Gtari M, Brusetti L, Cherif A, Boudabous A, Daffonchio D
Laboratoire Microorganismes et Biomolécules Actives, Département de Biologie, Faculté des Sciences de Tunis, Campus Universitaire, 2092 Tunis, Tunisia.
J Appl Microbiol. 2007 Oct;103(4):1031-40. doi: 10.1111/j.1365-2672.2007.03329.x.
Detection of polymorphisms in intergenic transcribed spacer (ITS) 16S-23S rRNA within single Frankia strains.
Polymorphisms in the 16S-23S rRNA ITS were investigated in single-colony subcultures of seven Frankia isolates. Multiple ITS-polymerase chain reaction (PCR) bands were detected solely in isolates BMG5.5 and BMG5.11. The slow-migrating bands in the ITS-PCR agarose gel electrophoresis profiles of the isolates were revealed to be heteroduplexes on the basis of their migration shift in different electrophoretic matrices, southern hybridization and the single-strand DNA mung bean endonuclease digestion. Laser-scanned capillary electrophoresis detected two ITS-PCR fragments differing in length by three and six nucleotide insertions/deletions in strains BMG5.5 and BMG5.11, respectively. Sequence analysis of the cloned ITS showed that in strain BMG5.5 the two ITS differed by the presence of three to four copies of the 3-bp tandem repeat 5'-TGG-3'. In strain BMG5.11, the two ITS differed by the presence of two to three copies of the 6-bp tandem repeat 5'-CTTGGG-3'.
We demonstrate the occurrence of ITS 16S-23S rRNa polymorphisms within single Frankia strains.
We reported the occurrence of ITS 16S-23S rRNA polymorphisms within single Frankia strains from Elaeagnus host group recognized as the more flexible strains within Frankia genus. Furthermore, we underscored the applied interest of strains BMG5.11 and BMG5.5 in future ecological studies using ITS 16S-23S rRNA as molecular marker.
检测单个弗兰克氏菌菌株中16S - 23S核糖体RNA基因间隔区(ITS)的多态性。
对7株弗兰克氏菌分离株的单菌落传代培养物中16S - 23S rRNA ITS的多态性进行了研究。仅在分离株BMG5.5和BMG5.11中检测到多个ITS - 聚合酶链反应(PCR)条带。基于其在不同电泳基质中的迁移变化、Southern杂交和单链DNA绿豆核酸酶消化,ITS - PCR琼脂糖凝胶电泳图谱中迁移缓慢的条带被证明是异源双链体。激光扫描毛细管电泳检测到菌株BMG5.5和BMG5.11中分别有两个长度相差3个和6个核苷酸插入/缺失的ITS - PCR片段。对克隆的ITS进行序列分析表明,在菌株BMG5.5中,两个ITS的差异在于存在3至4个拷贝的3 - bp串联重复序列5'-TGG-3'。在菌株BMG5.11中,两个ITS的差异在于存在2至3个拷贝的6 - bp串联重复序列5'-CTTGGG-3'。
我们证明了单个弗兰克氏菌菌株中存在ITS 16S - 23S rRNA多态性。
我们报道了在被认为是弗兰克氏菌属中更具灵活性的菌株——胡颓子宿主组的单个弗兰克氏菌菌株中存在ITS 16S - 23S rRNA多态性。此外,我们强调了菌株BMG5.11和BMG5.5在未来使用ITS 16S - 23S rRNA作为分子标记的生态学研究中的应用价值。