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中国甘薯由一种迪基氏菌(菊欧文氏菌)引起的细菌性茎基腐病和根腐病的首次报道

First Report of Bacterial Stem and Root Rot of Sweetpotato Caused by a Dickeya sp. (Erwinia chrysanthemi) in China.

作者信息

Huang L F, Fang B P, Luo Z X, Chen J Y, Zhang X J, Wang Z Y

机构信息

Crop Research Institute, Guangdong Academy of Agricultural Sciences, Guangzhou, 510640, China. Supported by the Agricultural Ministry of China (nyhyzx nycytx-16-B-5).

出版信息

Plant Dis. 2010 Dec;94(12):1503. doi: 10.1094/PDIS-06-10-0417.

DOI:10.1094/PDIS-06-10-0417
PMID:30743366
Abstract

Since 2006, stem and root rot of sweetpotato has been observed in fields at a number of sweetpotato-production areas in Huidong, Haifeng, Puning, and Zhanjiang counties and Guangzhou City in Guangdong Province of China. Initially, the leaves turn yellow, and a black, water-soaked rot occurs on the bottom of the stems that gradually extends to the top of the stems. Finally, the entire plant collapses and dies. Bacteria were consistently isolated from stems of diseased seedlings by streaking on nutrient agar. Twelve representative isolates were chosen for further characterization. All strains grew at 37°C, were gram negative, facultatively anaerobic, and rod shaped with peritrichous flagella. The strains were negative for oxidase and positive for catalase and tryptophanase (indole production) They fermented glucose, reduced nitrates to nitrites, degraded pectate, produced phosphatase and lecithinase, and utilized citrate, tartrate, malonate, glucose, sucrose, fructose, and maltose, but not trehalose and lactose. These characteristics were similar to those of Erwinia chrysanthemi (Pectobacterium chrysanthemi) (1). PCR was performed on the 16S rDNA gene from isolate H12 (1,503 bp; GenBank Accession No. GU252371) with primers 27f (5'-GAGAGTTTGATCCTGGCTCAG-3') and reverse primer (5'-GGCTACCTTGTTACGACTTC-3'). Subsequently, PCR products were sequenced. Results of sequence analysis showed the sequence of isolated strain H12 was 99% identical to that of E. chrysanthemi, 99% identical to that of type strain CFBP 1269T of Dickeya dadantii (Accession No. AF520707), and 98% identical to that of type strain CFBP 1200T of D. dianthicola (Accession No. AF520708). Recently, E. chrysanthemi was transferred to Dickeya gen. nov., but it was difficult to identify the species within the genus Dickeya. Seedlings (20 to 30 cm) were planted in 10-cm-diameter plastic pots containing sterilized field soil at room temperature. Four days later, five stem tops of sweetpotato were injected with a bacteria suspension (10 CFU/ml) of approximately 100 μl to fulfill Koch's postulates. Five control plants were inoculated with sterile distilled water. The experiment was conducted three times. All plants were incubated in a chamber at 30°C with high humidity. One to two days after inoculation, symptoms were observed in all inoculated plants and appeared to be identical to those observed in the field. No symptoms were noted on the control plants. The bacterium was reisolated from symptomatic stems of sweetpotato plants. This pathogen was previously reported on sweetpotato in the United States in 1974 (2). To our knowledge, this is the first report of a Dickeya sp. (E. chrysanthemi) causing bacterial stem and root rot of sweetpotato in China. References: (1) D. J. Brenner et al. Page 670 in: Bergey's Manual of Systematic Bacteriology. 2nd ed. Springer, New York, 2005. (2) N. W. Schaad et al. Phytopathology 67:302, 1977.

摘要

自2006年以来,在中国广东省惠东县、海丰县、普宁市、湛江市以及广州市的多个甘薯产区的田间均观察到甘薯茎基腐病。最初,叶片变黄,茎基部出现黑色、水渍状腐烂,并逐渐向上蔓延至茎顶。最终,整株植物枯萎死亡。通过在营养琼脂平板上划线,从患病幼苗的茎中持续分离出细菌。挑选了12个具有代表性的分离株进行进一步鉴定。所有菌株在37°C下生长,革兰氏阴性,兼性厌氧,杆状,具周生鞭毛。这些菌株氧化酶阴性,过氧化氢酶和色氨酸酶(吲哚产生)阳性。它们能发酵葡萄糖,将硝酸盐还原为亚硝酸盐,降解果胶酸盐,产生磷酸酶和卵磷脂酶,并利用柠檬酸盐、酒石酸盐、丙二酸盐、葡萄糖、蔗糖、果糖和麦芽糖,但不能利用海藻糖和乳糖。这些特征与菊欧文氏菌(果胶杆菌属)相似(1)。使用引物27f(5'-GAGAGTTTGATCCTGGCTCAG-3')和反向引物(5'-GGCTACCTTGTTACGACTTC-3')对分离株H12的16S rDNA基因(1503 bp;GenBank登录号GU252371)进行PCR扩增。随后,对PCR产物进行测序。序列分析结果显示,分离菌株H12的序列与菊欧文氏菌的序列相似度为99%,与达旦迪基氏菌模式菌株CFBP 1269T(登录号AF520707)的序列相似度为99%,与石竹迪基氏菌模式菌株CFBP 1200T(登录号AF520708)的序列相似度为98%。最近,菊欧文氏菌已被转移至迪基氏菌属,但在迪基氏菌属内难以鉴定该物种。将20至30厘米高的幼苗种植在直径为10厘米的装有灭菌田间土壤的塑料盆中,置于室温下。四天后,向五株甘薯的茎顶注射约100微升细菌悬液(10 CFU/ml)以满足科赫法则。五株对照植物接种无菌蒸馏水。该实验进行了三次。所有植物均在30°C、高湿度的培养箱中培养。接种后1至2天,所有接种植物均出现症状,且与田间观察到的症状相似。对照植物未出现症状。从有症状的甘薯植株茎中重新分离出该细菌。该病原菌于1974年在美国的甘薯上首次报道(2)。据我们所知,这是中国关于迪基氏菌属(菊欧文氏菌)引起甘薯细菌性茎基腐病的首次报道。参考文献:(1)D. J. Brenner等人。《伯杰氏系统细菌学手册》第2版,施普林格出版社,纽约,2005年,第670页。(2)N. W. Schaad等人。《植物病理学》67:302,1977年。