First report of strawberry root rot caused by Monosporascus eutypoides in China.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES Plant disease Pub Date : 2025-01-28 DOI:10.1094/PDIS-07-24-1465-PDN
Jiaqi Zhang, Lihong Dong, Yifan Fu, Qinggang Guo, Peipei Wang, Ping Ma
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Abstract

Strawberry (Fragaria × ananassa) is an important economic crop in Hebei, China. In May 2023, root rot was observed in strawberry plantations (cultivar 'Benihoppe') in Shijiazhuang (37°57'23″N, 115°16'34″E), Hebei, China. The incidence of the disease reached up to 30% in the field. The infected plants displayed symptoms of reduced vigor and stunted growth, yellowing leaves, blackened roots, and eventual rotting. Ten diseased strawberry plants were collected for pathogen isolation. Root tissues of symptomatic plants were surface sterilized sequentially in 70% ethanol (1 min), 3.125% NaOCl (6 min), and 70% ethanol (30 s), then they were rinsed in sterile water three times (Sahu et al. 2022). The sterilized roots were then cut into 3.0 × 3.0 mm pieces and placed on potato dextrose agar (PDA) medium supplemented with chloramphenicol (100 μg/mL). After 2 to 3 days incubated at 25℃ in darkness, single colonies from the initial isolates were streaked onto PDA agar plates to obtain pure cultures. The fungal colonies appeared milky white on PDA medium and exhibited only hyphae growth. Globose perithecia were observed on V8-juice medium after 30 days of incubation, with black, smooth, spherical ascospores 13.9 to 19.1 μm in diameter (n=50). For molecular analysis, the representative isolates ME10-2 and ME10-3 from different strawberry plants were selected for the amplification of internal transcribed spacer (ITS) and elongation factor 1-alpha (EF-1α) sequences using the primer sets ITS1/ITS4 (Bellemain et al. 2010) and EF1-688F/EF1-1251R (Alves et al. 2008). The sequences were deposited in GenBank (accession no. PP990210 and PP990211 for ITS, and PQ001579 and PQ001580 for EF-1α). BLASTn analysis revealed that the sequences of ITS had above 99% (504/511 bp and 503/506 bp) similarity to Monosporascus eutypoides (MK183805.1), the sequences of EF-1α had 94% (625/661 bp and 619/656 bp) similarity to Monosporascus eutypoides (JQ958959.1). Phylogenetic analysis based on concatenated sequences of ITS and EF-1α using the Maximum Likelihood method with IQ-TREE version 2.2.3 (Nguyen et al. 2015) also indicated that the two isolates clustered with M. eutypoides. To fulfill Koch's postulates, pathogenicity tests were performed (Chen et al. 2024). Due to challenges in ascospore production, an improved wheat grain medium (wheat grain with 2% dextrose) was used for fungal culture (Sainos et al. 2006). After 14 days of inoculation at 25℃, the medium was crushed and mixed into sterilized soil with a 10% ratio by weight. Four-week-old strawberry plants were transplanted into the inoculated soil and grown in a growth chamber at 25℃ (16 h light/8 h dark). Strawberry plants transplanted into sterilized uninoculated soil served as a negative control. Three weeks post-inoculation, the inoculated strawberry plants exhibited symptoms similar to those observed in field-infected, whereas no symptoms were observed on the control plants. The pathogen was reisolated from the symptomatic plants and identified as M. eutypoides based on colony morphology on a PDA plate and ITS sequences information. M. eutypoides has been found to cause Monosporascus root rot and vine decline on muskmelon, watermelon and cucumber (Martyn and Miller 1996; Salem I. B. et al. 2013). To our knowledge, this is the first report of M. eutypoides causing root rot on strawberry. This finding suggests a potential risk of strawberry root rot when planting subsequent to cucurbit crops and assists strawberry growers in the region in adjusting their planting and disease management decisions.

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草莓纯型单孢霉根腐病在国内首次报道。
草莓(Fragaria × ananassa)是河北省重要的经济作物。2023年5月,在中国河北省石家庄(37°57′23″N, 115°16′34″E)的‘Benihoppe’草莓种植园发现了根腐病。该病在田间的发病率高达30%。受感染的植物表现出活力下降、生长迟缓、叶子变黄、根变黑、最终腐烂的症状。收集10株草莓病株进行病原菌分离。对症植株的根组织依次用70%乙醇(1 min)、3.125% NaOCl (6 min)和70%乙醇(30 s)进行表面消毒,然后用无菌水冲洗3次(Sahu et al. 2022)。将灭菌后的根切成3.0 × 3.0 mm的小块,置于添加氯霉素(100 μg/mL)的马铃薯葡萄糖琼脂(PDA)培养基上。25℃黑暗培养2 ~ 3天后,将初始分离的单个菌落涂布在PDA琼脂板上获得纯培养物。在PDA培养基上菌落呈乳白色,菌丝仅生长。培养30 d后,在V8-juice培养基上观察到球形子囊孢子,孢子黑色,光滑,球形,直径13.9 ~ 19.1 μm (n=50)。在分子分析方面,选取不同草莓植株中具有代表性的ME10-2和ME10-3分离株,利用引物集ITS1/ITS4 (Bellemain et al. 2010)和EF1-688F/EF1-1251R (Alves et al. 2008)扩增内部转录间隔段(ITS)和伸长因子1- α (EF-1α)序列。测序结果存于GenBank(登录号:;PP990210和PP990211用于ITS, PQ001579和PQ001580用于EF-1α)。BLASTn分析结果显示,ITS序列与真型单孢子孢子虫(MK183805.1)的相似度在99%以上(504/511 bp和503/506 bp), EF-1α序列与真型单孢子孢子虫(JQ958959.1)的相似度在94% (625/661 bp和619/656 bp)。利用IQ-TREE 2.2.3版本的最大似然法(Nguyen et al. 2015)对ITS和EF-1α序列的串联进行系统发育分析也表明,这两个分离株与真型假芽孢杆菌聚集在一起。为了实现Koch的假设,进行了致病性测试(Chen et al. 2024)。由于子囊孢子生产方面的挑战,采用改良的小麦培养基(含2%葡萄糖的小麦)进行真菌培养(Sainos et al. 2006)。在25℃下接种14天后,将培养基粉碎,按10%的质量比混合到无菌土壤中。将4周大的草莓植株移栽到接种过的土壤中,在25℃(光照16 h /暗8 h)的生长室内生长。草莓植株移栽到无菌未接种土壤中作为阴性对照。接种3周后,接种草莓植株表现出与田间侵染植株相似的症状,而对照植株没有出现症状。根据PDA平板菌落形态和ITS序列信息,从有症状的植物中重新分离到该病原菌,并鉴定为真型芽孢杆菌(M. eutypoides)。在甜瓜、西瓜和黄瓜上发现了引起单孢霉病根腐病和葡萄藤枯萎病的真菌(Martyn and Miller 1996;Salem i.b. et al. 2013)。据我们所知,这是第一次报道的实型芽孢杆菌引起草莓根腐病。这一发现表明,在种植瓜类作物后种植草莓有潜在的根腐病风险,并有助于该地区的草莓种植者调整种植和病害管理决策。
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来源期刊
Plant disease
Plant disease 农林科学-植物科学
CiteScore
5.10
自引率
13.30%
发文量
1993
审稿时长
2 months
期刊介绍: Plant Disease is the leading international journal for rapid reporting of research on new, emerging, and established plant diseases. The journal publishes papers that describe basic and applied research focusing on practical aspects of disease diagnosis, development, and management.
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