Recombinase-aid amplification (RAA) thermostatic fluorescence detection method of infectious hypodermal and hematopoietic necrosis virus (IHHNV), and reagent

A technology for hematopoietic tissue and necrotic virus, applied in the field of molecular biology, can solve the problems of low detection sensitivity, limited application, complicated operation, etc., and achieve the effects of high sensitivity, simple identification and simple operation.

Active Publication Date: 2018-03-23
HANGZHOU ZHONGCE BIO SCI&TECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Although electron microscope counting can directly observe the presence of virus particles, the operation is complicated, time-consuming and costly
The HE staining method is based on pathological counts, and cannot directly detect the virus, but can only be detected by using the histopathological signs of the disease
Antibody detection method and nucleic acid probe hybridization method are used to detect the protein or nucleic acid components of the virus itself. The detection sensitivity is low and time-consuming, and can only be used for the detection of diseased shrimp or shrimps that are about to become diseased; IHHNV has not yet caused infection or in Infection is very early and difficult to detect with the above methods
Although the PCR detection method of IHHNV overcomes the shortcomings of the first four methods, it can achieve relatively fast and accurate detection of IHHNV under laboratory conditions, but because conventional PCR detection requires expensive PCR equipment, gel electrophoresis and imaging systems, And the detection time is long, which also greatly limits the popularization and application of PCR detection method in practice.
LAMP isothermal amplification technology also has high false positives and low accuracy, so its application in the detection of aquatic pathogens is still relatively limited

Method used

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  • Recombinase-aid amplification (RAA) thermostatic fluorescence detection method of infectious hypodermal and hematopoietic necrosis virus (IHHNV), and reagent
  • Recombinase-aid amplification (RAA) thermostatic fluorescence detection method of infectious hypodermal and hematopoietic necrosis virus (IHHNV), and reagent
  • Recombinase-aid amplification (RAA) thermostatic fluorescence detection method of infectious hypodermal and hematopoietic necrosis virus (IHHNV), and reagent

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029]The present invention searches the gene sequence of the infectious subcutaneous and hematopoietic tissue necrosis virus of prawns in the Genebank database, uses DNAMAN 6.0 software to compare multiple sequences, and finds the conserved segment. Four sets of primers and probes were designed in the conserved regions, and BLAST comparison was performed in the NCBI database. The sequences of the primers and probes are shown in Table 1. The positive sample amplification curve is as follows figure 1 shown.

[0030] Table 1 primers and probe sequences:

[0031]

[0032] Depend on figure 1 The results show that the amplification curves of the fourth group of primers and probes are the most typical, with obvious exponential phase and plateau phase, higher fluorescence intensity (ordinate value), and smaller CT value (the intersection of the curve and the threshold line Corresponding abscissa) result analysis is shown in Table 2. For other primers and probes, the rising hei...

example 3

[0044] Example 3: Kit of the present invention Enterococcus hepatica

[0045] 1. Extraction of sample nucleic acid

[0046] 1.1. Nucleic acid extraction: DNA extraction was performed using a marine animal tissue DNA extraction kit.

[0047] 2. The configuration of the RAA reaction system: each test sample corresponds to a RAA reaction dry powder tube, and the reaction components and the added volume in each RAA reaction dry powder tube are shown in Table 3.

[0048] table 3:

[0049] RAA reaction system components

Volume (μL)

A Buffer

12.5μL

B Buffer

2.5μL

primer mix

4μL

specific fluorescent probe

0.6μL

DNA template

2μL

wxya 2 o

28.4μL

total capacity

50μL

[0050] A Buffer is 20% PEG; B Buffer is 280mM MgAc

[0051] 3. Place the RAA reaction tube with the reaction system in the ABI7500 amplification instrument, and perform RAA amplification according to the following procedure: ...

Embodiment 4

[0054] Embodiment 4: Evaluation of the RAA detection kit of the present invention in clinical practice

[0055] The kit of the present invention is used to carry out a clinical blind sample experiment, and 500 prawns are detected; the experimental results show that the fourth primer pair of the present invention can distinguish Hepatocystis prawns, and the positive coincidence rate with nested PCR is very high. Among the 500 copies of nested PCR, 345 were positive results, 155 were negative results, 346 were positive by the RAA method, 154 were also negative results, and one positive result was different. The sample DNA was amplified by PCR and sequenced, and the sequencing result showed that the sample was positive, indicating that the RAA detection reagent of the present invention has a higher accuracy rate.

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Abstract

The invention discloses a recombinase-aid amplification (RAA) thermostatic fluorescence detection method of infectious hypodermal and hematopoietic necrosis virus (IHHNV) of prawns, and a detection kit. The detection kit comprises a forward primer shown in SEQ ID No. 1, a reverse primer shown in SEQ ID No. 2, a specific fluorescent probe shown in SEQ ID No. 3, a reaction solution, recombinant polymerase and a reference substance. The kit provided by the invention is high in specificity; the detection sensitivity is high, and can reach up to 0.32fg/mu L; the detection method has the advantagesof high accuracy, reliability, simple, convenient and fast operation, and suitability for field detection, thus having wide application prospect.

Description

technical field [0001] The invention belongs to the technical field of molecular biology, and relates to a detection method of marine aquaculture industry, in particular to a RAA constant-temperature fluorescence detection method and a kit for infectious subcutaneous and hematopoietic tissue necrosis virus of prawns. Background technique [0002] Infectious hypodermal and hematopoietic necrosis virus (IHHNV) is the source of disease causing shrimp infectious hypodermal and hematopoietic necrosis (IHHN), that is, causing chronic short stature syndrome ( Runt-deformity syndrome, the pathogen of DRS). The disease was first discovered in a farm in Hawaii, USA in 1981. It first broke out in Litopenaeus stylirostris (L. stylirostris). Subsequent investigations found that it also widely exists in shrimp cultured in Asia and America. This disease is particularly serious to the harm of juvenile shrimp, and it affects the development of whole prawn farming industry. Epidemic outbrea...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C12Q1/70C12Q1/6844
CPCC12Q1/6844C12Q1/701C12Q2563/107C12Q2521/507C12Q2522/101
Inventor 程奇钱冬黄震巨张建勋肖文余国君陶智勇徐锦余霍胜楠沈弘郑晓叶郑天伦沈伟良吕文浩
Owner HANGZHOU ZHONGCE BIO SCI&TECH CO LTD
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