Locht C, Bertin P, Menozzi F D, Renauld G
Laboratoire de Microbiologie Génétique et Moléculaire INSERM CJF9109, Lille, France.
Mol Microbiol. 1993 Aug;9(4):653-60. doi: 10.1111/j.1365-2958.1993.tb01725.x.
Filamentous haemagglutinin (FHA) is the major attachment factor produced by virulent Bordetella spp. Similar to the other virulence factors, its production is tightly regulated by a two-component system in response to environmental changes. Although of impressive size (c. 220 kDa), it is very efficiently released into the culture supernatant of Bordetella pertussis. Its biogenesis involves complex processing of a larger precursor with a calculated molecular mass of 370 kDa. Export of FHA into the culture medium depends on an outer membrane protein homologous to haemolysin accessory proteins. Purified extracellular FHA is able to increase the adherence of other pathogens to the host, which may contribute to super-infection in whooping cough. Although FHA- mutants colonize lungs as efficiently as the wild-type parent strains, immune responses against FHA appear to protect against colonization. Unlike many other adhesins, FHA expresses at least three different attachment activities, one specific for the CR3 integrins of macrophages, one involving a carbohydrate-binding site, specific for interactions with cilia, and a heparin-binding activity that may be important for interaction of B. pertussis with epithelial cells or extracellular matrices.
丝状血凝素(FHA)是由致病性博德特氏菌属产生的主要黏附因子。与其他毒力因子类似,其产生受双组分系统严格调控,以响应环境变化。尽管其分子量较大(约220 kDa),但它能非常有效地释放到百日咳博德特氏菌的培养上清中。其生物合成涉及对一个计算分子量为370 kDa的更大前体的复杂加工。FHA分泌到培养基中依赖于一种与溶血素辅助蛋白同源的外膜蛋白。纯化的细胞外FHA能够增加其他病原体对宿主的黏附,这可能导致百日咳中的重叠感染。尽管FHA突变体在肺部定殖的效率与野生型亲本菌株相同,但针对FHA的免疫反应似乎能防止定殖。与许多其他黏附素不同,FHA表现出至少三种不同的黏附活性,一种对巨噬细胞的CR3整合素具有特异性,一种涉及碳水化合物结合位点,对与纤毛的相互作用具有特异性,还有一种肝素结合活性,这可能对百日咳博德特氏菌与上皮细胞或细胞外基质的相互作用很重要。