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韩国罗勒上由长枝葡萄孢引起的黑茎病首次报道。

First Report of Black Stem Caused by Botryosporium longibrachiatum on Sweet Basil in Korea.

作者信息

Park J H, Park M J, Han K S, Shin H D

机构信息

Division of Environmental Science and Ecological Engineering, Korea University, Seoul 136-701, Korea.

Horticultural & Herbal Crop Environment Division, National Institute of Horticultural and Herbal Science, Suwon 441-440, Korea.

出版信息

Plant Dis. 2013 Mar;97(3):425. doi: 10.1094/PDIS-09-12-0852-PDN.

Abstract

Sweet basil, Ocimum basilicum L., is cultivated mainly for fresh consumption in Korea. In March 2009, in Icheon, Korea, several dozen plants showing symptoms of black stems were found in an organic farm that used polyethylene tunnels for production. The black stems were usually covered with a fungus that gave the appearance of hoar-frost on the stems, especially when plants were grown under a cool and humid environment. According to the farmer, black stems appear during the winter season of November to March when the tunnels were mostly closed. The relative humidity (RH) during that period was around 100% every night due to poor ventilation. Beginning the middle of April when both sides of the tunnels were open, providing good ventilation, no further disease development was observed. The fungus on the stems had an elongate, upright conidiophore, reaching 5 mm in length. At intervals along its length, the main axis of conidiophores produced lateral fertile branches in acropetal succession. Each lateral branch terminated in a cluster of four or five ampullae. Conidia were hyaline, oval, and 5.5 to 9.5 × 3.5 to 6 μm. The fungus was non-pigmented and colonies on potato dextrose agar were chalk white. Morphological and cultural characteristics of the fungus were consistent with the previous reports of Botryosporium longibrachiatum (Oudem.) Maire (3,4). Voucher specimens (n = 4) were housed at Korea University Herbarium (KUS). An isolate from KUS-F24010 was deposited in the Korean Agricultural Culture Collection (Accession No. KACC44849) and used for molecular analysis and pathogenicity tests. The complete internal transcribed spacer (ITS) region of rDNA was amplified with the primers ITS1/ITS4 and sequenced. The resulting sequence of 592 bp was deposited in GenBank (Accession No. JX666334). A BLAST search in GenBank showed that there was no comparable sequence of B. longibrachiatum and thus this was the first ITS sequence for the species submitted in GenBank. To confirm the pathogenicity, colonized mycelial plugs (3 mm in diameter) from 10-day-old PDA cultures were placed onto the stem apices (n = 10) of 2-month-old sweet basil pot plants, which were topped as normally harvested. Control plants were inoculated with uncolonized agar plugs. All plants were incubated at 22 ± 2°C in a humidified chamber with a 12-h photoperiod for 48 h, and then maintained in a greenhouse (22 ± 2°C). Three to four days after inoculation, necrotic lesions developed around the points of inoculation on all stems and expanded downwards, leading to black stems covered with the hoar-frost like fungus after 14 days. B. longibrachiatum was successfully reisolated from all inoculated stems, while control plants remained symptomless. The pathogenicity test was conducted twice with the same result. The association of B. longibrachiatum and sweet basil was previously reported (4). Several other plants including burley tobacco are also reported to be infected by this fungus (1,2). To our knowledge, this is the first etiological report of B. longibrachiatum on sweet basil globally as well as in Korea. References: (1) T. R. Anderson. Plant Dis. 67:1158, 1983. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Mycology & Microbiology Laboratory, ARS, USDA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/ , September 7, 2012. (3) C. V. Subramanian. Hyphomycetes. Indian Council of Agricultural Research, New Delhi, India, 1971. (4) H. T. Tribe and R. W. S. Weber. Mycologist 15:158, 2001.

摘要

甜罗勒(Ocimum basilicum L.)在韩国主要作为新鲜蔬菜进行种植。2009年3月,在韩国利川的一个使用聚乙烯大棚进行生产的有机农场中,发现了几十株出现黑茎症状的植株。黑茎上通常覆盖着一种真菌,在茎上呈现出白霜的外观,特别是当植株在凉爽潮湿的环境中生长时。据农民说,黑茎出现在11月至3月的冬季,此时大棚大多处于封闭状态。由于通风不良,那段时间每晚的相对湿度(RH)约为100%。从4月中旬开始,大棚两侧打开,通风良好,此后未观察到病害进一步发展。茎上的真菌有细长、直立的分生孢子梗,长度可达5毫米。在其长度上每隔一段距离,分生孢子梗的主轴以向顶顺序产生侧生可育分支。每个侧分支末端有一簇四到五个壶形结构。分生孢子无色,椭圆形,大小为5.5至9.5×3.5至6微米。该真菌无色素,在马铃薯葡萄糖琼脂上的菌落为白垩色。该真菌的形态和培养特征与之前关于长枝葡萄孢(Botryosporium longibrachiatum (Oudem.) Maire)的报道一致(3,4)。凭证标本(n = 4)保存在韩国大学植物标本馆(KUS)。从KUS - F24010分离得到的菌株保藏于韩国农业菌种保藏中心(保藏编号KACC44849),并用于分子分析和致病性测试。用引物ITS1/ITS4扩增rDNA的完整内部转录间隔区(ITS)并进行测序。得到的592 bp序列保存在GenBank(登录号JX666334)。在GenBank中进行的BLAST搜索显示,没有与长枝葡萄孢可比的序列,因此这是该物种在GenBank中提交的首个ITS序列。为了确认致病性,将来自10日龄PDA培养物的定殖菌丝块(直径3毫米)放置在2个月大的甜罗勒盆栽植株的茎尖(n = 10)上,这些植株按正常收获方式进行打顶处理。对照植株接种未定殖的琼脂块。所有植株在22 ± 2°C、湿度饱和、光照周期为12小时的培养箱中培养48小时,然后置于温室(22 ± 2°C)中。接种后三到四天,所有茎上接种点周围出现坏死斑,并向下扩展,14天后导致茎变黑并覆盖有霜状真菌。从所有接种的茎上成功重新分离出长枝葡萄孢,而对照植株无症状。致病性测试重复进行了两次,结果相同。此前已有关于长枝葡萄孢与甜罗勒关联的报道(4)。据报道,包括白肋烟在内的其他几种植物也受到这种真菌的感染(1,2)。据我们所知,这是全球以及韩国关于长枝葡萄孢侵染甜罗勒的首例病原学报道。参考文献:(1) T. R. Anderson. Plant Dis. 67:1158, 1983. (2) D. F. Farr and A. Y. Rossman. Fungal Databases. Systematic Mycology & Microbiology Laboratory, ARS, USDA. Retrieved from http://nt.ars-grin.gov/fungaldatabases/, September 7, 2012. (3) C. V. Subramanian. Hyphomycetes. Indian Council of Agricultural Research, New Delhi, India, 1971. (4) H. T. Tribe and R. W. S. Weber. Mycologist 15:158, 2001.

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