Wen A, Mallik I, Alvarado V Y, Pasche J S, Wang X, Li W, Levy L, Lin H, Scholthof H B, Mirkov T E, Rush C M, Gudmestad N C
Department of Plant Pathology, North Dakota State University, Fargo, ND 58108.
Department of Plant Pathology and Microbiology, Texas AgriLife, Texas A&M University, College Station, TX 77843.
Plant Dis. 2009 Nov;93(11):1102-1115. doi: 10.1094/PDIS-93-11-1102.
The specificity and sensitivity of polymerase chain reaction (PCR) primers developed for 'Candidatus Liberibacter solanacearum' and 'Candidatus Liberibacter psyllaurous' were evaluated in conventional and real-time PCR assays. All PCR primers were specific for 'Ca. L. psyllaurous' and 'Ca. L. solanacearum' insomuch as they did not detect other prokaryotic plant pathogens that affect potato except for the putative pathogens associated with psyllid-yellows and haywire. Conventional PCR assays were capable of detecting 0.19 to 1.56 ng of total DNA per reaction, and real-time PCR was found capable of detecting 1.56 to 6.25 ng of total DNA per reaction, depending on the specific PCR primer set used. 'Ca. Liberibacter' species associated with zebra complex disease (ZC) was confirmed in plants affected by this disease throughout Texas from 2005 to 2008, in seed tubers produced in Wyoming in 2007, and in Colorado, Kansas, Nebraska, and Mexico in 2008. A multiplex PCR assay using 'Ca. L. solanacearum'-specific primers and primers specific for the β-tubulin DNA regions from potato was developed, providing possible utility of the multiplex assay for 'Ca. Liberibacter' detection in different solanaceous plant species. Preliminary studies suggest silverleaf nightshade (Solanum elaeagnifolium), wolfberry (Lycium barbarum), black nightshade (S. ptychanthum), and jalapeno pepper (Capsicum annuum) as additional solanaceous hosts for the ZC-associated bacterium. The 'Ca. Liberibacter' species detected in all samples divided into two clusters sharing similarity of 99.8% in their partial 16S rRNA gene sequences and 99.3% in their partial intergenic spacer region (ISR)-23S rRNA gene sequences. Genetic variation in the 16S rDNA region consistently matched that of the ISR-23S rDNA region. In this partial 16S-ISR-23S rDNA region, there was a total of eight single nucleotide polymorphisms among 'Ca. L. psyllaurous' and 'Ca. L. solanacearum' "strains" investigated in this study. 'Ca. L. solanacearum' and 'Ca. L. psyllaurous' were shown to be very closely related bacteria, if not the same, by successful amplification using a combination of forward primer of 'Ca. L. solanacearum' and reverse primer of 'Ca. L. psyllaurous' in ZC-affected potato samples. This finding clarifies the current taxonomic status of 'Ca. L. solanacearum' and 'Ca. L. psyllaurous'. The detection of 'Ca. L. solanacearum' from haywire-symptomatic potato samples demonstrates that this bacterium might also be associated with this disease.
针对“番茄伪菌原体”和“木虱伪菌原体”开发的聚合酶链反应(PCR)引物,在常规PCR和实时PCR检测中进行了特异性和敏感性评估。所有PCR引物对“番茄伪菌原体”和“木虱伪菌原体”具有特异性,因为它们除了能检测到与木虱黄化病和紊乱病相关的假定病原体外,未检测到其他影响马铃薯的原核植物病原体。常规PCR检测每个反应能够检测到0.19至1.56纳克的总DNA,实时PCR检测发现每个反应能够检测到1.56至6.25纳克的总DNA,这取决于所使用的特定PCR引物组。2005年至2008年在得克萨斯州受斑马复合病(ZC)影响的植物中、2007年在怀俄明州生产的种薯中以及2008年在科罗拉多州、堪萨斯州、内布拉斯加州和墨西哥均确认了与斑马复合病相关的“伪菌原体”物种。开发了一种使用“番茄伪菌原体”特异性引物和马铃薯β - 微管蛋白DNA区域特异性引物的多重PCR检测方法,该多重检测方法可能有助于在不同茄科植物物种中检测“伪菌原体”。初步研究表明,银叶茄(Solanum elaeagnifolium)、枸杞(Lycium barbarum)、龙葵(S. ptychanthum)和墨西哥胡椒(Capsicum annuum)是与斑马复合病相关细菌的额外茄科寄主。在所有样本中检测到的“伪菌原体”物种分为两个簇,它们的部分16S rRNA基因序列相似度为99.8%,部分基因间隔区(ISR)- 23S rRNA基因序列相似度为99.3%。16S rDNA区域的遗传变异与ISR - 23S rDNA区域的遗传变异始终匹配。在该部分16S - ISR - 23S rDNA区域,本研究中调查的“木虱伪菌原体”和“番茄伪菌原体”“菌株”之间共有8个单核苷酸多态性。通过在受ZC影响的马铃薯样本中使用“番茄伪菌原体”正向引物和“木虱伪菌原体”反向引物的组合成功扩增,表明“番茄伪菌原体”和“木虱伪菌原体”是非常密切相关的细菌,即便不是同一种细菌。这一发现澄清了“番茄伪菌原体”和“木虱伪菌原体”目前的分类地位。从有紊乱症状的马铃薯样本中检测到“番茄伪菌原体”表明该细菌也可能与这种疾病有关。