Carnoy Christophe, Floquet Stephanie, Marceau Michael, Sebbane Florent, Haentjens-Herwegh Stephanie, Devalckenaere Annie, Simonet Michel
Equipe Mixte Inserm E9919-Université JE 2225-Institut Pasteur de Lille, Lille, France.
J Bacteriol. 2002 Aug;184(16):4489-99. doi: 10.1128/JB.184.16.4489-4499.2002.
Yersinia pseudotuberculosis produces YPM (Y. pseudotuberculosis-derived mitogen), a superantigenic toxin that exacerbates the virulence of the bacterium in vivo. To date, three alleles of the superantigen gene (ypmA, ypmB, and ypmC) have been described. These genes are not found in all Y. pseudotuberculosis strains and have a low GC content, suggesting their location on mobile genetic elements. To elucidate this question, the genetic environment of the superantigen-encoding genes was characterized and 11 open reading frames (ORFs) were defined. Sequence analysis revealed that the ypm genes were not associated with plasmids, phages, transposons, or pathogenicity islands and that the superantigen genes were always located in the chromosome between ORF3 and ORF4. Nonsuperantigenic strains exhibited the same genetic organization of the locus but lacked the ypm gene between ORF3 and ORF4. A new insertion sequence, designated IS1398, which displays features of the Tn3 family, was characterized downstream of the ypmA and ypmC genes. A 13.3-kb region containing the ypm genes was not found in the genome of Y. pestis (CO92 and KIM 5 strains). We experimentally induced deletion of the ypm gene from a superantigen-expressing Y. pseudotuberculosis: using the association of aph(3')-IIIa and sacB genes, we demonstrated that when these reporter genes were present in the ypm locus, deletion of these genes was about 250 times more frequent than when they were located in another region of the Y. pseudotuberculosis chromosome. These results indicate that unlike other superantigenic toxin genes, the Yersinia ypm genes are not associated with mobile genetic elements but are inserted in an unstable locus of the genome.
假结核耶尔森菌产生YPM(假结核耶尔森菌衍生的丝裂原),一种超抗原毒素,可增强该细菌在体内的毒力。迄今为止,已描述了超抗原基因的三个等位基因(ypmA、ypmB和ypmC)。并非所有假结核耶尔森菌菌株中都存在这些基因,且它们的GC含量较低,这表明它们位于可移动遗传元件上。为阐明这个问题,对超抗原编码基因的遗传环境进行了表征,并确定了11个开放阅读框(ORF)。序列分析表明,ypm基因与质粒、噬菌体、转座子或致病岛无关,且超抗原基因总是位于ORF3和ORF4之间的染色体上。非超抗原性菌株表现出该位点相同的遗传组织,但在ORF3和ORF4之间缺少ypm基因。在ypmA和ypmC基因下游鉴定出一种新的插入序列,命名为IS1398,它具有Tn3家族的特征。在鼠疫耶尔森菌(CO92和KIM 5菌株)的基因组中未发现包含ypm基因的13.3 kb区域。我们通过实验诱导表达超抗原的假结核耶尔森菌缺失ypm基因:利用aph(3')-IIIa和sacB基因的组合,我们证明当这些报告基因存在于ypm位点时,这些基因的缺失频率比它们位于假结核耶尔森菌染色体的其他区域时高约250倍。这些结果表明,与其他超抗原毒素基因不同,耶尔森菌ypm基因与可移动遗传元件无关,而是插入到基因组的一个不稳定位点。