GB/T 36833-2018 in English
VALIDDetection and identification of Potato virus X
- Issued on:2018-09-17
- Implemented on:2019-04-01
- File Format:PDF
- Delivery:Via email within 5 business days
$301.00
《GB/T 36833-2018马铃薯X病毒检疫鉴定方法》由TC271(全国植物检疫标准化技术委员会)归口,主管部门为国家标准化管理委员会。
Introduction
National Standard of the People's Republic of China GB/T 36833—2018
Potato virus X quarantine identification method
Background and significance of standard formulation
The formulation of GB/T 36833—2018 is based on the important position of potato in international trade and agricultural production. Potato virus X (PVX) is a quarantine disease that seriously affects potato yield and quality. The introduction of this standard fills the gap in the field of PVX detection methods in China, and provides a scientific basis for standardizing import and export plant quarantine and ensuring agricultural safety.
Detection principle and technical route
The genomic characteristics and immunogenicity of PVX are the main basis for its quarantine identification. The standard adopts a variety of molecular biology techniques and immunological methods, including:
- Reverse transcription PCR (RT-PCR)
- Real-time fluorescence reverse transcription PCR (Real-time RT-PCR)
- Reverse transcription loop-mediated isothermal amplification (RT-LAMP)
- Enzyme-linked immunosorbent assay (ELISA)
- Immunochromatographic test strip test
- Dot enzyme-linked immunosorbent assay (dot-ELISA)
Main instruments and equipment and function comparison table
| Instrument name | Model and specifications | Purpose | Detection sensitivity |
|---|---|---|---|
| Microplate reader | Micro-volume detection, suitable for ELISA and dot-ELISA | Optical density (OD) determination, sensitivity up to 0.001 | |
| PCR instrument | Variable temperature control, support gradient PCR | DNA amplification, suitable for RT-PCR and Real-time RT-PCR | Single copy detection level |
| Real-time fluorescence PCR instrument | Equipped with fluorescence detection module | Quantitative analysis of viral load, Ct value range: 15-40 | Ct ≤ 35 is positive |
| RT-LAMP detector | Constant temperature amplification, 65℃ | Rapid nucleic acid amplification, suitable for on-site detection | Colorimetric reaction to directly determine the result |
Sample preparation and sampling methods
The standard specifies a detailed sample preparation process, including:
- Cultivation and observation of tissue culture seedlings, miniature potatoes, and tubers
- Sowing and symptom monitoring of host plant seeds of the Solanaceae family
- Direct detection of samples with suspicious symptoms
Result determination and record keeping
The detection result is determined by a double confirmation mechanism:
- Negative samples must be negative by at least one method
- Positive samples must be positive by at least two methods
Implementation suggestions and precautions
In order to ensure the effective implementation of the standard, the following suggestions are put forward:
- Laboratory conditions:Equipped with Class II biosafety protection facilities.
- Staff training:Regularly conduct training on testing methods and quality control.
- Reagent management:Establish a reagent validity period and traceability record system.
- Data sharing:Promote the information management and sharing mechanism of quarantine results.

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