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马来西亚首次报道芥末果胶杆菌引起甘蓝软腐病。

First Report of Pectobacterium wasabiae Causing Soft Rot of Cabbage in Malaysia.

作者信息

Golkhandan E, Sijam K, Meon S, Ahmad Z A M, Nasehi A, Nazerian E

机构信息

Department of Plant Protection, Faculty of Agriculture, University Putra Malaysia, 43400 UPM, Serdang, Selangor Darul Ehsan.

出版信息

Plant Dis. 2013 Aug;97(8):1110. doi: 10.1094/PDIS-01-13-0112-PDN.

Abstract

Soft rot of cabbage (Brassica rapa) occurs sporadically in Malaysia, causing economic damage under the hot and wet Malaysian weather conditions that are suitable for disease development. In June 2011, 27 soft rotting bacteria were isolated from cabbage plants growing in the Cameron Highlands and Johor State in Malaysia where the economic losses exceeded 50% in severely infected fields and greenhouses. Five independent strains were initially identified as Pectobacterium wasabiae based on their inability to grow at 37°C, and elicit hypersensitive reaction (HR) on Nicotiana tabaccum and their ability to utilize raffinose and lactose. These bacterial strains were gram-negative, rod-shaped, N-acetylglucosaminyl transferase, gelatin liquefaction, and OPNG-positive and positive for acid production from D-galactose, lactosemelibiose, raffinose, citrate, and trehalose. All strains were negative for indole production, phosphatase activity, reducing sucrose, and negative for acid production from maltose, sorbitol, inositol, inolin, melezitose, α-methyl-D-glucoside, and D-arabitol. All the strains exhibited pectolytic activity on potato slices. PCR assays were conducted to distinguish P. wasabiae from P. carotovorum subsp. brasiliensis, P. atrosepticum, and other Pectobacterium species using primers Br1f/L1r (2), Eca1f/Eca2r (1), and EXPCCF/EXPCCR, respectively. DNA from strains did not yield the expected amplicon with the Br1f/L1r and Eca1f/Eca2r, whereas a 550-bp amplicon typical of DNA from P. wasabiae was produced with primers EXPCCF/EXPCCR. ITS-RFLP using the restriction enzyme, Rsa I, produced similar patterns for the Malaysian strains and the P. wasabiae type strain (SCRI488), but differentiated it from P. carotovora subsp. carotovora, P. atrosepticum, P. carotovorum subsp. brasiliensis, and Dickeya chrysanthemi type strains. BLAST analysis of the 16S rRNA DNA sequence (GenBank Accession No. KC445633) showed 99% identity to the 16S rRNA of Pw WPP163. Phylogenetic reconstruction using concatenated DNA sequences of mdh and gapA from P. wasabiae Cc6 (KC484657) and other related taxa (4) clustered Malaysian P. wasabiae strains with P. wasabiae SCRI488, readily distinguishing it from other closely related species of Pectobacterium. Pathogenicity assays were conducted on leaves and stems of four mature cabbage plants for each strain (var. oleifera) by injecting 10 μl of a bacterial suspension (10 CFU/ml) into either stems or leaves, and incubating them in a moist chamber at 80 to 90% relative humidity at 30°C. Water-soaked lesions similar to those observed in the fields and greenhouses were observed 72 h after injection and bacteria with similar characteristics were consistently reisolated. Symptoms were not observed on water-inoculated controls. The pathogenicity test was repeated with similar results. P. wasabiae was previously reported to cause soft rot of horseradish in Japan (3). However, to our knowledge, this is the first report of P. wasabiae infecting cabbage in Malaysia. References: (1) S. H. De Boer and L. J. Ward. Phytopathology 85:854, 1995. (2) V. Duarte et al. J. Appl. Microbiol. 96:535, 2004. (3) M. Goto and K. Matsumoto. Int. J. Syst. Bacteriol. 37:130, 1987. (4) B. Ma et al. Phytopathology 97:1150, 2007.

摘要

甘蓝(Brassica rapa)软腐病在马来西亚时有发生,在适合病害发展的炎热潮湿的马来西亚气候条件下会造成经济损失。2011年6月,从马来西亚金马仑高原和柔佛州种植的甘蓝植株上分离出27株软腐病菌,在严重感染的田地和温室中,经济损失超过50%。基于5个独立菌株在37°C下无法生长、对烟草引发过敏反应(HR)以及利用棉子糖和乳糖的能力,最初将它们鉴定为山葵果胶杆菌。这些细菌菌株为革兰氏阴性、杆状,具有N - 乙酰葡糖胺基转移酶、明胶液化能力,OPNG阳性,并且能利用D - 半乳糖、乳糖蜜二糖、棉子糖、柠檬酸盐和海藻糖产酸。所有菌株吲哚产生试验、磷酸酶活性试验、还原蔗糖试验均为阴性,利用麦芽糖、山梨醇、肌醇、菊糖、松三糖、α - 甲基 - D - 葡萄糖苷和D - 阿拉伯糖醇产酸试验也均为阴性。所有菌株在土豆片上均表现出果胶分解活性。分别使用引物Br1f/L1r (2)、Eca1f/Eca2r (1)和EXPCCF/EXPCCR进行PCR分析,以区分山葵果胶杆菌与胡萝卜果胶杆菌巴西亚种、黑胫果胶杆菌以及其他果胶杆菌属物种。菌株DNA使用Br1f/L1r和Eca1f/Eca2r未产生预期扩增子,而使用引物EXPCCF/EXPCCR产生了山葵果胶杆菌DNA典型的550 bp扩增子。使用限制性内切酶Rsa I进行的ITS - RFLP分析,马来西亚菌株和山葵果胶杆菌模式菌株(SCRI488)产生了相似的图谱,但将其与胡萝卜软腐果胶杆菌胡萝卜亚种、黑胫果胶杆菌、胡萝卜果胶杆菌巴西亚种和菊苣果胶杆菌模式菌株区分开来。对16S rRNA DNA序列(GenBank登录号KC445633)的BLAST分析显示,其与Pw WPP163的16S rRNA有99%的同源性。使用来自山葵果胶杆菌Cc6(KC484657)和其他相关分类单元的mdh和gapA串联DNA序列进行系统发育重建,将马来西亚山葵果胶杆菌菌株与山葵果胶杆菌SCRI488聚类在一起,很容易将其与其他密切相关的果胶杆菌属物种区分开来。对每个菌株(油用变种)的四株成熟甘蓝植株的叶片和茎进行致病性测定,通过向茎或叶中注射10 μl细菌悬液(10 CFU/ml),并将它们在30°C、相对湿度80%至90%的潮湿箱中培养。注射后72小时观察到与田间和温室中观察到的类似的水渍状病斑,并且始终能重新分离出具有相似特征的细菌。水接种对照未观察到症状。重复致病性试验,结果相似。此前有报道称山葵果胶杆菌在日本引起辣根软腐病(3)。然而,据我们所知,这是山葵果胶杆菌感染马来西亚甘蓝的首次报道。参考文献:(1) S. H. De Boer和L. J. Ward。植物病理学85:854,1995。(2) V. Duarte等人。应用微生物学杂志96:535,2004。(3) M. Goto和K. Matsumoto。国际系统与进化微生物学杂志37:130,1987。(4) B. Ma等人。植物病理学97:1150,2007。

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