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Isothermal Amplification Breakthrough: RAA Platform Accelerates Chikungunya Virus Research


Release Time:

2025-07-25

Since 2025, Chikungunya virus (CHIKV) has shown exceptionally active spread in tropical regions. Although traditional RT-PCR offers high sensitivity, its >2-hour amplification cycle and heavy reliance on specialized equipment have created bottlenecks for research teams needing critical data during outbreaks. Field traceability studies are further constrained by cold-chain transport requirements and laboratory dependencies.

Epidemic Research Faces Timeliness Challenges

Since 2025, Chikungunya virus (CHIKV) has shown exceptionally active spread in tropical regions. Although traditional RT-PCR offers high sensitivity, its >2-hour amplification cycle and heavy reliance on specialized equipment have created bottlenecks for research teams needing critical data during outbreaks. Field traceability studies are further constrained by cold-chain transport requirements and laboratory dependencies.

Limitations of Current Detection Technologies:

  • Virus Isolation: Time-consuming, labor-intensive, and incompatible with rapid screening
  • Serological Diagnosis: Low sensitivity for early-stage infections, leading to missed cases
  • RT-PCR: Requires expensive thermal cyclers and advanced labs; lacks portability
  • RT-LAMP: Needs multiple primers and suffers from poor specificity
  • NASBA: Lengthy 2-hour reaction time

Revolutionary Isothermal Amplification Technology

RAA technology, short for Recombinase Aided Amplification,is a technology that utilizes recombinase, single-stranded binding protein and DNA polymerase to perform nucleic acid amplification under isothermal conditions (the optimal temperature is 39℃).The specific principle is: Recombinases, single-stranded binding proteins, and primers form polymers to scan double-stranded DNA, unwind double-stranded DNA at sequences homologous to the primers, and single-stranded binding proteins (SSBS) bind to the untwisted single strand to prevent single-stranded DNA refolding. In the presence of

energy and dNTP, DNA polymerase completes the strand extension and repeats the process. The amplification can be detected by the instrument within 5-15 minutes.

Compatible detection methods include:

→ Electrophoresis Method

→ Test Strip Method

→ Fluorescent Method

RAA Scientifi Research Platform Kit:

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4d7a1002f66e67db78d57f092580e3b5

RAA Research Platform Kit Features:

Isothermal amplification39℃constant temperature (no thermal cycling)
High stabilityLyophilized format transport&store at room temperature
Rapid&convenient5-15 minute detection for field deployment
Efficient&sensitiveLoD: 10 copies/test (equivalent to qPCR)

Academic Impact Validation

Supported by 190+ international journal publications:

Representative PublicationsImpact Factor
Evaluation of recombinase-based isothermal amplification assays for point-of-need detection of SARS-CoV-2 in resource-limited settings20.999
A multi-country phase 2 study to evaluate the suitcase lab for rapid detection of SARS-CoV-2 in seven Sub-Saharan African countries:Lessons from the field14.481

Multiplex bacteria detection using one-pot CRISPR/Cas13a-based

droplet microfluidics

12.6

Certified Institutional Partners

✅ Sierra Leone-China Friendship Laboratory (Malaria Surveillance)

✅ CDC (Emerging Virus Screening Systems)

✅ Leipzig University, Germany


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