First Report of Alternaria alternata Causing Alternaria Leaf Spot of Black Nightshade in China.

IF 4.4 2区 农林科学 Q1 PLANT SCIENCES
Zhanjiang Tie, Shaohua Chen, Zhiqiang Zhang, Juanxu Zhan, Guiyuan Zhang, Chaoyang Ma, Shuyi Jia, Sifeng Zhao, Hui Xi
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引用次数: 0

Abstract

Black nightshade (Solanum nigrum L.) belongs to Solanaceae family, which is distributed all over China and has become one of the malignant weeds in cotton field in Xinjiang (Zhang et al., 2020; Zhang et al., 2021). During July 2016 to August 2023, leaf spot was observed on black nightshade in Hami and Shihezi city, Xinjiang, China. The spots appeared as brown circular or irregular, with some small black dots surrounded with yellow halos. Twenty five black nightshade plants were collected from a cotton field (100 m2) for pathogen isolation in Shihezi, July 2023. Leaf samples (2×2 mm) from the boundary between diseased tissue and healthy tissue, sterilized in 70% ethanol for 45 s, dipped in 2% NaClO for 30 s, rinsed three times with sterile distilled water, placed on potato dextrose agar (PDA) after dried and cultivated at 25°C in the dark for 4 days. Twenty-five fungal isolates were obtained and purified by using the single-spore isolation method, and all isolates were found to be similar in morphology, appeared as dark brown and produced dark brown pigmentation on PDA. Conidiophores were black brown, 8 to 58 × 10 to 20 μm, with 1 to 5 transverse septa and 0 to 3 longitudinal septa, the results similar to those of Alternaria alternata isolated from buckwheat (Li et al., 2021). To confirm this identification, total genomic DNA of the isolates were extracted by CTAB method (Doyle et al., 1987). The internal transcribed spacer (rDNA-ITS), Alternaria major allergen gene (Alt α1) and glyceraldehyde-3-phosphate dehydrogenase gene (GAPDH) of the A. alternata 26 were amplified using the primers ITS1/ITS4 (Glass et al., 1995), Altα1-F/Altα1-R (Li et al., 2024) and gpd-F/gpd-R (5'-CAACGGCTTCGGTCGCAT- TG-3' / 5'-GCCAAGCAGTTGGTTGTG-3'), respectively. The rDNA-ITS, Altα1 and GAPDH gene sequences were deposited in GenBank (KX904867, PP263361, PP263360), and showed 100% identity (rDNA-ITS: 572 out of 609 bp; Alt α1: 514 out of 516 bp; GAPDH: 619 out of 619 bp) to A. alternata (KU179665; MW522975; MK451977), respectively. The multi-gene phylogenetic tree showed that the representative isolate was grouped with A. alternata and identified as A. alternata. Black nightshade was used for pathogenicity assay. Fifteen plants at 3 to 4-leaf stage were selected and sprayed with the conidial suspension (1.0×106 spores/mL) of A. alternata 26 after wound the underside of leaves (2 mm length) with inoculating needle. Five plants were sprayed with sterilized water as control. After inoculation, placed the plants in a plastic box and covered with plastic wrap to keep 80% relative humidity for 3 days at 25℃ in the greenhouse, then removed the plastic box. Symptoms of leaf spots appeared within 12 - 15 days that were similar to the symptoms observed in the field, and the fungal pathogen that was re-isolated from symptomatic leaves was identical to original pathogen on the basis of morphological and molecular analysis to fulfill Koch's postulates. This experiment was repeated three times, and the disease incidence was above 80% after inoculation at each time. To our knowledge, this is the first report of A. alternata causing leaf spot of black nightshade in China. This report will help us to monitoring distribution of the disease and providing theoretical basis for disease prevention and control.

中国首次报告交替孢属交替孢属真菌导致黑夜来香叶斑病。
黑夜草(Solanum nigrum L.)属茄科,分布于中国各地,已成为新疆棉田的恶性杂草之一(Zhang et al.,2020;Zhang et al.,2021)。2016 年 7 月至 2023 年 8 月期间,在中国新疆哈密和石河子市观察到黑夜蛾叶斑病。病斑呈褐色圆形或不规则形,一些小黑点周围有黄色晕圈。2023 年 7 月,从石河子市的一块棉田(100 平方米)中采集了 25 株黑夜来香植株,用于病原分离。叶片样本(2×2 毫米)取自病组织与健康组织的交界处,在 70% 的乙醇中消毒 45 秒,在 2% 的 NaClO 中浸泡 30 秒,用无菌蒸馏水冲洗 3 次,干燥后置于马铃薯葡萄糖琼脂(PDA)上,在 25°C 黑暗中培养 4 天。通过单孢分离法获得并纯化了 25 个真菌分离物,发现所有分离物形态相似,呈黑褐色,在 PDA 上产生黑褐色色素沉着。分生孢子梗黑褐色,8-58×10-20 μm,有 1-5 个横隔膜和 0-3 个纵隔膜,结果与从荞麦中分离出的交替花叶病毒相似(Li 等,2021 年)。为确认这一鉴定结果,采用 CTAB 法(Doyle 等人,1987 年)提取了分离物的总基因组 DNA。使用引物 ITS1/ITS4 (Glass et al、1995)、Altα1-F/Altα1-R(Li 等人,2024)和 gpd-F/gpd-R (5'-CAACGGCTTCGGTCGCAT- TG-3' / 5'-GCCAAGCAGTTGGTTGTG-3')分别扩增。rDNA-ITS、Altα1 和 GAPDH 基因序列已存入 GenBank(KX904867、PP263361、PP263360),并显示出 100%的一致性(rDNA-ITS:分别与 A. alternata(KU179665;MW522975;MK451977)的基因序列(rDNA-ITS:572,共 609 bp;Alt α1:514,共 516 bp;GAPDH:619,共 619 bp)显示出 100%的一致性。多基因系统发育树显示,代表性分离株与交替花叶病毒(A. alternata)归为一类,并被鉴定为交替花叶病毒。黑夜莺被用于致病性检测。选取 15 株 3 至 4 叶期的植株,用接种针刺伤叶片背面(2 毫米长)后,喷洒交替穗霉 26 的分生孢子悬浮液(1.0×106 个孢子/毫升)。五株植物喷洒灭菌水作为对照。接种后,将植株放在塑料箱中,用保鲜膜覆盖,保持相对湿度为 80%,在 25℃的温室中放置 3 天,然后移开塑料箱。12 - 15 天内出现叶斑症状,与田间观察到的症状相似,从症状叶片中重新分离出的真菌病原体,根据形态学和分子分析,与原始病原体相同,符合科赫假说。该实验重复了三次,每次接种后的发病率都在 80% 以上。据我们所知,这是中国首次报道交替花叶病毒(A. alternata)引起黑夜来香叶斑病。该报告将有助于我们监测该病害的分布情况,为病害防控提供理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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