Falendysz Elizabeth A, Lopera Juan G, Lorenzsonn Faye, Salzer Johanna S, Hutson Christina L, Doty Jeffrey, Gallardo-Romero Nadia, Carroll Darin S, Osorio Jorge E, Rocke Tonie E
U.S. Geological Survey-National Wildlife Health Center, Madison, Wisconsin, United States of America.
Department of Pathobiological Science, School of Veterinary Medicine, University of Wisconsin, Madison, Wisconsin, United States of America.
PLoS Negl Trop Dis. 2015 Oct 30;9(10):e0004130. doi: 10.1371/journal.pntd.0004130. eCollection 2015.
Monkeypox is a zoonosis clinically similar to smallpox in humans. Recent evidence has shown a potential risk of increased incidence in central Africa. Despite attempts to isolate the virus from wild rodents and other small mammals, no reservoir host has been identified. In 2003, Monkeypox virus (MPXV) was accidentally introduced into the U.S. via the pet trade and was associated with the Gambian pouched rat (Cricetomys gambianus). Therefore, we investigated the potential reservoir competence of the Gambian pouched rat for MPXV by utilizing a combination of in vivo and in vitro methods. We inoculated three animals by the intradermal route and three animals by the intranasal route, with one mock-infected control for each route. Bioluminescent imaging (BLI) was used to track replicating virus in infected animals and virological assays (e.g. real time PCR, cell culture) were used to determine viral load in blood, urine, ocular, nasal, oral, and rectal swabs. Intradermal inoculation resulted in clinical signs of monkeypox infection in two of three animals. One severely ill animal was euthanized and the other affected animal recovered. In contrast, intranasal inoculation resulted in subclinical infection in all three animals. All animals, regardless of apparent or inapparent infection, shed virus in oral and nasal secretions. Additionally, BLI identified viral replication in the skin without grossly visible lesions. These results suggest that Gambian pouched rats may play an important role in transmission of the virus to humans, as they are hunted for consumption and it is possible for MPXV-infected pouched rats to shed infectious virus without displaying overt clinical signs.
猴痘是一种人畜共患病,在临床上与人类天花相似。最近的证据表明,中非存在发病率上升的潜在风险。尽管曾试图从野生啮齿动物和其他小型哺乳动物中分离出该病毒,但尚未确定其储存宿主。2003年,猴痘病毒(MPXV)通过宠物贸易意外传入美国,并与冈比亚有袋大鼠(Cricetomys gambianus)有关。因此,我们通过体内和体外方法相结合,研究了冈比亚有袋大鼠作为MPXV储存宿主的潜在能力。我们通过皮内途径接种了三只动物,通过鼻内途径接种了三只动物,每种途径设置一只假感染对照。利用生物发光成像(BLI)追踪感染动物体内复制的病毒,并通过病毒学检测(如实时PCR、细胞培养)确定血液、尿液、眼、鼻、口腔和直肠拭子中的病毒载量。皮内接种导致三只动物中有两只出现猴痘感染的临床症状。一只重病动物被安乐死,另一只受感染动物康复。相比之下,鼻内接种导致所有三只动物出现亚临床感染。所有动物,无论明显感染还是隐性感染,口腔和鼻腔分泌物中均排出病毒。此外,BLI在皮肤中发现了病毒复制,但没有明显可见的病变。这些结果表明,冈比亚有袋大鼠可能在将病毒传播给人类方面发挥重要作用,因为它们被猎杀以供食用,而且感染MPXV的有袋大鼠可能在不表现出明显临床症状的情况下排出传染性病毒。