Jeyachandran Arjit Vijey, Irudayam Joseph Ignatius, Dubey Swati, Chakravarty Nikhil, Daskou Maria, Zaiss Anne, Garcia Gustavo, Konda Bindu, Shah Aayushi, Venkatraman Aditi, Su Baolong, Wang Cheng, Cui Qi, Williams Kevin J, Srikanth Sonal, Kumar Ashok, Shi Yanhong, Deb Arjun, Damoiseaux Robert, Stripp Barry R, Ramaiah Arunachalam, Arumugaswami Vaithilingaraja
Department of Molecular and Medical Pharmacology, University of California, Los Angeles, California, United States of America.
Department of Epidemiology, University of California, Los Angeles, California, United States of America.
PLoS Pathog. 2025 Aug 26;21(8):e1013401. doi: 10.1371/journal.ppat.1013401. eCollection 2025 Aug.
Hantaviruses are zoonotically transmitted from rodents to humans through the respiratory route, with no currently approved antivirals or widely available vaccines. The recent discovery of interhuman-transmitted Andes virus (ANDV) necessitates the systematic identification of cell tropism, infective potential, and potent therapeutic agents. We utilized human primary lung endothelial cells, various pluripotent stem cell-derived heart and brain cell types, and established human lung organoid models to evaluate the tropisms of Old World Hantaan (HTNV) and New World ANDV and Sin Nombre (SNV) viruses. ANDV exhibited broad tropism for all cell types assessed. SNV readily infected pulmonary endothelial cells, while HTNV robustly amplified in endothelial cells, cardiomyocytes, and astrocytes. We also provide the first evidence of hantaviral infection in human 3D distal lung organoids, which effectively modeled these differential tropisms. ANDV infection transcriptionally promoted cell injury and inflammatory responses, and downregulated lipid metabolic pathways in lung epithelial cells. Evaluation of selected drug candidates and pharmacotranscriptomics revealed that the host-directed small molecule compound urolithin B inhibited ANDV infection and restored cellular metabolism with minimal changes in host transcription. Given the scarcity of academic BSL-4 facilities that enable in vivo hantaviral studies, this investigation presents advanced human cell-based model systems that closely recapitulate host cell tropism and responses to infection, thereby providing critical platforms to evaluate potential antiviral drug candidates.
汉坦病毒通过呼吸道从啮齿动物人畜共患传播给人类,目前尚无获批的抗病毒药物或广泛可用的疫苗。最近发现的人际传播的安第斯病毒(ANDV)使得有必要系统地确定细胞嗜性、感染潜力和有效的治疗药物。我们利用人原代肺内皮细胞、多种多能干细胞衍生的心脏和脑细胞类型,并建立了人肺类器官模型,以评估旧世界的汉滩病毒(HTNV)以及新世界的ANDV和辛诺柏病毒(SNV)的嗜性。ANDV对所有评估的细胞类型均表现出广泛的嗜性。SNV易于感染肺内皮细胞,而HTNV在内皮细胞、心肌细胞和星形胶质细胞中能强劲增殖。我们还提供了汉坦病毒在人三维远端肺类器官中感染的首个证据,该模型有效地模拟了这些不同的嗜性。ANDV感染在转录水平上促进细胞损伤和炎症反应,并下调肺上皮细胞中的脂质代谢途径。对选定候选药物和药物转录组学的评估表明,宿主导向的小分子化合物尿石素B可抑制ANDV感染并恢复细胞代谢,同时宿主转录变化最小。鉴于能够进行体内汉坦病毒研究的生物安全四级学术设施稀缺,本研究提出了先进的基于人类细胞的模型系统,该系统能紧密模拟宿主细胞嗜性和对感染的反应,从而为评估潜在的抗病毒候选药物提供关键平台。