Wolde-Meskel Endalkachew, Terefework Zewdu, Frostegård Åsa, Lindström Kristina
Norwegian University of Life Sciences, Department of Chemistry, Biotechnology and Food Science, PO Box 5040, N-1432 Ås, Norway.
Department of Applied Chemistry and Microbiology, Biocenter 1, FIN-0014 University of Helsinki, Finland.
Int J Syst Evol Microbiol. 2005 Jul;55(Pt 4):1439-1452. doi: 10.1099/ijs.0.63534-0.
The genetic diversity within 195 rhizobial strains isolated from root nodules of 18 agroforestry species (15 woody and three herbaceous legumes) growing in diverse ecoclimatic zones in southern Ethiopia was investigated by using PCR-RFLP of the ribosomal operon [16S rRNA gene, 23S rRNA gene and the internal transcribed spacer (ITS) region between the 16S rRNA and 23S rRNA genes] and 16S rRNA gene partial sequence (800 and 1350 bp) analyses. All of the isolates and the 28 reference strains could be differentiated by using these methods. The size of the ITS varied among test strains (500-1300 bp), and 58 strains contained double copies. UPGMA dendrograms generated from cluster analyses of the 16S and 23S rRNA gene PCR-RFLP data were in good agreement, and the combined distance matrices delineated 87 genotypes, indicating considerable genetic diversity among the isolates. Furthermore, partial sequence analysis of 67 representative strains revealed 46 16S rRNA gene sequence types, among which 12 were 100% similar to those of previously described species and 34 were novel sequences with 94-99% similarity to those of recognized species. The phylogenetic analyses suggested that strains indigenous to Ethiopia belonged to the genera Agrobacterium, Bradyrhizobium, Mesorhizobium, Methylobacterium, Rhizobium and Sinorhizobium. Many of the rhizobia isolated from previously uninvestigated indigenous woody legumes had novel 16S rRNA gene sequences and were phylogenetically diverse. This study clearly shows that the characterization of symbionts of unexplored legumes growing in previously unexplored biogeographical areas will reveal additional diversity.
通过对核糖体操纵子(16S rRNA基因、23S rRNA基因以及16S rRNA和23S rRNA基因之间的内部转录间隔区(ITS))进行PCR-RFLP分析以及16S rRNA基因部分序列(800和1350 bp)分析,研究了从埃塞俄比亚南部不同生态气候区生长的18种农林物种(15种木本和3种草本豆科植物)根瘤中分离出的195株根瘤菌菌株的遗传多样性。使用这些方法可以区分所有分离株和28株参考菌株。测试菌株中ITS的大小各不相同(500 - 1300 bp),58株含有双拷贝。从16S和23S rRNA基因PCR-RFLP数据的聚类分析生成的UPGMA树状图高度一致,合并的距离矩阵划分出87个基因型,表明分离株之间存在相当大的遗传多样性。此外,对67株代表性菌株的部分序列分析揭示了46种16S rRNA基因序列类型,其中12种与先前描述的物种100%相似,34种是新序列,与已知物种的相似性为94 - 99%。系统发育分析表明,埃塞俄比亚本土的菌株属于农杆菌属、慢生根瘤菌属、中生根瘤菌属、甲基杆菌属、根瘤菌属和中华根瘤菌属。从以前未研究过的本土木本豆科植物中分离出的许多根瘤菌具有新的16S rRNA基因序列,并且在系统发育上具有多样性。这项研究清楚地表明,对生长在以前未探索的生物地理区域的未开发豆科植物共生体进行表征将揭示更多的多样性。