Wu Yunfeng, Hao Xingan, Li Zhengnan, Gu Peiwen, An Fengqui, Xiang Jianye, Wang Haini, Luo Zhaopeng, Liu Junjun, Xiang Yu
Northwest A&F University - College of Plant Protection and Shaanxi Key Laboratory of Molecular Biology for Agriculture, Key Laboratory of Plant Protection Resources and Pest Management, Ministry of Education, Yangling, China.
Northwest A&F University, and Agriculture and Agri-Food Canada - Pacific Agri-Food Research Center, Summmerland, British Columbia, Canada.
Plant Dis. 2010 Aug;94(8):977-985. doi: 10.1094/PDIS-94-8-0977.
Wheat blue dwarf disease (WBD) was first reported in China in the 1960s. It has caused severe losses on several occasions in winter wheat (Triticum aestivum) in northwestern China, and the nature of the pathogenic agent has been unknown. Here we have shown that WBD was caused by a 16SrI-C phytoplasma transmitted by Psammotettix striatus. This finding was based on molecular diagnostics, insect transmission trials, and host-range determination. Portions of the 16S rRNA and ribosomal protein (rp) genes, rpsS (rps19), rplV (rpl22), and rpsC (rps3), were amplified from DNA samples of WBD-infected wheat seedlings by polymerase chain reaction (PCR) utilizing phytoplasma specific primer pairs. The nucleotide sequences of these amplicons showed high identity to these genes from phytoplasma strains in the aster yellows group (16SrI). Pairwise nucleotide sequence identities of WBD 16S rDNA compared to representative genes of 16SrI group strains ranged from 98.9 to 99.9%, whereas compared to 17 other phytoplasma groups (16SrII to 16SrXVIII), sequence identity ranged from 88.6 to 96.0%. Similarly, the sequence identities of rps19, rpl22, and rps3 between WBD and 16SrI group strains varied from 96.6 to 99.7%, but only 60.3 to 65% between WBD and other phytoplasma groups. Phylogenetic analyses were carried out on sequences from 16S rRNA and ribosomal protein genes (rps19, rpl22, and rps3), respectively, and both results indicated that WBD phytoplasma was a member of the 16SrI group and most closely related to subgroup 16SrI-C. WBD-infected P. striatus were present in wheat fields with WBD, and phytoplasma infection was verified by PCR detection followed by DNA sequencing. Insect transmission trials confirmed that P. striatus transmitted the WBD phytoplasmal agent from infected wheat to healthy wheat seedlings and seven other different plant species in the greenhouse. A survey of various weed species near WBD-infected wheat fields found 10 plant species in seven families to be positive for the presence of WBD phytoplasma.
小麦蓝矮病(WBD)于20世纪60年代在中国首次被报道。它曾多次在中国西北的冬小麦(普通小麦)上造成严重损失,而病原体的性质一直不明。在此我们证明,WBD是由条纹角蝉传播的16SrI-C植原体引起的。这一发现基于分子诊断、昆虫传播试验和寄主范围测定。利用植原体特异性引物对,通过聚合酶链反应(PCR)从感染WBD的小麦幼苗DNA样本中扩增出16S rRNA和核糖体蛋白(rp)基因rpsS(rps19)、rplV(rpl22)和rpsC(rps3)的部分片段。这些扩增子的核苷酸序列与翠菊黄化组(16SrI)中植原体菌株的这些基因具有高度同源性。与16SrI组菌株的代表性基因相比,WBD 16S rDNA的成对核苷酸序列同源性在98.9%至99.9%之间,而与其他17个植原体组(16SrII至16SrXVIII)相比,序列同源性在88.6%至96.0%之间。同样,WBD与16SrI组菌株之间rps19、rpl22和rps3的序列同源性在96.6%至99.7%之间,但WBD与其他植原体组之间仅为60.3%至65%。分别对16S rRNA和核糖体蛋白基因(rps19、rpl22和rps3)的序列进行了系统发育分析,结果均表明WBD植原体是16SrI组的成员,且与16SrI-C亚组关系最为密切。在有WBD的麦田中存在感染WBD的条纹角蝉,通过PCR检测及DNA测序验证了植原体感染。昆虫传播试验证实,条纹角蝉可将WBD植原体从感染的小麦传播至温室中的健康小麦幼苗及其他七种不同植物物种。对WBD感染麦田附近的各种杂草物种进行调查发现,七个科中的10种植物对WBD植原体呈阳性。