A rescued NADC30-like virus by reverse genetic manipulation exhibits moderate virulence and a promising application

Zhengda Cao1, Jinxia Chen2, Liwei Li2

  • 1Shanghai Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Shanghai, 200241, China; Shandong Agricultural University, Shandong, 271018, China.

Virus Research
|May 13, 2022
PubMed

Insights

Researchers created a viable clone of the NADC30-like Porcine Reproductive and Respiratory Syndrome Virus (PRRSV). This tool aids in studying PRRSV characteristics and developing new vaccines.

Area of Science:

  • Veterinary Virology
  • Molecular Biology
  • Animal Health

Background:

  • NADC30-like Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) strains are prevalent in China, showing high homology to US-isolated strains.
  • These strains exhibit a significant propensity for recombination with other PRRSV strains, including vaccine viruses, complicating disease control.
  • The increasing complexity of PRRSV prevention and control necessitates deeper molecular and virulence analyses.

Purpose of the Study:

  • To construct a full-length infectious clone of the NADC30-like PRRSV strain.
  • To analyze the molecular biology and pathogenicity of the NADC30-like PRRSV.
  • To provide a tool for future research on PRRSV biological characteristics and vaccine development.

Main Methods:

  • Construction and rescue of a full-length infectious clone of NADC30-like PRRSV using reverse genetics.
  • Virological characterization of the rescued virus (rZJqz) compared to its parental strain (ZJqz21).
  • Animal experiments to assess pathogenicity, clinical symptoms, and viral shedding of the rescued virus.

Main Results:

  • A rescued virus, rZJqz, was successfully generated and found indistinguishable from the parental ZJqz21 strain in virological characteristics.
  • The rescued virus rZJqz demonstrated similar pathogenicity to ZJqz21, inducing typical clinical symptoms and viral shedding.
  • The study provides a viable tool for investigating NADC30-like PRRSV strains.

Conclusions:

  • The rescued NADC30-like PRRSV clone (rZJqz) serves as a valuable tool for studying viral characteristics and pathogenicity.
  • These findings lay the groundwork for understanding PRRSV recombination and developing novel, effective universal vaccines.
  • Further research using this infectious clone can advance strategies for PRRSV prevention and control.

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