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schmallenberg disease introduction standard background schmallenberg virus quarantine protocol comprehensive quarantine technology system notifiable disease non-metallic blast-cleaning abrasives radial hydrocyclone units secondary fly ash
SN/T 4661-2016 in English

SN/T 4661-2016 in English

VALID

Quarantine protocol for Schmallenberg disease

  • Issued on:2016-12-12
  • Implemented on:2017-07-01
  • File Format:PDF
  • Delivery:Via email within 1~3 business days
Price(USD): $240.00
$233.00
Standard No: SN/T 4661-2016
Document status: VALID
Title in English: Quarantine protocol for Schmallenberg disease
Title in Chinese: 施马伦贝格病检疫技术规范
Language: English
File Format: Electronic (PDF)
Delivery: Via email within 1~3 business days
Issued on: 2016-12-12
Implemented on: 2017-07-01
Professional Classification: SN-Import&Export Inspection
Related Keywords: schmallenberg disease introduction standard background
schmallenberg virus
quarantine protocol
comprehensive quarantine technology system
notifiable disease
Related Topics: Quarantine technology
Border disease quarantine technology
Equine bubonic quarantine technology


Introduction

Standard Background and Technological Evolution

This standard was developed in response to the Schmallenberg virus (SBV), first reported in Europe in 2011. This virus, belonging to the genus Orthobunyavirus in the family Bunyaviridae, primarily causes fever and abortion in ruminants. As the outbreak spread, the OIE designated it a notifiable disease, and this standard establishes a comprehensive quarantine technology system.


Comparison of core detection methods

Method Sensitivity Specificity Time Consumption Applicable samples
Real-time RT-PCR 103 copies/μL 100% 2 hours Whole blood, tissue, semen
Blocking ELISA 1:32000 dilution 98.7% 4 hours Serum, plasma

Key Technical Points

Real-time Fluorescence RT-PCR

Using the AgPath-ID™ One-Step RT-PCR Kit, primer sequences:
Forward: TCAGATTGTCATGCCCCTTG
Reverse: TTCGGCCCCAGGTGCAAATC
Probe: FAM-TTAAGGGATGCACCTGGGCCGATGGT-BHQ1

Blocking ELISA

Key Parameters:
- Coating Antigen Concentration: 2μg/mL
- Positive Determination: PI≥50%
- Negative Determination: PI≤40%


Implementation Suggestions

  1. Samples must be transported in a cold chain maintained at 2-8℃ to avoid repeated freezing and thawing.
  2. Laboratories should operate in separate areas, and PCR product processing should comply with the requirements of GB 19489.
  3. It is recommended to use two methods in parallel to improve the detection rate.

Typical Application Case

During the 2014 Zambia epidemic, this standard was used to test bovine serum samples. A positive case with a Ct value of 28.3 was detected by RT-PCR, and sequencing confirmed that the homology with the European strain was 99.2%.

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