Department of Microbiology, Oregon State University, Corvallis, Oregon 97331-3804.
Appl Environ Microbiol. 1994 Aug;60(8):2772-8. doi: 10.1128/aem.60.8.2772-2778.1994.
An investigation was carried out to determine the genetic structure in soil populations of Rhizobium leguminosarum bv. trifolii and viciae at each of two Oregon sites (A and C) that were 1 km apart. Although the soils were similar, the plant communities were quite different because grazing by domestic animals had been allowed (site A) or prevented (site C). Analysis of allelic variation at 13 enzyme-encoding loci by multilocus enzyme electrophoresis delineated 202 chromosomal types (ETs) among a total of 456 isolates representing two populations of R. leguminosarum bv. trifolii (AT and CT) and two populations of R. leguminosarum bv. viciae (AV and CV). Regardless of their site of origin or biovar affiliation, isolates of the same ET were confirmed to be more closely related to each other than to isolates of other ETs by repetitive extragenic palindromic and enterobacterial repetitive intergeneric consensus sequences and the PCR technique. Despite the wide range in densities of the Rhizobium populations (<10 to >10/g of soil), their overall genetic diversities were similar (mean genetic diversity, 0.45 to 0.51), indicating that low-density populations of soil-borne bacterial species are not necessarily of little genetic diversity. Linkage disequilibrium analysis revealed significant multilocus structure (nonrandom associations of alleles) within each of the four populations. From a combination of cluster and linkage disequilibrium analyses, a total of eight distinct groups of ETs were defined in the four populations. Two groups (I and III) contributed significant numbers of ETs and isolates to each population. The two populations of R. leguminosarum bv. viciae (AV and CV) exhibited similar genetic structures despite existing at different densities, in different plant communities, and in the presence (CV) or absence (AV) of their local Vicia hosts. In contrast, total linkage disequilibrium was partitioned differently in two biovar populations occupying the same soil (AV and AT), with disequilibrium in the latter being due entirely to the presence of group V.
进行了一项调查,以确定在俄勒冈州的两个地点(A 和 C)的土壤根瘤菌群体中的遗传结构,这两个地点相距 1 公里。尽管土壤相似,但植物群落却大不相同,因为在一个地点(A)允许家畜放牧,而在另一个地点(C)则禁止放牧。通过多位点酶电泳分析等位基因变异,在总共 456 个代表两种根瘤菌 bv.trifolii(AT 和 CT)种群和两种根瘤菌 bv.viciae(AV 和 CV)种群的分离物中,描绘了 202 个染色体类型(ET)。无论其来源地或生物变种归属如何,同一 ET 的分离物通过重复外基因回文和肠杆菌属间重复共识序列和 PCR 技术被确认为彼此之间比其他 ET 的分离物更密切相关。尽管根瘤菌种群的密度范围很广(<10 至> 10/g 土壤),但它们的总体遗传多样性相似(平均遗传多样性为 0.45 至 0.51),这表明土壤传播细菌种群的低密度种群不一定遗传多样性小。连锁不平衡分析显示,四个种群中的每个种群都存在显著的多位点结构(等位基因的非随机关联)。通过聚类和连锁不平衡分析的组合,在四个种群中总共定义了 8 个不同的 ET 组。两个组(I 和 III)为每个种群提供了大量的 ET 和分离物。尽管在不同的密度、不同的植物群落中存在,并且存在(CV)或不存在(AV)其当地的 Vicia 宿主,两种根瘤菌 bv.viciae(AV 和 CV)种群仍表现出相似的遗传结构。相比之下,两种生物变种种群(AV 和 AT)在同一土壤中占据不同的总连锁不平衡被不同地划分,后者的不平衡完全是由于组 V 的存在所致。