Suzuki Nobuhiro, Maruyama Kazuyuki, Moriyama Miho, Nuss Donald L
Agrivirology Laboratory, Research Institute for Bioresources, Okayama University, Kurashiki, Okayama 710-0046, Japan.
J Virol. 2003 Nov;77(21):11697-707. doi: 10.1128/jvi.77.21.11697-11707.2003.
The prototypic hypovirus CHV1-EP713 attenuates virulence (hypovirulence) and alters several physiological processes of the chestnut blight fungus Cryphonectria parasitica. The papain-like protease, p29, and the highly basic protein, p40, derived, respectively, from the N-terminal and C-terminal portions of the CHV1-EP713-encoded open reading frame (ORF) A polyprotein, p69, both contribute to reduced pigmentation and sporulation. The p29 coding region was shown to suppress pigmentation and asexual sporulation in the absence of virus infection in transformed C. parasitica, whereas transformants containing the p40-coding domain exhibited a wild-type, untransformed phenotype. Deletion of either p29 or p40 from the viral genome also results in reduced accumulation of viral RNA. We now show that p29, but not p40, functions in trans to enhance genomic RNA accumulation and vertical transmission of p29 deletion mutant viruses. The frequency of virus transmission through conidia was found to decrease with reduced accumulation of viral genomic double-stranded RNA (dsRNA): from almost 100% for wild-type virus to approximately 50% for Deltap29, and 10 to 20% for Deltap69. When expressed from a chromosomally integrated cDNA copy, p29 elevated viral dsRNA accumulation and transmission for Deltap29 mutant virus to the level shown by wild-type virus. Increased viral RNA accumulation levels were also observed for a Deltap69 mutant lacking almost the entire ORF A sequence. Such enhancements were not detected in transgenic fungal colonies expressing p40. Mutation of p29 residues Cys(70) or Cys(72), strictly conserved in hypovirus p29 and potyvirus HC-Pro, resulted in the loss of both p29-mediated suppressive activity in virus-free transgenic C. parasitica and in trans enhancement of RNA accumulation and transmission, suggesting a linkage between these functional activities. These results suggest that p29 is an enhancer of viral dsRNA accumulation and vertical virus transmission through asexual spores.
原型低毒病毒CHV1-EP713可减弱毒力(低毒性),并改变栗疫病菌寄生隐孢壳菌的多个生理过程。分别源自CHV1-EP713编码的开放阅读框(ORF)A多聚蛋白N端和C端部分的类木瓜蛋白酶p29和高碱性蛋白p40,均有助于减少色素沉着和孢子形成。在转化的寄生隐孢壳菌中,p29编码区在无病毒感染时可抑制色素沉着和无性孢子形成,而含有p40编码域的转化体表现出野生型、未转化的表型。从病毒基因组中删除p29或p40也会导致病毒RNA积累减少。我们现在表明,p29而非p40可通过反式作用增强基因组RNA积累以及p29缺失突变病毒的垂直传播。发现病毒通过分生孢子传播的频率随病毒基因组双链RNA(dsRNA)积累减少而降低:野生型病毒几乎为100%,Δp29为约50%,Δp69为10%至20%。当从染色体整合的cDNA拷贝表达时,p29将Δp29突变病毒的病毒dsRNA积累和传播提高到野生型病毒所示水平。对于几乎缺失整个ORF A序列的Δp69突变体,也观察到病毒RNA积累水平增加。在表达p40的转基因真菌菌落中未检测到这种增强作用。低毒病毒p29和马铃薯Y病毒HC-Pro中严格保守的p29残基Cys(70)或Cys(72)发生突变,导致在无病毒的转基因寄生隐孢壳菌中p29介导的抑制活性丧失,以及在反式作用中RNA积累和传播增强,这表明这些功能活性之间存在联系。这些结果表明,p29是病毒dsRNA积累以及通过无性孢子进行病毒垂直传播的增强因子。