Bacteroides fragilis selective culture medium

A technology for selecting medium and Bacteroides fragilis, applied in the field of microbial inspection, can solve the problems of slow growth, complex experimental conditions, high cost, and achieve the effect of reliable detection and high separation rate

Inactive Publication Date: 2015-08-26
钟伟萍
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The clinical determination of BF is mainly based on PCR and cell culture. The sensitivity of PCR is high, and the result can be obtained within 5 hours. It has the characteristics of rapidity and sensitivity, but it has the following defects: ① Fecal samples contain PCR inhibitors, which can easily cause false negative results ; ② complex experimental conditions are required, and the cost is high
However, the BBE medium has the following defects: ① cannot inhibit the growth of Fusobacterium mutans and Fusobacterium dead; ② has no killing effect on aerobic bacteria and facultative anaerobic bacteria, so gentamicin 100mg / L should be added , but gentamicin also has a weak inhibitory effect on BF, resulting in slow growth; ③If gentamicin is not added, a strict anaerobic environment is required. Since most laboratory departments of primary hospitals lack absolute anaerobic testing equipment, Therefore, the "anaerobic tank culture method" is mostly used. The so-called anaerobic tank is a drying tank. The oxygen in the tank is exhausted through physical and chemical methods, resulting in an anaerobic environment.
Oxygen depletion in the anaerobic cylinder method takes time, affecting growth and isolation of obligate anaerobic bacteria BF

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

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0015] Example 1, the formula for preparing 1000ml medium contains: tryptone 10g; glucose 2g; yeast powder 5g; sodium chloride 5g; agar 15g; Bacterial calf serum 100ml; add distilled water to 1000ml. Preparation method: Weigh tryptone; glucose; yeast powder; sodium chloride; agar; , add sterile calf serum and mix evenly, dilute to 1000ml with sterilized distilled water and dispense.

[0016] The sterilized calf serum in this example only serves as a nutrient matrix and has no selective antibacterial effect.

Embodiment 2

[0017] Example 2, the formula for preparing 1000ml medium contains: tryptone 8g; glucose 5g; yeast powder 8g; sodium chloride 5g; agar 15g; Sterile heat deformed calf serum 50ml; add distilled water to 1000ml. Preparation method: Weigh tryptone; glucose; yeast powder; sodium chloride; agar; , add sterile heat-deformed calf serum and mix evenly, dilute to 1000ml with sterilized distilled water, and dispense.

[0018] The preparation method of the sterile heat-deformed calf serum is as follows: heat the sterile calf serum at 80°C for 10 minutes, add sterilized trypsin at 45°C for 90 minutes, and the mass ratio of enzyme to substrate is 1:150. The preparation method of the sterile heat-deformed calf serum in other examples is the same as that in Example 1.

Embodiment 3

[0019] Example 3, the formula for preparing 1000ml medium contains: tryptone 10g; glucose 3g; yeast powder 10g; sodium chloride 5g; agar 20g; -Homoarginine 0.1g; sterile heat deformed calf serum 80ml; distilled water added to 1000ml. Preparation method: Weigh tryptone; glucose; yeast powder; sodium chloride; agar; Sterilize for 15 minutes, cool to 45°C, add sterile heat-deformed calf serum and mix evenly, dilute to 1000ml with sterilized distilled water and dispense.

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 discloses a bacteroides fragilis culture medium, and belongs to the field of inspection microbe cultivation. The bacteroides fragilis culture medium is characterized by comprising casein tryptone, glucose, yeast powder, sodium chloride, agar, cimigenyl xyloside, pig gallbladder powder, valine, and the balance of distilled water for per 1000 ml. Compared with the prior art, the bacteroides fragilis culture medium has the advantages that the inspection result is reliable, and the separation rate of bacteroides fragilis is high.

Description

technical field [0001] The invention relates to the field of microbiology testing, in particular to a culture medium for Bacteroides fragilis. Background technique [0002] Bacteroides Fragilis (BF) is a Gram-negative short bacillus with capsules, no spores, some pili, obligate anaerobic. BF is an integral part of the normal flora of the human body, and is also an important clinically important conditional pathogen. It can cause infections in many parts of the human body. The symptoms of infection can be found in various clinical departments. The detection rate is high, accounting for 25% of clinical anaerobic isolates. Bacteroides isolates accounted for 50%, and the BF isolation rate in patients with diarrhea was 9.2%-26.8%. [0003] The clinical determination of BF is mainly based on PCR and cell culture. The sensitivity of PCR is high, and the result can be obtained within 5 hours. It has the characteristics of rapidity and sensitivity, but it has the following defects: ...

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): C12Q1/04C12R1/01
Inventor 钟伟萍
Owner 钟伟萍
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