Shi H, Zheng J
Institute of Biotechnology, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, China.
Plant Dis. 2013 Jun;97(6):852. doi: 10.1094/PDIS-10-12-0926-PDN.
Soybean cyst nematode (SCN) (Heterodera glycines) commonly infests soybean (Glycine max), but has also been reported to infest haricot bean, mung bean, adzuki bean, some species of Lespedeza and Melilotus (3), purple deadnettle (Lamium purpureum), henbit (Lamium amplexicaule), field pennycress (Thlaspi arvense), and shepherd's-purse (Capsella bursa-pastoris) (4). During 2009 to 2011, a survey for plant parasitic nematodes on tobacco was made in Xuchang, Henan Province, central China. Thirty six percent of 50 tobacco fields showed yellowing symptoms, and females and cysts of cyst-forming nematode were observed in the yellowing tobacco roots. The cysts were characterized by a lemon shape, with posterior protuberance, ambifenestrate, bullae, and underbridge present. The key morphometrics of cysts were fenestra length (38 to 44 μm) and width (34 to 40 μm), vulval silt (41 to 50 μm), and underbridge length (73 to 99 μm), all of which were similar to SCN (1). DNA was extracted by putting a single cracked cyst collected from the tobacco root to a 0.2-ml Eppendorf tube containing 10 μl double distilled water, 8 μl 10 × PCR Buffer (Mg-), and 2 μl of proteinase K (600 μg/ml) and frozen at -70°C for 30 min, then incubated at 65°C for 1 h and at 95°C for 10 min. After centrifugation at 12,000 rpm for 2 min, the DNA suspension was used for PCR amplification. Primers TW81 (5'-GTTTCCGTAGGTGAACCTGC-3') and AB28 (5'-ATATGCTTAAGTTCAGCGGGT-3') were used to amplify the rDNA internal transcribed spacer (ITS) region, and a PCR fragment of 1,030 bp was obtained. The sequence (GenBank Accession No. JX561139) showed 99% similarity to H. glycines strain Hg1-Ark1 (EF611124). Duplex PCR containing the universal primers D2A (5'-ACAAGTACCGTGAGGGAAAGTTG-3'), D3B (5'-TCGGAAGGAACCAGCTACTA-3') and SCAR primers SCNFI (5'-GGACCCTGACCAAAAAGTTTCCGC-3'), SCNRI (5'-GGACCCTGACGAGTTATGGGCCCG-3'), obtained a 477-bp fragment, which is specific for SCN populations (2). Based on both morphological and molecular identification, the populations of cyst-forming nematodes on tobacco from Henan, China were confirmed as SCN. Pathogenicity tests were conducted on 30 each of 50-day-old tobacco and 5-day-old soybean plants (one plant per pot), respectively, by adding 2 ml of a suspension of 1,000 eggs and J2 of cysts collected from tobacco roots. After 35 days, 20 to 35 white females could be detected in each of the tobacco roots, and the yellowing symptom on almost all of tobacco plants was observed. Although infection on soybean plants was observed, the nematodes infected in roots was just 10 to 20 per pot, and they all stayed in the infective J2 stage. Except for one J3 until 48 dpi, no mature females could be found, and the nematode population could not reproduce on soybean tested. This suggests that the cyst nematode population from tobacco is a new pathotype of SCN. To our knowledge, this is the first report of SCN parasitized on tobacco in naturally infected fields, which is a potential threat to tobacco growth and should attract worldwide attention. References: (1) R. H. Mulvey. Can. J. Zool. 50:1277, 1972. (2) S. Ou et al. Nematology 10:397, 2008. (3) R. D. Riggs. In: Biology and Management of the Soybean Cyst Nematode, p. 107-114, 1992. (4) R. Venkatesh et al. Weed Technol. 14:156, 2000.
大豆胞囊线虫(SCN)(大豆异皮线虫)通常侵染大豆(大豆),但也有报道称其侵染菜豆、绿豆、小豆、一些胡枝子属和草木樨属物种(3)、紫花野芝麻(野芝麻)、宝盖草(宝盖草)、田野勿忘草(遏蓝菜)和荠菜(荠菜)(4)。2009年至2011年期间,在中国中部河南省许昌市对烟草上的植物寄生线虫进行了调查。50块烟草田中36%出现黄化症状,在黄化的烟草根中观察到胞囊线虫的雌虫和胞囊。胞囊呈柠檬形,有后突起、双窗孔、泡状突起和下桥。胞囊的关键形态测量数据为窗孔长度(38至44μm)和宽度(34至40μm)、阴门缝(41至50μm)和下桥长度(73至99μm),所有这些数据均与大豆胞囊线虫相似(1)。从烟草根中收集单个破裂的胞囊,放入含有l0μl双蒸水、8μl 10×PCR缓冲液(含镁)和2μl蛋白酶K(600μg/ml)的0.2ml Eppendorf管中,在-70°C下冷冻30分钟,然后在65°C下孵育1小时,再在95°C下孵育10分钟,提取DNA。以12000rpm离心2分钟后,将DNA悬浮液用于PCR扩增。使用引物TW81(5'-GTTTCCGTAGGTGAACCTGC-3')和AB28(5'-ATATGCTTAAGTTCAGCGGGT-3')扩增核糖体DNA内转录间隔区(ITS),获得了1030bp的PCR片段。该序列(GenBank登录号JX561139)与大豆异皮线虫菌株Hg1-Ark1(EF611124)的相似性为99%。使用通用引物D2A(5'-ACAAGTACCGTGAGGGAAAGTTG-3')、D3B(5'-TCGGAAGGAACCAGCTACTA-3')和SCAR引物SCNFI(5'-GGACCCTGACCAAAAAGTTTCCGC-3')、SCNRI(5'-GGACCCTGACGAGTTATGGGCCCG-3')进行双重PCR,获得了一个477bp的片段,该片段对大豆胞囊线虫种群具有特异性(2)。基于形态学和分子鉴定,确认中国河南烟草上的胞囊线虫种群为大豆胞囊线虫。分别对50株50日龄烟草和5日龄大豆植株(每盆一株)进行致病性测试,方法是添加2ml从烟草根中收集的含1000个卵和J2期幼虫的悬浮液。35天后,在每株烟草根中可检测到20至35个白色雌虫,几乎所有烟草植株都出现了黄化症状。虽然观察到大豆植株受到感染,但每盆根中感染的线虫仅为10至20条,且它们都处于感染性J2期。除了在接种后第48天发现一条J3期幼虫外,未发现成熟雌虫,且测试的线虫种群在大豆上无法繁殖。这表明来自烟草的胞囊线虫种群是大豆胞囊线虫的一种新致病型。据我们所知,这是首次报道在自然感染田块中大豆胞囊线虫寄生烟草,这对烟草生长构成潜在威胁,应引起全球关注。参考文献:(1)R.H.Mulvey.Can.J.Zool.50:1277,1972.(2)S.Ou等.Nematology 10:397,2008.(3)R.D.Riggs.In:Biology and Management of the Soybean Cyst Nematode,p.107 - 114,1992.(4)R.Venkatesh等.Weed Technol.14:156,2000.