Key Amino Acids in RNA Polymerase and Helicase Proteins Regulate RNA Synthesis Efficiency in Porcine Reproductive and Respiratory Syndrome Virus.

Abstract

Porcine reproductive and respiratory syndrome virus (PRRSV) exhibits rapid evolution due to its high mutation rate and frequent recombination, posing significant challenges for disease control. In this study, we investigated the molecular mechanisms underlying strain-specific variations in PRRSV replication phenotypes. Using reverse genetics and molecular biology approaches, we established a non-infectious replicon model that simulates PRRSV genomic replication and subgenomic (sg) mRNA transcription at the cellular level. This model enabled the evaluation of regulatory effects of viral non-structural proteins (nsps) and transcription-regulating sequences (TRSs) on viral replication and transcription, revealing the crucial roles of nsp9 and nsp12 in RNA synthesis. Furthermore, we developed a subgenomic replicon system (sg-Rep-PRRSV) driven by a minimal replication-transcription complex (mini-RTC) to investigate the impact of specific mutations in PRRSV replicase-associated proteins on viral RNA synthesis efficiency. Our findings demonstrated that mini-RTC components derived from XM-2020 exhibited significantly higher transcriptional driving efficiency compared to those from GD strain (p < 0.01). Site-directed mutagenesis analysis identified critical amino acid residues contributing to differential RNA synthesis efficiency between strains: E141N, N416H, and S591A in nsp9, and S51D, L57T, and K349E in nsp10. These adaptive mutations likely modulate the catalytic conformations of RNA-dependent RNA polymerase (RdRp) and helicase, ultimately contributing to the distinct replication phenotypes observed among PRRSV strains. Our findings provide an insight into the molecular mechanisms underlying PRRSV evolution and adaptation, which have significant implications for mitigating future PRRS outbreak risks and maintaining sustainable development of the swine industry.