Suppr超能文献

尖孢镰孢九州专化型引起玉米茎腐病在中国的首次报道

First Report of Maize Stalk Rot Caused by Fusarium kyushuense in China.

作者信息

Cao Yanyong, Zhang Jie, Han Shengbo, Xia Laikun, Ma Juan, Wang Lifeng, Li Huiyong, Yang Lirong, Sun Suli, Zhu Zhendong, Duan Canxing

机构信息

Henan Academy of Agricultural Sciences, 74728, Institute of Cereal Crops, Henan provincial key laboratory of Maize Biology, Zhengzhou, Henan, China;

Hunan Academy of Agricultural Sciences, 441102, Institute of Plant Protection, Zhengzhou, Henan, China;

出版信息

Plant Dis. 2021 Apr 27. doi: 10.1094/PDIS-11-20-2342-PDN.

Abstract

During 2017 to 2019, a field survey for maize stalk rot was conducted in 21 counties (districts) across the Guangxi province of China. This disease caused yield losses ranging from 20% to 30%. Maize plants with stalk rot were collected during the late milk stage and pieces of diseased pith tissue were cultured as previously described (Shan et al. 2017). Fungal colonies and mycelia with morphological characteristics of Fusarium species were subcultured onto fresh potato dextrose agar (PDA) and carnation leaf agar (CLA) plates. Based on morphological characteristics and molecular detection by amplification of Fusarium genus-specific primers (Duan et al. 2016), 39 Fusarium isolates were identified. Among them, five isolates from Du'an, Pingguo, Debao, and Daxin had abundant, pale orange to yellow aerial mycelium with deep red pigments when grown on PDA (Fig. 1A; 1B). The average growth rate was 8.0 to 12.0 mm per day at 25°C in the dark. The fungi produced two types of spores on CLA. Microconidia were ovoid to clavate, generally 0- to 3-septate, and 4.6 to 9.4 μm in length (n = 30) (Fig. 1D); Macroconidia were slightly curved with an acute apical cell, mostly 3- to 4- septate, and 19.4 to 38.2 μm in length (n = 30) (Fig. 1C). No chlamydospores were observed. These five isolates were initially identified as Fusarium kyushuense based on morphological features. PCR was performed to amplify three phylogenetic genes (TEF1-α, RPB1, and RPB2) (O'Donnell et al. 1998) and species specific primers kyuR1F/kyuR1R (5-TTTTCCTCACCAAGGAGCAGATCATG-3/5-TCCAATGGACTGGGCAGCCAAAACACC-3), kyuR2F/kyuR2R (5-CAGATATACATTTGCCTCGACAC-3/5-TACTTGAGCACGGAGCTTG-3) were used to confirm species identity. The obtained sequences were deposited in GenBank under the accession numbers MT997084, MT997080, MT997081 (TEF1-α); MT550012, MT997085, MT997086 (RPB1); MT550009, MT997089, and MT997090 (RPB2), respectively. Using BLAST, sequences of TEF1-α, RPB1, and RPB2 of the isolates were 99.33% (MH582297.1) to 100% (MG282364.1) similar to those of F. kyushuense strains (Supplementary Table 1). Based on phylogenetic analysis with maximum likelihood methods using tools of the website of CIPRES (http://www.phylo.org), isolates GX27, GX167, and GX204 clustered with F. kyushuense with 100% bootstrap support (Fig. 2). The pathogenicity of the three isolates was tested using young seedlings and adult plants as previously described with modification (Ye et al. 2013; Zhang et al. 2016). The primary roots of three-leaf-old seedlings were inoculated by immersing the roots into a 1 × 106 macroconidia solution, incubating for 6 h at 25°C, and transferring to normal growth conditions (26°C, 16 h light/22°C, 8 h dark). The second or third internode above the soil surface of flowering stage plants grown in a greenhouse was bored with a Bosch electric drill to make a hole (ca. 8 mm in diameter) and inoculated with 0.5 mL of mycelia plug then sealed with petrolatum. The inoculum was created by homogenizing five plates of flourish hyphal mats (approximately 125 mL) with kitchen blender and adjusting to a final volume of 200 mL with sterilized ddH2O. No symptoms were observed in the seedlings or adult plants that were mock-inoculated with PDA plugs. Three days post-inoculation (dpi), roots of the infected seedling turned dark-brown and shrunk and the leaves wilted (Fig. 1E). Typical stalk rot symptoms observed in the inoculated plants were premature wilting of entire plant and hollow and weak stalks, leading to lodging; the longitudinal section of the internodes exhibited obvious dark brown necrosis and reddish discoloration at 14 dpi and 30 dpi, respectively (Fig. 1F). Fusarium kyushuense was re-isolated from the inoculated stalk lesions but not from the control. This is the first record of stalk rot caused by F. kyushuense on maize plants in China. However, F. kyushuense is known to cause maize ear rot in China (Wang et al. 2014) and can produce type A and type B trichothecene mycotoxins in kernels (Aoki and O'Donnell 1998). The occurrence of maize stalk rot and ear rot caused by F. kyushuense should be monitored in China due to the potential risk for crop loss and mycotoxin contamination.

摘要

2017年至2019年期间,在中国广西壮族自治区的21个县(区)开展了玉米茎腐病实地调查。这种病害导致的产量损失在20%至30%之间。在乳熟后期采集患有茎腐病的玉米植株,将患病的髓组织切块按照之前描述的方法进行培养(单等,2017年)。将具有镰刀菌形态特征的真菌菌落和菌丝体转接至新鲜的马铃薯葡萄糖琼脂(PDA)平板和香石竹叶琼脂(CLA)平板上。基于形态特征以及通过扩增镰刀菌属特异性引物进行分子检测(段等,2016年),鉴定出39株镰刀菌分离株。其中,来自都安、平果、德保和大新的5株分离株在PDA平板上生长时,气生菌丝丰富,呈浅橙色至黄色,带有深红色色素(图1A;1B)。在25℃黑暗条件下,平均生长速率为每天8.0至12.0毫米。这些真菌在CLA平板上产生两种类型的孢子。分生孢子呈卵形至棒形,通常0至3分隔,长度为4.6至9.4微米(n = 30)(图1D);大型分生孢子略微弯曲,顶端细胞尖锐,大多3至4分隔,长度为19.4至38.2微米(n = 30)(图1C)。未观察到厚垣孢子。基于形态特征,这5株分离株最初被鉴定为九州镰刀菌。进行PCR扩增三个系统发育基因(TEF1-α、RPB1和RPB2)(奥唐奈等,1998年),并使用物种特异性引物kyuR1F/kyuR1R(5-TTTTCCTCACCAAGGAGCAGATCATG-3/5-TCCAATGGACTGGGCAGCCAAAACACC-3)、kyuR2F/kyuR2R(5-CAGATATACATTTGCCTCGACAC-3/5-TACTTGAGCACGGAGCTTG-3)来确认物种身份。获得的序列分别以登录号MT997084、MT997080、MT997081(TEF1-α);MT550012、MT997085、MT997086(RPB1);MT550009、MT997089和MT997090(RPB2)存入GenBank。使用BLAST分析,这些分离株的TEF1-α、RPB1和RPB2序列与九州镰刀菌菌株的序列相似度为99.33%(MH582297.1)至100%(MG282364.1)(补充表1)。基于使用CIPRES网站工具(http://www.phylo.org)的最大似然法进行的系统发育分析,分离株GX27、GX167和GX204与九州镰刀菌聚类,自展支持率为100%(图2)。按照之前描述并略有修改的方法(叶等,2013年;张等,2016年),使用幼苗和成株对这三株分离株的致病性进行测试。将三叶期幼苗的初生根浸入1×106个大型分生孢子溶液中进行接种,在25℃下孵育6小时,然后转移至正常生长条件(26℃,16小时光照/22℃,8小时黑暗)。使用博世电钻在温室中生长的开花期植株土壤表面上方的第二或第三茎节处钻孔(直径约8毫米),接种0.5毫升菌丝体块,然后用凡士林密封。接种物是通过用厨房搅拌机将五平板旺盛生长的菌丝垫(约125毫升)匀浆,并加入无菌双蒸水调整至最终体积200毫升制备而成。用PDA块进行 mock接种的幼苗或成株未观察到症状。接种后3天(dpi),受感染幼苗的根变为深褐色并萎缩,叶片枯萎(图1E)。在接种植株上观察到的典型茎腐病症状是整株过早枯萎,茎中空且脆弱,导致倒伏;在14 dpi和30 dpi时,茎节的纵切面分别表现出明显的深褐色坏死和微红变色(图1F)。从接种的茎部病斑中重新分离出九州镰刀菌,但对照中未分离到。这是九州镰刀菌引起中国玉米植株茎腐病的首次记录。然而,已知九州镰刀菌在中国会引起玉米穗腐病(王等,2014年),并且能在玉米粒中产生A型和B型单端孢霉烯族毒素(青木和奥唐奈,1998年)。鉴于存在作物损失和霉菌毒素污染的潜在风险,在中国应监测由九州镰刀菌引起的玉米茎腐病和穗腐病的发生情况。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验