A test paper for identification and detection of strong and weak strains of Newcastle disease virus

A technology for Newcastle disease virus and anti-Newcastle disease virus, applied in the direction of measuring devices, instruments, scientific instruments, etc., can solve the problem of inability to prevent the replication and discharge of epidemic strain infection, difficulty in distinguishing immune attenuated virus and wild virus infection, unfavorable ND control and purification and other problems, to achieve the effect of easy large-scale promotion and application, simple and fast operation, and high labeling rate

Active Publication Date: 2017-11-10
HENAN ACAD OF AGRI SCI
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0003] At present, the prevention and control of Newcastle disease in my country still adopts a strategy based on vaccine immunization. Since the 1990s, attenuated ND vaccine strains have been frequently used on a large scale and in high doses in my country. Although the virulent epidemic strain can produce complete clinical protection, it cannot prevent the infection, replication and excretion of the epidemic strain in immunized chickens, and ND virulent infection still occurs in immunized chicken flocks. At the same time, due to the lack of serological markers and supporting Differential diagnosis method, its large-scale application in my country makes it difficult to distinguish immune attenuated virus from wild virus infection through antibody detection techniques such as hemagglutination inhibition test (HI) and enzyme-linked immunosorbent assay (ELISA), which is not conducive to the control and purification of ND
With the completion of the complete gene sequences of NDV wild strains and vaccine strains from different sources and regions and the development of molecular biology detection technology, scholars at home and abroad have conducted a lot of research on the identification and detection of NDV. Strain characteristic sites, respectively design strong and weak strain-specific primers or probes, and establish molecular identification detection methods such as RT-PCR and fluorescent quantitative PCR to distinguish strong and weak NDV, with high sensitivity and specificity , but these detection methods need to rely on PCR machines or fluorescent quantitative PCR machines, and have disadvantages such as relatively cumbersome operations, long time-consuming, and high detection costs, which limit their application in epidemiological investigations and veterinary clinics

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  • A test paper for identification and detection of strong and weak strains of Newcastle disease virus
  • A test paper for identification and detection of strong and weak strains of Newcastle disease virus

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specific Embodiment approach

[0017] DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT The test paper for differential detection of virulent and weak Newcastle disease virus can be widely used in the differential detection of virulent Newcastle disease virus infection and vaccine immunity of various poultry (such as chickens, ducks, geese, pigeons, etc.). To prepare Newcastle disease virus virulent and attenuated detection test strips, it is first necessary to prepare Newcastle disease virus immune antigen, and then prepare anti-Newcastle disease virus polyclonal antibody and monoclonal antibody, and screen the monoclonal antibody for distinguishing virulent and attenuated Newcastle disease virus. The monoclonal antibody mAb1 of virulent and weak Newcastle disease was used to prepare colloidal gold markers, and the monoclonal antibody mAb2, which recognized the virulent Newcastle disease but not the weak, was used to print the blot "│" of the detection line of strong Newcastle disease to identify strong Newca...

Embodiment 1

[0064]Example 1, rapid diagnosis of virulent Newcastle disease infection in poultry, collecting diseased tissues of sick (dead) poultry, including glandular stomach, lung, liver, spleen, kidney, trachea, small intestine, large intestine and lymph nodes, etc., at a ratio of 1:5 or 1 :10 Add an appropriate amount of PBS or water for simple grinding to prepare the solution to be tested, use the test paper to identify the strong and weak Newcastle disease virus strains and weak strains of Newcastle disease virus according to the operation method (15) to detect and judge the results, and differentially diagnose the strong virus of sick (dead) poultry Infection or vaccine immunity. The test paper shows three reddish-brown bands (strong virus detection line, weak virus test line and quality control line). Detection line and quality control line) "||" is positive for attenuated NDV, indicating that the poultry to be tested is immune to NDV vaccine; only one reddish-brown band (quality...

Embodiment 2

[0065] Example 2, Newcastle disease virus inspection and quarantine of live poultry, collect live poultry swabs (throat swab and anal swab) or feces, add appropriate amount of PBS or water at 1:5 or 1:10 for simple suspension, and prepare the solution to be tested , Use test strips to identify strong and weak Newcastle disease virus strains according to the operation method (15) for detection and result judgment, to identify and detect the strong virus contamination or vaccine immunity of live poultry. Three reddish-brown bands appear on the test paper (strong toxin detection line, weak toxin detection line and quality control line) "|||" is positive for NDV strong toxin, indicating that the poultry to be tested or the environment is NDV strong toxin pollution; two reddish-brown bands (Attenuated virus detection line and quality control line) "||" is positive for NDV attenuated virus, indicating that the poultry or the environment to be inspected has no strong NDV pollution, an...

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Abstract

The invention relates to a detecting appliance for distinguishing infection and immunization of diseases in poultry, and particularly relates to a test paper for distinguishing a virulent strain from an attenuated strain of a newcastle disease virus. The test paper is composed of a support plate, a sample pad, a gold pad, a detection membrane and an absorbent pad, wherein the detection membrane contains prints of a virulent detection line T1 '|', an attenuated detection line T2 '|' and a quality control line C '|'; when distinguishing detection is carried out, infection of the virulent newcastle disease virus is determined when three red strips '|||' appear on the detection membrane; immunization of a newcastle attenuated vaccine is determined when two red strips '||' appear; and a negative newcastle disease virus is determined when only one red strip '|' appears. The distinguishing detection test paper has the advantages of high specificity, high sensitivity, and wide response spectrum, is simple, convenient and fast to operate, can be widely applied to distinguishing detection of infection and immunization of the newcastle disease virus, and is easy to popularize and apply in production practice; and existing attenuated vaccine strains and most of popular virulent strains can be detected.

Description

technical field [0001] The invention relates to a differential detection instrument for poultry epidemic infection and immunity, in particular to a test paper for differential detection of strong and weak Newcastle disease virus. Background technique [0002] Newcastle disease (ND), also known as Asian chicken plague, is a highly contagious, acute septic avian infectious disease caused by Newcastle disease virus (NDV) with respiratory and gastrointestinal mucosal bleeding as typical lesions. In addition to poultry, at least 200 species of birds can be infected naturally or in laboratories, and it is one of the most serious infectious diseases threatening the poultry industry in the world. Since the disease was first reported in 1926, it is still prevalent in various parts of the world, with outbreaks from time to time, causing serious economic losses to the poultry industry. The World Health Organization (OIE) listed it as a notifiable disease, and my country listed it as a ...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): G01N33/577G01N33/569G01N33/558
CPCG01N33/558G01N33/56983G01N33/577G01N2333/183
Inventor 李青梅赵东孙亚宁王丽杨继飞柴书军邢广旭滕蔓郭军庆邓瑞广张改平
Owner HENAN ACAD OF AGRI SCI
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