Sate Key Laboratory of Biocontrol, School of Life Sciences, Sun Yat-sen University, Guangzhou, 510006, China.
Department of Medicine, Division of Infectious Diseases, Stanford University, Stanford, CA, 94305, USA.
Adv Sci (Weinh). 2024 Sep;11(34):e2402025. doi: 10.1002/advs.202402025. Epub 2024 Jul 8.
As a significant infectious disease in livestock, porcine reproductive and respiratory syndrome (PRRS) imposes substantial economic losses on the swine industry. Identification of diagnostic markers and therapeutic targets has been a focal challenge in PPRS prevention and control. By integrating metabolomic and lipidomic serum analyses of clinical pig cohorts through a machine learning approach with in vivo and in vitro infection models, lysophosphatidic acid (LPA) is discovered as a serum metabolic biomarker for PRRS virus (PRRSV) clinical diagnosis. PRRSV promoted LPA synthesis by upregulating the autotaxin expression, which causes innate immunosuppression by dampening the retinoic acid-inducible gene I (RIG-I) and type I interferon responses, leading to enhanced virus replication. Targeting LPA demonstrated protection against virus infection and associated disease outcomes in infected pigs, indicating that LPA is a novel antiviral target against PRRSV. This study lays a foundation for clinical prevention and control of PRRSV infections.
作为一种重要的家畜传染病,猪繁殖与呼吸综合征(PRRS)给养猪业造成了巨大的经济损失。鉴定诊断标志物和治疗靶点一直是 PRRS 预防和控制的焦点挑战。本研究通过整合临床猪群的代谢组学和脂质组学血清分析,采用机器学习方法与体内和体外感染模型相结合,发现溶血磷脂酸(LPA)是 PRRS 病毒(PRRSV)临床诊断的血清代谢标志物。PRRSV 通过上调自分泌酶(autotaxin)的表达来促进 LPA 的合成,自分泌酶(autotaxin)的表达会通过抑制视黄酸诱导基因 I(RIG-I)和 I 型干扰素反应来导致先天免疫抑制,从而导致病毒复制增强。靶向 LPA 可在感染猪中针对病毒感染和相关疾病结果提供保护,表明 LPA 是针对 PRRSV 的新型抗病毒靶标。本研究为 PRRSV 感染的临床预防和控制奠定了基础。