Bearden S W, Fetherston J D, Perry R D
Department of Microbiology and Immunology, University of Kentucky, Lexington 40536-0084, USA.
Infect Immun. 1997 May;65(5):1659-68. doi: 10.1128/iai.65.5.1659-1668.1997.
We have identified an approximately 22-kb region of the pgm locus of Yersinia pestis KIM6+ which encodes a number of iron-regulated proteins involved in the biosynthesis of the Y. pestis cognate siderophore, yersiniabactin (Ybt), and which is located immediately upstream of the pesticin/yersiniabactin receptor gene (psn). Sequence analysis and the construction of insertion and deletion mutants allowed us to determine the putative location of the irp1 gene and the positions of irp2, ybtT, and ybtE within the ybt operon. Mutations in the irp1, irp2, or ybtE gene yielded strains defective in siderophore production. Mutant strains were unable to grow on iron-deficient media at 37 degrees C but could be cross-fed by culture supernatants from yersiniabactin-producing strains of Y. pestis grown under iron-limiting conditions. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis of whole-cell extracts from Ybt+ and Ybt- strains grown in iron-deficient media revealed that expression of ybt-encoded proteins is not only iron regulated but also influenced by the presence of the siderophore itself. Finally, Y. pestis strains with mutations in either the psn or irp2 gene were avirulent in mice when inoculated subcutaneously.
我们已鉴定出鼠疫耶尔森氏菌KIM6 +的pgm基因座中一个约22 kb的区域,该区域编码许多参与鼠疫耶尔森氏菌同源铁载体yersiniabactin(Ybt)生物合成的铁调节蛋白,且位于杀鼠菌素/yersiniabactin受体基因(psn)的紧邻上游。序列分析以及插入和缺失突变体的构建使我们能够确定irp1基因的推定位置以及ybt操纵子内irp2、ybtT和ybtE的位置。irp1、irp2或ybtE基因的突变产生了铁载体产生缺陷的菌株。突变菌株在37℃的缺铁培养基上无法生长,但可以被在铁限制条件下生长的鼠疫耶尔森氏菌yersiniabactin产生菌株的培养上清液交叉喂养。对在缺铁培养基中生长的Ybt +和Ybt-菌株的全细胞提取物进行的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析表明,ybt编码蛋白的表达不仅受铁调节,还受铁载体本身存在的影响。最后,psn或irp2基因发生突变的鼠疫耶尔森氏菌菌株经皮下接种后在小鼠中无致病性。