National Emerging Infectious Diseases Laboratories Institute, Boston University School of Medicine, Boston, Massachusetts, United States of America.
PLoS One. 2010 May 18;5(5):e10690. doi: 10.1371/journal.pone.0010690.
Nipah virus (NiV) is an enigmatic emerging pathogen that causes severe and often fatal neurologic and/or respiratory disease in both animals and humans. Amongst people, case fatality rates range between 40 and 75 percent and there are no vaccines or treatments approved for human use. Guinea pigs, hamsters, cats, ferrets, pigs and most recently squirrel monkeys (New World monkey) have been evaluated as animal models of human NiV infection, and with the exception of the ferret, no model recapitulates all aspects of NiV-mediated disease seen in humans. To identify a more viable nonhuman primate (NHP) model, we examined the pathogenesis of NiV in African green monkeys (AGM). Exposure of eight monkeys to NiV produced a severe systemic infection in all eight animals with seven of the animals succumbing to infection. Viral RNA was detected in the plasma of challenged animals and occurred in two of three subjects as a peak between days 7 and 21, providing the first clear demonstration of plasma-associated viremia in NiV experimentally infected animals and suggested a progressive infection that seeded multiple organs simultaneously from the initial site of virus replication. Unlike the cat, hamster and squirrel monkey models of NiV infection, severe respiratory pathology, neurological disease and generalized vasculitis all manifested in NiV-infected AGMs, providing an accurate reflection of what is observed in NiV-infected humans. Our findings demonstrate the first consistent and highly pathogenic NHP model of NiV infection, providing a new and critical platform in the evaluation and licensure of either passive and active immunization or therapeutic strategies for human use.
亨德拉病毒(NiV)是一种神秘的新兴病原体,可导致动物和人类发生严重且常致命的神经和/或呼吸道疾病。在人群中,病死率在 40%至 75%之间,目前尚无获准用于人类的疫苗或治疗方法。豚鼠、仓鼠、猫、雪貂、猪和最近的松鼠猴(新世界猴)已被评估为人类 NiV 感染的动物模型,但除了雪貂之外,没有一种模型能重现人类 NiV 感染的所有方面。为了确定更可行的非人类灵长类动物(NHP)模型,我们研究了 NiV 在绿长尾猴(AGM)中的发病机制。八只猴子接触 NiV 后,所有八只动物均发生严重全身感染,其中七只动物因感染而死亡。挑战动物的血浆中检测到病毒 RNA,其中三分之二的动物在第 7 天至 21 天之间出现峰值,这首次明确证明了 NiV 实验感染动物的血浆相关病毒血症,并提示了一种从最初的病毒复制部位同时感染多个器官的进行性感染。与 NiV 感染的猫、仓鼠和松鼠猴模型不同,严重的呼吸道病理、神经疾病和全身性血管炎均在 NiV 感染的 AGM 中表现出来,准确反映了 NiV 感染人类的情况。我们的研究结果表明,这是 NiV 感染的首个一致且高致病性的 NHP 模型,为评估和批准被动和主动免疫或治疗策略用于人类提供了一个新的关键平台。