Al-Shihi A A, Akhtar S, Khan A J
Department of Crop Sciences, College of Agricultural and Marine Sciences, Sultan Qaboos University, Al-Khod 123, Sultanate of Oman.
Plant Dis. 2014 Apr;98(4):572. doi: 10.1094/PDIS-06-13-0678-PDN.
Petunias (Petunia × hybrida) are the most important ornamental plants in Oman. In 2012, petunias were observed in public parks and airport landscape in Dhofar region with symptoms of upward leaf curling, yellowing and vein clearing, and size reduction in leaves. Almost all plants in the surveyed landscape showed high infestation of Bemisia tabaci and symptoms that suggested infection with a begomovirus. Six symptomatic samples were collected from three different sites. All symptomatic samples were found PCR-positive with diagnostic primers for begomovirus (3) when DNA extracted from infected leaves was used as template. Nucleic acids extracted from the symptomatic leaves were used to amplify circular DNA molecules by rolling circle amplification method. The amplified concatameric products were digested with restriction enzyme PstI, which yielded a product ∼2.8 kb in size. The putative begomovirus fragment was cloned and sequenced in both orientations. Partial sequences of six clones were 99 to 100% similar and thus only two clones, PT-2 and PT-3, were fully sequenced. The whole genomes of both clones were 2,761 bp, and both were deposited in GenBank under accession numbers HF968755 and HF968756 for the isolates PT-2 and PT-3, respectively. Both sequences had six open reading frames; Rep, TrAP, REn, and C4 genes in complementary sense; and CP and V2 genes in virion-sense, typical of the begomovirus genome organization. Upon alignment, the two sequences showed 99.4% nucleotide identity with each other, thus representing isolates of a single begomovirus species. BlastN comparison showed PT-2 and PT-3 from petunia were 94 to 95% identical to the sequences of ChCLV from Oman (JN604490 to JN604500), which were obtained from other hosts. ClustalV multiple sequence alignment showed that isolates PT-2 and PT-3 shared maximum sequence identity of 93.3 and 92.8%, respectively, with an isolate of ChLCV-OM (JN604495). According to ICTV rules for begomoviruses, PT-3 should be considered to be a new strain of ChLCV-OM and PT-2 a variant of the already existing ChLCV-OM strain. We propose the name for this new strain as the "Petunia strain" of Chili leaf curl virus (ChLCV-Pet). Two infectious clones were constructed from the PT-2 and PT-3 sequences, clones as 1.75-genome sequences in a binary vector, suitable for agroinfection to confirm their infectivity. Both clones, PT-2 and PT-3, produced typical leaf curl disease symptoms upon inoculation on petunia 18 days post inoculation. The presence of the same virus in symptomatic field infected and inoculated petunia was confirmed by Southern blot using 650 bp DIG labeled probe prepared from CP region of PT-3 isolate. ChLCV-OM, a monopartite begomovirus, is widely associated with leaf curl disease of tomato and pepper in Oman, with its origin traced to the Indian subcontinent (2). Identification of a new strain of ChLCV from petunia provides evidence of an ongoing rapid evolution of begomoviruses in this region. Although petunia has been tested as an experimental host for some begomoviruses (1,4), this is the first report of petunia as natural host for ChLCV, a begomovirus previously reported in tomato and pepper in Oman. References: (1) Cui et al. J. Virol. 78:13966, 2004. (2) Khan et al. Virus Res. 177:87, 2013. (3) Khan et al. Plant Dis. 97:1396, 2013. (4) Urbino et al. Arch. Virol. 149:417, 2003.
矮牵牛(Petunia × hybrida)是阿曼最重要的观赏植物。2012年,在佐法尔地区的公园和机场景观中观察到矮牵牛出现向上卷叶、发黄、叶脉失绿症状,叶片尺寸减小。在所调查景观中的几乎所有植株都表现出烟粉虱的高度侵染,且症状表明感染了双生病毒。从三个不同地点采集了六个有症状的样本。当以感染叶片提取的DNA为模板时,所有有症状的样本用双生病毒诊断引物进行PCR检测均呈阳性。从有症状的叶片中提取核酸,通过滚环扩增法扩增环状DNA分子。扩增的串联产物用限制性内切酶PstI消化,产生一个大小约为2.8 kb的产物。推定的双生病毒片段进行克隆并双向测序。六个克隆的部分序列相似度为99%至100%,因此仅对两个克隆PT - 2和PT - 3进行了全序列测定。两个克隆的全基因组均为2761 bp,分离株PT - 2和PT - 3分别以登录号HF968755和HF968756保存在GenBank中。两个序列均有六个开放阅读框;互补链上的Rep、TrAP、REn和C4基因;以及病毒链上的CP和V2基因,这是双生病毒基因组结构的典型特征。经比对,这两个序列彼此的核苷酸同一性为99.4%,因此代表单一双生病毒物种的分离株。BlastN比较显示,矮牵牛的PT - 2和PT - 3与阿曼的ChCLV序列(JN604490至JN604500)的同一性为94%至95%,这些序列来自其他寄主。ClustalV多序列比对显示,分离株PT - 2和PT - 3与ChLCV - OM分离株(JN604495)的最大序列同一性分别为93.3%和92.8%。根据国际病毒分类委员会双生病毒的规则,PT - 3应被视为ChLCV - OM的一个新株系,PT - 2是已存在的ChLCV - OM株系的一个变体。我们提议将这个新株系命名为辣椒卷叶病毒(ChLCV)的“矮牵牛株系”(ChLCV - Pet)。根据PT - 2和PT - 3序列构建了两个感染性克隆,克隆为二元载体中的1.75基因组序列,适用于农杆菌介导的接种以确认其感染性。接种18天后,克隆PT - 2和PT - 3在矮牵牛上接种时均产生典型的卷叶病症状。使用从PT - 3分离株的CP区域制备的650 bp DIG标记探针,通过Southern杂交证实了有症状的田间感染和接种矮牵牛中存在相同病毒。ChLCV - OM是一种单分体双生病毒,在阿曼与番茄和辣椒的卷叶病广泛相关,其起源可追溯到印度次大陆(2)。从矮牵牛中鉴定出ChLCV新株系为该地区双生病毒正在进行的快速进化提供了证据。尽管矮牵牛已被用作一些双生病毒的实验寄主(1,4),但这是矮牵牛作为ChLCV自然寄主的首次报道,ChLCV是阿曼先前在番茄和辣椒中报道过的一种双生病毒。参考文献:(1)Cui等人,《病毒学杂志》78:13966,2004年。(2)Khan等人,《病毒研究》177:87,2013年。(3)Khan等人,《植物病害》97:1396,2013年。(4)Urbino等人,《病毒学档案》149:417,2003年。