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产生抗真菌化合物2,4-二乙酰基间苯三酚的生防荧光假单胞菌的多位点序列分析

Multilocus sequence analysis of biocontrol fluorescent Pseudomonas spp. producing the antifungal compound 2,4-diacetylphloroglucinol.

作者信息

Frapolli Michele, Défago Geneviève, Moënne-Loccoz Yvan

机构信息

Plant Pathology, Institute of Integrative Biology, ETH-Zürich, 8092 Zürich, Switzerland.

出版信息

Environ Microbiol. 2007 Aug;9(8):1939-55. doi: 10.1111/j.1462-2920.2007.01310.x.

DOI:10.1111/j.1462-2920.2007.01310.x
PMID:17635541
Abstract

The genetic and evolutionary relationship among 2,4-diacetylphloroglucinol (Phl)-producing pseudomonads that protect plants from soil-borne pathogens were investigated by multilocus sequence typing. A total of 65 pseudomonads consisting of 58 Phl-positive biocontrol strains of worldwide origin and seven Phl-negative representatives of characterized Pseudomonas species were compared using 10 housekeeping genes (i.e. rrs, dsbA, gyrB, rpoD, fdxA, recA, rpoB, fusA, rpsL and rpsG). Multilocus sequence typing differentiated 51 strains among 58 Phl-positive pseudomonads and proved to be as discriminative as enterobacterial repetitive intergenic consensus polymerase chain reaction profiling. As phylogenetic trees inferred from each locus were rather incongruent with one another, we derived the topology from all concatenated loci, which led to the identification of six main groups of Phl-producing Pseudomonas spp. Taxonomically, these groups could correspond to at least six different species. Linkage disequilibrium analysis pointed to a rather clonal structure, even when the analysis was restricted to Phl-producing pseudomonads from a same geographic location or a same phylogenetic group. Intragenic recombination was evidenced for gyrB, rpoD and fdxA, but was shown to be a weaker force than mutation in the origin of intragenetic diversity. This is the first multilocus assessment of the phylogeny and population structure of an ecologically important bacterial group involved in plant disease suppression.

摘要

通过多位点序列分型研究了能够保护植物免受土传病原体侵害的产2,4-二乙酰基间苯三酚(Phl)假单胞菌之间的遗传和进化关系。使用10个管家基因(即rrs、dsbA、gyrB、rpoD、fdxA、recA、rpoB、fusA、rpsL和rpsG)对总共65株假单胞菌进行了比较,其中包括58株来自世界各地的Phl阳性生防菌株和7株已鉴定的假单胞菌属Phl阴性代表菌株。多位点序列分型在58株Phl阳性假单胞菌中区分出51个菌株,并且证明其鉴别能力与肠杆菌重复基因间共识聚合酶链反应分析相当。由于从每个基因座推断出的系统发育树彼此相当不一致,我们从所有串联的基因座得出拓扑结构,这导致鉴定出六个主要的产Phl假单胞菌属组。在分类学上,这些组可能对应于至少六个不同的物种。连锁不平衡分析表明存在相当的克隆结构,即使分析仅限于来自同一地理位置或同一系统发育组的产Phl假单胞菌。在gyrB、rpoD和fdxA中证实了基因内重组,但在基因内多样性起源方面,其显示出比突变更弱的作用。这是对参与植物病害抑制的一个具有重要生态意义的细菌群体的系统发育和种群结构的首次多位点评估。

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