Li Yang, Shi Maoyin, Mo Zhenghai, Zhai Min, Shang Chu, Xuan Jiping, Hu Longjiao
No. 1, qianhuhou village, Xuanwu District, Nanjing City, Jiangsu ProvinceNanjing, China, 210014;
Nanchang, China;
Plant Dis. 2023 Mar 22. doi: 10.1094/PDIS-11-22-2611-PDN.
Pecan [Carya illinoinensis (Wangenh.) K. Koch] is an important nut tree species, which has been widely planted in Jiangsu and Anhui Provinces of China in recent years (Mo et al. 2018). In May 2022, a new leaf spot disease was observed on both young and old leaves of pecan trees in the Luhe area, Nanjing, Jiangsu Province. Approximately 30% of pecan trees suffered from the disease, which affected the growth of young trees and nut production to cause economic loss. Initially, the leaf spots were grayish black and round. Then, disease spots enlarged and joined together, forming irregular lesions with uneven edges. In the last stage, the leaflets were withered. To isolate the pathogen, three symptomatic leaves were collected from each of three different pecan trees. Leaf sections (3 to 4 mm) were excised from the margin of spots, surface sterilized in 75% alcohol for 30 s, then sterilized in 1.5% NaClO for 90 s. After rinsing three times with sterile distilled water, leaf sections were placed on potato dextrose agar (PDA) medium and incubated at 25 °C in a dark environment for 5 days. Pure cultures were obtained by monosporic isolation. A total of 20 isolates were obtained, and 12 isolates were identified as Stemphylium sp. with the same morphological features and ITS sequences. A representative isolate, named LH3-3, was selected for further study. Colonies on PDA were light yellow with dense mycelium and were brownish yellow on the reverse side. Conidia were 16.3 to 34.4 × 8.1 to 16.3 µm) (n=35), muriform, brown, with transverse and longitudinal septa, lightly deformed at the transverse septa. Ascomata were not observed. The morphological characteristics were consistent with the description of Stemphylium eturmiunum (Simmons 2001). The internal transcribed spacer region (ITS) and portions of genes for calmodulin (cmdA) and glyceraldehyde-3-phosphate dehydrogenase (gpd) were amplified and sequenced with the primers ITS1/ITS4 (White et al. 1990), CALDF1/CALDR2 (Xu et al. 2022) and GPD-F/R (Xie et al. 2019), respectively. Sequences were deposited in GenBank under accessions OP482492 (ITS), OP495734 (cmdA), and OP495735 (gpd). BLAST analysis showed that the sequences had 99.67-100% homology to ITS (525/525 bp) of S. eturmiunum strain ST14 (MH843733), cmdA (694/694 bp) of strain CBS122124 (KU850832), and gpd (299/300 bp) of isolate UMSe0030 (MK336876). MEGA 7.0 was used to construct a phylogenetic analysis based on concatenated sequences of ITS, cmdA, and gpd using the neighbor-joining method. The results showed that LH3-3 clustered on the branch of S. eturmiunum, and the support rate was 100%. A spore suspension in sterile water was made from strain LH3-3 grown on PDA, and adjusted to 1×106 spores/mL with a hemocytometer. To test pathogenicity, 20 µl drops of the spore suspension were placed on the left sides of four healthy detached leaflets of mature pecan trees and leaves of three 3-month-old seedlings. The right side of each leaflet was inoculated with 20 µl drops of sterile distilled water as the control. All inoculated seedlings and detached leaflets were covered with a transparent plastic bag and cultured in a greenhouse at 25 °C, 80% relative humidity, and a 12 h light cycle until symptom appeared. The experiment was repeated three times. After 7 days of inoculation, grayish black lesions appeared on all inoculation sites with the spore suspension but not in the controls. The leaf spot symptoms were similar to those observed in orchards. The same fungus, identified by morphological characteristics and sequencing of ITS, cmdA, and gpd, was re-isolated from the diseased spots of the inoculated leaflets to complete Koch's postulates. S. eturmiunum has been reported to infect garlic (Dumin et al. 2022) and tomato (Prencipee et al. 2021), but this is the first report of S. eturmiunum causing leaf spot of C. illinoinensis. This study provides a basis for further study on the biology, epidemiology, and management of the disease.
山核桃[Carya illinoinensis (Wangenh.) K. Koch]是一种重要的坚果树种,近年来在中国江苏省和安徽省广泛种植(Mo等人,2018年)。2022年5月,在江苏省南京市六合地区的山核桃树幼叶和老叶上均观察到一种新的叶斑病。约30%的山核桃树感染此病,影响幼树生长和坚果产量,造成经济损失。最初,叶斑为灰黑色,圆形。随后,病斑扩大并融合在一起,形成边缘不齐的不规则病斑。在后期,小叶枯萎。为分离病原菌,从三棵不同的山核桃树上各采集三片有症状的叶片。从病斑边缘切取3至4毫米的叶片切片,在75%乙醇中表面消毒30秒,然后在1.5%次氯酸钠中消毒90秒。用无菌蒸馏水冲洗三次后,将叶片切片置于马铃薯葡萄糖琼脂(PDA)培养基上,在25℃黑暗环境中培养5天。通过单孢分离获得纯培养物。共获得20个分离株,其中12个分离株被鉴定为链格孢属(Stemphylium sp.),具有相同的形态特征和ITS序列。选择一个代表性分离株,命名为LH3-3,进行进一步研究。PDA培养基上的菌落浅黄色,菌丝浓密,背面棕黄色。分生孢子大小为16.3至34.4×8.1至16.3微米(n = 35),砖格状,褐色,有横隔和纵隔,在横隔处轻度变形。未观察到子囊壳。形态特征与埃氏链格孢(Stemphylium eturmiunum)的描述一致(Simmons,2001年)。分别用引物ITS1/ITS4(White等人,1990年)、CALDF1/CALDR2(Xu等人,2022年)和GPD-F/R(Xie等人,2019年)扩增并测序了内部转录间隔区(ITS)以及钙调蛋白(cmdA)和甘油醛-3-磷酸脱氢酶(gpd)基因的部分序列。序列已存入GenBank,登录号分别为OP482492(ITS)、OP495734(cmdA)和OP495735(gpd)。BLAST分析表明,这些序列与埃氏链格孢菌株ST14(MH843733)的ITS(525/525 bp)、菌株CBS122124(KU850832)的cmdA(694/694 bp)和分离株UMSe0030(MK336876)的gpd(299/300 bp)具有99.67 - 100%的同源性。使用MEGA 7.0软件,采用邻接法基于ITS、cmdA和gpd的串联序列构建系统发育分析。结果表明,LH3-3聚类在埃氏链格孢的分支上,支持率为100%。用在PDA培养基上生长的菌株LH3-3制备无菌水孢子悬浮液,并用血细胞计数板将其调整至1×106个孢子/毫升。为测试致病性,将20微升孢子悬浮液滴在四片成熟山核桃树健康离体小叶和三株3个月大幼苗的叶片左侧。每片小叶右侧接种20微升无菌蒸馏水作为对照。所有接种的幼苗和离体小叶均用透明塑料袋覆盖,在25℃、相对湿度80%、12小时光照周期的温室中培养,直至出现症状。该实验重复三次。接种7天后,接种孢子悬浮液的所有接种部位均出现灰黑色病斑,而对照未出现。叶斑症状与果园中观察到的症状相似。通过形态特征以及ITS、cmdA和gpd测序鉴定,从接种小叶的病斑中重新分离出相同的真菌,从而完成了柯赫氏法则验证。据报道,埃氏链格孢可感染大蒜(Dumin等人,2022年)和番茄(Prencipee等人,2021年),但这是埃氏链格孢引起山核桃叶斑病的首次报道。本研究为进一步研究该病的生物学、流行病学和防治提供了依据。