Genov N, Mitrović J, Genov M, Duduk B
Department of Plant Protection, Institute of Viticulture and Enology, Pleven, Bulgaria.
Institute of Pesticides and Environmental Protection, Belgrade, Serbia.
Plant Dis. 2014 Jul;98(7):991. doi: 10.1094/PDIS-12-13-1220-PDN.
Corn reddening (CR) or maize redness is a severe disease of corn (Zea mays L.) associated with 'Candidatus Phytoplasma solani' or stolbur phytoplasma (16SrXII-A). In Serbia, CR is continually present at a low frequency, while two outbreaks occurred in the late 1950s and 1990s. Its etiology was molecularly determined in 2006 (1). The first severe outbreak in Bulgaria was observed in Kneja in 1992, and in 2010 typical CR symptoms (leaf reddening, premature drying, and shriveled grains) were observed from Byala Slatina to Pleven. Although the number of CR affected plants was highly variable in different fields, the disease incidence in most cases was 30 to 50%, with an estimated yield reduction of about 20%. Leaf samples from four symptomatic corn plants were collected from Kneja, northwestern Bulgaria, in mid-August 2013. Extraction of DNA was performed from the main leaf midrib tissues using the CTAB method. Separate PCRs were carried out for amplification of the phytoplasma 16S rDNA and tuf genes using the phytoplasma specific primers P1/P7 and TufAyf/r, respectively. DNA from asymptomatic corn plants and reactions without template DNA were employed as negative controls, while DNA from periwinkle tissue infected with 'Ca. P. asteris' was used as a positive control. Amplicons of the expected sizes (1.7 and 0.9 kbp, respectively) were produced with DNA from three out of four symptomatic corn samples, while no amplification was observed with DNA from one symptomatic corn sample (probably because samples were collected during a drought period) nor the DNA from asymptomatic plants and negative control. RFLP analyses performed on 16S rDNA and tuf gene amplicons using Tru1I and HpaII restriction enzymes, respectively, revealed the presence of 'Ca. P. solani' (16SrXII-A, tuf type b) in all three positive samples (3). Both amplicons of a selected representative sample 241/13 were directly sequenced by a commercial service and the obtained sequences were deposited in NCBI GenBank under the accession number KF907506 for the16S rDNA (1,684 bp) and KF907507 for the tuf gene (896 bp). The 16S rDNA sequence of phytoplasma detected in Bulgarian corn shared a complete sequence identity with 'Ca. P. solani' strain from Serbian corn (JQ730750.1) and >99.7% sequence identity with the reference strain STOL (AF248959), while the tuf gene nucleotide sequence shared complete sequence identity with several 'Ca. P. solani' (e.g., Serbian strain 284/09, FO393427), thus confirming, with both genes, the affiliation of phytoplasmas in Bulgarian corn to 'Ca. P. solani'. This study adds new information on CR prevalence, previously reported in neighboring countries. Further studies will investigate the roles of Hyalesthes obsoletus and Reptalus panzeri, both polyphagous Cixiidae reported as CR vectors (2,4) in disease transmission in Bulgaria. References: (1) B. Duduk and A. Bertaccini. Plant Dis. 90:1313, 2006. (2) J. Jović et al. Eur. J. Plant Pathol. 118:85, 2007. (3) I.-M. Lee et al. Int. J. Syst. Bacteriol. 48:1153, 1998. (4) N. Mori et al. Bull. Insectol. 66:245, 2013.
玉米变红(CR)或玉米红化病是玉米(Zea mays L.)的一种严重病害,与“Ca. Phytoplasma solani”或 stolbur 植原体(16SrXII - A)有关。在塞尔维亚,CR 一直以低频率存在,而在 20 世纪 50 年代末和 90 年代发生过两次疫情爆发。其病因在 2006 年通过分子手段得以确定(1)。保加利亚的首次严重疫情爆发于 1992 年在 Kneja 被观察到,并且在 2010 年从 Byala Slatina 到 Pleven 观察到了典型的 CR 症状(叶片变红、过早干枯和籽粒皱缩)。尽管在不同田块中受 CR 影响的植株数量差异很大,但在大多数情况下发病率为 30%至 50%,估计产量降低约 20%。2013 年 8 月中旬,从保加利亚西北部的 Kneja 采集了四株有症状玉米植株的叶片样本。使用 CTAB 方法从主要叶片中脉组织提取 DNA。分别使用植原体特异性引物 P1/P7 和 TufAyf/r 进行单独的 PCR,以扩增植原体 16S rDNA 和 tuf 基因。来自无症状玉米植株的 DNA 和无模板 DNA 的反应用作阴性对照,而来自感染“Ca. P. asteris”的长春花组织的 DNA 用作阳性对照。四个有症状玉米样本中的三个样本的 DNA 产生了预期大小的扩增子(分别为 1.7 和 0.9 kbp),而一个有症状玉米样本的 DNA(可能因为样本是在干旱时期采集的)以及无症状植株的 DNA 和阴性对照均未观察到扩增。分别使用 Tru1I 和 HpaII 限制性内切酶对 16S rDNA 和 tuf 基因扩增子进行的 RFLP 分析表明,所有三个阳性样本中均存在“Ca. P. solani”(16SrXII - A,tuf 类型 b)(3)。所选代表性样本 241/13 的两个扩增子均由商业服务直接测序,获得的序列分别以登录号 KF907506(1,684 bp)存入 NCBI GenBank 用于 16S rDNA,以登录号 KF907507(896 bp)存入用于 tuf 基因。在保加利亚玉米中检测到的植原体的 16S rDNA 序列与来自塞尔维亚玉米的“Ca. P. solani”菌株(JQ730750.1)具有完全的序列同一性,与参考菌株 STOL(AF248959)的序列同一性>99.7%,而 tuf 基因核苷酸序列与几个“Ca. P. solani”(例如塞尔维亚菌株 284/09,FO393427)具有完全的序列同一性,从而通过两个基因证实了保加利亚玉米中的植原体属于“Ca. P. solani”。本研究增加了关于 CR 在邻国流行情况的新信息。进一步的研究将调查 Hyalesthes obsoletus 和 Reptalus panzeri 的作用,这两种多食性蜡蝉科昆虫均被报道为 CR 的传播媒介(2,4),在保加利亚的疾病传播中所起的作用。参考文献:(1)B. Duduk 和 A. Bertaccini。植物病害。90:1313,2006。(2)J. Jović 等人。欧洲植物病理学报。118:85,2007。(3)I.-M. Lee 等人。国际系统细菌学杂志。48:1153,1998。(4)N. Mori 等人。昆虫学通报。66:245,2013。