Botten Jason, Mirowsky Katy, Ye Chunyan, Gottlieb Keith, Saavedra Melissa, Ponce Liana, Hjelle Brian
Infectious Diseases and Inflammation Program and Departments of Pathology, University of New Mexico, Albuquerque, New Mexico 87131, USA.
J Virol. 2002 Aug;76(15):7587-94. doi: 10.1128/jvi.76.15.7587-7594.2002.
The mechanism(s) by which Sin Nombre (SN) hantavirus is maintained in deer mouse populations is unclear. Field studies indicate that transmission occurs primarily if not exclusively via a horizontal mechanism. Using an experimental deer mouse infection model in an outdoor laboratory, we tested whether infected rodents shed SN virus in urine, feces, and saliva, whether infected mice transmit infection to naïve cage mates, and whether infected dams are able to vertically transmit virus or antibody to offspring. Using pooled samples of urine, feces, and saliva collected from mice infected 8 to 120 days postinoculation (p.i.), we found that a subset of saliva samples, collected between 15 and 90 days p.i., contained viral RNA. Parallel studies conducted on wild-caught, naturally infected deer mice showed a similar pattern of intermittent positivity, also only in saliva samples. Attempts to isolate virus through inoculation of cells or naïve deer mice with the secreta or excreta of infected mice were uniformly negative. Of 54 attempts to transmit infection by cohousing infected deer mice with seronegative cage mates, we observed only a single case of transmission, which occurred between 29 and 42 days p.i. Dams passively transferred antibodies to neonatal pups via milk, and those antibodies persisted for at least 2 months after weaning, but none transmitted infection to their pups. Compared to other hantavirus models, SN virus is shed less efficiently and transmits inefficiently among cage mates. Transmission of SN virus among reservoir rodents may require factors that are not required for other hantaviruses.
辛诺柏(SN)汉坦病毒在鹿鼠种群中得以维持的机制尚不清楚。野外研究表明,即便传播并非完全通过水平传播机制,但其传播主要是通过该机制。在户外实验室中,我们使用实验性鹿鼠感染模型,测试了受感染的啮齿动物是否通过尿液、粪便和唾液排出SN病毒,受感染的小鼠是否将感染传播给未感染的同笼伙伴,以及受感染的母鼠是否能够将病毒或抗体垂直传播给后代。我们使用接种后8至120天(p.i.)从受感染小鼠收集的尿液、粪便和唾液混合样本,发现接种后15至90天收集的一部分唾液样本含有病毒RNA。对野生捕获的自然感染鹿鼠进行的平行研究显示出类似的间歇性阳性模式,同样仅在唾液样本中出现。通过用受感染小鼠的分泌物或排泄物接种细胞或未感染的鹿鼠来分离病毒的尝试均呈阴性。在54次将受感染的鹿鼠与血清阴性的同笼伙伴同笼饲养以传播感染的尝试中,我们仅观察到1例传播病例,发生在接种后29至42天。母鼠通过乳汁将抗体被动转移给新生幼崽,这些抗体在断奶后至少持续2个月,但没有一只母鼠将感染传播给幼崽。与其他汉坦病毒模型相比,SN病毒的排出效率较低,在同笼伙伴之间的传播效率也较低。SN病毒在储存宿主啮齿动物之间的传播可能需要其他汉坦病毒不需要的因素。