Hu P, Elliott J, McCready P, Skowronski E, Garnes J, Kobayashi A, Brubaker R R, Garcia E
Human Genome Center, Biology and Biotechnology Research Program, Lawrence Livermore National Laboratory, Livermore, California 94550, USA.
J Bacteriol. 1998 Oct;180(19):5192-202. doi: 10.1128/JB.180.19.5192-5202.1998.
The complete nucleotide sequence and gene organization of the three virulence plasmids from Yersinia pestis KIM5 were determined. Plasmid pPCP1 (9,610 bp) has a GC content of 45.3% and encodes two previously known virulence factors, an associated protein, and a single copy of IS100. Plasmid pCD1 (70,504 bp) has a GC content of 44.8%. It is known to encode a number of essential virulence determinants, regulatory functions, and a multiprotein secretory system comprising the low-calcium response stimulation that is shared with the other two Yersinia species pathogenic for humans (Y. pseudotuberculosis and Y. enterocolitica). A new pseudogene, which occurs as an intact gene in the Y. enterocolitica and Y. pseudotuberculosis-derived analogues, was found in pCD1. It corresponds to that encoding the lipoprotein YlpA. Several intact and partial insertion sequences and/or transposons were also found in pCD1, as well as six putative structural genes with high homology to proteins of unknown function in other yersiniae. The sequences of the genes involved in the replication of pCD1 are highly homologous to those of the cognate plasmids in Y. pseudotuberculosis and Y. enterocolitica, but their localization within the plasmid differs markedly from those of the latter. Plasmid pMT1 (100,984 bp) has a GC content of 50.2%. It possesses two copies of IS100, which are located 25 kb apart and in opposite orientations. Adjacent to one of these IS100 inserts is a partial copy of IS285. A single copy of an IS200-like element (recently named IS1541) was also located in pMT1. In addition to 5 previously described genes, such as murine toxin, capsule antigen, capsule anchoring protein, etc., 30 homologues to genes of several bacterial species were found in this plasmid, and another 44 open reading frames without homology to any known or hypothetical protein in the databases were predicted.
测定了来自鼠疫耶尔森氏菌KIM5的三种毒力质粒的完整核苷酸序列和基因组织。质粒pPCP1(9610 bp)的GC含量为45.3%,编码两个先前已知的毒力因子、一个相关蛋白和单拷贝的IS100。质粒pCD1(70504 bp)的GC含量为44.8%。已知它编码许多必需的毒力决定因素、调节功能以及一个多蛋白分泌系统,该系统包括与另外两种对人类致病的耶尔森氏菌(假结核耶尔森氏菌和小肠结肠炎耶尔森氏菌)共有的低钙应答刺激。在pCD1中发现了一个新的假基因,该假基因在小肠结肠炎耶尔森氏菌和假结核耶尔森氏菌衍生的类似物中以完整基因形式存在。它对应于编码脂蛋白YlpA的基因。在pCD1中还发现了几个完整和部分插入序列和/或转座子,以及六个与其他耶尔森氏菌中功能未知的蛋白质具有高度同源性的假定结构基因。参与pCD1复制的基因序列与假结核耶尔森氏菌和小肠结肠炎耶尔森氏菌中的同源质粒高度同源,但其在质粒中的定位与后者明显不同。质粒pMT1(100984 bp)的GC含量为50.2%。它有两个拷贝的IS100,它们相距25 kb且方向相反。其中一个IS100插入片段旁边是IS285的部分拷贝。在pMT1中还定位了一个单拷贝的类IS200元件(最近命名为IS1541)。除了5个先前描述的基因,如鼠毒素、荚膜抗原、荚膜锚定蛋白等,在该质粒中还发现了30个与几种细菌物种基因的同源物,另外预测了44个与数据库中任何已知或假设蛋白质无同源性的开放阅读框。