Verhoeven J Th J, Jansen C C C, Werkman A W, Roenhorst J W
Plant Protection Service, Unit Virology, P.O. Box 9102, 6700 HC Wageningen, the Netherlands.
Plant Dis. 2007 Mar;91(3):324. doi: 10.1094/PDIS-91-3-0324B.
In November 2005, 13 accessions of Petunia hybrida from the United States of America entered the post-entry quarantine station of the Plant Protection Service in the Netherlands. The plants were inspected and tested for quarantine organisms according to Directives 95/44 and 97/46 of the European Union. No virus and viroid symptoms were observed in the imported plants or in mechanically inoculated plants of Chenopodium quinoa, Nicotiana benthamiana, and N. occidentalis-P1 (3). Testing for pospiviroids by return-polyacrylamide gel electrophoresis (1) and reverse transcriptase-PCR with universal pospiviroid primers Pospi1-RE/FW (2) indicated the presence of pospiviroids in 3 and 11 P. hybrida accessions, respectively. The 196-bp amplicons of six accessions were sequenced. Sequence analysis showed the highest identity for all amplicons to both isolates of Tomato chlorotic dwarf viroid (TCDVd) in NCBI GenBank, Accession Nos. AF162131and AY372399, from Canada and the United States, respectively. Additional RT-PCRs with the Pospi1-RE/FW primers in opposite order and the semi-universal pospiviroid primers Vid-RE/FW (2) for one isolate, followed by sequence analysis, confirmed the identity as TCDVd. The isolate consisted of 359 nucleotides (GenBank Accession No. DQ859013) and showed sequence identities of 98.6 and 96.1% to the Canadian and American tomato isolates of this viroid, respectively. The next highest sequence identity was 90.0% to two accessions of Potato spindle tuber viroid (GenBank Accession Nos. AJ593449 and AY962324). On the basis of these results, the viroid from P. hybrida was identified as TCDVd. To our knowledge, this is the first report of TCDVd in this plant species. Reference: (1) J. W. Roenhorst et al. EPPO Bull. 30:453, 2000. (2) J. Th. J. Verhoeven et al. Eur. J. Plant Pathol. 110:823, 2004. (3) J. Th. J. Verhoeven and J. W. Roenhorst. EPPO Bull. 33:305, 2003.
2005年11月,13份来自美国的矮牵牛品种进入了荷兰植物保护局的入境后检疫站。根据欧盟第95/44号和第97/46号指令,对这些植物进行了检疫性有害生物的检查和检测。在进口植物以及藜麦、本氏烟草和西方烟草-P1的机械接种植物中未观察到病毒和类病毒症状。通过反向聚丙烯酰胺凝胶电泳(1)以及使用通用类病毒引物Pospi1-RE/FW(2)进行逆转录聚合酶链反应检测类病毒,结果分别表明在3份和11份矮牵牛品种中存在类病毒。对6个品种的196碱基对扩增子进行了测序。序列分析表明,所有扩增子与美国国立生物技术信息中心基因库中分别来自加拿大和美国的番茄褪绿矮缩类病毒(TCDVd)的两个分离株的一致性最高,登录号分别为AF162131和AY372399。对一个分离株使用Pospi1-RE/FW引物以相反顺序进行额外的逆转录聚合酶链反应,以及使用半通用类病毒引物Vid-RE/FW(2),随后进行序列分析,证实其为TCDVd。该分离株由359个核苷酸组成(基因库登录号DQ859013),与该类病毒的加拿大和美国番茄分离株的序列一致性分别为98.6%和96.1%。其次最高的序列一致性为90.0%,与马铃薯纺锤块茎类病毒的两个品种(基因库登录号AJ593449和AY962324)。基于这些结果,将来自矮牵牛的类病毒鉴定为TCDVd。据我们所知,这是该植物物种中首次报道TCDVd。参考文献:(1)J. W. Roenhorst等人,《欧洲和地中海植物保护组织通报》30:453,2000年。(2)J. Th. J. Verhoeven等人,《欧洲植物病理学杂志》110:823,2004年。(3)J. Th. J. Verhoeven和J. W. Roenhorst,《欧洲和地中海植物保护组织通报》33:305,2003年。