A capsidless (+)RNA yadokarivirus hosted by a dsRNA virus is infectious as particles, cDNA, and dsRNA.

IF 3.8 2区 医学 Q2 VIROLOGY Journal of Virology Pub Date : 2025-03-18 Epub Date: 2025-02-13 DOI:10.1128/jvi.02166-24
Muhammad Fadli, Sakae Hisano, Guy Novoa, José R Castón, Hideki Kondo, Nobuhiro Suzuki
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Abstract

Capsidless yadokariviruses (members of the order Yadokarivirales) with (+)RNA genomes divert the capsid of their partner icosahedral double-stranded RNA (dsRNA) viruses in different families of the order Ghabrivirales into the replication site. A yadokarivirus, AfSV2, has been reported from a German strain of the ascomycete fungus Aspergillus foetidus coinfected by two dsRNA viruses, a victorivirus (AfSV1, family Pseudototiviridae) and an alternavirus (AfFV, family Alternaviridae). Here, we identified AfSV1 as the partner of AfSV2 in a Japanese A. foetidus strain after showing the infectiousness of AfSV2 in three forms: virus particles (heterocapsid), transforming full-length complementary DNA (cDNA), and purified replicated form (RF) dsRNA that is believed to be inactive as a translational template. Virion transfection of virus-free A. foetidus protoplasts resulted in the generation of two strains infected either by AfSV1 alone or by both AfSV1 and AfSV2. Transformants with AfSV2 full-length cDNA launched AfSV2 infection only in the presence of AfSV1, but not those with AfSV2 RNA-directed RNA polymerase mutant cDNA. The purified fractions containing AfSV2 RF dsRNA also launched infection when transfected into protoplasts infected by AfSV1. Treatment with dsRNA-specific RNase III, but not with proteinase K, S1 nuclease, or DNase I, abolished the infectivity of AfSV2 RF dsRNA. Furthermore, we confirmed the infectiousness of gel-purified AfSV2 RF dsRNA in the presence of AfSV1. Taken together, our results show the unique infectious entity of AfSV2 and the expansion of yadokarivirus partners in the family Pseudototiviridae and provide interesting evolutionary insights.IMPORTANCEThe viral phylum Pisuviricota accommodates members with both double-stranded RNA (dsRNA) and (+)RNA genomes. Some members of the second group display peculiar virus lifestyles. These include (+)RNA yadkariviruses, which are capsidless and highjack the capsid of their partner dsRNA viruses in the order Ghabrivirales of a different phylum Duplornaviricota. We identified the partner dsRNA virus (AfSV1, a victorivirus) of a yadokarivirus (AfSV2) from the ascomycete Aspergillus foetidus. AfSV2 is infectious in the presence of AfSV1 in three forms: purified particles, transforming full-length complementary DNA, and, surprisingly, the purified replicative form dsRNA. These combined results expand yadokarivirus partner viruses to the family Pseudototiviridae and provide evidence for AfSV2 as a unique infectious entity as well as interesting evolutionary insights.

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一种由dsRNA病毒宿主的无衣壳(+)RNA崖粒病毒作为颗粒、cDNA和dsRNA具有传染性。
具有(+)RNA基因组的无衣壳yadokarivirae病毒(yadokarivirae目成员)将其不同亚麻布目科伙伴二十面体双链RNA (dsRNA)病毒的衣壳转移到复制位点。一种由两种dsRNA病毒(维多利亚病毒(AfSV1,假假病毒科)和替代病毒(AfFV,替代病毒科)共同感染的子囊菌真菌胎儿曲霉德国菌株中发现了一种yadokarivirus, AfSV2。在此,我们通过三种形式确定了AfSV2的感染性,即病毒颗粒(异衣壳)、转化全长互补DNA (cDNA)和纯化的复制形式(RF) dsRNA,该复制形式被认为是无活性的翻译模板,从而确定了AfSV1是日本a . foetidus菌株中AfSV2的伴侣。用病毒粒子转染脱毒的原质体可产生两种菌株,一种是单独感染AfSV1,另一种是同时感染AfSV1和AfSV2。携带AfSV2全长cDNA的转化子仅在AfSV1存在的情况下启动了AfSV2感染,而携带AfSV2 RNA定向RNA聚合酶突变cDNA的转化子则不启动。将含有AfSV2 RF dsRNA的纯化组分转染到被AfSV1感染的原生质体中,也能启动感染。用dsRNA特异性RNase III治疗,而不是用蛋白酶K、S1核酸酶或DNase I治疗,可以消除AfSV2 RF dsRNA的感染性。此外,我们证实了凝胶纯化的AfSV2 RF dsRNA在存在AfSV1的情况下具有传染性。综上所述,我们的研究结果显示了AfSV2的独特感染实体和假托病毒科中yadokarivirus伙伴的扩展,并提供了有趣的进化见解。病毒门Pisuviricota容纳双链RNA (dsRNA)和(+)RNA基因组的成员。第二组的一些成员表现出特殊的病毒生活方式。这些病毒包括(+)RNA yadkarivirus,它们是无衣壳的,并劫持它们的伙伴dsRNA病毒的衣壳。我们鉴定出子囊菌胎儿曲霉芽胞病毒(AfSV2)的伴侣dsRNA病毒(AfSV1,一种维多利亚病毒)。在AfSV1存在的情况下,AfSV2以三种形式具有传染性:纯化颗粒,转化全长互补DNA,以及令人惊讶的纯化复制形式dsRNA。这些综合结果将yadokarivirus伴侣病毒扩展到假托病毒科,并为AfSV2作为一种独特的感染实体以及有趣的进化见解提供了证据。
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来源期刊
Journal of Virology
Journal of Virology 医学-病毒学
CiteScore
10.10
自引率
7.40%
发文量
906
审稿时长
1 months
期刊介绍: Journal of Virology (JVI) explores the nature of the viruses of animals, archaea, bacteria, fungi, plants, and protozoa. We welcome papers on virion structure and assembly, viral genome replication and regulation of gene expression, genetic diversity and evolution, virus-cell interactions, cellular responses to infection, transformation and oncogenesis, gene delivery, viral pathogenesis and immunity, and vaccines and antiviral agents.
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