First report of Diaporthe pescicola causing leaf spot on tea (Camellia sinensis) in China.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES Plant disease Pub Date : 2025-03-03 DOI:10.1094/PDIS-01-25-0119-PDN
Yongtian Zhao, Hong Wang, Taifeng Huang, Ruixing Wang, Li Yang, Yuxin Yang, Lingyu Yang, Fen Wang, Xing'e Wang
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Abstract

Duyun Maojian Tea mainly cultivated in Duyun City is one of the ten famous teas in China. A brown leaf spot was discovered in March 2023 in Qiannan Normal University for Nationalities' Maojian Tea experimental field (26.29°N, 107.52°E). The incidence of the disease is about 40% surveyed on about 300 m2 of tea plants. Infected leaves showed light brown, round or irregular lesions. With disease progression, they enlarged and merged, creating dark brown necrotic zones along leaf edges. To identify the responsible pathogen, three symptomatic leaves from the tea nursery base were collected. The samples were cut 3 mm x 3 mm tissues with 75% ethanol for 30 s and 5% sodium hypochlorite for 60 s, rinsing three times with sterile water. Tissues were taken to potato dextrose agar (PDA) medium and incubated dark at 28 °C for 3 days. Three isolates (TF1, TF3 and TF5) with similar morphology were obtained from three samples, respectively. The colony showed white, with short, villous hyphae expanding radially. Notably, mycelium near the disc was erect and sparse 2 cm away. After 30 days, conidia were observed. Alpha conidia (5.9 to 8.6 μm × 2.0 to 2.8 μm (n = 50)) were colorless and transparent, no septum, ellipsoid to spindle-shaped. Beta conidia (11.1 to 25.3 μm × 1.0 to 1.8 μm (n = 50)) were transparent, no septum, filiform, hooklike, tapering towards the ends. The isolates were identified as Diaporthe pescicola based on the morphology (Zhang et al. 2022). Genomic DNA was extracted, the internal transcribed spacer region (ITS), β-tubulin (tub2), and translation elongation factor 1-alpha (TEF) genes were amplified with primer pairs ITS1/ITS4 (White et al. 1990), Bt2a/Bt2b (Glass and Donaldson 1995), and EF1-728F/EF1-986R (Carbone and Kohn 1999), respectively, and sequenced. The ITS (PQ163865, PQ685064 and PQ685065), tub2 (PQ197032, PV055438 and PV055439), and TEF (PQ197029, PV055440 and PV055441) sequences of isolates (TF1, TF3 and TF5) were deposited in GenBank, respectively. BLAST searches showed >97% nucleotide identity to sequences of D. pescicola MFLUCC 16-0105 (ITS, 98.40% to KU557555.1; tub2, 97.40% to KU557579.1; and TEF, 97.63% to KU557623.1). The phylogenetic tree of ITS, tub2, and TEF gene sequences was constructed using MEGA 6 software with the neighbour-joining method (NJ), and the bootstrap method was employed for 1,000 repeated tests. Isolates TF1, TF3, TF5, and D. pescicola DT 1-1 were grouped together in a node with a bootstrap value of 99. Isolates were identified as D. pescicola. Since large quantities of conidia are difficult to produce in cultures, pathogenicity on the wounded leaves of 5-year-old tea plants of Duyun Maojian Tea local population was conducted by inoculating 6 mm mycelium discs of TF1. The control group and the treatment group were inoculated with 3 tea plants, repeated 2 times. All tea plants were incubated at 25 ± 1 °C, 70% humidity, and natural daylight. The onset of symptoms appeared 7 days later. Lesions were brown, similar to field symptoms. In contrast, the control were healthy. A strain exhibiting the same morphology as TF1 was re-isolated from the diseased portion. ITS, tub2, and TEF gene sequences were consistent with TF1, completing Koch's postulates. D. pescicola as a pathogen has caused leaf spot on Kerria japonica (Zhang et al. 2022), dieback on Prunus persica (Dissanayake et al. 2017) and Vitis vinifera (Manawasinghe et al. 2019), and shoot canker on Pyrus plants (Guo et al. 2020). To our knowledge, this is the first report of tea leaf spot caused by D. pescicola in China and worldwide. It is imperative to develop and implement control measures to manage the disease.

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引起茶树叶斑病的紫斑蝶蚜在国内首次报道。
都匀毛尖茶主要产于都匀市,是中国十大名茶之一。黔南民族师范大学毛尖茶试验田(26.29°N, 107.52°E)于2023年3月发现褐斑病。在约300平方米的茶树上调查,该病发病率约为40%。叶片呈浅棕色,呈圆形或不规则。随着疾病的进展,它们扩大并合并,在叶子边缘形成深棕色的坏死区。为了鉴定病原菌,从茶园基地采集了3片有症状的叶子。样品用75%乙醇30 s, 5%次氯酸钠60 s切割3mm × 3mm组织,用无菌水冲洗三次。将组织置于马铃薯葡萄糖琼脂(PDA)培养基中,28℃暗色孵育3天。从3份样品中分别分离得到形态相似的3株菌株(TF1、TF3和TF5)。菌落呈白色,菌丝呈短绒毛状呈放射状扩张。值得注意的是,菌丝在离菌盘2 cm处直立且稀疏。30 d后观察分生孢子。α分生孢子(5.9 ~ 8.6 μm × 2.0 ~ 2.8 μm (n = 50))无色透明,无隔,椭球形至纺锤形。β分生孢子(11.1 ~ 25.3 μm × 1.0 ~ 1.8 μm (n = 50))透明,无隔,丝状,钩状,向末端逐渐变细。根据形态鉴定该分离株为psicola Diaporthe (Zhang et al. 2022)。提取基因组DNA,分别用引物对ITS1/ITS4 (White et al. 1990)、Bt2a/Bt2b (Glass and Donaldson 1995)和EF1-728F/EF1-986R (Carbone and Kohn 1999)扩增内部转录间隔区(ITS)、β-微管蛋白(tub2)和翻译伸长因子1- α (TEF)基因,并进行测序。分离株(TF1、TF3和TF5)的ITS序列(PQ163865、PQ685064和PQ685065)、tub2序列(PQ197032、PV055438和PV055439)和TEF序列(PQ197029、PV055440和PV055441)分别存入GenBank。BLAST检索显示,与D. pescicola MFLUCC 16-0105 (ITS)序列同源性为98.40%,与KU557555.1序列同源性为98.97%;tub2, 97.40%至KU557579.1;TEF, 97.63%至KU557623.1)。采用MEGA 6软件,采用邻域连接法(NJ)构建ITS、tub2和TEF基因序列的系统发育树,并采用自举法进行1000次重复检测。分离株TF1、TF3、TF5和D. pescicola DT 1-1聚在一个节点,引导值为99。分离株鉴定为青霉菌。由于在培养中难以产生大量分生孢子,采用接种6 mm菌丝盘TF1对杜匀毛尖茶当地种群5年生茶树的伤叶进行致病性研究。对照组和处理组分别接种3株茶树,重复接种2次。所有茶树在25±1℃、70%湿度和自然光条件下孵育。7天后出现症状。病灶呈棕色,与野外症状相似。相比之下,对照组是健康的。从患病部分重新分离出一株与TF1形态相同的菌株。ITS、tub2和TEF基因序列与TF1一致,完成了Koch的假设。d.p escicola作为一种病原菌,引起了粳稻叶斑病(Zhang et al. 2022)、桃李枯死(Dissanayake et al. 2017)和葡萄枯死(Manawasinghe et al. 2019)和梨枝溃疡病(Guo et al. 2020)。据我们所知,这是中国和世界上第一次报道由紫霉引起的茶叶斑病。必须制定和实施控制措施来管理该病。
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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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