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6K1-CI 区的单个氨基酸变化可以促进李和烟草传播李痘病毒 C 分离物对任一宿主的替代适应。

Single amino acid changes in the 6K1-CI region can promote the alternative adaptation of Prunus- and Nicotiana-propagated Plum pox virus C isolates to either host.

出版信息

Mol Plant Microbe Interact. 2014 Feb;27(2):136-49. doi: 10.1094/MPMI-08-13-0242-R.

DOI:10.1094/MPMI-08-13-0242-R
PMID:24200075
Abstract

Plum pox virus (PPV) C is one of the less common PPV strains and specifically infects cherry trees in nature. Making use of two PPV-C isolates that display different pathogenicity features, i.e., SwCMp, which had been adapted to Nicotiana species, and BY101, which had been isolated from cherry rootstock L2 (Prunus lannesiana) and propagated only in cherry species, we have generated two infective full-length cDNA clones in order to determine which viral factors are involved in the adaptation to each host. According to our results, the C-P3(PIPO)/6K1/N-CI (cylindrical inclusion) region contains overlapping but not coincident viral determinants involved in symptoms development, local viral amplification, and systemic movement capacity. Amino acid changes in this region promoting the adaptation to N. benthamiana or P. avium have trade-off effects in the alternative host. In both cases, adaptation can be achieved through single amino acid changes in the NIapro protease recognition motif between 6K1 and CI or in nearby sequences. Thus, we hypothesize that the potyvirus polyprotein processing could depend on specific host factors and the adaptation of PPV-C isolates to particular hosts relies on a fine regulation of the proteolytic cleavage of the 6K1-CI junction.

摘要

李痘病毒(PPV)C 是较少见的 PPV 株系之一,其在自然界中特异性侵染樱桃树。利用两个具有不同致病性特征的 PPV-C 分离株,即 SwCMp,其已适应烟属植物,和 BY101,其从樱桃砧木 L2(李属)中分离出来且仅在樱桃属中繁殖,我们生成了两个感染性全长 cDNA 克隆,以确定哪些病毒因子参与适应各自的宿主。根据我们的结果,C-P3(PIPO)/6K1/N-CI(圆柱包含体)区域包含重叠但不相同的病毒决定因素,涉及症状发展、局部病毒扩增和系统运动能力。该区域中的氨基酸变化促进了对 N. benthamiana 或 P. avium 的适应,但在替代宿主中具有权衡效应。在这两种情况下,通过在 6K1 和 CI 之间或附近序列中的 NIapro 蛋白酶识别基序中的单个氨基酸变化,可以实现适应。因此,我们假设,马铃薯 Y 病毒属多蛋白加工可能依赖于特定的宿主因子,并且 PPV-C 分离株对特定宿主的适应依赖于 6K1-CI 连接点的蛋白水解切割的精细调节。

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