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引起富贵草叶斑病的拟舟形柱盘孢的首次报道

First Report of Cylindrocladium pseudonaviculatum Causing Leaf Spot of Pachysandra terminalis.

作者信息

LaMondia J A, Li D W, Marra R E, Douglas S M

机构信息

The Connecticut Agricultural Experiment Station, Windsor, CT 06095, and New Haven, CT 06504.

出版信息

Plant Dis. 2012 Jul;96(7):1069. doi: 10.1094/PDIS-03-12-0235-PDN.

Abstract

Cylindrocladium pseudonaviculatum Crous, J.Z., Groenew. & C.F. Hill 2002 was recently reported infecting common boxwood, Buxus sempervirens L., in Connecticut (2). We isolated the pathogen from leaf and stem lesions of B. sempervirens and obtained single-spored cultures on half-strength potato dextrose agar (½PDA). The pathogen was identified as C. pseudonaviculatum by morphological characteristics (1). Colony size reached 71 mm in diameter after 14 days at room temperature on ½PDA, and was fluffy with white aerial hyphae, mars brown, and reverse color chestnut brown at the center fading to pale brown forming concentric bands. Macroconidiophores were solitary or in a group of up to three, comprised a stipe, a sterile elongation, and one to three penicillate fertile branches. The stipe was up to nine septate, 90 to 250 μm long, colorless, smooth, terminating in a naviculate or broadly ellipsoidal vesicle with a pointed or papillate apex, and 27 to 50 × 6.5 to 9 μm. Primary branches were zero- to one-septate, 20 to 36 × 4 to 5 μm; secondary branches were aseptate and 11 to 20 × 3 to 4.5 μm; tertiary branches were rare, each terminal branch producing two to five phialides; phialides were doliiform or reniform, colorless, 12 to 18 μm. Conidia were cylindrical, rounded at both ends, straight, smooth, colorless, two-celled, 48 to 55 × 4.5 to 5.5 μm, and in colorless slimy cylindrical clusters. Microconidiophores were not observed. Chlamydospores were golden to dark brown, thick-walled, and smooth or rough. Microsclerotia were present on ½PDA. Primers T1 and T22 (3) were used to amplify a portion of the β-tubulin gene from isolates Cps-CT-L1 and Cps-CT-S1. Amplified sequences were used in a BLAST search against the GenBank database to demonstrate 100% sequence identity only with other C. pseudonaviculatum strains. Both sequences were deposited in GenBank (Accession Nos. JQ866628 and JQ866629), using corresponding gene data from C. pseudonaviculatum strain STE-U 3399 (GenBank Accession No. AF449455) to distinguish coding from noncoding regions. Healthy plants of Japanese spurge, Pachysandra terminalis, with three plants per 10 cm diameter pot, were inoculated with water alone or a conidial suspension of C. pseudonaviculatum isolate Cps-CT-L1 (ATCC MYA-4891) (1.0 × 10 conidia/plant) with a handheld sprayer until runoff. Plants were kept moist in a plastic bag for 48 h at laboratory temperature and then transferred to the greenhouse. Circular lesions (1- to 4-mm diameter) were evident on leaves after 10 days. All 12 inoculated plants developed lesions, and no lesions were observed on noninoculated plants. Leaves with lesions were surface sterilized in 0.5% NaOCl for 30 s, rinsed twice in sterile water, and lesion margins plated onto water agar or ½PDA. The pathogen was reisolated from at least one leaf per plant. Koch's postulates were performed again with isolate Cps-CT-S1 (ATCC MYA-4890). After 3 weeks, many of the leaves with lesions yellowed and dropped to the soil surface and heavy sporulation of C. pseudonaviculatum and microsclerotia were observed. To our knowledge, this is the first report of C. pseudonaviculatum causing a leaf spot disease on P. terminalis. Pachysandra is a widely grown ground cover suitable for shady, humid environmental conditions that may be conducive for the development of disease. References: (1) P. Crous, et al. Sydowia 54:23, 2002. (2) K. Ivors et al. Plant Disease. 96:X, 2012. (3) K. O'Donnell and E. Cigelnik Mol. Phylogenet. Evol. 7:103, 1997.

摘要

圆柱状枝孢菌(Cylindrocladium pseudonaviculatum Crous, J.Z., Groenew. & C.F. Hill 2002)最近被报道在康涅狄格州感染了欧洲黄杨(Buxus sempervirens L.)(2)。我们从欧洲黄杨的叶片和茎部病斑中分离出病原体,并在半强度马铃薯葡萄糖琼脂(½PDA)上获得了单孢培养物。通过形态特征(1)将病原体鉴定为假舟形圆柱状枝孢菌。在室温下于½PDA上培养14天后,菌落直径达到71毫米,菌落蓬松,有白色气生菌丝,呈栗褐色,背面颜色为栗棕色,中心逐渐褪色为浅棕色,形成同心环带。大型分生孢子梗单生或成簇,每簇最多三个,由一个梗、一个不育的延伸部分和一到三个帚状可育分支组成。梗最多有九个隔膜,长90至250微米,无色,光滑,末端为舟形或宽椭圆形囊泡,顶端尖锐或有乳头状突起,大小为27至50×6.5至9微米。初生分支有零到一个隔膜,长20至36×4至5微米;次生分支无隔膜,长11至20×3至4.5微米;三生分支很少见,每个末端分支产生两到五个瓶梗;瓶梗呈桶形或肾形,无色,长12至18微米。分生孢子呈圆柱形,两端圆形,直,光滑,无色,双细胞,大小为48至55×4.5至5.5微米,呈无色粘滑的圆柱形簇状。未观察到小型分生孢子梗。厚垣孢子呈金黄色至深褐色,壁厚,表面光滑或粗糙。在½PDA上存在微菌核。使用引物T1和T22(3)从分离株Cps-CT-L1和Cps-CT-S1中扩增β-微管蛋白基因的一部分。扩增序列用于在GenBank数据库中进行BLAST搜索,结果表明仅与其他假舟形圆柱状枝孢菌菌株具有100%的序列同一性。这两个序列都已存入GenBank(登录号JQ866628和JQ866629),使用来自假舟形圆柱状枝孢菌菌株STE-U 3399(GenBank登录号AF449455)的相应基因数据来区分编码区和非编码区。日本玉簪(Pachysandra terminalis)的健康植株,每10厘米直径的花盆中种植三株,分别用清水或假舟形圆柱状枝孢菌分离株Cps-CT-L1(ATCC MYA-4891)的分生孢子悬浮液(每株1.0×10个分生孢子)用手持喷雾器喷雾直至径流。植株在实验室温度下用塑料袋保湿48小时,然后转移到温室中。10天后,叶片上出现明显的圆形病斑(直径1至4毫米)。所有12株接种的植株都出现了病斑,未接种的植株未观察到病斑。带有病斑的叶片在0.5%次氯酸钠中进行表面消毒30秒,在无菌水中冲洗两次,然后将病斑边缘接种到水琼脂或½PDA上。从每株至少一片叶子上重新分离出病原体。使用分离株Cps-CT-S1(ATCC MYA-4890)再次进行柯赫氏法则验证。3周后,许多带有病斑的叶片变黄并掉落到土壤表面,观察到假舟形圆柱状枝孢菌大量产孢和形成微菌核。据我们所知,这是假舟形圆柱状枝孢菌引起玉簪叶斑病的首次报道。玉簪是一种广泛种植的地被植物,适合在阴凉、潮湿的环境条件下生长,这种环境可能有利于病害的发生。参考文献:(1)P. Crous等人,《Sydowia》54:23,2002。(2)K. Ivors等人,《植物病害》96:X,2012。(3)K. O'Donnell和E. Cigelnik,《分子系统发育与进化》7:103,1997。

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