Kang Yeonglim, Choi Jong-Chul, Lee Joong-Bok, Park Seung-Yong, Oh Changin
Laboratory of Infectious Diseases, College of Veterinary Medicine, Konkuk University, Seoul, Republic of Korea.
Department of Genetics, Yale University School of Medicine, New Haven, Connecticut, United States of America.
PLoS One. 2025 May 20;20(5):e0324500. doi: 10.1371/journal.pone.0324500. eCollection 2025.
Rottlerin exerts antiviral activity against various enveloped viruses, yet the mechanism by which it inhibits viral replication and the associated signaling pathways remains unclear. Here, we investigated the mechanisms for the antiviral effects of rottlerin against Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) in vitro. We demonstrate that PRRSV enters host cells via macropinocytosis. Rottlerin, a PKCδ inhibitor, partially inhibits PRRSV entry by decreasing actin polymerization, as evidenced by alterations in actin dynamics. LIM domain kinase 1 (LIMK1) is essential for PRRSV replication, and PRRSV infection-induced cofilin activation, which was reversed by rottlerin treatment. Our findings suggest that a subset of PRRSV utilizes PKCδ-mediated actin dynamics to enter cells via macropinocytosis, and that rottlerin is a potential antiviral molecule targeting this entry pathway.
rottlerin对多种包膜病毒具有抗病毒活性,但其抑制病毒复制的机制及相关信号通路仍不清楚。在此,我们研究了rottlerin在体外对猪繁殖与呼吸综合征病毒(PRRSV)抗病毒作用的机制。我们证明PRRSV通过巨胞饮作用进入宿主细胞。rottlerin是一种PKCδ抑制剂,通过降低肌动蛋白聚合作用部分抑制PRRSV进入,肌动蛋白动力学的改变证明了这一点。LIM结构域激酶1(LIMK1)对PRRSV复制至关重要,rottlerin处理可逆转PRRSV感染诱导的丝切蛋白激活。我们的研究结果表明,一部分PRRSV利用PKCδ介导的肌动蛋白动力学通过巨胞饮作用进入细胞,并且rottlerin是靶向该进入途径的潜在抗病毒分子。