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基于 16S rRNA 基因、ITS 区以及 glnII、recA、atpD 和 dnaK 基因的多位点序列分析对多种 Bradyrhizobium 菌株的系统发育和分类学研究。

Phylogeny and taxonomy of a diverse collection of Bradyrhizobium strains based on multilocus sequence analysis of the 16S rRNA gene, ITS region and glnII, recA, atpD and dnaK genes.

机构信息

Embrapa Soja, Cx Postal 231, 86001-970 Londrina, Paraná, Brazil.

出版信息

Int J Syst Evol Microbiol. 2009 Dec;59(Pt 12):2934-50. doi: 10.1099/ijs.0.009779-0. Epub 2009 Jul 23.

Abstract

The genus Bradyrhizobium encompasses a variety of bacteria that can live in symbiotic and endophytic associations with legumes and non-legumes, and are characterized by physiological and symbiotic versatility and broad geographical distribution. However, despite indications of great genetic variability within the genus, only eight species have been described, mainly because of the highly conserved nature of the 16S rRNA gene. In this study, 169 strains isolated from 43 different legumes were analysed by rep-PCR with the BOX primer, by sequence analysis of the 16S rRNA gene and the 16S-23S rRNA intergenic transcribed spacer (ITS) and by multilocus sequence analysis (MLSA) of four housekeeping genes, glnII, recA, atpD and dnaK. Considering a cut-off at a level of 70 % similarity, 80 rep-PCR profiles were distinguished, which, together with type strains, were clustered at a very low level of similarity (24 %). In both single and concatenated analyses of the 16S rRNA gene and ITS sequences, two large groups were formed, with bootstrap support of 99 % in the concatenated analysis. The first group included the type and/or reference strains of Bradyrhizobium japonicum, B. betae, B. liaoningense, B. canariense and B. yuanmingense and B. japonicum USDA 110, and the second group included strains related to Bradyrhizobium elkanii USDA 76(T), B. pachyrhizi PAC48(T) and B. jicamae PAC68(T). Similar results were obtained with MLSA of glnII, recA, atpD and dnaK. Greatest variability was observed when the atpD gene was amplified, and five strains related to B. elkanii revealed a level of variability never reported before. Another important observation was that a group composed of strains USDA 110, SEMIA 5080 and SEMIA 6059, all isolated from soybean, clustered in all six trees with high bootstrap support and were quite distinct from the clusters that included B. japonicum USDA 6(T). The results confirm that MLSA is a rapid and reliable way of providing information on phylogenetic relationships and of identifying rhizobial strains potentially representative of novel species.

摘要

慢生根瘤菌属包含了多种能够与豆科植物及其它非豆科植物共生和内生的细菌,其特点是具有生理和共生的多功能性以及广泛的地理分布。然而,尽管该属内存在巨大的遗传变异性迹象,但仅描述了 8 个种,主要是因为 16S rRNA 基因高度保守。在这项研究中,用 BOX 引物通过重复扩增多态性 DNA(rep-PCR)分析、16S rRNA 基因和 16S-23S rRNA 基因间转录间隔区(ITS)序列分析以及 4 个看家基因(glnII、recA、atpD 和 dnaK)的多位点序列分析(MLSA)对从 43 种不同豆科植物中分离出的 169 株菌株进行了分析。考虑到 70%相似性的截断水平,区分出了 80 种 rep-PCR 图谱,这些图谱连同模式株一起,在非常低的相似性水平(24%)上聚类。在 16S rRNA 基因和 ITS 序列的单序列和串联分析中,形成了两个大组,在串联分析中支持度为 99%。第一组包括慢生根瘤菌、大豆慢生根瘤菌、辽宁慢生根瘤菌、坎那慢生根瘤菌和元明串珠菌的模式和/或参考菌株以及大豆慢生根瘤菌 USDA110,第二组包括与慢生根瘤菌 elkanii USDA76(T)、大豆慢生根瘤菌 PAC48(T)和野葛慢生根瘤菌 PAC68(T)相关的菌株。glnII、recA、atpD 和 dnaK 的 MLSA 也得到了类似的结果。当扩增 atpD 基因时观察到最大的变异性,并且与慢生根瘤菌 elkanii 相关的 5 株菌株显示出了以前从未报道过的变异性水平。另一个重要的观察结果是,由菌株 USDA110、SEMLA5080 和 SEMIA6059 组成的一组,均从大豆中分离出来,在所有六棵树中以高支持度聚类,并与包含大豆慢生根瘤菌 USDA6(T)的聚类明显不同。结果证实,MLSA 是一种快速可靠的方法,可以提供关于系统发育关系的信息,并识别可能代表新种的根瘤菌株。

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