Suppr超能文献

中国多室链核盘菌引起李树褐腐病的首次报道。

First Report of Brown Rot on Plum Caused by Monilia polystroma in China.

作者信息

Zhu X Q, Guo L Y

机构信息

Department of Plant Pathology, China Agricultural University, Beijing 100193, China.

出版信息

Plant Dis. 2010 Apr;94(4):478. doi: 10.1094/PDIS-94-4-0478A.

Abstract

In August 2008, mummies of dwarf sweet plum (Prunus aitianli) fruit covered with grayish, conidial tufts were found in an orchard in Mudanjiang City of Heilongjiang in China. Conidial masses were touched with a sterilized wire loop and streaked onto the surface of water agar (WA) plates. After incubating at 22 ± 2°C for 16 to 24 h, individual germinated spores were picked out with a sterilized scalpel blade under a microscope in a laminar flow cabinet, and transferred to potato dextrose agar (PDA) in petri dishes. Mycelium grew an average of 10.7 mm per day on PDA and formed a white-to-grayish colony with irregular, black stroma 12 days after incubation at 22 ± 2°C under 12-h light/12-h dark. The average size of stroma was 8.19 cm per petri dish 37 days after incubation in the dark. The conidia were one-celled, hyaline, lemon-shaped, 15.2 (10.8 to 18.9) × 10.9 (8.3 to 16.3) μm, and arranged in branched monilioid chains on inoculated apples. The PCR products of internal transcribed spacer (ITS) region 1 and 2 and 5.8S gene of the ribosomal RNA amplified with primers ITS1 and ITS4 was directly sequenced in both directions using the PCR primers. The sequence of the Monilia polystroma isolate (GenBank Accession No. GU067539) was identical to the reference isolate of M. polystroma (CBS102686), containing five nucleotides that distinguish it from Monilinia fructigena (1,3). The pathogen was identified as M. polystroma on the basis of morphological characteristics (3) and the sequence of internal transcribed spacer (ITS) region 1 and 2 and 5.8S gene of the ribosomal RNA. Pathogenicity was confirmed by inoculating surface-sterilized, mature plum and apple fruit wounded with a nail, with a mycelial plug (5 mm in diameter) of the fungus at each wound. Fruit treated with plain PDA plugs were used as a control. Inoculated fruits were placed in a sterilized moist chamber at room temperature (23 to 28°C). Fifteen plums and nine apples were used in each of two replicated tests. All inoculated fruit developed typical brown rot symptoms 4 days after inoculation, while the control fruit remained healthy. M. polystroma was reisolated from the inoculated fruit and identified by the above methods. M. polystroma was first reported on apple in Japan (3) and it was recently discovered in an apple orchard in Hungary (2). Although the occurrence of Monilinia fructicola, Monilinia laxa, and Monilinia fructigena (teleomorphs of the three Monilia spp.) in China have been documented, to our knowledge, this is the first report of the occurrence of M. polystroma in China. References: (1) C. E. Fulton et al. Eur. J. Plant Pathol. 105:495, 1999. (2) M. Petróczy and L. Palkovics. Eur. J. Plant Pathol. 125:343, 2009. (3) G. C. M. van Leeuwen et al. Mycol. Res. 106:444, 2002.

摘要

2008年8月,在中国黑龙江省牡丹江市的一个果园里发现了被灰色分生孢子簇覆盖的矮李(Prunus aitianli)果实木乃伊。用无菌接种环触碰分生孢子团,然后划线接种到水琼脂(WA)平板表面。在22±2°C下培养16至24小时后,在层流柜的显微镜下用无菌手术刀挑出单个萌发的孢子,并转移到培养皿中的马铃薯葡萄糖琼脂(PDA)上。在22±2°C、12小时光照/12小时黑暗条件下培养12天后,菌丝体在PDA上平均每天生长10.7毫米,并形成一个白色至灰色的菌落,带有不规则的黑色子座。在黑暗中培养37天后,每个培养皿中子座的平均大小为8.19厘米。分生孢子单细胞,无色透明,柠檬形,大小为15.2(10.8至18.9)×10.9(8.3至16.3)微米,在接种的苹果上排列成分枝状的念珠状链。用引物ITS1和ITS4扩增核糖体RNA的内部转录间隔区(ITS)1、2和5.8S基因的PCR产物,使用PCR引物进行双向直接测序。多子座链核盘菌分离株(GenBank登录号GU067539)的序列与多子座链核盘菌参考分离株(CBS102686)相同,含有五个将其与果生链核盘菌区分开的核苷酸(1,3)。根据形态特征(3)以及核糖体RNA的内部转录间隔区(ITS)1、2和5.8S基因序列,将该病原菌鉴定为多子座链核盘菌。通过用该真菌的菌丝体小块(直径5毫米)接种用钉子刺伤的表面消毒的成熟李子和苹果果实来确认致病性,每个伤口接种一块。用普通PDA小块处理的果实作为对照。接种后的果实置于室温(23至28°C)的无菌保湿箱中。在两个重复试验中,每个试验使用15个李子和9个苹果。接种后4天,所有接种的果实都出现了典型的褐腐症状,而对照果实保持健康。从接种的果实中重新分离出多子座链核盘菌,并通过上述方法进行鉴定。多子座链核盘菌首次在日本的苹果上被报道(3),最近在匈牙利的一个苹果园中被发现(2)。虽然中国已记录了果生链核盘菌、核果链核盘菌和果生链核盘菌(三种链核盘菌属的有性型)的发生情况,但据我们所知,这是中国首次报道多子座链核盘菌的发生。参考文献:(1)C. E. Fulton等人,《欧洲植物病理学杂志》105:495,1999年。(2)M. Petróczy和L. Palkovics,《欧洲植物病理学杂志》125:343,2009年。(3)G. C. M. van Leeuwen等人,《真菌学研究》106:444,2002年。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验