Primers and probe sequence for edwardsiella tarda LAMP-LFD detection and application of primers and probe

A LAMP-LFD, Edwards tarda technology, applied in the field of primers and probe sequences for the detection of Edwardsiella tarda, can solve problems such as delayed diagnosis and detection, and achieve personal and environmental safety, high detection sensitivity, and short detection time. Effect

Active Publication Date: 2015-10-21
NINGBO UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, this technology has been successfully applied to Taura virus ( Taura syndrome virus , TSV), infectious myonecrosis virus ( Infectious myonecrosis virus , IMNV), infectious spleen and kidney necrosis virus ( Infectious spleen and kidney necrosis virus , ISKNV), Vibrio vulnificus ( Vibrio vulnificus ), and Streptococcus iniae ( Strepstococcus iniae ) and other aquatic pathogenic microorganisms, there have been no reports at home and abroad that this technology has been applied to the diagnosis and detection of Edwardsiella tarda

Method used

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  • Primers and probe sequence for edwardsiella tarda LAMP-LFD detection and application of primers and probe
  • Primers and probe sequence for edwardsiella tarda LAMP-LFD detection and application of primers and probe
  • Primers and probe sequence for edwardsiella tarda LAMP-LFD detection and application of primers and probe

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] Establishment of a method for the detection of Edwardsiella tarda by LAMP-LFD technique

[0037] 1. Primer design: Design according to the coding sequence of Edwardsiella tarda outer membrane protein A (GenBank accession number: EF528483) published in NCBI, where the primer sequence is as follows:

[0038] EtaompA-F3: 5'-CATTAGCAGTGGCACTGG-3'

[0039] EtaompA-B3: 5'-TGCCTTGAACTTACCGTTC-3',

[0040] EtaompA-FIP: 5'-TCGGATGAGACTTCGTGGAGTttttGTAGGTGGTAAACTGGGTTG-3',

[0041] EtaompA-BIP: 5'-CGGTGCTTTCTTCGGTTACCAttttCCAGTCGTAGCCCATTTC-3',

[0042] EtaompA-LF: 5'-AAGCTGTTACCGATGTAGTGG-3',

[0043] EtaompA-LB: 5'-CTAATCCGTACCTGGGCTTC-3',

[0044] Probe EtaompA-HP: 5'-ATACGAATCAGCTGGGCGC-3',

[0045] Among them, the 5' end of EtaompA-FIP is labeled with biotin; the 5' end of probe EtaompA-HP is labeled with fluorescein isothiocyanate.

[0046] 2. Sample DNA extraction: Streak the Edwardsiella tarda strain (E. tarda MCCC235) stored at -70°C for a long time on LB solid med...

Embodiment 2

[0053] Specificity determination of Edwardsiella tarda LAMP-LFD detection using primers and probes of the invention

[0054] Using the designed specific primers and probes, Edwardsiella tarda MCCC235, Aeromonas salmonicida ATCC 33658, Aeromonas hydrophila ATCC 7966, Vibrio vulnificus ATCC 27562, Vibrio harveyi ATCC 33866 , Vibrio riverina ATCC 33809, Pseudomonas putida MCCC 1A01082, Streptococcus iniae ATCC 29178, Vibrio alginolyticus ATCC 33787, Vibrio anguillarum ayu-H080701, Vibrio rotiferus DSM 17186T, Listeria monocytogenes ATCC 19115, Genomic DNA of Pseudomonas aeruginosa ATCC 9027 etc. was used as a template, and LAMP-LFD reaction was performed according to steps 3 and 4 of the above-mentioned Example 1 to verify the specificity of primers and probes, and double distilled water was used as a negative control. The result is as figure 1 and figure 2 As shown, using the electrophoresis method ( figure 1 ) and LFD ( figure 2 ) can only be amplified from the genomic ...

Embodiment 3

[0056] Sensitivity determination of Edwardsiella tarda LAMP-LFD detection using primers and probes of the present invention

[0057] Adopt the method of step 2 of above-mentioned embodiment 1 to extract the genomic DNA of Edwardsiella tarda, carry out 10 times serial dilution, select 3.50 * 10 7 , 3.50×10 6 , 3.50×10 5 , 3.50×10 4 , 3.50×10 3 , 3.50×10 2 , 3.50×10 1 cfu / mL was used as a template, and the LAMP-LFD reaction was performed according to steps 3 and 4 of the above-mentioned Example 1 to verify the sensitivity of the primers and probes, and double-distilled water was used as a negative control. The result is as image 3 , Figure 4 and Figure 5 As shown, the sensitivity of the LAMP-LFD detection using the primers and probes provided by the invention is 3.50×10 2 cfu / mL ( Figure 4 ), consistent with the sensitivity obtained by agarose gel electrophoresis detection of LAMP amplification products ( image 3 ), which is 100 times that of the conventional P...

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Abstract

The invention discloses primers and a probe for edwardsiella tarda LAMP-LFD (Loop-Mediated Isothermal Amplification-Lateral Flow Dipstick) detection and application of the primers and the probe. The primers and the probe are characterized by comprising three pairs of primers, namely EtaompA-F3, EtaompA-B3; EtaompA-FIP, EtaompA-BIP; EtaompA-LF and EtaompA-LB, of LAMP, and a probe EtaompA-HP, wherein the nucleotide sequence is shown as SEQ NO1-NO7; the visible detection of edwardsiella tarda is realized by utilizing the primers and the probe, and an amplification step of an LAMP reaction system, a hybridization step of the probe and an LAMP reaction product, and an LFD detecting step; the primers and the probe have the advantages that the rapidness, specificity and sensitivity are higher, the instrument requirement is simple, the primers and the probe are favourable for the early diagnosis and detection of the edwardsiella tarda, and the requirements on the detection of a primary detecting mechanism and an on-site epidemic focus can be met.

Description

technical field [0001] The invention relates to a primer and a probe sequence for detecting Edwardsiella tarda, in particular to a primer and a probe sequence for detecting Edwardsiella tarda LAMP-LFD and the application of the primer and the probe. Background technique [0002] Edwardsiella tarda ( Edwardsiella tarda ) is a Gram-negative short bacillus belonging to the family Enterobacteriaceae and the genus Edwardsiella. It has a wide host range and can infect fish, amphibians, reptiles, and mammals including humans. The bacterium is ubiquitous in freshwater and seawater environments, and water transmission is an important transmission route of Edwardsiella tarda. The deterioration of the water environment can easily lead to the outbreak of the disease. Fish is the most common host of Edwardsiella tarda, which can infect more than 20 types of marine and freshwater fish including flounder, turbot, eel, carp, tilapia, etc., resulting in thick sores on the body surface, skin...

Claims

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Application Information

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IPC IPC(8): C12Q1/68C12Q1/04C12R1/01
CPCC12Q1/6844C12Q1/689C12Q2531/119
Inventor 陈炯周前进
Owner NINGBO UNIV
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