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暹罗炭疽菌引起中国百日草炭疽病的首次报道

First Report of Colletotrichum siamense Causing Anthracnose on Zinnia elegans Jacq. in China.

作者信息

Li Wen, He Yue-Qiu, Fu Tao, Lin Li, Liu Feng, Wang Long Zhi, Wang Guo Liang

机构信息

Xuefu Road, Ningbo, Zhejiang, ChinaNingbo, China, 315100;

Ningbo, China;

出版信息

Plant Dis. 2020 Oct 19. doi: 10.1094/PDIS-04-20-0803-PDN.

DOI:10.1094/PDIS-04-20-0803-PDN
PMID:33074074
Abstract

Zinnia elegans (syn. Zinnia violacea), known as common zinnia, is one of the most spectacular ornamental plants in the family Asteraceae. Zinnia plants are widely cultivated in China for their impressive range in flower colours and profuse bloom over a long period. In April 2019, Zinnia plants grown in Ningbo Botanical Garden (29°56'57″N, 121°36'20″E) were found to have many circular necrotic lesions. In the early infection stage, the lesions appeared as small circular specks which developed later into large spots (15 to 32 mm diameter). Typical symptoms appeared to be grayish white centers with a chlorotic edges and disease incidence reached approximately 80% of plants in the affected field. Moreover, the growth of Zinnia plants was seriously affected by the disease. To identify the causative pathogen associated with the disease, 10 symptomatic leaves were collected from ten different Zinnia plants. Leaf tissues were cut from the lesion margins, surface sterilized with 75% ethanol for 30 seconds and rinsed three times in sterile distilled water. The leaf tissues were then dipped into 10% sodium hypochlorite for 2-3 minutes, washed three times in distilled water and dried on a sterile filter paper. After drying, the surface-sterilized leaf discs were transferred to potato dextrose agar (PDA) plates and incubated at 28°C for 2 to 3 days under the 12 h photoperiod. A total of ten pure fungal isolates were obtained and all the isolates displayed the same colony structure. Afterwards, three pure strains were randomly selected (F1, F3 and F5) for further study. The fungal colonies showed gray to brownish aerial mycelia with pink-colored masses of conidia. Conidia were one-celled, hyaline, cylindrical to subcylindrical, spindle-shaped with obtuse ends, measuring from 15.6 to 17.3 × 4.6 to 5.1 μm with both ends rounded. These morphological characteristics were consistent with the description of Colletotrichum gloeosporioides complex (Weir et al. 2012). The identity of a representative isolate, F3, was confirmed by a multilocus approach. Genomic DAN of isolate F3 was extracted and partial sequences of actin (ACT), chitin synthase (CHS), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), ribosomal internal transcribed spacer (ITS), manganese-superoxide dismutase (SOD2) , glutamine synthatase (GS), beta-tubulin (TUB2) and calmodulin (CAL) were amplified and sequenced as previously described (Weir et al. 2012). These nucleotide sequences were deposited in GenBank (accession MN972436 to MN972440, and MT266559 to MT266561; all sequences in FASTA format are shown (Supplementary S1). BLAST analysis of ITS, ACT, CHS, GAPDH and GS sequences from the F3 isolate revealed similarity to C. gloeosporioides voucher strain ZH01 with 100%, 100%,99%, 99% and 99% identity, respectively. SOD, TUB2 and CAL sequences showed similarity to C. siamense with 100%, 100% and 100% identity, respectively. The phylogenetic trees were constructed by Maximum Likelihood method (ML) using JTT model implemented in the MEGA 7. Results inferred from the concatenated sequences (ACT, CHS, GAPDH, ITS, SOD, GS, TUB2 and CAL) placed the isolate F3 within the C. siamense cluster (Supplementary S2). To confirm pathogenicity of the fungus, Koch's postulates were conducted by spraying 20 Zinnia plants (60-day-old) with a 1 × 106 conidia/ml suspension. Plants were maintained in the growth chamber at 25°C and 85% relative humidity. After 10 to 15 days, symptoms were observed on all inoculated leaves and resembled those observed in the field, whereas the control plants remained asymptomatic. Here, C. siamense was isolated only from the infected Zinnia leaves and identified by morphological and gene sequencing analyses. C. siamense has been reported in many crops in China (Yang et al. 2019; Chen et al. 2019; Wang et al. 2019). However, to our knowledge, this is the first report of anthracnose caused by C. siamense on Zinnia elegans in China. References Chen, X., Wang, T., Guo, H., Zhu, P. K., and Xu, L. 2019. First report of anthracnose of Camellia sasanqua caused by Colletotrichum siamense in China. Plant Dis. 103:1423-1423. Wang, Y., Qin, H. Y., Liu, Y. X., Fan, S. T., Sun, D., Yang, Y. M., Li, C. Y., and Ai, J. 2019. First report of anthracnose caused by Colletotrichum siamense on Actinidia arguta in China. Plant Dis. 103:372-373. Weir, B. S., Johnston, P. R., and Damm, U. 2012. The Colletotrichum gloeosporioides species complex. Stud. Mycol. 73: 115-180. Yang, S., Wang, H. X., Yi, Y. J., and Tan, L. L. 2019. First report that Colletotrichum siamense causes leaf spots on Camellia japonica in China. Plant Dis. 103:2127-2127.

摘要

百日草(学名:Zinnia elegans,异名:Zinnia violacea),又称普通百日草,是菊科中最引人注目的观赏植物之一。百日草在中国广泛种植,因其花色丰富多样且花期长、花量大。2019年4月,宁波植物园(北纬29°56'57″,东经121°36'20″)种植的百日草被发现有许多圆形坏死斑。在感染初期,病斑呈小圆形斑点,随后发展成大斑点(直径15至32毫米)。典型症状表现为灰白色中心,边缘黄化,发病田块中约80%的植株受影响。此外,百日草的生长受到该病害的严重影响。为鉴定与该病害相关的致病病原体,从10株不同的百日草植株上采集了10片有症状的叶片。从病斑边缘切取叶片组织,用75%乙醇表面消毒30秒,然后在无菌蒸馏水中冲洗三次。接着将叶片组织浸入10%次氯酸钠中2至3分钟,用蒸馏水冲洗三次,在无菌滤纸上晾干。干燥后,将表面消毒的叶盘转移到马铃薯葡萄糖琼脂(PDA)平板上,在12小时光周期下于28°C培养2至3天。共获得10个纯真菌分离株,所有分离株均表现出相同的菌落结构。随后,随机选择三个纯菌株(F1、F3和F5)进行进一步研究。真菌菌落呈现出灰色至褐色的气生菌丝体,带有粉红色的分生孢子团。分生孢子单细胞,透明,圆柱形至近圆柱形,纺锤形,两端钝圆,大小为15.6至17.3×4.6至5.1μm,两端圆形。这些形态特征与胶孢炭疽菌复合体(Weir等人,2012年)的描述一致。通过多位点方法确认了一个代表性分离株F3的身份。提取分离株F3的基因组DNA,按照先前描述的方法(Weir等人,2012年)扩增并测序肌动蛋白(ACT)、几丁质合成酶(CHS)、甘油醛-3-磷酸脱氢酶(GAPDH)、核糖体内部转录间隔区(ITS)、锰超氧化物歧化酶(SOD2)、谷氨酰胺合成酶(GS)、β-微管蛋白(TUB2)和钙调蛋白(CAL)的部分序列。这些核苷酸序列已存入GenBank(登录号MN972436至MN972440,以及MT266559至MT266561;所有序列均以FASTA格式显示(补充材料S1)。对F3分离株的ITS、ACT、CHS、GAPDH和GS序列进行BLAST分析,结果显示与胶孢炭疽菌模式菌株ZH01的相似性分别为100%、100%、99%、99%和99%。SOD、TUB2和CAL序列与暹罗炭疽菌的相似性分别为100%、100%和100%。使用MEGA 7中实现的JTT模型,通过最大似然法(ML)构建系统发育树。从串联序列(ACT、CHS、GAPDH、ITS、SOD、GS、TUB2和CAL)推断的结果将分离株F3置于暹罗炭疽菌簇内(补充材料S2)。为确认该真菌的致病性,通过向20株60日龄的百日草植株喷洒1×10⁶个分生孢子/毫升的悬浮液来进行柯赫氏法则验证。植株置于生长室中,温度为25°C,相对湿度为85%。10至15天后,在所有接种的叶片上观察到症状,与田间观察到的症状相似,但对照植株仍无症状。在此,暹罗炭疽菌仅从感染的百日草叶片中分离得到,并通过形态学和基因测序分析进行鉴定。暹罗炭疽菌在中国的许多作物中都有报道(Yang等人,2019年;Chen等人,20

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