Fluorescent quantitative PCR method for simultaneous detection of streptococcus suis subtype 2 (SS2) extracellular protein factor and hemolysin gene

A technology of streptococcus suis and extracellular protein, which is applied in the field of multiplex fluorescent quantitative PCR, can solve the problems of high price and strong specificity, and achieve the effects of avoiding pollution and dispersing toxins, low detection cost, and strong versatility of reagents

Inactive Publication Date: 2011-11-02
INST OF ANIMAL SCI & VETERINARY MEDICINE SHANDONG ACADEMY OF AGRI SCI
View PDF0 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The Taqman probe method has strong specificity, and needs to design s

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
  • Fluorescent quantitative PCR method for simultaneous detection of streptococcus suis subtype 2 (SS2) extracellular protein factor and hemolysin gene
  • Fluorescent quantitative PCR method for simultaneous detection of streptococcus suis subtype 2 (SS2) extracellular protein factor and hemolysin gene
  • Fluorescent quantitative PCR method for simultaneous detection of streptococcus suis subtype 2 (SS2) extracellular protein factor and hemolysin gene

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] The design and synthesis of embodiment 1 primer

[0029] According to the EF and SLY gene sequences of Streptococcus suis type 2 published in GenBank, the conserved sequences were selected through gene sequence comparison, and the GeneBank accession numbers of the selected EF and SLY public sequences were DQ417121.1 and DQ443530.1, respectively. EF and SLY primers were designed by Primer PremierS 5.0 and Oligo 6 software, and the primers were synthesized by Shanghai Sangon Biotechnology Company.

[0030] The upstream primer of EF is: 5'-GAAGAAGAACCCAAGGAACC-3'; the downstream primer of EF is: 5'-ACATTCTGACCACTCGCATC-3'. The size of the amplified EF fragment is 158bp, and the Tm value of the product is 84°C.

[0031] The upstream primer of SLY is: 5'-TTCCGATTTCGTATTCAACC-3'; the downstream primer of SLY is: 5'-AACTGTTTCCACCACTCCC-3'. The size of the amplified SLY fragment is 338bp, and the Tm value of the product is 80°C.

Embodiment 2

[0032] The extraction of embodiment 2 bacterial DNA

[0033] Inoculate sterilized Todd-Hewitt broth medium with a single colony of Streptococcus suis type 2 HA9801 strain, culture overnight at 37°C, take 1 mL of the bacterial solution, centrifuge at 12,000 rpm for 2 min, and resuspend the precipitate with 567 μL of TE buffer (pH 8.0). Add 30 μL of 10% SDS and 3 μL of 20 mg / mL proteinase K, mix well, bathe in 37°C water for 1 hour, add 100 μL of 5mol / L NaCl, mix well, then add 80 μL CTAB / NaCl solution, mix well, bathe in water at 65°C for 10 min , add an equal volume of phenol: chloroform: isoamyl alcohol (25:24:1) and mix evenly, centrifuge at 12000rpm for 10min, absorb the supernatant and add an equal volume of chloroform:isoamylalcohol (24:1) and mix evenly, centrifuge at 12000rpm for 10min, Aspirate the supernatant, add 0.6 volume of isopropanol, place at -20°C for 20 minutes to fully precipitate the DNA, centrifuge at 12,000 rpm for 10 minutes, wash the precipitate twice w...

Embodiment 3

[0035] Example 3 Establishment of Multiplex Fluorescent Quantitative PCR of Streptococcus suis Type 2 EF and SLY Genes

[0036] Fluorescent PCR reaction system:

[0037] The fluorescent quantitative PCR reaction system of the present invention is a 20ul system, operated on ice, and the following reagents are added in order:

[0038]

[0039] Among them, Master Mix is ​​SYBR Green I dye, polymerase, dNTP, Mg 2+ , PCR buffer mixture. Fluorescent PCR reaction conditions:

[0040] Pre-denaturation: 95°C, 5min

[0041] Fluorescent PCR amplification for 40-45 cycles: denaturation at 95°C for 10s; annealing at 55°C for 20s; extension at 72°C for 30s

[0042] Melting curve reaction program: 95°C, 5s; 65°C, 1min; 97°C, continuous; heating rate 2.2°C / s, start collecting fluorescence signals continuously at 65°C until 97°C.

[0043] Cooling: 40°C, 10s

[0044] Fluorescent PCR reaction criteria:

[0045] According to the Ct value and Tm value, the detection results of Streptococ...

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

No PUM Login to view more

Abstract

The invention relates to a fluorescent quantitative PCR method for simultaneous detection of an extracellular protein factor EF and a hemolysin gene SLY of SS2 based on SYBR Green dye solubility curve method. According to the invention, two pairs of specific primers are designed and synthesized based on conserved sequences of the SS2 EF and SLY gene disclosed by GenBank, the PCR reaction system and reaction conditions are optimized, and the fluorescent quantitative PCR method for simultaneous detection of an EF and an SLY gene of SS2 based on SYBR Green dye method is established through analysis of an amplification curve and a solubility curve. On such bases, the mol ratio of EF primers and SLY primers are optimized and the amplification efficiency of the two pairs of primers is adjusted,which enables the two product peaks in the solubility curve to be of similar size. Utilization of the established SYBR Green dye solubility curve method enables convenient and simultaneous detection of SS2 EFs and SLY genes.

Description

technical field [0001] The invention relates to a multiple fluorescence quantitative PCR method for detecting the extracellular protein factor and hemolysin gene of Streptococcus suis type 2 by a SYBR Green dye dissolution curve analysis method, belonging to the field of nucleic acid detection. technical background [0002] Streptococcus suis (SS) is an important zoonotic pathogen with a worldwide distribution, and it is one of the main infectious diseases that have plagued the pig industry for many years. Acute infection of pigs often manifests as hemorrhagic septicemia and meningitis, and chronic infection manifests as arthritis, endocarditis, and suppurative lymph nodes. Toxic shock and meningitis in humans infected with Streptococcus. Streptococcus suis not only seriously hinders the healthy development of pig industry, but also threatens the safety of human life. Therefore, it is necessary to closely monitor the epidemiological changes of Streptococcus suis. [0003] ...

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): C12Q1/68C12R1/46
Inventor 颜世敢朱丽萍陆承平陈正涛崔道石张秀美胡北侠许传田杨少华张琳
Owner INST OF ANIMAL SCI & VETERINARY MEDICINE SHANDONG ACADEMY OF AGRI SCI
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap