CN102220285A - Monoclonal antibody of outer membrane protein of chlamydia abortus and application thereof - Google Patents
Monoclonal antibody of outer membrane protein of chlamydia abortus and application thereof Download PDFInfo
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Abstract
The invention relates to monoclonal antibody of N-terminal protein of chlamydia abortus POMP18D as well as a preparation method and application thereof. The monoclonal antibody is secreted by a hybridoma cell strain 1F10D4 with the collection number of CGMCC No.4658. The invention also provides application of the monoclonal antibody in direct fluorescence immune or indirect fluorescence immune detection of chlamydia abortus. The monoclonal antibody of N-terminal protein of chlamydia abortus POMP18D has strong specificity and fluorescent characteristic, and is suitable for being used as a fluorescence antibody to establish a direct fluorescence detection method or indirect immune fluorescence detection method.
Description
Technical field
The invention belongs to field of biological detection, relate to a kind of miscarriage preferendum chlamydozoan monoclonal antibody and preparation method thereof and application, relate in particular to a kind of miscarriage preferendum chlamydozoan POMP18D N end protein monoclonal antibody and preparation method thereof and application.
Background technology
Miscarriage preferendum chlamydozoan (Chlamydia abortus, C.abortus) be the entozoic prokaryotic organism of obligate eukaryotic cell that large numbers of and Gram-negative bacteria have substantial connection, it can cause various animal and humans' infection, and the livestock industry production of many countries is caused enormous economic loss and influences public health.Miscarriage preferendum chlamydozoan is the more common pathogenic agent that causes the dam miscarriage; in recent years; people such as Qiu Changqing show the investigation of the pig chlamydiosis that the large-scale pig farm of present domestic each province carries out; the pig choamydiae infection is totally in rising trend; infection rate as Sichuan in 1987 is 11.45%; 1989 be to rise to 80% in 15.52%, 2003 year, already cause serious economy loss for intensive pig production.
Aspect the chlamydozoan diagnosis, use antigenic major outer membrane albumen (MOMP) and the lipopolysaccharides (LPS) of remaining at most at present.Comprise the antigenic polymerase chain reaction of detection (PCR) technology of setting up according to ompA gene conservative property, according to detecting the direct immunofluorescence antibody test technology that the LPS specificity is set up, as the chlamydozoan fluorescence detection reagent kit of Britain OXOID company, and amplify enzyme-linked immunosorbent assay (PCE-ELISA) method.Detecting the test kit of antibody, as the indirect fluorescent test kit (Israel Savyon Diagnostics) with LPS bag quilt, is enzyme-linked immunosorbent assay kit (French IDVET) antibody assay kit etc. of envelope antigen with MOMP.But the round pcr interval between diagnosis is long, narrow application range, is unfavorable for clinical expansion, though and import antibody assay kit confidence level is higher, cost is also high, also be unfavorable for clinical popularizing.
Summary of the invention
The purpose of this invention is to provide a kind of miscarriage preferendum MOMP-E monoclonal antibody and preparation method thereof and application.
Miscarriage preferendum MOMP-E monoclonal antibody provided by the invention is produced by hybridoma cell strain 1F10D4, its immunogen is to be immunogen with first section recombinant protein POMP18D-1 of POMP18D N end for miscarriage preferendum chlamydozoan (C.abortus) outer membrane protein, immunity Balb/c mouse, the hybridoma cell strain that filters out then.Hybridoma cell strain 1F10D4 provided by the invention, in 2011 03 month No. 10 at China Committee for Culture Collection of Microorganisms common micro-organisms center (address: No. 3, A, DaTun Road, Chaoyang District, BeiJing City, Institute of Microorganism, Academia Sinica, postcode 100101) preservation, preserving number are CGMCC No.4658.
The present invention also provides miscarriage preferendum chlamydozoan MONOCLONAL ANTIBODIES SPECIFIC FOR method, it is as the antigen immune mouse with miscarriage preferendum MOMP-E POMP18D N end protein, mouse boosting cell after the immunity and myeloma cell are merged the hybridoma that obtains secretion miscarriage preferendum chlamydozoan POMP18D N end protein monoclonal antibody, and preferendum chlamydozoan POMP18D N end protein monoclonal antibody obtains miscarrying.
Wherein, described miscarriage preferendum MOMP-E POMP18D N end protein is the freezing powder of draining, and when immunity is with an amount of PBS solution dilution.
Miscarriage preferendum MOMP-E POMP18D N end protein, called after POMP18D-1, for:
1) protein of the composition of the aminoacid sequence shown in the SEQ ID No.2;
2) aminoacid sequence of SEQ ID No.2 is through adding sequence label deutero-protein.
In order to make 1) POMP18D-1 protein be convenient to purifying, can connect label as shown in table 1 at proteinic N-terminal or the C-terminal that the aminoacid sequence shown in the SEQ ID No.2 is formed.
Table 1. sequence label
| Label | Residue | Sequence |
| Poly-Arg | 5-6 (being generally 5) | RRRRR |
| Poly-His | 2-10 (being generally 6) | HHHHHH |
| FLAG | 8 | DYKDDDDK |
| Strep-tag II | 8 | WSHPQFEK |
| c-myc | 10 | EQKLISEEDL |
Above-mentioned 2) but in POMP18D-1 protein synthetic, also can synthesize its encoding gene earlier, carry out biology again and express and to obtain.Encode above-mentioned 2) in the proteinic gene of POMP18D-1 can be by the encoding sequence that its 5 ' end and/or 3 ' end connects the label shown in the table 1 of the dna sequence dna shown in the SEQ ID No.1 be obtained.
Miscarriage preferendum MOMP-E POMP18D N end protein monoclonal anti physical efficiency of the present invention detects at C.abortus POMP18D-1 albumen, has very strong specificity, can be used for detecting miscarriage preferendum chlamydozoan.
Miscarriage preferendum chlamydozoan POMP18D N end protein monoclonal antibody of the present invention also has good fluorescent characteristic, suits to set up direct fluorescence or the chlamydial method of indirect immunofluorescence detection miscarriage preferendum as fluorescence antibody.
The chlamydial method of direct fluoroscopic examination miscarriage preferendum of the present invention, be directly to combine, under fluorescent microscope, detect specific fluorescence and detect miscarriage preferendum chlamydozoan with corresponding antigens in the histocyte with fluorescein-labeled above-mentioned miscarriage preferendum chlamydozoan POMP18D N end protein monoclonal antibody.Concrete steps comprise: (1) preparation pathological material of disease section: take doubtful C.abortus pathological material of disease, as get tissues such as air bag, lungs, spleen, liver, uterine mucosa, uterine cervix, larynx mucus and cut in right amount, after grinding under 4 ℃ of conditions, gentamicin room temperature treatment 30min, 1,000r/min, centrifugal 10min, abandon precipitation, infect the McCoy cell (placing cover glass in advance in the 24 porocyte plates) that has grown to individual layer with supernatant, infect 24～48h, take out the cover glass that infects, fix 10～20min with the methyl alcohol or the dehydrated alcohol of precooling; Perhaps above-mentioned tissue is cooked the frozen section of 0.1～0.3mm thickness, paster is crossed on the slide in cold alcohol immersion; The suspicious respiratory tract or the vaginal swab that perhaps will collect are smeared sheet, are positioned in the cold acetone to fix, and taking-up is dried, and-20 ℃ of preservations are standby; (2) foundation of direct immunofluorescence diagnostic method: take out the slide for preparing, drip PBS earlier and soak into 10min, drip the fluorescent mark C.abortus monoclonal antibody of 0.15～15 μ g/ml of about 25 μ L then, pack in the wet box, hatch 30min for 37 ℃, taking-up is washed 3 times with PBS, each 5min, after washing finishes, lucifuge seasoning 5～10min, with volume fraction 50% glycerine mounting, fluorescence microscope.Simultaneously with the positive contrast of the positive slide of choamydiae infection, with the negative contrast of not infecting of slide.
Indirect fluorescent of the present invention detects the chlamydial method of miscarriage preferendum, be to be one anti-with above-mentioned miscarriage preferendum chlamydozoan POMP18D N end protein monoclonal antibody, with fluorescently-labeled rabbit anti-mouse igg is two anti-, carries out the indirect IF staining method and detects miscarriage preferendum chlamydozoan.Specifically comprise the steps: the section of (1) preparation pathological material of disease: method and step are with aforementioned; (2) foundation of indirect immunofluorescence diagnostic method: take out the slide for preparing, drip the C.abortus POMP18D-1 protein monoclonal antibody of 2～20 μ g/ml of 25 μ L, in the wet box of packing into, hatch 1h for 37 ℃, taking-up is washed 3 times with PBST, each 5min, and the anti-mouse fluorescence two of rabbit that drips the 15 μ g/ml of 25 μ L then resists, pack in the wet box, hatch 1h for 37 ℃, take out with PBST washing 3 times each 5min, with volume fraction 50% glycerine mounting, fluorescence microscope.Simultaneously with the positive contrast of mouse positive serum, with the negative contrast of not infecting of McCoy cell.
In order to make the aforesaid method operation simpler, the present invention also provides direct fluorescent reagent box and indirect immunofluorescence test kit.
Direct fluorescent reagent box of the present invention contains fluorescein-labeled described miscarriage preferendum MOMP-E POMP18D N end protein monoclonal antibody.
Direct fluorescent reagent box of the present invention also can contain positive control serum, negative control sera, phosphoric acid salt and/or mounting medium.
Indirect fluorescent test kit of the present invention contains above-mentioned miscarriage preferendum MOMP-E POMP18D N end protein monoclonal antibody.
Indirect fluorescent test kit of the present invention also can contain fluorescently-labeled rabbit anti-mouse igg, positive control serum, negative control sera, phosphoric acid salt, polysorbas20 and/or mounting medium.
The prokaryotic expression pig that the present invention obtains with purifying is miscarried preferendum chlamydozoan POMP18D-1 recombinant protein as the antigen immune mouse, by the indirect ELISA method screening positive clone, obtained the hybridoma of secretion at the monoclonal antibody of miscarriage preferendum chlamydozoan POMP18D-1 recombinant protein.From hybridoma chromosome number, biological characteristics after continuous passage is cultivated and be frozen, and the type of monoclonal antibody, subclass and aspect such as tire, the monoclonal antibody biological characteristics that is obtained has been carried out system's evaluation, the result shows that the ability of the hybridoma secretory antibody that is obtained is strong and stable, the monoclonal antibody height of tiring.Directly fluorescence and indirect fluorescent test experience result show that the monoclonal antibody that is obtained all can detect at C.abortusPOMP18D-1 albumen, have very strong specificity and fluorescent characteristic, suit to set up direct fluorescence detection method or indirect immunofluorescence detection method as fluorescence antibody.
Description of drawings
Figure 1 shows that the chromosome map of 1F10D4 hybridoma.
Figure 2 shows that the indirect immunofluorescence assay result of 1F10D4 monoclonal antibody to miscarriage choamydiae infection swine disease material.Wherein, the negative contrast of A, B is the sample detection result.
Embodiment
Following examples are used to illustrate the present invention, but are not used for limiting the scope of the invention.The preparation method of embodiment 1 miscarriage preferendum chlamydozoan POMP18D protein monoclonal antibody
Pig miscarriage preferendum chlamydozoan CP16 bacterial strain is available from China Veterinery Drug Inspection Office culture presevation chamber, and BALB/c mouse is available from Beijing's Experimental Animal Center.
HAT substratum, HT substratum, foetal calf serum, DMEM high glucose medium, RPMI1640 substratum, horseradish peroxidase (HRP) and HRP mark rabbit anti-mouse igg, fluorescein (FITC) mark rabbit anti-mouse igg are all available from Sigma company.
Miscarriage preferendum chlamydozoan POMP18D proteic preparation (specifically can be referring to junjing Yang et al.Bull Vet Inst Pulawy, 2009,53 (4), 621-625):
Pig is had a liking for miscarriage chlamydozoan CP16 bacterial strain lyophilized powder dilute, be inoculated in the SPF chicken embryo of 6 ages in days, every piece of egg inoculation 0.2mL with 1 milliliter of sterile saline.Collect the yolk cyst membrane of 5 days dead chicken embryos, the chick embryo yolk sac film of results is added PBS (pH7.4) in ice bath, grind to form 20% suspension; Take out 100 μ L, 4 ℃, the centrifugal 10min of 3000rpm, abandon precipitation and keep supernatant, supernatant is chlamydozoan bacterium liquid, with supernatant in 4 ℃, the centrifugal 20min of 14000rpm, abandon supernatant and stay precipitation, extract the test kit step by DNA of bacteria afterwards and carry out genome extraction (the Qiagen genome extracts test kit, Germany).Have a liking for the POMP18D gene order of miscarriage chlamydozoan S26/3 bacterial strain with reference to the sheep of NCBI login, design associated clip primer, the primer sequence is as follows: F:TCTTGGGAAAATCTAGATACC (SEQ IDNo.8); R:GGGCAGTGTAACCACCTCAT (SEQ ID No.9).Genome with said extracted is a template, amplification purpose fragment.Reclaim the purpose fragment, after PBS-T II cloning vector is connected, do further screening, doubtful positive colony is checked order, sequence shown in SEQ ID No.1, the albumen shown in the SEQ ID No.2 of encoding.With containing SalI and NotI restriction enzyme site primer carries out the pcr amplification second time, the gene fragment of 509～1842bp of the POMP18D gene shown in the aforementioned SEQ ID No.1 that increases.Primer sequence is
F：GTCGACGG TCTTGGGAAAATCTAGATACC(SEQ ID No.10)，
R：GCGGCCGCAGGGCAGTGTAACCACCTCAT(SEQ ID No.11)。
The PCR product is cut through SalI and NotI enzyme, is connected acquisition recombinant expression vector pET-POMP18D-1 with pET-32a (+) expression vector that same enzyme is cut.Recombinant expression vector changes BL21 (DE3) over to, induces express recombinant protein POMP18D-1 down at IPTG.
The result shows, is 37 ℃ at inducing temperature, when inductor IPTG final concentration is 1.0mmol/L, the target protein great expression, and when inducing 5 hours the expression amount maximum, target protein size is 65.3kD (containing carrier pET-32a (+) label protein), and is suitable with theoretical value.Afterwards with target protein through Ni-NTA purification column (Invitrogen) purifying under the sex change condition, then through the dialysis renaturation, again through measuring concentration behind the ultrafiltration and concentration, according to the protein concentration calculation formula:
Protein concentration (mg/mL)=1.45OD
280-0.74OD
260
After obtaining protein concentration, packing.And carry out freezing draining, and make lyophilized powder ,-80 ℃ of preservations are standby.
Animal immune:
POMP18D-1 albumen after concentrating with renaturation is as antigen immune Balb/c mouse in 6 age in week, immunity is 6 times altogether, each 1～2 week at interval, carry out immunity after being emulsified into water-in-oil with antigen and equivalent Freund's complete adjuvant for the first time, immunizing dose is 200 μ g/, totally 2, immunization route is the subcutaneous injection of belly multiple spot.Carry out second time immunity after two weeks, carry out immunity for the third time at interval a week, all use the equivalent Freund's incomplete adjuvant twice, immunizing dose be 100 μ g/ only, immunization route is the subcutaneous injection of belly multiple spot.Carry out four in one week of every interval and exempt from and five exempt from, use the antigen liquid immunity instead, dosage be 100 μ g/ only, immunization route is an abdominal injection.Five exempt from one week of back, and mouse tail is taken a blood sample in a small amount, detect antibody titer, select to tire the high order of magnitude 10
7Above mouse is cooked booster immunization in first three sky of fusion, uses the antigen liquid abdominal injection, and dosage is 100 μ g/.
Cytogamy:
Merged recovery SP2/0 myeloma cell preceding 3 days.Under aseptic condition, get the spleen after the above-mentioned immunity of mouse, the preparation splenocyte, and draw 1 * 10 respectively
8Individual splenocyte and 2 * 10
7Individual myeloma cell's suspension under fusogen PEG4000 effect, merges.Fused cell is selected to cultivate suspension with HAT be covered with in the 96 porocyte plates of feeder cell even also the adding, every hole 100 μ L place 5%CO
2Cultivate in the incubator.Every day observed and recorded cell growing state; Note replenishing volume fraction 1%HAT substratum.
Hybridoma screening and subclone:
After cell clone after waiting to merge grows into and covers cell hole bottom 1/4～1/3, there is the culture supernatant of clonal growth to detect to all with setting up good indirect ELISA method.To detecting to strong positive hole employing limiting dilution assay carries out subclone, negative hole detects once after 3 days again, then abandons it as if still negative.Cultivate through 4 times screenings and cloning, obtaining 6 strains can the stably excreting C.abortus POMP18D-1 protein monoclonal antibody and the high hybridoma of tiring.
The preparation of odd contradictive hydroperitoneum:
With the hybridoma that screens, be inoculated in and use ages inductor silica gel H (or sterilising liq paraffin, 0.5mL/ is only) to handle 10 days healthy Balb/c mouse peritoneal in 10 weeks in advance, 0.5mL/ only (contains 5 * 10
5～1 * 10
6Individual hybridoma), through 14 days, visible mouse web portion obviously increased, and gathered ascites this moment and with the ascites 3000r/min that collects, centrifugal 10min removes grease and post precipitation and is odd contradictive hydroperitoneum, and is standby in-80 ℃ of preservations.
The evaluation of monoclonal antibody:
Adopt Sigma company mouse monoclonal antibody parting kit, use agar diffusion test mensuration and show that 6 hybridoma excretory monoclonal antibodies of acquisition have 5 to be the IgG1 type, have one to be the IgG3 type.
Use indirect ELISA method and detect tiring of Hybridoma Cell Culture supernatant liquor.The result shows C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 (IgG1 type), and (1:4096K) antibody titer is the highest, the hybridoma cell strain of this antibody of secretion is preserved in China Committee for Culture Collection of Microorganisms common micro-organisms center (abbreviation CGMCC on March 10th, 2011, address: No. 3, Yard 1, BeiChen xi Road, Chaoyang District, Beijing City, Institute of Microorganism, Academia Sinica, postcode 100101), preserving number is CGMCC No.4658.
Utilize the colchicine cracking process.Getting goes down to posterity cultivates the cell of 24h, adds 0.1mL 1% colchicine, puts 37 ℃ of water-bath 4h, collecting cell, 2000r/min, centrifugal 10min abandons supernatant, adds 0.075mol/L KCl 10mL in the precipitation, even with the suction pipe pressure-vaccum, put 37 ℃ of water-bath 15～20min, make cellular swelling.Centrifugal abandon supernatant after, cell precipitation is with the fixing 20min of the mixed solution 10mL of 3 parts of methyl alcohol, 1 part in Glacial acetic acid, with 2000r/min, centrifugal 10min gets the cell precipitation smear after abandoning supernatant, dyes oily spectroscopy after the seasoning with Giemsa.100～108 of hybridoma 1F10D4 karyomit(e)s (Fig. 1).As can be seen from Figure 1, chromosome number is 104, shows that the cultured cells that goes down to posterity does not morph.
The mouse ascites of finally collecting is carried out western blot test, and two resist the anti-mouse IgG of rabbit for the HRP mark that dilutes at 1: 1000 with antibody diluent (5% skim-milk, TBST preparation).Simultaneously, sample segment carries out SDS-PAGE.The result shows in SDS-PAGE, the very thick purpose band about a 65KDa is arranged, with the albumen sizableness behind the expression and purification; In western blot test, after the DAB colour developing, the brown purpose band about a 65KDa is arranged on the PVDF transfer film, with the used albumen sizableness of preparation monoclonal antibody, and have immunogenicity.
Adopt the ELISA method to measure the mouse ascites of the C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 that collects and the cross reactivity of expression vector pET-32a (+) target protein.The result shows, gained C.abortus POMP18D-N protein monoclonal antibody and carrier proteins no cross reaction.
Carry out fluorescent mark respectively with the C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 ascites purifying for preparing, and according to the known method antagonist, prepare fluorescence antibody.Grow to the McCoy cell of individual layer on C.abortus CP16 strain infection 96 orifice plates, behind 24～48h, supernatant discarded, with dehydrated alcohol fixing after, PBS washing 3 times adds the corresponding fluorescence antibody of 25 μ L, 1.5 μ g/ml in 96 orifice plates, 37 ℃ of reaction 30min in wet box, PBS washing 3 times, fluorescent microscope is observed down, with PBS as negative control.The person is judged to the positive the green fluorescence, and no fluorescence person is judged to feminine gender.Observe and find, the positive hole McCoy cell of CP16 strain infection and the McCoy cell in the monoclonal antibody hole all present tangible green fluorescence, and the McCoy cell does not have tangible green fluorescence in the negative hole, shows that C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 has good fluorescent characteristic.
Grow to the McCoy cell of individual layer on C.abortus CP16 strain infection 96 orifice plates, behind the 48h, supernatant discarded, with dehydrated alcohol fixing after, PBS washing 3 times adds the monoclonal antibody 1F10D4 for preparing the 4 μ g/ml of 25 μ L in 96 orifice plates, 37 ℃ of reaction 1h, PBS washs 3 times, adds the rabbit anti-mouse igg of the FITC mark of 25 μ L, 15 μ g/ml, 37 ℃ of reaction 30min, PBS washing 3 times, fluorescent microscope is observed down, and as negative control, the mouse positive serum is as positive control with PBS.The person is judged to the positive the green fluorescence, and no fluorescence person is judged to feminine gender.Observe and find, the positive hole McCoy cell of CP16 strain infection and the McCoy cell in the monoclonal antibody hole all present tangible green fluorescence, and the McCoy cell does not have tangible green fluorescence in the negative hole, shows that C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 has good fluorescent characteristic.
The foundation of embodiment 2C.abortus POMP18D-1 protein monoclonal antibody direct immunofluorescence detection method
Tissue samples is handled: gets doubtful miscarriage chlamydozoan pathological material of disease, gets proper amount of fresh lungs, spleen, uterine mucosa, vaginal mucosa, make the frozen section of 0.1～0.3mm, and after cold acetone is fixed 10 minutes, the lucifuge examine.
Cell sample is handled: after grinding under 4 ℃ of conditions of pathological material of disease tissue, 200UI/mL gentamicin room temperature treatment 30min, 1,000r/min, centrifugal 10min, abandon precipitation, infect the McCoy cell (placing cover glass in advance in the 24 porocyte plates) that has grown to individual layer, infect 48h with supernatant, take out cover glass, with the fixing 10min of the methyl alcohol of precooling or dehydrated alcohol, taking-up is dried, and-20 ℃ of preservations are standby;
Take out the above-mentioned slide for preparing, drip PBS earlier and soak into 10min, drip 1.5 μ g/mL C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 of about 25 μ L fluorescein isothiocyanate (FITC) marks then, pack in the wet box, hatch 30min for 37 ℃, take out with PBS washing 3 times each 5min, simultaneously with the positive contrast of the positive slide of choamydiae infection, with the negative contrast of not infecting of slide.After washing finished, lucifuge seasoning 5～10min was with 50% glycerine mounting, fluorescence microscope.Utilize C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 to experimentize, detect sample clinically, and the commercial kit detected result of direct immunofluorescence diagnostic result and chlamydiaceae specificity lipopolysaccharides (LPS) bag quilt is done coincidence rate relatively.
Utilize fluorescently-labeled C.abortus POMP18D-1 protein monoclonal antibody that 50 collected duplicate samples are detected, miscarriage preferendum chlamydozoan is distributed with the light-emitting particles of ellipse, bright green, systematicness in cytoplasm under fluorescent microscope.Detect (IMAGEN with the commercial kit of chlamydiaceae specificity lipopolysaccharides (LPS) bag quilt
TMCHLAMYDIA, Oxoid Ltd, Britain) result relatively sees Table 2.
The direct fluorescent method diagnosis of table 2C.abortus POMP18D-1 protein monoclonal antibody is compared with the immunofluorescence technique detected result that LPS wraps quilt
| Pathological material of disease | POMP18D-1 | LPS | Coincidence rate |
| Positive | 49 | 50 | 98％ |
| Negative | 1 | 0 | 100％ |
The foundation of embodiment 3C.abortus POMP18D-1 protein monoclonal antibody indirect immunofluorescence detection method
Take doubtful C.abortus pathological material of disease, cut an amount of lungs, spleen, uterine mucosa, vaginal mucosa, after grinding under 4 ℃ of conditions, 200UI/mL gentamicin room temperature treatment 30min, 1.000r/min centrifugal 10min abandons precipitation, infect the McCoy cell (placing cover glass in advance in the 24 porocyte plates) that has grown to individual layer with supernatant, infect 48h, take out cover glass, the methyl alcohol of usefulness precooling or dehydrated alcohol be 10min fixedly, taking-up is dried, and-20 ℃ of preservations are standby.
The slide that taking-up prepares drips the C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 of 25 μ L, 10 μ g/ml, in the wet box of packing into, hatch 1h for 37 ℃, taking-up is with PBST washing 3 times, and each 5min drips the FITC mark rabbit anti-mouse igg of 25 μ L, 15 μ g/ml then, pack in the wet box, hatch 1h for 37 ℃, take out with PBST washing 3 times each 5min, with volume fraction 50% glycerine mounting, fluorescence microscope.With the positive contrast of C.abortus mouse positive serum, with the negative contrast of not infecting of McCoy cell.If positive then can be observed the light-emitting particles of ellipse, bright green, systematicness, feminine gender does not then have (Fig. 2).
Utilize C.abortus POMP18D-1 protein monoclonal antibody 1F10D4 anti-as one, 30 parts of miscarriage chlamydozoan pathological material of diseases of clinical censorship have been detected, with PCR detected result (Zhang FM, et al, Zoonose and Public Health, 2009, positive coincidence rate 56:71-76) is 92%, with PCR as a result negative match-rate be 100% (table 3).
The comparison of indirect fluorescent method diagnosis of table 3C.abortus POMP18D-1 protein monoclonal antibody and PCR diagnostic result
| Pathological material of disease | PCR | The indirect fluorescent method | Coincidence rate |
| Positive | 25 | 23 | 92％ |
| Negative | 5 | 6 | 100％ |
In sum, C.abortus POMP18D-1 protein monoclonal antibody can be used for quick diagnosis miscarriage preferendum chlamydiosis.
The above only is a preferred implementation of the present invention; should be pointed out that for those skilled in the art, under the prerequisite that does not break away from the technology of the present invention principle; can also make some improvements and modifications, these improvements and modifications also should be considered as protection scope of the present invention.
Claims (9)
1. miscarriage preferendum chlamydozoan POMP18D N end protein monoclonal antibody hybridoma cell strain 1F10D4, its deposit number is: CGMCC No.4658.
2. the miscarriage preferendum MOMP-E monoclonal antibody that produces by the described hybridoma cell strain of claim 1.
3. monoclonal antibody according to claim 2, its immunogen is:
1) the miscarriage preferendum MOMP-E POMP18D N end protein of forming by the aminoacid sequence shown in the SEQ ID No.2 in the sequence table; Or
2) aminoacid sequence of SEQ ID No.2 process is added sequence label and deutero-miscarriage preferendum MOMP-E POMP18D N end protein in the sequence table.
4. the application of the described miscarriage preferendum of claim 2 MOMP-E POMP18D N end protein monoclonal antibody in miscarriage preferendum chlamydozoan detects.
5. the direct chlamydial method of fluoroscopic examination miscarriage preferendum, it comprises with the described monoclonal antibody of fluorescein-labeled claim 2 and directly combining with corresponding antigens in the histocyte that the detection specific fluorescence detects the preferendum chlamydozoan of miscarrying under fluorescent microscope.
6. indirect fluorescent detects the chlamydial method of miscarriage preferendum, and it comprises with the described monoclonal antibody of claim 2 is one anti-, is two anti-with fluorescein-labeled rabbit anti-mouse igg, carries out the indirect IF staining method and detects miscarriage preferendum chlamydozoan.
7. the direct immunofluorescence test kit that contains the described monoclonal antibody of fluorescein-labeled claim 2.
8. the indirect immunofluorescence test kit that contains the described monoclonal antibody of claim 2.
9. indirect fluorescent test kit according to claim 8 is characterized in that, also contains fluorescein-labeled rabbit anti-mouse igg, positive control serum, negative control sera, phosphoric acid salt, polysorbas20 and/or mounting medium.
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| CN104130326A (en) * | 2014-08-01 | 2014-11-05 | 中国农业科学院兰州兽医研究所 | Monoclonal antibody of Chlamydophila abortus macrophage infectivity potentiator and hybridoma cell thereof |
| CN108486066A (en) * | 2018-02-27 | 2018-09-04 | 中国农业大学 | A kind of monoclonal antibody of the anti-current of hybridoma cell strain and its secretion production Chlamydia |
| CN110129278A (en) * | 2019-05-31 | 2019-08-16 | 湖北省农业科学院畜牧兽医研究所 | Hybridoma cell strain CMOMP-5D7 and its monoclonal antibody and application of secretion |
| CN112358545A (en) * | 2020-11-10 | 2021-02-12 | 中国农业大学 | Preparation method and application of pigeon trichomonas and candida albicans bigeminal egg yolk antibody powder |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104130326A (en) * | 2014-08-01 | 2014-11-05 | 中国农业科学院兰州兽医研究所 | Monoclonal antibody of Chlamydophila abortus macrophage infectivity potentiator and hybridoma cell thereof |
| CN108486066A (en) * | 2018-02-27 | 2018-09-04 | 中国农业大学 | A kind of monoclonal antibody of the anti-current of hybridoma cell strain and its secretion production Chlamydia |
| CN108486066B (en) * | 2018-02-27 | 2021-07-27 | 中国农业大学 | Hybridoma cell strain and monoclonal antibody secreted by hybridoma cell strain and resisting chlamydia abortus |
| CN110129278A (en) * | 2019-05-31 | 2019-08-16 | 湖北省农业科学院畜牧兽医研究所 | Hybridoma cell strain CMOMP-5D7 and its monoclonal antibody and application of secretion |
| CN112358545A (en) * | 2020-11-10 | 2021-02-12 | 中国农业大学 | Preparation method and application of pigeon trichomonas and candida albicans bigeminal egg yolk antibody powder |
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| CN102220285B (en) | 2012-12-12 |
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