Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Biochip for detecting pathogenesis fungus

A technology of biochips and pathogenic fungi, applied in the determination/testing of microorganisms, biochemical equipment and methods, etc.

Inactive Publication Date: 2005-11-16
INST OF HYGIENE & ENVIRONMENTAL MEDICINE PLA ACAD OF MILITARY MEDICAL
View PDF0 Cites 24 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The detection of pathogenic fungi or conditional pathogenic fungi by gene chip technology belongs to the frontier field of clinical testing. The scientific nature of the technology has been recognized; the innovation lies in the fact that the gene chip technology is a new technology invented in the 1990s and developed vigorously after 2000. Up to now, there has been no relevant research on the use of gene chip technology to detect pathogenic fungi or Reports on opportunistic fungi

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
  • Biochip for detecting pathogenesis fungus
  • Biochip for detecting pathogenesis fungus
  • Biochip for detecting pathogenesis fungus

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0079] Establishment of fungal culture conditions

[0080] 1. Yeast (Candida and Cryptococcus)

[0081] Apply Sandcastle solid or liquid medium and culture at 30°C for 2 days

[0082] Recipe: Glucose 40g

[0083] Peptone 10g

[0084] Agar 20g

[0085] Distilled water 1000ml

[0086] Mix the above ingredients, heat until completely dissolved, adjust the pH to about 5.6, and steam sterilize at 115°C for 30 minutes for later use

[0087] Note: liquid medium without agar

[0088] 2. Filamentous fungi and superficial dermatophytes

[0089] Use potato solid or liquid medium for cultivation at 30°C for 5-7 days

[0090] Recipe: Boil 200 peeled and chopped potatoes with 700ml of water for 20 minutes, filter with gauze, and keep the filtrate

[0091] Add glucose 20g

[0092] Agar 15g

[0093] Add water to 1000ml,

Embodiment 2

[0095] Establishment of DNA Extraction Method from Fungi

[0096] Extraction of Fungal DNA Using Benzyl Chloride

[0097] 1. Principle

[0098]

[0099] ROH stands for chitin in the cell wall, above for PhcH 2 cL in the reaction formula of various polysaccharides

[0100] 2. Method

[0101] (1) Scrape 0.1-0.3g of colonies with a volume of about 100ul into a 1.5ml centrifuge tube

[0102] (2) Add 600μl DNA extraction solution, shake and mix

[0103] (3) Add 10% SDS 50ul shake and mix

[0104] (4) Add 300ul benzyl chloride and shake to mix

[0105] (5) 50-55 ℃ water bath for 1 hour and mix every 10 minutes

[0106] (6) Add 60ul of 3M sodium acetate to each tube and bathe in ice for 20 minutes

[0107] (7) Centrifuge at 4°C, 13000rpm for 10 minutes

[0108] (8) Take the supernatant, add an equal volume of phenol chloroform, and centrifuge at 13,000 rpm for 10 minutes at 4°C

[0109] (9) Take the supernatant, add 1 / 10 sodium acetate and an equal volume of isopropan...

Embodiment 3

[0116] Target gene selection

[0117] Whether in fungi or bacteria, cellular ribosomal ribonucleic acid (rRNA) genes are commonly used targets for molecular analysis. The ribosomal ribonucleic acid (rRNA) gene and its adjacent spacer are collectively referred to as rDNA. Fungal cell rDNA has dozens or even hundreds of copies, and the fungal ribosomal DNA (rRNA gene) operator includes three functional genes, namely 18S rDNA, 5.8S rDNA, and 28S rDNA, which are connected head to tail on the chromosome, arranged in series, and mutually Between the internal transcribed spacer (internal transcribed spacer) division. Including the internal transcribed spacer-1 (ITS-1) between 18S rDNA and 5.8S rDNA, and the internal transcribed spacer-1 (ITS-2) between 5.8S rDNA and 28S rDNA. (See Figure 2)

[0118] The nuclear rDNA of eukaryotes is a multi-gene cluster, arranged in tandem repeat units, and a typical rDNA repeat unit is about 8-12kb. They are located in nucleolar organizer region...

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

A biochip for detecting the pathogenic funguses features that the DNA probes respectively for detecting one of 20 pathogenic funguses including Candida albicans, Aspergillus fumigatus, etc are immobilized on the glass plate, silicon chip, or high-molecular material.

Description

technical field [0001] The invention relates to a biochip, in particular to a biochip for detecting fungi. Background technique [0002] At present, the harm of pathogenic microbial infectious diseases to human beings continues unabated, and the infections caused by fungi are also becoming more and more prominent due to the increasing number of immunocompromised hosts. With the widespread application of radiotherapy, chemotherapy, broad-spectrum antibiotics and immune agents for tumors, systemic and opportunistic fungal infections are increasing, especially in hematological malignancies, tumors and bone marrow transplantation and organ transplantation; for example, 18% -50% of patients develop invasive fungal infection after bone marrow transplantation; the prevalence of fungal infection in organ transplant recipients and patients with malignant tumors is as high as 20% to 40%; and fungal infections are often fatal infections, and the case fatality rate is sharp Rising tren...

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): C12Q1/68
Inventor 李君文黄爱华王新为谌志强金敏
Owner INST OF HYGIENE & ENVIRONMENTAL MEDICINE PLA ACAD OF MILITARY MEDICAL
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
Eureka Blog
Learn More
PatSnap group products