Willems R J, Geuijen C, van der Heide H G, Renauld G, Bertin P, van den Akker W M, Locht C, Mooi F R
Molecular Microbiology Unit, National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.
Mol Microbiol. 1994 Jan;11(2):337-47. doi: 10.1111/j.1365-2958.1994.tb00314.x.
The chromosome of Bordetella pertussis harbours a region of 27 contiguous kb, which contains the bvg, fha and fim genes, involved in the co-ordinate regulation of virulence genes, FHA production and fimbriae production, respectively. The linkage of FHA and fimbrial genes has resulted in some confusion concerning the existence and location of genes required for the production of FHA and the function of the fimbrial genes fimB-D, which were proposed to be involved in both FHA and fimbriae biosynthesis. Through the use of non-polar mutations in each of these genes, we found that fimB-D are required for the production of both serotype 2 and 3 fimbriae, but not for FHA biosynthesis. Furthermore, a large open reading frame, designated fhaC, was identified downstream of fimD. It was shown that fhaC is essential for FHA production but not for fimbriae biogenesis. We propose that insertion mutations in fimB-D affect FHA production because of polar effects on fhaC expression. An insertion in the region downstream of fhaC had only a slight effect on FHA and fimbriae production. The fhaC gene product shows homology with ShIB and HpmB, two outer membrane proteins involved in export and activation of the haemolysins, ShIA and HpmA, of Serratia marcescens and Proteus mirabilis, respectively. Homology is also observed between the N-termini of FHA, ShIA and HpmA. Export of the haemolysins requires the N-termini of these molecules, and when this region was removed from FHA by an in-frame deletion, FHA biosynthesis was abolished. These results suggest that the N-terminus of FHA interacts with FhaC, and that as a result FHA is transported across the outer membrane.
百日咳博德特氏菌的染色体含有一个27 kb的连续区域,其中包含bvg、fha和fim基因,分别参与毒力基因的协同调控、丝状血凝素(FHA)的产生和菌毛的产生。FHA基因和菌毛基因的连锁导致了一些关于FHA产生所需基因的存在和位置以及菌毛基因fimB - D功能的混淆,有人提出fimB - D参与FHA和菌毛的生物合成。通过在这些基因中的每一个中使用非极性突变,我们发现fimB - D是2型和3型菌毛产生所必需的,但不是FHA生物合成所必需的。此外,在fimD下游鉴定出一个大的开放阅读框,命名为fhaC。结果表明,fhaC对FHA的产生至关重要,但对菌毛的生物发生不是必需的。我们提出,fimB - D中的插入突变由于对fhaC表达的极性效应而影响FHA的产生。在fhaC下游区域的插入对FHA和菌毛的产生只有轻微影响。fhaC基因产物与ShIB和HpmB具有同源性,ShIB和HpmB分别是参与粘质沙雷氏菌和奇异变形杆菌溶血素ShIA和HpmA的输出和激活的两种外膜蛋白。在FHA、ShIA和HpmA的N端之间也观察到同源性。溶血素的输出需要这些分子的N端,当通过框内缺失从FHA中去除该区域时,FHA的生物合成被废除。这些结果表明,FHA的N端与FhaC相互作用,从而使FHA穿过外膜运输。