Bailey Adam L, Lauck Michael, Ghai Ria R, Nelson Chase W, Heimbruch Katelyn, Hughes Austin L, Goldberg Tony L, Kuhn Jens H, Jasinska Anna J, Freimer Nelson B, Apetrei Cristian, O'Connor David H
Department of Pathology and Laboratory Medicine, University of Wisconsin-Madison, Madison, Wisconsin, USA.
Wisconsin National Primate Research Center, Madison, Wisconsin, USA.
J Virol. 2016 Jul 11;90(15):6724-6737. doi: 10.1128/JVI.00573-16. Print 2016 Aug 1.
Nonhuman primates (NHPs) are a historically important source of zoonotic viruses and are a gold-standard model for research on many human pathogens. However, with the exception of simian immunodeficiency virus (SIV) (family Retroviridae), the blood-borne viruses harbored by these animals in the wild remain incompletely characterized. Here, we report the discovery and characterization of two novel simian pegiviruses (family Flaviviridae) and two novel simian arteriviruses (family Arteriviridae) in wild African green monkeys from Zambia (malbroucks [Chlorocebus cynosuros]) and South Africa (vervet monkeys [Chlorocebus pygerythrus]). We examine several aspects of infection, including viral load, genetic diversity, evolution, and geographic distribution, as well as host factors such as age, sex, and plasma cytokines. In combination with previous efforts to characterize blood-borne RNA viruses in wild primates across sub-Saharan Africa, these discoveries demonstrate that in addition to SIV, simian pegiviruses and simian arteriviruses are widespread and prevalent among many African cercopithecoid (i.e., Old World) monkeys.
Primates are an important source of viruses that infect humans and serve as an important laboratory model of human virus infection. Here, we discover two new viruses in African green monkeys from Zambia and South Africa. In combination with previous virus discovery efforts, this finding suggests that these virus types are widespread among African monkeys. Our analysis suggests that one of these virus types, the simian arteriviruses, may have the potential to jump between different primate species and cause disease. In contrast, the other virus type, the pegiviruses, are thought to reduce the disease caused by human immunodeficiency virus (HIV) in humans. However, we did not observe a similar protective effect in SIV-infected African monkeys coinfected with pegiviruses, possibly because SIV causes little to no disease in these hosts.
非人灵长类动物(NHPs)一直是重要的人畜共患病毒来源,也是许多人类病原体研究的金标准模型。然而,除了猿猴免疫缺陷病毒(SIV)(逆转录病毒科)外,这些野生动物携带的血源病毒仍未得到充分表征。在此,我们报告了在赞比亚(绿猴[Chlorocebus cynosuros])和南非(黑长尾猴[Chlorocebus pygerythrus])的野生非洲绿猴中发现并鉴定了两种新型猿猴pegiviruses病毒(黄病毒科)和两种新型猿猴动脉炎病毒(动脉炎病毒科)。我们研究了感染的几个方面,包括病毒载量、遗传多样性、进化和地理分布,以及宿主因素,如年龄、性别和血浆细胞因子。结合此前在撒哈拉以南非洲野生灵长类动物中表征血源RNA病毒的努力,这些发现表明,除了SIV外,猿猴pegiviruses病毒和猿猴动脉炎病毒在许多非洲猕猴(即旧世界猴)中广泛存在且普遍流行。
灵长类动物是感染人类的病毒的重要来源,也是人类病毒感染的重要实验室模型。在此,我们在来自赞比亚和南非的非洲绿猴中发现了两种新病毒。结合此前的病毒发现工作,这一发现表明这些病毒类型在非洲猴子中广泛存在。我们的分析表明,其中一种病毒类型,即猿猴动脉炎病毒,可能有在不同灵长类物种之间传播并引发疾病的潜力。相比之下,另一种病毒类型,即pegiviruses病毒,被认为可减轻人类免疫缺陷病毒(HIV)在人类中引起的疾病。然而,我们在感染SIV的非洲猴子与pegiviruses病毒共感染时未观察到类似的保护作用,可能是因为SIV在这些宿主中几乎不引起疾病。