A virus associated with the zoonotic pathogen Plasmodium knowlesi causing human malaria is a member of a diverse and unclassified viral taxon.

IF 5.5 2区 医学 Q1 VIROLOGY
Virus Evolution Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.1093/ve/veae091
Mary E Petrone, Justine Charon, Matthew J Grigg, Timothy William, Giri S Rajahram, Jacob Westaway, Kim A Piera, Mang Shi, Nicholas M Anstey, Edward C Holmes
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引用次数: 0

Abstract

The Apicomplexa are a phylum of single-celled eukaryotes that can infect humans and include the mosquito-borne parasite Plasmodium, the cause of malaria. Viruses that infect non-Plasmodium spp. disease-causing protozoa affect the pathogen life cycle and disease outcomes. However, only one RNA virus (Matryoshka RNA virus 1) has been identified in Plasmodium, and none have been identified in zoonotic Plasmodium species. The rapid expansion of the known RNA virosphere via metagenomic sequencing suggests that this dearth is due to the divergent nature of RNA viruses that infect protozoa. We leveraged newly uncovered data sets to explore the virome of human-infecting Plasmodium species collected in Sabah, east (Borneo) Malaysia. From this, we identified a highly divergent RNA virus in two human-infecting P. knowlesi isolates that is related to the unclassified group 'ormycoviruses'. By characterizing 15 additional ormycoviruses identified in the transcriptomes of arthropods, we show that this group of viruses exhibits a complex ecology as noninfecting passengers at the arthropod-mammal interface. With the addition of viral diversity discovered using the artificial intelligence-based analysis of metagenomic data, we also demonstrate that the ormycoviruses are part of a diverse and unclassified viral taxon. This is the first observation of an RNA virus in a zoonotic Plasmodium species. By linking small-scale experimental data to advances in large-scale virus discovery, we characterize the diversity and confirm the putative genomic architecture of an unclassified viral taxon. This approach can be used to further explore the virome of disease-causing Apicomplexa and better understand how protozoa-infecting viruses may affect parasite fitness, pathobiology, and treatment outcomes.

与引起人类疟疾的人畜共患病原体诺氏疟原虫相关的一种病毒是一个多样化且未分类的病毒分类群的成员。
顶复合体是单细胞真核生物的一个门,可以感染人类,包括蚊子传播的寄生虫疟原虫,疟疾的病因。感染非疟原虫致病原生动物的病毒会影响病原体的生命周期和疾病结果。然而,在疟原虫中只鉴定出一种RNA病毒(1型套氏RNA病毒),而在人畜共患疟原虫中未发现任何病毒。通过宏基因组测序,已知RNA病毒圈的迅速扩大表明,这种缺乏是由于感染原生动物的RNA病毒的不同性质造成的。我们利用新发现的数据集来探索在马来西亚东部(婆罗洲)沙巴收集的人类感染疟原虫物种的病毒组。由此,我们在两个感染人类的诺氏疟原虫分离株中发现了一种高度分化的RNA病毒,该病毒与未分类的“或分枝病毒”群有关。通过表征节肢动物转录组中鉴定的另外15种或分枝病毒,我们表明这组病毒作为节肢动物-哺乳动物界面的非感染乘客表现出复杂的生态。随着使用基于人工智能的宏基因组数据分析发现的病毒多样性的增加,我们也证明了或分枝病毒是多样化和未分类的病毒分类群的一部分。这是首次在人畜共患疟原虫物种中观察到RNA病毒。通过将小规模实验数据与大规模病毒发现的进展联系起来,我们表征了多样性并确认了一个未分类病毒分类群的假定基因组结构。该方法可用于进一步探索致病顶复虫的病毒组,并更好地了解感染原生动物的病毒如何影响寄生虫的适应性、病理生物学和治疗效果。
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来源期刊
Virus Evolution
Virus Evolution Immunology and Microbiology-Microbiology
CiteScore
10.50
自引率
5.70%
发文量
108
审稿时长
14 weeks
期刊介绍: Virus Evolution is a new Open Access journal focusing on the long-term evolution of viruses, viruses as a model system for studying evolutionary processes, viral molecular epidemiology and environmental virology. The aim of the journal is to provide a forum for original research papers, reviews, commentaries and a venue for in-depth discussion on the topics relevant to virus evolution.
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