filing Date
US10/500,435 Abandoned US20050181363A1 (en) 2002-05-21 2003-05-21 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith
US11/656,575 Expired - Fee Related US7935483B2 (en) 2002-05-21 2007-01-23 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith

Family Applications After (1)

Application Number Title Priority Date Filing Date
US11/656,575 Expired - Fee Related US7935483B2 (en) 2002-05-21 2007-01-23 Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith

Country Status (9)

Country Link
US (2) US20050181363A1 (en)
EP (1) EP1506995B1 (en)
JP (1) JP3910198B2 (en)
KR (1) KR100633808B1 (en)
CN (1) CN1656211B (en)
AT (1) ATE445697T1 (en)
AU (1) AU2003242353A1 (en)
DE (1) DE60329676D1 (en)
WO (1) WO2003097816A1 (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20100055082A1 (en) * 2008-09-04 2010-03-04 Jacques Alain Bauer Immunomodulatory extracts from lactobacillus bacteria and methods of manufacturing and use thereof
US10435735B2 (en) 2014-03-07 2019-10-08 Dna Genotek Inc. Composition and method for stabilizing nucleic acids in biological samples
US11002646B2 (en) 2011-06-19 2021-05-11 DNA Genotek, Inc. Devices, solutions and methods for sample collection
US11572581B2 (en) 2002-06-07 2023-02-07 DNA Genotek, Inc. Compositions and methods for obtaining nucleic acids from sputum

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5916610B2 (en) 2009-09-03 2016-05-11 ベクトン・ディキンソン・アンド・カンパニーＢｅｃｔｏｎ， Ｄｉｃｋｉｎｓｏｎ Ａｎｄ Ｃｏｍｐａｎｙ Methods and compositions for direct chemical dissolution
JP5568968B2 (en) * 2009-11-30 2014-08-13 東洋紡株式会社 Lysing method of acid-fast bacterium
JP5714291B2 (en) * 2010-10-15 2015-05-07 独立行政法人農業・食品産業技術総合研究機構 Extraction and purification of mycobacterial DNA
KR101370140B1 (en) * 2012-06-08 2014-03-04 포항공과대학교 산학협력단 Acid Fast Bacilli Detecting Apparatus and Method therefor

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5712095A (en) * 1994-06-16 1998-01-27 Becton Dickinson And Company Rapid and sensitive detection of antibiotic-resistant mycobacteria using oligonucleotide probes specific for ribosomal RNA precursors
US6251659B1 (en) * 1998-10-19 2001-06-26 Hitachi, Ltd. Biological sample treating apparatus
US6979450B2 (en) * 1998-02-06 2005-12-27 Japan Bcg Laboratory Method and compositions for detection and diagnosis of infectious diseases

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU664050B2 (en) * 1991-12-18 1995-11-02 Becton Dickinson & Company Process for lysing mycobacteria
CA2176496C (en) * 1993-11-29 1999-09-28 Kathleen A. Clark Method for extracting nucleic acids from a wide range of organisms
JPH09178752A (en) 1995-12-26 1997-07-11 Lion Corp Method for detecting microorganism and inspection set for detection
JP3093164B2 (en) * 1997-05-07 2000-10-03 三光純薬株式会社 Cell lysis method for acid-fast bacterium and nucleic acid extraction method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5712095A (en) * 1994-06-16 1998-01-27 Becton Dickinson And Company Rapid and sensitive detection of antibiotic-resistant mycobacteria using oligonucleotide probes specific for ribosomal RNA precursors
US6979450B2 (en) * 1998-02-06 2005-12-27 Japan Bcg Laboratory Method and compositions for detection and diagnosis of infectious diseases
US6251659B1 (en) * 1998-10-19 2001-06-26 Hitachi, Ltd. Biological sample treating apparatus

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11572581B2 (en) 2002-06-07 2023-02-07 DNA Genotek, Inc. Compositions and methods for obtaining nucleic acids from sputum
US20100055082A1 (en) * 2008-09-04 2010-03-04 Jacques Alain Bauer Immunomodulatory extracts from lactobacillus bacteria and methods of manufacturing and use thereof
US11002646B2 (en) 2011-06-19 2021-05-11 DNA Genotek, Inc. Devices, solutions and methods for sample collection
US11536632B2 (en) 2011-06-19 2022-12-27 DNA Genotek, Inc. Biological collection system
US11549870B2 (en) 2011-06-19 2023-01-10 DNA Genotek, Inc. Cell preserving solution
US11592368B2 (en) 2011-06-19 2023-02-28 DNA Genotek, Inc. Method for collecting and preserving a biological sample
US10435735B2 (en) 2014-03-07 2019-10-08 Dna Genotek Inc. Composition and method for stabilizing nucleic acids in biological samples
US11198899B2 (en) 2014-03-07 2021-12-14 Dna Genotek Inc. Composition and method for stabilizing nucleic acids in biological samples

Also Published As

Publication number Publication date
WO2003097816A1 (en) 2003-11-27
US7935483B2 (en) 2011-05-03
ATE445697T1 (en) 2009-10-15
EP1506995A4 (en) 2005-06-22
KR20040101234A (en) 2004-12-02
DE60329676D1 (en) 2009-11-26
JPWO2003097816A1 (en) 2005-09-15
CN1656211A (en) 2005-08-17
KR100633808B1 (en) 2006-10-13
JP3910198B2 (en) 2007-04-25
US20070178508A1 (en) 2007-08-02
EP1506995A1 (en) 2005-02-16
AU2003242353A1 (en) 2003-12-02
CN1656211B (en) 2010-04-28
EP1506995B1 (en) 2009-10-14

Similar Documents

Publication Publication Date Title
US7935483B2 (en) Method of effecting lysis of acid-fast bacteria and method of performing gene amplification or detection therewith
Vandeventer et al. Mechanical disruption of lysis-resistant bacterial cells by use of a miniature, low-power, disposable device
US20070015185A1 (en) Lysis and stabilization buffer suitable for inclusion in PCR reactions
US20110281272A1 (en) Processing and analysis of viscous liquid biological samples
US10604787B2 (en) Composition for reducing inhibition of nucleic acid amplification
EP0547789A1 (en) Process for lysing mycobacteria
EP1574564B1 (en) Microorganism or cell collecting method, and microorganism or cell collecting implement used for the method
JP2781749B2 (en) Mycobacterial lysis method
Omar et al. Laboratory evaluation of a specimen transport medium for downstream molecular processing of sputum samples to detect Mycobacterium tuberculosis
US11168352B2 (en) Process for cell lysis and nucleic acid amplification
WO2015183811A1 (en) Apparatus and methods for detecting and identifying nucleic acid sequences in biological samples
JP5434199B2 (en) Method for amplifying mycobacterial genes
JP2014097051A (en) Bacteriolytic reagent for acid-fast bacteria and method of detecting acid-fast bacteria with the same
US20050239045A1 (en) Microorganism or cell collecting method, and microorganism or cell collecting implement used for the method
Bowman et al. Evaluation of commercial DNA extraction methods for biosecurity applications
JP3093164B2 (en) Cell lysis method for acid-fast bacterium and nucleic acid extraction method
JP2020130131A (en) Method for detecting microorganisms
JP2004344108A (en) Method for pre-treating acid-fast bacterium and method for amplifying or detecting gene by using the same
US20180298437A1 (en) Method for fragmenting double-stranded rna and use of the same
WO2024048755A1 (en) Rapid sterility test method
JP2009136221A (en) Nucleic acid extraction method
Chen ENHANCING THE qPCR DETECTION OF CANDIDATUS LIBERIBACTER ASIATICUS
Beissner et al. Detection of viable
JP2011110025A (en) Method for dissolving acid fast bacteria
JP2001190279A (en) Method for detecting pseudomonas bacterium

Legal Events

Date Code Title Description
AS Assignment

Owner name: ARKRAY, INC., JAPAN

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:KAMATA, TATSUO;IZUMIZAWA, YUJI;REEL/FRAME:016530/0075

Effective date: 20040322

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION

点击 这是indexloc提供的php浏览器服务，不要输入任何密码和下载