GB/T 36851-2018 in English
VALIDDetection and identification of Xanthomonas vesicatoria
- Issued on:2018-09-17
- Implemented on:2019-04-01
- File Format:PDF
- Delivery:Via email within 1~3 business days
$214.00
《GB/T 36851-2018辣椒细菌性斑点病菌检疫鉴定方法》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
1. Background and significance of standard formulation
The formulation of the National Standard of the People's Republic of China GB/T 36851-2018 "Quarantine and Identification Methods for Pepper Bacterial Spot Disease" aims to standardize the quarantine and identification process of pepper bacterial spot disease (Xanthomonas vesicatoria) in pepper and its products, and ensure the safety of agricultural production and the smooth progress of international trade. This standard was proposed and managed by the National Technical Committee for Plant Quarantine and Standardization, and the main drafting units include the China Institute of Inspection and Quarantine, the Suifenhe Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China, etc.
2. Basic information of bacterial spot of pepper
| Classification information | Transmission route | Host range | Geographical distribution |
|---|---|---|---|
| Xanthomonas vesicatoria | Infected seeds, plant residues, rain splash | Pepper, tomato, various Solanaceae crops | Major agricultural areas in the world, including China |
| Bacterial leaf spot of pepper | - Long-distance transmission: infected seeds | - Contact transmission: seedling transplanting | Africa, America, Asia, Europe, Oceania |
3. Interpretation of quarantine identification methods
Detection of Xanthomonas vesicatoria usually includes three parts: symptom inspection, isolation culture and molecular biological detection.
3.1 Symptom inspection and sample preparation
Preliminary judgment is made based on the symptoms of the host plant, focusing on the characteristics of the lesions on the leaves and fruits. Plants with typical symptoms need to be photographed and sent to the laboratory for testing.
3.2 Molecular biological detection
PCR gel electrophoresis or real-time fluorescence PCR technology is used for detection. Specific primers (such as Bs-XvF and Bs-XvR) were used in the PCR reaction system, and the size of the amplified product was 138 bp.
3.3 Isolation, culture and identification
The mTMB and CKTM selective culture media were used for isolation and culture, and the characteristics of the colonies included yellow and viscous. Combined with the Biolog system for automatic identification of microorganisms.
4. Implementation suggestions
- Choose appropriate detection technology:Choose PCR or real-time fluorescence PCR method according to laboratory conditions, and ensure sufficient supply of reagents and equipment.
- Optimize sample collection and preparation:Strictly follow the standard operating procedures (SOP) for plant and seed sample processing to avoid contamination.
- Strengthen laboratory capacity building:Equip with necessary instruments and equipment (such as PCR instruments, real-time fluorescence PCR instruments, autoclaves, etc.), and conduct regular staff training.
- Establish a data sharing mechanism:Unify the recording format of test results, promote data sharing and analysis, and improve quarantine efficiency across the country.

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