Sohel I, Puente J L, Ramer S W, Bieber D, Wu C Y, Schoolnik G K
Department of Microbiology and Immunology, Stanford University School of Medicine, California 94305, USA.
J Bacteriol. 1996 May;178(9):2613-28. doi: 10.1128/jb.178.9.2613-2628.1996.
Sequence flanking the bfpA locus on the enteroadherent factor plasmid of the enteropathogenic Escherichia coli (EPEC) strain B171-8 (O111:NM) was obtained to identify genes that might be required for bundle-forming pilus (BFP) biosynthesis. Deletion experiments led to the identification of a contiguous cluster of at least 12 open reading frames, including bfpA, that could direct the synthesis of a morphologically normal BFP filament. Within the bfp gene cluster, we identified open reading frames that share homology with other type IV pilus accessory genes and with genes required for transformation competence and protein secretion. Immediately upstream of the bfp gene cluster, we identified a potential replication origin including genes that are predicted to encode proteins homologous with replicase and resolvase. Restriction fragment length polymorphism analysis of DNA from six additional EPEC serotypes showed that the organization of the bfp gene cluster and its juxtaposition with a potential plasmid origin of replication are highly conserved features of the EPEC biotype.
获得了肠致病性大肠杆菌(EPEC)菌株B171-8(O111:NM)的粘附因子质粒上bfpA基因座侧翼的序列,以鉴定可能是束状菌毛(BFP)生物合成所必需的基因。缺失实验导致鉴定出至少12个开放阅读框的连续簇,包括bfpA,其可指导形态正常的BFP细丝的合成。在bfp基因簇内,我们鉴定出与其他IV型菌毛辅助基因以及转化能力和蛋白质分泌所需基因具有同源性的开放阅读框。在bfp基因簇的紧邻上游,我们鉴定出一个潜在的复制起点,包括预计编码与复制酶和解旋酶同源蛋白质的基因。对另外六种EPEC血清型的DNA进行的限制性片段长度多态性分析表明,bfp基因簇的组织及其与潜在质粒复制起点的并置是EPEC生物型的高度保守特征。