Villar M T, Hirschberg R L, Schaefer M R
Division of Molecular Biology and Biochemistry, School of Biological Sciences, University of Missouri-Kansas City, Kansas City, Missouri 64110, USA.
J Bacteriol. 2001 Jan;183(1):55-62. doi: 10.1128/JB.183.1.55-62.2001.
The human pathogen Eikenella corrodens expresses type IV pili and exhibits a phase variation involving the irreversible transition from piliated to nonpiliated variants. On solid medium, piliated variants form small (S-phase), corroding colonies whereas nonpiliated variants form large (L-phase), noncorroding colonies. We are studying pilus structure and function in the clinical isolate E. corrodens VA1. Earlier work defined the pilA locus which includes pilA1, pilA2, pilB, and hagA. Both pilA1 and pilA2 predict a type IV pilin, whereas pilB predicts a putative pilus assembly protein. The role of hagA has not been clearly established. That work also confirmed that pilA1 encodes the major pilus protein in this strain and showed that the phase variation involves a posttranslational event in pilus formation. In this study, the function of the individual genes comprising the pilA locus was examined using a recently developed protocol for targeted interposon mutagenesis of S-phase variant VA1-S1. Different pilA mutants were compared to S-phase and L-phase variants for several distinct aspects of phase variation and type IV pilus biosynthesis and function. S-phase cells were characterized by surface pili, competence for natural transformation, and twitching motility, whereas L-phase cells lacked these features. Inactivation of pilA1 yielded a mutant that was phenotypically indistinguishable from L-phase variants, showing that native biosynthesis of the type IV pilus in strain VA1 is dependent on expression of pilA1 and proper export and assembly of PilA1. Inactivation of pilA2 yielded a mutant that was phenotypically indistinguishable from S-phase variants, indicating that pilA2 is not essential for biosynthesis of functionally normal pili. A mutant inactivated for pilB was deficient for twitching motility, suggesting a role for PilB in this pilus-related phenomenon. Inactivation of hagA, which may encode a tellurite resistance protein, had no effect on pilus structure or function.
人类病原体腐蚀艾肯菌表达IV型菌毛,并呈现出一种相变,涉及从有菌毛变体到无菌毛变体的不可逆转变。在固体培养基上,有菌毛变体形成小的(S期)、具有腐蚀作用的菌落,而无菌毛变体形成大的(L期)、无腐蚀作用的菌落。我们正在研究临床分离株腐蚀艾肯菌VA1中菌毛的结构和功能。早期工作确定了pilA基因座,其中包括pilA1、pilA2、pilB和hagA。pilA1和pilA2均预测为IV型菌毛蛋白,而pilB预测为一种假定的菌毛组装蛋白。hagA的作用尚未明确确定。该工作还证实pilA1编码该菌株中的主要菌毛蛋白,并表明相变涉及菌毛形成过程中的翻译后事件。在本研究中,使用最近开发的针对S期变体VA1-S1的靶向插入诱变方案,研究了构成pilA基因座的各个基因的功能。将不同的pilA突变体与S期和L期变体在相变、IV型菌毛生物合成和功能的几个不同方面进行了比较。S期细胞的特征是表面有菌毛、具有自然转化能力和颤动运动性,而L期细胞缺乏这些特征。pilA1的失活产生了一个在表型上与L期变体无法区分的突变体,表明菌株VA1中IV型菌毛的天然生物合成依赖于pilA1的表达以及PilA1的正确输出和组装。pilA2的失活产生了一个在表型上与S期变体无法区分的突变体,表明pilA2对于功能正常的菌毛生物合成不是必需的。pilB失活的突变体缺乏颤动运动性,表明PilB在这种与菌毛相关的现象中起作用。hagA可能编码一种亚碲酸盐抗性蛋白,其失活对菌毛结构或功能没有影响。