Tas E, Leinonen P, Saano A, Räsänen L A, Kaijalainen S, Piippola S, Hakola S, Lindström K
Department of Applied Chemistry and Microbiology, University of Helskinki, Finland.
Appl Environ Microbiol. 1996 Feb;62(2):529-35. doi: 10.1128/aem.62.2.529-535.1996.
Competition between effective and ineffective Rhizobium galegae strains nodulating Galega orientalis was examined on the basis of plant growth, nodulation, antibiotic resistance, and PCR results. In a preliminary experiment in Leonard's jars, ineffective R. galegae strains HAMBI 1207 and HAMBI 1209 competed in similar manners with the effective strain R. galegae HAMBI 1174. In a pot experiment, soil was inoculated with 0 to 10(5) HAMBI 1207 cells per g before G. orientalis was sown. Seeds of G. orientalis were surface inoculated with 2 x 10(4) and 2 x 10(5) cells of HAMBI 1174 per seed (which represent half and fivefold the commercially recommended amount of inoculant, respectively). Plant yield and nodulation by the effective strain were significantly reduced, with as few as 10(2) ineffective rhizobia per g of soil, and the inoculation response was not improved by the 10-fold greater dose of the inoculant. Bacteria occupying the nodules were identified by antibiotic resistance and PCR with primers specific for R. galegae HAMBI 1174, R. galegae, and genes coding for bacterial 16S rRNA (bacterial 16S rDNA). Sixty-two large nodules examined were occupied by the effective strain HAMBI 1174, as proven by antibiotic resistance and amplification of the strain-specific fragment. From 20 small nodules, only the species-specific fragment could be amplified, and isolated bacteria had the same antibiotic resistance and 16S PCR restriction pattern as strain HAMBI 1207. PCR with our strain-specific and species-specific primers provides a powerful tool for strain identification of R. galegae directly from nodules without genetic modification of the bacteria.
基于植物生长、结瘤、抗生素抗性和聚合酶链式反应(PCR)结果,对东方山羊豆上有效和无效的根瘤菌菌株之间的竞争进行了研究。在伦纳德氏罐的初步实验中,无效的山羊豆根瘤菌菌株HAMBI 1207和HAMBI 1209与有效菌株山羊豆根瘤菌HAMBI 1174的竞争方式相似。在盆栽实验中,在播种东方山羊豆之前,每克土壤接种0至10⁵个HAMBI 1207细胞。东方山羊豆种子表面接种每粒种子2×10⁴和2×10⁵个HAMBI 1174细胞(分别代表商业推荐接种量的一半和五倍)。每克土壤中低至10²个无效根瘤菌时,有效菌株的植物产量和结瘤就会显著降低,接种量增加10倍也无法改善接种反应。通过抗生素抗性以及使用针对山羊豆根瘤菌HAMBI 1174、山羊豆根瘤菌和编码细菌16S核糖体RNA(细菌16S rDNA)的基因的引物进行PCR,鉴定占据根瘤的细菌。经抗生素抗性和菌株特异性片段扩增证明,所检查的62个大根瘤由有效菌株HAMBI 1174占据。从20个小根瘤中,仅能扩增出物种特异性片段,分离出的细菌具有与菌株HAMBI 1207相同的抗生素抗性和16S PCR限制性图谱。使用我们的菌株特异性和物种特异性引物进行PCR,为直接从根瘤中鉴定山羊豆根瘤菌菌株提供了一种强大的工具,而无需对细菌进行基因改造。