Read T D, Dowdell M, Satola S W, Farley M M
Veterans Affairs Medical Center, Department of Medicine, Emory University School of Medicine, Decatur, Georgia 30033, USA.
J Bacteriol. 1996 Nov;178(22):6564-70. doi: 10.1128/jb.178.22.6564-6570.1996.
Brazilian purpuric fever (BPF) is a recently described pediatric septicemia caused by a strain of Haemophilus influenzae biogroup aegyptius. The pilus specified by this bacterium may be important in BPF pathogenesis, enhancing attachment to host tissue. Here, we report the cloning of two haf (for H. influenzae biogroup aegyptius fimbriae) gene clusters from a cosmid library of strain F3031. We sequenced a 6.8-kb segment of the haf1 cluster and identified five genes (hafA to hafE). The predicted protein products, HafA to HafD, are 72, 95, 98, and 90% similar, respectively, to HifA to HifD of the closely related H. influenzae type b pilus. Strikingly, the putative pilus adhesion, HifE, shares only 44% identity with HafE, suggesting that the proteins may differ in receptor specificity. Insertion of a mini-gammadelta transposon in the hafE gene eliminated hemadsorption. The nucleotide sequences of the haf1 and haf2 clusters are more than 99% identical. Using the recently published sequence of the H. influenzae Rd genome, we determined that the haf1 complex lies at a unique position in the chromosome between the pmbA gene and a hypothetical open reading frame, HI1153. The location of the haf2 cluster, inserted between the purE and pepN genes, is analogous to the hif genes on H. influenzae type b. BPF fimbrial phase switching appears to involve slip-strand mispairing of repeated dinucleotides in the pilus promoter. The BPF-associated H. influenzae biogroup aegyptius pilus system generally resembles other H. influenzae, but the possession of a second fimbrial gene cluster, which appears to have arisen by a recent duplication event, and the novel sequence of the HafE adhesin may be significant in the unusual pathogenesis of BPF.
巴西紫癜热(BPF)是一种最近发现的由埃及生物群流感嗜血杆菌菌株引起的小儿败血症。该细菌产生的菌毛可能在BPF发病机制中起重要作用,可增强对宿主组织的附着。在此,我们报告从菌株F3031的黏粒文库中克隆了两个haf(埃及生物群流感嗜血杆菌菌毛)基因簇。我们对haf1基因簇的一个6.8kb片段进行了测序,并鉴定出五个基因(hafA至hafE)。预测的蛋白质产物HafA至HafD分别与密切相关的b型流感嗜血杆菌菌毛的HifA至HifD有72%、95%、98%和90%的相似性。引人注目的是,假定的菌毛黏附蛋白HifE与HafE的同源性仅为44%,这表明这些蛋白质在受体特异性上可能存在差异。在hafE基因中插入一个微型γδ转座子消除了血细胞吸附。haf1和haf2基因簇的核苷酸序列有超过99%的同一性。利用最近公布的流感嗜血杆菌Rd基因组序列,我们确定haf1复合体位于染色体上pmbA基因和一个假定的开放阅读框HI1153之间的独特位置。haf2基因簇插入在purE和pepN基因之间,其位置类似于b型流感嗜血杆菌上的hif基因。BPF菌毛相转变似乎涉及菌毛启动子中重复二核苷酸的滑链错配。与BPF相关的埃及生物群流感嗜血杆菌菌毛系统总体上类似于其他流感嗜血杆菌,但拥有第二个菌毛基因簇(似乎是最近通过复制事件产生的)以及HafE黏附素的新序列可能在BPF不寻常的发病机制中具有重要意义。