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Genome Sequence, Full-Length Infectious cDNA Clone, and Mapping of Viral Double-Stranded RNA Accumulation Determinant of Hypovirus CHV1-EP721▿

机译:慢病毒CHV1-EP721的基因组序列,全长感染性cDNA克隆以及病毒双链RNA累积决定子的定位

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摘要

Cryphonectria parasitica strain EP721 is infected with a strain of hypovirus CHV1, CHV1-EP721, and exhibits typical hypovirulence-associated traits such as reduced pigmentation and reduced asexual sporulation. However, the accumulation of the viral double-stranded RNA (dsRNA) in this hypovirus-infected C. parasitica strain is atypically low. We now report the complete nucleotide sequence and construction of a full-length infectious cDNA clone for hypovirus CHV1-EP721. The genome sequence of CHV1-EP721 was determined to be 12,724 bp in length and to share extensive homology with two other hypovirus strains, CHV1-Euro7 and CHV1-EP713, with an average of 99% and 90% identities at the nucleotide level and 99% and 92% identities at the amino acid level, respectively. CHV1-EP721 was successfully introduced into virus-free fungal host strain EP721(-v) by transfection with transcripts derived from a full-length viral cDNA. The transfected strain had a phenotype indistinguishable from that of EP721, and the accumulation of CHV1-EP721 dsRNA in the transfectant was lower than those transfected by CHV1-Euro7 and CHV1-EP713 transcripts. Through the construction of chimeric viruses by domain swapping using infectious cDNA clones of CHV1-EP721, CHV1-EP713, and CHV1-Euro7 hypoviruses, the determinant for the low level of viral dsRNA accumulation in CHV1-EP721 was mapped to the second of two CHV1-EP721 open reading frames (ORFs), ORF B. Further refined swapping of domains within ORF B identified a 2.5-kb coding region between p48 and the polymerase domain of CHV1-EP721 as being responsible for the low viral dsRNA accumulation. Evidence is also provided that low rates of hypovirus transmission through conidial spores correlates with low viral dsRNA accumulation.
机译:寄生性隐孢子虫菌株EP721感染了次病毒CHV1,CHV1-EP721菌株,并表现出典型的与低毒力相关的性状,例如色素沉着减少和无性孢子形成减少。但是,在这种经次病毒感染的寄生虫梭状芽胞杆菌菌株中病毒双链RNA(dsRNA)的积累非典型地低。我们现在报告完整的核苷酸序列,并为慢病毒CHV1-EP721构建全长感染性cDNA克隆。已确定CHV1-EP721的基因组序列长度为12,724 bp,并与其他两种低毒病毒株CHV1-Euro7和CHV1-EP713具有广泛的同源性,在核苷酸水平上的平均同一性为99%和90%。分别在氨基酸水平上的%同一性和92%同一性。通过用衍生自全长病毒cDNA的转录本转染,将CHV1-EP721成功导入无病毒的真菌宿主菌株EP721(-v)。转染的菌株具有与EP721不能区别的表型,并且CHV1-EP721 dsRNA在转染子中的积累低于通过CHV1-Euro7和CHV1-EP713转录本转染的菌株。通过使用CHV1-EP721,CHV1-EP713和CHV1-Euro7次流感病毒的感染性cDNA克隆通过域交换构建嵌合病毒,CHV1-EP721中低水平病毒dsRNA积累的决定因素被映射到两个CHV1中的第二个-EP721开放阅读框(ORF),ORFB。ORFB中结构域的进一步精细交换确定p48和CHV1-EP721聚合酶结构域之间的2.5 kb编码区是低病毒dsRNA积累的原因。还提供证据表明,通过分生孢子孢子传播的低速病毒与低病毒dsRNA积累有关。

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