Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Method for isolated culture of strain of helicobacter pylori

A technology for the separation of Helicobacter pylori and strains, applied in the field of biomedicine, can solve the problems of too strict time limit, variation, bacterial death form, etc., and achieve the effect of improving the positive rate

Inactive Publication Date: 2019-06-14
GUIZHOU MEDICAL UNIV
View PDF1 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the above-mentioned technical scheme has the following problems: during the transfer process, Helicobacter pylori is under stress conditions (that is, the environmental conditions that are not suitable for the growth of Helicobacter pylori), and the excessively long transfer time will cause bacterial death or morphological variation
Therefore, the time limit for transferring the sample to the laboratory for isolation and culture after sampling is about 4 hours, which is too strict
For the situation where the sampling site and the experimental culture site are far apart, the transfer of the sample takes a long time, which leads to a large number of deaths or morphological changes of the isolated Helicobacter pylori to be cultured, and finally the positive rate of bacterial culture is low. and a large number of "false negative" cases

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
  • Method for isolated culture of strain of helicobacter pylori
  • Method for isolated culture of strain of helicobacter pylori
  • Method for isolated culture of strain of helicobacter pylori

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] Embodiment 1: Adopt the method of the present invention to the isolation culture of wild-type Helicobacter pylori

[0044] (1) Materials and instruments

[0045] Microaerophilic culture tank and microaerophilic gas bag, ultra-clean bench (Mitsubishi, Japan); trigas incubator, disposable inoculation loop, Columbia agar (OXOID, UK); Brooke's broth, Gram stain solution (Anhui Chaohu Hongci Medical Company, China), urease test paper (Guangdong Zhuhai Kedi Technology Company, China); fetal bovine serum, cysteine, soluble starch, activated carbon, cyclodextrin, phosphate (PBS) buffer liquid, defibrinated sheep whole blood (Youkang Biotechnology Co., Ltd., China); deoxyribonuclease DNase Ⅰ, ribonuclease RNaseA, tris (hydroxymethyl) aminomethane hydrochloride Tris-HCL (TAKARA); the standard strain NCTC11639 was obtained from Gift from China Helicobacter pylori Strain Management and Preservation Center.

[0046] (1.1) Preparation of Helicobacter pylori lipopolysaccharide extra...

Embodiment 2

[0062] Embodiment 2: Adopt the method of the present invention to the isolation culture of wild-type Helicobacter pylori

[0063] The present embodiment Helicobacter pylori isolation culture material, instrument and process are basically the same as embodiment 1, the difference is:

[0064] (1) Different from (1.2) transport liquid preparation in embodiment 1, the method that present embodiment adopts is:

[0065] To prepare the hpLPS solution, dissolve 15 g of hpLPS in 100 ml of sterile distilled water, and use a 0.22 μm filter membrane to filter and sterilize. Weigh 281g of Brinell broth powder, heat and stir to dissolve in distilled water, add distilled water to the final volume of 100ml to obtain Brinell broth medium, then add 0.5g of activated carbon particles, dissolve and mix well, and then autoclave at 121°C . After cooling, 8 ml of aseptically treated hpLPS solution and 0.1 ml of aseptically treated 0.5 g / ml cysteine ​​solution were added. Then aseptically dispense...

Embodiment 3

[0070] Embodiment 3: Adopt the method of the present invention to the isolation culture of wild-type Helicobacter pylori

[0071] The present embodiment Helicobacter pylori isolation culture material, instrument and process are basically the same as embodiment 1, the difference is:

[0072] (1) Different from (1.2) transport liquid preparation in embodiment 1, the method that present embodiment adopts is:

[0073] To prepare the hpLPS solution, dissolve 15 g of hpLPS in 100 ml of sterile distilled water, and use a 0.22 μm filter membrane to filter and sterilize. Weigh 281g of Brooke’s broth powder, heat and stir to dissolve in distilled water, add distilled water to the final volume of 100ml to obtain Brooke’s broth medium, then add 1g of cyclodextrin, dissolve and mix well, and then autoclave at 121°C . After cooling, 3 ml of aseptically treated hpLPS solution and 0.1 ml of aseptically treated 0.5 g / ml cysteine ​​solution were added. Then aseptically dispense the Brooke's ...

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
diameteraaaaaaaaaa
Login to View More

Abstract

The invention belongs to the field of biomedicine, and relates to a method for separating and cultivating bacteria, in particular to a method for isolated culture of a strain of helicobacter pylori. In a sample transfer process of the method, a sample suspected of containing helicobacter pylori is stored in a transport liquid; and the transport liquid includes a brucella broth medium, an adsorbent, a reducing agent, and a helicobacter pylori lipopolysaccharide extract. The helicobacter pylori lipopolysaccharide extract has an inhibitory effect on sundry fungi and has a protective effect on helicobacter pylori thalluses. The method can prolong the transfer time for sample transfer to a bacterial culture research unit and maintain the activity of the helicobacter pylori, so that the difficulty of isolated culture of wild helicobacter pylori strains is reduced, and the positive rate of bacterial culture is improved. The method for culture of the helicobacter pylori can be applied to studies such as bacterial typing, pathogenic mechanism research, construction of animal models, and determination of pathogenic factors.

Description

technical field [0001] The invention belongs to the field of biomedicine and relates to a method for isolating and cultivating bacteria, in particular to a method for isolating and cultivating Helicobacter pylori strains. Background technique [0002] Helicobacter pylori (H.pylori) is a spiral-shaped Gram-negative microaerophilic bacterium that infects half of the world's population and is the main pathogen that causes gastritis, peptic ulcer, and gastric cancer. The discovery of Helicobacter pylori It has deepened human understanding of the relationship between chronic infection, inflammation and cancer, and has been listed as a class I carcinogen for human gastric cancer by the World Health Organization. The isolated and cultured clinical strains of Helicobacter pylori can be used in basic research such as bacterial typing, research on pathogenic mechanism, construction of animal models and determination of pathogenic factors. However, Helicobacter pylori has very strict ...

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
Patent Type & Authority Applications(China)
IPC IPC(8): C12N1/20C12N1/02C12R1/01
Inventor 周建奖谢渊
Owner GUIZHOU MEDICAL UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com