Variation in type IV pilus stability modulates DNA-uptake and biofilm formation.

IF 4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yafan Yu,Rabab Mahdi,Ahmad Al-Hilfy Leon,Nam Vo,Reese Lofgren,Jean Luc Mutabazi,Kurt H Piepenbrink
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引用次数: 0

Abstract

Type IV pili are helical filaments composed of protein subunits which are produced by numerous taxa of bacteria, including Acinetobacter. Type IV pili are extended out from the cell by extension enzyme complexes, which extract subunits from the membrane and insert them into the base of the filament, but can also be retracted by reverse rotation catalyzed by a retraction enzyme. Type IV pili have diverse functions, including twitching motility and DNA-uptake, which require retraction, and host adhesion and bacterial aggregation, which do not. Acinetobacter bacteria, including International Clone I (IC-I) and International Clone II (IC-II) strains, show variable phenotypes in assays of type IV pilus-dependent functions. Here, we show this variation is the result of differentiation of type IV pilus subtypes in Acinetobacter, which we defined based on the sequence of the major subunit, PilA. These subtypes show variable efficiency in pilus retraction between pilus subtypes, and from that, a differential balance between retraction-dependent and retraction-independent functions. In both naturally-occurring pilA variants from the IC-I and IC-II groups and isogenic strains complemented with IC-I or IC-II pilA, the IC-I pilus subtype promotes greater twitching motility and DNA-uptake while the IC-II pilus subtype promotes biofilm formation while showing reduced capacity for DNA-uptake and twitching motility, similar to a retraction-deficient mutant and consistent with the hypothesis that pilus retraction of the IC-II pilus is naturally deficient. This defect in retraction was sufficient to increase the level of piliation on the cell surface when we compared the yields of T4P sheared from the cell surface from IC-I pilA and IC-II pilA complements in an isogenic background. Complementation with IC-II pilA results in greater levels of surface PilA per cell than equivalent complementation with an IC-I pilA gene. Additionally, direct comparisons of pilus stability between type IV pili isolated from IC-I pilA and IC-II pilA complements show greater thermostability for the IC-II pili, supporting the hypothesis that pilus stability can impede retraction and increase piliation.
IV型菌毛稳定性的变化调节dna摄取和生物膜的形成。
IV型毛是由蛋白质亚基组成的螺旋状细丝,由许多细菌分类群产生,包括不动杆菌。IV型毛通过延伸酶复合物从细胞中伸出,延伸酶复合物从膜中提取亚基并将其插入丝的基部,但也可以通过收缩酶催化的反向旋转收缩。IV型菌毛具有多种功能,包括抽搐运动和dna摄取,这些功能需要收缩,而寄主粘附和细菌聚集则不需要收缩。不动杆菌,包括国际克隆I (IC-I)和国际克隆II (IC-II)菌株,在IV型菌依赖功能的检测中显示出可变的表型。在这里,我们表明这种变异是不动杆菌IV型菌毛亚型分化的结果,我们根据主要亚基PilA的序列定义了IV型菌毛亚型。这些亚型在不同亚型之间的毛缩回中表现出不同的效率,由此,在缩回依赖和不缩回功能之间存在差异平衡。在来自IC-I和IC-II组的自然发生的菌毛变异以及与IC-I或IC-II菌毛互补的等基因菌株中,IC-I菌毛亚型促进更大的抽搐运动性和dna摄取,而IC-II菌毛亚型促进生物膜的形成,同时显示出dna摄取和抽搐运动性的能力降低,类似于收缩缺陷突变体,与IC-II菌毛的毛收缩自然缺陷的假设一致。当我们比较在等基因背景下从IC-I和IC-II pilA补体中从细胞表面剪切的T4P的产量时,这种缩回缺陷足以增加细胞表面的pilip水平。与IC-I基因的互补相比,IC-II基因的互补导致每个细胞的表面pilA水平更高。此外,直接比较IC-I型和IC-II型菌毛补体分离的IV型菌毛的菌毛稳定性表明,IC-II型菌毛的热稳定性更强,这支持了菌毛稳定性可以阻碍回缩和增加菌毛的假设。
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来源期刊
Journal of Biological Chemistry
Journal of Biological Chemistry Biochemistry, Genetics and Molecular Biology-Biochemistry
自引率
4.20%
发文量
1233
期刊介绍: The Journal of Biological Chemistry welcomes high-quality science that seeks to elucidate the molecular and cellular basis of biological processes. Papers published in JBC can therefore fall under the umbrellas of not only biological chemistry, chemical biology, or biochemistry, but also allied disciplines such as biophysics, systems biology, RNA biology, immunology, microbiology, neurobiology, epigenetics, computational biology, ’omics, and many more. The outcome of our focus on papers that contribute novel and important mechanistic insights, rather than on a particular topic area, is that JBC is truly a melting pot for scientists across disciplines. In addition, JBC welcomes papers that describe methods that will help scientists push their biochemical inquiries forward and resources that will be of use to the research community.
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