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闪亮柳作为梨叶锈孢菌寄主植物的首次报道。

First Report of Shining Willow as a Host Plant for Septoria musiva.

作者信息

Feau N, Bernier L

机构信息

Centre de Recherche en Biologie Forestière, Université Laval, Sainte-Foy (QC), Canada, G1K 7P4.

出版信息

Plant Dis. 2004 Jul;88(7):770. doi: 10.1094/PDIS.2004.88.7.770B.

DOI:10.1094/PDIS.2004.88.7.770B
PMID:30812495
Abstract

During the summer of 2001, leaf spots resembling those caused by Septoria musiva Peck. were observed on shining willow (Salix lucida Mühl. subsp. lucida) at Leclerville, Québec, Canada (46°34'19″N,71°59'35″W). Affected leaves had brown, necrotic leaf spots (>5mm in diameter) surrounded by a darker brown halo. Conidia were cylindrical, straight to curved with 1 to 4 septa, 28 to 54 × 3.5 to 4 μm, and were produced in pycnidia located on the abaxial surface in the center of the leaf spots. The causal agent of this disease was successfully isolated by germinating the conidia on corn meal agar that was supplemented with streptomycin (50mg/ml) and chloramphenicol (300mg/ml) and followed with the transfer of the germinated conidia to potato dextrose agar. Leaf symptoms and morphology matched those of S. musiva, the cause of leaf spot and stem canker of hybrid poplars in North America (2,4). The internal transcribed spacers and the 5.8S portion of the rDNA were amplified using PCR with the ITS1 (5'-TCC GTA GGT GAA CCT GCG G-3') and ITS2 (5'-GCT GCG TTC TTC ATC GAT GC-3') primer pair on total genomic DNA extracted from a pure culture of the pathogen. The rDNA sequence obtained (GenBank Accession No. AY555277) had 100% identity at 506 base positions with the ITS1, 5.8S, and ITS2 of three S. musiva isolates from Québec and one from Wisconsin (GenBank Accession Nos. AY549464 to AY549467). To test for pathogenicity, excised leaf disks from plants propagated by softwood cuttings of the source plant and from one hybrid poplar clone (Populus maximowiczii × P. xjackii) were inoculated with 3 μl of a suspension of ground mycelium or sterile water (control). Disks were placed in a 24-well tissue culture plate with 1 ml of distilled water per well and incubated in a growth room maintained at 22°C with a 16-h photoperiod. After 1 month, symptoms were similar to those previously observed. Isolates collected from shining willow or hybrid poplar were able to induce S. musiva leaf spot symptoms on leaf disks excised from shining willow or the hybrid poplar clone. From symptomatic leaf disks, S. musiva was consistently reisolated. To our knowledge, this is the first report of S. musiva on a member of the genus Salix. S. didyma, S. salicicola, and S. salicina have been reported from leaves of species of Salix (1,3). Only a vague morphological description of S. didyma was found (3). Moreover, conidia of S. salicicola (20 to 50 × 2.5 to 3.5 μm) and S. salicina (40 to 60 μm long, unspecified width) overlap dimensions of S. musiva conidia (1). There is a need to reexamine the relationships between these species of Septoria. Evidently, the complete host range of S. musiva is not yet known. References: (1) L. Lanier et al. Mycologie et Pathologie Forestières. Masson. Paris, 1978. (2) M. E. Ostry. Eur. J. For. Pathol. 17:158, 1987. (3) P. A. Saccardo. Sylloge fungurum omnium hucusque cognitorum. Patavii: Sumptibus Auctoris, 1882. (4) L. J. Spielman et al. Plant Dis. 70:968, 1986.

摘要

2001年夏天,在加拿大魁北克省勒克莱尔维尔(北纬46°34'19″,西经71°59'35″)的亮叶柳(Salix lucida Mühl. subsp. lucida)上观察到类似由穆氏壳针孢(Septoria musiva Peck.)引起的叶斑。受影响的叶片有褐色坏死叶斑(直径>5毫米),周围有深褐色晕圈。分生孢子圆柱形,直或弯曲,有1至4个隔膜,28至54×3.5至4微米,在叶斑中心背面的分生孢子器中产生。通过在添加了链霉素(50毫克/毫升)和氯霉素(300毫克/毫升)的玉米粉琼脂上使分生孢子萌发,成功分离出这种病害的病原菌,随后将萌发的分生孢子转移到马铃薯葡萄糖琼脂上。叶片症状和形态与北美杂交杨树叶斑和茎溃疡病的病原菌穆氏壳针孢相符(2,4)。使用引物对ITS1(5'-TCC GTA GGT GAA CCT GCG G-3')和ITS2(5'-GCT GCG TTC TTC ATC GAT GC-3')通过PCR扩增从病原菌纯培养物中提取的总基因组DNA的内部转录间隔区和rDNA的5.8S部分。获得的rDNA序列(GenBank登录号AY555277)在506个碱基位置与来自魁北克的三个穆氏壳针孢分离株和来自威斯康星州的一个分离株(GenBank登录号AY549464至AY549467)的ITS1、5.8S和ITS2具有100%的同一性。为了测试致病性,将源植物软木扦插繁殖的植株以及一个杂交杨树克隆(Populus maximowiczii×P. xjackii)的离体叶片圆盘接种3微升研磨菌丝体悬浮液或无菌水(对照)。将圆盘放入24孔组织培养板中,每孔加入1毫升蒸馏水,在温度为22°C、光周期为16小时的生长室中培养。1个月后,症状与之前观察到的相似。从亮叶柳或杂交杨树上采集的分离株能够在从亮叶柳或杂交杨树克隆上切下的叶片圆盘上诱导出穆氏壳针孢叶斑症状。从有症状的叶片圆盘中,始终能重新分离出穆氏壳针孢。据我们所知,这是穆氏壳针孢在柳属植物上的首次报道。曾有文献报道在柳属植物的叶片上发现过双壳针孢(S. didyma)、柳叶壳针孢(S. salicicola)和柳生壳针孢(S. salicina)(1,3)。仅发现了对双壳针孢的模糊形态描述(3)。此外,柳叶壳针孢(20至50×2.5至3.5微米)和柳生壳针孢(长40至60微米,宽度未提及)的分生孢子尺寸与穆氏壳针孢分生孢子的尺寸有重叠(1)。有必要重新审视这些壳针孢属物种之间的关系。显然,穆氏壳针孢的完整寄主范围尚不清楚。参考文献:(1)L. Lanier等人,《森林真菌学与病理学》,马松出版社,巴黎,1978年。(2)M. E.奥斯特里,《欧洲森林病理学杂志》,17:158,1987年。(3)P. A.萨卡尔多,《所有已知真菌的编目》,帕塔维:作者自费出版,1882年。(4)L. J.斯皮尔曼等人,《植物病害》,7:968,1986年。