Perry R D, Straley S C, Fetherston J D, Rose D J, Gregor J, Blattner F R
Department of Microbiology and Immunology, University of Kentucky, Lexington, Kentucky 40536-0084, USA.
Infect Immun. 1998 Oct;66(10):4611-23. doi: 10.1128/IAI.66.10.4611-4623.1998.
The low-Ca2+-response (LCR) plasmid pCD1 of the plague agent Yersinia pestis KIM5 was sequenced and analyzed for its genetic structure. pCD1 (70,509 bp) has an IncFIIA-like replicon and a SopABC-like partition region. We have assigned 60 apparently intact open reading frames (ORFs) that are not contained within transposable elements. Of these, 47 are proven or possible members of the LCR, a major virulence property of human-pathogenic Yersinia spp., that had been identified previously in one or more of Y. pestis or the enteropathogenic yersiniae Yersinia enterocolitica and Yersinia pseudotuberculosis. Of these 47 LCR-related ORFs, 35 constitute a continuous LCR cluster. The other LCR-related ORFs are interspersed among three intact insertion sequence (IS) elements (IS100 and two new IS elements, IS1616 and IS1617) and numerous defective or partial transposable elements. Regional variations in percent GC content and among ORFs encoding effector proteins of the LCR are additional evidence of a complex history for this plasmid. Our analysis suggested the possible addition of a new Syc- and Yop-encoding operon to the LCR-related pCD1 genes and gave no support for the existence of YopL. YadA likely is not expressed, as was the case for Y. pestis EV76, and the gene for the lipoprotein YlpA found in Y. enterocolitica likely is a pseudogene in Y. pestis. The yopM gene is longer than previously thought (by a sequence encoding two leucine-rich repeats), the ORF upstream of ypkA-yopJ is discussed as a potential Syc gene, and a previously undescribed ORF downstream of yopE was identified as being potentially significant. Eight other ORFs not associated with IS elements were identified and deserve future investigation into their functions.
对鼠疫杆菌KIM5的低钙应答(LCR)质粒pCD1进行了测序,并分析了其遗传结构。pCD1(70,509 bp)具有类IncFIIA复制子和类SopABC分区区域。我们确定了60个明显完整的开放阅读框(ORF),它们不包含在转座元件内。其中,47个是LCR的已证实或可能成员,LCR是人类致病性耶尔森菌属的主要毒力特性,先前已在鼠疫杆菌或肠道致病性耶尔森菌小肠结肠炎耶尔森菌和假结核耶尔森菌中的一种或多种中鉴定出来。在这47个与LCR相关的ORF中,35个构成一个连续的LCR簇。其他与LCR相关的ORF散布在三个完整的插入序列(IS)元件(IS100以及两个新的IS元件IS1616和IS1617)和许多有缺陷或部分的转座元件之间。GC含量百分比的区域差异以及LCR效应蛋白编码ORF之间的差异是该质粒复杂历史的额外证据。我们的分析表明,可能有一个新的编码Syc和Yop的操纵子添加到与LCR相关的pCD1基因中,并且不支持YopL的存在。YadA可能不表达,就像鼠疫杆菌EV76的情况一样,并且在小肠结肠炎耶尔森菌中发现的脂蛋白YlpA基因在鼠疫杆菌中可能是一个假基因。yopM基因比以前认为的要长(多了一个编码两个富含亮氨酸重复序列的序列),ypkA - yopJ上游的ORF被讨论为一个潜在的Syc基因,并且在yopE下游鉴定出一个先前未描述的ORF可能具有重要意义。还确定了另外八个与IS元件无关的ORF,值得未来对其功能进行研究。