Long Cynthia D, Tobiason Deborah M, Lazio Matthew P, Kline Kimberly A, Seifert H Steven
Department of Microbiology-Immunology, Northwestern University Medical School, Chicago, Illinois 60611, USA.
Infect Immun. 2003 Nov;71(11):6279-91. doi: 10.1128/IAI.71.11.6279-6291.2003.
The gonococcal pilus is a major virulence factor that has well-established roles in mediating epithelial cell adherence and DNA transformation. Gonococci expressing four gonococcal pilin variants with distinct piliation properties under control of the lac regulatory system were grown in different levels of the inducer isopropyl-beta-D-thiogalactopyranoside (IPTG). These pilin variants expressed various levels of pilin message and pilin protein in response to the level of IPTG in the growth medium. Moreover, posttranslational modifications of the variant pilin proteins were detected, including S-pilin production and glycosylation. The ratio of the modified and unmodified pilin forms did not substantially change with different levels of pilin expression, showing that these modifications are not linked to pilin expression levels. DNA transformation competence was also influenced by IPTG levels in the growth medium. Substantial increases in transformation competence over an isogenic, nonpiliated mutant were observed when limited amounts of three of the pilin variants were expressed. Immunoelectron microscopy showed that when limited amounts of pilin are expressed, pili are rare and do not explain the pilin-dependent transformation competence. This pilin-dependent transformation competence required prepilin processing, the outer membrane secretin PilQ, and the twitching-motility-regulating protein PilT. These requirements show that a fully functional pilus assembly apparatus is required for DNA uptake when limited pilin is produced. We conclude that the pilus assembly apparatus functions to import DNA into the bacterial cell in a pilin-dependent manner but that extended pili are not required for transformation competence.
淋菌菌毛是一种主要的毒力因子,在介导上皮细胞黏附和DNA转化方面具有公认的作用。在乳糖调节系统的控制下,表达四种具有不同菌毛形成特性的淋菌菌毛蛋白变体的淋球菌,在不同浓度的诱导剂异丙基-β-D-硫代半乳糖苷(IPTG)中生长。这些菌毛蛋白变体根据生长培养基中IPTG的浓度表达不同水平的菌毛蛋白信息和菌毛蛋白。此外,还检测到了变体菌毛蛋白的翻译后修饰,包括S-菌毛蛋白的产生和糖基化。修饰和未修饰菌毛形式的比例并没有随着菌毛表达水平的不同而发生实质性变化,这表明这些修饰与菌毛表达水平无关。生长培养基中的IPTG水平也会影响DNA转化能力。当表达有限量的三种菌毛蛋白变体时,与同基因的非菌毛突变体相比,转化能力有显著提高。免疫电子显微镜显示,当表达有限量的菌毛蛋白时,菌毛很少见,无法解释菌毛依赖性转化能力。这种菌毛依赖性转化能力需要前菌毛加工、外膜分泌素PilQ和调节颤动运动的蛋白PilT。这些需求表明,当产生有限的菌毛蛋白时,DNA摄取需要一个功能完整的菌毛组装装置。我们得出结论,菌毛组装装置的功能是以菌毛蛋白依赖性方式将DNA导入细菌细胞,但转化能力并不需要延长的菌毛。