Willems R J, van der Heide H G, Mooi F R
Molecular Microbiology Unit, National Institute of Health and Environmental Protection, Bilthoven, The Netherlands.
Mol Microbiol. 1992 Sep;6(18):2661-71. doi: 10.1111/j.1365-2958.1992.tb01443.x.
The biosynthesis of fimbriae is a complex process requiring multiple genes which are generally found clustered on the chromosome. In Bordetella pertussis, only major fimbrial subunit genes have been identified, and no evidence has yet been found that they are located in a fimbrial gene cluster. To locate additional genes involved in the biosynthesis of B. pertussis fimbriae, we used TnphoA mutagenesis. A PhoA+ mutant (designated B176) was isolated which was affected in the production of both serotype 2 and 3 fimbriae. Cloning and sequencing of the DNA region harbouring the transposon insertion revealed the presence of at least three additional fimbrial genes, designated fimB, fimC and fimD. The transposon was found to be located in fimD. Analysis of PhoA activity indicated that the fimbrial gene cluster was positively regulated by the bvg locus. A potential binding site for BvgA was observed upstream of fimB. FimB showed homology with the so-called chaperone-like fimbrial proteins, while FimC was homologous with a class of fimbrial proteins located in the outer membrane and presumed to be involved in transport and anchorage of fimbrial subunits. An insertion mutation in fimB abolished the expression of fimbrial subunits, implicating this gene in the biosynthesis of both serotype 2 and 3 fimbriae. Upstream of fimB a pseudogene (fimA) was observed which showed homology with the three major fimbrial subunit genes, fim2, fim3 and fimX. The construction of a phylogenetic tree suggested that fimA may be the primordial major fimbrial subunit gene from which the other three were derived by gene duplication. Interestingly, the fimbrial gene cluster was found to be located directly downstream from the gene coding for the filamentous haemagglutinin, an important B. pertussis adhesin, possibly suggesting co-operation between the two loci in the pathogenesis of pertussis.
菌毛的生物合成是一个复杂的过程,需要多个基因参与,这些基因通常成簇地位于染色体上。在百日咳博德特氏菌中,仅鉴定出了主要的菌毛亚基基因,尚未发现它们位于菌毛基因簇中的证据。为了定位参与百日咳博德特氏菌菌毛生物合成的其他基因,我们使用了TnphoA诱变技术。分离出了一个PhoA+突变体(命名为B176),该突变体在2型和3型菌毛的产生方面受到影响。对含有转座子插入的DNA区域进行克隆和测序,发现至少存在另外三个菌毛基因,分别命名为fimB、fimC和fimD。发现转座子位于fimD中。对PhoA活性的分析表明,菌毛基因簇受bvg位点的正向调控。在fimB上游观察到一个潜在的BvgA结合位点。FimB与所谓的伴侣样菌毛蛋白具有同源性,而FimC与一类位于外膜的菌毛蛋白同源,推测其参与菌毛亚基的转运和锚定。fimB中的插入突变消除了菌毛亚基的表达,表明该基因参与2型和3型菌毛的生物合成。在fimB上游观察到一个假基因(fimA),它与三个主要的菌毛亚基基因fim2、fim3和fimX具有同源性。系统发育树的构建表明,fimA可能是原始的主要菌毛亚基基因,其他三个基因是通过基因复制从该基因衍生而来的。有趣的是,发现菌毛基因簇直接位于编码丝状血凝素(一种重要的百日咳博德特氏菌粘附素)的基因下游,这可能表明这两个位点在百日咳发病机制中存在协同作用。