Metagenomic discovery and co-infection of diverse wobbly possum disease viruses and a novel hepacivirus in Australian brushtail possums.

One Health Outlook Pub Date : 2019-12-12 eCollection Date: 2019-01-01 DOI:10.1186/s42522-019-0006-x
Wei-Shan Chang, John-Sebastian Eden, William J Hartley, Mang Shi, Karrie Rose, Edward C Holmes
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引用次数: 20

Abstract

Background: Australian brushtail possums (Trichosurus vulpecula) are an introduced pest species in New Zealand, but native to Australia where they are protected for biodiversity conservation. Wobbly possum disease (WPD) is a fatal neurological disease of Australian brushtail possums described in New Zealand populations that has been associated with infection by the arterivirus (Arteriviridae) wobbly possum disease virus (WPDV-NZ). Clinically, WPD-infected possums present with chronic meningoencephalitis, choroiditis and multifocal neurological symptoms including ataxia, incoordination, and abnormal gait.

Methods: We conducted a retrospective investigation to characterise WPD in native Australian brushtail possums, and used a bulk meta-transcriptomic approach (i.e. total RNA-sequencing) to investigate its potential viral aetiology. PCR assays were developed for case diagnosis and full genome recovery in the face of extensive genetic variation.

Results: We identified genetically distinct lineages of arteriviruses from archival tissues of WPD-infected possums in Australia, termed wobbly possum disease virus AU1 and AU2. Phylogenetically, WPDV-AU1 and WPDV-AU2 shared only ~ 70% nucleotide similarity to each other and the WPDV-NZ strain, suggestive of a relatively ancient divergence. Notably, we also identified a novel and divergent hepacivirus (Flaviviridae) - the first in a marsupial - in both WPD-infected and uninfected possums, indicative of virus co-infection.

Conclusions: We have identified marsupial-specific lineages of arteriviruses in mainland Australia that are genetically distinct from that in New Zealand, in some cases co-infecting animals with a novel hepacivirus. Our study provides new insight into the hidden genetic diversity of arteriviruses, the capacity for virus co-infection, and highlights the utility of meta-transcriptomics for disease investigation in a One Health context.

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多种摇摆负鼠病病毒和一种新型肝病毒在澳大利亚帚尾负鼠中的宏基因组发现和共感染。
背景:澳大利亚帚尾负鼠(Trichosurus vulpecula)是新西兰引进的一种有害生物,但原产于澳大利亚,在澳大利亚受到生物多样性保护。摇摆负鼠病(WPD)是在新西兰种群中描述的澳大利亚刷尾负鼠的一种致命神经系统疾病,与动脉病毒(动脉病毒科)摇摆负鼠病病毒(WPDV-NZ)感染有关。临床上,感染wpd的负鼠表现为慢性脑膜脑炎、脉膜炎和多灶性神经系统症状,包括共济失调、不协调和步态异常。方法:我们进行了回顾性调查,以表征澳大利亚本土刷尾负鼠的WPD,并使用大量元转录组学方法(即总rna测序)来调查其潜在的病毒病因。在广泛的遗传变异面前,开发了病例诊断和全基因组恢复的PCR检测。结果:我们从澳大利亚感染wpd的负鼠档案组织中鉴定出遗传上不同的动脉病毒谱系,称为摇摆负鼠病病毒AU1和AU2。在系统发育上,WPDV-AU1和WPDV-AU2与WPDV-NZ毒株的核苷酸相似性仅为~ 70%,表明两者存在较早的分化。值得注意的是,我们还在wpd感染和未感染的负鼠中发现了一种新的和不同的肝炎病毒(黄病毒科)-首次在有袋类动物中发现,表明病毒共感染。结论:我们已经在澳大利亚大陆发现了有袋动物特有的动脉病毒谱系,它们在遗传上与新西兰的动脉病毒谱系不同,在某些情况下,动物与一种新型肝病毒共同感染。我们的研究为动脉病毒隐藏的遗传多样性、病毒共感染的能力提供了新的见解,并强调了在“同一个健康”背景下,meta转录组学在疾病调查中的应用。
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