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GeXP quick detection multi-primers and detection method for detecting akabane viruses, bovine viral diarrhea viruses and blue tongue viruses

A technology for bovine viral diarrhea and Akabane disease, applied in the field of biotechnology applications, can solve the problems of inability to meet detection requirements, cumbersome operation, and long measurement cycle.

Inactive Publication Date: 2016-05-11
ANIMAL & PLANT & FOOD INSPECTION CENT OF TIANJIN ENTRY EXIT INSPECTION & QUARANTINE BUREAU
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  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Virus isolation and culture is the gold standard for diagnosis, but there are problems such as long test period and cumbersome operation; virus neutralization test requires specific standard serum or virus strain, which has certain limitations in practical application; imported enzyme-linked immunosorbent immunoassay Kits are generally expensive; molecular biology methods such as ordinary PCR and fluorescent quantitative PCR are all aimed at the detection of a single virus, which cannot meet the detection needs of differential diagnosis of mixed infections with multiple pathogens
Multiplex PCR technology has been applied to the differential diagnosis of various pathogens, but due to the problem of amplification preference, it is impossible to realize high-throughput detection in the true sense

Method used

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  • GeXP quick detection multi-primers and detection method for detecting akabane viruses, bovine viral diarrhea viruses and blue tongue viruses
  • GeXP quick detection multi-primers and detection method for detecting akabane viruses, bovine viral diarrhea viruses and blue tongue viruses
  • GeXP quick detection multi-primers and detection method for detecting akabane viruses, bovine viral diarrhea viruses and blue tongue viruses

Examples

Experimental program
Comparison scheme
Effect test

specific Embodiment approach

[0025] Example 1 Primer Verification

[0026] The singleplex RT-PCR products were analyzed by capillary electrophoresis with GeXP system. The size of the amplified fragments of each target gene was BTV: 306-308bp, AKAV: 267-269bp, BVDV: 349-353bp, and the size of the amplified fragments was consistent with the design.

Embodiment 2

[0027] Example 2 Establishment of Multiplex Detection System and Verification Results of Single Template Specificity

[0028]In the multi-primer detection system, only a specific fragment of a single virus template was amplified in each reaction without cross-reaction, suggesting that this method has strong specificity and can distinguish and distinguish each virus according to the size of the amplified fragment. The results are shown in Figure 1-Figure 4 .

Embodiment 3

[0029] Embodiment 3 multiple detection system single template sensitivity test result

[0030] Using cloned plasmids to transcribe RNA in vitro as a template, the detection limit of each virus was 100 copies / μL.

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PUM

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Abstract

The invention discloses GeXP quick detection multi-primers and a detection method for detecting akabane viruses, bovine viral diarrhea viruses and blue tongue viruses. The GeXP quick detection multi-primers and the detection method have the advantages that the detection method is created for detecting diversified epidemic diseases of cows on the basis of GeXP multi-gene expression genetic analysis systems, so that problems that serological methods are low in sensitivity, only single pathogens can be detected by the aid of conventional PCR (polymerase chain reaction), gene chip methods are high in cost and the like when diversified epidemic diseases of cows are about to be detected at present can be solved, and reference of RNA (ribonucleic acid) positive samples of three epidemic diseases of the cows is created; 10-times continuous dilution reference of reference RNA is used as a detection object, and the detection sensitivity can reach 100 copies; cross reaction between the GeXP quick detection multi-primers and the other epidemic diseases of the cows and false-negative results can be prevented; monitoring and screening requirements on large quantities of diversified epidemic diseases of cows can be met by 600 actual detection samples.

Description

technical field [0001] The invention relates to the application field of biotechnology, in particular to the simultaneous detection and identification of three imported cow virus diseases. Background technique [0002] Akabane Disease (AKA), Bovine Viral Diarrhea (BVD) and Bluetongue (Bluetongue, BT) are three viral diseases that require isolation and quarantine for imported dairy cows. In recent years, as the national demand for high-quality dairy products has increased, the number of imported dairy cows has increased year by year, which has brought a certain amount of work pressure and financial burden to animal disease testing laboratories at dairy cow entry ports. Therefore, it is of great significance to establish a high-throughput rapid detection method that can simultaneously differentially diagnose multiple dairy cow diseases to reduce the workload of the inspection laboratory at the port of entry of dairy cows, reduce the cost of inspection, and carry out epidemiolo...

Claims

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Application Information

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IPC IPC(8): C12Q1/70C12Q1/68C12N15/11C12R1/93
CPCC12Q1/686C12Q1/701C12Q2600/16C12Q2537/143C12Q2565/125
Inventor 王乃福刘洋吴冬雪黄晨陈小金王万骞董志珍赵祥平
Owner ANIMAL & PLANT & FOOD INSPECTION CENT OF TIANJIN ENTRY EXIT INSPECTION & QUARANTINE BUREAU
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