Verhoeven J Th J, Botermans M, Jansen C C C, Roenhorst J W
Plant Protection Service, P.O. Box 9102, 6700 HC Wageningen, the Netherlands.
Plant Dis. 2010 Jun;94(6):791. doi: 10.1094/PDIS-94-6-0791A.
In 2009, in the framework of surveying for pospiviroids, samples of various ornamental plants from the Netherlands were tested by reverse transcription (RT)-PCR with the primer pairs Pospi1-RE/FW and Vid-RE/FW (2). With primer pair Pospi1-RE/FW, amplicons of the expected size were obtained in two samples of symptomless plants of Lycianthes rantonnetii and Streptosolen jamesonii. Sequencing of the amplicons, which were expected to correspond with partial pospiviroid genomes, showed identities of 100 and 98% to the sequence of Tomato apical stunt viroid (TASVd), NCBI GenBank Accession No. AM777161 (3). For the amplification of the complete viroid genomes, RT-PCRs were performed with primer pair CEVd-FW/RE (1). Sequencing of these amplicons yielded sequences of 364 nt and identities to TASVd AM777161 of 100 and 98.1%, respectively. Therefore, both isolates were identified as TASVd. The sequence variant from S. jamesonii was submitted to the NCBI GenBank as No. GU911351. In addition, both isolates were mechanically inoculated to four tomato plants (Solanum lycopersicum) of cv. Moneymaker. All inoculated plants developed chlorosis and growth reduction after 4 weeks and TASVd infections were confirmed in a bulked sample by RT-PCR with primer pair CEVd-FW/RE after 6 weeks. Hence, two more ornamental host plant species have been identified that may act as symptomless sources of pospiviroid inoculum. References: (1) N. Önelge. Turk. J. Agric. For. 21:419, 1997. (2) J. Th. J. Verhoeven et al. Eur. J. Plant Pathol. 110:823, 2004. (3) J. Th. J. Verhoeven et al. Plant Dis. 92:973, 2008.
2009年,在对马铃薯纺锤块茎类病毒进行检测的框架下,采用逆转录(RT)-PCR技术,使用引物对Pospi1-RE/FW和Vid-RE/FW(2)对来自荷兰的各种观赏植物样本进行了检测。使用引物对Pospi1-RE/FW时,在两种无症状的蓝花茄(Lycianthes rantonnetii)和金钮扣(Streptosolen jamesonii)植物样本中获得了预期大小的扩增子。对预期与马铃薯纺锤块茎类病毒部分基因组相对应的扩增子进行测序后发现,其与番茄顶枯类病毒(TASVd)序列(NCBI GenBank登录号AM777161)的同一性分别为100%和98%(3)。为了扩增完整的类病毒基因组,使用引物对CEVd-FW/RE进行了RT-PCR(1)。对这些扩增子进行测序后得到了364 nt的序列,其与TASVd AM777161的同一性分别为100%和98.1%。因此,这两个分离株均被鉴定为TASVd。来自金钮扣的序列变体已作为编号GU911351提交至NCBI GenBank。此外,将这两个分离株机械接种到4株“Money maker”品种的番茄(Solanum lycopersicum)植株上。所有接种的植株在4周后出现黄化和生长减缓现象,6周后通过使用引物对CEVd-FW/RE进行RT-PCR在混合样本中确认了TASVd感染。因此,又鉴定出了两种可能作为马铃薯纺锤块茎类病毒无症状接种源的观赏寄主植物物种。参考文献:(1)N. Önelge。《土耳其农业与林业杂志》21:419,1997年。(2)J. Th. J. Verhoeven等人。《欧洲植物病理学报》110:823,2004年。(3)J. Th. J. Verhoeven等人。《植物病害》92:973,2008年。