CN110361460A - A kind of discrimination method of laying duck stress situation - Google Patents

A kind of discrimination method of laying duck stress situation Download PDF

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CN110361460A
CN110361460A CN201910527954.0A CN201910527954A CN110361460A CN 110361460 A CN110361460 A CN 110361460A CN 201910527954 A CN201910527954 A CN 201910527954A CN 110361460 A CN110361460 A CN 110361460A
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laying duck
cage
stress
group
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张昊
吴艳
陈芳
梁振华
皮劲松
潘爱銮
梁逸夫
杜金平
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Institute of Animal Science and Veterinary of Hubei Academy of Agricultural Sciences
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    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
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    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N30/00—Investigating or analysing materials by separation into components using adsorption, absorption or similar phenomena or using ion-exchange, e.g. chromatography or field flow fractionation
    • G01N30/02—Column chromatography
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    • G01N2030/027—Liquid chromatography

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Abstract

The present invention provides a kind of laying duck stress situation discrimination methods, which comprises (1) cage farming egg ducks blood is handled obtained blood plasma as to be measured group of sample, and it is control sample that flat feeding laying duck blood, which is handled obtained blood plasma,；(2) Spectrometry is used, mass spectral results are obtained；(3) after analyzing lower machine database, the qualification result and metabolin abundance result of metabolin are obtained；(4) T- inspection is carried out to the expression quantity of the characteristic indication object in be measured group of sample and control sample；To be measured group of sample is compared with control sample, if significant downward (P < 0.05) occurs in the expression quantity of 2- arachidonic acyl glycerol, i.e. laying duck is in the cage stress reaction phase；Otherwise laying duck be in cage stress convalescence.This method being capable of simplicity, accurately identification laying duck stress situation.

Description

A kind of discrimination method of laying duck stress situation
Technical field
The present invention relates to poultry breedings and healthy aquaculture technical field more particularly to a kind of identification side of laying duck stress situation Method.
Background technique
China's laying duck cultivation amount accounts for 70% of the world or more.As the continuous popularization of facilityization cultivation and the people want environmental protection The increasingly raising asked, traditional laying duck water support mode because its production efficiency is low, and environmental pollution is big, is gradually challenged.Currently, from Water cultivation becomes main laying duck cultivation means.Laying duck mainly uses three kinds of modes from water cultivation, is respectively as follows: ground drought and supports mould Formula, net bed aquaculture model and cage mode.Cage mode is because of its high production efficiency, and egg product cleanliness is good, and waste is easily handled, by Gradually received by large-scale breeding enterprise and factory family.
But cage farming egg ducks there are problems that upper cage stress, mainly due to by environmental restrictions, laying duck natural natural instincts are difficult to full Foot, stress reaction are obvious.Laying duck stress show as weight loss, body weight gains decline, feed intake decline, premunition reduction etc., answer The damage of physical stress caused by swashing needs a period of time that can restore.It therefore, can stress by physiological caused by cage in laying duck Be divided into the stress reaction phase and stress two periods of convalescence: first stage laying duck generates directly reaction and compensation response to stimulation； Second stage laying duck adapts to cage conditions.The science in above-mentioned two stage locating for laying duck individual is identified, it can be extensive Selection and anti-cage applied to cage farming egg ducks kind stress laying duck new varieties (being) breeding, also in breeding process Reply stress provide new target spot, have important theory significance and practice significance.But increased based on weight, feed intake, body A series of indexs such as weight, serum (slurry) glucocorticoid content, serum (slurry) oxidative stress index, intestinal mucosa oxidative stress Comprehensive detection, sampling is complicated, and measurement difficulty is big, also to butcher to individual sometimes, cannot achieve vivo assessment.
Summary of the invention
The object of the present invention is to provide the discrimination method of laying duck stress situation, can accurate and effective identification stress shape State, it is easy, objective, accurate, and facilitate disclose laying duck cage stress during body acknowledgement mechanism.
To achieve the above object, the present invention is implemented as follows:
The object of the present invention is to provide a kind of discrimination methods of laying duck stress situation, with 2- arachidonic acyl glycerol work For the characteristic indication object for identifying laying duck stress situation.
The method specifically comprises the following steps:
Step 1, cage farming egg ducks blood are handled obtained blood plasma as to be measured group of sample, and the flat feeding laying duck blood in ground is through locating Managing obtained blood plasma is control sample；
Step 2, using to be measured group of sample described in Spectrometry, obtain mass spectral results；
Step 3 after analyzing the lower machine database in mass spectral results, obtains the qualification result and metabolin of metabolin Abundance result；
Step 4 carries out T- inspection, the spy to the expression quantity of the characteristic indication object in be measured group of sample and control sample Sign marker is 2- arachidonic acyl glycerol；
To be measured group of sample is compared with control sample, if the expression quantity of the 2- arachidonic acyl glycerol of to be measured group of sample occurs It lowers, and significant difference P < 0.05, then it represents that laying duck is in the cage stress reaction phase；Otherwise laying duck be in cage stress Convalescence.
The beneficial effect that the present invention has is:
1, the discrimination method of a kind of laying duck stress situation provided by the invention, it is determined that using 2- arachidonic acyl glycerol as Identify the characteristic indication object of laying duck stress situation, the present invention screens the mark metabolin 2- arachidonic acyl glycerol obtained, can Accurate and effective identify stress situation, and facilitate disclose laying duck cage stress during acknowledgement mechanism, indicate metabolin Determining keeps analysis easier, objective, accurate.
The present invention identifies chaste tree as the mark metabolin for identifying laying duck stress situation using 2- arachidonic acyl glycerol River laying duck three series mating commercial generation laying duck (embodiment 2), mountain sheldrake (embodiment 3), Dual Gold (embodiment 4) and conventional method " changes of weight data, body weight gains data, feed intake situation data, D-ALPHA-Hydroxypropionic acid situation in serum, endotoxin situation, blood in serum Clear glucocorticoid delta data, serum oxidative stress index, a series of index results such as intestinal mucosa oxidative stress index " identify Result it is consistent.
2, the present invention is for the first time by the triple level four bars of non-targeted high performance liquid chromatography -/super high field Orbitrap mass spectrum (LC-MS) Technology is applied to the acquisition of laying duck cage stress situation metabolic markers and stress situation identifies；
3, the discrimination method of a kind of laying duck stress situation provided by the invention, can be widely applied to the choosing of cage farming egg ducks kind It selects and the breeding of resisting stress cage farming egg ducks new varieties (being), stress also provide new target spot for the reply in breeding process, To improve China's laying duck facility breeding level with important theory significance and practice significance.
Detailed description of the invention
Fig. 1 be in embodiment 1 cage stress 5 days (CR5) groups, cage stress 10 days (CR10) groups, cage stress be 15 days (CR15) it organizes and the PCA of ground control (TB) group in the negative ion mode analyzes result；Wherein number 23-27 is TB group sample； 13-18 is CR5 group sample；1-6 is CR10 group sample；7-12 is CR15 group sample；19-21 is Quality Control group sample；Horizontal seat in figure Mark PC1 and ordinate PC2 respectively indicates the score to rank the first with second principal component, fiducial confidence ellipse 95%；
Fig. 2 be respectively in embodiment 1 cage stress 5 days (CR5) groups, cage stress be organized for 10 days (CR10) and cage stress 15 Its (CR15) group compare with ground metabolite analysis volcano figure that (TB) organize (wherein (A) figure be stress 5 days groups and ground control group Between difference metabolin volcano figure；(B) figure be stress difference metabolin volcano figure between 10 days groups and ground control group；(C) figure For stress difference metabolin volcano figure between 15 days groups and ground control group)；
Fig. 3 be embodiment 1 in 2- arachidonic acyl glycerol cage stress 10 days ROC curves obtained compared with the control group Figure；
Fig. 4 is the mass spectrogram for indicating metabolin 2- arachidonic acyl glycerol in embodiment 2；Wherein (A) figure is 1 grade of mass spectrum Figure, (B) figure is 2 grades of mass spectrograms.
Specific embodiment
Embodiment 1 is used to identify the acquisition of the mark metabolin of laying duck stress situation
1, the 500 μ l of laying duck blood for extracting known upper cage number of days is experimental group (to be identified group), is extracted and upper cage laying duck day The flat feeding 500 μ l of laying duck blood in age close (± 8d) is control group.Blood sample heparin sodium is anticoagulant, 5000rpm, 4 DEG C of centrifugation 10min Afterwards, 200 μ L blood plasma are obtained, liquid nitrogen cryopreservation is spare.
2, take step 1 part plasma sample mixed in equal amounts prepare Quality Control sample, the plasma sample that step 1 is obtained and 100 μ L/ sample of Quality Control sample, is placed in EP pipe, and 80% methanol aqueous solution that 500 μ L contain 0.1% formic acid is added, and is vortexed after concussion, Ice bath stands 5min, 15000rpm, 4 DEG C of centrifugation 10min, takes to reset and add mass spectrum grade water on a certain amount of and be diluted to methanol content and is 60%, it is placed in 15000g in the centrifuge tube with 0.22 μm of filter membrane, 4 DEG C of centrifugation 10min, collects filtrate, carries out efficient liquid phase The triple level four bars of chromatography -/super high field Orbitrap mass spectrum (LC-MS) detection.The high performance liquid chromatography uses Accucore HILIC column chromatographic column, scanning of the mass spectrum range select m/z 100-1500.Lower machine data are searched into library analysis and peak area point After analysis, obtain metabolin qualification result and with each metabolin abundance result.
3, the data of every group of standard sample are analyzed using Principal Component Analysis (PCA), is indicated with tentatively judging Whether metabolin measures stress situation variation feasible: upper cage stress after a certain period of time, and laying duck feed intake and weight have begun It rises, if experimental group data and control group data are gathered in respective 95% confidence limit ellipse figure, and two groups of data can be complete Separation, then tentatively judge the stage still in the stress reaction phase；The result is shown in Figure 1, it is known that exist and distinguish stress reaction phase and stress The mark metabolin of convalescence.
Fig. 1 is sample P CA analysis chart, and PCA analysis chart is the peak for obtaining all experiment samples and QC sample extraction, warp PCA analysis is carried out after Pareto-scaling processing.Wherein the number 23-27 in Fig. 1 is TB group sample；13-18 is CR5 group sample Product；1-6 is CR10 group sample；7-12 is CR15 group sample；19-21 is Quality Control group sample；Abscissa PC1 and ordinate in Fig. 1 PC2 respectively indicates the score to rank the first with second principal component, fiducial confidence ellipse 95%.
4, experimental group and control group data are analyzed, according to the variable drop different degree of PLS-DA model first principal component (Variable Importance in the Projection, VIP) value, and the P value (P-value) of T inspection is combined to find Differential expression metabolin, is provided with threshold value are as follows: VIP > 1.0, fold differences (Fold Change, FC) > 2.0 or FC < 0.5 and P value < 0.05.
5, logarithm is taken the bottom of for 2 to each metabolin fold differences, P value is taken with 10 the bottom of for the absolute value of logarithm, drawn Volcano figure further screens characteristic indication object from the potential marker described in step 4.The volcano figure is with log2(fold It change) is abscissa ,-log10(P-value) it is ordinate, and takes Fold change > 2, and the number of P-value < 0.05 Value mapping, is as a result shown in Fig. 2.
Fig. 2 is that volcano figure takes p-value value with 10 with 2 to be that bottom takes logarithm by each metabolin fold differences the bottom of for The absolute value of logarithm is made.This metabolin is the metabolin that negative ion mode identification obtains, therefore it provides volcano figure be with negative The volcano figure drawn based on the metabolin abundance that ion mode identification obtains.In figure: the difference of abscissa expression difference metabolin Different multiple (log2 value), the longitudinal axis indicate p-value (- log10 value), and black (figure inner underside region) represents difference inapparent generation It thanks object (NoDiff), red (upper right side region in scheming) represents upregulating metabolic object (UP), and green (region is surveyed in upper left in scheming) represents It lowers metabolin (DW), the size of figure orbicular spot represents VIP numerical value.
6, according to the analysis of experimental group and control group as a result, drawing recipient's operating characteristic curve (receiver Operating characteristic curve, ROC curve) as shown in figure 3, and calculate AUC value, it is corresponding with maximum AUC value Substance as the mark metabolin that can be used for identifying laying duck cage stress situation.Finally obtain 2- arachidonic acyl glycerol conduct For identifying the mark metabolin of laying duck stress situation.From the figure 3, it may be seen that the marker AUC value is 1, indicating stress as differentiation The reaction phase and stress convalescence mark metabolin.Exclusive use sample can be distinguished, and have good sensitivity and Specificity.(ordinate indicates that true positive rate, abscissa indicate false positive rate).
Below it is 2- arachidonic acyl glycerol as the mark metabolin for identifying laying duck stress situation and identifies Jingjiang Laying duck three series mating commercial generation laying duck (embodiment 2), mountain sheldrake (embodiment 3), Dual Gold (embodiment 4).
Embodiment 2
One, the identification of Jingjiang laying duck stress situation
The acquisition of step 1, sample: choosing 120 age in days Jingjiang laying duck three series mating commercial generation laying ducks, acquires in laying duck respectively The flat blood sample for supporting group laying duck in 5 days groups of cage, 10 days groups, 15 days groups and ground, every group 6, sample.Blood sample heparin sodium is anticoagulant, After 5000rpm, 4 DEG C of centrifugation 10min, 200 μ L blood plasma are obtained, liquid nitrogen cryopreservation is spare.
Step 2, Spectrometry: the part plasma sample mixed in equal amounts of step 1 is taken to prepare Quality Control sample, by step 1 The 100 μ L/ sample of plasma sample and Quality Control sample of acquisition, is placed in EP pipe, and 80% methanol that 500 μ L contain 0.1% formic acid is added Aqueous solution is vortexed after concussion, and ice bath stands 5min, and 15000rpm, 4 DEG C of centrifugation 10min take and reset and add mass spectrum grade water on a certain amount of Being diluted to methanol content is 60%, is placed in 15000g in the centrifuge tube with 0.22 μm of filter membrane, 4 DEG C of centrifugation 10min, collects filter Liquid carries out the triple level four bars of high performance liquid chromatography -/super high field Orbitrap mass spectrum (LC-MS) detection.
High performance liquid chromatography uses Thermo Scientific Accucore HILIC column chromatographic column, column temperature: 40 ℃；Flow velocity: 0.2mL/min.In holotype: with 0.1% formic acid, 95% acetonitrile, 10mM ammonium acetate is mobile phase A: 0.1% first Acid, 50% acetonitrile, 10mM ammonium acetate are Mobile phase B.In negative mode: 95% acetonitrile, 10mM ammonium acetate are mobile phase A；50% second Nitrile, 10mM ammonium acetate are Mobile phase B, and negative mode A, B mobile phase pH is 9.0.The gradient elution are as follows: 0-1.5min: 98%A, 2%B；1.5-12min:98%A, 2%B；12-14min:100%B；14-16min:98%A, 2%B.
Scanning of the mass spectrum range selects m/z 100-1500, and Mass Spectrometry Conditions are provided that spray voltage: 3.2kV；Sheath stream Gas, assist gas pressure power are respectively 35arb and 10arb；Ion transfer tube temperature are as follows: 320 DEG C.Polarity: anode, cathode；MS/MS bis- Grade scanning is that data dependence type scans.
Step 3 searches lower machine data importing CD (compound discover) in library software, carries out retention time, matter lotus Than etc. parameters simple screening, peak pair then is carried out according to retention time deviation 0.1min and mass deviation 5ppm to different samples Together, make to identify it is more acurrate, then according to the mass deviation 5ppm of setting, signal strength variance 30%, signal-to-noise ratio 3, minimum signal The information such as intensity 100000, adduction ion carry out peak extraction, while quantifying to peak area, then conformity goal ion, then The prediction of molecular formula is carried out by molecular ion peak and fragment ion and is compared with mzCloud and Chemspider database It is right, background ions are removed with blank sample, and quantitative result is normalized, finally obtains metabolin qualification result and determine Measure result.The mass spectrogram of 2- arachidonic acyl glycerol is shown in Fig. 4.
Step 4 carries out T- inspection to the expression quantity of the characteristic indication object in be measured group of sample and control sample: to Jingjiang Laying duck ternary forms a complete set of 5 days groups of upper cage, 10 days groups, the 2- arachidonic acyl glycerol (2- of 15 days groups and ground group Arachidonoylglycerol after expression quantity) carries out T inspection, see Table 1 for details for experimental result.
Table 1
Right shoulder letter is different in table 1 indicates significant difference (P < 0.05).
As shown in Table 1,2- arachidonic acyl glycerol is during stress reaction, the group expression in 10 days of 5 days groups of upper cage and upper cage There is significant downward (P < 0.05) compared with the control group in amount, shows that the laying duck of 5 days groups of upper cage and 10 days groups of upper cage is in cage The stress reaction phase.
Compared with the control group, the difference of the expression quantity of 2- arachidonic acyl glycerol is not significant, table for 15 days group expression quantity of upper cage The laying duck of bright 15 days groups of upper cage is in stress convalescence.
Two, identify the Accuracy Verification of the method for laying duck stress situation
1, it obtains after metabolin qualification result and quantitative result using Principal Component Analysis (PCA) to every group of standard sample Data are analyzed: upper cage laying duck weight stress not yet be begun to ramp up after 5 days, indicate it still in the stress reaction phase；Upper cage 10 After it, laying duck feed intake and weight have begun rising, and 10 days group data of upper cage are gathered in respective with ground control group data In 95% confidence limit ellipse figure, two groups of data can be kept completely separate, and judge the stage still in the stress reaction phase；Upper cage 15 days Afterwards, 15 days experimental group data of upper cage and ground control group data are gathered in respective 95% confidence limit ellipse figure, two groups of data It can not be kept completely separate, judge the stage still in stress convalescence.
2, it is formed a complete set of upper cage 5 days based on Jingjiang laying duck ternary, 10 days, the changes of weight data of 15 heaven and earth face groups, body Increase weight data, feed intake situation data, D-ALPHA-Hydroxypropionic acid situation in serum, endotoxin situation, serum glucocorticoid variation in serum Data, serum oxidative stress index, a series of indexs such as intestinal mucosa oxidative stress index the result shows that, laying duck upper cage the 5th day, It is within 10th day the stress reaction phase, the 15th day is stress convalescence.With the identification of laying duck stress situation provided in this embodiment The result of method is consistent.
Embodiment 3
One, the identification of mountain sheldrake stress situation
Step 1, the kind are mountain sheldrake, and cage age in days is 100 days in laying duck, and the evaluation phase is the 6th day and the 12nd after upper cage It.The 6th day and the 12nd day laying duck sample to be evaluated of cage in acquisition, while acquisition is every with the ground cultivation group laying duck sample of age in days Group 6, sample.Blood sample heparin sodium is anticoagulant, after 5000rpm, 4 DEG C of centrifugation 10min, obtains 200 μ L blood plasma, liquid nitrogen cryopreservation is spare.
100 μ L/ sample of step 2, the plasma sample for taking acquisition and Quality Control sample, is placed in EP pipe, and 500 μ L are added and contain 80% methanol aqueous solution of 0.1% formic acid is vortexed after concussion, and ice bath stands 5min, and 15000rpm, 4 DEG C of centrifugation 10min take one Resetting and adding mass spectrum grade water on quantitative to be diluted to methanol content is 60%, is placed in the centrifuge tube with 0.22 μm of filter membrane 15000g, 4 DEG C of centrifugation 10min collect filtrate, carry out the triple level four bars of high performance liquid chromatography -/super high field Orbitrap mass spectrum (LC-MS) it detects.
High efficiency chromatography analysis is carried out using Thermo Scientific Accucore HILIC column chromatographic column, column Temperature: 40 DEG C；Flow velocity: 0.2mL/min.In holotype: with 0.1% formic acid, 95% acetonitrile, 10mM ammonium acetate is mobile phase A: 0.1% formic acid, 50% acetonitrile, 10mM ammonium acetate are Mobile phase B.In negative mode: 95% acetonitrile, 10mM ammonium acetate are mobile phase A； 50% acetonitrile, 10mM ammonium acetate are Mobile phase B, and negative mode A, B mobile phase pH is 9.0.The gradient elution are as follows: 0- 1.5min:98%A, 2%B；1.5-12min:98%A, 2%B；12-14min:100%B；14-16min:98%A, 2%B.
Scanning of the mass spectrum range selects m/z 100-1500；Mass Spectrometry Conditions are provided that spray voltage: 3.2kV；Sheath stream Gas, assist gas pressure power are respectively 35arb and 10arb；Ion transfer tube temperature are as follows: 320 DEG C.Polarity: anode, cathode；MS/MS bis- Grade scanning is that data dependence type scans.
Step 3 searches lower machine data importing CD (compound discover) in library software, carries out retention time, matter lotus Than etc. parameters simple screening, peak pair then is carried out according to retention time deviation 0.1min and mass deviation 5ppm to different samples Together, make to identify it is more acurrate, then according to the mass deviation 5ppm of setting, signal strength variance 30%, signal-to-noise ratio 3, minimum signal The information such as intensity 100000, adduction ion carry out peak extraction, while quantifying to peak area, then conformity goal ion, then The prediction of molecular formula is carried out by molecular ion peak and fragment ion and is compared with mzCloud and Chemspider database It is right, background ions are removed with blank sample, and quantitative result is normalized, finally obtains metabolin qualification result and determine Measure result.The same Fig. 4 of the mass spectrogram of D- phenyl-lactic acid.
Step 4, to the expression quantity of the characteristic indication object 2- arachidonic acyl glycerol in be measured group of sample and control sample Carry out T- inspection；To the 6th day group of cage and the 12nd day group in the sheldrake kind of mountain and ground group 2- arachidonic acyl glycerol (2- Arachidonoylglycerol after expression quantity) carries out T inspection, see Table 2 for details for experimental result.
Table 2
Difference metabolin TB CR6 CR12
2-arachidonoylglycerol 96623±49203a 9681±2686b 8309±4235b
Right shoulder letter is different in table 2 indicates significant difference (P < 0.05).
As shown in Table 2, in mountain sheldrake kind the 2- arachidonic acyl glycerol of 6 days groups of cage and 12 days groups expression magnitude with compare Group is compared to there are significant changes, i.e., 6 days groups of cage and 12 days groups are in the cage stress reaction phase in expression mountain sheldrake kind.
Two, identify the Accuracy Verification of the method for laying duck stress situation
Based on cage 6 days on the sheldrake of mountain, the changes of weight data of 12 heaven and earth face groups, body weight gains data, feed intake situation number According to endotoxin situation, serum glucocorticoid delta data, serum oxidative in D-ALPHA-Hydroxypropionic acid situation in, serum, serum stress index, A series of indexs such as intestinal mucosa oxidative stress index the result shows that, mountain sheldrake kind was at upper cage the 6th day, the 12nd day stress be anti- Ying Qi.It is consistent with the result of discrimination method of laying duck stress situation that embodiment provides.
Embodiment 4
One, the identification of Dual Gold stress situation
Step 1, the kind are Dual Gold, and upper cage age in days is 90 days, and the evaluation phase is the 6th day and the 12nd day after upper cage.It adopts The 6th day and the 12nd day laying duck sample to be evaluated of cage on collection, while acquiring every group of laying duck sample of ground cultivation group of close age in days 3, sample.Blood sample heparin sodium is anticoagulant, after 5000rpm, 4 DEG C of centrifugation 10min, obtains 200 μ L blood plasma, liquid nitrogen cryopreservation is spare.
Step 2, using to be measured group of sample described in the triple level four bars of high performance liquid chromatography -/super high field Orbitrap mass spectral analysis Product obtain mass spectral results: taking the 100 μ L/ sample of plasma sample and Quality Control sample of acquisition, be placed in EP pipe, 500 μ L are added and contain 80% methanol aqueous solution of 0.1% formic acid is vortexed after concussion, and ice bath stands 5min, and 15000rpm, 4 DEG C of centrifugation 10min take one Resetting and adding mass spectrum grade water on quantitative to be diluted to methanol content is 60%, is placed in the centrifuge tube with 0.22 μm of filter membrane 15000g, 4 DEG C of centrifugation 10min collect filtrate, carry out the triple level four bars of high performance liquid chromatography -/super high field Orbitrap mass spectrum (LC-MS) it detects.
High efficiency chromatography analysis is carried out using Thermo Scientific Accucore HILIC column chromatographic column, column Temperature: 40 DEG C；Flow velocity: 0.2mL/min.In holotype: with 0.1% formic acid, 95% acetonitrile, 10mM ammonium acetate is mobile phase A: 0.1% formic acid, 50% acetonitrile, 10mM ammonium acetate are Mobile phase B.In negative mode: 95% acetonitrile, 10mM ammonium acetate are mobile phase A； 50% acetonitrile, 10mM ammonium acetate are Mobile phase B, and negative mode A, B mobile phase pH is 9.0.The gradient elution are as follows: 0- 1.5min:98%A, 2%B；1.5-12min:98%A, 2%B；12-14min:100%B；14-16min:98%A, 2%B.
Scanning of the mass spectrum range selects m/z 100-1500；Mass Spectrometry Conditions are provided that spray voltage: 3.2kV；Sheath stream Gas, assist gas pressure power are respectively 35arb and 10arb；Ion transfer tube temperature are as follows: 320 DEG C.Polarity: anode, cathode；MS/MS bis- Grade scanning is that data dependence type scans.
Step 3 after analyzing the lower machine database in mass spectral results, obtains the qualification result and metabolin of metabolin Abundance result: lower machine data importing CD (compound discover) is searched in library software, carries out retention time, mass-to-charge ratio etc. Then the simple screening of parameter carries out peak alignment according to retention time deviation 0.1min and mass deviation 5ppm to different samples, Make to identify it is more acurrate, then according to the mass deviation 5ppm of setting, signal strength variance 30%, signal-to-noise ratio 3, minimum signal strength 100000, the information such as ion are summed it up and carries out peak extraction, while peak area quantified, then conformity goal ion, then passed through Molecular ion peak and fragment ion carry out the prediction of molecular formula and are compared with mzCloud and Chemspider database, use Blank sample removes background ions, and quantitative result is normalized, and finally obtains metabolin qualification result and quantitative knot Fruit.The same Fig. 4 of the mass spectrogram of D- phenyl-lactic acid.
Step 4, to the expression quantity of the characteristic indication object 2- arachidonic acyl glycerol in be measured group of sample and control sample T- inspection is carried out, to the 6th day group of cage on Dual Gold and the 12nd day group and ground group 2- arachidonic acyl glycerol (2- Arachidonoylglycerol after expression quantity) carries out T inspection, see Table 3 for details for experimental result.
Table 3
Difference metabolin TB CR6 CR12
2-arachidonoylglycerol 56720±20689a 8909±5009b 10498±9605a
Right shoulder letter is different in table 3 indicates significant difference (P < 0.05).
As shown in Table 3, the 2- arachidonic acyl glycerol expression magnitude of the 6th day group of cage occurs compared with the control group on Dual Gold It is significant to lower, indicate that the 6th day group of cage is in the cage stress reaction phase on Dual Gold.The 2- peanut of the 12nd day group of cage on Dual Gold Tetraene acyl glycerol expression magnitude does not occur significantly lowering compared with the control group, indicates that the 12nd day group of cage is in cage on Dual Gold It stress convalescence.
Two, carry out identifying the accuracy of the method for laying duck stress situation using 2- arachidonic acyl glycerol as characteristic indication object Verifying
Based on cage 6 days on Dual Gold, the changes of weight data of 12 heaven and earth face groups, body weight gains data, feed intake situation number According to endotoxin situation, serum glucocorticoid delta data, serum oxidative in D-ALPHA-Hydroxypropionic acid situation in, serum, serum stress index, A series of indexs such as intestinal mucosa oxidative stress index the result shows that, laying duck Dual Gold was respectively at cage at upper cage the 6th day, the 12nd day It supports the stress reaction phase and cage stress convalescence.It is consistent with the result of discrimination method of laying duck stress situation provided by the invention.
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the invention, all in essence of the invention Within mind and principle, any modification, equivalent replacement, improvement and so on be should all be included in the protection scope of the present invention.

Claims (7)

1. a kind of discrimination method of laying duck stress situation, which is characterized in that answered using 2- arachidonic acyl glycerol as laying duck is identified Swash the characteristic indication object of state.
2. the discrimination method of laying duck stress situation as described in claim 1, which is characterized in that the method specifically includes as follows Step:
Step 1, cage farming egg ducks blood are handled what obtained blood plasma was obtained as to be measured group of sample, flat feeding laying duck blood through processing Blood plasma is control sample；
Step 2, using to be measured group of sample described in Spectrometry, obtain mass spectral results；
Step 3 after analyzing the lower machine database in mass spectral results, obtains the qualification result and metabolin abundance of metabolin As a result；
Step 4 carries out the expression quantity of the characteristic indication object 2- arachidonic acyl glycerol in be measured group of sample and control sample T- is examined；
To be measured group of sample is compared with control sample, if under the expression quantity of the 2- arachidonic acyl glycerol of to be measured group of sample occurs It adjusts, and significant difference P < 0.05, then it represents that laying duck is in the cage stress reaction phase；Otherwise laying duck be in cage stress be extensive The multiple phase.
3. the discrimination method of laying duck stress situation as claimed in claim 2, which is characterized in that blood is through locating in the step 1 Reason obtains the specific steps of blood plasma are as follows: blood sample is first anticoagulant through heparin sodium, then after 5000rpm, 4 DEG C of centrifugation 10min, obtains blood Slurry, liquid nitrogen cryopreservation are spare.
4. the discrimination method of laying duck stress situation as claimed in claim 2, which is characterized in that in the step 1 known to acquisition The cage farming egg ducks plasma sample of age in days and upper cage number of days is as to be measured group of sample；Control sample be and to be measured group of sample cage group Kind is identical, the flat feeding laying duck plasma sample of the close ± 8d of age in days；Every group 3-10 parts of sample number, ibid cage number of days is not difference To be measured group of sample.
5. the discrimination method of laying duck stress situation as claimed in claim 2, which is characterized in that chromatography-mass spectroscopy in the step 2 In design parameter are as follows:
Chromatography uses Accucore HILIC column chromatographic column, column temperature: 40 DEG C；Flow velocity: 0.2mL/min；
With 0.1% formic acid in holotype, 95% acetonitrile, 10mM ammonium acetate is mobile phase A；0.1% formic acid, 50% acetonitrile, 10mM Ammonium acetate is Mobile phase B；
With 95% acetonitrile in negative mode, 10mM ammonium acetate is mobile phase A；50% acetonitrile, 10mM ammonium acetate are Mobile phase B, negative norm Formula A, B mobile phase pH is 9.0；
Gradient elution are as follows: 0-1.5min:98%A, 2%B；1.5-12min:98%A, 2%B；12-14min:100%B；14- 16min:98%A, 2%B.
6. the discrimination method of laying duck stress situation as claimed in claim 2, which is characterized in that chromatography-mass spectroscopy in the step 2 In design parameter are as follows:
Scanning of the mass spectrum range selects m/z 100-1500；Mass Spectrometry Conditions are provided that spray voltage: 3.2kV；Sheath gas, it is auxiliary Helping atmospheric pressure is respectively 35arb and 10arb；Ion transfer tube temperature are as follows: 320 DEG C；Polarity: anode, cathode；MS/MS second level is swept It retouches as the scanning of data dependence type.
7. the discrimination method of laying duck stress situation as claimed in claim 2, which is characterized in that mass spectrum knot in the step 3 The specific steps that lower machine database in fruit is analyzed are as follows:
S1, lower machine data importing CD is searched in library software, carries out the simple screening of retention time, mass-to-charge ratio parameter；
S2, peak alignment, subsequent basis then are carried out according to retention time deviation 0.1min and mass deviation 5ppm to different samples The mass deviation 5ppm of setting, signal strength variance 30%, signal-to-noise ratio 3, minimum signal strength 100000, the information such as ion are summed it up Peak extraction is carried out, while peak area is quantified；
Then S3, again conformity goal ion carry out prediction and and the mzCloud of molecular formula by molecular ion peak and fragment ion It is compared with Chemspider database, removes background ions with blank sample, and quantitative result is normalized, most After obtain metabolin qualification result and quantitative result.
CN201910527954.0A 2019-06-18 2019-06-18 A kind of discrimination method of laying duck stress situation Pending CN110361460A (en)

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Application publication date: 20191022