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人参疫霉对甲霜灵的敏感性及致病性的首次报道——从西洋参(Panax quinquefolium)中分离得到的柑橘疫霉

First Report of Mefenoxam Sensitivity and Pathogenicity of Phytophthora citricola Isolated from American Ginseng (Panax quinquefolium).

作者信息

Hill S N, Hurtado-Gonzales O P, Lamour K H, Hausbeck M K

机构信息

Michigan State University, East Lansing 48824.

University of Tennessee, Knoxville 37996.

出版信息

Plant Dis. 2008 Dec;92(12):1706. doi: 10.1094/PDIS-92-12-1706A.

Abstract

In March of 2004, stratified ginseng seeds from commercial Wisconsin gardens were planted in sterilized silica sand in a research greenhouse at Michigan State University. Following emergence, seedlings exhibiting wilting, damping off, and black stem lesions were observed. In the laboratory, symptomatic seedlings were rinsed with distilled water. Tissue samples were excised and embedded in water agar amended with ampicillin (100 mg/liter) and incubated at 25°C. In addition to the isolation of Phytophthora cactorum, a known pathogen of ginseng, P. citricola, (five isolates) also was identified from single-zoospore cultures based on morphology (2). One-week-old, dilute V8 agar cultures were used to obtain single zoospores. Cultures were flooded with 20 ml of sterilized distilled water chilled to 10°C and incubated at 25°C for 25 min to induce zoospore release. Zoospore suspensions were spread onto water agar plates, and after 24 h at 25°C, single germinating zoospores were selected at random and transferred to benomyl, ampicillin, rifampicin, and pentachloronitrobenzene (BARP)-amended V8 agar plates. Sequence analysis of the internal transcribed spacer (ITS) region 1 and 2 of the rDNA was also used to distinguish P. citricola from P. cactorum. A representative sequence for the isolates of P. citricola (NCBI Accession No. FJ217388) matched (100% similarity) a P. citricola isolate deposited in GenBank (Accession No. DQ486661). To screen P. citricola for in vitro response to mefenoxam, agar plugs (7-mm diameter) from 1-week-old V8 agar cultures incubated at 25°C under fluorescent lighting were placed in the center of each of two V8 agar plates amended with 0 and 100 ppm of mefenoxam (Ridomil Gold EC, 48% a.i., suspended in sterile distilled water and added to V8 agar cooled to 49°C). The plates were incubated at 25°C for 3 days under fluorescent lighting. Isolates were assigned a mefenoxam sensitivity rating based on the percentage of radial mycelial growth on the amended V8 agar when compared with the unamended control. Each of the five isolates was scored as mefenoxam resistant with growth on 100-ppm plates >30% of the controls. Koch's postulates were conducted for the isolates of P. citricola recovered from ginseng seedlings to confirm pathogenicity. Previously, P. citricola was reported as nonpathogenic to ginseng (1). Three-week-old, healthy ginseng seedlings were planted into 89- × 64-mm pots filled with autoclaved medium-particle vermiculite and maintained in the greenhouse under 63% shade cloth with temperatures between 18 and 26°C. Pots were arranged in a completely randomized block design with eight seedlings per isolate as replicates and watered as needed. A 2-ml inoculum suspension (approximately 10 zoospores) was injected into the potting medium at the stem base of each seedling. All of the isolates were pathogenic to ginseng seedlings with 60% of inoculated seedlings per isolate exhibiting wilting, damping off, and blackened stems within 3 weeks after inoculation. P. citricola was reisolated from all inoculated plants. To our knowledge, this is the first report of P. citricola pathogenic on ginseng. References: (1) T. W. Darmono et al. Plant Dis. 75:610, 1991. (2) D. C. Erwin and O. K. Ribeiro. Page 96 in: Phytophthora Diseases Worldwide. The American Phytopathological Society, St. Paul, MN. 1996.

摘要

2004年3月,将来自威斯康星州商业种植园的分层人参种子种植于密歇根州立大学研究温室的无菌硅砂中。出苗后,观察到幼苗出现萎蔫、猝倒和黑色茎部病斑。在实验室中,有症状的幼苗用蒸馏水冲洗。切取组织样本并嵌入添加氨苄青霉素(100毫克/升)的水琼脂中,于25°C下培养。除了分离出已知的人参病原菌恶疫霉外,还基于形态学从单游动孢子培养物中鉴定出了柑橘疫霉(5个分离株)(2)。使用一周龄的稀释V8琼脂培养物来获取单个游动孢子。向培养物中加入20毫升冷却至10°C的无菌蒸馏水,于25°C下培养25分钟以诱导游动孢子释放。将游动孢子悬浮液涂布于水琼脂平板上,在25°C下培养24小时后,随机选择单个萌发的游动孢子并转移至添加了苯菌灵、氨苄青霉素、利福平和平氯硝基苯(BARP)的V8琼脂平板上。还利用核糖体DNA的内部转录间隔区(ITS)1和2的序列分析来区分柑橘疫霉和恶疫霉。柑橘疫霉分离株的代表性序列(NCBI登录号FJ217388)与GenBank中保存的柑橘疫霉分离株(登录号DQ486661)匹配(相似度100%)。为筛选柑橘疫霉对甲霜灵的体外反应,从在25°C荧光灯下培养一周的V8琼脂培养物中切取直径7毫米的琼脂块,置于两个分别添加0和100 ppm甲霜灵(瑞毒霉金乳油,有效成分48%,悬浮于无菌蒸馏水中并添加到冷却至49°C的V8琼脂中)的V8琼脂平板中央。平板在25°C荧光灯下培养3天。根据与未添加对照相比,在添加甲霜灵的V8琼脂上的径向菌丝生长百分比为分离株指定甲霜灵敏感性评级。五个分离株中的每一个在100 ppm平板上的生长均超过对照的30%,被评为对甲霜灵耐药。对从人参幼苗中分离得到的柑橘疫霉分离株进行柯赫氏法则验证以确认致病性。此前,柑橘疫霉被报道对人参无致病性(1)。将三周龄的健康人参幼苗种植于装满经高压灭菌的中等颗粒蛭石的89×64毫米花盆中,置于温室中63%遮光布下,温度保持在18至26°C。花盆采用完全随机区组设计,每个分离株有八株幼苗作为重复,并根据需要浇水。向每株幼苗茎基部的盆栽基质中注射2毫升接种物悬浮液(约10个游动孢子)。所有分离株对人参幼苗均具有致病性,接种后3周内,每个分离株接种的幼苗中有60%表现出萎蔫、猝倒和茎部变黑。从所有接种植物中再次分离出柑橘疫霉。据我们所知,这是柑橘疫霉对人参致病的首次报道。参考文献:(1)T. W. Darmono等人,《植物病害》75:610,1991年。(2)D. C. Erwin和O. K. Ribeiro,《全球疫霉病害》第96页,美国植物病理学会,明尼苏达州圣保罗,1996年。

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