Colloidal gold immunization test strip and detection method for detecting plum pox virus

A technology of plum pox virus and colloidal gold, which is applied in the direction of antiviral immunoglobulin, viral peptides, botanical equipment and methods, etc., can solve the problems of long cycle, complicated operation and low accuracy

Inactive Publication Date: 2013-04-17
陈定虎
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although enzyme-linked immunosorbent assay (ELISA) is still the main method for detection of fruit tree virus diseases at ports, ELISA requires specialized equipment and professionals to perform detection and judgment. The operation is cumbersome and takes a long time , there is an urgent need for a simpler, faster and more sensitive detection method to be more suitable for the requirements of quick inspection and release at ports
[0004] At present, the detection methods of plant viruses in foreign countries mainly include the following five kinds: one is the traditional biological method, which is characterized by long cycle, low accuracy, small number of detected viruses, and high labor intensity; the other is the electron microscope method, but It can only observe the shape of virions, but cannot identif

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Colloidal gold immunization test strip and detection method for detecting plum pox virus
  • Colloidal gold immunization test strip and detection method for detecting plum pox virus
  • Colloidal gold immunization test strip and detection method for detecting plum pox virus

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0098] The colloidal gold immunity test strip that the present invention detects plum pox virus is prepared by the following steps:

[0099] 1. Identification and storage of virus samples

[0100] Identification: The collected samples are first detected by serological methods, mainly ELISA, and confirmed by modern molecular biological methods such as PCR detection according to the serological test results. Preservation: Two methods are mainly used. One is to select leaf specimens with typical symptoms and freeze-dry them and store them in a -80°C refrigerator; the other is to extract the total DNA and RNA of the diseased plants and store them in a -80°C refrigerator.

[0101] 1.1 The serological detection method of PPV is carried out by indirect ELISA method, and the steps are as follows:

[0102] (1) Take 0.1 g of the sample to be tested, crush it with a pestle, add 1 mL of antigen coating buffer, transfer it to a 1.5 mL centrifuge tube, centrifuge at 2700 g, and take the su...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

PropertyMeasurementUnit
Sensitiveaaaaaaaaaa
Login to view more

Abstract

The invention discloses a colloidal gold immunization test strip and a detection method for detecting plum pox viruses. The colloidal gold immunization test strip is formed by the steps of: A. extracting RNA (Ribonucleic Acid) of plum pox viruses from materials infected by the plum pox viruses; B. cloning coat protein genes of the plum pox viruses by an RT-PCR (Reverse Transcription-Polymerase Chain Reaction) method, connecting the coat protein genes on a prokaryotic expression vector pET29(a) to obtain pET29a-PPV (porcine parvovirus) recombinant vectors, orderly measuring and finally verifying the recombinant vectors with correct reading frames, carrying out the inducible expression with the coat protein genes of the plum pox viruses, and transforming escherichia coli BL21 (DE3) with the pET29a-PPV recombinant vectors; C. recovering specific expression protein by an affinity column method, and making the rabbits immune to obtain plum pox virus antiserum; and D. adopting the above antiserum to prepare the colloidal gold immunization test strip used for detecting the plum pox viruses by the prepared antiserum. The invention aims to provide the convenient colloidal gold immunization test strip for rapidly detecting the plum pox viruses and the method for detecting plum pox viruses by adopting the test strip.

Description

technical field [0001] The invention relates to a colloidal gold immune test strip for detecting plum pox virus, and also relates to a method for detecting plum pox virus by using the colloidal gold immune test strip. Background technique [0002] Plumpox virus (PPV) is the latest quarantine pathogen promulgated by my country, belonging to the Potyvirus genus (Potyvirus) in the family Potyviridae (Potyviridae), and it is one of the most dangerous viruses for stone fruit trees (Dunez , Sutic, 1988; Nemeth, 1994), its natural hosts are mainly woody plants of the genus Prunus, such as apricot (PrunusarmeniacaL.), peach (P.persicaL.) and plums (P.domesticaL. and P. salicinaLindl.) and sweet cherry (P.aviumL.) and sour cherry (P.cerasusL.) and so on. Once the fruit tree is infected by it, the leaves will be distorted and chlorotic, the veins will be yellowed, especially the fruit will be deformed and become smaller, and mottled will appear, resulting in a decline in quality, and a...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
IPC IPC(8): G01N33/569C12N15/40C12N15/70C07K14/08C07K16/10C07K16/06
Inventor 陈定虎王勇杨雷亮刘恭源刘军
Owner 陈定虎
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products