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意大利首次报道立枯丝核菌AG-4引起非洲雏菊猝倒病

First Report of Damping-Off on African Daisy Caused by Rhizoctonia solani AG-4 in Italy.

作者信息

Aiello D, Castello I, Vitale A, Lahoz E, Nicoletti R, Polizzi G

机构信息

Dipartimento di Scienze e Tecnologie Fitosanitarie, University of Catania, Italy.

CRA, Unità di Ricerca per le Colture Alternative al Tabacco, Scafati, Salerno, Italy.

出版信息

Plant Dis. 2008 Sep;92(9):1367. doi: 10.1094/PDIS-92-9-1367B.

Abstract

Osteospermum (African Daisy or Cape Daisy) is a genus belonging to the Calendulae with a large number of perennial plant species. In February of 2007, a severe damping-off occurred on 3- to 4-month-old potted cuttings of Osteospermum 'Impassion Rose Purple', 'Impassion White', 'Impassion Purple', and 'Impassion White Rose' cultivated in a nursery in eastern Sicily. More than 30% of the plants were infected. Disease symptoms consisted of extensive water-soaked lesions at the base of the stem followed by wilt and collapse of the plant. Isolations from diseased tissues on potato dextrose agar (PDA) amended with streptomycin sulfate at 100 mg/l consistently recovered a fungus with morphological characteristics of Rhizoctonia solani. Fungal colonies were initially white, turned brown after 2 to 3 days, and produced irregularly shaped, brown sclerotia after 1 week. Microscopic examination revealed that hyphae had right angle branching patterns, were constricted at the base of the branch near the union with main hyphae, and septate near the constriction. The number of nuclei per hyphal cell was determined on cultures grown at 25°C on 2% water agar in petri plates. Mycelium was stained with 0.5% aniline blue solution (4) and examined with a microscope at ×400. The hyphal cells were all multinucleate. Anastomosis groups were determined by pairing isolates (3) with tester isolates of AG-1 IA, AG-2-2-1, AG-2-2IIIB, AG-2-2IV, AG-3, AG-4, AG-5, AG-6, and AG-11. Anastomosis was observed only with tester isolates of AG-4, giving C2 reactions (1) at a high frequency. The identification of group AG-4 within R. solani had been obtained by electrophoretic patterns of pectic enzymes (polygalacturonases) in vertical pectin-acrylamide gel stained with ruthenium red (2). All isolates of R. solani collected from infected plants were paired in all combinations on PDA plus 1% activated charcoal and examined for somatic interaction. All paired colonies merged without producing visible tufts of aerial mycelium. Absence of tufts and the lack of formation of heterokaryon at the hyphal interaction zone indicated that all isolates belonged to the same mating type with the same mating alleles (3). Pathogenicity tests were performed by placing plugs of PDA from 5-day-old mycelial cultures in the soil near the base of the stem on 20 potted, healthy, 2-month-old cuttings of Osteospermum cv. Impassion Rose Purple. The same number of plants treated with 1/cm PDA plugs served as controls. Following inoculation, all plants were maintained in a growth chamber at 25°C and 95% relative humidity on a 12-h fluorescent light/dark regimen. Wilt symptoms and lesions at the base of stem identical to those observed in the nursery developed 7 days after inoculation, and all inoculated plants died within 20 days. Control plants remained symptomless. R. solani AG-4 was consistently reisolated from symptomatic tissues, completing Koch's postulates. To our knowledge, this is the first report of damping-off on the genus Osteospermum caused by R. solani. References: (1) D. E. Carling. Page 37 in: Grouping in Rhizoctonia solani by Hyphal Anastomosis Reactions. Kluwer Academic Publishers, the Netherlands, 1996. (2) R. H. Cruickshank and G. C. Wade. Anal. Biochem. 107:177, 1980. (3) M. C. Juliàn et al. Phytopathology 86:566, 1996. (4) C. C. Tu and J. W. Kimbrough. Mycologia 65:941, 1973.

摘要

蓝目菊(非洲雏菊或海角雏菊)是金盏花属的一个包含大量多年生植物物种的属。2007年2月,西西里岛东部一家苗圃中种植的3至4月龄的盆栽蓝目菊品种‘热情玫瑰紫’、‘热情白’、‘热情紫’和‘热情白玫瑰’发生了严重的猝倒病。超过30%的植株受到感染。病害症状包括茎基部广泛的水渍状病斑,随后植株枯萎和倒伏。在添加了100mg/l硫酸链霉素的马铃薯葡萄糖琼脂(PDA)上对病组织进行分离,始终能分离出一种具有立枯丝核菌形态特征的真菌。真菌菌落最初为白色,2至3天后变为褐色,1周后产生不规则形状的褐色菌核。显微镜检查显示,菌丝具有直角分支模式,在与主菌丝结合处附近的分支基部缢缩,在缢缩处附近有隔膜。在培养皿中25°C下2%水琼脂上生长的培养物上测定每个菌丝细胞的细胞核数量。菌丝体用0.5%苯胺蓝溶液染色(4),并在×400显微镜下检查。菌丝细胞均为多核。通过将分离株与AG-1 IA、AG-2-2-1、AG-2-2IIIB、AG-2-2IV、AG-3、AG-4、AG-5、AG-6和AG-11的测试分离株配对来确定融合群(3)。仅在与AG-4的测试分离株配对时观察到融合,高频出现C2反应(1)。通过用钌红染色的垂直果胶-丙烯酰胺凝胶中果胶酶(多聚半乳糖醛酸酶)的电泳图谱确定了立枯丝核菌内的AG-4群(2)。从受感染植物中收集的所有立枯丝核菌分离株在添加1%活性炭的PDA上以所有组合配对,并检查体细胞相互作用。所有配对菌落融合,未产生可见的气生菌丝簇。气生菌丝簇的缺失以及菌丝相互作用区异核体的未形成表明所有分离株属于具有相同交配等位基因的相同交配型(3)。通过将5日龄菌丝体培养物的PDA菌块放置在20盆健康的2月龄蓝目菊品种‘热情玫瑰紫’扦插苗茎基部附近的土壤中进行致病性测试。相同数量的用1/cm PDA菌块处理的植株作为对照。接种后,所有植株在生长室中保持在25°C和95%相对湿度下,采用12小时荧光光照/黑暗周期。接种7天后出现与苗圃中观察到的相同的枯萎症状和茎基部病斑,所有接种植株在20天内死亡。对照植株无症状。从有症状的组织中始终能重新分离出立枯丝核菌AG-4,从而完成了柯赫氏法则。据我们所知,这是立枯丝核菌引起蓝目菊属植物猝倒病的首次报道。参考文献:(1)D. E. Carling。载于:《通过菌丝融合反应对立枯丝核菌进行分组》,第37页。Kluwer学术出版社,荷兰,1996年。(2)R. H. Cruickshank和G. C. Wade。《分析生物化学》107:177,1980年。(3)M. C. Juliàn等人。《植物病理学》86:566,1996年。(4)C. C. Tu和J. W. Kimbrough。《真菌学》65:941,1973年。

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