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phytoplasma pytoplasma pyri candidatus phytoplasma candidatus phytoplasma pear decline phytoplasma quarantine real-time fluorescence pcr detection pear decline phytoplasma classification status chinese name english name host range bacteria centralized air-conditioning energy efficiency sheet resistance technical concepts patent control
GB/T 36843-2018 in English

GB/T 36843-2018 in English

VALID

Detection and identification of Candidatus Phytoplasma pyri

  • Issued on:2018-09-17
  • Implemented on:2019-04-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $250.00
$243.00

《GB/T 36843-2018梨衰退植原体检疫鉴定方法》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 the standard

GB/T 36843-2018 "Pear decline phytoplasma quarantine and identification method" is an important standard for pear decline disease in China, aiming to standardize the quarantine and identification process and prevent the spread of the disease. The standard was proposed by the National Technical Committee for Plant Quarantine Standardization and approved by the National Standardization Administration.


2. Basic information of pear decline phytoplasma

Classification status Chinese name English name Host range
Bacteria, Firmicutes, Soft-coated Fungi, Nonsteroidal Mycoplasmas, Phytoplasma Pytoplasma pyri Candidatus Phytoplasma pyri Various plants in the Rosaceae, Apocynaceae, etc.

3. Detection methods and technical points

This standard mainly adopts molecular biological detection technology, including:

  • Nested PCR amplification and detection: Use universal primers P1/P7 and specific primers fPD/rPDs for amplification.
  • Electronic restriction endonuclease pattern (RFLP) analysis: Establish a fingerprint map through sequencing results and compare it with the standard map.
  • Real-time fluorescence PCR detection: Specific amplification of 16S rDNA sequence.

4. Implementation suggestions

Recommended steps:

  1. On-site symptom observation: Focus on symptoms such as leaf curling and discoloration.
  2. Sample collection and storage: Suspected samples need to be stored in low temperature in time.
  3. Laboratory testing: Real-time fluorescence PCR technology is preferred to ensure the accuracy of the results.

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