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考氏肠杆菌引起巴西本土森林物种马贝木细菌性斑点病的首次报告。

First Report of Enterobacter cowanii Causing Bacterial Spot on Mabea fistulifera, a Native Forest Species in Brazil.

作者信息

Furtado G Q, Guimarães L M S, Lisboa D O, Cavalcante G P, Arriel D A A, Alfenas A C, Oliveira J R

机构信息

Departamento de Fitopatologia, Universidade Federal de Viçosa, Viçosa, Minas Gerais, 36570-000, Brazil.

出版信息

Plant Dis. 2012 Oct;96(10):1576. doi: 10.1094/PDIS-02-12-0160-PDN.

DOI:10.1094/PDIS-02-12-0160-PDN
PMID:30727327
Abstract

In the summer of 2011, in a nursery located in Viçosa City, Minas Gerais State, brownish, necrotic, irregular spots were observed on leaves of Mabea fistulifera Mart. (Euphorbiaceae), an indigenous forest species commonly found in Brazil. Around 6,300 seedlings were evaluated and as many as 60% of them showed disease symptoms, including severe defoliation and plant death. Leaves with coalescing lesions turned papery in texture and had a blighted appearance. Bacterial colonies were isolated from these symptomatic leaves on King B's medium and identified based on biochemical and molecular analysis, as a member of the Enterobacteriaceae family. Like other members of the Enterobacteriaceae family, the bacteria were facultative anaerobic, gram-negative, cream-colored on YDC medium, urease and oxidase negative, as well as catalase and asparagine positive. Bacterial DNA was extracted from pure culture grown overnight in liquid 523 medium at 28°C using the Wizard Genomic DNA Purification kit (Promega) and conserved sequences in 16S rDNA (3) and rpoB (1) were amplified by PCR. The sequence of the 1,300-bp 16S rDNA fragment and the 750-bp rpoB gene were analyzed by NCBI BLAST. Related sequences were aligned and analyzed by ClustalW in MEGA 5 software. Phylogenetic analysis by maximum likelihood, using PAUP version 4.0 and TBR algorithm with 1,000 bootstrap replications, grouped the isolate in a clade with Enterobacter cowanii and the result showed 99% and 98% identity to the 16s rDNA and rpoB, respectively. The isolate clustered closely with the type strain of E. cowanii in both phylogenetic trees constructed. Pathogenicity tests were carried out by inoculating leaves of healthy seedlings either by spraying or cutting with a scissor previously dipped into a 10 CFU/ml bacterial suspension. The experiment was in a completely randomized design, with six replications. A pot with one plant was considered one experimental unit. Control seedlings were sprayed or cut with a scissor treated with saline solution. Prior to and after inoculation, plants were kept in a humid chamber for 24 h at 26°C in the dark and at room temperature. Subsequently, plants were transferred to growth chamber at 26°C, under a 12-h photoperiod (40 μmol/s/m). Consistent with the symptoms observed originally, 7 days after inoculation, all seedlings developed leaf spots. No characteristic symptoms could be observed in the negative control. Furthermore, Koch's postulates were confirmed by reisolation of the bacterium from symptomatic tissues. In summary, the phenotypic, biochemical, and molecular tests identified the pathogen as E. cowanii. Recently, E. cowanii was isolated from Eucalyptus trees with symptoms of bacterial blight, although its pathogenicity was not demonstrated (2). To the best of our knowledge, this is the first report of a member of the Enterobacteriaceae family causing disease in M. fistulifera. The result has a great importance to better understand the role of E. cowanii as a pathogen-causing disease on a forest species. References: (1) C. L. Brady et al. Syst. Appl. Microbiol. 31:447, 2008. (2) C. L. Brady et al. Lett. Appl. Microbiol. 49:461, 2009. (3) W. G. Weisburg et al. J. Bacteriol. 173:697, 1991.

摘要

2011年夏天,在米纳斯吉拉斯州维索萨市的一家苗圃里,人们在巴西常见的本土森林物种管叶马比木(大戟科)的叶片上观察到褐色、坏死的不规则斑点。大约6300株幼苗接受了评估,其中多达60%表现出病害症状,包括严重落叶和植株死亡。病斑合并的叶片质地变为纸质,呈现枯萎状。从这些有症状的叶片上在King B培养基上分离出细菌菌落,并通过生化和分子分析鉴定为肠杆菌科的一员。与肠杆菌科的其他成员一样,该细菌为兼性厌氧、革兰氏阴性,在YDC培养基上呈奶油色,脲酶和氧化酶阴性,过氧化氢酶和天冬酰胺阳性。使用Wizard基因组DNA纯化试剂盒(Promega)从在28°C的液体523培养基中过夜培养的纯培养物中提取细菌DNA,并通过PCR扩增16S rDNA(3)和rpoB(1)中的保守序列。对1300bp的16S rDNA片段和750bp的rpoB基因序列进行NCBI BLAST分析。相关序列在MEGA 5软件中通过ClustalW进行比对和分析。使用PAUP 4.0版本和TBR算法以及1000次重复的自展分析,通过最大似然法进行系统发育分析,将该分离株归入与考氏肠杆菌同一进化枝,结果显示其与16S rDNA和rpoB的同源性分别为99%和98%。在构建的两个系统发育树中,该分离株都与考氏肠杆菌的模式菌株紧密聚类。通过用先前浸入10 CFU/ml细菌悬液中的剪刀剪叶或喷雾接种健康幼苗的叶片进行致病性测试。实验采用完全随机设计,重复6次。一盆一株植物被视为一个实验单位。对照幼苗用经盐溶液处理的剪刀剪叶或喷雾。接种前后,将植物在黑暗中于26°C的潮湿箱中放置24小时,然后在室温下培养。随后,将植物转移到26°C、12小时光周期(40 μmol/s/m)的生长室中。与最初观察到的症状一致,接种7天后,所有幼苗都出现了叶斑。阴性对照未观察到特征性症状。此外,通过从有症状的组织中再次分离出该细菌,证实了科赫法则。总之,表示型、生化和分子测试确定病原体为考氏肠杆菌。最近,从有细菌性枯萎症状的桉树中分离出了考氏肠杆菌,但其致病性尚未得到证实(2)。据我们所知,这是首次报道肠杆菌科的成员在管叶马比木上引起病害。该结果对于更好地了解考氏肠杆菌作为一种在森林物种上引起病害的病原体的作用具有重要意义。参考文献:(1)C.L.布雷迪等人,《系统与应用微生物学》31:447,2008年。(2)C.L.布雷迪等人,《应用微生物学快报》49:461,2009年。(3)W.G.魏斯堡等人,《细菌学杂志》173:697,1991年。

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