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Divergent Simian Arteriviruses Cause Simian Hemorrhagic Fever of Differing Severities in Macaques

机译:猿猴不同的猿猴病毒引起猿猴严重程度不同的猿猴出血热

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ABSTRACT Simian hemorrhagic fever (SHF) is a highly lethal disease in captive macaques. Three distinct arteriviruses are known etiological agents of past SHF epizootics, but only one, simian hemorrhagic fever virus (SHFV), has been isolated in cell culture. The natural reservoir(s) of the three viruses have yet to be identified, but African nonhuman primates are suspected. Eleven additional divergent simian arteriviruses have been detected recently in diverse and apparently healthy African cercopithecid monkeys. Here, we report the successful isolation in MARC-145 cell culture of one of these viruses, Kibale red colobus virus 1 (KRCV-1), from serum of a naturally infected red colobus ( Procolobus [ Piliocolobus ] rufomitratus tephrosceles ) sampled in Kibale National Park, Uganda. Intramuscular (i.m.) injection of KRCV-1 into four cynomolgus macaques ( Macaca fascicularis ) resulted in a self-limiting nonlethal disease characterized by depressive behavioral changes, disturbance in coagulation parameters, and liver enzyme elevations. In contrast, i.m. injection of SHFV resulted in typical lethal SHF characterized by mild fever, lethargy, lymphoid depletion, lymphoid and hepatocellular necrosis, low platelet counts, increased liver enzyme concentrations, coagulation abnormalities, and increasing viral loads. As hypothesized based on the genetic and presumed antigenic distance between KRCV-1 and SHFV, all four macaques that had survived KRCV-1 injection died of SHF after subsequent SHFV injection, indicating a lack of protective heterotypic immunity. Our data indicate that SHF is a disease of macaques that in all likelihood can be caused by a number of distinct simian arteriviruses, although with different severity depending on the specific arterivirus involved. Consequently, we recommend that current screening procedures for SHFV in primate-holding facilities be modified to detect all known simian arteriviruses. IMPORTANCE Outbreaks of simian hemorrhagic fever (SHF) have devastated captive Asian macaque colonies in the past. SHF is caused by at least three viruses of the family Arteriviridae : simian hemorrhagic fever virus (SHFV), simian hemorrhagic encephalitis virus (SHEV), and Pebjah virus (PBJV). Nine additional distant relatives of these three viruses were recently discovered in apparently healthy African nonhuman primates. We hypothesized that all simian arteriviruses are potential causes of SHF. To test this hypothesis, we inoculated cynomolgus macaques with a highly divergent simian arterivirus (Kibale red colobus virus 1 [KRCV-1]) from a wild Ugandan red colobus. Despite being only distantly related to red colobuses, all of the macaques developed disease. In contrast to SHFV-infected animals, KRCV-1-infected animals survived after a mild disease presentation. Our study advances the understanding of an important primate disease. Furthermore, our data indicate a need to include the full diversity of simian arteriviruses in nonhuman primate SHF screening assays.
机译:摘要猿猴出血热(SHF)是圈养猕猴中的一种高度致死性疾病。过去的SHF流行病是已知的三种不同的小动脉病毒,但在细胞培养中仅分离出一种猿猴出血热病毒(SHFV)。三种病毒的天然贮藏库尚未确定,但怀疑是非洲非人类灵长类动物。最近在多样化且看似健康的非洲头足类猕猴中发现了另外11种发散的猿猴小动脉病毒。在这里,我们报道了从一种自然感染的红色疣猴(Procolobus [Piliocolobus] rufomitratus tephrosceles)的血清中,从MARC-145细胞培养物中成功分离出其中一种病毒,即Kibale红疣猴病毒1(KRCV-1)。乌干达公园。肌内(i.m.)注射KRCV-1到四个猕猴(Macaca fascicularis)中导致了一种自限性非致死性疾病,其特征是抑郁行为改变,凝血参数紊乱和肝酶升高。相反,我注射SHFV会导致典型的致命SHF,其特征为轻度发烧,嗜睡,淋巴样耗竭,淋巴样和肝细胞坏死,血小板计数低,肝酶浓度增加,凝血异常和病毒载量增加。根据KRCV-1和SHFV之间的遗传距离和推测的抗原距离进行假设,在随后的SHFV注射后,所有在KRCV-1注射中存活下来的四只猕猴都死于SHF,表明缺乏保护性异型免疫。我们的数据表明,SHF是猕猴的一种疾病,很可能是由许多不同的猿猴小动脉病毒引起的,尽管严重程度取决于所涉及的特定小动脉病毒。因此,我们建议修改目前在灵长类动物收容设施中对SHFV的筛查程序,以检测所有已知的猿猴小动脉病毒。重要事项过去,猿猴出血热(SHF)的爆发毁灭了圈养的亚洲猕猴殖民地。 SHF至少由Arteriviridae家族的三种病毒引起:猿猴出血热病毒(SHFV),猿猴出血性脑炎病毒(SHEV)和Pebjah病毒(PBJV)。最近在明显健康的非洲非人类灵长类动物中发现了这三种病毒的另外9个远亲。我们假设所有猿猴小动脉病毒都是引起SHF的潜在原因。为了检验这一假设,我们用来自野生乌干达红疣猴的高度分化的猿猴小动脉病毒(Kibale红疣猴病毒1 [KRCV-1])接种了猕猴。尽管只与红色的短尾猴有很远的联系,但所有猕猴都患有这种疾病。与SHFV感染动物相反,KRCV-1感染动物在出现轻度疾病后存活。我们的研究提高了对重要的灵长类动物疾病的认识。此外,我们的数据表明有必要在非人类灵长类动物SHF筛选分析中包括猿猴小动脉病毒的全部多样性。

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