Rouvier C, Prin Y, Reddell P, Normand P, Simonet P
Laboratoire d'Ecologie Microbienne du Sol, Villeurbanne, France.
Appl Environ Microbiol. 1996 Mar;62(3):979-85. doi: 10.1128/aem.62.3.979-985.1996.
DNA extracted directly from nodules was used to assess the genetic diversity of Frankia strains symbiotically associated with two species of the genus Casuarina and two of the genus Allocasuarina naturally occurring in northeastern Australia. DNA from field-collected nodules or extracted from reference cultures of Casuarina-infective Frankia strains was used as the template in PCRs with primers targeting two DNA regions, one in the ribosomal operon and the other in the nif operon. PCR products were then analyzed by using a set of restriction endonucleases. Five distinct genetic groups were recognized on the basis of these restriction patterns. These groups were consistently associated with the host species from which the nodules originated. All isolated reference strains had similar patterns and were assigned to group 1 along with six of the eight unisolated Frankia strains from Casuarina equisetifolia in Australia. Group 2 consisted of two unisolated Frankia strains from C. equisetifolia, whereas groups 3 to 5 comprised all unisolated strains from Casuarina cunninghamiana, Allocasuarina torulosa, and Allocasuarina littoralis, respectively. These results demonstrate that, contrary to the results of previous molecular studies of isolated strains, there is genetic diversity among Frankia strains that infect members of the family Casuarinacaeae. The apparent high homogeneity of Frankia strains in these previous studies probably relates to the single host species from which the strains were obtained and the origin of these strains from areas outside the natural geographic range of members of the family Casuarinaceae, where genetic diversity could be lower than in Australia.
直接从根瘤中提取的DNA用于评估与澳大利亚东北部自然生长的两种木麻黄属植物和两种异木麻黄属植物共生的弗兰克氏菌菌株的遗传多样性。从田间采集的根瘤中提取的DNA或从感染木麻黄的弗兰克氏菌菌株的参考培养物中提取的DNA用作PCR模板,PCR引物靶向两个DNA区域,一个在核糖体操纵子中,另一个在固氮酶操纵子中。然后使用一组限制性内切酶分析PCR产物。根据这些限制性图谱识别出五个不同的遗传组。这些组始终与根瘤来源的宿主物种相关。所有分离的参考菌株具有相似的图谱,并与来自澳大利亚木麻黄的八个未分离的弗兰克氏菌菌株中的六个一起被归入第1组。第2组由来自木麻黄的两个未分离的弗兰克氏菌菌株组成,而第3至5组分别包括来自细枝木麻黄、串珠异木麻黄和滨海异木麻黄的所有未分离菌株。这些结果表明,与之前对分离菌株的分子研究结果相反,感染木麻黄科成员的弗兰克氏菌菌株之间存在遗传多样性。这些先前研究中弗兰克氏菌菌株明显的高度同质性可能与获得这些菌株的单一宿主物种以及这些菌株来自木麻黄科成员自然地理范围之外的地区有关,在这些地区遗传多样性可能低于澳大利亚。