Rodio Maria-Elena, Delgado Sonia, Flores Ricardo, Serio Francesco Di
Dipartimento di Protezione delle Piante e Microbiologia Applicata, Università degli Studi and Istituto di Virologia Vegetale del CNR, Sezione di Bari, Via Amendola 165/A, 70126 Bari, Italy.
Instituto de Biología Molecular y Celular de Plantas (UPV-CSIC), Universidad Politécnica de Valencia, 46022 Valencia, Spain.
J Gen Virol. 2006 Jan;87(Pt 1):231-240. doi: 10.1099/vir.0.81356-0.
Previous characterization of Peach latent mosaic viroid (PLMVd) variants from a single peach calico (PC) isolate showed that PC symptoms are induced by variants with a 12-13 nt insertion at a specific position and folding into a hairpin with a U-rich loop. Here, this study was extended to two other PC isolates. PLMVd variants with insertions similar to those reported previously (type 1), predominated in one isolate (PC-P2). The second (PC-P1), in addition to these variants, contained others with insertions in the same position and of the same size, but with the hairpin capped by a GA-rich loop (type 2). When symptomatic and non-symptomatic tissues from both isolates were used to inoculate GF-305 peach seedlings, they reproduced the phenotype of the inoculum source, indicating that variants differing in pathogenicity are unevenly distributed within single plants. Moreover, characterization of the progeny from inoculations with the PC-P1 source showed that variants with insertions of type 1 and 2 were predominant in the symptomatic and non-symptomatic seedlings, respectively, confirming the association between PC and variants with type 1 but not type 2 insertions. Inoculations with dimeric in vitro transcripts from PLMVd variants with type 1, type 2 and with a chimeric insertion showed that the variant with type 2 insertion was latent and established that the U-rich capping loop has a major role in PC, although the adjacent stem may also have some influence. Insertions can be acquired and lost during infection, suggesting that latent variants can evolve into pathogenic variants and vice versa.
先前对来自单个桃杂色叶病(PC)分离株的桃潜隐花叶类病毒(PLMVd)变体的特征分析表明,PC症状是由在特定位置有12 - 13个核苷酸插入并折叠成富含U环的发夹结构的变体诱导的。在此,本研究扩展到另外两个PC分离株。在一个分离株(PC - P2)中,与先前报道的具有相似插入序列的PLMVd变体(1型)占主导。在第二个分离株(PC - P1)中,除了这些变体之外,还包含其他在相同位置有相同大小插入但发夹结构由富含GA环封端的变体(2型)。当使用来自这两个分离株的有症状和无症状组织接种GF - 305桃树苗时,它们再现了接种源的表型,表明致病性不同的变体在单株植物内分布不均。此外,对来自PC - P1源接种后代的特征分析表明,有症状和无症状幼苗中分别以1型和2型插入变体为主,证实了PC与1型而非2型插入变体之间的关联。用来自1型、2型PLMVd变体以及嵌合插入的二聚体体外转录本进行接种表明,2型插入变体是潜伏性的,并确定富含U的封端环在PC中起主要作用,尽管相邻的茎也可能有一些影响。插入在感染过程中可以获得和丢失,这表明潜伏性变体可以演变成致病性变体,反之亦然。