引起扁豆叶斑病的cantlous Alternaria (Lens culinaris)首次报道

Q3 Agricultural and Biological Sciences
M. E. A. Kouadri, A. A. Bekkar, S. Zaim
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引用次数: 0

摘要

在2019年5月的一项调查中,扁豆(Lens culinaris)的死亡率为2%。在阿尔及利亚提亚雷特的一块空地上栽培的植物出现褪绿叶斑病,发病率约为10%。症状开始时是小的、不规则的病变,随着时间的推移从叶子边缘扩展到叶子中心。为确定致病因子,将患病叶片用2% NaOCl消毒3分钟,用无菌水冲洗3次,涂于马铃薯葡萄糖琼脂上,在25±1℃下孵育7天。菌落呈深灰色,生长致密。分生孢子为棕色,直立,单生或分枝,2.5 ~ 3.75 × 21-42.5 μm。分生孢子多为卵球形或椭圆形,浅至深褐色,有1 ~ 3个横隔和0 ~ 2个纵隔,大小为8.75 ~ 17.5 × 7.5 ~ 15 μm (n = 25)(图1)。根据形态特征鉴定菌株为Alternaria sp. (Simmons, 2007)。为了确认真菌的身份,对代表性分离物ST2的ITS和tef1区域进行了PCR扩增(White et al., 1990;Carbone & Kohn, 1999)。获得的序列(GenBank登录号:OQ256241, OQ269665)用BLASTn进行分析,与Alternaria cantlous (CBS 123007)的ITS (KC584245)和tef1 (KC584739)前型序列的同源性分别为99.58和99.52%,479/481(99%)和209/210(99%)对匹配。利用最大似然法对ITS和tef1串联序列进行系统发育分析,分离株ST2与cantlous Alternaria前型菌株(Wang Yong bis & X.G. Zhang) (Woudenberg et al., 2013)聚类一致,bootstrap支持度为96%(图2)。基于BLAST搜索和系统发育分析,鉴定分离株ST2为cantlous Alternaria。在温室条件下,将105个分生孢子/ml的分生孢子悬浮液喷施于3个扁豆的成熟叶片上,进行致病性试验。叙利亚的植物。对照植株喷洒了无菌水。所有植物都用透明塑料袋覆盖72小时。20天后,接种植株表现出与田间相似的症状(图3),而对照植株没有出现症状。从所有接种的植物中重新分离出真菌,以满足科赫的假设。据我们所知,这是阿尔及利亚和世界范围内第一次报道扁豆叶斑病。作者谨向马斯卡拉Mustapha Stambouli大学地球科学系Madani Benouycef教授表示最诚挚的感谢,感谢他为研究工作提供了必要的设施和设备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The first report of Alternaria cantlous causing leaf spot on lentil (Lens culinaris)
During a survey in May 2019, lentil (Lens culinaris cv. Syria 229) plants cultivated in an open field in Tiaret, Algeria showed chlorotic leaf spots with an incidence of about 10%. The symptoms began as small, irregular lesions and expanded with time from the edge to the centre of the leaves. To identify the causal agent, diseased leaves were disinfected in 2% NaOCl for three minutes, rinsed thrice with sterile water, plated onto potato dextrose agar and incubated at 25±1°C for seven days. Fungal colonies were dark grey with dense growth. Conidiophores were brown, erect, simple or branched, 2.5-3.75 × 21–42.5 μm. Conidia were mostly ovoid or ellipsoidal, light to dark brown with 1 to 3 transverse septa and 0 to 2 longitudinal septa and ranged in size from 8.75-17.5 × 7.5-15 μm (n = 25) (Fig. 1). Based on morphological characters, isolates were identified as Alternaria sp. (Simmons, 2007). To confirm the identity of the fungus, a PCR was done to amplify ITS and tef1 regions of a representative isolate, ST2 (White et al., 1990; Carbone & Kohn, 1999). The obtained sequences (GenBank Accession Nos. OQ256241, OQ269665) were analysed with BLASTn and had 99.58 and 99.52% identity, 479/481(99%) and 209/210 (99%) pairs matching, with the ex-type sequences of Alternaria cantlous (CBS 123007) for ITS (KC584245) and tef1 (KC584739), respectively. Phylogenetic analysis of concatenated sequences of ITS and tef1 using the maximum likelihood method, clustered isolate ST2 consistently with the ex-type strain of Alternaria cantlous (Yong Wang bis & X.G. Zhang) (Woudenberg et al., 2013), with bootstrap support of 96% (Fig. 2). Based on the BLAST search and phylogenetic analysis, isolate ST2 was identified as Alternaria cantlous. A pathogenicity test was performed under greenhouse conditions by spraying a conidial suspension of 105 conidia/ml onto mature leaves of three lentil (cv. Syria 229) plants. Control plants were sprayed with sterile water. All plants were covered with a transparent plastic bag for 72 hours. After 20 days, the inoculated plants showed similar symptoms to those observed in the field (Fig. 3), while no symptoms were observed on control plants. The fungus was reisolated from all inoculated plants to fulfill Koch's postulates. To the best of our knowledge this is the first report of A. cantlous causing leaf spot on lentil in Algeria and worldwide. The authors wish to express their sincerest gratitude to Professor Madani Benouycef from University Mustapha Stambouli of Mascara, Department of Earth Sciences for providing the necessary facilities and equipment for the research work.
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来源期刊
New Disease Reports
New Disease Reports Agricultural and Biological Sciences-Agronomy and Crop Science
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