CN201285399Y - Dipstick for detecting pathogen of pig breeding disordered virus infectious disease - Google Patents
Dipstick for detecting pathogen of pig breeding disordered virus infectious disease Download PDFInfo
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- CN201285399Y CN201285399Y CNU200820148807XU CN200820148807U CN201285399Y CN 201285399 Y CN201285399 Y CN 201285399Y CN U200820148807X U CNU200820148807X U CN U200820148807XU CN 200820148807 U CN200820148807 U CN 200820148807U CN 201285399 Y CN201285399 Y CN 201285399Y
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Abstract
The utility model discloses a test paper for detecting the causal factor of a pig propagation barrier virus communicable disease, comprising a supporting layer which can not absorb water and an absorption layer which is attached to the supporting layer, wherein the absorption layer is formed by sequentially splicing an absorption fiber layer, a gold-labelled antibody fiber layer, a fibrino film layer and a water absorption layer, the fibrino film layer is marked with a comparing print which includes pig/mouse resistant IgG and at least one detecting print which includes pig propagation barrier virus antibodies, the pig propagation barrier virus antibodies are at least one of PRRSV, PPV and JEV monoclonal antibodies/polyclonal antibodies, and gold-labelled polyclonal antibodies/ monoclonal antibodies of a resistant pig propagation barrier virus communicable disease corresponding to the antibody of the barrier virus communicable disease antibody included by the detecting print are attached to the gold-labelled antibody fiber layer. The test paper has strong particularity and high sensitivity without additional equipment and reagent during detection, can be operated by anyone, and is suitable for fast distinguishing and diagnosing the pig propagation barrier virus communicable disease on the field.
Description
Technical field
The utility model relates to a kind of utensil that detects pig virus infectious disease cause of disease, particularly relates to a kind of test strips that detects pig breeding disorder virus epidemic pathogen.
Technical background
China is the production and consumption big country of live pig.Increase year by year along with large, medium and small large scale of pig farm field, boar number; the pig breeding dysfunction disease has become one of most important disease of China's large-scale pig farm; incidence of disease average out to causes enormous economic loss more than 30%, and is seriously restricting the development of pig industry.The pig breeding is to cause three kinds of important viruses of pig breeding dysfunction with breathing syndrome virus (PRRSV), pig parvoviral (PPV) and pig japanese b encephalitis virus (JEV).PRRSV causes porcine reproductive and respiratory syndrome (PRRS), mainly show as and infect the sow heating, apocleisis, miscarry later stage of pregnancy, stillborn foetus, mummy tire and weak son etc., infect piglet have difficulty in breathing (pneumonia), immunodeficiency disease and high mortality, blue because of the ear of the sick pig of part, claim blue otopathy again.Blue otopathy is spread wide in China in recent years, thinks now that as " hyperpyrexia disease " that the swinery of more than 10 province in China north and south in 2006 (city, district) is taken place highly pathogenic PRRSV strain causes, the morbidity swinery reaches 2,000,000, dead 400,000.Therefore, PRRSV is considered to one of principal disease that causes pork rise in price in recent years.PPV causes porcine parvovirus, mainly show as infected sow, particularly the negative multiparity sow of first farrowing sow and serology miscarry, stillborn foetus, monster, mummy tire and weak son and join infertilely repeatly, and do not show tangible clinical symptoms after the infection of the pig at other ages.Porcine parvovirus is spread wide in China swinery at present, infects the pig farm at great majority and is the popular and very difficult purification of region, thereby caused the economic loss that continues, and has seriously hindered the sound development of pig industry.JEV causes zoonosis-Japanese Type-B encephalitis.Pig japanese b encephalitis mainly shows as infected pigs heating, apocleisis, and sow is miscarried suddenly later stage of pregnancy, stillborn foetus, mummy tire and weak son etc., and newborn piglet is very different, mortality ratio is high, and orchitis appears in the infection boar.Pig japanese b encephalitis is mainly propagated by viruliferous bite by mosquitos, mainly is distributed in countries in Asia, and the most of area of China all has this disease to take place.
Quick diagnosis is the basis of effective prevention and control disease.But aborning; the breeding difficulty disease that PRRSV, PPV and JEV cause; clinical symptoms is similar; and often mixed infection; often can not in time correctly diagnose only according to the clinical pathology variation; make a definite diagnosis at last and depend on laboratory examination, as detect the existence of cause of disease in the disease pig sample or its specific antibody even copy clinical case with the cause of disease that is separated to.The method that these three kinds of viruses are detected in present laboratory has: (1) virus is separated and is identified, aseptic disease pig sample inoculation pulmonary alveolar macrophage or MarC-145 cell (to PRRSV), the pig nephrocyte (to PPV and JEV) that goes down to posterity of getting is cultivated corresponding virus, with the virus in enzyme or the fluorescein trace antibody test cellular incubation, or use the neutralizing antibody identifying virus; (2) with the specific antibody in indirect enzyme-linked immunosorbent assay (ELISA) the detection PRRSV infected pigs serum, with the specific antibody in hemagglutination-inhibition test (HI) detection PPV or the JEV infected pigs serum; (3) with PRRSV or JEV nucleic acid in reverse transcription-PCR (RT-PCR) detection cell culture or the sick pig sample, with the PPV nucleic acid in PCR detection cell culture or the sick pig sample.
Virus separation and evaluation and PCR detection technique complicated operation, the time that needs instrument and grow, be not suitable for producing or on-the-spot quick diagnosis needs.ELISA and HI separate with evaluation and round pcr easyly, quick than viral, are commonly used to detect PRRSV (ELISA), JEV and PPV (HI) and antibody thereof, but still are not easy to China basic unit or the scene is generally applied.Because ELISA still needs microplate reader and reagent, than complicated operations step and experience, HI also needs fresh cavy or goose red blood cell; These instruments, reagent perhaps lack operating personnel and preservation condition in basic unit or shortage.For this reason, the someone studies and has reported with spot immune gold percolation and detect PPV, JEV and PRRSV.This method utilizes the diafiltration of miillpore filter to concentrate and capillarity, antigen-antibody response forwarded on the solid phase filter membrane by traditional liquid phase environment of ELISA or HI carry out fast, and adopt the collaurum trace to replace enzyme trace and red blood cell trace, the judged result with the colour developing situation of naked eyes Direct observation collaurum is therefore easier, quick and practical than ELISA and HI.But the spot immune of report gold percolation once only detects a kind of swine disease cause of disease at present, even like this, also need add 2 reagent at least and wash 2 ability obtaining the result; If the above-mentioned three kinds of swine disease viruses of antidiastole then need plurality of reagents box and tens operation stepss simultaneously, non-professional basic staff uses and still seems inconvenient.
A kind of test strips that detects pig breeding and respiration syndrome antibody and preparation method thereof is disclosed among the patent documentation CN 101216488A, it is to diagnose by detecting PRRSV antibody, rather than the existence of directly detection virus, and can only diagnose indirectly in three kinds of main pig breeding dysfunction venereal disease poison a kind of (PRRSV), significant limitation is arranged.
The utility model content
The technical problems to be solved in the utility model provides a kind of intuitive display as a result, detects the test strips of pig breeding disorder virus epidemic pathogen accurately, this test strip and spot immune gold percolation is the same special, responsive but operation is easier, quick and practical, and it is more cheap to detect cost.
For solving the problems of the technologies described above, the technical solution adopted in the utility model is:
A kind of test strips that detects pig breeding disorder virus epidemic pathogen, at least comprise the supporting layer that does not absorb water, attached to the adsorbed layer on the supporting layer, described adsorbed layer is by sample adsorbing fiber layer, gold labeling antibody fibrage, cellulose rete and water accepting layer are spliced successively, be marked with one/bar on the described cellulose membrane and contain the contrast trace of anti-pig/mouse IgG, and at least one/bar contains pig breeding dysfunction venereal disease poison detection of antibodies trace, and described pig breeding dysfunction venereal disease poison antibody is anti-porcine reproductive and respiratory syndrome virus PRRSV, pig parvoviral PPV, at least a in the pig japanese b encephalitis virus JEV monoclonal antibody (abbreviation monoclonal antibody)/polyclonal antibody (be called for short many anti-); It is corresponding and with the polyclonal antibody/monoclonal antibody of the anti-pig breeding dysfunction venereal disease poison of colloid gold label to be attached with and to detect the contained pig breeding dysfunction venereal disease of trace poison antibody on the described golden labeling antibody fibrage.On the described golden labeling antibody fibrage as adhere to anti-pig breeding dysfunction venereal disease poison gold mark monoclonal antibody, then correspondingly with the how anti-marker detection trace of anti-this virus, and with anti-mouse IgG solution mark contrast trace; How anti-on the gold labeling antibody fibrage as adhering to antiviral gold mark, contrast trace then correspondingly with anti-this viral monoclonal antibody marker detection trace, and with anti-pig IgG solution mark.
On described cellulose rete, be marked with respectively contain PRRSV how anti-/ monoclonal antibody, PPV how anti-/ monoclonal antibody, JEV how the three/bar of anti-/ monoclonal antibody detect trace; Be attached with corresponding mixing gold labeling antibody on the described golden labeling antibody fibrage, it is with anti-PRRSV, the PPV of colloid gold label and JEV monoclonal antibody/many anti-potpourris.
There is two/bar to detect trace in described cellulose rete subscript note, contain how anti-/ monoclonal antibody, PPV anti-/ monoclonal antibody how of PRRSV respectively, or contain how anti-/ monoclonal antibody, JEV anti-/ monoclonal antibody how of PRRSV respectively, or contain how anti-/ monoclonal antibody, JEV anti-/ monoclonal antibody how of PPV respectively, on described golden labeling antibody fibrage, be attached with the monoclonal antibody of corresponding anti-PRRSV, PPV with colloid gold label/or how anti-, or the monoclonal antibody of anti-PRRSV, JEV/or how anti-, or the monoclonal antibody of PPV, JEV/or how anti-.
When described cellulose rete subscript note has one/to detect trace, its permutation and combination with the contrast trace be " ‖ ", "=", " // ", " | ", "+",
"
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In any one; When cellulose rete subscript note had two/to detect trace, its spread pattern with the contrast trace was
" ///",
" ± ", " ... ",
"
" in any one; When cellulose rete subscript note has three/to detect traces, its spread pattern with the contrast trace be " | | | | ", " // // ", " king ", "
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" in any one.
Described cellulose rete is made by in nitrocellulose filter, pure cellulose film, carboxylation cellulose membrane, the PVDF membrane any one.
Described sample adsorbing fiber layer is made by in glass wool, nylon fiber, the dacron any one.
Described supporting layer is made by hard plastic sheet that does not absorb water or cardboard bar.
Described water accepting layer is made with thieving paper.
Described golden labeling antibody fiber rete is made by in glass wool, nylon fiber, the dacron any one.
On described sample adsorbing fiber layer, golden labeling antibody fibrage and water accepting layer, be laid with diaphragm, and deflection sample adsorbed layer one side 0.3～0.7cm place is printed with the sample mark line on the sample adsorbing fiber layer diaphragm corresponding with golden labeling antibody fibrage intersection.
The beneficial effects of the utility model are:
(1) detection specificity is strong, the susceptibility height.This quick detection test paper bar is that the basis is prepared from specific monoclonal antibody/resist of collaurum trace high-affinity more, no covalent bond formation between gold grain and the antibody molecule in the gold labeling antibody, the two combines by the Van der Waals force between the charges of different polarity, how anti-the collaurum mark is very little to monoclonal antibody/specificity and affinity (adhesion) influence, and have higher trace rate.Therefore, the quick detection test paper bar has higher specificity and susceptibility, can detect the albumen of the corresponding virus of 2 nanograms.
(2) easy and simple to handle, fast.Need not additional any Other Instruments and reagent when using this test strips, as long as its test lead was inserted in the clarification sample liquid to be checked about 30 seconds, is the decidable testing result about 5 minutes then.
(3) intuitive display, accurately as a result.With the test strips that detects three kinds of pig breeding disorder virus epidemic pathogens simultaneously is example, to show that henna detection trace and contrast trace are as the positive and the negative trace that detect, promptly on cellulose membrane, only show one/brownish red contrast trace C, represent that these three kinds of swine disease viruses all do not detect in detected sample liquid, show that on cellulose membrane one/brownish red contrast trace C and three/brownish reds detect trace R, P, J, then be illustrated in and all detect this three kinds of swine disease viruses in the detected sample liquid, testing result is positive; The result judges intuitively, accurately, simple and clear, be not prone to the erroneous judgement of false negative and false positive.
(4) reduce investment and detection cost.Use this quick detection test paper bar, do not need to join Other Instruments, equipment and reagent in addition, save big measuring appratus, equipment and additive reagent expense; Article one, test paper once can detect 1～3 kind of swine disease virus (former), and specialty and layman all can carry out scene whenever and wherever possible and detect, and need not to pay the expert diagnosis Laboratory Fee or feeding sample removes the travelling expenses of diagnosis room, saving detection cost, and testing cost is low.
(5) applied range is convenient to generally apply.The utility model is manipulated simply, become " single step " or " foolproof ", and be convenient for carrying and preserve, can satisfy different levels personnel's needs, comprise that professional chemical examination, customs quarantine control, health and epidemic prevention, quality monitoring, livestock products processing, intensive culture arrive individual breed etc., have vast market prospect and bigger economical, societal benefits.
Description of drawings
Fig. 1 is a kind of side-looking structural representation that detects the test strips of pig breeding disorder virus epidemic pathogen.
Fig. 2 is the plan structure synoptic diagram of Fig. 1.
Embodiment
Embodiment 1: a kind of test strips that detects three kinds of pig breeding disorder virus epidemic pathogens simultaneously, referring to Fig. 1 and Fig. 2,1 is the supporting layer made from the plastic slice bar among the figure, 2 is the sample adsorbed layer made from glass wool, 3 for being attached with the anti-PRRSV (code name R) of colloid gold label, the microglass fiber layer of anti-PPV (code name P) and anti-JEV (code name J) monoclonal antibody (Wi), 4 is nitrocellulose filter, 5 is the water accepting layer of being made by absorbent filter, to number 2,3,4,5 each layers stick on the supporting layer 1 successively, Pin Jie the intersection fiber infiltration that crosses one another each other.On nitrocellulose filter 4, mark detection trace 6-1,6-2, the 6-3 of three kinds of viruses respectively with anti-PRRSV, anti-PPV, anti-JEV polyclonal antibody IgG solution (Xi), and mark contrast trace (C) 7 with the anti-mouse IgG of sheep (rabbit) solution; The spread pattern that detects trace and contrast trace is " | | | | ".8-1 is the white diaphragm that covers sample adsorbing fiber layer 2 and the test lead above the golden labeling antibody fibrage 3; on the diaphragm 8-1 of sample adsorbed layer 2 and golden labeling antibody fibrage 3 intersection correspondences, be partial to sample adsorbed layer 2 one side 0.5cm places and be printed on trace line 9; 9 right-hand member is printed on arrow and max printed words, is coated with other color (as yellow) diaphragm 8-2 on the water accepting layer 5 (handle end).
Be used to contrast the anti-mouse of sheep (or rabbit)/pig IgG antibody of trace, and it is as follows to be used to detect the preparation method of routine of the polyclonal antibody of trace and the fibrolaminar anti-PRRSV of golden labeling antibody, anti-PPV and anti-JEV and monoclonal antibody:
1) preparation of the anti-mouse/pig IgG of sheep (or rabbit)
Extract IgG in mouse/porcine blood serum with the saturated ammonium sulfate method: get 1 part of serum and add 2 parts of PBS liquid (pH7.2) mixing, add equal-volume saturated ammonium sulfate liquid mixing, put in 4 ℃ of refrigerators 2 hours,, abandon supernatant at 4 ℃, the centrifugal 15min of 10000r/min; With an amount of PBS liquid (pH7.2) dissolution precipitation, adding saturated ammonium sulfate liquid to its ultimate density is 33%, put in 4 ℃ of refrigerators 2 hours, centrifugal 15min under 4 ℃, 10000r/min condition abandons supernatant, with a small amount of PBS liquid (pH7.2) dissolution precipitation, put in 4 ℃ of refrigerators with PBS liquid (pH7.2) dialyzed overnight, change liquid 2～3 times, centrifugal 15min under 4 ℃, 10000r/min condition, collect supernatant, measure its protein concentration with ultraviolet spectrophotometer.With 50 μ g～100 μ g (IgG)/kg body weight through subcutaneous or intramuscular injection negative antibody Healthy Sheep or rabbit 3～4 times, the last immunity is after 20 days, venous blood collection, measure its serum antibody titer more than 1:2000 with ELISA, its hyper-immune serum is collected in heart blood sampling or arteria carotis bloodletting, and (its extracting method is identical with said extracted mice serum IgG to extract the IgG of the anti-mouse/pig of sheep (rabbit) with the saturated ammonium sulfate method, no longer repeat), be used for the contrast trace of mark test strips of the present invention.
2) preparation of anti-PRRSV, anti-PPV and anti-JEV monoclonal antibody (Wi)
With 50～100 μ g/ PRRSV (PPV or JEV) protein immunization Balb/c only is mouse three times, each 15～30 days at interval; Behind the booster immunization 3～4 days for the third time, with the bloodletting of immune mouse eyeball, draw neck to cause death, in 75% alcohol-pickled 5～10min, aseptic its splenocyte of getting; Shred and through 100 order nylon net filters, the centrifugal 10min of 1000r/min collects splenocyte; With 1 * 10
8Splenocyte and 2 * 10
7～5 * 10
7NSO plasmacytoma mixing with cells, 1000r/min is centrifugal, and 10min abandons supernatant, cell precipitation slowly adds 40%～50%PEG4000 (pH8.5～9.0) effect 1min of 0.7～1mL in 37 ℃ water-soluble, slowly add serum-free 1640 nutrient culture media 15ml then, to stop the effect of PEG, 37 ℃ of water-bath 5～10min, 1000r/min is centrifugal, and 10min abandons supernatant, cell precipitation is resuspended in HAT selects in the nutrient culture media, and add 96 well culture plates (100～200 μ L/ hole), place 37 ℃ of 5%CO
2After cultivating 7～10 days in the incubator, by 96 hole ELISA Plate, detect the culture supernatant of hybridoma, picking strong positive cell clone (OD with enzyme linked immunosorbent assay (ELISA) with purifying PRRSV (PPV or JEV) the albumen bag of 5～10 μ g/mL
450〉=0.5), carry out continuous three times limiting dilution assay cloning, the hybridoma chromosome number of being produced is 92～98, the monoclonal antibody W1 (W2 or W3) of the anti-PRRSV of its secretion (PPV or JEV) reacts with PRRSV (PPV or JEV) specifically, and with other swine disease virus cross reaction does not take place, affinity constant reaches 10
9～10, light chain subtype is κ or λ, the heavy chain hypotype is IgG
1, IgG
2a, IgG
2b, IgG
3, the monoclonal antibody of these three kinds of viruses (Wi) all is used to prepare gold mark monoclonal antibody (Wi).
3) preparation of anti-PRRSV, anti-PPV and anti-JEV gold mark monoclonal antibody (Wi) and gold mark monoclonal antibody tunica fibrosa
Prepare aurosol with the sodium citrate reducing process, promptly in 0.01～0.05% aqueous solution of chloraurate of 50～100mL boiling, add 0.5～2% citric acid three sodium solution of 2～4mL, obtain the collaurum about diameter 15nm.K with 0.1mol/L
2CO
3Transfer collaurum pH value to 8.5～9.5, with the trace of 1:1000～1300 than the anti-PRRSV that will treat trace (or PPV, or JEV) monoclonal antibody W1 (W2 or W3) adds in the aurosol of pH8.5～9.5, behind the trace 10min, add 20%PEG10000 to final concentration 0.05%, under 4 ℃, the centrifugal 20min of 1500～3000r/min, remove unconjugated colloid gold particle, under 4 ℃, centrifugal 1 hour of 15000r/min, abandon supernatant, obtain preliminary purification gold labeling antibody protein mixture after, with propylene glucosan S-400 column chromatography, the separation and purification gold is marked albumen, obtains the anti-PRRSV of collaurum trace respectively, the monoclonal antibody of anti-PPV and anti-JEV.In processed glass cotton (nylon fiber or dacron), 4 ℃ of following low-temperature vacuum dryings promptly make gold mark monoclonal antibody tunica fibrosa with 2～3 kinds of mixing and absorption in the said monoclonal antibody of the collaurum trace of 1:100～500 dilution.
4) preparation of anti-PRRSV, anti-PPV and anti-JEV polyclonal antibody (Xi)
Adopt the inactivated vaccine or the attenuated vaccine at these three kinds of swine diseases of state approval respectively, separately immunity inoculation negative antibody health pig repeatedly.Last immunity posterior vein blood sampling in 20 days, measure its serum antibody titer at 1:2000 or more than the 1:1024 with ELISA or HI, then heart blood sampling or arteria carotis bloodletting, collect its hyper-immune serum, extract IgG antibody in the serum (method is identical with extraction mice serum IgG, does not repeat) with the saturated ammonium sulfate method.
5) the detecting operation method of above-mentioned test strip
The preparation of a test sample liquid is aseptic gets the tissues such as brain, lung, intestines, liver, lymph node of disease pig or aborted fetus, and it is shredded, grinds, and makes 1:2～5 times detected sample suspension with physiological saline, puts 4 ℃ or room temperature clarification or centrifugal; If get the blood of disease pig, separation of serum then, and it is to be measured to do 1:10～50 times dilution with physiological saline.
The b detecting operation inserts this quick detection test paper bar test lead in detected sample clarified solution or the serum, and insertion depth is no more than trace line 9, takes out test strips after about 30 seconds, about 1～5 minute of horizontal positioned, observations simultaneously.
Only demonstrate one/brownish red contrast trace C if c result judges on the test strip cellulose membrane, expression is surveyed the inspection result and is negative, and illustrates not detect PRRSV, PPV and JEV in test sample liquid; If the cellulose membrane on the test strip henna contrast trace C occurs and detects trace R or P or J, the expression testing result is positive, and promptly detects corresponding PRRSV or PPV or JEV in sample to be checked; If detection trace R, P, J occur simultaneously, be illustrated in and detect PRRSV, PPV, these three kinds of swine disease viruses of JEV in the sample to be checked simultaneously; If show without any the brownish red trace on the cellulose membrane, show that then test strips had lost efficacy or operates wrong.
6) described test strip testing principle is as follows:
After this quick detection test paper bar test lead (sample adsorption band) inserts detected sample solution, solution to be checked spreads to nitrocellulose filter together by the golden labeling antibody that siphon drives in swine disease virus to be checked and the golden labeling antibody tunica fibrosa, and finally infiltrate in the handle end filter paper, swine disease virus to be checked can combine with the corresponding gold mark of this virus monoclonal antibody in the diffusion process, and then with cellulose membrane on detect anti-this virus in the trace how anti-IgG combine, thereby demonstrate henna detection trace R, P, J; The anti-mouse IgG of goat-anti in the contrast trace or rabbit then can mark monoclonal antibody (Wi) with gold and combine, and forms brownish red contrast trace C.If do not have PRRSV, PPV, these three kinds of swine disease viruses of JEV in the sample liquid to be checked, test strips only demonstrates (individual) brownish red contrast trace C; Contain PRRSV (PPV or JEV) in the sample solution, then corresponding with it respectively gold mark monoclonal antibody Wi combination, again with cellulose membrane on antiviral how anti-IgG detect trace R (P or J) and combine, demonstrate brownish red detection trace, positive trace; If show without any the brownish red trace on the cellulose membrane, show that then test strips had lost efficacy or misoperation.
Embodiment 2: a kind of test strips that detects three kinds of pig breeding disorder virus epidemic pathogens simultaneously, its structure, preparation method are substantially the same manner as Example 1, and difference is: adhere to the anti-PRRSV with colloid gold label, anti-PPV and anti-JEV gold mark polyclonal antibody (Xi) on the golden labeling antibody fibrage of being made by nylon fiber 3 (R+P+J); On nitrocellulose filter 4, spray out three with anti-PRRSV, anti-PPV and anti-JEV monoclonal antibody IgG solution (Wi) respectively and detect trace (R+P+J), and go out to contrast trace C with the anti-pig IgG solution spraying of sheep (or rabbit), the spread pattern that detects trace and contrast trace be " // // ", " king ", "
", "
", "
" in any one.Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1, does not repeat.
Embodiment 3: a kind ofly detect two kinds of pig breeding disorder virus epidemic pathogen test strips simultaneously, its structure, preparation method are substantially the same manner as Example 1, and difference is: only be attached with anti-PRRSV, anti-PPV gold mark monoclonal antibody (Wi) on the golden labeling antibody fibrage of being made by dacron; Anti-PRRSV, anti-PPV polyclonal antibody IgG solution (Xi) with correspondence marks two detection traces respectively on the cellulose rete 4 that polyvinylidene fluoride is made, and stamping the contrast trace with the anti-mouse IgG of sheep (or rabbit) solution, the spread pattern that detects trace and contrast trace is
" ///", "
", " ± ", "
",
In any one.Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1.
Embodiment 4: a kind ofly detect two kinds of pig breeding disorder virus epidemic pathogen test strips simultaneously, its structure, preparation method are substantially the same manner as Example 3, and difference is: adhere to anti-PRRSV, anti-PPV gold mark polyclonal antibody (Wi) on the gold mark fibrage of being made by nylon fiber; Print out two with anti-PRRSV, the anti-PPV monoclonal antibody IgG solution (Xi) of correspondence respectively on the polyvinylidene fluoride cellulose rete 4 and detect trace "/", and mark contrast trace “ " with the anti-pig IgG solution of sheep (or rabbit).
Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1.
Embodiment 5: a kind ofly detect two kinds of pig breeding disorder virus epidemic pathogen test strips simultaneously, its structure, preparation method are substantially the same manner as Example 2, and difference is: only be attached with anti-PPV and anti-JEV gold mark polyclonal antibody (Xi) on the golden labeling antibody fibrage; Mark two with anti-PPV of correspondence and anti-JEV monoclonal antibody IgG solution (Xi) respectively on the pure cellulose rete 4 and detect trace
And with the anti-pig IgG solution of sheep (or rabbit) on the pure cellulose film, print the contrast trace
Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1.
Embodiment 6: a kind ofly detect two kinds of pig breeding disorder virus epidemic pathogen test strips simultaneously, its structure, preparation method are substantially the same manner as Example 1, and difference is: only be attached with anti-PRRSV, anti-JEV gold mark polyclonal antibody (Xi) on the golden labeling antibody fibrage that glass wool is made; On the carboxylation cellulose rete 4 respectively with anti-PRRSV and anti-JEV monoclonal antibody IgG solution (Xi) print out corresponding two detect traces "
On the carboxylation cellulose membrane, print the contrast trace with the anti-pig IgG solution of sheep (or rabbit)
Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1.
Embodiment 7: two kinds of pig breeding disorder virus epidemic pathogen test strips of a kind of detection, its structure, preparation method are substantially the same manner as Example 1, and difference is: the gold mark polyclonal antibody (Xi) that is attached with anti-PRRSV and anti-PPV on the golden labeling antibody fibrage that glass wool is made; On the cellulose nitrate rete respectively with anti-PRRSV, anti-PPV gold mark monoclonal antibody IgG solution (Xi) mark two detect traces "
And with the anti-pig IgG solution of sheep (or rabbit) on nitrocellulose filter, print the contrast trace
Embodiment 8: two kinds of pig breeding disorder virus epidemic pathogen test strips of a kind of detection, its structure, preparation method are substantially the same manner as Example 1, and difference is: the golden standard gold mark monoclonal antibody (Xi) that is attached with anti-JEV and anti-PPV on the golden labeling antibody fibrage; On the cellulose nitrate rete, spray out two with anti-JEV and anti-PPV gold mark polyclonal antibody IgG solution (Wi) respectively and detect trace
And on nitrocellulose filter, stamp the contrast trace with the anti-mouse IgG of sheep (or rabbit) solution
Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1.
Embodiment 9: a kind of detection pig breeding disorder virus epidemic pathogen test strips, its structure, preparation method are substantially the same manner as Example 3, and difference is: be attached with anti-PRRSV gold mark polyclonal antibody (Wi) on the gold mark fibrage of being made by nylon fiber; On the cellulose rete 4 that polyvinylidene fluoride is made, print out one/bar and detect trace with the anti-PRRSV monoclonal antibody IgG solution (Xi) of correspondence, and mark the contrast trace with the anti-pig IgG solution of sheep (or rabbit), the permutation and combination that detects trace and contrast trace be " || ", "=", " // ", " | ", "+",
"
", "
", " ≈ ",
In any one.
Embodiment 10: a kind of detection pig breeding disorder virus epidemic pathogen test strips, its structure, preparation method are substantially the same manner as Example 1, and difference is: only be attached with anti-PPV gold mark monoclonal antibody (Wi) on the golden labeling antibody fibrage of being made by dacron; Anti-PPV polyclonal antibody IgG solution (Xi) with correspondence on the cellulose rete 4 that polyvinylidene fluoride is made marks a detection trace " ", and stamps contrast trace " " with the anti-mouse IgG of sheep (or rabbit) solution.Other comprises that test sample preparation, method of operating and judgement as a result etc. are all identical with embodiment 1.
Embodiment 11: a kind of detection pig breeding disorder virus epidemic pathogen test strips, its structure, preparation method are substantially the same manner as Example 1, and difference is: only be attached with anti-JEV gold mark polyclonal antibody (Xi) on the golden labeling antibody fibrage that glass wool is made; Print out one with anti-JEV monoclonal antibody IgG solution (Xi) on the carboxylation cellulose rete 4 and detect trace
And with the anti-pig IgG solution of sheep (or rabbit) on the carboxylation cellulose membrane, print the contrast trace
Embodiment 12: a kind of detection pig breeding disorder virus epidemic pathogen test strips, its structure, preparation method are substantially the same manner as Example 1, and difference is: be attached with anti-JEV gold standard gold mark monoclonal antibody (Xi) on the golden labeling antibody fibrage of being made by glass wool; On the cellulose nitrate rete, spray out one and detect trace with anti-JEV and anti-PPV gold mark polyclonal antibody IgG solution (Wi)
And on nitrocellulose filter, stamp the contrast trace with the anti-mouse IgG of sheep (or rabbit) solution
Embodiment 13: this quick detection test paper bar structure and embodiment 1 are basic identical, and difference is: supporting layer 1 is made by the cardboard bar that does not absorb water, and test lead sample adsorbing fiber layer 2 is made by nylon fiber, and cellulose rete 4 adopts the pure cellulose films to make.
Embodiment 14: this quick detection test paper bar structure and embodiment 1 are basic identical, and difference is: sample adsorbing fiber layer 2 is made by the dacron film, and cellulose rete 4 adopts the carboxylation cellulose membranes.Other comprises that test sample preparation, method of operating and judgement as a result etc. all with the detecting operation method in the embodiment 1, do not repeat.
Embodiment 15: this quick detection test paper bar structure and embodiment 3 are basic identical, and difference is: the sample adsorbing fiber layer 2 usefulness nylon fiber of test lead are made, and cellulose rete 4 adopts polyvinylidene fluoride (PVDF) tunica fibrosa.
Embodiment 16: this quick detection test paper bar structure and embodiment 7 are basic identical, and difference is: sample adsorption band 2 dacron film, cellulose rete 4 adopts the pure cellulose film.Other comprises that test sample preparation, method of operating and judgement as a result etc. all with the detecting operation method among the embodiment 1, do not repeat.
Claims (10)
1. test strips that detects pig breeding disorder virus epidemic pathogen, comprise the supporting layer that does not absorb water, attached to the adsorbed layer on the supporting layer, described adsorbed layer is by sample adsorbing fiber layer, gold labeling antibody fibrage, cellulose rete and water accepting layer are spliced successively, it is characterized in that: described cellulose rete subscript note has one/bar to contain the contrast trace of anti-pig/mouse IgG, and at least one/bar contains pig breeding dysfunction venereal disease poison detection of antibodies trace, and described pig breeding dysfunction venereal disease poison antibody is anti-pig breeding and breathing syndrome virus PRRSV, pig parvoviral PPV, at least a in pig japanese b encephalitis virus JEV monoclonal antibody/polyclonal antibody; It is corresponding and with the polyclonal antibody/monoclonal antibody of the anti-pig breeding dysfunction venereal disease poison of colloid gold label to be attached with and to detect the contained pig breeding dysfunction venereal disease of trace poison antibody on the described golden labeling antibody fibrage.
2. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 1 is characterized in that: on described cellulose rete, be marked with respectively contain PRRSV how anti-/ monoclonal antibody, PPV how anti-/ monoclonal antibody, JEV how the three/bar of anti-/ monoclonal antibody detect trace; Be attached with corresponding anti-PRRSV, PPV and JEV monoclonal antibody/many anti-potpourris on the described golden labeling antibody fibrage with colloid gold label.
3. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 1, it is characterized in that: have two/bar to detect trace in described cellulose rete subscript note, contain PRRSV respectively resists/monoclonal antibody more, PPV resists/monoclonal antibody more, or contain how anti-/ monoclonal antibody of PRRSV respectively, JEV resists/monoclonal antibody more, or contain how anti-/ monoclonal antibody of PPV respectively, JEV resists/monoclonal antibody more, on described golden labeling antibody fibrage, be attached with corresponding anti-PRRSV with colloid gold label, the monoclonal antibody of PPV/or how anti-, or anti-PRRSV, the monoclonal antibody of JEV/or how anti-, or PPV, the monoclonal antibody of JEV/or how anti-.
4. according to the test strips of any described detection pig breeding disorder virus epidemic pathogen of claim in the claim 1 to 3, it is characterized in that: when described cellulose rete subscript note has one/to detect trace, its permutation and combination with the contrast trace be " ‖ ", "=", " // ", " | ", "+", " ⊥ ", "
", among " ", " ≈ ", " ︽ " any one; When cellulose rete subscript note has two/to detect traces, its spread pattern with the contrast trace be "
", " ///", " ≡ ", " ± ", " ", " ∵ ", "
" in any one; When cellulose rete subscript note has three/to detect traces, its spread pattern with the contrast trace be " || || ", " // // ", " king ", "
", among " ", " ∷ " any one.
5. according to the test strips of the described detection pig breeding disorder virus epidemic pathogen of claim 4, it is characterized in that: described cellulose rete is made by in nitrocellulose filter, pure cellulose film, carboxylation cellulose membrane, the PVDF membrane any one.
6. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 5 is characterized in that: described sample adsorbing fiber layer is made by in glass wool, nylon fiber, the dacron any one.
7. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 6 is characterized in that: described supporting layer is made by hard plastic sheet that does not absorb water or cardboard bar.
8. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 7 is characterized in that: described water accepting layer is made with thieving paper.
9. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 8 is characterized in that: described golden labeling antibody fiber rete is made by in glass wool, nylon fiber, the dacron any one.
10. the test strips of detection pig breeding disorder virus epidemic pathogen according to claim 9; it is characterized in that: on described sample adsorbing fiber layer, golden labeling antibody fibrage and water accepting layer, be laid with diaphragm, and deflection sample adsorbed layer one side 0.3～0.7cm place is printed with the sample mark line on the sample adsorbing fiber layer diaphragm corresponding with golden labeling antibody fibrage intersection.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNU200820148807XU CN201285399Y (en) | 2008-08-28 | 2008-08-28 | Dipstick for detecting pathogen of pig breeding disordered virus infectious disease |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNU200820148807XU CN201285399Y (en) | 2008-08-28 | 2008-08-28 | Dipstick for detecting pathogen of pig breeding disordered virus infectious disease |
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| CN201285399Y true CN201285399Y (en) | 2009-08-05 |
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| CNU200820148807XU Expired - Lifetime CN201285399Y (en) | 2008-08-28 | 2008-08-28 | Dipstick for detecting pathogen of pig breeding disordered virus infectious disease |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101339191A (en) * | 2008-08-28 | 2009-01-07 | 河南省农业科学院 | Test paper for detecting pig breeding disorder virus epidemic pathogen |
| CN101915846A (en) * | 2010-08-13 | 2010-12-15 | 扬州大学 | ELISA kit for detecting porcine reproductive and respiratory syndrome virus and using method |
| CN103995136A (en) * | 2014-06-06 | 2014-08-20 | 武汉中博生物股份有限公司 | Rapid colloidal gold detection test strip for pig porcine reproductive and respiratory syndrome virus |
| CN106370849A (en) * | 2016-10-21 | 2017-02-01 | 北京康思润业生物技术有限公司 | Immune-lateral-chromatography detecting system and preparing method thereof |
-
2008
- 2008-08-28 CN CNU200820148807XU patent/CN201285399Y/en not_active Expired - Lifetime
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101339191A (en) * | 2008-08-28 | 2009-01-07 | 河南省农业科学院 | Test paper for detecting pig breeding disorder virus epidemic pathogen |
| CN101915846A (en) * | 2010-08-13 | 2010-12-15 | 扬州大学 | ELISA kit for detecting porcine reproductive and respiratory syndrome virus and using method |
| CN103995136A (en) * | 2014-06-06 | 2014-08-20 | 武汉中博生物股份有限公司 | Rapid colloidal gold detection test strip for pig porcine reproductive and respiratory syndrome virus |
| CN106370849A (en) * | 2016-10-21 | 2017-02-01 | 北京康思润业生物技术有限公司 | Immune-lateral-chromatography detecting system and preparing method thereof |
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