CN106093435A - The application of Echinococcus granulosus Glutaredoxin 1 - Google Patents

Abstract

The present invention relates to biological technical field, specifically disclose the application in the immunizing antigen and/or test kit of preparation detection echinococcosis granulosa of the Echinococcus granulosus Glutaredoxin 1, it can be by the sheep positive serum identification of natural infection echinococcosis granulosa as immunizing antigen, when being applied to indirect ELISA detection, possessing higher specificity and sensitivity, Clinical detection coincidence rate is up to 97.9%.For the detection method that immunizing antigen is set up, there is good diagnosis effect with Echinococcus granulosus Glutaredoxin 1, may be used for the Preliminary screening of epidemic-stricken area sheep echinococcosis granulosa.

Description

The application of Echinococcus granulosus glutaredoxin-1

Technical field

The present invention relates to biological technical field, more particularly to Echinococcus granulosus glutaredoxin-1 should With.

Background technology

Echinococcus granulosus (Echinococcus granulosus) Shu Dai section (Taeniidae) Echinococcus (Echinococcus), wherein silk ribbon phase parasitized larvae caused Echinococcus Granulosus Cysts in animal and the liver of people, lung and other organs Disease, also known as capsule echinococcosis, is a kind of Amphixenosis, and main parasitic is in the multiple mammal body such as people and domestic animal.90% Above Echinococcus Granulosus Cysts encapsulation is grown on the liver of host, lungs or is grown on liver lung simultaneously.Echinococcosis granulosa is generation Criticality is distributed, and causes a series of economy and public health problem.In some Prevalent district, its infection rate may be up to 5-10%, Mortality rate is up to 2-4%.According to estimates, people from whole world capsule echinococcosis the most at least loses 1-3.6 million disability adjusted life years (DALYs), and the economic loss that animal capsule echinococcosis causes every year is at least 2,000,000,000 dollars.Therefore, World Health Organization (WHO) Echinococcosis is classified as " unheeded tropical disease ", as its 2008-2015 keypoint control plan.

At present, the research of echinococcosis granulosa immunologic diagnosis is concentrated mainly on thick cyst fluid antigen, but its complicated component, Have and be difficult to defects such as purifying in a large number, antigenic source is unstable, cost is high, specificity is low.Shortage standard is the most special Property recombinant antigen is a difficult problem the most unsolved in echinococcosis granulosa immunologic diagnosis.

Summary of the invention

In view of this, it is an object of the invention to provide the application of Echinococcus granulosus glutaredoxin-1 (Eg-Grx1), Can be there is good immunogenicity by the sheep positive serum identification of natural infection echinococcosis granulosa, and have Higher specificity and sensitivity, reduce the cross reaction with other Taeniidae disease positive serums.

Glutaredoxin (glutaredoxin, Grx), also known as thioltransferase (thioltmnsferase), be sulfydryl- The important component of disulfide bond oxidoreduction enzyme family.Glutaredoxin family and thioredoxin family together maintain organism The balance of internal oxidition reduction, is two important system of the sulfhydryl oxidase reduction-state regulation participating in protein.Grx using GSH as Direct electron donor, NADPH is as original electron donor, the regulation cell oxygen containing sulfydryl (mainly being provided by cysteine) albumen Change reducing condition, play a significant role during cell signalling.

Research currently, with respect to glutaredoxin is concentrated mainly on trypanosomicide and plasmodium, plasmodium Grx1 (Pf-Grx1) It is located in Cytoplasm, there is HEDS activity and reduce the characteristics such as ribonucleotide reductase.Tripathi etc. study discovery Pf-Grx1 can denaturant high temperature resistant, resistance to and the feature of resistance to PH change.The clonal expressions such as Marquez go out the Grx egg of trypanosoma bocagei In vain, find that it plays a significant role in the oxidoreduction metabolism of parasite.But, about glutaredoxin on parasite Report more rare.Therefore, the present invention has carried out bioinformatics to Echinococcus granulosus glutaredoxin-1 (Eg-Grx1) Analyze, and give expression to rEg-Grx1 albumen by reverse transcription, prepare the polyclonal antibody of anti-rEg-Grx1, this albumen is carried out Immunoblotting assay shows that it can be had good immunogen by the sheep positive serum identification of natural infection echinococcosis granulosa Property, utilize rEg-Grx1 albumen to set up echinococcosis granulosa indirect ELISA diagnostic method, the prevention and control for echinococcosis granulosa provide Monitoring means.

Therefore, the present invention proposes the Echinococcus granulosus glutaredoxin-1 immunity at preparation detection echinococcosis granulosa Application in antigen and/or test kit.

Wherein, as preferably, described test kit is ELISA detection kit or immune-blotting method test kit.

Meanwhile, present invention also offers a kind of ELISA detection kit detecting echinococcosis granulosa, including particulate spine ball Cestode glutaredoxin-1 (being coated as antigen) and ELISA detection kit conventional constituents.Between described test kit foundation Connect ELISA Cleaning Principle.

As preferably, described ELISA detection kit conventional constituents includes antigen coated liquid, ELISA Plate, confining liquid, HRP The two of labelling resist and tmb substrate.

It is further preferred that described confining liquid is 5% defatted milk powder；The two of described HRP labelling resist the goat for HRP labelling Or sheep anti-rabbit two resists.

During concrete ELISA detection, antigen coated optimum condition be 4 DEG C overnight, antigen optium concentration is 1.6 μ The every hole of g/, optimal serum-dilution concentration is 1:320, and optimal confining liquid and sealing condition are that 5% defatted milk powder 37 DEG C closes 1h, blood Hatching clearly Best Times is 37 DEG C of 1.5h, and two anti-to hatch Best Times be 37 DEG C of 1h, and two time to resist optimal diluted concentration be 1:3000, The optimum condition of substrate colour developing is 37 DEG C of 15min, and in the above conditions, the P/N value recording yin and yang attribute serum is 3.04

As preferably, described ELISA detection kit conventional constituents also includes chromogenic reaction stop buffer H₂SO₄, cleaning mixture PBST and diluent PBS.

The present invention first extracts Echinococcus granulosus total serum IgE, then carries out reverse transcription and obtains cDNA, according to GeneDB The Eg-Grx1's (EgrG_000124800) announced in (http://www.genedb.org/Homepage/Egranulosus) Gene order, by Primer Premier 5.0 software design primer amplification purpose fragment, then carries out sequence verification, its with In GeneDB, the sequence homology of Eg-Grx1 (EgrG_000124800) reaches 100%.It is finally coupled in expression vector, turns Enter expression in escherichia coli, it is thus achieved that the reverse transcription recombiant protein rEg-Grx1 of Echinococcus granulosus glutaredoxin-1.

Immunoblotting display rEg-Grx1 can be had good by the sheep positive serum identification of natural infection echinococcosis granulosa Good immunogenicity.Result of indirect ELISA shows, the cut-off value of the method is 0.481, and specificity and sensitivity are respectively 64.3% (9/14) and 1:3200, and with sheep brain Echinococcus hydatid cyst serum no cross reaction.

From above technical scheme, the invention provides Echinococcus granulosus glutaredoxin-1 at preparation detection particulate Application in the immunizing antigen of echinococcosis and/or test kit, it can be by natural infection Echinococcus Granulosus Cysts as immunizing antigen Sick sheep positive serum identification, when being applied to indirect ELISA detection, possesses higher specificity and sensitivity, Clinical detection Coincidence rate is up to 97.9%.Have good with the detection method that Echinococcus granulosus glutaredoxin-1 is set up for immunizing antigen Diagnosis effect, may be used for the Preliminary screening of epidemic-stricken area sheep echinococcosis granulosa.

Accompanying drawing explanation

Fig. 1 show Eg-Grx1PCR and expands gel figure；Wherein, M is DNA molecular quality standard DL2000；1 is Eg- Grx1cDNA PCR primer；2 is blank；

Fig. 2 show the western blot gel figure of rEg-Grx1；Wherein, M is Protein standards；1 is recombinant bacterium The expression of middle rEg-Grx1；2 is rEg-Grx1 after purification；3 is that the anti-rEg-Grx1-IgG of rabbit identifies rEg-Grx1；4 is healthy Rabbit anteserum identification rEg-Grx1；The sheep positive serum identification rEg-Grx1 that 5 is natural infection echinococcosis granulosa；6 is healthy Sheep serum identification rEg-Grx1；7 is that the anti-rEg-Grx1-IgG of rabbit identifies the thick leach protein of protoscolex；8 is Healthy Rabbits serum identification The thick leach protein of protoscolex；

Fig. 3 show the indirect ELISA specificity analyses figure to rEg-Grx1；Wherein, abscissa is followed successively by from left to right Sheep anti-cenurus cerebralis positive serum, goat anti-cysticercus tenuicollis positive serum, sheep anti-Echinococcus Granulosus Cysts positive serum； Cuto-off value represents marginal value；

Fig. 4 show the clinical test results figure of indirect ELISA；Wherein, abscissa is followed successively by positive serum from left to right And negative serum；Cuto-off value represents marginal value.

Detailed description of the invention

The invention discloses the application of Echinococcus granulosus glutaredoxin-1, those skilled in the art can use for reference herein Content, is suitably modified technological parameter and realizes.Special needs to be pointed out is, all similar replacements and change are to people in the art Being apparent from for Yuan, they are considered as being included in the present invention.Preferred embodiment has been passed through in application of the present invention Being described, application as herein described substantially can be carried out in without departing from present invention, spirit and scope by related personnel Change or suitably change and combination, realize and apply the technology of the present invention.

In the specific embodiment of the invention, material and reagent involved by each test are as follows:

1, main agents

Total RNA from animal tissues extraction agent box (TRIzol.R.Total RNA Isolation.Reagent) and reverse transcription Test kit (RevertAid First Strand cDNA Synthesis Kit), purchased from GIBCOBRL company；DNA Marker, Protein Marker, restricted enzyme (BamH I, Hind III, EcoRI, Xho I), T4DNA ligase, Purchased from TaKaRa company；Agarose gel reclaims test kit, Ni-NTA Agarose, purchased from Qiagen company；TaqPCR MasterMix, plasmid extraction agent box, HRP-DAB substrate colour reagent box in a small amount, purchased from sky, Beijing limited public affairs of root biochemical technology Department；The goat anti-rabbit igg antibody of HRP labelling, the rabbit anti goat igg antibody of HRP labelling, the rabbit anti-sheep IgG antibody of HRP labelling, The goat anti-rabbit igg antibody of FITC labelling is purchased from Wuhan doctor moral biology company limited；IPTG, Freund's complete adjuvant and Freund are the completeest Full adjuvant, purchased from Sigma company；HiTrap Protein A HP, purchased from Bio-Rad company, PCR primer synthesis and order-checking by Shanghai handsome biological engineering company limited completes；Other reagent is domestic analytical pure.

2, bacterial strain and plasmid vector

Host Strains bacillus coli DH 5 alpha, e. coli bl21 (DE3), pMD19-T Vector are purchased from TaKaRa company； PET32a (+) carrier provides by Sichuan Agricultural University animal parasitosis laboratory.

3, conventional buffer solution and the preparation of culture medium

PBS Buffer is 1.: weigh following reagent respectively in beaker: NaCl 8g, KCl 0.2g, Na₂HPO₄1.42g, KH₂PO₄0.27g.Add the mixing of about 500mL sterilizing distilled water to dissolve, add dense HCl and make pH reach 7.4, constant volume to 1L.High pressure Room temperature preservation after sterilizing.

Electrophoretic buffer (50 × TAE Buffer): weigh 242g Tris and 37.2g Na₂EDTA·2H₂O in beaker, Add 500mL sterilizing distilled water and mix dissolving, adding the CH of 58mL₃COOH is sufficiently stirred for again, constant volume to 1L room temperature preservation.

EB: added by 0.1gEB in the sterilizing distilled water of 100mL, after subpackage, room temperature preserves.

LB culture medium: liquid culture medium: weigh Triptone 10g, 5g Yeast Extract, 10g NaCl respectively and add Enter beaker is dissolved in 500mL sterilizing H₂PH to 7.0, autoclaving after constant volume to 1L, 4 DEG C of preservations are regulated in O and with Caustic soda.LB puts down Plate: add 15g agar powder, autoclaving, 4 DEG C of preservations in every 1L solution.

IPTG solution: electronic balance weighs the isopropylthiogalactoside of 2g and is dissolved in 8mL ultra-pure water, is sufficiently stirred for molten Add water after solution 10mL, is stored in-20 DEG C with after 0.45 μm membrane filtration with EP pipe subpackage.

30% polyacrylamide solution: weigh the Acrylamide of Bis-acrylamide and 29.2g of 0.8g, adds The mixing of 50mL deionized water is dissolved, and add water 100mL, with 0.22 μm membrane filtration.

1M Tris-HCl (pH 6.8): weigh the Tris of 12.11g in beaker, add 80mL distilled water and be sufficiently stirred for molten Solving, add water after adding concentrated hydrochloric acid and using acidometer adjustment pH to 6.8 100mL, with 0.22 μm membrane filtration.

1.5M Tris-HCl (pH 8.8): take the Tris of 19g in beaker, adds 50mL distilled water and is sufficiently stirred for dissolving, add Concentrated hydrochloric acid also uses acidometer to adjust after pH to 8.8 to add water 100mL, 4 DEG C of preservations.

10% sodium lauryl sulphate (SDS) solution: weigh the SDS of 10g in beaker, adds 80mL distilled water and fully stirs It is settled to 100mL after mixing dissolving, preserves with room temperature after 0.45 μm membrane filtration.

10% ammonium persulfate solution: weigh the APS of 0.1g, the constant volume that adds water preserves to 1mL, room temperature.

Coomassie brilliant blue staining liquid: weigh 0.1g Coomassie brilliant blue powder in 20mL ethanol with electronic balance, take 100mL Strong phosphoric acid, to 200mL, preserves with room temperature after 0.45 μm membrane filtration.

Ampicillin sodium solution (AMP): use electronic balance to weigh 1gAmpicilin powder, draw 9mL ultra-pure water abundant Being settled to 10mL after stirring and dissolving, degerming with 0.22 μm filtering with microporous membrane, subpackage EP manages-20 DEG C of preservations.

4, experimental animal

2 healthy new zealand rabbits, 1.4～2.2kg, purchased from Sichuan Agricultural University's experimental animal center.

Below in conjunction with embodiment, the present invention is expanded on further.

Embodiment 1: the extraction of Echinococcus Granulosus Cysts total serum IgE

Middle silk ribbon phase larva (Echinococcus Granulosus Cysts) encapsulation of Echinococcus granulosus comes from the sheep liver of natural infection, sample Pick up from Xining, Qinghai or Szechwan Ganzi, Liquid nitrogen storage.

Taking out the Echinococcus Granulosus Cysts of Liquid nitrogen storage, ground with mortar, the animal tissue RNA referring next to sky root extracts Test kit description extracts total serum IgE.

(1) every 10-20mg protoscolex adds 300 μ L lysates, uses grinding rod to grind；

(2) in homogenate, Proteinase K (10 μ L) and RNase-Free ddH2O (590 μ L) is added, anti-after mixing Answer 15min (56 DEG C).

(3) centrifugal 5min (12,000rpm), transfers to supernatant in clean pipe；0.5 times of supernatant is added in pipe The dehydrated alcohol of volume, proceeds to after mixing in adsorption column, abandons waste liquid after centrifugal 1min (12,000rpm).

(4) in adsorption column, add Deproteinization matter liquid RW1 (350 μ L), after centrifugal 1min (12,000rpm), abandon waste liquid.

(5) DNase I working solution (80 μ L) is added adsorption column, room temperature placing response 15min；Add Deproteinization matter liquid subsequently RW1 (350 μ L), abandons waste liquid after centrifugal 1min (12,000rpm).

(6) 500 μ L rinsing liquid RW add in adsorption column, place 2min (room temperature), abandon useless after centrifugal 1min (12,000rpm) Liquid.

(7) (6) are repeated.

(8) empty from, abandon waste liquid, dry remaining rinsing liquid.

(9) adsorption column is put in a new centrifuge tube, with RNase-Free ddH2O (30-100 μ L) eluting, stand 2min (room temperature), obtains Echinococcus Granulosus Cysts Total RNAs extraction liquid after centrifugal 2min (12,000rpm).

The synthesis of embodiment 2: the first chain cDNA

With the Echinococcus Granulosus Cysts total serum IgE of extracting as template, with Oligo dT (18) as reverse transcription primer, public with reference to Thermo Department's Reverse Transcription box description operates:

(1) reactant mixture is prepared on ice

Oligo dT₁₈ 1μL

Template ribonucleic acid 1 μ L

DEPC ddH₂O 1μL

(2) after 70 DEG C (5min) hatch, cooled on ice is forwarded to

(3) following reactant is added in order on ice:

5reaction buffer 4μL

Ribonuclease inhibitor 1 μ L

10dNTP mixture 2 μ L

(4) 37 DEG C (5min) adds RevertAid after hatching^TMReverse transcription 1 μ L.

(5) PCR program: 42 DEG C, 1h；70 DEG C, 10min.

(6) cDNA obtained is in-80 DEG C of preservations.

The amplification of embodiment 3:Eg-Grx1 gene

According to the Eg-Grx1 announced in GeneDB (http://www.genedb.org/Homepage/Egranulosus) (EgrG_000124800) gene order, with Primer Premier 5.0 software design primer:

Upstream: 5 '-CCGGAATTCATGTGGCGCTTTTTATC-3 ' underscore is EcoR I

Downstream: 5 '-CCGCTCGAGCTCTAAAAGTTCAGCAAGTG-3 ' underscore Xho I

Amplification system (25 μ L): each 1 μ L of DNA profiling, each 1 μ L of upstream and downstream primer, PCR Mixture 12.5 μ L, sterilizing is double Steam water 9.5 μ L.

Amplification condition: denaturation: 95 DEG C of 5min；38 circulations (degeneration: 95 DEG C, 40s；Annealing: 54 DEG C, 45s；Extend: 72 DEG C, 45s)；Finally extend: 72 DEG C, 10min.

The band (Fig. 1) of an about 351bp is gone out with the cDNA of Echinociccus granulosus protoscolex for template amplification.

The recovery of embodiment 4:PCR product

To cut containing the gel of purpose band, put in EP pipe, weigh.Use gel DNA to reclaim test kit and reclaim mesh Fragment.After every 100mg gel adds 400 μ LPC Buffer, 55 DEG C of water-bath colloidal sols.After gel is completely dissolved, move into absorption In post, centrifugal 60sec (12000rpm), after being subsequently added centrifugal 2 times of Washing Buffer washing, empty centrifugal 2min (12000rpm).Dry ethanol abnormal smells from the patient in adsorption column, in adsorption column, add 30 μ L Elution Buffer, centrifugal 2min (12000rpm), target DNA fragment is obtained.

Embodiment 5:Eg-Grx1 gene cloning and sequencing and comparison

(1) following reagent is mixed: the template DNA of Solution 1, the 3.5 μ L of 4 μ L, the pMD19-T of 0.5 μ L Vector, put into centrifuge wink from after be put in 16 DEG C of thermostatted waters and connect overnight.

(2) going out competent cell from-70 DEG C, room temperature takes 30 μ L after melting and puts in sky EP pipe, is produced by the 8 μ L connected overnight Thing adds EP pipe and blows and beats mixing gently with micro sample-adding rifle, puts into mixture of ice and water ice bath 30min at once.42 DEG C of water-bath 90s Ice bath 5min immediately.Adding the LB solution of 600 μ L in each EP pipe, in 37 DEG C, 180r/min cultivates 1.5h.Solution by mixing Being poured on LB flat board, 37 DEG C of cooling 1h make dry tack free, instead flat board is overnight.

(3) picking colony is in empty EP pipe, adds 1mL LB solution and 1 μ LAMP solution, and 160r/min concussion cultivates 6h extremely It is muddy.Observe after drawing 1 μ L bacterium solution amplification and product being run electrophoresis.The bacterium solution choosing electrophoresis observation positive delivers to English Weihe River victory base Company checks order.

The purpose fragment sequence that order-checking is obtained puts into comparison in GeneDB data base, through the sequence that obtains of order-checking with In GeneDB, the sequence homology of Eg-Grx1 (EgrG_000124800) reaches 100%.

Embodiment 6:Eg-Grx1 gene is cloned, is identified and convert

1, plasmid extraction

After sequencing result comparison is correct, by bacterial strain amplification culture, carry reagent with reference to the plasmid of sky root biochemistry company limited is little Box operating instruction is carried out:

(1) 3-5mL bacterium solution, centrifugal collecting precipitation are taken；

(2) add suspension P1 suspension thalline, and add lysate P2 bacterium solution is cracked；

(3) add P3 and produce precipitation, upset mixing, centrifugal 15min (12,000rpm) after standing 10min；

(4) take supernatant in collecting pipe, add 600 μ L rinsing solution PW, stand 2min, centrifugal 1min (12,000rpm), abandon Waste liquid；

(5) (4) are repeated；

(6) plasmid is reclaimed with 90 μ L eluents after drying rinsing liquid.

2, plasmid enzyme restriction reclaims

The pMD19-T-Eg-Grx1 Takara EcoR I and Xho I of extraction is cut enzyme double digestion, 37 DEG C of enzyme action soon 12min, system cumulative volume is 10 μ L:T cloned plasmids 8 μ L, 10X QuickCut Green Buffer 1 μ L, QuickBamH I With Xho I 0.5 μ L.After mixing with micro sample-adding rifle wink from, take out rapidly point sample after 37 DEG C of water bath with thermostatic control 15min and carry out 1% Agarose gel electrophoresis glue reclaim.

3, purpose fragment connects expression vector

By the fragment of the Eg-Grx1 mesh of double digestion and pET28a (+) 22 DEG C of carrier connects 1.5h, connect product subsequently and convert E.coli DH5 α competent cell, and be applied on the LB culture medium flat plate of amicillin resistance, cultivate 12h for 37 DEG C.Picking list Individual bacterium colony, carries out PCR qualification.

4, pET28a-Eg-Grx1 recombiant plasmid double digestion is identified

Recombiant plasmid carries out double digestion qualification, and method is with reference to " 2, plasmid enzyme restriction reclaim ".

Embodiment 7: restructuring Eg-Grx1 expression in escherichia coli

1, the expression of recombiant protein

(1) by the correct recombiant plasmid pET28a of order-checking (+)-Grx1 proceeds to BL21 (DE3) and expresses bacterium.

(2) being inoculated in expressing bacterium in two bottles of fresh LB (containing AMP 100 μ g/mL) culture fluid containing 100mL, 37 DEG C are shaken 3h (160r/min) cultivated by bed, is to add derivant IPTG (1mmol/L), 37 DEG C of induction 5h (160r/ after 0.6 to bacterium solution OD590 Min), another bottle is not added with IPTG and does comparison cultivation.

(3) taking bacterium solution 1.5mL later respectively in two new EP pipes, 4 DEG C of centrifugal 1min (12,000r/min) are received Collection thalline, is separately added into 10 μ L 5 × SDS loadings Buffer and 40 μ L PBS solution, fully mixes.

(4) boiling water boiling 10min, so that thalline fully ruptures, 4 DEG C of centrifugal 10min (12,000r/min), take supernatant and carry out SDS-PAGE。

(5) use coomassie brilliant blue staining 1h, after decolouring, observe expression.

2, the soluble analysis of recombiant protein

Bacterium of expressing containing recombiant plasmid Pet28a-Eg-Grx1 is inoculated in the 500mL fluid medium containing ammonia benzyl, 37 DEG C of cultivations (170rpm), to about OD600=0.6, add optimal IPTG concentration, induce 6h.Bacterium solution is centrifuged 10min (8000rpm), abandoning supernatant, precipitation lysate (20mM Tris-Cl, pH8.0) suspends, ultrasonication thalline.After broken Cellular lysate liquid is centrifugal 10min (12,000rpm), precipitation separation and supernatant under the conditions of 4 DEG C；Precipitation adds appropriate 8M carbamide Dissolve.Upper cleer and peaceful precipitation respectively takes 40 μ L, adds 10 μ L 5 × sds gel sample-loading buffers respectively, boils 10min, centrifugal 10min (12,000rpm), carry out SDS-PAGE electrophoresis, analyze whether rEg-Grx1 is solubility expression.

3, SDS-PAGE electrophoresis detection

By protein electrophorese instrument (Bio-Rad) description, assemble electrophoresis tank.The separation gel of preparation 12% and the concentration of 5% Glue；Gel is vertically arranged in electrophoretic buffer, sample and protein Marker are added in sample well；Regulation constant voltage is 80V, 20min；Adjusting voltage subsequently is 200V.Taking out gel after electrophoresis, use coomassie brilliant blue staining 1h, boiling water bath decolours 15min, finally in gel imaging system, photograph is observed.

4, the purification of recombiant protein

According to above-mentioned steps to recombinant bacterium abduction delivering, it is thus achieved that a large amount of recombiant protein bacterium solution.

(1) 1 is taken, 000mL bacterium solution, centrifugal 10min (8,000rpm), abandons supernatant, collects thalline.

(2) in thalline, lysate is added.

(3) ultrasonic disruption, until bacterium solution is clarified.

(4) centrifugal 10min (12,000rpm), stays supernatant.

(5) take nickel ion affinity chromatograph post, balance 5-10 bed volume with Banding Buffer；

(6) by sample loading after 0.22 μm membrane filtration；

(7) 5-10 bed volume is washed with Banding Buffer；

(8) carry out eluting with the imidazole elution containing different gradients, and collect each eluting peak；

(9), after cleaning with 400mM imidazole elution, the washing with alcohol with 20% to ion concentration is 0, by pillar in 4 DEG C Preserve.

(10) albumen super filter tube is carried out ultrafiltration and concentration, repeatedly add PBS and carry out the displacement of solution, original to remove Imidazoles；

(11), after protein concentration, SDS-PAGE inspection is carried out, and with BCA quantification of protein kit measurement protein compression Degree.

5, result

Eg-Grx1 fragment is successfully connected on pET-28a carrier, converts and enters abduction delivering in BL21 escherichia coli.? Under the conditions of 37 DEG C, when inducing 6h with 1mM IPTG, expression is maximum.The recombiant protein size expressed is about 19kDa, meets pre- Phase size.Soluble analysis result shows, rEg-Grx1 is expressed as soluble protein.Recombiant protein after purification is single band (Fig. 2).

Embodiment 8: Analysis of Immunogenicity

1, the preparation of the anti-rEg-Grx1-IgG of rabbit

REg-Grx1 albumen after purification is mixed according to 1:1 ratio with Freund's complete adjuvant and incomplete Freund's adjuvant respectively Emulsion Seedling is prepared in conjunction.Two new zealand rabbits are carried out subcutaneous four injecting immunes, two all immunity of every minor tick once, for the first time With Freund's complete adjuvant and the immunity of 200 μ g recombiant protein subcutaneous injections, all recombinate with incomplete Freund's adjuvant and 200 μ g for latter three times The immunity of protein skin hemostasis.

After immunity terminates, use HiTrap ProteinA 1mL prepacked column and HPLC purification system (Bio-Rad) purification blood Clearly, flow velocity is adjusted to 1.0mL/min, uses A2Buffer to wash pillar 10min.The serum that 0.45 μm NC membrane filtration is crossed is put into In pillar, 0.5mL/min.With the B Buffer eluting of 10-20ml, collect the IgG eluted, and regulate with the Tris of 50mM The PH of the IgG solution eluted.After balance with 20% ethanol wash pillar, until ion concentration reduces to 0.Pass through SDS- PAGE identifies antibody purification situation.

2, immunoblotting

(1) prepare protein electrophorese gel according to the method described above, albumen after purification is carried out SDS-PAGE electrophoresis.

(2), after protein electrophorese terminates, take the corresponding gel position at protein place, put in transferring film buffer and put down Weighing apparatus, totally 3 times, each 4min.

(3) nitrocellulose filter (NC film) and 24 metafiltration paper are placed in transfering buffering liquid immersion 5min.

(4) in order cathode electrode plate, 24 metafiltration paper, gel, NC film, 24 metafiltration paper are placed in Bio-Rad half dry type and turn In print groove, cover anode electrode plate.

(5) electrotransfer device is received on electroporation, and add transfering buffering liquid 35mA transfer 30min.

(6) after transfer terminates, take out NC film, be immersed in the TBST of 3%BSA, close overnight for 4 DEG C.

(7) after closing terminates, cutting off NC film, negative separated with the positive, the one of addition 1: 1000 dilution is anti-, and room temperature is incubated After educating 2h, outwell one and resist, quickly wash film with TBST 3 times, 5min/ time.

(8), after the Goat-anti-sheep IgG of HRP labelling is pressed 1:1000 dilution, NC film, incubated at room 2h are added After, outwell two and resist, quickly wash film with TBST 3 times, 5min/ time.

(9) NC film being placed in plate, rinsing with fresh substrate nitrite ion until developing the color.

(10), after colour developing, rinse NC film color development stopping with distilled water, and result is carried out Taking Pictures recording.

3, result

Immunoblotting shows, rEg-Grx1 can by echinococcosis granulosa positive sheep serum identification, and be single band (figure 2), illustrate that rEg-Grx1 has preferable immunogenicity.Protoscolex crude protein extracting solution is identified with the anti-rEg-Grx1-IgG of rabbit, aobvious Show the most single band, size consistent with natural Eg-Grx1 (13.2kDa), illustrate that the recombiant protein expressed is really for rEg- Grx1。

Embodiment 9: the foundation of indirect ELISA method

1, indirect ELISA operating procedure

(1) with antigen coated liquid by ratio row dilution rEg-Grx1 albumen, every hole 100 μ L adds in 96 ELISA Plate and wraps Quilt；

(2) outwell and be coated liquid, pat dry liquid in hole, wash with PBST, be repeated four times；

(3), after adding confining liquid (defatted milk powder of 5%) closing, wash four times；

(4) with after PBS in proportion dilute serum, add enzyme mark hole and hatch, outwell liquid, wash four times；

(5) goat or the sheep anti-rabbit two that add the HRP labelling diluted resist, and hatch, wash four times；

(6) under the conditions of lucifuge, in hole, add solubility one pack system substrate TMB and carry out chromogenic reaction；

(7) in hole, add 100 μ L 2M H₂SO₄Terminate reaction, measure its OD value when ultraviolet absorptivity is 450nm.

(8) liquid is outwelled, after patting dry, by washing four times, each 3min shown in (2)；

(9) outwell liquid, after patting dry, under the conditions of lucifuge, carry out color reaction, add at the bottom of solubility one pack system in hole Thing TMB, every hole 100 μ L, incubated at room 10～20min；

(10) in hole, add 100 μ L 2M H again₂SO₄Terminate reaction, immediately 96 orifice plates are placed in microplate reader, in ultraviolet Absorbance is to measure its OD value during 450nm.

2, optimum condition is determined

(1) determining optimal antigen and serum-dilution concentration by Checkerboard titration method, the protein concentration of rEg-Grx1 is set to: 0.2 μ The every hole of g/, the 0.4 every hole of μ g/, the 0.8 every hole of μ g/, the 1.6 every holes of μ g/, the 3.2 every holes of μ g/, the 6.4 every holes of μ g/, serum-dilution ratio: 1: 20,1:40,1:80,1:160,1:320,1:640, with positive serum OD450 close to 1, condition maximum for P/N is as most preferably.

The optium concentration of (2) two anti-effects and time, set 1:1000,1:2000,1:3000,1:4000,1:5000 respectively Five diluted concentrations are groped.Be set to for two anti-action times 37 DEG C 0.5 hour, 1 hour, 1.5 hours, 2 hours four groups, With positive serum OD₄₅₀Close to 1, condition maximum for P/N is as most preferably.

(3) the antigen coated time determines, with being coated liquid dilution recombinant antigen, is coated by optimal diluted concentration, is coated Time is respectively 37 DEG C of 1h, 37 DEG C of 2h and 4 DEG C overnight 3 groups, with positive serum OD₄₅₀Close to 1, condition maximum for P/N is as Good.

(4) confining liquid and the determination of off-period, respectively with 1%BSA, 3%BSA, 5%BSA, 1% skim milk, 3% skim milk, 5% skim milk is closed.37 DEG C are closed off 1 hour, 2 hours, 3 hours and 4 DEG C with optimal confining liquid Overnight 4, with positive serum OD₄₅₀Close to 1, condition maximum for P/N is as most preferably.

(5) determination of positive and negative seroreaction time, according to the condition determined to screen most preferably incubating of positive and negative serum Educate the time, be set to 37 DEG C 0.5 hour, 1 hour, 1.5 hours, 2 hours 4 groups, with positive serum OD₄₅₀Close to 1, P/N maximum Concentration is as most preferably.

(6) determination of substrate developing time, 37 DEG C of conditions divide into 5 minutes, 10 minutes, 15 minutes, 20 minutes, 25 minutes and 30 minutes developing times, measure OD₄₅₀Value, with positive serum OD₄₅₀Close to 1, P/N maximum time is as most preferably.

Result of indirect ELISA shows, P/N value reach the highest antigen coated optimum condition be 4 DEG C overnight, antigen is optimal Concentration is the 1.6 every holes of μ g/, and the optimal diluted concentration of serum is 1:320, and optimal confining liquid and sealing condition are 5% defatted milk powder 37 DEG C closing 1h, sera incubation Best Times is 37 DEG C of 1.5h, and two anti-to hatch Best Times be 37 DEG C of 1h, and two resist optimal diluted concentration During for 1:3000, the optimum condition of substrate colour developing is 37 DEG C of 15min, and in the above conditions, the P/N value recording yin and yang attribute serum is 3.04。

3, the determination of marginal value

At optimum conditions, the OD of 24 parts of sheep echinococcosis granulosa negative serums is measured₄₅₀.Three repetitions are set.According to Marginal value=meansigma methods+3 times standard deviation calculates.

OD with 24 parts of sheep negative serum samples₄₅₀Value determines marginal value, by statistical analysis, calculates 24 parts of silk flosses Sheep negative serum sample OD₄₅₀The meansigma methods of value is 0.296, and standard deviation is 0.0615.According to computing formula: marginal value=feminine gender Sample OD₄₅₀+ 3 times of standard deviations of meansigma methods, show that marginal value is 0.481, i.e. OD₄₅₀> 0.481 time, can determine that as the positive in theory, OD₄₅₀< 0.481 can determine that as feminine gender.

4, replica test in criticizing

Take the coated plank of same batch, detect 5 parts and be known as the sheep serum that echinococcosis granulosa is positive, every part of setting 3 repeating holes, according to the ELISA method having built up, repeat test in carrying out criticizing, and calculate the coefficient of variation, detection the method Repeatability in batch.

In batch, replica test result shows, the coefficient of variation in plate is between 0.583%-2.014%, and meansigma methods is 1.191%.

5, criticize between replica test

Take 3 coated planks of batch, at optimum conditions, detect the sheep serum that 3 parts of echinococcosis granulosas are positive, often Part arranges 3 repeating holes, according to the ELISA method having built up, repeats test between carrying out criticizing, calculates the coefficient of variation, and detection is somebody's turn to do Method batch between repeatability.

Between Pi, replica test result shows, between plate, the coefficient of variation is between 0.914%-1.558%, and meansigma methods is 1.153%.

6, specific test

Enter with the indirect ELISA cysticercus tenuicollis positive serum anti-to goat respectively set up, sheep anti-cenurus cerebralis serum Row detection, detects its specificity.

Indirect ELISA cenurus cerebralis serum anti-to sheep respectively and goat anti-cysticercus tenuicollis positive serum with setting up enter Row detection, result shows and only there is cross reaction with a sheep brain Echinococcus hydatid cyst serum, with four goat Cysticercosis Tenuicollis serum There is cross reaction (Fig. 3), therefore, its specificity is 64.3% (9/14).

7, sensitivity test

3 parts of positive serums are made doubling dilution, from 1:100 to 1:201800, according to criterion, determines its sensitivity.

3 parts of positive serums are made doubling dilution, and result shows when diluting 3200 times, OD₄₅₀Meansigma methods is 0.567, still belongs to In the positive, and when dilution 6400 times, OD₄₅₀Meansigma methods is 0.392, less than marginal value, accordingly, it is determined that its sensitivity is 1: 3200。

8, clinical trial

With the indirect ELISA method set up respectively to 24 parts of echinococcosis granulosa feminine gender sheep serums and 24 points of particulate spine balls Larva of a tapeworm or the cercaria of a schistosome disease positive sheep serum detects, and judges the reliability of the method according to marginal value.

With 24 parts of sheep echinococcosis granulosa positive serums and 24 parts of negative serums, the indirect ELISA method set up is carried out Clinical detection (is shown in Table 1 and Fig. 4), and result shows the OD of 23 parts of sheep echinococcosis granulosa positive serums₄₅₀It is all higher than marginal value, 24 parts of negative serum OD₄₅₀Being respectively less than marginal value, the coincidence rate of detection is up to 97.9%.

Table 1 clinical serum sample OD₄₅₀

The above is only the preferred embodiment of the present invention, it is noted that for the ordinary skill people of the art For Yuan, under the premise without departing from the principles of the invention, it is also possible to make some improvements and modifications, these improvements and modifications also should It is considered as protection scope of the present invention.

Claims (7)

1. Echinococcus granulosus glutaredoxin-1 is in the immunizing antigen and/or test kit of preparation detection echinococcosis granulosa Application.

Apply the most according to claim 1, it is characterised in that described test kit is ELISA detection kit or immunoblotting Detection kit.

3. the ELISA detection kit detecting echinococcosis granulosa, it is characterised in that include Echinococcus granulosus paddy oxygen also Albumen-1 and ELISA detection kit conventional constituents.

Test kit the most according to claim 3, it is characterised in that described ELISA detection kit conventional constituents includes antigen It is coated two anti-and tmb substrates of liquid, ELISA Plate, confining liquid, HRP labelling.

Test kit the most according to claim 4, it is characterised in that described confining liquid is 5% defatted milk powder.

Test kit the most according to claim 4, it is characterised in that the two of described HRP labelling resist the goat for HRP labelling or silk floss Goat-anti rabbit two resists.

7. according to test kit described in claim 4-6 any one, it is characterised in that described ELISA detection kit routine group Divide and also include chromogenic reaction stop buffer H₂SO₄, cleaning mixture PBST and diluent PBS.