Bourhy Pascale, Frangeul Lionel, Couvé Elisabeth, Glaser Philippe, Saint Girons Isabelle, Picardeau Mathieu
Laboratoire des Spirochètes, Institut Pasteur, 25 rue du docteur Roux, 75724 Paris Cedex 15, France.
J Bacteriol. 2005 Jun;187(12):3931-40. doi: 10.1128/JB.187.12.3931-3940.2005.
The first and, to date, only extrachromosomal circular replicon identified in the spirochete Leptospira is the LE1 prophage from Leptospira biflexa. The 74-kb LE1 genome has a GC content of 36%, which is similar to the GC content of Leptospira spp. Most of the 79 predicted open reading frames (ORFs) showed no similarities to known ORFs. However 21 ORFs appeared to be organized in clusters that could code for head and tail structural proteins and immunity repressor proteins. In addition, the pattern of gene expression showed that several LE1 genes are expressed specifically either in LE1 prophage or in L. biflexa late after infection. Since the LE1 prophage replicates autonomously as a circular replicon in L. biflexa, we were able to engineer an L. biflexa-Escherichia coli shuttle vector from a 5.3-kb DNA fragment of LE1 (Saint Girons et al., J. Bacteriol. 182:5700-5705, 2000), opening this genus to genetic manipulation. In this study, base compositional asymmetry confirms the location of the LE1 replication region and suggests that LE1 replicates via a bidirectional Theta-like replication mechanism from this unique origin. By subcloning experiments, the replication region can be narrowed down to a 1-kb region. This minimal replication region consists of a rep encoding a protein of 180 amino acids. Upstream from rep, putative partitioning genes, called parA and parB, were found to be similar to the par loci in Borrelia plasmids. A significant increase of plasmid stability in L. biflexa can be seen only when both parA and parB are present. These results enable the construction of new shuttle vectors for studying the genetics of Leptospira spp. This study will also contribute to a better knowledge of phages unrelated to lambdoid phages.
在螺旋体钩端螺旋体中鉴定出的首个也是迄今唯一的染色体外环状复制子是来自双曲钩端螺旋体的LE1原噬菌体。74kb的LE1基因组的GC含量为36%,这与钩端螺旋体属的GC含量相似。79个预测的开放阅读框(ORF)中的大多数与已知的ORF没有相似性。然而,21个ORF似乎成簇排列,可能编码头部和尾部结构蛋白以及免疫阻遏蛋白。此外,基因表达模式表明,几个LE1基因在LE1原噬菌体中或在感染后期的双曲钩端螺旋体中特异性表达。由于LE1原噬菌体在双曲钩端螺旋体中作为环状复制子自主复制,我们能够从LE1的一个5.3kb DNA片段构建一个双曲钩端螺旋体-大肠杆菌穿梭载体(Saint Girons等人,《细菌学杂志》182:5700-5705,2000),从而开启了对该属进行基因操作的大门。在本研究中,碱基组成不对称证实了LE1复制区域的位置,并表明LE1通过双向θ样复制机制从这个独特的起点进行复制。通过亚克隆实验,复制区域可以缩小到一个1kb的区域。这个最小的复制区域由一个编码180个氨基酸的蛋白质的rep组成。在rep的上游,发现了假定的分区基因,称为parA和parB,它们与疏螺旋体质粒中的par位点相似。只有当parA和parB都存在时,才能在双曲钩端螺旋体中看到质粒稳定性的显著增加。这些结果有助于构建新的穿梭载体来研究钩端螺旋体属的遗传学。本研究也将有助于更好地了解与λ样噬菌体无关的噬菌体。