CN104328207A - Rapid detection kit of Salmonella and application of rapid detection kit - Google Patents

Rapid detection kit of Salmonella and application of rapid detection kit Download PDF

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Publication number
CN104328207A
CN104328207A CN201410679477.7A CN201410679477A CN104328207A CN 104328207 A CN104328207 A CN 104328207A CN 201410679477 A CN201410679477 A CN 201410679477A CN 104328207 A CN104328207 A CN 104328207A
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salmonellas
reaction
sample
kit
dna
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张辉
陈曦
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WUHAN MINGMAN GENE ENGINEERING Co Ltd
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WUHAN MINGMAN GENE ENGINEERING Co Ltd
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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6876Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes
    • C12Q1/6888Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms
    • C12Q1/689Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes for detection or identification of organisms for bacteria
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING 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
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/68Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
    • C12Q1/6844Nucleic acid amplification reactions

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  • Life Sciences & Earth Sciences (AREA)
  • Organic Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
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  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)

Abstract

The invention discloses a visual Salmonella loop-mediated isothermal amplification (LAMP) detection kit and an application thereof. The kit consists of a reaction pre-mixed solution, a fluorescent chromogenic agent and a detection pipe with a sterilization filter paper piece adhered to an inner cover, wherein the reaction pre-mixed solution comprises a BstDNA polymerase, a reaction buffer, dNTP, magnesium sulfate, a specific primer group, betaine and sterile double distilled water. The application of the kit lies in that Salmonella in a sample can be rapidly detected by simply treating the sample by using the kit. The visual Salmonella LAMP detection kit disclosed by the invention has the advantages of simplicity and convenience in operation, high speed, convenience in result determination, strong specificity, high sensitivity, low cost and the like.

Description

The quick detection kit of a kind of Salmonellas and application thereof
Technical field
The invention belongs to microbial molecules detection technique Application Areas, be specifically related to a kind of highly sensitive, visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit of high specificity and application thereof.
Background technology
Salmonellas (Salmonella spp.) is a class Gram-negative bacteria, is distributed widely in nature, is common infecting both domestic animals and human type pathogenic bacterium.Salmonellas known is at present more than 2000 kinds, and nearly all Salmonellas can cause serious food poisoning, is the main pathogenic fungi causing poisoning by food.According to statistics, in all kinds of bacterial food poisonings of countries in the world, the normal row umber one of salmonellal food poisoning.In recent years, the harm that Salmonellas causes in the world is continuous ascendant trend and causes great financial loss.Traditional microbial culture, biochemical reaction, Serologic test supervisor are mostly continued to use in the detection of current Salmonellas, are necessary to set up a kind of accurate, quick, sensitive detection method.
Ring mediated isothermal amplification (Loop-mediated isothermal amplification, LAMP) technology is a kind of Novel isothermal nucleic acid amplification method (International Patent Publication No. WO 00/28082) that Notomi equals report in 2000,4 LAMP primer are designed in 6 sites for target gene, utilize a kind of archaeal dna polymerase (Bst archaeal dna polymerase) with strand-displacement activity, amplified target sequence fast, efficiently, specifically under constant temperature, can reach 10 in 1h 9target sequence copies, and is developed the color by fluorescence dye, visual inspection judged result under natural light, is suitable for the on-the-spot and better simply laboratory of experiment condition and fast detects.
Summary of the invention
An object of the present invention is to be to provide a kind of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit.According to the hilA gene conserved regions sequences Design loop-mediated isothermal amplification (LAMP) primer of Salmonellas, application PrimerExplorer V4(http: //primerexplorer.jp/elamp4.0.0/index.html) online software design Auele Specific Primer group, utilize the specific region of LAMP technology amplified target gene, the rapid detection of Salmonellas is realized from molecular level, for Salmeterol fluticasone propionate provides effectively and nucleic acid screening detection method fast, the detection method of alternative traditional Salmonellas, has wide market outlook and larger economical, societal benefits.
Another object of the present invention is the application being to provide a kind of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit, only need a water-bath or metal bath can in 2 hours, just can Salmonellas in rapid detection sample by simply processing sample.
To achieve these goals, the present invention is by the following technical solutions:
a kind of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit
This test kit by reacting premixed liquid, fluorescent color-developing agent, inner cap form with the detector tube of sterilizing filter paper, reaction premixed liquid wherein comprises Bst archaeal dna polymerase, reaction buffer, dNTP, magnesium sulfate, Auele Specific Primer group, trimethyl-glycine and aseptic double-distilled water.
Described Auele Specific Primer group comprises outer primer F3 and B3, inner primer FIP and BIP, and its nucleotide sequence is as shown in SEQ ID NO 1-4.
a kind of application of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit
Using method comprises the extraction of DNA of bacteria, ring mediated isothermal amplification and colour developing result and judges:
1, the extraction of DNA of bacteria:
Adopt DNA rapid fractionation method, boil by sample diluting liquid, supernatant liquor is as the DNA profiling of loop-mediated isothermal amplification.
2, LAMP amplification:
Adopt 25 μ l reaction systems: each 1.6 μMs of inner primer FIP and BIP, each 0.2 μM of outer primer F3 and B3, dNTP 1mM, trimethyl-glycine 0.5M, magnesium sulfate 6mM, Bst archaeal dna polymerase 8U, template DNA 5 μ l, 10 × ThermoPol Reaction Buffer 2.5 μ l, selects 64 DEG C of lucifuges to react 60 minutes.
3, detected result judges:
Detector tube is inverted whipping, and reaction solution and the interior filter paper covered fully are mixed, and room temperature places 2 minutes; Positive postpone is exerted oneself whipping detector tube, makes the reaction solution being mixed with fluorescent color-developing agent in pipe gather bottom detector tube, observing response liquid color under colorimetric card background: yellow-green colour then in interpret sample containing Salmonellas, brown, there is no Salmonellas in interpret sample.
compared with prior art, the present invention has the following advantages:
1, specificity is good, effectively can detect in sample and whether there is Salmonellas specific gene fragment, and then determines whether there is Salmonellas in sample;
2, rapidly and efficiently, detection (not comprising the sample cultivation time) can be completed less than 2 hours;
3, do not need to use expensive, accurate plant and instrument, only need common metal bath or water-bath, testing cost is low;
4, identify convenient and simple, under natural light, can result judgement be carried out by gross visualization reaction solution colour-change;
5, whole process does not relate to toxic reagent, ensure that the safety of operator and environment.
Accompanying drawing explanation
Fig. 1 is the vertical view of test kit detector tube of the present invention, and the sterilizing filter paper of display inner cap attachment with the addition of fluorescent color-developing agent.
Fig. 2 is the side-view of test kit detector tube of the present invention, display packing without colour response premixed liquid.
Fig. 3 is the schematic diagram of test kit applying detection result of the present invention.
Observing response liquid color under colorimetric card background: yellow-green colour (left side) then in interpret sample containing Salmonellas, brown (right side) does not then have Salmonellas in interpret sample.
Embodiment
Following Examples further illustrates the present invention, but should not regard limitation of the present invention.
embodiment 1:
A kind of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit
This test kit by reacting premixed liquid, fluorescent color-developing agent, inner cap form with the detector tube of sterilizing filter paper, reaction premixed liquid wherein comprises Bst archaeal dna polymerase, reaction buffer, dNTP, magnesium sulfate, Auele Specific Primer group, trimethyl-glycine and aseptic double-distilled water.
Described Auele Specific Primer group comprises outer primer F3 and B3, inner primer FIP and BIP, and its nucleotide sequence is as shown in SEQ ID NO 1-4.
embodiment 2:
A kind of optimization of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit
The optimizer of test kit of the present invention is: screen the suitableeest Auele Specific Primer group, the optimal concentration ratio of interior outer primer, optimal reactive temperature, magnesium sulfate concentration, trimethyl-glycine concentration, dNTP concentration, in the reaction times, all answers amplified production by negate, with 2%(w/v, identical below) agarose gel electrophoresis after, be placed in gel imaging system imaging, the power according to electrophoresis picture display LAMP characteristic scalariform band determines top condition.Finally optimize the consumption of fluorescent color-developing agent.Illustrate with the example that is optimized for of optimal reactive temperature below.
One, the preparation of DNA of bacteria template:
Aseptic technique, by 1:1000(v/v) inoculate Salmonellas pure growth in sterilizing LB liquid nutrient medium, put 36 ± 1 DEG C and cultivate 16 ± 1 hours; Aseptic technique, gets in 0.1ml to 0.9ml sterile saline from above-mentioned nutrient solution; Be placed in 100 DEG C of boiling water insulation 5 minutes, room temperature cooling rearmounted 4 DEG C for subsequent use, the same day uses.
Two, the reaction system of LAMP amplification:
Adopt 25 μ l reaction systems: each 0.2 μM of each 1.6 μMs of inner primer FIP and BIP, outer primer F3 and B3, dNTP 1mM, trimethyl-glycine 0.5M, magnesium sulfate 6mM, Bst archaeal dna polymerase 8U, template DNA 5 μ l, 10 × ThermoPol Reaction Buffer 2.5 μ l, aseptic double-distilled water supplies surplus.
Three, the reaction conditions of LAMP amplification:
Reaction tubes is placed in 60,61,62,63,64,65,66 DEG C of incubations 60 minutes respectively.
Four, result judges:
Get 8 μ l amplified productions, after the agarose gel electrophoresis of 2%, be placed in gel imaging system imaging, when electrophoresis picture shows 64 DEG C, result is best.
embodiment 3:
A kind of application of visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit
The sensitivity detected in conjunction with test kit of the present invention and the requirement of correlation detection standard, optimize the process of measuring samples.
One, the extraction of DNA of bacteria in measuring samples:
Aseptic technique, takes in measuring samples 25g or 25ml to 225ml sterilizing LB liquid nutrient medium, puts 36 ± 1 DEG C and cultivates 16 ± 1 hours; Aseptic technique, gets in 0.1ml to 0.9ml sterile saline from above-mentioned nutrient solution; Be placed in 100 DEG C of boiling water insulation 5 minutes, room temperature cooling rearmounted 4 DEG C for subsequent use, the same day uses.
Two, LAMP amplification:
Aseptic technique, the rear diluent supernatant that boils getting the above-mentioned preparation of 5 μ l responds in the detector tube of premixed liquid, fluorescent color-developing agent to packing.64 DEG C of lucifuges react 60 minutes.
Three, detected result judges:
Detector tube is inverted whipping, and reaction solution and the interior filter paper covered fully are mixed, and room temperature places 2 minutes; Positive postpone is exerted oneself whipping detector tube, makes the reaction solution being mixed with fluorescent color-developing agent in pipe gather bottom detector tube, observing response liquid color under colorimetric card background: yellow-green colour then in interpret sample containing Salmonellas, brown, there is no Salmonellas in interpret sample.
Set up the Standard PCR detection technique using outer primer F3 and B3 in addition, 40 cyclic amplifications, consistent with the detected result of test kit of the present invention to the detected result of measuring samples.
  
SEQUENCE LISTING
<110> Wuhan Ming Man genetically engineered company limited
The quick detection kit of a <120> Salmonellas and application thereof
The quick detection kit of a <130> Salmonellas and application thereof
<160> 4
<170> PatentIn version 3.1
<210> 1
<211> 20
<212> DNA
<213> Salmonellas
<400> 1
ACCACAATAA TCCACAAGCT 20
<210> 2
<211> 22
<212> DNA
<213> Salmonellas
<400> 2
GGTCCAATTT TAAACACTCG TT 22
<210> 3
<211> 49
<212> DNA
<213> Salmonellas
<400> 3
TTGAATAGCA AACTCCCGAC GTTTTGATTA CTGGGGCTAA TTAATACGA 49
<210> 4
<211> 43
<212> DNA
<213> Salmonellas
<400> 4
TACTTTCGCC CATTTCTGCA GTTTTTAAGG CCTCCTCCAA CTG 43

Claims (2)

1. visual Salmonellas ring mediated isothermal amplification (LAMP) detection kit, it is characterized in that, be made up of with the detector tube of sterilizing filter paper reaction premixed liquid, fluorescent color-developing agent, inner cap, reaction premixed liquid wherein comprises Bst archaeal dna polymerase, reaction buffer, dNTP, magnesium sulfate, Auele Specific Primer group, trimethyl-glycine and aseptic double-distilled water;
Described Auele Specific Primer group comprises outer primer F3 and B3, inner primer FIP and BIP, and its nucleotide sequence is as follows:
F3:5’-ACCACAATAATCCACAAGCT-3’
B3:5’-GGTCCAATTTTAAACACTCGTT-3’
FIP:5’-TTGAATAGCAAACTCCCGACGTTTTGATTACTGGGGCTAATTAATACGA-3’
BIP:5’-TACTTTCGCCCATTTCTGCAGTTTTTAAGGCCTCCTCCAACTG-3’。
2. the application of test kit described in, is characterized in that, just can Salmonellas in rapid detection sample by simply processing sample; Using method comprises the extraction of DNA of bacteria, ring mediated isothermal amplification and colour developing result and judges:
1), the extraction of DNA of bacteria:
Adopt DNA rapid fractionation method, boil by sample diluting liquid, supernatant liquor is as the DNA profiling of loop-mediated isothermal amplification;
2), LAMP amplification:
Adopt 25 μ l reaction systems: each 1.6 μMs of inner primer FIP and BIP, each 0.2 μM of outer primer F3 and B3, dNTP 1mM, trimethyl-glycine 0.5M, magnesium sulfate 6mM, Bst archaeal dna polymerase 8U, template DNA 5 μ l, 10 × ThermoPol Reaction Buffer 2.5 μ l, selects 64 DEG C of lucifuges to react 60 minutes;
3), detected result judges:
Detector tube is inverted whipping, and reaction solution and the interior filter paper covered fully are mixed, and room temperature places 2 minutes; Positive postpone is exerted oneself whipping detector tube, makes the reaction solution being mixed with fluorescent color-developing agent in pipe gather bottom detector tube, observing response liquid color under colorimetric card background: yellow-green colour then in interpret sample containing Salmonellas, brown, there is no Salmonellas in interpret sample.
CN201410679477.7A 2014-11-24 2014-11-24 Rapid detection kit of Salmonella and application of rapid detection kit Pending CN104328207A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109402271A (en) * 2017-08-14 2019-03-01 中国科学院微生物研究所 For detecting the primer system and kit and their application and the method for detecting salmonella of salmonella
CN109468396A (en) * 2018-12-28 2019-03-15 四川大学 A kind of primer sets, purposes, kit and its detection method detecting salmonella
WO2019114374A1 (en) * 2017-12-12 2019-06-20 新希望双喜乳业(苏州)有限公司 Rapid detection method for salmonella in dairy product

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009147435A1 (en) * 2008-06-03 2009-12-10 Health Protection Agency Salmonella detection assay

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009147435A1 (en) * 2008-06-03 2009-12-10 Health Protection Agency Salmonella detection assay

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
张敬平: "PCR检测沙门菌hilA基因的方法研究", 《中国卫生检验杂志》 *
朱胜梅: "环介导等温扩增技术快速检测沙门菌", 《现代食品科技》 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109402271A (en) * 2017-08-14 2019-03-01 中国科学院微生物研究所 For detecting the primer system and kit and their application and the method for detecting salmonella of salmonella
WO2019114374A1 (en) * 2017-12-12 2019-06-20 新希望双喜乳业(苏州)有限公司 Rapid detection method for salmonella in dairy product
CN109468396A (en) * 2018-12-28 2019-03-15 四川大学 A kind of primer sets, purposes, kit and its detection method detecting salmonella

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