SN/T 5228.2-2019 in English
VALIDRapid detection of pathogens in export food-MALDI-TOF MS method- Part 2: Clostridium perfringens
- Issued on:2019-12-27
- Implemented on:2020-07-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$97.00
Introduction
Technical background and significance of the standard
With the growth of international trade, the timeliness requirements for foodborne pathogen detection are increasing. The traditional culture method takes 5-7 days to detect Clostridium perfringens, while MALDI-TOF MS technology shortens the detection cycle to within 24 hours. As the second part of the SN/T 5228 series, this standard complements the GB 4789.13 method to meet the needs of rapid customs clearance of exported food.
Analysis of the core method
Key points of the detection process
| Steps | Technical parameters | Quality control requirements |
|---|---|---|
| Sample preparation | 5-10mg bacteria + 300μL water + 900μL ethanol | Centrifugal force ≥13,000g |
| Protein extraction | 30-50μL 70% formic acid + equal volume of acetonitrile | Vortex and mix thoroughly |
| Spot detection | 1μL supernatant + 1μL CHCA matrix | BTS calibration error <0.03% |
Instrument parameter settings
- Detection mode: Linear positive ion mode
- Mass range: 2,000-20,000 Da
- Laser parameters: 60Hz frequency, 40 accumulations
Result judgment criteria
The detection case of an export meat company shows that when the Biotyper software matching score is ≥2.300, the consistency rate with the traditional PCR method is 98.7%; the score in the range of 1.700-2.299 needs to be verified in combination with biochemical tests.
Implementation recommendations
- Laboratories should establish a regular calibration system for MALDI-TOF MS
- Pretreatment solutions should be optimized for high-fat samples
- It is recommended to set up negative/positive controls for each batch of tests
Technology evolution analysis
Compared with the 2015 version of the industry standard, this method increases the detection sensitivity to 103 CFU/mL, and for the first time clarifies the optimal conditions for anaerobic culture for 18-24h. In the future, it can form a methodological complement with whole genome sequencing technology.

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