Involvement of ArlI, ArlJ, and CirA in archaeal type IV pilin-mediated motility regulation.

IF 2.7 3区 生物学 Q3 MICROBIOLOGY
Journal of Bacteriology Pub Date : 2024-06-20 Epub Date: 2024-05-31 DOI:10.1128/jb.00089-24
Priyanka Chatterjee, Marco A Garcia, Jacob A Cote, Kun Yun, Georgio P Legerme, Rumi Habib, Manuela Tripepi, Criston Young, Daniel Kulp, Mike Dyall-Smith, Mecky Pohlschroder
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引用次数: 0

Abstract

Many prokaryotes use swimming motility to move toward favorable conditions and escape adverse surroundings. Regulatory mechanisms governing bacterial flagella-driven motility are well-established; however, little is yet known about the regulation underlying swimming motility propelled by the archaeal cell surface structure, the archaella. Previous research showed that the deletion of the adhesion pilins (PilA1-6), subunits of the type IV pili cell surface structure, renders the model archaeon Haloferax volcanii non-motile. In this study, we used ethyl methanesulfonate mutagenesis and a motility assay to identify motile suppressors of the ∆pilA[1-6] strain. Of the eight suppressors identified, six contain missense mutations in archaella biosynthesis genes, arlI and arlJ. In trans expression of arlI and arlJ mutant constructs in the respective multi-deletion strains ∆pilA[1-6]∆arlI and ∆pilA[1-6]∆arlJ confirmed their role in suppressing the ∆pilA[1-6] motility defect. Additionally, three suppressors harbor co-occurring disruptive missense and nonsense mutations in cirA, a gene encoding a proposed regulatory protein. A deletion of cirA resulted in hypermotility, while cirA expression in trans in wild-type cells led to decreased motility. Moreover, quantitative real-time PCR analysis revealed that in wild-type cells, higher expression levels of arlI, arlJ, and the archaellin gene arlA1 were observed in motile early-log phase rod-shaped cells compared to non-motile mid-log phase disk-shaped cells. Conversely, ∆cirA cells, which form rods during both early- and mid-log phases, exhibited similar expression levels of arl genes in both growth phases. Our findings contribute to a deeper understanding of the mechanisms governing archaeal motility, highlighting the involvement of ArlI, ArlJ, and CirA in pilin-mediated motility regulation.IMPORTANCEArchaea are close relatives of eukaryotes and play crucial ecological roles. Certain behaviors, such as swimming motility, are thought to be important for archaeal environmental adaptation. Archaella, the archaeal motility appendages, are evolutionarily distinct from bacterial flagella, and the regulatory mechanisms driving archaeal motility are largely unknown. Previous research has linked the loss of type IV pili subunits to archaeal motility suppression. This study reveals three Haloferax volcanii proteins involved in pilin-mediated motility regulation, offering a deeper understanding of motility regulation in this understudied domain while also paving the way for uncovering novel mechanisms that govern archaeal motility. Understanding archaeal cellular processes will help elucidate the ecological roles of archaea as well as the evolution of these processes across domains.

ArlI、ArlJ 和 CirA 参与了古生动物 IV 型柔毛蛋白介导的运动调节。
许多原核生物利用游动运动来趋向有利条件和逃避不利环境。细菌鞭毛驱动运动的调控机制已得到公认,但人们对古细菌细胞表面结构--古细菌--所推动的游泳运动的调控机制却知之甚少。以前的研究表明,缺失第四型纤毛虫细胞表面结构的亚基--粘附纤毛蛋白(PilA1-6)会使模型古细菌 Haloferax volcanii 失去运动能力。在这项研究中,我们使用甲基磺酸乙酯诱变和运动性试验来鉴定ΔpilA[1-6]菌株的运动性抑制因子。在确定的八个抑制因子中,有六个包含弓形虫生物合成基因 arlI 和 arlJ 的错义突变。在各自的多重缺失菌株 ∆pilA[1-6]∆arlI 和 ∆pilA[1-6]∆arlJ 中反式表达 arlI 和 arlJ 突变构建体,证实了它们在抑制 ∆pilA[1-6] 运动缺陷中的作用。此外,三个抑制因子中的 cirA(一个编码拟调控蛋白的基因)同时发生了错义和无义突变。cirA的缺失导致运动能力减弱,而cirA在野生型细胞中的反式表达则导致运动能力减弱。此外,定量实时聚合酶链反应分析表明,在野生型细胞中,与非运动性的中生期盘状细胞相比,运动性的早生期杆状细胞中 arlI、arlJ 和弓形蛋白基因 arlA1 的表达水平较高。相反,ΔcirA 细胞在早生期和中生期都形成杆状细胞,在两个生长阶段都表现出相似的 arl 基因表达水平。我们的研究结果有助于加深对古细菌运动机制的理解,突出了 ArlI、ArlJ 和 CirA 在柔毛蛋白介导的运动调控中的参与。重要意义古细菌是真核生物的近亲,发挥着重要的生态作用。某些行为,如游泳运动,被认为对古细菌的环境适应非常重要。古细菌(Archaella)是古细菌的运动附属物,在进化过程中与细菌鞭毛截然不同,而驱动古细菌运动的调控机制在很大程度上是未知的。以前的研究将 IV 型纤毛虫亚基的缺失与古细菌运动抑制联系起来。这项研究揭示了三种参与纤毛蛋白介导的运动调控的火山石蜡虫蛋白,从而加深了对这一未被充分研究领域的运动调控的理解,同时也为揭示支配古生物运动的新机制铺平了道路。了解古菌的细胞过程将有助于阐明古菌的生态作用以及这些过程的跨领域进化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bacteriology
Journal of Bacteriology 生物-微生物学
CiteScore
6.10
自引率
9.40%
发文量
324
审稿时长
1.3 months
期刊介绍: The Journal of Bacteriology (JB) publishes research articles that probe fundamental processes in bacteria, archaea and their viruses, and the molecular mechanisms by which they interact with each other and with their hosts and their environments.
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