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中国北方由新月弯孢菌引起的花生荚腐病首次报道

First Report of Peanut Pod Rot Caused by Neocosmospora vasinfecta in Northern China.

作者信息

Sun W M, Feng L N, Guo W, Liu D Q, Li Y N, Ran L X

机构信息

Biological Control Center of Plant Diseases and Plant Pests of Hebei Province, College of Plant Protection, College of Life Sciences, Agricultural University of Hebei, Baoding 071000, China.

出版信息

Plant Dis. 2012 Mar;96(3):455. doi: 10.1094/PDIS-03-11-0240.

Abstract

From 2006 to 2010, peanut (Arachis hypogaea) pod rot became more prevalent in northern China, especially in the Sha River drainage area. The incidence of pod rot ranged from 30 to 100%. Typical symptoms were black rot of the pods, but no obvious morphological abnormality of the aboveground parts of infected plants was observed. Brown or black spots appeared on many pods when initially infected and then all peanut pods became black and rotten. The same fungus was isolated from 54 surface-disinfested lesions (85.2% of all lesions) on potato dextrose agar (PDA) media. One isolate, designated as HBXLb, was chosen for further characterization. In culture, both anamorph and teleomorph were present. Mycelia of the fungus grew quickly (colonies were 3.2 cm in diameter in 3 days) and became white and floccose on PDA at 28°C. The hyaline, elongated-to-cylindrical conidia aggregated on the slimy heads of conidiogenous cells that developed on undifferentiated hyphae after incubation for 3 to 4 days. Conidial sizes varied from 5 to 10 × 1.5 to 3 μm (n = 50) and were mostly single celled. Some conidia appeared slightly curved. The morphology was consistent with Acremonium spp. Numerous ascomata (perithecia) formed within 10 to 14 days when incubated at 28°C under light and dark conditions. Perithecia were orange-brown, strawberry shaped (300 to 400 μm in diameter), and ostiolate on the top. Cylindrical asci, with an average size of 90 to 110 × 7.5 to 9 μm, were present inside the ascomata with each containing eight ascospores in a row. The ascospores were brownish, spherical to ellipsoidal, and 10 to 15 × 8 to 12 μm. The cultural and morphological characteristics of isolate HBXLb matched the description of N. vasinfecta (2). The internal transcribed spacer (ITS) region of rDNA was amplified by the primer pairs ITS4/ITS5. A 525-bp amplicon (ITS4-5.8s-ITS5) was obtained and sequenced (GenBank Accession No. HM461901). The ITS sequence was a 100% match to N. vasinfecta strain N-JXLN01 (GenBank Accession No. GU213063) by BLASTn in GenBank. Pathogenicity tests were conducted on detached pods of peanut cultivar Jihua 4. Forty surface-disinfested peanut pods were soaked in a conidial suspension (10 conidia per ml) for 2 min and 40 pods were soaked in sterile water as a control. Then all peanut pods were maintained in moist petri dishes under darkness for 14 days at 28°C. Brown or black spots appeared on all pods inoculated with the fungus within 10 days, while the controls remained healthy. Symptoms were similar to those originally observed in the field, and N. vasinfecta could be reisolated from all infected pods. This fungus previously has been reported as the pathogen of foot rot of peanut in South Africa (1), Taiwan (4), and Australia (3). To our knowledge, this is the first report of peanut pod rot caused by N. vasinfecta in China. References: (1) S. W. Baard et al. Phytophylactica 17:49, 1985. (2) O. A. Cornely et al. Emerg. Infect. Dis. 7:149, 2001. (3) M. F. Fuhlbohm et al. Australas. Plant Dis. Notes 2:3, 2007. (4) J. W. Huang et al. Plant Pathol. Bull. 1:203, 1992.

摘要

2006年至2010年期间,花生荚腐病在中国北方地区,尤其是在沙河排水区更为普遍。荚腐病的发病率在30%至100%之间。典型症状是荚果黑腐,但未观察到受感染植株地上部分有明显的形态异常。最初感染时,许多荚果上出现褐色或黑色斑点,随后所有花生荚果都变黑腐烂。在马铃薯葡萄糖琼脂(PDA)培养基上,从54个表面消毒的病斑中分离出相同的真菌(占所有病斑的85.2%)。选择了一个分离株,命名为HBXLb,进行进一步鉴定。在培养过程中,无性型和有性型均存在。该真菌的菌丝生长迅速(在28°C下3天内在PDA上菌落直径达3.2厘米),在PDA上28°C时变为白色且呈絮状。透明、细长至圆柱形的分生孢子聚集在产孢细胞的黏液头部,产孢细胞在培养3至4天后在未分化的菌丝上形成。分生孢子大小为5至10×1.5至3微米(n = 50),大多为单细胞。一些分生孢子略显弯曲。其形态与枝顶孢属真菌一致。在28°C光照和黑暗条件下培养10至14天内形成大量子囊壳(子囊腔)。子囊壳呈橙褐色,草莓形(直径300至400微米),顶部有孔口。子囊壳内有圆柱形子囊,平均大小为90至110×7.5至9微米,每个子囊内有8个呈一排的子囊孢子。子囊孢子呈褐色,球形至椭圆形,大小为10至15×8至12微米。分离株HBXLb的培养和形态特征与大豆疫霉的描述相符(2)。rDNA的内部转录间隔区(ITS)用引物对ITS4/ITS5进行扩增。获得了一个525碱基对的扩增片段(ITS4 - 5.8s - ITS5)并进行测序(GenBank登录号HM461901)。通过GenBank中的BLASTn分析,ITS序列与大豆疫霉菌株N - JXLN01(GenBank登录号GU213063)100%匹配。对花生品种冀花4号的离体荚果进行致病性测试。40个表面消毒的花生荚果在分生孢子悬浮液(每毫升10个分生孢子)中浸泡2分钟,40个荚果浸泡在无菌水中作为对照。然后将所有花生荚果在黑暗中于28°C的潮湿培养皿中保存14天。接种真菌的所有荚果在10天内出现褐色或黑色斑点,而对照保持健康。症状与最初在田间观察到的相似,并且可以从所有受感染的荚果中重新分离出大豆疫霉。此前该真菌已被报道为南非(1)、台湾(4)和澳大利亚(3)花生根腐病的病原菌。据我们所知,这是中国关于大豆疫霉引起花生荚腐病的首次报道。参考文献:(1)S. W. Baard等人,《植物保护》17:49,1985年。(2)O. A. Cornely等人,《新发传染病》7:149,2001年。(3)M. F. Fuhlbohm等人,《澳大利亚植物病害笔记》2:3,2

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