Du Q, Zhao S F, Wu C L, Kong L, Zhang P
The Key Laboratory of Prevention and Control for Oasis Crop Disease, Shihezi University, Shihezi, Xinjiang, 832003, China.
Institute of Agriculture Science and Technology of Division No. 2 of Xinjiang Production and Construction Group, Korla, Xinjiang, 841000, China.
Plant Dis. 2013 Dec;97(12):1661. doi: 10.1094/PDIS-11-12-1040-PDN.
Ziziphus jujuba Mill. (Rhamanaceae), commonly known as Chinese jujube, is a plant that is native to China and widely distributed in China and South Korea. Chinese jujube is a traditional Chinese medicine and food that has been used for thousands of years. From spring 2011 to spring 2012, Chinese jujube trees (<4 years old) from commercial orchards in Kashi and Akzo developed symptoms of severe wilting, chlorosis, and stunting. The taproot and lateral roots exhibited black, sunken, necrotic lesions, and progression of these symptoms eventually caused mortality of infected trees. In April 2011 and 2012, 15 trees with root rot symptoms were collected from different orchards, and a fungus was recovered consistently from symptomatic rhizome samples that had been surface-sterilized with 0.1% mercuric chloride and plated onto potato dextrose agar (PDA). Thirteen isolates were obtained. Colony growth on PDA was initially white but gradually turned grayish yellow-brown, with the lower side of the plate turning a deep yellow-brown. Colony texture was felty and slightly raised with no concentric growth zones. Pycnidia formed abundantly after 30 days, and each exuded a dull orange cirrhus containing conidia. The conidiomatal stromata were immersed in the bark, erumpent, discoid, convex to conical, and 1.53 ± 0.13 mm in diameter. Discs were dark brown or grey, nearly flat, circular, and up to 0.6 mm in diameter, with one to eight lateral ostioles. Ostioles were brown, 40 to 80 mm in diameter, and located above the disc surface. Locules were globose, with four to eight in a stroma, undivided, and did not share common walls. Conidia were hyaline, eguttulate, and allantoid, with sizes of 12 to 20 × 1.0 to 1.5 μm. The agar culture and conidiomatal stromata morphology were in accordance with descriptions of Cytospora sacculus (1,4). PCR amplification of the internal transcribed (ITS) spacer region of rDNA (using primers ITS1/4), combined with amplification of the β-tubulin gene (using primers BT1a/BT1b) (2,3), followed by sequencing of the amplified DNA, led to identification of isolate 6T-17 as Valsa ceratosperma (anamorph C. sacculus). The sequence of the ITS1-5.8s-ITS2 region of rDNA (GenBank Accession No. JX560175) matched the ITS sequence of V. ceratosperma Accession AB369475 with 99% similarity, and the β-tubulin gene sequence (KC840674) resulted in a 99% match with that of V. ceratosperma Accession EU219136. Mycelial plugs of a culture of each fungal isolate on PDA were inoculated onto 10 rhizomes of 2-month-old seedlings of Z. jujube, and maintained in a greenhouse at 25 to 30°C. Ten rhizomes of 2-month-old seedlings of Z. jujuba were inoculated with non-colonized PDA plugs as the control treatment. After 2 months, all inoculated seedlings showed chlorotic leaves and root rot symptoms similar to those observed in the original commercial orchards. No symptoms were observed on the control plants. The pathogen was reisolated successfully from symptomatic plants but not from the control plants, fulfilling Koch's postulates. To our knowledge, this is the first report of C. sacculus causing a root rot of Z. jujuba trees in China. References: (1) G. C. Adams et al. Stud. Mycol. 52:83, 2005. (2) G. M. Arruda et al. Plant Pathol. 54:53, 2005. (3) J. Baskarathevan et al. Eur. J. Plant Pathol. 132:549, 2012. (4) J. B. Kepley et al. J. Arbor. 26:326, 2000.
枣(鼠李科),通常称为中国枣,是一种原产于中国并在中国和韩国广泛分布的植物。中国枣是一种已有数千年使用历史的传统中药和食品。从2011年春季到2012年春季,喀什和阿克苏商业果园中树龄小于4年的枣树出现了严重萎蔫、黄化和生长受阻的症状。主根和侧根出现黑色、凹陷、坏死的病斑,这些症状的发展最终导致受感染树木死亡。在2011年4月和2012年,从不同果园收集了15株有根腐症状的树,并且从用0.1%氯化汞进行表面消毒后接种到马铃薯葡萄糖琼脂(PDA)上的有症状根茎样本中持续分离出一种真菌。获得了13个分离株。在PDA上的菌落生长最初为白色,但逐渐变为灰黄棕色,平板底部变为深黄棕色。菌落质地似毡状且略有凸起,没有同心生长带。30天后大量形成分生孢子器,每个分生孢子器分泌出含有分生孢子的暗橙色分生孢子角。分生孢子座埋生于树皮中,突出,盘状,凸起至圆锥形,直径1.53±0.13毫米。盘为深棕色或灰色,近扁平,圆形,直径达0.6毫米,有1至8个侧生小孔。小孔为棕色,直径40至80毫米,位于盘表面上方。腔室为球形,在一个子座中有4至8个,未分隔,且没有共用壁。分生孢子无色,具油滴,腊肠形,大小为12至20×1.0至1.5微米。琼脂培养物和分生孢子座形态与囊孢壳菌(1,4)的描述一致。对核糖体DNA的内部转录间隔区(ITS)进行PCR扩增(使用引物ITS1/4),并结合β-微管蛋白基因的扩增(使用引物BT1a/BT1b)(2,3),随后对扩增的DNA进行测序,鉴定分离株6T-17为榆壳囊孢菌(无性型为囊孢壳菌)。核糖体DNA的ITS1-5.8s-ITS2区域序列(GenBank登录号JX560175)与榆壳囊孢菌登录号AB369475的ITS序列相似度为99%,β-微管蛋白基因序列(KC840674)与榆壳囊孢菌登录号EU219136的序列匹配度为99%。将每个真菌分离株在PDA上的培养物的菌丝块接种到10株2月龄枣树幼苗的根茎上,并在25至30°C的温室中培养。将10株2月龄枣树幼苗的根茎接种未定植的PDA块作为对照处理。2个月后,所有接种的幼苗都出现了与原始商业果园中观察到的类似的叶片黄化和根腐症状。对照植株未观察到症状。从有症状的植株上成功重新分离出病原体,但从对照植株上未分离出,满足柯赫氏法则。据我们所知,这是囊孢壳菌在中国引起枣树根腐病的首次报道。参考文献:(1)G.C.亚当斯等人,《真菌学研究》52:83,2005年。(2)G.M.阿鲁达等人,《植物病理学》54:53,2005年。(3)J.巴斯卡拉特万等人,《欧洲植物病理学杂志》132:549,2012年。(4)J.B.凯普利等人,《树木学杂志》26:326,2000年。