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Indirect ELISA (enzyme-linked immuno sorbent assay) kit for detecting haemophilus parasuis antibody

A technology of Haemophilus suis and a kit, which is applied in molecular biology, microbiology, detection of animal infectious diseases, and prevention and control of Haemophilus parasuis disease, achieving high biological safety, high homology, and good specificity Effect

Active Publication Date: 2014-07-23
SOUTHWEST UNIVERSITY FOR NATIONALITIES
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, Zhao Qian (2010) showed that the gene sequence of outer membrane protein P5 in the 15 serotypes of H. The middle homology is high and conservation is good, while the homology of the outer membrane protein P2 is low, and some serotype gene sequences have segmental base deletions and multiple point mutations, which may affect its versatility as an envelope protein
Zhang Bin (2013) and others showed that the expressed outer membrane protein P5 protein can react with the positive sera of 15 serotype reference strains of Haemophilus parasuis by immunoblotting. The outer membrane protein P5 protein has good versatility, but indirect ELISA detection The results showed that the ELISA plates expressing the outer membrane protein P5 protein can cross-react with the positive sera of bacteria such as Pasteurella and Actinobacillus pleurodes, and the protein specificity is poor, which may cause false positive results

Method used

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  • Indirect ELISA (enzyme-linked immuno sorbent assay) kit for detecting haemophilus parasuis antibody
  • Indirect ELISA (enzyme-linked immuno sorbent assay) kit for detecting haemophilus parasuis antibody
  • Indirect ELISA (enzyme-linked immuno sorbent assay) kit for detecting haemophilus parasuis antibody

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Experimental program
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Effect test

Embodiment 1

[0040] 1. Cloning, sequencing, expression and purification of Haemophilus parasuis CDT-C protein

[0041] 1.1 Primer design and synthesis

[0042] According to the SH0165 (accession number CP001321) H. parasuis CDT-C complete gene sequence in GenBank, design a pair of expression primers, P (CDTC-BamHI-F): CGC GGATCC ATGCTAAAGCGTTTTACTTT, under P (CDTC-SalI-R): ACGT GTC GAC The upstream and downstream primers of TTATAATAACCTACTAGGTC introduced BamHI and SalI restriction sites (underlined) respectively to amplify the CDT-C OFR sequence. The expected fragment size is 531bp.

[0043] 1.2 Cloning and sequencing analysis of the CDT-C gene of Haemophilus parasuis

[0044] Using the extracted H. parasuis serum type 1-15 DNA as a template, P up and P down were used as primers. The total reaction system is 25 μL, Taq enzyme: 0.25 μL; MgCl2 buffer: 2.5 μL; MgCl2: 2.5 μL; dNTP: 2 μL; F1: 1 μL; R1: 1 μL; ddH2O: 13.75 μL; DNA template 2 μL. The reaction program was: 94 °C pre-...

Embodiment 2

[0064] Development of an indirect ELISA kit for detecting antibodies against Haemophilus parasuis

[0065] 1. Expression, extraction, purification and storage of antigens in Haemophilus parasuis ELISA antibody detection kit

[0066] Inoculate the production-use Escherichia coli seeds carrying Haemophilus parasuis CDT-C protein in LB liquid medium (containing 100 μg / mL ampicillin sodium), cultivate overnight at 37 °C, and transfer to LB liquid medium at a ratio of 1:100 (containing 100 μg / mL ampicillin sodium), shake culture at 37°C until OD 600nm When the value reaches about 0.6, add the final concentration of 0.5mM IPTG to the bacterial liquid, place it in a shaker at 16°C to induce expression for 24 hours, collect the bacterial liquid, freeze and thaw three times at -70°C and 37°C, and then ultrasonically break (300W , work for 5 s, interval of 10 s) 70 times. The collected protein was purified with Octave? Ni-NTA SF Columns affinity chromatography column. Purified protei...

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Abstract

The invention discloses an indirect ELISA (enzyme-linked immuno sorbent assay) kit for detecting a haemophilus parasuis antibody. The kit consists of an ELISA coating plate with haemophilus parasuis cytolethal distending toxin)-C protein serving as a coating antigen, a to-be-detected sample dilution plate, a positive contrast serum, a negative contrast serum, 20-time concentrated washing liquid, a serum sample dilution solution, an enzyme-labeled antibody working solution, a developing solution and a terminating solution. A judgment standard is that if an S / P value is less than 0.200, a sample to be detected is negative; if the S / P value is greater than or equal to 0.200, the to-be-detected sample is positive; the S / P value is obtained according to a formula: S / P value=(the mean value of the to-be-detected sample OD450nm-the mean value of a negative contrast OD450nm) / (the mean value of a positive sample OD450nm-the mean value of the negative contrast OD450nm). Due to the specificity test, the sensitivity test, the repetitiveness test, the coincidence rate test, the test for comparing the kit disclosed by the invention with a kit on sale, the clinical application test and the like, the kit disclosed by the invention has the characteristics of high specificity, high sensitivity, high repetitiveness and the like and is high in coincidence rate to the same type of products on sale home and abroad; the indirect ELISA kit can be used for clinical large-scale detection and epidemiological investigation for the haemophilus parasuis antibodies.

Description

[0001] technical field [0002] The invention relates to the technical fields of molecular biology, microbiology and animal infectious disease detection, in particular to an indirect ELISA kit for detecting antibodies to Haemophilus parasuis, and belongs to the field of prevention and control of Haemophilus parasuis disease. Background technique [0003] Haemophilus parasuis disease is an infectious disease caused by Haemophilus parasuis. Haemophilus parasuis ( H. parasuis ) is an NAD-dependent, non-motile, Gram-negative bacillus belonging to the genus Haemophilus of the Pasteurellaceae family. The bacterium is a commensal bacterium in the upper respiratory tract of pigs, which can invade the body under certain conditions and cause a serious systemic disease—Glasser's Disease, which is clinically manifested as polyserositis in pigs , arthritis and meningitis. H. parasuis Susceptible to young pigs aged 2 weeks to 4 months, the disease mainly occurs before and after we...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): G01N33/68
CPCG01N33/56911G01N33/6803G01N2333/285
Inventor 岳华汤承张斌王远微张焕容
Owner SOUTHWEST UNIVERSITY FOR NATIONALITIES
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