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引起土耳其爱琴海地区马铃薯褐腐病的青枯雷尔氏菌生物变种2的爆发。

Outbreak of Ralstonia solanacearum Biovar 2 Causing Brown Rot on Potato in the Aegean Region of Turkey.

作者信息

Ustun N, Ozakman M, Karahan A

机构信息

Plant Protection Research Institute, Bornova, Izmir, Turkey.

Plant Protection Central Research Institute, Ankara, Turkey.

出版信息

Plant Dis. 2008 Jun;92(6):973. doi: 10.1094/PDIS-92-6-0973B.

Abstract

Ralstonia solanacearum (Smith) Yabuuchi, Kosako, Yano, Hotta, and Nishiuchi, the cause of brown rot of potato (Solanum tuberosum), was detected for the first time in Turkey in 1995 in five potato fields in the Nevsehir Province of the central Anatolia Region and was eradicated under measures mandated by the government. Occurrence of the pathogen was not reported in other parts of the country. However, in 2006, brown rot symptoms were observed in potato (cv. Marabel) fields in the Balikesir Province of the Aegean Region. Symptoms and signs included wilting, browning of stem vascular tissues, and ooze exudation from the transversely cut stem. On tubers, brown discoloration of the vascular ring was observed. Creamy bacterial ooze emerged from the vascular ring a few minutes after cutting. In advanced stages, bacterial slime oozed from the tuber heel end (stolon) and "eyes" causing soil particles to adhere. Isolation of bacteria from diseased stem and tuber tissues on mSMSA medium (1) consistently resulted in white, fluid colonies with red coloration in the center. On the basis of biochemical, immunofluorescence (IF), and real-time PCR tests, 10 representative isolates (one per affected field) were identified as Ralstonia solanacearum. They were further identified as biovar 2 according to metabolization of maltose, lactose, and D (+) cellobiose but not mannitol, sorbitol, and dulcitol. In the IF tests, fluorescent cells were observed at antibody dilutions from 200 to 12,800. The expected real-time PCR products were generated using biovar 2-specific primers (2). Pathogenicity tests were performed by injecting a bacterial suspension (10 CFU/ml) into the stem of 2-week-old tomato seedlings (cv. Alta F1). Inoculated plants (five plants per isolate) were incubated for up to 2 weeks at 25°C and 70 to 80% humidity. Wilting symptoms developed within 5 to 10 days. No symptoms were observed on controls inoculated with sterile water. The bacterium was reisolated and identified as R. solanacearum biovar 2 as described above. The incidence of the disease in the affected fields varied between 20 and 40%, and surveys showed that approximately 163 ha were infested. Phytosanitary measures that were taken included a prohibition of production of host plants in the infested areas, tracing and testing programs to identify the source of the bacterium, and measures to prevent any further spread of the bacterium to new areas. To our knowledge, this is the first report of R. solanacearum biovar 2 on potato in the Aegean Region of Turkey. References: (1) J. G. Elphinstone et al. EPPO Bull. 26:663, 1996. (2) M. Ozakman and N. W.Schaad. Can. J. Plant Pathol. 25:232, 2003.

摘要

茄科雷尔氏菌(拉氏菌)(Smith)Yabuuchi、Kosako、Yano、Hotta和Nishiuchi是马铃薯(Solanum tuberosum)褐腐病的病原菌,1995年在土耳其中部安纳托利亚地区内夫谢希尔省的5个马铃薯田首次被发现,并在政府规定的措施下被根除。该国其他地区未报告该病原菌的发生情况。然而,2006年,在爱琴海地区巴勒克埃西尔省的马铃薯(品种Marabel)田观察到褐腐病症状。症状和病征包括萎蔫、茎维管束组织褐变以及从横切茎部渗出黏液。在块茎上,观察到维管束环褐变。切割后几分钟,奶油状细菌黏液从维管束环中渗出。在发病后期,细菌黏液从块茎根端(匍匐茎)和“芽眼”渗出,导致土壤颗粒附着。在mSMSA培养基(1)上从患病茎和块茎组织中分离细菌,始终得到白色、液体状菌落,中心呈红色。根据生化、免疫荧光(IF)和实时PCR检测,10个代表性分离株(每个受影响田块1个)被鉴定为茄科雷尔氏菌。根据麦芽糖、乳糖和D(+)纤维二糖的代谢情况,但不包括甘露醇、山梨醇和卫矛醇的代谢情况,它们进一步被鉴定为生物变种2。在IF检测中,在抗体稀释度为200至12800时观察到荧光细胞。使用生物变种2特异性引物(2)产生了预期的实时PCR产物。通过将细菌悬浮液(10 CFU/ml)注射到2周龄番茄幼苗(品种Alta F1)的茎中进行致病性测试。接种的植株(每个分离株5株)在25°C和70至80%湿度下培养长达2周。5至10天内出现萎蔫症状。接种无菌水的对照未观察到症状。该细菌被重新分离,并如上所述被鉴定为茄科雷尔氏菌生物变种2。受影响田块的发病率在20%至40%之间,调查显示约163公顷土地受到侵染。采取的植物检疫措施包括禁止在受侵染地区种植寄主植物、追踪和检测计划以确定细菌来源,以及防止细菌进一步传播到新地区的措施。据我们所知,这是土耳其爱琴海地区马铃薯上茄科雷尔氏菌生物变种2的首次报告。参考文献:(1)J.G.Elphinstone等人,《欧洲和地中海植物保护组织通报》26:663,1996年。(2)M.Ozakman和N.W.Schaad,《加拿大植物病理学杂志》25:232,2003年。

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